Presentations

2023 🐰

<Domestic>

1.    ML-assisted Screening for Efficient Electrochemical Synthesis of Multiple PHAs Towards Higher Chiroptical Features (Poster)

*Mohamed S. H. Salem, Masaru Kondo, Hiroaki Sasai, Shinobu Takizawa; The 3rd result report meeting of Academic Transformation A "Digital Organic Synthesish, Osaka, 27th-28th January 2023.

 

2.    Electrochemical Synthesis of Hetero[7]helicenes, Dehydro hetero[7]helicenes and Hetero[8]circulenes with Intriguing Optical Features (Oral)

*Mohamed S. H. Salem, Md. Imrul Khalid, Ahmed Sabri, Hiroaki Sasai, Shinobu Takizawa; The 103rd CSJ Annual Meeting, Chiba, 22nd-25th March 2023.

 

3.    Azobenzene Based Chiral Photoswitchable Vanadium Catalyst: Design and its Application to Enantioselective Synthesis (Oral)

*Meghna Sasi, Chandu G Krishnan, Masaru Kondo, Hiroaki Sasai, Shinobu Takizawa; The 103rd CSJ Annual Meeting, Chiba, 22nd-25th March 2023.

 

4.    ƒxƒCƒYÅ“K‰ŧ‚É‚æ‚éļ–§—L‹@‡Ž”―‰žðŒ‚Ė’Tõiĩ‘Ōu‰‰j

–‘ęāV”E; The 103rd CSJ Annual Meeting, Chiba, 22nd-25th March 2023.

 

5.    Electrochemical Synthesis of [7]helicenes, dehydro[7]helicenes and [8]circulenes iOralj

*Ahmed Sabri, Mohamed S. H. Salem, Md. Imrul Khalid, Masaru Kondo, Makoto Sako, Hiroaki Sasai, Shinobu Takizawa; 142nd Annual Meeting the Pharmaceutical Society of Japan (PSJ), Hokkaido, 25th-28th March 2023.

 

6.    Å­ŠwKƒf[ƒ^‚É‚æ‚éƒf[ƒ^‹ė“ŪŒ^ļ–§—L‹@‡Ž”―‰ž‚ĖŠJ”­@`ƒxƒCƒYÅ“K‰ŧ‚É‚æ‚é”―‰žðŒ‚Ėv‘ŽÅ“K‰ŧ`(ĩ‘Ōu‰‰)

*‘ęāV”E; 142nd Annual Meeting the Pharmaceutical Society of Japan (PSJ), Hokkaido, 25th-28th March 2023.

 

<International>

1.    Two-step Synthesis, Structure and Optical Features of a Double Hetero[7]helicene (Poster)

*Ishani Uditha Weadge, Mohamed S. H. Salem, Ahmed Sabri, Md. Imrul Khalid, Shinobu Takizawa; The 26th SANKEN International Symposium GREEN TRANSFORMATION For a Sustainable Society, Osaka 11th-12th January 2023.

 

2.    Asymmetric Synthesis of Eight-membered N-heterocycles: Autoorganocatalyzed Ring Expansion via Kinetic Resolution (Poster)

*Aye, T. Z.; Takizawa, S.; Sasai, H., The 26th SANKEN International Symposium GREEN TRANSFORMATION For a Sustainable Society, Osaka 11th-12th January 2023.

 

2022 🐯

<Domestic>

1.    “ņdŠˆŦ‰ŧŒ^•sÄG”}‚Ė‘nŧiĩ‘Ōu‰‰j

*ųˆäG–ū —L‹@‡ŽVtu‰‰‰ïyƒIƒ“ƒ‰ƒCƒ“ŠJÃz, 1ŒŽ17“ú 2022”N.

 

2.    Asymmetric synthesis of eight-membered N-heterocycles: Auto-organocatalyzed ring expansion of tetrahydrocarbolines with kinetic resolution (Oral)

*Aye, T. Z.; Kondo, K.; Takizawa, S.; Sasai, H. “ú–{‰ŧŠw‰ï ‘æ102”N‰ïi2022jyƒIƒ“ƒ‰ƒCƒ“ŠJÃz, 3ŒŽ23“ú, 2022”N.

 

3.    ŒõŠwŠˆŦ‚ȩóBINOLŽO—Ę‘Ė‚Ė‘I‘ð“I‡ŽiŒû“Š”­•\j

*™›―WŦ; ‘ęāV”E; ųˆäG–ū “ú–{‰ŧŠw‰ï ‘æ102”N‰ïi2022jyƒIƒ“ƒ‰ƒCƒ“ŠJÃz, 3ŒŽ24“ú, 2022”N.

 

4.   ‹@ŠBŠwK‹ė“ŪŒ^ƒ}ƒ‹ƒ`ƒpƒ‰ƒ[ƒ^ƒXƒNƒŠ[ƒjƒ“ƒO‚É‚æ‚éƒPƒ`ƒ~ƒ“‚Ė“d‰ð‡Ž‚Ė”―‰žðŒÅ“K‰ŧiŒû“Š”­•\j

*‹ß“ĄŒ’; ™›―WŦ; Khalid Md Imrul; H. D. P. Wathsala; Îėˆęé; Œī‘; ‘鍇F”V; ˜h”ö—ē; ‘ęāV”E; ųˆäG–ū “ú–{‰ŧŠw‰ï ‘æ102”N‰ïi2022jyƒIƒ“ƒ‰ƒCƒ“ŠJÃz, 3ŒŽ24“ú, 2022”N.

 

5.   Œõ‰ž“šŒ^ƒuƒŒƒ“ƒXƒeƒbƒhŽ_•sÄG”}‚Ė‘nŧŒĪ‹†iŒû“Š”­•\j

*ˆĀ“cC; ‹ß“ĄŒ’; ‘ęāV”E; ųˆäG–ū “ú–{‰ŧŠw‰ï ‘æ102”N‰ïi2022jyƒIƒ“ƒ‰ƒCƒ“ŠJÃz, 3ŒŽ26“ú, 2022”N.

       

6.   A chiral vanadium(V) complex-catalyzed enantioselective oxidative coupling of hydroxycarbazoles (Oral)

*Kamble, G. T.; Salem, M. S. H.; Sugizaki, A.; Park, H.; Sako, M.; Takizawa, S.; Sasai, H. “ú–{‰ŧŠw‰ï ‘æ102”N‰ïi2022jyƒIƒ“ƒ‰ƒCƒ“ŠJÃz, 3ŒŽ26“ú, 2022”N.

 

7.   Enantioselective synthesis of hetero[9]helicenes using a chiral dinuclear vanadium(V) catalyst (Oral)

*Kumar, A.; Sako, M.; Tamori, Y.; Takizawa, S.; Sasai, H. “ú–{‰ŧŠw‰ï ‘æ102”N‰ïi2022jyƒIƒ“ƒ‰ƒCƒ“ŠJÃz, 3ŒŽ26“ú, 2022”N.

 

8.    Ž_‰ŧ“IƒwƒeƒƒJƒbƒvƒŠƒ“ƒOE’E…ŠÂ‰ŧE’E…‘fŠÂ‰ŧ”―‰ž‚É‚æ‚éŒõŠwŠˆŦƒAƒUƒIƒLƒTƒfƒqƒhƒ[7]ƒwƒŠƒZƒ“—Þ‚Ėƒhƒ~ƒm‡ŽŒĪ‹†iŒû“Š”­•\j

*‘ęāV”E; Khalid Md. Imrul ; Salem H. Mohamed; ‹ß“ĄŒ’; ēŒÃ^; ųˆäG–ū “ú–{–ōŠw‰ï ‘æ142”N‰ïi2022jyƒIƒ“ƒ‰ƒCƒ“ŠJÃz, 3ŒŽ26“ú, 2022”N.

 

9.   Photoswitchable phase transfer catalyst: Design and application to enantioselective synthesis (Oral)

*Krishnan, C. G.; Kondo, M.; Nakamura, K.; Takizawa, S.; Sasai, H. “ú–{–ōŠw‰ï ‘æ142”N‰ïi2022jyƒIƒ“ƒ‰ƒCƒ“ŠJÃz, 3ŒŽ26“ú, 2022”N.

 

10. Electrochemical Synthesis of Dehydrohelicenes (Poster)

*Ahmed Sabri, Md. Imrul Khalid, Mohamed S. H. Salem, Makoto Sako, Masaru Kondo, Hiroaki Sasai, Shinobu Takizawa; 11th JACI/GSC Symposium (Japan Association for Chemical Innovation/Green and Sustainable Chemistry), yOnlinez, 16th June 2022.

 

11. A chiral vanadium (V) complex catalyzed enantioselective oxidative homo- and heterocoupling of hydroxycarbazoles(Poster)

*Ganesh Tatya Kamble, Makoto Sako, Hiroaki Sasai, Shinobu Takizawa;“ú–{ƒvƒƒZƒX‰ŧŠw‰ï2022ƒTƒ}[ƒVƒ“ƒ|ƒWƒEƒ€, Toyama, 30th Jun-1st July 2022.

 

12. ‹@ŠBŠwKƒxƒCƒYÅ“K‰ŧ‚ðŠˆ—p‚·‚éƒPƒ`ƒ~ƒ“‚Ė“d‰ð‡Ž”―‰žðŒÅ“K‰ŧ (Poster)

*Md. Imrul Khalid, Masaru Kondo, ™›―ļŦCH. D. P. Wathsala, ÎėˆęéCŒī‘C‘éF”VC˜h”ö—ēCHiroaki Sasai, Shinobu Takizawa; “ú–{ƒvƒƒZƒX‰ŧŠw‰ï2022ƒTƒ}[ƒVƒ“ƒ|ƒWƒEƒ€, Toyama, 30th Jun-1st July 2022.

 

13. Asymmetric Synthesis of Eight-membered N-heterocycles: Auto-organocatalyzed Amplification (Poster)

*Tin Zar Aye, Masaru Kondo, Hiroaki Sasai, Shinobu Takizawa; “ú–{ƒvƒƒZƒX‰ŧŠw‰ï2022ƒTƒ}[ƒVƒ“ƒ|ƒWƒEƒ€, Toyama, 30th Jun-1st July 2022.

 

14. Electrochemical synthesis of hetero[8]circulene derivatives (Poster)

*Ahmed Sabri, Md. Imrul Khalid, Mohamed S. H. Salem, Makoto Sako, Masaru Kondo, Hiroaki Sasai, Shinobu Takizawa; 51st Congress of Heterocyclic Chemistry, Osaka University, 15th-17th September 2022.

 

15. ’‚‘fEŽ_‘fE—°‰ĐŒīŽq‚ðŠÜ‚Þƒwƒeƒ[9]ƒwƒŠƒZƒ“‚ĖƒGƒiƒ“ƒ`ƒI‘I‘ð“I‡Ž(Poster)

*Ankit Kumar, ēŒÃ ^, ųˆäG–ū, ‘ęāV ”E; 51st Congress of Heterocyclic Chemistry, Osaka University, 15th-17th September 2022.

 

16. •sÄ‘•‚𔚂ĪŒõŠwŠˆŦŠÜ’‚‘f‚WˆõŠÂ‚Ė‡ŽŒĪ‹†(Poster)

*‘ęāV ”E, Tin Zar Aye, ‹ß“Ą Œ’, ųˆäG–ū; 51st Congress of Heterocyclic Chemistry, Osaka University, 15th-17th September 2022.

 

17. Å­ŠwKƒf[ƒ^‚É‚æ‚éƒf[ƒ^‹ė“ŪŒ^ļ–§—L‹@‡Ž”―‰ž‚ĖŠJ”­iĩ‘Ōu‰‰j

*‘ęāV”E; ŽYŒĪŽŸĒ‘ã—L‹@‰ŧŠwƒZƒ~ƒi[, ‘åã‘åŠw, 2022”N9ŒŽ26“ú

 

18. Electrochemical Syntheses of Dehydrohelicenes and Other Polycyclic Heteroaromatics (PHAs) (Poster)

*Mohamed S. H. Salem, Hiroaki Sasai, Shinobu Takizawa; The 38th Seminar on Synthetic Organic Chemistry, Fukuoka, 28th-30th September 2022.

 

19. ’PŠj‚Ļ‚æ‚Ņ“ņŠjƒoƒiƒWƒEƒ€G”}”―‰ž‚É‚æ‚éŽē•sÄ‰ŧ‡•Ļ‚ĖƒGƒiƒ“ƒ`ƒI‘I‘ð“I‡Ž(Poster)

*Ankit KumarAųˆäG–ūA‘ęāV”E; The 38th Seminar on Synthetic Organic Chemistry, Fukuoka, 28th-30th September 2022.

 

20. Å­ŠwKƒf[ƒ^‚É‚æ‚éƒf[ƒ^‹ė“ŪŒ^ļ–§—L‹@‡Ž”―‰ž‚ĖŠJ”­iĩ‘Ōu‰‰j

*‘ęāV”E; ‹ß‹E‰ŧŠw‹Ķ‰ï ‡Ž•”‰ï ƒtƒ[Eƒ}ƒCƒNƒ‡ŽŒĪ‹†‰ï ‘æ96‰ņŒĪ‹†‰ï, ‘åã‰ČŠw‹ZpƒZƒ“ƒ^[, 2022”N11ŒŽ18“ú

 

21. A Chiral Vanadium(V) Complex-catalyzed Hetero-coupling of ƒĀ-Naphthylamines via Photoactivation (Poster)

*Duona Fan, Ganesh T. Kamble, Hiroaki Sasai, Shinobu Takizawa; ‘æ48‰ņ”―‰ž‚ƍ‡Ž‚Ėi•āƒVƒ“ƒ|ƒWƒEƒ€CChiba, 28th-29th November 2022.

 

22. Synthesis of Eight-membered N-Heterocycles via Auto-organocatalyzed Asymmetric Amplification (Poster)

*‘ęāV ”E, Tin Zar Aye, ‹ß“Ą Œ’, ųˆäG–ū; ‘æ48‰ņ”―‰ž‚ƍ‡Ž‚Ėi•āƒVƒ“ƒ|ƒWƒEƒ€CChiba, 28th-29th November 2022.

 

23. ‹@ŠBŠwK‚ðŠˆ—p‚·‚éļ–§—L‹@‡Ž”―‰žðŒ‚ĖÅ“K‰ŧ(ĩ‘Ōu‰‰)

*‘ęāV”E; ‘æ105‰ņŽYŒĪƒeƒNƒmƒTƒƒ“, ‘åã‘åŠw, 2022”N12ŒŽ19“ú

 

24. Å­ŠwKƒf[ƒ^‚É‚æ‚éƒf[ƒ^‹ė“ŪŒ^ļ–§—L‹@‡ŽF”―‰žŠJ”­‚ð‰Á‘Ž‚·‚é‹@ŠBŠwKƒxƒCƒYÅ“K‰ŧ‚É‚æ‚é”―‰žðŒÅ—Į‰ŧ(ĩ‘Ōu‰‰)

*‘ęāV”E; uAI‚Æ—L‹@‡Ž‰ŧŠwv‘æ10‰ņ•Ũ‹­‰ï, ‚Ļ’ƒ‚Ė…ƒ†ƒjƒIƒ“ƒrƒ‹, 2022”N12ŒŽ22“úu‰‰j

 

<International>

1.    Machine-learning-assisted multi-parameter screening for flow and electrochemical reactions (Poster)

*Takizawa, S.; Wathsala, H. D. P.; Kondo, M.; Sugizaki, A.; Khalid, M. I.; Ishikawa, K.; Hara, S.; Takaai, T.; Washio, T.; Sasai, H. The 25th SANKEN International Symposium, The 20th SANKEN Nanotechnology International Symposium, The 9th Kansai Nanoscience and nanotechnology International Symposium, The 17th Handai Nanoscience and nanotechnology International Symposium, The 3rd AIRC-ISIR International Symposium, yƒIƒ“ƒ‰ƒCƒ“ŠJÃz, 1ŒŽ7“ú, 2022”N.

 

2.    Sustainable Approaches to Fine Chemical Synthesis (Invited)

*Shinobu Takizawa; 2022 International Conference on Recent Advances in Chemical Sciences [RACS-2022], yƒIƒ“ƒ‰ƒCƒ“ŠJÃz, 11th-12th November 2022.

 

3.    Electrochemical Synthesis of Helicenes, Dehydrohelicenes, and Circulenes (Poster)

*Mohamed S. H. Salem, Md. Imrul Khalid, Ahmed Sabri, Hiroaki Sasai, Shinobu Takizawa; International Symposium on Innovative Reactions through Controlling Electrons (ISIRCE) Nara, 23rd-24th November 2022.

 

4.    Electrochemical Synthesis of Dehydrohelicenes(Poster)

*Md. Imrul Khalid, Shinobu Takizawa; 2022 The 7th Conference of Bangladesh Crystallographic Association, Bangladesh, 8th-9th December 2022.

 

2021 🐮

<Domestic>

1.  ‹@ŠBŠwK‚Æ—L‹@‡Ž‰ŧŠwiĩ‘Ōu‰‰j

*ųˆäG–ū@—L‹@‡Ž2ŒŽƒZƒ~ƒi[u—L‹@‡Ž‚Ėƒjƒ…[ƒgƒŒƒ“ƒh2021vyWEB”zMz, 2ŒŽ5“ú, 2021”N.

 

2.  Enantioselective synthesis of hetero[9]helicenes via oxidative coupling/dehydrative cyclization sequence using a chiral dinuclear vanadium(V) catalyst (Oral)

*Kumar, A.; Sako, M.; Mattan, I.; Takizawa, S.; Hiroaki, S. “ú–{‰ŧŠw‰ï@‘æ101t‹G”N‰ïi2021jyƒIƒ“ƒ‰ƒCƒ“ŠJÃz, 3ŒŽ19“ú, 2021”N.

 

3.  Chemo- and Enantioselective Hetero-coupling of 3-Hydroxycarbazoles Catalyzed by a Chiral Vanadium(V) Complex (Oral)

*Kamble, G. T.; Sako, M.; Higashida, K.; Kumar, A.; Takizawa, S.; Sasai, H. “ú–{‰ŧŠw‰ï@‘æ101t‹G”N‰ïi2021jyƒIƒ“ƒ‰ƒCƒ“ŠJÃz, 3ŒŽ19“ú, 2021”N.

 

4.  Œõ‰ž“šŒ^•sÄ‘ŠŠÔˆÚ“ŪG”}‚ĖŠJ”­iŒû“Š”­•\j

*’†‘šŒ°“l; ‹ß“ĄŒ’; Krishnan, C.; ‘ęāV”E; ųˆäG–ū “ú–{‰ŧŠw‰ï@‘æ101t‹G”N‰ïi2021jyƒIƒ“ƒ‰ƒCƒ“ŠJÃz, 3ŒŽ19“ú, 2021”N.

 

5.  Enantioselective Synthesis of Spirooxindoles via Sequential ReactionsiOralj

*Aye, T. Z.; Matsuyama, N.; Mattan, I.; Kondo, M.; Takizawa, S.; Sasai, H. “ú–{‰ŧŠw‰ï@‘æ101t‹G”N‰ïi2021jyƒIƒ“ƒ‰ƒCƒ“ŠJÃz, 3ŒŽ21“ú, 2021”N.

 

6.  Electrochemical Synthesis of Azaoxa[7]helicenes via Oxidative Hetero-coupling/Dehydrative Cyclization Sequence of ArenolsiOralj

*Salem, M. S. H.; Khalid, Md. I.; Sako, M.; Takizawa, S.; Sasai, H. “ú–{‰ŧŠw‰ï@‘æ101t‹G”N‰ïi2021jyƒIƒ“ƒ‰ƒCƒ“ŠJÃz, 3ŒŽ21“ú, 2021”N.

 

7.  ŒÅ’č‰ŧƒoƒiƒWƒEƒ€G”}V-MPS4‚É‚æ‚éC-HŠŊ”\‰ŧƒwƒeƒƒrƒAƒŠ[ƒ‹ƒJƒbƒvƒŠƒ“ƒO–@‚ĖŠJ”­‚Æ‚ŧ‚Ė‰ž—piŒû“Š”­•\j*Š}ŠÔŒšŒá; “ú“ė—D–į; Gamal. A. I. M.; ēŒÃ^; ‘ęāV”E; ųˆäG–ū; ÔˆäŽüŽi “ú–{–ōŠw‰ï@‘æ141”N‰ïiL“‡jyƒIƒ“ƒ‰ƒCƒ“ŠJÃz, 3ŒŽ28“ú, 2021”N.

 

8.  ‹@ŠBŠwK‚ðŠˆ—p‚·‚éƒtƒ[‡Ž‚Ė‰Â•Ïƒpƒ‰ƒ[ƒ^[Å“K‰ŧiĩ‘Ōu‰‰j*ųˆäG–ū ‹ß‹E‰ŧŠw‹Ķ‰ï‡Ž•”‰ïƒtƒ[Eƒ}ƒCƒNƒ‡ŽŒĪ‹†‰ï ‘æ35‰ņŒöŠJu‰‰‰ïi‘æ91‰ņŒĪ‹†‰ïjyƒIƒ“ƒ‰ƒCƒ“ŠJÃz, 8ŒŽ6“ú 2021”N

 

9.  Stereoselective synthesis of C3-spirooxindole- and C2-spiropseudoindoxyl-pyrrolidines via organocatalyzed Pictet-Spengler reaction/oxidative rearrangement sequenceiƒ|ƒXƒ^[j

*Tin Zar Aye; ‹ß“ĄŒ’; žŽRŪŽũ; Irshad Mattan; ‘ęāV”E; ųˆäG–ū ‘æ47‰ņ”―‰ž‚ƍ‡Ž‚Ėi•āƒVƒ“ƒ|ƒWƒEƒ€yƒIƒ“ƒ‰ƒCƒ“ŠJÃz, 10ŒŽ2“ú, 4“ú 2021”N

 

10.  “d‰ð˜A‘ą”―‰ž‚É‚æ‚éŠÂóƒfƒqƒhƒƒIƒLƒTƒwƒŠƒZƒ“‚Ė‡ŽiŒû“Š”­•\j

*Mohamed S. H. Salem; Md. Imrul Khalid; ēŒÃ^; ‹ß“ĄŒ’; ‘ęāV”E; ųˆäG–ū ‘æ50‰ņ•Ą‘fŠÂ‰ŧŠw“Ē˜_‰ïyƒIƒ“ƒ‰ƒCƒ“ŠJÃz, 10ŒŽ9“ú 2021”N

 

11.  Photoswitchable chiral phase transfer catalyst: Design and applicationiŒû“Š”­•\j

*Chandu G. Krishnan; ‹ß“ĄŒ’; ’†‘šŒ°; ‘ęāV”E; ųˆäG–ū ‘æ14‰ņ—L‹@G”}ƒVƒ“ƒ|ƒWƒEƒ€ yƒIƒ“ƒ‰ƒCƒ“ŠJÃz, 11ŒŽ24“ú 2021”N

 

<International>

1.    Machine-Learning-Assisted Multi-Parameter Screening for Flow and Electrochemical Reactions (Poster)

*Wathsala, H. D. P.; Kondo, M.; Sugizaki, A.; Khalid, M. I.; Ishikawa, K.; Hara, S.; Takaai, T.; Washio, T.; Sasai. PACIFICHEM 2021 (2021 International Chemical Congress of Pacific Basin Societies), yƒnƒCƒuƒŠƒbƒhŠJÃz, 12ŒŽ18“ú, 2021”N

 

2020@🐭

<Domestic>

1.  Development of Organocatalyzed Umpolung C-C Bond Forming Reactions of Alkynyl Esters (Oral)
*Furukawa, T.; Sako, M.; Takizawa, S.; Sasai, H.
“ú–{‰ŧŠw‰ï‘æ100t‹G”N‰ïC“Œ‹ž—‰Č‘åŠw@–ė“cƒLƒƒƒ“ƒpƒXiį—tjC3ŒŽ22“ú`3ŒŽ25“úC2020”ND

2.  Chiral Vanadium Complex-catalyzed Enantioselective Oxidative Coupling of 4-Hydroxycarbazoles (Oral)
*Park, H.; Sako, M.; Takizawa, S.; Sasai, H.
“ú–{‰ŧŠw‰ï‘æ100t‹G”N‰ïC“Œ‹ž—‰Č‘åŠw@–ė“cƒLƒƒƒ“ƒpƒXiį—tjC3ŒŽ22“ú`3ŒŽ25“úC2020”ND

3.  Exploration of Flow Reaction Conditions Using Machine-learning for Enantioselective Organocatalyzed Rauhut-Currier/[3+2] Annulation Sequence (Oral)
*Wathsala, H. D. P.; Kondo, M.; Sako, M.; Hanatani, Y.; Ishikawa, K.; Hara, S.; Takaai, T.; Washio, T.; Takizawa, S.; Sasai, H.
“ú–{‰ŧŠw‰ï‘æ100t‹G”N‰ïC“Œ‹ž—‰Č‘åŠw@–ė“cƒLƒƒƒ“ƒpƒXiį—tjC3ŒŽ22“ú`3ŒŽ25“úC2020”ND

4.  Vanadium Complex-catalyzed Enantioselective Synthesis of Hetero[9]helicenes and Their Physical Properties (Oral)
*Sako, M.; Kumar, A.; Takizawa, S.; Sasai, H.
“ú–{‰ŧŠw‰ï‘æ100t‹G”N‰ïC“Œ‹ž—‰Č‘åŠw@–ė“cƒLƒƒƒ“ƒpƒXiį—tjC3ŒŽ22“ú`3ŒŽ25“úC2020”ND

5.  Development of Asymmetric Catalyst Bearing Dithienylethene and Application (Oral)
*Wakabayashi, Y.; Nakamura, K.; Kondo, M.; Sasai, H.
“ú–{‰ŧŠw‰ï‘æ100t‹G”N‰ïC“Œ‹ž—‰Č‘åŠw@–ė“cƒLƒƒƒ“ƒpƒXiį—tjC3ŒŽ22“ú`3ŒŽ25“úC2020”N

6.  Development of Photoresponsive Chiral Pyridine-Oxazoline Ligand (Oral)
*Nakamura, K.; Wakabayashi, Y.; Kondo, M.; Sasai, H.
“ú–{‰ŧŠw‰ï‘æ100t‹G”N‰ïC“Œ‹ž—‰Č‘åŠw@–ė“cƒLƒƒƒ“ƒpƒXiį—tjC3ŒŽ22“ú`3ŒŽ25“úC2020”N

7.  Development of a Novel Photoisomerizable Organocatalyst (Oral)
*Kondo, M.; Nakamura, K.; Wakabayashi, Y.; Sasai, H.
“ú–{‰ŧŠw‰ï‘æ100t‹G”N‰ïC“Œ‹ž—‰Č‘åŠw@–ė“cƒLƒƒƒ“ƒpƒXiį—tjC3ŒŽ22“ú`3ŒŽ25“úC2020”N

8.  Electrochemical Synthesis of Heterohelicenes via Oxidative Hetero-coupling/Intramolecular Cyclization Sequence (Oral)
*Khalid, M. I.; Sako, M.; Takizawa, S.; Sasai H.
“ú–{‰ŧŠw‰ï‘æ100t‹G”N‰ïC“Œ‹ž—‰Č‘åŠw@–ė“cƒLƒƒƒ“ƒpƒXiį—tjC3ŒŽ22“ú`3ŒŽ25“úC2020”ND

9.  ƒLƒ‰ƒ‹ƒoƒiƒWƒEƒ€G”}‚ð—p‚Ē‚éƒAƒŒƒm[ƒ‹—Þ‚ĖŽ_‰ŧ“IƒwƒeƒƒJƒbƒvƒŠƒ“ƒO”―‰žiŒû“Šj
*
“Œ“cŒbŒÞAēŒÃ^A‘ęāV”EAųˆäG–ūC“ú–{–ōŠw‰ï‘æ140”N‰ïC‘—§‹ž“s‘Û‰ïŠŲ@‘ži‹ž“sjC3ŒŽ25“ú`3ŒŽ28“úC2020”N.

10.  Asymmetric Synthesis of Spirooxindoles via Pictet-Spengler Reaction and Oxidative Rearrangement (Oral)
*Tin Zar Aye; Matsuyama, N.; Mattan, I.; Kondo, M.; Takizawa, S.; Sasai, H.
“ú–{–ōŠw‰ï‘æ140”N‰ïC‘—§‹ž“s‘Û‰ïŠŲ@‘ži‹ž“sjC3ŒŽ25“ú`3ŒŽ28“úC2020”N.

11.  Development of Anionic Octahedral Salicylimine-based Cobalt(III) Catalysts for Enantioselective Reactions (Oral)
*Salem, M.; Takizawa, S.; Sasai, H.
“ú–{–ōŠw‰ï‘æ140”N‰ïC‘—§‹ž“s‘Û‰ïŠŲ@‘ži‹ž“sjC3ŒŽ25“ú`3ŒŽ28“úC2020”N.

 

12.  ƒvƒƒpƒ‹ƒMƒ‹ƒAƒZƒe[ƒg‚Ė•sÄŠÂ‰ŧ|ƒJƒ‹ƒ{ƒjƒ‹‰ŧ”―‰ž‚ðŠî”Õ‚Æ‚ĩ‚―(|)-Graminin A‚Ė‘S‡ŽiŒû“Š”­•\j

*“ú‰š•”‘ūˆę; ˆÉ“Ą—zˆę; ‚‹īŒ\‰î; Dhage, T. D.; â“cŒ’; ųˆäG–ū; ‰Á“ĄŒb‰î@‘æ117‰ņ—L‹@‡ŽƒVƒ“ƒ|ƒWƒEƒ€2020”NyƒIƒ“ƒ‰ƒCƒ“z, 10ŒŽ29“ú`10ŒŽ30“ú, 2020”N.

 

13.  ‹@ŠBŠwK‚ðŠˆ—p‚·‚éļ–§ƒtƒ[•sÄ‡Ž‚ĖÅ“KðŒ’TõiŒû“Š”­•\j

*‹ß“ĄŒ’; Wathsala, H. D. P.; ēŒÃ^; ‰Ô’J—D‘ū˜N; Îėˆęé;Œī‘; ‘鍇F”V; ˜h”ö—ē; ‘ęāV”E; ųˆäG–ū@‘æ117‰ņ—L‹@‡ŽƒVƒ“ƒ|ƒWƒEƒ€2020”NyƒIƒ“ƒ‰ƒCƒ“z, 10ŒŽ29“ú`10ŒŽ30“ú, 2020”N.

 

14.  Vanadium Complex-catalyzed Enantioselective Oxidative Coupling of HydroxycarbazolesiŒû“Š”­•\j

––pŠØúŲ; ēŒÃ^; ‘ęāV”E; ųˆäG–ū@@‘æ117‰ņ—L‹@‡ŽƒVƒ“ƒ|ƒWƒEƒ€2020”NyƒIƒ“ƒ‰ƒCƒ“z, 10ŒŽ29“ú`10ŒŽ30“ú, 2020”N.


<International>

1.  Efficient Synthesis of Hetero-helicenes and Their Chiroptical PropertiesiKeynote Lecturej

*Sasai, H. Molecular Chirality Asia 2020 online, Oct. 31st Nov. 2nd, 2020.

 

2.  Development of Dithienylethene Based Photoswitchable Chiral Catalyst (Poster)

*Yasuda, O.; Wakabayashi, Y.; Kondo, M.; Sasai, H. Molecular Chirality Asia 2020 online, Oct. 31st Nov. 2nd, 2020.

 

3.  Stereoselective Complexation of Anionic Octahedral Cobalt(III) Complexes and Their Application to Enantioselective Iodocyclization Reaction (Poster)

*Salem, M. S. H.; Abe, T.; Takizawa, S.; Sasai, H. Molecular Chirality Asia 2020 online, Oct. 31st Nov. 2nd, 2020.

 

4.  Chemo-, Regio- and Enantioselective Hetero-coupling of 3-Hydroxycarbazoles Catalyzed by Chiral Vanadium(V) Complexes (Poster)

*Kamble, G. T.; Sako, M.; Higashida, K.; Kumar, A.; Takizawa, S.; Sasai, H. Molecular Chirality Asia 2020 online, Oct. 31st Nov. 2nd, 2020.

 

5.  Enantioselective Synthesis of Spirooxindoles via Pictet-Spengler Reaction and Oxidative Rearrangement (Poster)

*Aye, T. Z.; Matsuyama, N.; Mattan, I.; Kondo, M.; Takizawa, S.; Sasai, H. Molecular Chirality Asia 2020 online, Oct. 31st Nov. 2nd, 2020.

 

6.  Short Step Synthesis of Chiral Spirooxindoles via Sequential Reactions (Poster)
*Tin Zar Aye, Matsuyama, N.; Mattan, I.; Kondo, M.; Takizawa, S.; Sasai, H., The 23rd SANKEN International Symposium, Chemistry Awaji Yumebutai International Conference Center, January 9-10, 2020.

7.  Machine]learning assisted efficient exploration of suitable flow reaction conditions for organocatalyzed domino reaction (Poster)
Kondo, M.; Wathsala, H. D. P.; Sako, M.; Hanatani, Y.; Ishikawa, K.; Hara, S.; Takaai, T.; Washio, T.; Takizawa, S.; Sasai, H., The 23rd SANKEN International Symposium, Chemistry Awaji Yumebutai International Conference Center, January 9-10, 2020.

2019@🐗

<Domestic>

1.  Enantioselective Organocatalytic Construction of a Chiral Quaternary Carbon Center (Oral)
*Hanatani, Y.; Kondo, M.; Takizawa, S.; Sasai, H.
“ú–{‰ŧŠw‰ï‘æ99t‹G”N‰ïCb“ė‘åŠwi•šŒÉjC3ŒŽ16“ú`3ŒŽ19“úC2019”ND

2.  Development of New Chiral Ligands Based on a Tetraphenylene Backbone (Oral)
*Kataoka, K.; Takenaka, K.; Sasai, H.
“ú–{‰ŧŠw‰ï‘æ99t‹G”N‰ïCb“ė‘åŠwi•šŒÉjC3ŒŽ16“ú`3ŒŽ19“úC2019”ND

3.  Facile Synthesis of Allylamines via Intermolecular Aza-Wacker-Type Reaction Promoted by a Pd-SPRIX Catalyst (Oral)
Sen, A.; *Takenaka, K.; Sasai, H.
“ú–{‰ŧŠw‰ï‘æ99t‹G”N‰ïCb“ė‘åŠwi•šŒÉjC3ŒŽ16“ú`3ŒŽ19“úC2019”ND

4.  Enantioselective Synthesis of Spirooxindoles via Pictet-Spengler, Oxidative and Wagner-Meerwein Rearrangements of Isotryptamine (Oral)
*Matsuyama, N.; Kondo, M.; Takizawa, S.; Sasai, H.
“ú–{‰ŧŠw‰ï‘æ99t‹G”N‰ïCb“ė‘åŠwi•šŒÉjC3ŒŽ16“ú`3ŒŽ19“úC2019”ND

5.  Effect of Phosphine Ligands on Pd-catalyzed Cyclative Hydroamination (Oral)
*Kusaba, M.; Takenaka, K.; Sasai, H.
“ú–{‰ŧŠw‰ï‘æ99t‹G”N‰ïCb“ė‘åŠwi•šŒÉjC3ŒŽ16“ú`3ŒŽ19“úC2019”ND

6.  Synthetic Study of Bismurayaquinone-A Using Chiral Vanadium Catalyst (Oral)
*Park, H.; Sako, M.; Takizawa, S.; Sasai, H.
“ú–{‰ŧŠw‰ï‘æ99t‹G”N‰ïCb“ė‘åŠwi•šŒÉjC3ŒŽ16“ú`3ŒŽ19“úC2019”ND

7.  Chiral Vanadium Complex-catalyzed Enantioselective Oxidative Hetero-coupling Reactions of Phenols (Oral)
*Higashida, K.; Sako, M.; Takizawa, S.; Sasai, H.
“ú–{‰ŧŠw‰ï‘æ99t‹G”N‰ïCb“ė‘åŠwi•šŒÉjC3ŒŽ16“ú`3ŒŽ19“úC2019”ND

8.  Chiral Vanadium Complex-Catalyzed Efficient Synthesis of Heterohelicenes (Oral)
*Tamori, Y.; Sako, M.; Takizawa, S.; Sasai, H.
“ú–{‰ŧŠw‰ï‘æ99t‹G”N‰ïCb“ė‘åŠwi•šŒÉjC3ŒŽ16“ú`3ŒŽ19“úC2019”ND

9.  Vanadium Complex-catalyzed One-pot Synthesis of Nitrogen Containing Aromatic Compounds (Oral)
*Takiishi, T.; Sako, M.; Takizawa, S.; Zumbrägel, N.; Gröger, H.; Sasai, H.
“ú–{‰ŧŠw‰ï‘æ99t‹G”N‰ïCb“ė‘åŠwi•šŒÉjC3ŒŽ16“ú`3ŒŽ19“úC2019”ND

10.              Vanadium Complex-catalyzed Enantioselective oxa-Piancatelli Rearrangement Reaction (Oral)
*Sako, M.; Schober, L.; Takizawa, S.; Gröger, H.; Sasai, H.
“ú–{‰ŧŠw‰ï‘æ99t‹G”N‰ïCb“ė‘åŠwi•šŒÉjC3ŒŽ16“ú`3ŒŽ19“úC2019”ND

11.              Development of Novel Photoswitchable Chiral Catalyst (Oral)
*Kondo, M.; Nakamura K.; Sasai, H.
“ú–{‰ŧŠw‰ï‘æ99t‹G”N‰ïCb“ė‘åŠwi•šŒÉjC3ŒŽ16“ú`3ŒŽ19“úC2019”ND

12.              Development of Novel Photoswitchable Chiral Oxazoline Catalyst (Oral)
*Nakamura K.; Kondo, M.; Sasai, H.
“ú–{‰ŧŠw‰ï‘æ99t‹G”N‰ïCb“ė‘åŠwi•šŒÉjC3ŒŽ16“ú`3ŒŽ19“úC2019”ND

13.              ƒOƒŠ[ƒ“ƒPƒ~ƒXƒgƒŠ[ŽuŒüŒ^•sÄ‡Ž”―‰ž‚ĖŠJ”­‚Æ‘―ŠŊ”\Ŧ•Ą‘fŠÂœŠi\’z‚Ö‚Ė‰ž—pi“ú–{–ōŠw‰ï@ŠwpU‹ŧÜŽóÜu‰‰jiŒû“Šj
*
‘ęāV”EC“ú–{–ōŠw‰ï‘æ139”N‰ïC–‹’ĢƒƒbƒZ@‘žiį—tjC3ŒŽ20“ú`3ŒŽ23“úC2019”ND

14.              ƒLƒ‰ƒ‹ƒoƒiƒWƒEƒ€G”}‚ð—p‚Ē‚éƒGƒiƒ“ƒ`ƒI‘I‘ð“IŽ_‰ŧƒJƒbƒvƒŠƒ“ƒO‚ĖŠJ”­‚Ɖž—piŒû“Šj
*
ēŒÃ^CÂ–؍FŒ›C‘ęāV”ECųˆäG–ūC“ú–{–ōŠw‰ï‘æ139”N‰ïC–‹’ĢƒƒbƒZ@‘žiį—tjC3ŒŽ20“ú`3ŒŽ23“úC2019”ND

15.              ƒtƒ[ƒVƒXƒeƒ€‚ð—p‚Ē‚éG”}“I•sÄ˜A‘ą”―‰ž‚ĖŠJ”­iŒû“Šj
*Piyumi HETTIARACHCHIGE DONA
CēŒÃ^CŠÝ“S”nC‘ęāV”ECųˆäG–ūC“ú–{–ōŠw‰ï‘æ139”N‰ïC–‹’ĢƒƒbƒZ@‘žiį—tjC3ŒŽ20“ú`3ŒŽ23“úC2019”ND

16.              ƒoƒiƒWƒEƒ€G”}‚ðŠˆ—p‚·‚éŠÜ’‚‘f–F‘°‰ŧ‡•Ļ‚Ėƒƒ“ƒ|ƒbƒg‡ŽiŒû“Šj
*
‘ëÎ•ü‘åCēŒÃ^C‘ęāV”ECNadine ZUMBRAEGELCHarald GROEGERCųˆäG–ūC“ú–{–ōŠw‰ï‘æ139”N‰ïC–‹’ĢƒƒbƒZ@‘žiį—tjC3ŒŽ20“ú`3ŒŽ23“úC2019”ND

17.              ‹@ŠBŠwK‚É‚æ‚é”―‰žðŒÅ“K‰ŧ‚ðŠˆ—p‚·‚éƒXƒsƒƒIƒLƒVƒCƒ“ƒh[ƒ‹—Þ‰‘Ė‚Ėļ–§ƒtƒ[•sÄ‡Žiƒ|ƒXƒ^[j
*
‹ß“ĄŒ’AēŒÃ^AųˆäG–ūA‘ęāV”ECVŠwp—ĖˆæŒĪ‹†u”―‰žWÏ‰ŧ‚Š“ą‚­’†•ŠŽqí—Š:‚ŽŸķ•Ļ‹@”\•ŠŽq‚Ė‘nŧv‘æ8‰ņŽ‰Ę•ņ‰ïC‹ž“s‘åŠwŒjƒLƒƒƒ“ƒpƒX‘Dˆäï—Į‹L”Ou“°i‹ž“sjC5ŒŽ31`6ŒŽ1“úC2019”ND

18.              ƒLƒ‰ƒ‹ƒoƒiƒWƒEƒ€G”}‚ð—p‚Ē‚éƒtƒFƒm[ƒ‹—Þ‚ĖŽ_‰ŧ“IƒwƒeƒƒJƒbƒvƒŠƒ“ƒO”―‰žiŒû“Šj
*
“Œ“cŒbŒÞAēŒÃ^A‘ęāV”EAųˆäG–ūC‘æ115‰ņ—L‹@‡ŽƒVƒ“ƒ|ƒWƒEƒ€C“Œ–k‘åŠwÂ—tŽRƒRƒ‚ƒ“ƒYi‹{éjC6ŒŽ3“ú`4“úC2019”ND

19.              ˜A‘ą”―‰ž‚ð—˜—p‚·‚éƒXƒsƒƒIƒLƒVƒCƒ“ƒh[ƒ‹—Þ‚Ė’ZH’ö•sÄ‡Žiƒ|ƒXƒ^[j
*
žŽRŪŽũA‹ß“ĄŒ’A‘ęāV”EAųˆäG–ūC‘æ115‰ņ—L‹@‡ŽƒVƒ“ƒ|ƒWƒEƒ€C“Œ–k‘åŠw Â—tŽRƒRƒ‚ƒ“ƒYi‹{éjC6ŒŽ3“ú`4“úC2019”ND

20.              ƒLƒ‰ƒ‹ƒoƒiƒWƒEƒ€ö‘Ė‚ĖŽ_G”}”\‚ðŠˆ—p‚·‚é•sÄ”―‰ž‚ĖŠJ”­iŒû“Šj
*
ēŒÃ^A‘ëÎ•ü‘åALukas SchoberAHarald GrögerA‘ęāV”EAųˆäG–ūCƒVƒ“ƒ|ƒWƒEƒ€ ƒ‚ƒŒƒLƒ…ƒ‰[EƒLƒ‰ƒŠƒeƒB[2019C‹ā‘ōĪH‰ï‹cŠiÎėjC6ŒŽ14“ú`15“úC2019”ND

21.              AIŠˆ—p‚É‚æ‚éļ–§ƒtƒ[•sÄ‡Ž‚Ė”―‰žÅ“K‰ŧiƒ|ƒXƒ^[j
*
‹ß“ĄŒ’AH. D. P. WathsalaAēŒÃ^A‰Ô’J—D‘ū˜NAÎėˆęéAŒī‘A‘鍇F”VA˜h”ö—ēA‘ęāV”EAųˆäG–ūC‘æ8‰ņJACI/GSCƒVƒ“ƒ|ƒWƒEƒ€C“Œ‹ž‘ÛƒtƒH[ƒ‰ƒ€i“Œ‹žjC6ŒŽ24“ú`6ŒŽ25“úC2019”ND

22.              ƒpƒ‰ƒWƒEƒ€ƒGƒmƒ‰[ƒg‚Ė‹ÉŦ“]Š·Œ^‹Šj“IƒAƒ~ƒm‰ŧ”―‰ž‚ĖŠJ”­iƒ|ƒXƒ^[j
*
‘ę–Ē—ˆA–ė–{—T–įA’|’†˜a_AųˆäG–ūC‘æ52‰ņ—L‹@‹ā‘ŪŽáŽč‚Ė‰ï‰Ä‚ĖŠwZA‘q•~‚đ‚Æ‚Ī‚ŋŽ™“‡ƒzƒeƒ‹i‰ŠŽRjA6ŒŽ24“ú`26“úA2019”ND

23.              ‹@ŠBŠwK‚ð—p‚Ē‚éļ–§ƒtƒ[•sÄ‡Ž‚ĖÅ“KðŒ—\‘ŠiŒû“Šj
*
‹ß“ĄŒ’CŽY‹Æ‰ČŠwAIƒZƒ“ƒ^[”­‘Ŧ‹L”OƒLƒbƒNƒIƒtu‰‰‰ïAŽY‹Æ‰ČŠwŒĪ‹†Šu“°i‘åãjA7ŒŽ6“úA2019”ND

24.              Œõ‰ž“šŦ•sÄG”}‚ĖŠJ”­‚Ɖž—p (ƒ|ƒXƒ^[)
*
Žá—Ņ—Į’mA‹ß“ĄŒ’AųˆäG–ūC‘æ39‰ņ—L‹@‡ŽŽáŽčƒZƒ~ƒi[C‘åã•{—§‘åŠw@’†•Sã’đƒLƒƒƒ“ƒpƒXi‘åãjC8ŒŽ8“úC2019”ND

25.              •ŠŽqŠÔ‹ÉŦ“]Š·Œ^•sÄƒhƒ~ƒm”―‰ž‚ĖŠJ”­ŒĪ‹†iƒ|ƒXƒ^[j
*
ŒÃė’q‘åAēŒÃ^A‰Ô’J—D‘ū˜NA‹ß“ĄŒ’A‘ęāV”EAųˆäG–ūC‘æ39‰ņ—L‹@‡ŽŽáŽčƒZƒ~ƒi[C‘åã•{—§‘åŠw@’†•Sã’đƒLƒƒƒ“ƒpƒXi‘åãjC8ŒŽ8“úC2019”ND

26.              Facile synthesis of chiral aza-bicyclo[3.1.0]hexanes via allylic substitution/oxidative cyclization (Poster)
*Zhu, L.; Chaki, B. M.; Takenaka, K.; Takizawa, S.; Sasai, H.
C‘æ39‰ņ—L‹@‡ŽŽáŽčƒZƒ~ƒi[C‘åã•{—§‘åŠw@’†•Sã’đƒLƒƒƒ“ƒpƒXi‘åãjC8ŒŽ8“úC2019”ND

27.              ƒLƒ‰ƒ‹ƒoƒiƒWƒEƒ€G”}‚ð—p‚Ē‚éƒtƒFƒm[ƒ‹—Þ‚ĖŽ_‰ŧ“IƒwƒeƒƒJƒbƒvƒŠƒ“ƒO”―‰žiŒû“Šj
*
ēŒÃ^A“Œ“cŒbŒÞA‘ęāV”EAųˆäG–ūC‘æ66‰ņ—L‹@‹ā‘Ū‰ŧŠw“Ē˜_‰ïCŽņ“s‘åŠw“Œ‹ž@“ė‘å‘ōƒLƒƒƒ“ƒpƒXi“Œ‹žjC9ŒŽ14“ú`9ŒŽ16“úC2019”ND

28.              ‹ÉŦ“]Š·Œ^ƒGƒiƒ“ƒ`ƒI‘I‘ð“Iƒhƒ~ƒm”―‰ž‚ĖŠJ”­‚ƃLƒ‰ƒ‹‘æŽl‹‰’Y‘f\’z‚Ö‚Ė‰ž—piƒ|ƒXƒ^[j
*
‰Ô’J—D‘ū˜NA‹ß“ĄŒ’AŒÃė’q‘åAēŒÃ^A‘ęāV”EAųˆäG–ūC‘æ45‰ņ”―‰ž‚ƍ‡Ž‚Ėi•āƒVƒ“ƒ|ƒWƒEƒ€-ƒ‰ƒCƒtƒTƒCƒGƒ“ƒX‚ðŽuŒü‚ĩ‚―—˜_C”―‰ž‚Ļ‚æ‚Ņ‡Ž-C‘q•~ŽsŒ|•ķŠŲi‰ŠŽRjC10ŒŽ28“ú`10ŒŽ29“úC2019”ND

29.              V‹KŒõ‰ž“šŒ^•sÄ”zˆĘŽq‚ĖŠJ”­iƒ|ƒXƒ^[j
*
’†‘šŒ°“lA‹ß“ĄŒ’AųˆäG–ūC‘æ45‰ņ”―‰ž‚ƍ‡Ž‚Ėi•āƒVƒ“ƒ|ƒWƒEƒ€-ƒ‰ƒCƒtƒTƒCƒGƒ“ƒX‚ðŽuŒü‚ĩ‚―—˜_C”―‰ž‚Ļ‚æ‚Ņ‡Ž-C‘q•~ŽsŒ|•ķŠŲi‰ŠŽRjC10ŒŽ28“ú`10ŒŽ29“úC2019”ND

30.              ˜A‘ą”―‰ž‚ð—˜—p‚·‚éƒXƒsƒƒIƒLƒVƒCƒ“ƒh[ƒ‹—Þ‚Ė’ZH’ö•sÄ‡Žiƒ|ƒXƒ^[j
*
žŽRŪŽũA‹ß“ĄŒ’ATin Zar AyeA‘ęāV”EAųˆäG–ūC‘æ45‰ņ”―‰ž‚ƍ‡Ž‚Ėi•āƒVƒ“ƒ|ƒWƒEƒ€-ƒ‰ƒCƒtƒTƒCƒGƒ“ƒX‚ðŽuŒü‚ĩ‚―—˜_C”―‰ž‚Ļ‚æ‚Ņ‡Ž-C‘q•~ŽsŒ|•ķŠŲi‰ŠŽRjC10ŒŽ28“ú`10ŒŽ29“úC2019”ND

31.              ƒLƒ‰ƒ‹ƒoƒiƒWƒEƒ€ö‘Ė‚ð—p‚Ē‚é•sÄG”}”―‰ž‚ĖŠJ”­iƒ|ƒXƒ^[j
*
ēŒÃ^A‘ęāV”EAųˆäG–ūC‘æ7‰ņƒAƒ‰ƒCƒAƒ“ƒXŽáŽčŒĪ‹†Œð—Ž‰ïC‘åã‘åŠwŽY‹Æ‰ČŠwŒĪ‹†Ši‘åãjC11ŒŽ12“ú`13“úC2019”ND

32.              Exploration of Flow Reaction Conditions Using Machine-learning for Enantioselective Organocatalyzed Rauhut-Currier/[3+2] Annulation Sequence (Œû“Š)
Kondo, M.; Wathsala, H. D. P.; Sako, M.; Hanatani, Y.; Ishikawa, K.; Hara, S.; Takaai, T.; Washio, T.; *Takizawa, S.; Sasai, H.
‘æ12‰ņ—L‹@G”}ƒVƒ“ƒ|ƒWƒEƒ€C‹ž“s‘åŠw–ōŠwŒĪ‹†‰Č@ˆã–ōŒn‘‡ŒĪ‹†“@“Ą‘―‹L”Oƒz[ƒ‹EƒAƒEƒgƒŠ[ƒ`ƒGƒŠƒAi‹ž“sjC12ŒŽ4“ú~12ŒŽ5“úC2019”ND

33.              Development of Enantioselective Umpolung Domino Reaction (ƒ|ƒXƒ^[)
*Furukawa, T.; Sako, M.; Hanatani, Y.; Kondo, M.; Takizawa, S.; Sasai, H.
‘æ12‰ņ—L‹@G”}ƒVƒ“ƒ|ƒWƒEƒ€C‹ž“s‘åŠw–ōŠwŒĪ‹†‰Č@ˆã–ōŒn‘‡ŒĪ‹†“@“Ą‘―‹L”Oƒz[ƒ‹EƒAƒEƒgƒŠ[ƒ`ƒGƒŠƒAi‹ž“sjC12ŒŽ4“ú~12ŒŽ5“úC2019”ND

34.              Facile Synthesis of Chiral Spirooxindoles via Sequential Reactions (ƒ|ƒXƒ^[)
*Matsuyama, N. Kondo, M.; Tin Zar Aye, Mattan, I.; Takizawa, S.; Sasai, H.
‘æ12‰ņ—L‹@G”}ƒVƒ“ƒ|ƒWƒEƒ€C‹ž“s‘åŠw–ōŠwŒĪ‹†‰Č@ˆã–ōŒn‘‡ŒĪ‹†“@“Ą‘―‹L”Oƒz[ƒ‹EƒAƒEƒgƒŠ[ƒ`ƒGƒŠƒAi‹ž“sjC12ŒŽ4“ú~12ŒŽ5“úC2019”ND

<International>

1.  Catalytic Asymmetric Synthesis of Cedarmycins Using Chiral Iridium Complex (Poster)
*Suzuki, T.; Ismiyarto; Kishi, N.; Adachi, Y.; Zhou, D.-Y.; Asano, K.; Obora, Y.; Sasai, H. The 22nd SANKEN International Symposium/17th SANKEN Nanotechnology International Symposium, Osaka, Japan, January 15-16, 2019.

2.  Efficient Optimization of Enantioselective Domino Reaction Based on Bayesian Optimization (Poster)
*Wathsala, H. D. P.; Kondo, M.; Sako, M.; Hara, S.; Ishikawa, K.; Takaai, T.; Takizawa, S.; Washio, T.; Sasai, H. The 22nd SANKEN International Symposium/17th SANKEN Nanotechnology International Symposium, Osaka, Japan, January 15-16, 2019.

3.  Chiral Dinuclear Vanadium Complex-mediated Oxidative Coupling of Resorcinols (Poster)
Sako, M.; Aoki, T.; Zumbrägel, N.; Schober, L.; Gröger, H.; Takizawa, S.; Sasai, H. THE 47th NAITO CONFERENCE ON C-H Bond Activation and Transformation, CHÂTERAISÉ Gateaux Kingdom SAPPORO, Hokkaido, Japan, July 2-5, 2019

4.  Facile Enantioselective Synthesis of Hetero[9]helicenes Using Redox/acid Cooperative Catalysts (Oral)
Sako, M.; Tamori, Y.; Higashida, K.; *Takizawa, S.; Sasai, H. 31st International Symposium on Chirality, Bordeaux, France, July 14-17, 2019

5.  Organocatalytic Umpolung Michael Process: Synthesis of Highly Functionalized Ketones Bearing a Chiral Quaternary Carbon Center (Poster)
*Hanatani, Y.; Kondo, M.; Takizawa, S.; Sasai, H.
31st International Symposium on Chirality, Bordeaux, France, July 14-17, 2019

6.  Synthesis and Application of Novel Photoswitchable Chiral Catalyst (Poster)
*Nakamura K.; Kondo, M.; Sasai, H. 31st International Symposium on Chirality, Bordeaux, France, July 14-17, 2019

7.  Palladium Enolate Umpolung: Cyclative Hydroamination of Alkynyl Cyclohexadienones (Poster)
*Kusaba, M.; Nomoto, Y.; Takenaka, K.; Sasai, H., 20th IUPAC International Symposium on Organometallic Chemistry Directed Towards Organic Synthesis (OMCOS 20), Heidelberg, Germany, July 21-25, 2019
<Poster AwardŽóÜ>

8.  Development of Vanadium-catalyzed Organic Reaction in Water (Poster)
*Sako, M.; Zumbrägel, N.; Takiishi, T.; Schober, S.; Gröger, H.; Takizawa, S.; Sasai, H., The 4th International Symposium on Process Chemistry, Kyoto, Japan, July 24-26, 2019.
<Selected as Short Talk (10 min)>

9.  AI-Assisted Optimization for Synthesis of Spirooxindole Analogues via Enantioselective Domino Reaction in Flow System (Poster)
*Wathsala, H. D. P.; Kondo, M.; Sako, M.; Hanatani, Y.; Hara, S.; Ishikawa, K.; Takaai, T.; Washio, T.; Takizawa, S.; Sasai, H., The 4th International Symposium on Process Chemistry, Kyoto, Japan, July 24-26, 2019.

10.              Recent Progress in Chiral Cooperative Vanadium Catalysis (Keynote Lecture)
*Sasai, H., International Congress on Pure and Applied Chemistry (ICPAC) Yangon 2019, Rose Garden Hotel, Yangon, Myanmar, August 6-9, 2019.

11.              Asymmetric Synthesis of Spirooxindoles via Pictet-Spengler Reaction, Oxidative and Wagner-Meerwein Rearrangement (Poster)
*Tin Zay Aye; Matsuyama, N.; Kondo, M.; Takizawa, S.; Sasai, H., International Congress on Pure and Applied Chemistry (ICPAC) Yangon 2019, Rose Garden Hotel, Yangon, Myanmar, August 6-9, 2019.

12.              Enantioselective Synthesis of Highly Functionalized Heterocycles via Organocatalyzed Domino Reactions (Oral)
*Takizawa, S.; Sako, M.; Wathsala, H. D. P.; Hanatani, Y.; Furukawa, T.; Matsuyama, N.; Tin Zar Aye; Sasai, H., 27th International Society of Heterocyclic Chemistry Congress, ROHM Theatre Kyoto & Miyakomesse, Kyoto, Japan, September 1-6, 2019.

13.              Facile Synthesis of Chiral Spirooxindoles via Pictet-Spengler/Oxidative Rearrangement (Flash Talk & Poster)
*Matsuyama, N.; Kondo, M.; Tin Zar Aye, Takizawa, S.; Sasai, H., 27th International Society of Heterocyclic Chemistry Congress, ROHM Theatre Kyoto & Miyakomesse, Kyoto, Japan, September 1-6, 2019.

14.              Chiral Vanadium Complex-catalyzed Enantioselective Oxidative Hetero-coupling Reactions of Arenols (Flash Talk & Poster)
*Higashida, K.; Sako, M.; Takizawa, S.; Sasai, H., 27th International Society of Heterocyclic Chemistry Congress, ROHM Theatre Kyoto & Miyakomesse, Kyoto, Japan, September 1-6, 2019.

15.              Asymmetric Reactions Using Chiral Vanadium Complex as Acid Catalyst (Poster)
*Sako, H.; Takiishi, T.; Schober, L.; Park, H.; Gröger, H.; Takizawa, S.; Sasai, H., 27th International Society of Heterocyclic Chemistry Congress, ROHM Theatre Kyoto & Miyakomesse, Kyoto, Japan, September 1-6, 2019.

16.              Room-Temperature, Metal-Free and One-Pot Preparation of 2H-indazoles via a Mills Reaction and Cyclization Sequence (Poster)
*Kondo, M.; Takizawa, S.; Jiang, Y.; Sasai, H., 27th International Society of Heterocyclic Chemistry Congress, ROHM Theatre Kyoto & Miyakomesse, Kyoto, Japan, September 1-6, 2019.

17.              Development of Umpolung Michael Reaction of Alkynyl Acid Esters (poster)
*Hanatani, Y.; Kondo, M.; Furukawa, T.; Sako, M.; Takizawa, S.; Sasai, H., ISONIS-12, ISMMS-5, ICAMS-2, and ICSFC; 12th International Joint Symposium on Synthetic Organic Chemistry Awaji Yumebutai International Conference Center, November 21-23, 2019.

18.              Efficient Prediction of Flow Reaction Conditions Using Machine-Learning for Enantioselective Domino Reaction (Oral)
*Kondo, M.; Wathsala, H. D. P.; Sako, M.; Hanatani, U.; Ishikawa, K.; Hara, S.; Takaai, T.; Washio, T.; Takizawa, S.; Sasai, H., 13th International CeBiTec Symposium - Multi-Step Syntheses in Biology & Chemistry, An International Young Investigator Conference -, Center for Interdisciplinary Research (ZiF), Bielefeld University, Germany, December 2-4, 2019.

19.              Chiral Vanadium Complex-mediated oxa-Piancatelli Reaction and PictetSpengler Reaction/Aromatization Sequence (Oral)
*Sako, M.; Schober, L.; Takiishi, T.; Gröger, H.; Takizawa, S.; Sasai, H., 13th International CeBiTec Symposium - Multi-Step Syntheses in Biology & Chemistry, An International Young Investigator Conference -, Center for Interdisciplinary Research (ZiF), Bielefeld University, Germany, December 2-4, 2019.

20.              Enantioselective Organocatalytic Synthesis of 1,3-Disubstituted Isoindolines by Betti/Azamichael Sequence (Poster)
* Wathsala, H. D. P.; Sako, M.; Abozeid, M. A.; Kishi, K.; Hirata, S.; Murai, K.; Fujioka, H.; Takizawa, S. Sasai, H., 13th International CeBiTec Symposium - Multi-Step Syntheses in Biology & Chemistry, An International Young Investigator Conference -, Center for Interdisciplinary Research (ZiF), Bielefeld University, Germany, December 2-4, 2019.
<Catalysts Poster Prize>

21.              Development of Chiral Spiro Bis(isoxazoline) Ligand (SPRIX) (Keynote Lecture)
*Sasai, H., 13th International CeBiTec Symposium - Multi-Step Syntheses in Biology & Chemistry, An International Young Investigator Conference -, Center for Interdisciplinary Research (ZiF), Bielefeld University, Germany, December 2-4, 2019.

 


2018@🐶

<Domestic>

1.  ‘―‹@”\G”}‚ðŠˆ—p‚·‚éŽĀ—p“I•sÄ•ŠŽq•ÏŠ·iƒ|ƒXƒ^[j
*
‘ęāV”ECVŠwp—ĖˆæŒĪ‹†@”―‰žWÏ‰ŧ‚Š“ą‚­’†•ŠŽqí—Š@‚ŽŸķ•Ļ‹@”\•ŠŽq‚Ė‘nŧ@‘æ‚T‰ņŒöŠJŽ‰Ę•ņ‰ïC‘åã‘åŠw–L’†ƒLƒƒƒ“ƒpƒX“ė•”—zˆę˜Yƒz[ƒ‹i‘åãjC1ŒŽ26“ú`27“úC2018”ND

2.  Organocatalytic Enantioselective Sequential C-C Bond Forming Reaction in Flow SystemiŒû“Šj
*H. D. P. Wathsala
AŠÝ“S”nAQingwen ChenA‘ęāV”EAųˆäG–ūC“ú–{‰ŧŠw‰ï‘æ98t‹G”N‰ïC“ú–{‘åŠwiį—tjC3ŒŽ20`23“úC2018”ND

3.  Development of New Spiro-type Chiral Ligands Bearing a Functional Side ArmiŒû“Šj
*
V‹“c‹ąÍA’|’†˜a_AųˆäG–ūC“ú–{‰ŧŠw‰ï‘æ98t‹G”N‰ïC“ú–{‘åŠwiį—tjC3ŒŽ20`23“úC2018”ND

4.  Palladium Enolate Umpolung: Approach to ƒŋ-Aminocarbonyl CompoundsiŒû“Šj
*
–ė–{—T–įA’|’†˜a_AųˆäG–ūC“ú–{‰ŧŠw‰ï‘æ98t‹G”N‰ïC“ú–{‘åŠwiį—tjC3ŒŽ20`23“úC2018”ND

5.  Enantioselective Synthesis of Nitrogen Heterocycles via aza-Wacker-type Reaction Catalyzed by Pd-SPRIX ComplexiŒû“Šj
*Abhijit Sen
A’|’†˜a_AųˆäG–ūC“ú–{‰ŧŠw‰ï‘æ98t‹G”N‰ïC“ú–{‘åŠwiį—tjC3ŒŽ20`23“úC2018”ND

6.  Enantioselective Synthesis of Bicyclic Pyrrolidine Derivatives via One-Pot Organo and Palladium Catalysis RelayiŒû“Šj
*Bijan M. Chaki
AJianfei BaiA’|’†˜a_A‘ęāV”EAųˆäG–ūC“ú–{‰ŧŠw‰ï‘æ98t‹G”N‰ïC“ú–{‘åŠwiį—tjC3ŒŽ20`23“úC2018”ND

7.  Facile synthesis of spirooxindoles via an enantioselective organocatalyzed sequential reactioniŒû“Šj
*
‘ę–Ē—ˆAŠÝ“S”nA‘ęāV”EAJianfei BaiAųˆäG–ūC“ú–{‰ŧŠw‰ï‘æ98t‹G”N‰ïC“ú–{‘åŠwiį—tjC3ŒŽ20`23“úC2018”ND

8.  Irö‘Ė‚ðG”}‚Æ‚ĩ‚―ƒeƒBƒVƒ…ƒ`ƒFƒ“ƒRŒ^”―‰ž‚É‚æ‚éƒGƒ“ƒeƒƒ‰ƒNƒgƒ“‚ĖG”}“I•sÄ‡Žiƒ|ƒXƒ^[j
—é–ØŒ’”VA*‘Ŧ—§—S‹MAŠÝMŠóAŽü‘å—gA’Đ–ė–FDAųˆäG–ūC“ú–{‰ŧŠw‰ï‘æ98t‹G”N‰ïC“ú–{‘åŠwiį—tjC3ŒŽ20`23“úC2018”ND

9.  Development and Application of Organocatalyzed Stereoselective Umpolung Double Michael ReactioniŒû“Šj
*
ŠÝ“S”nA‘ęāV”EAųˆäG–ūC“ú–{‰ŧŠw‰ï‘æ98t‹G”N‰ïC“ú–{‘åŠwiį—tjC3ŒŽ20`23“úC2018”ND

10.              Chiral Vanadium Complex-catalyzed Enantioselective Oxidative Coupling Reactions of Polycyclic PhenolsiŒû“Šj
*
™›―WŦAēŒÃ^A‘ęāV”EAųˆäG–ūC“ú–{‰ŧŠw‰ï‘æ98t‹G”N‰ïC“ú–{‘åŠwiį—tjC3ŒŽ20`23“úC2018”ND

11.              Chiral Vanadium Complex-catalyzed Enantioselective Oxidative Coupling Reactions of HydroxycarbazolesiŒû“Šj
*
ēŒÃ^A‘ęāV”EAųˆäG–ūC“ú–{‰ŧŠw‰ï‘æ98t‹G”N‰ïC“ú–{‘åŠwiį—tjC3ŒŽ20`23“úC2018”ND

12.              Chiral Vanadium Complex-catalyzed Enantioselective Oxidative Coupling Reactions of Monocyclic PhenolsiŒû“Šj
*
Â–؍FŒ›AēŒÃ^A‘ęāV”EAųˆäG–ūC“ú–{‰ŧŠw‰ï‘æ98t‹G”N‰ïC“ú–{‘åŠwiį—tjC3ŒŽ20`23“úC2018”ND
 

13.              —L‹@•ŠŽqG”}‚ð—p‚Ē‚éƒXƒsƒƒIƒLƒVƒCƒ“ƒh[ƒ‹—Þ‰‘Ė‚Ė’ZH’ö•sÄ‡ŽiŒû“Šj
*
‘ę–Ē—ˆAŠÝ“S”nA‘ęāV”EAJianfei BaiAųˆäG–ūC“ú–{–ōŠw‰ï‘æ138”N‰ïCÎėŒ§—§‰đŠy“°@‘žiÎėjC3ŒŽ25`28“úC2018”N.
 

14.              ƒAƒ~ƒh‰ŧ/Rauhut-Currier˜A‘ą”―‰ž‚É‚æ‚éƒŋ-ƒƒ`ƒŠƒfƒ“-ƒÁ-ƒ‰ƒNƒ^ƒ€‚ĖG”}“I•sÄ‡ŽiŒû“Šj
*
ŠÝ“S”nAFernando Arteaga-ArteagaA‘ęāV”EAJianfei BaiAųˆäG–ūC“ú–{–ōŠw‰ï‘æ138”N‰ïCÎėŒ§—§‰đŠy“°@‘žiÎėjC3ŒŽ25`28“úC2018”N.
<“ú–{–ōŠw‰ï‘æ138”N‰ïŠwķ—DG”­•\ÜiŒû“Š”­•\‚Ė•”j>
 

15.              —L‹@•ŠŽqG”}‚É‚æ‚é1,3-cis-ƒCƒ“ƒhƒŠƒ“‰ŧ‡•Ļ‚ĖƒGƒiƒ“ƒ`ƒI‘I‘ð“Iƒƒ“ƒ|ƒbƒg‡ŽiŒû“Šj
*H. D. P. Wathsala
A‘ęāV”EAēŒÃ^AŠÝ“S”nA•―“cCˆęA‘šˆäŒ’ˆęA“Ą‰ŠO“đAųˆäG–ūC“ú–{–ōŠw‰ï‘æ138”N‰ïCÎėŒ§—§‰đŠy“°@‘žiÎėjC3ŒŽ25`28“úC2018”N.

16.              ƒoƒiƒWƒEƒ€G”}‚ð—p‚Ē‚éƒJƒ‹ƒoƒ][ƒ‹—U“ą‘Ė‚ĖƒGƒiƒ“ƒ`ƒI‘I‘ð“IŽ_‰ŧƒJƒbƒvƒŠƒ“ƒO”―‰ž‚ĖŠJ”­iŒû“Šj
*
‘ęāV”EAēŒÃ^Aˆę”VĢ˜a–íAųˆäG–ūC“ú–{–ōŠw‰ï‘æ138”N‰ïCÎėŒ§—§‰đŠy“°@‘žiÎėjC3ŒŽ25`28“úC2018”N.

17.              ƒIƒLƒ\ƒƒ^ƒ‹’†S‚ĖƒLƒ‰ƒŠƒeƒB[§Œä‚ðŠî”Õ‚Æ‚·‚é‘―‹@”\•sÄG”}‚Ė‘nŧiƒ|ƒXƒ^[j
*
‘ęāV”ECVŠwp—ĖˆæŒĪ‹†u”zˆĘƒAƒVƒ“ƒƒgƒŠ[v‘æ‚R‰ņ—Ėˆæ‘S‘Ė‰ï‹cC‹ãB‘åŠw•a‰@’n‹æ•S”Nu“°i•Ÿ‰ŠjC5ŒŽ8“ú`9“úC2018”N.

18.              ŠÂóƒWƒGƒmƒ“‚Ė”ņ‘ΏĖ‰ŧ‚ðŒŪH’ö‚Æ‚·‚éƒGƒiƒ“ƒ`ƒI‘I‘ð“I RauhutCurrier ˜A‘ą”―‰ž‚ĖŠJ”­‚Ɖž—piŒû“Šj
*
‘ęāV”EA‹g“c‘ŨŽuAFernando Arteaga ArteagaAŠÝ“S”nAųˆä G–ūCSymposium on Molecular Chirality 2018Cį—t‘åŠwžį—tƒLƒƒƒ“ƒpƒX‚Ŋ‚â‚Ŧ‰ïŠŲiį—tjC5ŒŽ11“ú`12“úC2018”N.

19.              ƒtƒ[ƒVƒXƒeƒ€‚ð—p‚Ē‚éG”}“I•sÄ˜A‘ą”―‰ž‚ĖŠJ”­iƒ|ƒXƒ^[j
*H. D. P. Wathsala
AŠÝ“S”nAēŒÃ^A‘ęāV”EAųˆä G–ūCSymposium on Molecular Chirality 2018Cį—t‘åŠwžį—tƒLƒƒƒ“ƒpƒX‚Ŋ‚â‚Ŧ‰ïŠŲiį—tjC5ŒŽ11“ú`12“úC2018”N.

20.              ƒoƒiƒWƒEƒ€G”}‚ðŠˆ—p‚·‚éƒwƒeƒƒwƒŠƒZƒ“‚ĖƒGƒiƒ“ƒ`ƒI‘I‘ð“I‡Žiƒ|ƒXƒ^[j
*
“cX—T‹MA™›―WŦAēŒÃ^A‘ęāV”EAųˆä G–ūCSymposium on Molecular Chirality 2018Cį—t‘åŠwžį—tƒLƒƒƒ“ƒpƒX‚Ŋ‚â‚Ŧ‰ïŠŲiį—tjC5ŒŽ11“ú`12“úC2018”N.

21.              —L‹@•ŠŽq−ƒpƒ‰ƒWƒEƒ€˜A‘ąG”}”―‰ž‚ðŠˆ—p‚·‚é“ņŠÂŽŪƒsƒƒŠƒWƒ“—U“ą‘Ė‚ĖƒGƒiƒ“ƒ`ƒI‘I‘ð“Iƒƒ“ƒ|ƒbƒg‡Žiƒ|ƒXƒ^[j
*
’|’†˜a_ABijan Mohon ChakiAJianfei BaiA‘ęāV”EAųˆäG–ūCSymposium on Molecular Chirality 2018Cį—t‘åŠwžį—tƒLƒƒƒ“ƒpƒX‚Ŋ‚â‚Ŧ‰ïŠŲiį—tjC5ŒŽ11“ú`12“úC2018”N.

22.              ‹ÉŦ“]Š·Œ^ƒ_ƒuƒ‹ƒ}ƒCƒPƒ‹•t‰Á”―‰ž‚É‚æ‚éƒqƒhƒƒCƒ“ƒh[ƒ‹‹y‚Ņƒqƒhƒƒxƒ“ƒ[ƒ“ƒtƒ‰ƒ“-2-ƒJƒ‹ƒ{ƒ“Ž_ƒGƒXƒeƒ‹‚Ė‡Žiƒ|ƒXƒ^[j
*
‘ęāV”ECVŠwp—ĖˆæŒĪ‹†@”―‰žWÏ‰ŧ‚Š“ą‚­’†•ŠŽqí—Š@‚ŽŸķ•Ļ‹@”\•ŠŽq‚Ė‘nŧ@‘æ6‰ņŒöŠJŽ‰Ę•ņ‰ïC‘ˆî“c‘åŠw‘Û‰ï‹cęi“Œ‹žjC6ŒŽ1“ú`6ŒŽ2“úC2018”N.

23.              —L‹@•ŠŽq•sÄG”}‚ð—p‚Ē‚éƒXƒsƒƒIƒLƒVƒCƒ“ƒh[ƒ‹œŠi‚ĖƒGƒiƒ“ƒ`ƒI‘I‘ð“I\’ziƒ|ƒXƒ^[j
*
‘ę–Ē—ˆAŠÝ“S”nA‘ęāV”EAųˆäG–ūC‘æ 7 ‰ņ JACI/GSC ƒVƒ“ƒ|ƒWƒEƒ€CANAƒNƒ‰ƒEƒ“ƒvƒ‰ƒUƒzƒeƒ‹_ŒËi•šŒÉjC6ŒŽ14“ú`6ŒŽ15“úC2018”N.
<—DGƒ|ƒXƒ^[ÜŽóÜ>

24.              ƒoƒiƒWƒEƒ€G”}‚ðŠˆ—p‚·‚é’PŠÂŽŪƒtƒFƒm[ƒ‹‚Ė•sÄƒJƒbƒvƒŠƒ“ƒO”―‰ž‚ĖŠJ”­iƒ|ƒXƒ^[j
*
ēŒÃ^AÂ–؍FŒ›A‘ęāV”EAųˆäG–ūC‘æ 7 ‰ņ JACI/GSC ƒVƒ“ƒ|ƒWƒEƒ€CANAƒNƒ‰ƒEƒ“ƒvƒ‰ƒUƒzƒeƒ‹_ŒËi•šŒÉjC6ŒŽ14“ú`6ŒŽ15“úC2018”N.

25.              ƒtƒ[ƒVƒXƒeƒ€‚ð—p‚Ē‚éG”}“I•sÄ˜A‘ą”―‰ž‚ĖŠJ”­iƒ|ƒXƒ^[j
*
‘ęāV”EAH. D. P. WathsalaAēŒÃ^AŠÝ“S”nAųˆäG–ūC“ú–{ƒvƒƒZƒX‰ŧŠw‰ï2018ƒTƒ}[ƒVƒ“ƒ|ƒWƒEƒ€Cƒ^ƒ[ƒz[ƒ‹‘D–xi“Œ‹žjC7ŒŽ26“ú`7ŒŽ27“úC2018”ND

26.              ˜A‘ąG”}ƒvƒƒZƒX‚É‚æ‚é“ņŠÂŽŪƒsƒƒŠƒWƒ“—U“ą‘Ė‚ĖƒGƒiƒ“ƒ`ƒI‘I‘ð“Iƒƒ“ƒ|ƒbƒg‡Žiƒ|ƒXƒ^[j
–’|’†˜a_ABijan Mohon ChakiAJianfei BaiA‘ęāV”EAųˆäG–ūC“ú–{ƒvƒƒZƒX‰ŧŠw‰ï2018ƒTƒ}[ƒVƒ“ƒ|ƒWƒEƒ€Cƒ^ƒ[ƒz[ƒ‹‘D–xi“Œ‹žjC7ŒŽ26“ú`7ŒŽ27“úC2018”ND

27.              ƒtƒ[ƒŠƒAƒNƒ^[‚ðŠˆ—p‚·‚éG”}“I•sÄƒhƒ~ƒm”―‰ž‚ĖŠJ”­iƒ|ƒXƒ^[j
*
‘ę–Ē—ˆAH. D. P. WathsalaAēŒÃ^AŠÝ“S”nA‘ęāV”EAųˆäG–ūC‘æ38‰ņ—L‹@‡ŽŽáŽčƒZƒ~ƒi[CŠÖžŠw‰@‘åŠw@ž‹{ãƒ–ŒīƒLƒƒƒ“ƒpƒXi•šŒÉjC8ŒŽ7“úC2018”ND

28.              V‹KŒõ‰ž“šŒ^ƒrƒXƒIƒLƒTƒ]ƒŠƒ“”zˆĘŽq‚ĖŠJ”­iƒ|ƒXƒ^[j
*
’†‘šŒ°“lA‹ß“ĄŸAųˆäG–ūC‘æ38‰ņ—L‹@‡ŽŽáŽčƒZƒ~ƒi[CŠÖžŠw‰@‘åŠw@ž‹{ãƒ–ŒīƒLƒƒƒ“ƒpƒXi•šŒÉjC8ŒŽ7“úC2018”ND

29.              ƒoƒiƒWƒEƒ€G”}‚ðŠˆ—p‚·‚éƒwƒeƒƒwƒŠƒZƒ“‚ĖŒø—Ķ“I‡Žiƒ|ƒXƒ^[j
*
“cX—T‹MAēŒÃ^A‘ęāV”EAųˆäG–ūC‘æ38‰ņ—L‹@‡ŽŽáŽčƒZƒ~ƒi[CŠÖžŠw‰@‘åŠw@ž‹{ãƒ–ŒīƒLƒƒƒ“ƒpƒXi•šŒÉjC8ŒŽ7“úC2018”ND

30.              ƒLƒ‰ƒ‹ƒoƒiƒWƒEƒ€G”}‚ð—p‚Ē‚éŽ_‰ŧ“IƒwƒeƒƒJƒbƒvƒŠƒ“ƒO”―‰ž‚ĖŠJ”­iƒ|ƒXƒ^[j
*
“Œ“cŒbŒÞAēŒÃ^A‘ęāV”EAųˆäG–ūC‘æ38‰ņ—L‹@‡ŽŽáŽčƒZƒ~ƒi[CŠÖžŠw‰@‘åŠw@ž‹{ãƒ–ŒīƒLƒƒƒ“ƒpƒXi•šŒÉjC8ŒŽ7“úC2018”ND

31.              ƒoƒiƒWƒEƒ€G”}‚ðŠˆ—p‚·‚é’PŠÂŽŪƒtƒFƒm[ƒ‹‚Ė•sÄƒJƒbƒvƒŠƒ“ƒO”―‰ž‚ĖŠJ”­iŒû“Šj
*
ēŒÃ^AÂ–؍FŒ›A‘ęāV”EAųˆäG–ūC‘æ‚T‰ņ VŠwp—ĖˆæŒĪ‹†u”―‰žWÏ‰ŧ‚Š“ą‚­’†•ŠŽqí—ŠF‚ŽŸķ•Ļ‹@”\•ŠŽq‚Ė‘nŧvŽáŽčƒVƒ“ƒ|ƒWƒEƒ€CƒV[ƒpƒ‹{–i•šŒÉjC8ŒŽ17“úC2018”ND

32.              ƒLƒ‰ƒ‹ƒoƒiƒWƒEƒ€G”}‚ð—p‚Ē‚éƒwƒeƒƒwƒŠƒZƒ“‚ĖŒø—Ķ“I‡Žiƒ|ƒXƒ^[j
*
“cX—T‹MAēŒÃ^A‘ęāV”EAųˆäG–ūC‘æ48‰ņ@•Ą‘fŠÂ‰ŧŠw“Ē˜_‰ïC’·čƒuƒŠƒbƒNƒz[ƒ‹@‘Û‰ï‹cęi’·čjC9ŒŽ3“ú`9ŒŽ5“úC2018”ND

33.              ƒGƒiƒ“ƒ`ƒI‘I‘ð“Iƒpƒ‰ƒWƒEƒ€2‰ŋ–4‰ŋG”}”―‰ž‚ðŠî”Õ‚Æ‚·‚é“ņŠÂŽŪƒsƒƒŠƒWƒ“—U“ą‘Ė‚Ėƒƒ“ƒ|ƒbƒg‡Žiƒ|ƒXƒ^[j
*
’|’†˜a_ABijan Mohon ChakiALinpeng ZHUAJianfei BaiA‘ęāV”EAųˆäG–ūC‘æ65‰ņ—L‹@‹ā‘Ū‰ŧŠw“Ē˜_‰ïC“ŊŽuŽÐ‘åŠwĄoėZ’n@Žš’ŽƒLƒƒƒ“ƒpƒXi‹ž“sjC9ŒŽ19“ú`9ŒŽ21“úC2018”ND

34.              Pd-SPRIXG”}‚ð—p‚Ē‚éaza-WackerŒ^”―‰ž‚ĖŠJ”­iƒ|ƒXƒ^[j
*Abhijit Sen
A’|’†˜a_AųˆäG–ūC‘æ65‰ņ—L‹@‹ā‘Ū‰ŧŠw“Ē˜_‰ïC“ŊŽuŽÐ‘åŠwĄoėZ’n@Žš’ŽƒLƒƒƒ“ƒpƒXi‹ž“sjC9ŒŽ19“ú`9ŒŽ21“úC2018”ND

35.              ‹ÉŦ“]Š·Œ^ƒ_ƒuƒ‹ƒ}ƒCƒPƒ‹•t‰Á”―‰ž‚É‚æ‚éƒqƒhƒƒCƒ“ƒh[ƒ‹‹y‚Ņƒqƒhƒ•Ų‚žƒtƒ‰ƒ“-2-ƒJƒ‹ƒ{ƒ“Ž_ƒGƒXƒeƒ‹‚Ė‡ŽiŒû“Šj
*
‘ęāV”EAŠÝ“S”nAųˆäG–ūC‘æ44‰ņ”―‰ž‚ƍ‡Ž‚Ėi•āƒVƒ“ƒ|ƒWƒEƒ€|ƒ‰ƒCƒtƒTƒCƒGƒ“ƒX‚ðŽuŒü‚ĩ‚―—˜_A”―‰ž‚Ļ‚æ‚Ņ‡Ž|CŽs–Ŋ‰ïŠŲƒVƒA[ƒYƒz[ƒ€–ēƒz[ƒ‹iŒF–{jC11ŒŽ5“ú`6“úC2018”ND

36.              ƒIƒLƒ\ƒƒ^ƒ‹’†S‚ĖƒLƒ‰ƒŠƒeƒB[§Œä‚ƏWÏ‰ŧ‚ðŠî”Õ‚Æ‚·‚é‘―‹@”\•sÄG”}‚Ė‘nŧiŒû“Šj
*
‘ęāV”ECVŠwp—ĖˆæŒĪ‹†u”zˆĘƒAƒVƒ“ƒƒgƒŠ[v‘æ‚S‰ņ—Ėˆæ‘S‘Ė‰ï‹cC‹ā‘ōĪH‰ï‹cŠ‰ïŠŲiÎėjC11ŒŽ29“ú`11ŒŽ30“úC2018”ND

37.              ‹ÉŦ“]Š·Œ^•sÄG”}”―‰ž‚É‚æ‚éƒLƒ‰ƒ‹‘æŽl‹‰’Y‘f‚Ė\’ziƒ|ƒXƒ^[j
*
‰Ô’J—D‘ū˜NA‹ß“ĄŒ’A‘ęāV”EAųˆäG–ūC‘æ11 ‰ņ—L‹@G”}ƒVƒ“ƒ|ƒWƒEƒ€CŠwK‰@‘n—§•SŽü”N‹L”O‰ïŠŲi“Œ‹žjC12ŒŽ3“ú`12ŒŽ4“úC2018”N



<International>

1.  Catalytic Enantioselective Sequential C-C Bond Forming Reactions in Flow System (Poster)
*Wathsala, H. D. P.; Kishi, K.; Chen, Q.; Sako, M.; Takizawa, S.; Sasai, H.  21st SANKEN International Symposium/16th SANKEN Nanotechnology International Symposium/5th Kansai Nanoscience and Nanotechnology International Symposium/13th Handai Nanoscience and Nanotechnology International Symposium, Osaka, Japan, January 16-17, 2018.

2.  Enantioselective Synthesis of Bicyclic Pyrrolidine Derivatives via One-pot Sequential Organo- and Pd-Catalysis (Poster)
*Chaki, B. M.; Bai, J.; Takenaka, K.; Takizawa, S.; Sasai, H. 21st SANKEN International Symposium/16th SANKEN Nanotechnology International Symposium/5th Kansai Nanoscience and Nanotechnology International Symposium/13th Handai Nanoscience and Nanotechnology International Symposium, Osaka, Japan, January 16-17, 2018.

3.  Catalytic Enantioselective Sequential C-C Bond Forming Reactions in Flow System (Poster)
*Wathsala, H. D. P.; Kishi K.; Chen, Q.; Takizawa, S.; Sasai, H. The First International Conference on Automated Flow and Microreactor Synthesis (ICAMS-1), Osaka, Japan, January 18-20, 2018.

4.  Vanadium Complex-catalyzed Enantioselective Synthesis of Oxa[9]helicenes (Poster)
*Sako, M.; Takizawa, S.; Sasai, H. IRCCS-JST CREST Joint Symposium, Fukuoka, Japan, January 24-26, 2018.

5.  Enantioselective CC Bond Forming Reactions Catalyzed by a Vanadium Complex (Poster)
Sako, M.; Aoki, T.; Sugizaki, A.; *Tamori, Y.; Takizawa, S.; Sasai, H. IRCCS-JST CREST Joint Symposium, Fukuoka, Japan, January 24-26, 2018

6.  Facile Synthesis of Spirooxindoles via Enantioselective Double Michael Reaction (Poster)
*Kusaba, M.; Kishi, K.; Takizawa, S.; Bai, J.; Sasai, H. Biotechnology and Chemistry for Green Growth (JSPS Japanese-German Graduate Externship Program), Awaji Island, Japan, March 13-14, 2018.

7.  Catalytic and Enantioselective Sequential Reaction in Flow System (Poster)
* Wathsala, H. D. P.; Kishi, K.; Chen, Q.; Sako, M.; Takizawa, S.; Sasai, H. Biotechnology and Chemistry for Green Growth (JSPS Japanese-German Graduate Externship Program), Awaji Island, Japan, March 13-14, 2018.

8.  Enantioselective Synthesis of Bicyclic Pyrrolidine Derivatives via One-Pot Organo and Palladium Catalysis (Poster)
*Chaki, B. M.; Bai, J.; Takenaka, K.; Takizawa, S.; Sasai, H. Biotechnology and Chemistry for Green Growth (JSPS Japanese-German Graduate Externship Program), Awaji Island, Japan, March 13-14, 2018.

9.  Chiral Vanadium Complex-catalyzed Enantioselective Oxidative Coupling Reactions of Polycyclic Phenol (Poster)
*Sugizaki, A.; Sako, M.; Takizawa, S.; Sasai, H. Biotechnology and Chemistry for Green Growth (JSPS Japanese-German Graduate Externship Program), Awaji Island, Japan, March 13-14, 2018.

10.              Chiral Dinuclear Vanadium Complex-mediated Oxidative Coupling of Monocyclic Phenols (Oral)
*Sako, M.; Aoki, T.; Takizawa, S.; Sasai, H. 43rd International Conference on Coordination Chemistry (ICCC 2018), Sendai, Japan, July 30
August 4, 2018.

11.              Enantioselective Oxidative C-H/C-H Coupling Catalyzed by Chiral Dinuclear Vanadium(V) Complex (Poster)
*Sako, M.; Aoki, T.; Takizawa, S.; Sasai, H. The 4th International Symposium on C-H Activation (ISCHA4), Kanagawa, Japan, August 30
September 2, 2018.
<Poster AwardŽóÜ>

12.              Enantioselective Synthesis of Tetrahydrocyclopenta[b]indole Bearing a Chiral Quaternary Carbon Center via Pd(II)-SPRIX-catalyzed C-H Activation (Poster)
*Takizawa, S.; Abozeid, M. A.; Sasai, H. The 4th International Symposium on C-H Activation (ISCHA4), Kanagawa, Japan, August 30
September 2, 2018.

13.              Chiral Catalyzed Domino Reactions (Poster)
*Kusaba, M.; Wathsala, H. D. P.; Sako, M.; Kishi, K.; Takizawa, S.; Sasai, H. Biotechnology and Chemistry for Green Growth (JSPS Japanese-German Graduate Externship Program), Awaji Island, Japan, September 10-11, 2018.

14.              Vanadium(V) Complex-catalyzed Oxidative Hetero-coupling Reactions (Poster)
*Jiang, Y.; Sako, M.; Takizawa, S.; Sasai, H. Biotechnology and Chemistry for Green Growth (JSPS Japanese-German Graduate Externship Program), Awaji Island, Japan, September 10-11, 2018.

15.              Chiral Dinuclear Vanadium Complex-mediated Oxidative Coupling of Phenols (Poster)
*Sako, M.; Aoki, T.; Takizawa, S.; Sasai, H.
The 14th International Kyoto Conference on New Aspects of Organic Chemistry (IKCOC-14), Kyoto, Japan, November 12-16, 2018.

16.              Enantioselective Synthesis of Bicyclic Pyrrolidine Derivatives via One-Pot Sequential Organo and Palladium Catalysis (Poster)
Chaki, B. M.; *Zhu, L.; Takenaka, K.; Bai, J.; Takizawa, S.; Sasai, H. The 14th International Kyoto Conference on New Aspects of Organic Chemistry (IKCOC-14), Kyoto, Japan, November 12-16, 2018.

17.              Catalytic Enantioselective Sequential C-C Bond Forming Reactions in Flow System (Poster)
*Wathsala, H. D. P.; Sako, M.; Kishi, K.; Takizawa, S.; Sasai, H. The 14th International Kyoto Conference on New Aspects of Organic Chemistry (IKCOC-14), Kyoto, Japan, November 12-16, 2018.

18.              Facile Synthesis of Spirooxindoles via Enantioselective Double Michael Reaction (Poster)
*Kusaba, M.; Kishi, K.; Bai, J.; Takizawa, S.; Sasai, H. The 14th International Kyoto Conference on New Aspects of Organic Chemistry (IKCOC-14), Kyoto, Japan, November 12-16, 2018.

19.              Catalytic Cyclative Hydroamination Based on Palladium Enolate Umpolung (Poster)
Nomoto, Y.; *Kusaba, M.; Takenaka, K.; Sasai, H. International Research Training Group
gSELECTIVITY IN CHEMO- AND BIOCATALYSISh FINAL AACHEM-OSAKA SYMPOSIUM, Aachen, Germany, November 26-27, 2018.

TopŠ

 

2017@🐓

<Domestic>

1.  ‰EŽčŒn‚Ė‰ŧ‡•Ļ‚ū‚Ŋ‚ð‡Ž‚·‚é•û–@ `ŒõŠwŠˆŦ‰ŧ‡•Ļ‚Ė“­‚Ŧ`iĩ‘Ōj
*
ųˆäG–ūCƒtƒ@ƒCƒ“ƒPƒ~ƒJƒ‹ƒYŒĪ‹†‰ïCKKRƒzƒeƒ‹‘åãi‘åãjC3ŒŽ2“úC2017”ND

2.  Enantioselective aza-Wacker Reaction Promoted by Pd-SPRIXiŒû“Šj
*Abhijit Sen
A’|’†˜a_AųˆäG–ūC“ú–{‰ŧŠw‰ï‘æ97t‹G”N‰ïCŒcœä‘åŠwi_“ސėjC3ŒŽ16`19“úC2017”ND

3.  Pd(II)-SPRIX Catalyzed Enantioselective Annulation of Alkenylindoles: Allyl Group Assisted Construction of Quaternary Carbon CenteriŒû“Šj
*Mohamed A. Abozeid
A‘ęāV”EA’|’†˜a_AųˆäG–ūC“ú–{‰ŧŠw‰ï‘æ97t‹G”N‰ïCŒcœä‘åŠwi_“ސėjC3ŒŽ16`19“úC2017”ND

4.  Development of Novel Spiro-type Chiral Ligands Bearing Pyrazole DonorsiŒû“Šj
*
dM‹§ŽuA’|’†˜a_AųˆäG–ūC“ú–{‰ŧŠw‰ï‘æ97t‹G”N‰ïCŒcœä‘åŠwi_“ސėjC3ŒŽ16`19“úC2017”ND

5.  Synthetic Study of Sorazolon E2 Using Chiral Vanadium CatalystiŒû“Šj
*
ˆę”VĢ˜a–íAēŒÃ^A‘ęāV”EAųˆäG–ūC“ú–{‰ŧŠw‰ï‘æ97t‹G”N‰ïCŒcœä‘åŠwi_“ސėjC3ŒŽ16`19“úC2017”ND

6.  Facile Synthesis of Spirooxindoles via an Enantioselective Organocatalyzed Sequential Reaction of Oxindole Derivatives with YnonesiŒû“Šj
*
‘ę–Ē—ˆAŠÝ“S”nAJianfei BaiA‘ęāV”EAųˆäG–ūC“ú–{‰ŧŠw‰ï‘æ97t‹G”N‰ïCŒcœä‘åŠwi_“ސėjC3ŒŽ16`19“úC2017”ND

7.  Enantioselective Synthesis of Bicyclic Pyrrolidine Derivatives via Sequential Organo- and Pd-CatalysisiŒû“Šj
*Bijan M. Chaki
AJianfei BaiA’|’†˜a_A‘ęāV”EAųˆäG–ūC“ú–{‰ŧŠw‰ï‘æ97t‹G”N‰ïCŒcœä‘åŠwi_“ސėjC3ŒŽ16`19“úC2017”ND

8.  Development of Enantioselective Reactions Using Fe CatalystsiŒû“Šj
*
•ÄŽRSAV‹“c‹ąÍA’|’†˜a_A‘ęāV”EAųˆäG–ūC“ú–{‰ŧŠw‰ï‘æ97t‹G”N‰ïCŒcœä‘åŠwi_“ސėjC3ŒŽ16`19“úC2017”ND

9.  ƒŋ-Functionalization of Carbonyl Compounds Based on Palladium Enolate UmpolungiŒû“Šj
*
–ė–{—T–įAāV“c˜a–íA’|’†˜a_AųˆäG–ūC“ú–{‰ŧŠw‰ï‘æ97t‹G”N‰ïCŒcœä‘åŠwi_“ސėjC3ŒŽ16`19“úC2017”ND

10.              Phosphine-Catalyzed Umpolung Tandem Michael Addition of Alkynyl EsteriŒû“Šj
*
ŠÝ“S”nA‘ęāV”EA‘ę–Ē—ˆAųˆäG–ūC“ú–{‰ŧŠw‰ï‘æ97t‹G”N‰ïCŒcœä‘åŠwi_“ސėjC3ŒŽ16`19“úC2017”ND

11.              Chiral Vanadium (V) Complex-catalyzed Enantioselective C-C Bond Forming Reactions (1)iŒû“Šj
*
ēŒÃ^A™›―WŦA‘ęāV”EAųˆäG–ūC“ú–{‰ŧŠw‰ï‘æ97t‹G”N‰ïCŒcœä‘åŠwi_“ސėjC3ŒŽ16`19“úC2017”ND

12.              Chiral Vanadium (V) Complex-catalyzed Enantioselective C-C Bond Forming Reactions (2)iŒû“Šj
*
Â–؍FŒ›A‘ęāV”EAēŒÃ^AųˆäG–ūC“ú–{‰ŧŠw‰ï‘æ97t‹G”N‰ïCŒcœä‘åŠwi_“ސėjC3ŒŽ16`19“úC2017”ND

13.              ƒJƒ‹ƒoƒ][ƒ‹—U“ą‘Ė‚ĖƒGƒiƒ“ƒ`ƒI‘I‘ð“IŽ_‰ŧƒJƒbƒvƒŠƒ“ƒO”―‰ž‚ĖŠJ”­‚Ɖž—piƒ|ƒXƒ^[j
*
ēŒÃ^Aˆę”VĢ˜a–íA‘ęāV”EAųˆäG–ūC‘æ111‰ņ—L‹@‡ŽƒVƒ“ƒ|ƒWƒEƒ€C‰ŠŽR‘åŠw‘n—§ŒÜ\Žü”N‹L”OŠŲi‰ŠŽRjC6ŒŽ8`9“úC2017”ND

14.              ƒGƒiƒ“ƒ`ƒI‘I‘ð“Iƒhƒ~ƒm”―‰ž‚É‚æ‚éƒXƒsƒƒIƒLƒVƒCƒ“ƒh[ƒ‹—U“ą‘Ė‡Žiƒ|ƒXƒ^[j
*
‘ę–Ē—ˆAŠÝ“S”nA‘ęāV”EABai JianfeiAųˆäG–ūC‘æ111‰ņ—L‹@‡ŽƒVƒ“ƒ|ƒWƒEƒ€C‰ŠŽR‘åŠw‘n—§ŒÜ\Žü”N‹L”OŠŲi‰ŠŽRjC6ŒŽ8`9“úC2017”ND

15.              ƒpƒ‰ƒWƒEƒ€ƒGƒmƒ‰[ƒg‚Ė‹ÉŦ“]Š·‚ð—˜—p‚·‚é‘―ŠŊ”\ŦƒJƒ‹ƒ{ƒjƒ‹‰ŧ‡•Ļ‚ĖŒø—Ķ‡Žiƒ|ƒXƒ^[j
*
–ė–{—T–įA’|’†˜a_AāV“c˜a–íASuman C. MohantaAųˆäG–ūC‘æ111‰ņ—L‹@‡ŽƒVƒ“ƒ|ƒWƒEƒ€C‰ŠŽR‘åŠw‘n—§ŒÜ\Žü”N‹L”OŠŲi‰ŠŽRjC6ŒŽ8`9“úC2017”ND

16.              Ž_‘f‚ð‹ĪŽ_‰ŧÜ‚Æ‚·‚éƒJƒ‹ƒoƒ][ƒ‹‚Ė•sÄƒJƒbƒvƒŠƒ“ƒO”―‰ž‚ĖŠJ”­iƒ|ƒXƒ^[j
*
ēŒÃ^A‘ęāV”EAųˆäG–ūC‘æ6‰ņ JACI/GSCƒVƒ“ƒ|ƒWƒEƒ€C“Œ‹ž‘ÛƒtƒH[ƒ‰ƒ€i“Œ‹žjC7ŒŽ3`4“úC2017”ND
<—DGƒ|ƒXƒ^[ÜŽóÜ>

17.              ƒŒƒhƒbƒNƒXEŽ_‹Ķ“ŊG”}‚ðŠˆ—p‚·‚éƒIƒLƒTƒwƒŠƒZƒ“‚ĖŒø—Ķ“I‚ČƒGƒiƒ“ƒ`ƒI‘I‘ð“I‡Žiƒ|ƒXƒ^[j
ēŒÃ^A*‘ęāV”EAųˆäG–ūC‘æ6‰ņ JACI/GSCƒVƒ“ƒ|ƒWƒEƒ€C“Œ‹ž‘ÛƒtƒH[ƒ‰ƒ€i“Œ‹žjC7ŒŽ3`4“úC2017”ND

18.              Development of Asymmetric Umpolung Tandem Michael Addition iŒû“Šj
–ŠÝ“S”nC‘æ3‰ņ–ėˆËƒtƒH[ƒ‰ƒ€ŽáŽčˆįŽmC–žŒÃ‰Ū‘åŠw@–ėˆË‹L”O•ĻŽŋ‰ŧŠwŒĪ‹†ŠŲiˆĪ’mjC7ŒŽ20`21“úC2017”ND

19.              ƒLƒ‰ƒ‹‚ČƒoƒiƒWƒEƒ€G”}‚ð—p‚Ē‚éƒqƒhƒƒLƒVƒJƒ‹ƒoƒ][ƒ‹—Þ‚Ė•sÄŽ_‰ŧƒJƒbƒvƒŠƒ“ƒO”―‰ž‚ĖŠJ”­iƒ|ƒXƒ^[j
*
ēŒÃ^A‘ęāV”EAųˆäG–ūC“ú–{ƒvƒƒZƒX‰ŧŠw‰ï2017ƒTƒ}[ƒVƒ“ƒ|ƒWƒEƒ€C‘åã‘ÛŒð—ŽƒZƒ“ƒ^[i‘åãjC8ŒŽ3`4“úC2017”ND

20.              Enantioselective Aza-Wacker-Type Reaction Promoted by Pd-SPRIX Catalystiƒ|ƒXƒ^[j
*Abhijit Sen
A’|’†˜a_AųˆäG–ūC“ú–{ƒvƒƒZƒX‰ŧŠw‰ï2017ƒTƒ}[ƒVƒ“ƒ|ƒWƒEƒ€C‘åã‘ÛŒð—ŽƒZƒ“ƒ^[i‘åãjC8ŒŽ3`4“úC2017”ND

21.              ƒoƒiƒWƒEƒ€G”}‚ð—p‚Ē‚éƒtƒFƒm[ƒ‹—Þ‚ĖŽ_‰ŧ“I•sÄƒJƒbƒvƒŠƒ“ƒO”―‰žiƒ|ƒXƒ^[j
*
Â–؍FŒ›AēŒÃ^A‘ęāV”EAųˆäG–ūC“ú–{ƒvƒƒZƒX‰ŧŠw‰ï2017ƒTƒ}[ƒVƒ“ƒ|ƒWƒEƒ€C‘åã‘ÛŒð—ŽƒZƒ“ƒ^[i‘åãjC8ŒŽ3`4“úC2017”ND

22.              ƒŋ-ƒAƒ~ƒmƒJƒ‹ƒ{ƒjƒ‹‰ŧ‡•Ļ‚ð—^‚Ķ‚éƒpƒ‰ƒWƒEƒ€ƒGƒmƒ‰[ƒg‚Ė‹ÉŦ“]Š·Œ^‹Šj“IƒAƒ~ƒm‰ŧ”―‰ž‚ĖŠJ”­iƒ|ƒXƒ^[j
*
–ė–{—T–įA’|’†˜a_AųˆäG–ūC“ú–{ƒvƒƒZƒX‰ŧŠw‰ï2017ƒTƒ}[ƒVƒ“ƒ|ƒWƒEƒ€C‘åã‘ÛŒð—ŽƒZƒ“ƒ^[i‘åãjC8ŒŽ3`4“úC2017”ND

23.              ƒwƒŠƒZƒ“œŠi‚ðŽ‚Â—L‹@•ŠŽqG”}‹y‚Ņ•sÄ”zˆĘŽq‚Ė‡ŽŒĪ‹†iƒ|ƒXƒ^[j
*
“cX—T‹MAēŒÃ^A‘ęāV”EAųˆäG–ūC‘æ37‰ņ—L‹@‡ŽŽáŽčƒZƒ~ƒi[C“ŊŽuŽÐ‘åŠwŽš’ŽƒLƒƒƒ“ƒpƒXi‹ž“sjC8ŒŽ9“úC2017”ND

24.              Pd-SPRIXG”}‚ð—p‚Ē‚éƒGƒiƒ“ƒ`ƒI‘I‘ð“I•ŠŽq“āaza-WackerŒ^ŠÂ‰ŧ”―‰žiƒ|ƒXƒ^[j
Sen Abhijit
A*•Ð‰Šq—CA’|’†˜a_AųˆäG–ūC‘æ37‰ņ—L‹@‡ŽŽáŽčƒZƒ~ƒi[C“ŊŽuŽÐ‘åŠwŽš’ŽƒLƒƒƒ“ƒpƒXi‹ž“sjC8ŒŽ9“úC2017”ND

25.              “ņŠjƒoƒiƒWƒEƒ€G”}‚ð—p‚Ē‚é’PŠÂŽŪƒtƒFƒm[ƒ‹—U“ą‘Ė‚ĖŽ_‰ŧ“I•sÄƒJƒbƒvƒŠƒ“ƒO”―‰žiƒ|ƒXƒ^[j
*
Â–؍FŒ›AēŒÃ^A‘ęāV”EAųˆäG–ūC‘æ37‰ņ—L‹@‡ŽŽáŽčƒZƒ~ƒi[C“ŊŽuŽÐ‘åŠwŽš’ŽƒLƒƒƒ“ƒpƒXi‹ž“sjC8ŒŽ9“úC2017”ND
<—DGƒ|ƒXƒ^[ÜŽóÜ>

26.              IrG”}‚ð—p‚Ē‚郁ƒ\Œ^ƒWƒI[ƒ‹‚ƃAƒ‹ƒfƒqƒh‚Ė•sÄƒ^ƒ“ƒfƒ€ƒJƒbƒvƒŠƒ“ƒO”―‰žiƒ|ƒXƒ^[j
—é–ØŒ’”VA*‘Ŧ—§—S‹MAųˆäG–ūC‘æ37‰ņ—L‹@‡ŽŽáŽčƒZƒ~ƒi[C“ŊŽuŽÐ‘åŠwŽš’ŽƒLƒƒƒ“ƒpƒXi‹ž“sjC8ŒŽ9“úC2017”ND

27.              ƒJƒ‹ƒoƒ][ƒ‹—U“ą‘Ė‚ĖƒGƒiƒ“ƒ`ƒI‘I‘ð“IƒJƒbƒvƒŠƒ“ƒO”―‰ž‚ĖŠJ”­‚Ɖž—piŒû“Šj
*
ēŒÃ^A‘ęāV”EAųˆäG–ūC‘æŽl‰ņ@VŠwp—ĖˆæŒĪ‹†u”―‰žWÏ‰ŧ‚Š“ą‚­’†•ŠŽqí—ŠF‚ŽŸķ•Ļ‹@”\•ŠŽq‚Ė‘nŧvŽáŽčƒVƒ“ƒ|ƒWƒEƒ€CH•ÛƒŠƒ][ƒg@ƒzƒeƒ‹ƒNƒŒƒZƒ“ƒgi‹{éjC8ŒŽ18`19“úC2017”ND

28.              Development of Catalytic Synthetic Method for ƒŋ-Amino Carbonyl Compounds Based on Palladium Enolate Umpolungiƒ|ƒXƒ^[j
*
’|’†˜a_A–ė–{—T–įAųˆäG–ūC‘æ64‰ņ—L‹@‹ā‘Ū‰ŧŠw“Ē˜_‰ïC“Œ–k‘åŠwė“āƒLƒƒƒ“ƒpƒXi‹{éjC9ŒŽ7`9“úC2017”ND

29.              Chiral Vanadium(V) Complex-catalyzed Enantioselective Oxidative Coupling of Phenol DerivativesiŒû“Šj
*
ēŒÃ^AÂ–؍FŒ›A‘ęāV”EAųˆäG–ūC‘æ64‰ņ—L‹@‹ā‘Ū‰ŧŠw“Ē˜_‰ïC“Œ–k‘åŠwė“āƒLƒƒƒ“ƒpƒXi‹{éjC9ŒŽ7`9“úC2017”ND

30.              Enantioselective aza-Wacker-Type Reaction Promoted by Pd-SPRIX Catalystiƒ|ƒXƒ^[j
*Sen Abhijit
A’|’†˜a_AųˆäG–ūC‘æ34‰ņ—L‹@‡Ž‰ŧŠwƒZƒ~ƒi[C‹ā‘ōŽs•ķ‰ŧƒz[ƒ‹iÎėjC9ŒŽ12`14“úC2017”ND

31.              ƒLƒ‰ƒ‹‚ČƒoƒiƒWƒEƒ€G”}‚ð—p‚Ē‚é’PŠÂŽŪƒtƒFƒm[ƒ‹—Þ‚ĖŽ_‰ŧ“I•sÄƒJƒbƒvƒŠƒ“ƒO”―‰žiƒ|ƒXƒ^[j
*
Â–؍FŒ›AēŒÃ^A‘ęāV”EAųˆäG–ūC‘æ34‰ņ—L‹@‡Ž‰ŧŠwƒZƒ~ƒi[C‹ā‘ōŽs•ķ‰ŧƒz[ƒ‹iÎėjC9ŒŽ12`14“úC2017”ND

32.              ƒAƒ‹ƒLƒjƒ‹ƒGƒXƒeƒ‹‚Ė‹ÉŦ“]Š·Œ^ƒ^ƒ“ƒfƒ€ƒ}ƒCƒPƒ‹•t‰Á‚É‚æ‚é•Ą‘fŠÂ‰ŧ‡•Ļ‚Ė‡Žiƒ|ƒXƒ^[j
*
ŠÝ“S”nA‘ęāV”EA‘ę–Ē—ˆAųˆäG–ūC‘æ34‰ņ—L‹@‡Ž‰ŧŠwƒZƒ~ƒi[C‹ā‘ōŽs•ķ‰ŧƒz[ƒ‹iÎėjC9ŒŽ12`14“úC2017”ND

33.              “ņdŠˆŦ‰ŧŒ^•sÄG”}‚Ė‘nŧi“Á•Ęu‰‰j
*
ųˆäG–ūC•―Ž29”N“x—L‹@‡Ž‰ŧŠw–k—ĪƒZƒ~ƒi[C‚܂‚âįįi•ŸˆäjC10ŒŽ6`7“úC2017”ND

34.              ƒoƒiƒWƒEƒ€ö‘Ė‚ðG”}‚Æ‚·‚é‘―ŠÂŽŪ•Ą‘fŠÂ‚ĖŽ_‰ŧ“I•sÄƒJƒbƒvƒŠƒ“ƒO”―‰ž‚ĖŠJ”­iƒ|ƒXƒ^[j
*
™›―WŦAēŒÃ^A‘ęāV”EAųˆäG–ūC•―Ž29”N“x—L‹@‡Ž‰ŧŠw–k—ĪƒZƒ~ƒi[C‚܂‚âįįi•ŸˆäjC10ŒŽ6`7“úC2017”ND

35.              ‚P,3-ƒVƒX-ƒCƒ\ƒCƒ“ƒhƒŠƒ“‰ŧ‡•Ļ‚ĖƒGƒiƒ“ƒ`ƒI‘I‘ð“Iƒƒ“ƒ|ƒbƒg‡Žiƒ|ƒXƒ^[j
*
‘ëÎ•ü‘åAH. D. P. WathsalaAŠÝ“S”nAMohamed Ahmed AbozeidA•―“cCˆęAēŒÃ^A‘šˆäŒ’ˆęA“Ą‰ŠO“đA‘ęāV”EAųˆäG–ūC•―Ž29”N“x—L‹@‡Ž‰ŧŠw–k—ĪƒZƒ~ƒi[C‚܂‚âįįi•ŸˆäjC10ŒŽ6`7“úC2017”ND

36.              ƒAƒ~ƒh‰ŧ/Rauhut-Currier ˜A‘ą”―‰ž‚É‚æ‚é ƒŋ-ƒƒ`ƒŠƒfƒ“-ƒÁ-ƒ‰ƒNƒ^ƒ€‚ĖG”}“I•sÄ‡ŽiŒû“Šj
*
ŠÝ“S”nAFernando Arteaga-ArteagaA‘ęāV”EAųˆäG–ūC‘æ67‰ņ“ú–{–ōŠw‰ï‹ß‹EŽx•”‘‰ïE‘å‰ïC•šŒÉˆã—ÑåŠwi•šŒÉjC10ŒŽ14“úC2017”ND

37.              ’PŠÂŽŪƒtƒFƒm[ƒ‹—U“ą‘Ė‚ĖŽ_‰ŧ“I•sÄƒJƒbƒvƒŠƒ“ƒO”―‰ž\ƒLƒ‰ƒ‹ƒoƒiƒWƒEƒ€G”}‚ð—p‚Ē‚éŠÂ‹Ŧ’ᕉ‰ŨŒ^‡Ž–@\iŒû“Šj
*
‘ęāV”EAÂ–؍FŒ›AēŒÃ^AųˆäG–ūC‘æ67‰ņ“ú–{–ōŠw‰ï‹ß‹EŽx•”‘‰ïE‘å‰ïC•šŒÉˆã—ÑåŠwi•šŒÉjC10ŒŽ14“úC2017”ND

38.              ƒoƒiƒWƒEƒ€G”}‚ð—p‚Ē‚é•sÄŽ_‰ŧ“IƒJƒbƒvƒŠƒ“ƒO”―‰ž‚ĖŠJ”­‚Ɖž—piŒû“Šj
*
ēŒÃ^A‘ęāV”EAųˆäG–ūC‘æ47‰ņ•Ą‘fŠÂ‰ŧŠw“Ē˜_‰ïC‚’mŒ§—§Œ§–Ŋ•ķ‰ŧƒz[ƒ‹i‚’mjC10ŒŽ26`28“úC2017”ND

39.              ‘―ŠÂŽŪƒtƒFƒm[ƒ‹‚ĖŽ_‰ŧƒJƒbƒvƒŠƒ“ƒO”―‰ž‚ðŠî”Õ‚Æ‚·‚é–F‘°•Ą‘fŠÂ‰ŧ‡•Ļ‚ĖG”}“I•sÄ‡Žiƒ|ƒXƒ^[j
*
‘ęāV”EAēŒÃ^Aˆę”VĢ˜a–íA’ŌŒī“N–įA‰Í–ė•xˆęAųˆäG–ūC‘æ43‰ņ”―‰ž‚ƍ‡Ž‚Ėi•āƒVƒ“ƒ|ƒWƒEƒ€\ƒ‰ƒCƒtƒTƒCƒGƒ“ƒX‚ðŽwŒü‚ĩ‚―—˜_C”―‰ž‹y‚Ņ‡Ž\C•xŽR‘Û‰ï‹cęi•xŽRjC11ŒŽ6`7“úC2017”ND

40.              ƒGƒiƒ“ƒ`ƒI‹y‚ŅƒWƒAƒXƒeƒŒƒI‘I‘ð“IBetti/aza-Michael˜A‘ą”―‰ž‚ĖŠJ”­‚Æ1,3-“ņ’uŠ·ƒCƒ\ƒCƒ“ƒhƒŠƒ“œŠi\’z‚Ö‚Ė‰ž—piƒ|ƒXƒ^[j
‘ęāV”EA‘šˆäŒ’ˆęA*H. D. P. WathsalaAēŒÃ^AŠÝ“S”nA•―“cCˆęA“Ą‰ŠO“đAųˆäG–ūC‘æ43‰ņ”―‰ž‚ƍ‡Ž‚Ėi•āƒVƒ“ƒ|ƒWƒEƒ€\ƒ‰ƒCƒtƒTƒCƒGƒ“ƒX‚ðŽwŒü‚ĩ‚―—˜_C”―‰ž‹y‚Ņ‡Ž\C•xŽR‘Û‰ï‹cęi•xŽRjC11ŒŽ6`7“úC2017”ND

41.              ƒzƒXƒtƒBƒ“G”}‚É‚æ‚é‹ÉŦ“]Š·Œ^ƒ_ƒuƒ‹ƒ}ƒCƒPƒ‹•t‰Á”―‰ž‚ðŠˆ—p‚·‚éƒqƒhƒƒCƒ“ƒh[ƒ‹‹y‚Ņƒqƒhƒƒxƒ“ƒ]ƒtƒ‰ƒ“-2-ƒJƒ‹ƒ{ƒ“Ž_ƒGƒXƒeƒ‹‚Ė‡Žiƒ|ƒXƒ^[j
*
ŠÝ“S”nA‘ęāV”EAųˆäG–ūC‘æ10‰ņ—L‹@G”}ƒVƒ“ƒ|ƒWƒEƒ€C“Œ–k‘åŠw‘åŠw‰@—ŠwŒĪ‹†‰Č‘åu‹`Žši‹{éjC11ŒŽ30“ú`12ŒŽ1“úC2017”ND

 

<International>

1.  Vanadium(V) Complex-Catalyzed Enantioselective CC Bond Forming Reactions (Poster)
*Sako, M.; Takizawa, S.; Sasai, H. Biotechnology and Chemistry for Green Growth (JSPS Japanese-German Graduate Externship Program), Awaji Island, Japan, March 6-7, 2017.

2.  Development of Novel Spiro-Type Chiral Ligands Bearing Pyrazole Donors (Poster)
*Shigenobu, M.; Takenaka, K.; Sasai, H. Biotechnology and Chemistry for Green Growth (JSPS Japanese-German Graduate Externship Program), Awaji Island, Japan, March 6-7, 2017.

3.  Phosphine-Catalyzed Umpolung Tandem Michael Addition of Alkynylester (Poster)
*Kishi, K.; Takizawa, S.; Kusaba, M.; Sasai, H. Biotechnology and Chemistry for Green Growth (JSPS Japanese-German Graduate Externship Program), Awaji Island, Japan, March 6-7, 2017.

4.  Enantioselective Aza-Wacker Reaction Promoted by Pd-SPRIX Catalyst (Poster)
*Sen, A.; Takenaka, K.; Sasai, H. Biotechnology and Chemistry for Green Growth (JSPS Japanese-German Graduate Externship Program), Awaji Island, Japan, March 6-7, 2017.

5.  Chiral Iron Catalysts Bearing SPRIX Ligand (Poster)
*Niida, Y.; Takenaka, K.; Takizawa, S.; Sasai, H. Biotechnology and Chemistry for Green Growth (JSPS Japanese-German Graduate Externship Program), Awaji Island, Japan, March 6-7, 2017.

6.  Oxidative Coupling of Polycyclic Phenols Promoted by a Chiral Vanadium Catalyst (Oral)
*Sasai, H. International Symposium on Green Chemistry 2017 (ISGC-2017), La Rochelle, France, May 16-19, 2017.

7.  Vanadium(V) Complex-catalyzed Enantioselective C-C Bond Forming Reactions (Poster)
*Sako, M.; Takizawa, S.; Sasai, H. the 19th IUPAC International Symposium on Organometallic Chemistry Directed Towards Organic Synthesis (OMCOS 19), Jeju, Korea, June 25-29, 2017.

8.  Oxidative Coupling of Polycyclic Phenols Promoted by Chiral Vanadium Catalysts (Invited)
*Sasai, H. Chirality 2017, Tokyo, Japan, July 9-12, 2017.

9.  Enantioselective Synthesis of Highly Functionalized Heterocycles via the Chiral Phosphine-catalyzed Domino Reaction (Poster)
*Takizawa, S.; Kishi, K.; Kusaba, M.; Sasai, H. Chirality 2017, Tokyo, Japan, July 9-12, 2017.

10.              Vanadium(V) Complex-catalyzed Enantioselective Oxidative Coupling of Monocyclic Phenol Derivatives (Poster)
*Aoki, T.; Sako, M.; Takizawa, S.; Sasai, H. Chirality 2017, Tokyo, Japan, July 9-12, 2017.

11.              Enantioselective Aza-Wacker-Type Reaction Promoted by Pd-SPRIX Catalyst (Poster)
*Sen, A.; Takenaka, K.; Sasai, H. Chirality 2017, Tokyo, Japan, July 9-12, 2017.

12.              Highly Enantioselective Oxidative Coupling of Polycyclic Phenols Using a Chiral Vanadium(V) Catalyst (Invited)
*Sasai. H. The 5th International Conference on Catalysis, Guilin, China, August 23-25, 2017.

13.              Oxidative Coupling of Phenol Derivatives Catalyzed by a Chiral Vanadium(V) Complex (Oral)
*Sasai, H. RWTH Aachen Univ.-Osaka Univ. Joint Symposium, Aachen, Germany, September 19-21, 2017.

14.              Enantioselective Synthesis of ƒŋ-Methylidene-ƒÁ-Lactams via Amidation and Rauhut-Currier Reaction Sequence (Poster)
*Takizawa, S.; Kishi, K.; Sasai, H. The 11th International Symposium on Integrated Synthesis (ISONIS-11), The 3rd International Symposium on Middle Molecular Strategy (ISMMS-3), Awaji Island, Japan, November 15-17, 2017.

15.              Enantioselective Aza-Wacker-Type Reaction Promoted by Pd-SPRIX Catalyst (Poster)
*Sen, A.; Takenaka, K.; Sasai, H. The 11th International Symposium on Integrated Synthesis (ISONIS-11), The 3rd International Symposium on Middle Molecular Strategy (ISMMS-3), Awaji Island, Japan, November 15-17, 2017.

TopŠ

 

2016@🐵

<Domestic>

1.  ƒGƒiƒ“ƒ`ƒI‘I‘ð“I”ņ‘ΏĖ‰ŧ‚ðŠî”Õ‚Æ‚·‚é“ņ˜A‘ą•sÄ’Y‘f‚ð—L‚·‚é•Ą‘fŠÂ‰ŧ‡•Ļ‚Ė‡Žiƒ|ƒXƒ^[j
*
ŠÝ“S”nA‘ęāV”EA‹g“c‘ŨŽuAųˆäG–ūC
u—L‹@•ŠŽqG”}‚É‚æ‚é–Ē—ˆŒ^•ŠŽq•ÏŠ·v‘æ6‰ņŒöŠJƒVƒ“ƒ|ƒWƒEƒ€C‘åã‰ČŠw‹ZpƒZƒ“ƒ^[i‘åãjC1ŒŽ22`23“úC2016”N.
<—DGƒ|ƒXƒ^[ÜŽóÜ>

2.  Palladium Enolate Umpolung: Cyclative Haloacetoxylation of Alkynyl CyclohexadienonesiŒû“Šj
*
’|’†˜a_ASuman C. MohantaAųˆäG–ūC“ú–{‰ŧŠw‰ï‘æ96t‹G”N‰ïC“ŊŽuŽÐ‘åŠwi‹ž“sjC3ŒŽ24`27“úC2016”ND

3.  Palladium Enolate Umpolung: Cyclative Hydroacyloxylation of Alkynyl CyclohexadienonesiŒû“Šj
*
āV“c˜a–íASuman C. MohantaA’|’†˜a_AųˆäG–ūC“ú–{‰ŧŠw‰ï‘æ96t‹G”N‰ïC“ŊŽuŽÐ‘åŠwi‹ž“sjC3ŒŽ24`27“úC2016”ND

4.  Efficient Synthesis of Spiro-type Chiral Ligands Based on Direct C5 Arylation of IsoxazolesiŒû“Šj
*
dM‹§ŽuA’|’†˜a_AųˆäG–ūC“ú–{‰ŧŠw‰ï‘æ96t‹G”N‰ïC“ŊŽuŽÐ‘åŠwi‹ž“sjC3ŒŽ24`27“úC2016”ND

5.  Catalytic Asymmetric Synthesis of Natural Products Using Ir Catalyzed Tishchenko-type ReactioniŒû“Šj
—é–ØŒ’”VA*“yˆä‹M—TAIsmiyartoAŽü‘å—gA’Đ–ė–FDAųˆäG–ūC“ú–{‰ŧŠw‰ï‘æ96t‹G”N‰ïC“ŊŽuŽÐ‘åŠwi‹ž“sjC3ŒŽ24`27“úC2016”ND

6.  Development of Enantioselective Reaction Using Abundant Transition MetalsiŒû“Šj
*
•ÄŽRSA’|’†˜a_A‘ęāV”EAųˆäG–ūC“ú–{‰ŧŠw‰ï‘æ96t‹G”N‰ïC“ŊŽuŽÐ‘åŠwi‹ž“sjC3ŒŽ24`27“úC2016”ND

7.  Chiral Amine-Catalyzed Enantioselective Rauhut-Currier ReactioniŒû“Šj
*
ŠÝ“S”nA‘ęāV”EAFernando Arteaga-ArteagaAųˆäG–ūC“ú–{‰ŧŠw‰ï‘æ96t‹G”N‰ïC“ŊŽuŽÐ‘åŠwi‹ž“sjC3ŒŽ24`27“úC2016”ND

8.  Asymmetric Synthesis of Spiro-type Chiral Ligands via Catalytic DesymmetrizationiŒû“Šj
*Bijan M. Chaki
A˜e“c˜a•FA’|’†˜a_A‘ęāV”EAųˆäG–ūC“ú–{‰ŧŠw‰ï‘æ96t‹G”N‰ïC“ŊŽuŽÐ‘åŠwi‹ž“sjC3ŒŽ24`27“úC2016”ND

9.  Pd(II)-SPRIX Catalyzed Enantioselective Fujiwara-Moritani Annulation of AlkenylindolesiŒû“Šj
*Mohamed A. Abozeid
A‘ęāV”EAųˆäG–ūC“ú–{‰ŧŠw‰ï‘æ96t‹G”N‰ïC“ŊŽuŽÐ‘åŠwi‹ž“sjC3ŒŽ24`27“úC2016”ND

10.              Catalytic and Enantioselective Synthesis of Heterohelicene DerivativesiŒû“Šj
*
ˆę”VĢ˜a–íAēŒÃ^A‘ęāV”EAųˆäG–ūC“ú–{‰ŧŠw‰ï‘æ96t‹G”N‰ïC“ŊŽuŽÐ‘åŠwi‹ž“sjC3ŒŽ24`27“úC2016”ND

11.              Enantioselective and Aerobic Oxidative Coupling of 2-Naphthols Derivatives Using Chiral Dinuclear Vanadium(V) Complex in WateriŒû“Šj
*
ēŒÃ^A‘ęāV”EA‹g“c‘ŨŽuAųˆäG–ūC“ú–{‰ŧŠw‰ï‘æ96t‹G”N‰ïC“ŊŽuŽÐ‘åŠwi‹ž“sjC3ŒŽ24`27“úC2016”ND

12.              The Development of Enantioselective Oxidative Coupling Reactions of 1-Naphthol Derivatives Catalyzed by Vanadium(V) ComplexiŒû“Šj
*
âˆä’qOAŽŽ›ƒ•―A‘ęāV”EAųˆäG–ūC“ú–{‰ŧŠw‰ï‘æ96t‹G”N‰ïC“ŊŽuŽÐ‘åŠwi‹ž“sjC3ŒŽ24`27“úC2016”ND

13.              Efficient Enantioselective Synthesis of Oxahelicenes Using Redox/Acid Cooperative CatalystsiŒû“Šj
*
‘ęāV”EC‘æ‚Q‚S‰ņ•ŠŽq‡Ž‰ŧŠwƒZƒ~ƒi[CÛ’ËŽE‰Ô‚Ė—Ē‰·ōEŽR…ŠŲi‘åãjC6ŒŽ11`12“úC2016”ND

14.              “ņdŠˆŦ‰ŧŒ^G”}‚Ė‘nŧ‚ðŠî”Õ‚Æ‚·‚éV‹K•ŠŽqœŠi\’z”―‰ž‚ĖŠJ”­iĩ‘Ōj
*
ųˆäG–ūC‘n–ōŒĪ‹†ƒZƒ“ƒ^[ƒVƒ“ƒ|ƒWƒEƒ€C“Œ–kˆã‰Č–ō‰Č‘åŠwi‹{éjC6ŒŽ18“úC2016”ND

15.              “ņdŠˆŦ‰ŧŒ^•sÄG”}‚Ė‘nŧ‚Æ“WŠJiĩ‘Ōj
*
ųˆäG–ūC‘æ11‰ņ—L‹@‡Ž‰ŧŠw‚Ėƒtƒƒ“ƒeƒBƒAC—‰ŧŠwŒĪ‹†Š—é–Ø”~‘ū˜Yƒz[ƒ‹ié‹ĘjC6ŒŽ24“úC2016”ND

16.              ƒpƒ‰ƒWƒEƒ€ƒGƒmƒ‰[ƒg‚Ė‹ÉŦ“]Š·‚ðŠîŽē‚Æ‚·‚é‘―ŠŊ”\ŦƒJƒ‹ƒ{ƒjƒ‹‰ŧ‡•Ļ‚ĖŒø—Ķ“I‡Žiƒ|ƒXƒ^[jC
*
’|’†˜a_AāV“c˜a–íASuman C. MohantaAųˆäG–ūC“ú–{ƒvƒƒZƒX‰ŧŠw‰ï2016ƒTƒ}[ƒVƒ“ƒ|ƒWƒEƒ€C–žŒÃ‰Ū‘Û‰ï‹cęiˆĪ’mjC7ŒŽ28`29“úC2016”ND

17.              —L‹@•ŠŽqG”}‚É‚æ‚éŠÜ’‚‘f•Ą‘fŠÂ‚ĖƒGƒiƒ“ƒ`ƒI‘I‘ð“I\’ziƒ|ƒXƒ^[j
*
ŠÝ“S”nA‘ęāV”EAFernando Arteaga-ArteagaAųˆäG–ūC“ú–{ƒvƒƒZƒX‰ŧŠw‰ï2016ƒTƒ}[ƒVƒ“ƒ|ƒWƒEƒ€C–žŒÃ‰Ū‘Û‰ï‹cęiˆĪ’mjC7ŒŽ28`29“úC2016”ND

18.              ƒoƒiƒWƒEƒ€G”}‚ðŠˆ—p‚·‚éƒGƒiƒ“ƒ`ƒI‘I‘ð“I’Y‘f|’Y‘fŒ‹‡Œ`Ž”―‰ž‚ĖŠJ”­‚Ɖž—piƒ|ƒXƒ^[j
*
ēŒÃ^A‘ęāV”EAųˆäG–ūC“ú–{ƒvƒƒZƒX‰ŧŠw‰ï2016ƒTƒ}[ƒVƒ“ƒ|ƒWƒEƒ€C–žŒÃ‰Ū‘Û‰ï‹cęiˆĪ’mjC7ŒŽ28`29“úC2016”ND

19.              ƒoƒiƒWƒEƒ€G”}‚ðŠˆ—p‚·‚éƒwƒeƒƒwƒŠƒZƒ“—U“ą‘Ė‚ĖŒø—Ķ“I‡Žiƒ|ƒXƒ^[j
ēŒÃ^A*ˆę”VĢ˜a–íA‘ęāV”EAųˆäG–ūC‘æ36‰ņ—L‹@‡ŽŽáŽčƒZƒ~ƒi[C‹ž“s–ō‰Č‘åŠwi‹ž“sjC8ŒŽ9“úC2016”ND
<ƒ|ƒXƒ^[ÜŽóÜ>

20.              ƒpƒ‰ƒWƒEƒ€ƒGƒmƒ‰[ƒg‚Ė‹ÉŦ“]Š·‚ðŠîŽē‚Æ‚·‚é‘―ŠŊ”\ŦƒJƒ‹ƒ{ƒjƒ‹‰ŧ‡•Ļ‚ĖŒø—Ķ“I‡Žiƒ|ƒXƒ^[j
*
–ė–{—T–įA’|’†˜a_AāV“c˜a–íASuman C. MohantaAųˆäG–ūC‘æ36‰ņ—L‹@‡ŽŽáŽčƒZƒ~ƒi[C‹ž“s–ō‰Č‘åŠwi‹ž“sjC8ŒŽ9“úC2016”ND

21.              •Ą‘fŠÂ‚ð—L‚·‚é‘―ŠÂŽŪƒtƒFƒm[ƒ‹—Þ‚Ė•sÄŽ_‰ŧ“IƒJƒbƒvƒŠƒ“ƒO”―‰ž‚ĖŠJ”­iƒ|ƒXƒ^[j
*
™›―WŦAēŒÃ^A‘ęāV”EAųˆäG–ūC‘æ36‰ņ—L‹@‡ŽŽáŽčƒZƒ~ƒi[C‹ž“s–ō‰Č‘åŠwi‹ž“sjC8ŒŽ9“úC2016”ND

22.              —L‹@G”}‚Ė‹Ī–ðƒAƒ‹ƒLƒ“‚Ö‚Ė•t‰Á‚ðŒŪ‚Æ‚·‚éƒhƒ~ƒm”―‰ž‚ĖŠJ”­iƒ|ƒXƒ^[j
*
‘ę–Ē—ˆAŠÝ“S”nA‘ęāV”EAJianfei BaiAųˆäG–ūC‘æ36‰ņ—L‹@‡ŽŽáŽčƒZƒ~ƒi[C‹ž“s–ō‰Č‘åŠwi‹ž“sjC8ŒŽ9“úC2016”ND

23.              “ņdŠˆŦ‰ŧŒ^•sÄG”}‚Ė‘noiĩ‘Ōj
*
ųˆäG–ūC•ŠŽqŒĪŒĪ‹†‰ï@—L‹@‹ā‘Ū‰ŧŠw‚Ė‘å’Š—ŽC‰ŠčƒRƒ“ƒtƒ@ƒŒƒ“ƒXƒZƒ“ƒ^[iˆĪ’mjC9ŒŽ2`3“úC2016”ND

24.              Pd(II)-SPRIX Catalyzed Enantioselective Annulation of Alkenylindolesiƒ|ƒXƒ^[j
*Mohamed A. Abozeid
A‘ęāV”EAųˆäG–ūC‘æ63‰ņ—L‹@‹ā‘Ū‰ŧŠw“Ē˜_‰ïC‘ˆî“c‘åŠwž‘ˆî“cƒLƒƒƒ“ƒpƒXi“Œ‹žjC9ŒŽ14`16“úC2016”ND

25.              Palladium Enolate Umpolung: Catalytic Cyclative Hydroacyloxylation of Alkynyl CyclohexadienonesiŒû“Šj
*
’|’†˜a_AāV“c˜a–íASuman C. MohantaAųˆäG–ūC‘æ63‰ņ—L‹@‹ā‘Ū‰ŧŠw“Ē˜_‰ïC‘ˆî“c‘åŠwž‘ˆî“cƒLƒƒƒ“ƒpƒXi“Œ‹žjC9ŒŽ14`16“úC2016”ND

26.              ƒpƒ‰ƒWƒEƒ€ƒGƒmƒ‰[ƒg‚Ė‹ÉŦ“]Š·‚ðŠˆ—p‚·‚éƒJƒ‹ƒ{ƒjƒ‹‰ŧ‡•Ļ‚ĖG”}“IŠÂ‰ŧŠŊ”\Šî‰ŧ”―‰žiŒû“Šj
*
’|’†˜a_AāV“c˜a–íASuman C. MohantaAųˆäG–ūC‘æ46‰ņ•Ą‘fŠÂ‰ŧŠw“Ē˜_‰ïC‹ā‘ō‰ĖŒ€ĀiÎėjC9ŒŽ26`28“úC2016”ND

27.              “ņdŠˆŦ‰ŧŒ^•sÄG”}‚Ė‘no‚Ɖž—piĩ‘Ōj
*
ųˆäG–ūCiŒöj‰ČŠw‹ZpŒð—Žā’c@ƒOƒŠ[ƒ“ƒPƒ~ƒXƒgƒŠ[‚ɍŠ·‚ĩ‚―—L‹@‡ŽŽč–@ŒĪ‹†‰ïC–žŒÃ‰ŪH‹Æ‘åŠwiˆĪ’mjC9ŒŽ30“úC2016”ND

28.              ƒAƒ~ƒh‰ŧERauhutCurrier˜A‘ą”―‰ž‚É‚æ‚éƒŋ]ƒƒ`ƒŠƒfƒ“]ƒÁ]ƒ‰ƒNƒ^ƒ€‚ĖG”}“I•sÄ‡ŽiŒû“Šj
*
ŠÝ“S”nA‘ęāV”EAųˆäG–ūC‘æ110‰ņ—L‹@‡ŽƒVƒ“ƒ|ƒWƒEƒ€C‘ˆî“c‘åŠw‘Û‰ï‹cęi“Œ‹žjC11ŒŽ10`11“úC2016”ND

29.              ƒAƒ~ƒh‰ŧ^•ŠŽq“āRauhutCurrier (RC) ˜A‘ą”―‰ž‚É‚æ‚éƒŋ]ƒƒ`ƒŠƒfƒ“]ƒÁ]ƒ‰ƒNƒ^ƒ€œŠi‚ĖƒGƒiƒ“ƒ`ƒI‘I‘ð“IG”}‡Žiƒ|ƒXƒ^[j
*
‘ęāV”EAŠÝ“S”nAųˆäG–ūC‘æ9‰ņ—L‹@G”}ƒVƒ“ƒ|ƒWƒEƒ€C–žŒÃ‰Ū‘åŠwiˆĪ’mjC12ŒŽ1`2“úC2016”ND

<International>

1.  Spiro Chiral Ligand-Pd(II) Complex Catalyzed Enantioselective Construction of Heterocycles (Poster)
*Abozeid, M. A.; Takizawa, S.; Sasai, H. The 8th Takeda Science Foundation Symposium on PharmaSciences, Osaka, Japan, January 21-22, 2016.

2.  Enantioselective Organocatalyzed Synthesis of Tetrahydrobenzofuranones Bearing a Tetrasubstituted Stereogenic Center (Poster)
*Kishi, K.; Takizawa, S.; Yoshida, Y.; Mader, S.; Rueping, M.; Sasai, H. The 8th Takeda Science Foundation Symposium on PharmaSciences, Osaka, Japan, January 21-22, 2016.


3.  Synthetic Studies on Heterohelicene Derivatives Using Vanadium-catalyzed Oxidative Reaction (Oral)
*Sako, M.; Ichinose, K.; Takizawa, S.; Sasai, H.
Aachen-Osaka Joint Symposium gBiotechnology and Chemistry for Green Growthh, Osaka, Japan, March 9-10, 2016.

4.  Enantioselective Organocatalyzed [3+2] Annulation via Umpolung Domino Reaction of Allenoates (Oral)
*Kishi, K.; Takizawa, S.; Yoshida, Y.; Mader, S.; Rueping, M.; Sasai, H.
Aachen-Osaka Joint Symposium gBiotechnology and Chemistry for Green Growthh, Osaka, Japan, March 9-10, 2016.

5.  Palladium Enolate Umpolung: Catalytic Cyclative Difunctionalization of Alkynyl Cyclohexadienones Using SPRIX Ligand
*Mohanta, S. C.; Takenaka, K.; Sasai, H. 16th Asian Chemical Congress (16ACC), Dhaka, Bangladesh, March 16-19, 2016.

6.  Vanadium(V)-Catalyzed Enantioselective Synthesis of Oxa[9]helicene (Poster)
*Sako, M.; Takizawa, S.; Takeuchi, Y.; Tsujihara, T.; Ichinose, K.; Kodera, J.; Yoneyama, S.; Kawano, T.; Sasai, H. Molecular Chirality Asia 2016, Osaka, Japan, April 20-22, 2016.
<Poster AwardŽóÜ>

7.  Facile Synthesis of ƒŋ-Methylidene-ƒÁ-Lactams via Amidation and Rauhut-Currier Reaction Sequence (Poster)
*Kishi, K.; Takizawa, S.; Arteaga, F. A.; Sasai, H. Molecular Chirality Asia 2016, Osaka, Japan, April 20-22, 2016.

8.  Pd(II)-SPRIX Catalyzed Enantioselective Fujiwara-Moritani Annulation of Alkenylindoles (Poster)
*Abozeid, M. A.; Takizawa, S.; Sasai, H. Molecular Chirality Asia 2016, Osaka, Japan, April 20-22, 2016.

9.  Palladium Enolate Umpolung: Catalytic Cyclative Difunctionalization of Alkynyl Cyclohexadienones Using SPRIX Ligand (Poster)
*Takenaka, K.; Mohanta, S. C.; Sasai, H. Molecular Chirality Asia 2016, Osaka, Japan, April 20-22, 2016.

10.              Recent Progress in Enantioselective Pd-SPRIX Catalysis (Invited)
*Sasai, H. 27th International Conference on Organometallic Chemistry, Melbourne, Australia, July 17-22, 2016.

11.              Construction of Highly Functionalized Compounds via Metal Free Transformations (Invited)
*Sasai, H. International Conference on Organic Chemistry, Las Vegas, USA, August 10-11, 2016.

12.              Pd(II)-SPRIX Catalyzed Enantioselective Annulation of Alkenylindoles (Oral)
Abozeid, M. A.; Takizawa, S.; *Sasai, H. Selectivity in Chemo- and Biocatalysis (Aachen-Osaka Joint Symposium), Aachen, Germany, September 5-7, 2016.

13.              Enantioselective Synthesis of ƒŋ-Methylidene-ƒÁ-Lactams via Amidation and Rauhut-Currier Reaction Sequence (Oral)
*Kishi, K.; Takizawa, S.; Mader, S.; Rueping, M.; Sasai, H. Selectivity in Chemo- and Biocatalysis (Aachen-Osaka Joint Symposium), Aachen, Germany, September 5-7, 2016.

14.              Recent Progress in Pd-SPRIX Catalyzed Enantioselective Reactions (Oral)
Takenaka, K.; Mohanta, S. C.; Abozeid, M. A.; Takizawa, S.; *Sasai, H. JSPS core-to-core Workshop Program -Green Process-, Dijon, France, September 22-23, 2016.

15.              Efficient Enantioselective Synthesis of Oxahelicenes Using Redox/Acid Cooperative Catalysts (Oral)
*Takizawa, S.; Sako, M.; Sasai, H. JSPS core-to-core Workshop Program -Green Process-, Dijon, France, September 22-23, 2016.

16.              Synthesis of Heterocyclic Compounds through Organocatalytic Domino Reaction (Oral)
*Kusaba, M.; Kishi, K.; Takizawa, S.; Sasai, H. JSPS core-to-core Workshop Program -Green Process-, Dijon, France, September 22-23, 2016.

17.              Chiral Iron Catalysts Bearing SPRIX Ligand (Poster)
*Niida, Y.; Takenaka, K.; Takizawa, S.; Sasai, H. JSPS core-to-core Workshop Program -Green Process-, Dijon, France, September 22-23, 2016.

18.              Enantioselective Oxidative Coupling of Phenol Derivatives Using Chiral Vanadium(V) catalysts (Poster)
*Aoki, T.; Sako, M.; Takizawa, S.; Sasai, H. JSPS core-to-core Workshop Program -Green Process-, Dijon, France, September 22-23, 2016.

19.              Enantioselective Carbon-Carbon Bond-Forming Reactions Catalyzed by Vanadium(V) Complexes (Invited)
*Takizawa, S.; Sako, M.; Sasai, H. The 10th International Vanadium Symposium Chemistry, Biological Chemistry & Toxicology (V10), Taipei, Taiwan, November, 6-9, 2016.

20.              Exploration of Organocatalytic Enantioselective [n+2] Type Annulations (Invited)
*Sasai, H. International Symposium on Catalysis and Fine Chemicals 2016 (C&FC 2016), Taipei, Taiwan, November 10-14, 2016.

21.              Recent Progress on Pd ̶SPRIX Catalyzed Enantioselective Reactions (Poster)
*Chaki, B. M.; Mohanta, S. C.; Abozeid, M. A.; Takenaka, K.; Takizawa, S.; Sasai, H. The 10th International Symposium on Integrated Synthesis (ISONIS-10), Awaji Island, Japan, November 18-19, 2016.

22.              Efficient Enantioselective Synthesis of Oxahelicenes Using Redox/Acid Cooperative Catalysts (Poster)
*Takizawa, S.; Sako, M.; Sasai, H. The 10th International Symposium on Integrated Synthesis (ISONIS-10), Awaji Island, Japan, November 18-19, 2016.

23.              Synthesis of Heterocyclic Compounds through Organocatalytic Double Michael Reaction (Poster)
Kusaba, M.; Kishi, K.; *Wathsala, H. D. P.; Takizawa, S.; Sasai, H. The 10th International Symposium on Integrated Synthesis (ISONIS-10), Awaji Island, Japan, November 18-19, 2016.

 

TopŠ

 

2015

<Domestic>

1.  ƒpƒ‰ƒWƒEƒ€G”}‚ð—p‚Ē‚éƒAƒ‹ƒPƒjƒ‹ƒIƒLƒVƒ€‚ĖƒGƒiƒ“ƒ`ƒI‘I‘ð“IŠÂ‰ŧ\ŠÂ‰ŧ•t‰Á”―‰žiŒû“Šj
*Mohamed A. Abozeid
A‘ęāV”EAųˆäG–ūC“ú–{–ōŠw‰ï‘æ135”N‰ïC_ŒËŠw‰@‘åŠwi•šŒÉjC3ŒŽ25`28“úC2015”ND

2.  V‹KƒXƒsƒŒ^ƒLƒ‰ƒ‹ƒCƒ~ƒ_ƒ][ƒ‹”zˆĘŽq‚ĖŠJ”­‚Ɖž—piŒû“Šj
*
āV“c˜a–íA‚’JC•―A’|’†˜a_AųˆäG–ūC“ú–{–ōŠw‰ï‘æ135”N‰ïC_ŒËŠw‰@‘åŠwi•šŒÉjC3ŒŽ25`28“úC2015”ND

3.  Stereoselective Construction of Chiral Tetrasubstituted Carbon Stereogenic Centers Via Organocatalytic RauhutCurrier Reactioni“Á•Ęu‰‰j
*
‘ęāV”EAųˆäG–ūC“ú–{‰ŧŠw‰ï‘æ95t‹G”N‰ïC“ú–{‘åŠwiį—tjC3ŒŽ26`29“úC2015”ND

4.  Development of Enantioselective Organocatalyzed Formal [n+2] Cycloaddition of Allenic Ester with OlefinsiŒû“Šj
*
‹g“c‘ŨŽuA‘ęāV”EAFernando Arteaga-ArteagaAŠÝ“S”nAųˆäG–ūC“ú–{‰ŧŠw‰ï‘æ95t‹G”N‰ïC“ú–{‘åŠwiį—tjC3ŒŽ26`29“úC2015”ND

5.  Vanadium(V) Complex-Catalyzed Enantioselective Synthesis of Oxa[9]heliceneiŒû“Šj
*
ēŒÃ^A‘ęāV”EA’ŌŒī“N–įA‹g“c‘ŨŽuAŽŽ›ƒ•―A‰Í–ė•xˆęAųˆäG–ūC“ú–{‰ŧŠw‰ï‘æ95t‹G”N‰ïC“ú–{‘åŠwiį—tjC3ŒŽ26`29“úC2015”ND

6.  Enantioselective RauhutCurrier Reaction Promoted by an Immobilized OrganocatalystiŒû“Šj
*
•―“cCˆęAŠÝ“S”nA‘ęāV”EAųˆäG–ūC“ú–{‰ŧŠw‰ï‘æ95t‹G”N‰ïC“ú–{‘åŠwiį—tjC3ŒŽ26`29“úC2015”ND

7.  Enantioselective Synthesis of Hetero Helicenes Bearing 1,2,3-Triazole UnitsiŒû“Šj
*
âˆä’qOA‹g“c‘ŨŽuA‘ęāV”EAųˆäG–ūC“ú–{‰ŧŠw‰ï‘æ95t‹G”N‰ïC“ú–{‘åŠwiį—tjC3ŒŽ26`29“úC2015”ND

8.  Novel Chiral Benzimidazole Ligands Having a Spiro Skeleton: Design, Preparation and ApplicationiŒû“Šj
*
‚’JC•―AāV“c˜a–íA’|’†˜a_AųˆäG–ūC“ú–{‰ŧŠw‰ï‘æ95t‹G”N‰ïC“ú–{‘åŠwiį—tjC3ŒŽ26`29“úC2015”ND

9.  2‰ŋƒpƒ‰ƒWƒEƒ€‚ðŠˆŦŽí‚Æ‚·‚é•sÄG”}”―‰ž‚ĖV“WŠJi“Á•Ęu‰‰j
*
’|’†˜a_C“ú–{‰ŧŠw‰ï‘æ95t‹G”N‰ïC“ú–{‘åŠwiį—tjC3ŒŽ26`29“úC2015”ND
<Žá‚ĒĒ‘ã‚Ė“Á•Ęu‰‰‰ï>

10.              Enantioselective Synthesis of Chiral Spiro Compounds and Their Applications to OrganocatalysisiŒû“Šj
*
•“ā–FŽũALulu FanA‘ęāV”EAųˆäG–ūC“ú–{‰ŧŠw‰ï‘æ95t‹G”N‰ïC“ú–{‘åŠwiį—tjC3ŒŽ26`29“úC2015”ND

11.              Divergent Synthesis of SPRIX Ligands Having Oxygen FunctionalitiesiŒû“Šj
*
—ŅŒŦĄA’|’†˜a_AųˆäG–ūC“ú–{‰ŧŠw‰ï‘æ95t‹G”N‰ïC“ú–{‘åŠwiį—tjC3ŒŽ26`29“úC2015”ND

12.              Ir-Catalyzed Asymmetric Tishchenko Type ReactioniŒû“Šj
—é–ØŒ’”VA*IsmiyartoAŽü‘å—gA’Đ–ė–FDAųˆäG–ūC“ú–{‰ŧŠw‰ï‘æ95t‹G”N‰ïC“ú–{‘åŠwiį—tjC3ŒŽ26`29“úC2015”ND

13.              [n+2]•sÄŠÂ‰ŧ”―‰ž‚É‚æ‚éƒLƒ‰ƒ‹Žl’uŠ·’Y‘f‚Ė\’ziƒ|ƒXƒ^[j
*
ŠÝ“S”nA‘ęāV”EA‹g“c‘ŨŽuAFernando Arteaga-ArteagaAųˆäG–ūC‘æ8‰ņ—L‹@G”}ƒVƒ“ƒ|ƒWƒEƒ€i
u—L‹@•ŠŽqG”}‚É‚æ‚é–Ē—ˆŒ^•ŠŽq•ÏŠ·v‘æ5‰ņŒöŠJƒVƒ“ƒ|ƒWƒEƒ€jC‰Ŧ“ęŒ§Žs’Ž‘šŽĐŽĄ‰ïŠŲi‰Ŧ“ęjC5ŒŽ10`11“úC2015”ND

14.              ƒoƒiƒWƒEƒ€G”}‚ðŠˆ—p‚·‚éƒGƒiƒ“ƒ`ƒI‘I‘ð“I’Y‘f|’Y‘fŒ‹‡Œ`Ž”―‰ž‚ĖŠJ”­‚Ɖž—piŒû“Šj
*
ēŒÃ^A•“ā–FŽũA‘ęāV”EA’ŌŒī“N–įA‹g“c‘ŨŽuAŽŽ›ƒ•―A‰Í–ė•xˆęAųˆäG–ūC‘æ107‰ņ—L‹@‡ŽƒVƒ“ƒ|ƒWƒEƒ€CŒc‰ž‹`m‘åŠw–ōŠw•”ƒ}ƒ‹ƒ`ƒƒfƒBƒAu“°i“Œ‹žjC6ŒŽ9`10“úC2015”ND

15.              —L‹@•ŠŽqG”}‚ð—p‚Ē‚éƒGƒiƒ“ƒ`ƒI‘I‘ð“I[2+2]ŠÂ‰ŧ”―‰ž‚É‚æ‚éŽlˆõŠÂ‚Ė\’ziƒ|ƒXƒ^[j
*
ŠÝ“S”nA‘ęāV”EAFernando Arteaga-ArteagaA‹g“c‘ŨŽuA—é–Ø’Ę‹ąAųˆäG–ūCSymposium on Molecular Chirality 2015C‘ˆî“c‘åŠwž‘ˆî“cƒLƒƒƒ“ƒpƒXi“Œ‹žjC6ŒŽ12`13“úC2015”ND

16.              “SG”}‚ð—p‚Ē‚éƒtƒŠ[ƒfƒ‹EƒNƒ‰ƒtƒc”―‰ž‚ĖŠJ”­iƒ|ƒXƒ^[j
*
•ÄŽRSA‘ęāV”EAųˆäG–ūC‘æ35‰ņ—L‹@‡ŽŽáŽčƒZƒ~ƒi[C‹ž“s•{—§‘åŠw‰šŠ›ƒLƒƒƒ“ƒpƒXi‹ž“sjC8ŒŽ1“úC2015”ND

17.              ƒpƒ‰ƒWƒEƒ€ƒGƒmƒ‰[ƒg‚Ė‹ÉŦ“]Š·‚ðŠîŽē‚Æ‚·‚éŠÂ‰ŧ“IŠŊ”\Šî‰ŧ”―‰ž‚ĖŠJ”­iƒ|ƒXƒ^[j
Suman C. Mohanta
AāV“c˜a–íA*V‹“c‹ąÍA’|’†˜a_AųˆäG–ūC‘æ35‰ņ—L‹@‡ŽŽáŽčƒZƒ~ƒi[C‹ž“s•{—§‘åŠw‰šŠ›ƒLƒƒƒ“ƒpƒXi‹ž“sjC8ŒŽ1“úC2015”ND

18.              Catalytic Cyclative Haloacetoxylation of Alkynyl Cyclohexadienones Based on Pd Enolate UmpolungiŒû“Šj
*
’|’†˜a_ASuman C. MohantaAųˆäG–ūC‘æ62‰ņ—L‹@‹ā‘Ū‰ŧŠw“Ē˜_‰ïCŠÖž‘åŠwį—ĒŽRƒLƒƒƒ“ƒpƒXi‘åãjC9ŒŽ7`9“úC2015”ND

19.              Ir Catalyzed Asymmetric Tandem Reaction of meso-Diolsiƒ|ƒXƒ^[j
—é–ØŒ’”VA*IsmiyartoAÎâ—FAŽü‘å—gA’Đ–ė–FDAųˆäG–ūC‘æ62‰ņ—L‹@‹ā‘Ū‰ŧŠw“Ē˜_‰ïCŠÖž‘åŠwį—ĒŽRƒLƒƒƒ“ƒpƒXi‘åãjC9ŒŽ7`9“úC2015”ND

20.              Carbon-Carbon Bonds Cleavage by Vanadium Catalyzed Aerobic Oxidationiƒ|ƒXƒ^[j
*
‹ËŒīģ”VAŠâˆä—˜–ūAž“‡—Č“ņA‘šž—R—˜A‘吙—œ‰hA‹gė—tA—é–Ø—œŽŅA‘ęāV”EC‘æ62‰ņ—L‹@‹ā‘Ū‰ŧŠw“Ē˜_‰ïCŠÖž‘åŠwį—ĒŽRƒLƒƒƒ“ƒpƒXi‘åãjC9ŒŽ7`9“úC2015”ND

21.              ƒoƒiƒWƒEƒ€G”}‚ðŠˆ—p‚·‚éƒIƒLƒTƒwƒŠƒZƒ“—Þ‚ĖƒGƒiƒ“ƒ`ƒI‘I‘ð“I‡Žiƒ|ƒXƒ^[j
*
‘ęāV”EAēŒÃ^A•“ā–FŽũAˆę”VĢ˜a–íA’ŌŒī“N–įAŽŽ›ƒ•―A‰Í–ė•xˆęAųˆäG–ūC•―Ž27”N“x—L‹@‡Ž‰ŧŠw–k—ĪƒZƒ~ƒi[C•xŽRŠÏŒõƒzƒeƒ‹i•xŽRjC10ŒŽ2`3“úC2015”N.

22.              —L‹@•ŠŽqG”}‚É‚æ‚é”ņ‘ΏĖ‰ŧ‚ðŠî”Õ‚Æ‚·‚é“ņ˜A‘ą•sÄ’Y‘f‚Ė\’ziƒ|ƒXƒ^[j
*
ŠÝ“S”nA‘ęāV”EA‹g“c‘ŨŽuASteffen MaderAMagnus RuepingAųˆäG–ūC•―Ž27”N“x—L‹@‡Ž‰ŧŠw–k—ĪƒZƒ~ƒi[C•xŽRŠÏŒõƒzƒeƒ‹i•xŽRjC10ŒŽ2`3“úC2015”ND

23.              ƒoƒiƒWƒEƒ€G”}‚ðŠˆ—p‚·‚éƒwƒeƒƒwƒŠƒZƒ“—U“ą‘Ė‚ĖƒGƒiƒ“ƒ`ƒI‘I‘ð“I‡Ž–@‚ĖŠJ”­iƒ|ƒXƒ^[j
ēŒÃ^A•“ā–FŽũA*ˆę”VĢ˜a–íA‘ęāV”EA’ŌŒī“N–įAŽŽ›ƒ•―A‰Í–ė•xˆęAųˆäG–ūC‘æ5‰ņCSJ‰ŧŠwƒtƒFƒXƒ^Cƒ^ƒ[ƒz[ƒ‹‘D–xi“Œ‹žjC10ŒŽ13`15“úC2015”N.

24.              •sÄ—L‹@•ŠŽqG”}‚ð—p‚Ē‚é[n+2]ŠÂ‰ŧ”―‰ž‚É‚æ‚éƒeƒgƒ‰ƒqƒhƒƒxƒ“ƒ]ƒtƒ‰ƒmƒ“—U“ą‘Ė‚Ė‡ŽiŒû“Šj
*
‘ęāV”EAŠÝ“S”nA‹g“c‘ŨŽuASteffen MaderAFernando Arteaga-ArteagaAMagnus RuepingAųˆäG–ūC‘æ41‰ņ”―‰ž‚ƍ‡Ž‚Ėi•āƒVƒ“ƒ|ƒWƒEƒ€C‹ß‹E‘åŠw“Œ‘åãƒLƒƒƒ“ƒpƒXi‘åãjC10ŒŽ26`27“úC2015”N.

25.              ŽŸˆŸ‰–‘fŽ_ƒiƒgƒŠƒEƒ€‚ð—p‚Ē‚éƒCƒ~ƒ“Ž_‰ŧ‚É‚æ‚éƒIƒLƒTƒWƒŠƒWƒ“‡Žiƒ|ƒXƒ^[j
*
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26.              ƒoƒiƒWƒEƒ€G”}‚ðŠˆ—p‚·‚éƒwƒeƒƒwƒŠƒZƒ“—U“ą‘Ė‚ĖƒGƒiƒ“ƒ`ƒI‘I‘ð“I‡Ž–@‚ĖŠJ”­iƒ|ƒXƒ^[j
*
ˆę”VĢ˜a–íAēŒÃ^A•“ā–FŽũA‘ęāV”EA’ŌŒī“N–įAŽŽ›ƒ•―A‰Í–ė•xˆęAųˆäG–ūC‘æ41‰ņ”―‰ž‚ƍ‡Ž‚Ėi•āƒVƒ“ƒ|ƒWƒEƒ€C‹ß‹E‘åŠw“Œ‘åãƒLƒƒƒ“ƒpƒXi‘åãjC10ŒŽ26`27“úC2015”N.

<International>

1.  Palladium-Catalyzed Direct C5 Arylation of Isoxazoles: Mechanistic Study and Application (Oral)
*Shigenobu, M.; Takenaka, K.;
Sasai, H. Biotechnology and Chemistry for Green Growth (Aachen-Osaka Joint Symposium), Osaka, Japan, March 10-11, 2015.

2.  Palladium-Catalyzed Direct CH Arylation of Isoxazoles at The 5-Position (Poster)
*
Shigenobu, M.; Takenaka, K.; Sasai, H. 18th IUPAC International Symposium on Organometallic Chemistry Directed Towards Organic Synthesis (OMCOS18), Barcelona, Spain, June 28-July 2nd July, 2015.

3.  Vanadium Complex Catalyzed Enantioselective Synthesis of Oxa[9]helicene (Poster)
*Takizawa, S.; Sako, M.; Takeuchi, Y.; Tsujihara, T.; Yoshida, Y.; Kodera, J.; Kawano, T.; Sasai, H.
18th IUPAC International Symposium on Organometallic Chemistry Directed Towards Organic Synthesis (OMCOS18), Barcelona, Spain, June 28-July 2nd July, 2015.

4.  Ir Catalyzed Asymmetric Tandem Reaction of meso-Diols (Poster)
*Suzuki, T.; Ismiyarto; Ishizaka, Y; Zhou, D-Y; Asano, K.; Sasai, H. Chirality 2015, Boston, USA, June 28-July 1, 2015.

5.  Enantioselective Organocatalyzed Formal Cycloaddition Reactions Based on the aza-Morita-Baylis-Hillman Process (Poster)
*Takizawa, S.; Sasai, H. The 39th Naito Conference, Hokkaido, Japan, July 6-9 2015.

6.  Enantioselective Multicatalytic Synthesis of ƒŋ-Benzylidene-ƒÁ-Hydroxy-1-Tetralone (Poster)
*Suzuki, T.; Ismiyarto; Ishizaka, Y; Zhou, D-Y; Asano, K.; Sasai, H. 17th International Symposium on Relations between Homogeneous and Heterogeneous Catalysis (ISHHC 17), Utrecht, the Netherlands, July 12-15, 2015.

7.  Enantioselective and Aerobic Oxidative Coupling of 2-Naphthol Derivatives Using Chiral Dinuclear Vanadium Complex in Water (Poster)
*Sako, M.; Takizawa, S.; Yoshida, Y.;
Sasai, H. The 3rd International Symposium on Process Chemistry, Kyoto, Japan, July 13-15, 2015.

8.  Enantioselective Synthesis of Oxa[9]helicenes Using Chiral Vanadium Catalysts (Poster)
*Takizawa, S.; Sako, M.; Takeuchi, Y.; Tsujihara, T.; Kodera, J.; Kawano, T.;
Sasai, H. 15th International Conference on Chiroptical Spectroscopy, Hokkaido, Japan, August 30-September 3, 2015.

9.  Catalytic Cyclative Haloacetoxylation Based on Palladium Enolate Umpolung (Oral)
*Takenaka, K.; Mohanta, S. C.;
Sasai, H. Aachen-Osaka Joint Symposium gBiological and Chemical Methods for Selective Catalysish, Aachen, Germany, September 1-2, 2015.

10.              Vanadium(V)-Catalyzed Enantioselective CC Bond Forming Reactions (Oral)
*Sako, M.; Takizawa, S.; Yoshida, Y.; Sasai, H.
Aachen-Osaka Joint Symposium gBiological and Chemical Methods for Selective Catalysish, Aachen, Germany, September 1-2, 2015.

11.              Spiro Chiral Ligand-Pd(II) Complex Catalyzed Enantioselective Construction of Heterocycles (Poster)
*Abozeid, M. A.; Takizawa, S.; Sasai, H. The 13th International Kyoto Conference on New Aspects of Organic Chemistry (IKCOC-13), Kyoto, Japan, November 9-13, 2015.

12.              Organocatalyzed Synthesis Of Heterocycles Bearing a Chiral Tetrasubstituted Carbon Center (Poster)
*Takizawa, S.; Kishi, K.; Sasai, H. The 13th International Kyoto Conference on New Aspects of Organic Chemistry (IKCOC-13), Kyoto, Japan, November 9-13, 2015.

13.              Recent Progress of Enantioselective Pd-Catalysis Promoted by Spiro-type Chiral Ligands (Poster)
Mohanta, S. C.; Shigenobu, M.; Wakita, K.; Takenaka, K.; *Chaki, B. M.; Sasai, H. The 13th International Kyoto Conference on New Aspects of Organic Chemistry (IKCOC-13), Kyoto, Japan, November 9-13, 2015.

 

TopŠ

 

2014

<Domestic>

1.  ƒLƒ‰ƒ‹ƒ}ƒ“ƒKƒ“G”}‚ð—p‚Ē‚é2|ƒiƒtƒg[ƒ‹—Þ‚ĖƒGƒiƒ“ƒ`ƒI‘I‘ð“I”―‰ž‚ĖŠJ”­iŒû“Šj
*
‘ęāV”EAųˆäG–ūC“ú–{‰ŧŠw‰ï‘æ94t‹G”N‰ïC–žŒÃ‰Ū‘åŠwiˆĪ’mjC3ŒŽ27`30“úC2014”ND

2.  ƒCƒ~ƒ_ƒ][ƒ‹‚ð”zˆĘ•”ˆĘ‚Æ‚ĩ‚Ä—L‚·‚éV‹KƒLƒ‰ƒ‹ƒXƒsƒŒ^”zˆĘŽq‚ĖŠJ”­iŒû“Šj
*
‚’JC•―A’|’†˜a_AųˆäG–ūC“ú–{‰ŧŠw‰ï‘æ94t‹G”N‰ïC–žŒÃ‰Ū‘åŠwiˆĪ’mjC3ŒŽ27`30“úC2014”ND

3.  ƒrƒX1,2,3|ƒgƒŠƒAƒ][ƒ‹ƒ†ƒjƒbƒg‚ð—L‚·‚éƒwƒeƒƒwƒŠƒZƒ“‚ĖƒGƒiƒ“ƒ`ƒI‘I‘ð“I‡Ž‚Æ•sÄG”}‚Ö‚Ė‰ž—piŒû“Šj
*
‹g“c‘ŨŽuA‘ęāV”EAųˆäG–ūC“ú–{‰ŧŠw‰ï‘æ94t‹G”N‰ïC–žŒÃ‰Ū‘åŠwiˆĪ’mjC3ŒŽ27`30“úC2014”ND

4.  —L‹@•ŠŽqG”}‚É‚æ‚éƒWƒGƒmƒ“‚Æ2,3|ƒuƒ^ƒWƒGƒ“Ž_ƒGƒXƒeƒ‹‚Æ‚ðŠîŽŋ‚Æ‚·‚éƒGƒiƒ“ƒ`ƒI‘I‘ð“IŒ`ŽŪ“I[3+2]ŠÂ‰ŧ”―‰ž‚ĖŠJ”­iŒû“Šj
*
—é–Ø’Ę‹ąAFernando Arteaga-ArteagaATue
M.-N. NguyenA‘ęāV”EAųˆäG–ūC“ú–{‰ŧŠw‰ï‘æ94t‹G”N‰ïC–žŒÃ‰Ū‘åŠwiˆĪ’mjC3ŒŽ27`30“úC2014”ND

5.  ƒpƒ‰ƒWƒEƒ€G”}‚É‚æ‚éC-HŒ‹‡ŠˆŦ‰ŧ‚ðŒo‚éƒCƒ\ƒIƒLƒTƒ][ƒ‹ŠÂ5ˆĘ‚Å‚Ė’žÚ“IƒAƒŠ[ƒ‹‰ŧ”―‰žiŒû“Šj
*
dM‹§ŽuA’|’†˜a_AųˆäG–ūC“ú–{‰ŧŠw‰ï‘æ94t‹G”N‰ïC–žŒÃ‰Ū‘åŠwiˆĪ’mjC3ŒŽ27`30“úC2014”ND

6.  ‘æŽO‹‰ƒAƒŠƒ‹ƒAƒ‹ƒR[ƒ‹‚Ėƒtƒb‘f‰ŧ‚É‚æ‚é‘―ŠŊ”\ŦŽl’uŠ·ƒIƒŒƒtƒBƒ“‚Ė—§‘Ė‘I‘ð“I‡ŽiŒû“Šj
*
ŠÝ“S”nA‘ęāV”EAFernando Arteaga-ArteagaAųˆäG–ūC“ú–{‰ŧŠw‰ï‘æ94t‹G”N‰ïC–žŒÃ‰Ū‘åŠwiˆĪ’mjC3ŒŽ27`30“úC2014”ND

7.  Development of Ni-SPRIX Catalysts toward Enantioselective Michael-type Reaction of Indoles with NitroolefinsiŒû“Šj
*Priyabrata Das
A’|’†˜a_AųˆäG–ūC“ú–{‰ŧŠw‰ï‘æ94t‹G”N‰ïC–žŒÃ‰Ū‘åŠwiˆĪ’mjC3ŒŽ27`30“úC2014”ND

8.  5‰ŋ‚ĖƒoƒiƒWƒEƒ€G”}‚ð—p‚Ē‚éƒGƒiƒ“ƒ`ƒI‘I‘ð“I’Y‘f|’Y‘fŒ‹‡Œ`Ž”―‰ž‚ĖŠJ”­‚Ɖž—piŒû“Šj
*
‘ęāV”EA’ŌŒī“N–įAŽŽ›ƒ•―AH“cŽOrA‹g“c‘ŨŽuAēŒÃ^A“yˆä‹M—TA”Đ’†–ŦAųˆäG–ūC“ú–{‰ŧŠw‰ï‘æ94t‹G”N‰ïC–žŒÃ‰Ū‘åŠwiˆĪ’mjC3ŒŽ27`30“úC2014”ND

9.  •sÄŠÂ‹Ŧ‚Ė‹y‚Ú‚·SPRIX”zˆĘŽq‚Ė’uŠ·ŠîŒø‰ĘiŒû“Šj
*
—ŅŒŦĄA’|’†˜a_AųˆäG–ūC“ú–{‰ŧŠw‰ï‘æ94t‹G”N‰ïC–žŒÃ‰Ū‘åŠwiˆĪ’mjC3ŒŽ27`30“úC2014”ND

10.              ƒXƒsƒ‰ŧ‡•Ļ‚ĖƒGƒiƒ“ƒ`ƒI‘I‘ð“I‡Ž–@‚ĖŠJ”­‚Æ—L‹@•ŠŽqG”}‚Ö‚Ė“WŠJiŒû“Šj
*
•“ā–FŽũALulu FanA‘ęāV”EAųˆäG–ūC“ú–{‰ŧŠw‰ï‘æ94t‹G”N‰ïC–žŒÃ‰Ū‘åŠwiˆĪ’mjC3ŒŽ27`30“úC2014”ND

11.              Enantioselective Organocatalyzed Synthesis of Cyclobutanes via Formal [2+2] CycloadditioniŒû“Šj
*Fernando Arteaga-Arteaga
A‘ęāV”EAųˆäG–ūC“ú–{‰ŧŠw‰ï‘æ94t‹G”N‰ïC–žŒÃ‰Ū‘åŠwiˆĪ’mjC3ŒŽ27`30“úC2014”ND

12.              Enantioselective Palladium(II) Catalyzed Cyclization-Cycloaddition Cascade ReactionsiŒû“Šj
*Abozeid Mohamed Ahmed
A‘ęāV”EAųˆäG–ūC“ú–{‰ŧŠw‰ï‘æ94t‹G”N‰ïC–žŒÃ‰Ū‘åŠwiˆĪ’mjC3ŒŽ27`30“úC2014”ND

13.              ƒwƒŠƒZƒ“‹y‚ŅƒwƒŠƒZƒ“—l‰ŧ‡•Ļ‚ĖŒø—Ķ“I•sÄ‡Ž–@‚ĖŠJ”­iƒ|ƒXƒ^[j
‘ęāV”EA‹g“c‘ŨŽuAŽŽ›ƒ•―AēŒÃ^A
*“yˆä‹M—TAųˆäG–ūCSymposium on Molecular Chirality 2014Aå‘䍑ÛƒZƒ“ƒ^[i‹{éjC6ŒŽ6`7“úC2014”ND
<ƒ|ƒXƒ^[ÜŽóÜ>

14.              ‘―‹@”\—L‹@•ŠŽqG”}‚ð—p‚Ē‚éƒGƒiƒ“ƒ`ƒI‘I‘ð“Iƒhƒ~ƒm”―‰ž‚ĖŠJ”­iŒû“Šj
*‘ęāV”ECu—L‹@•ŠŽqG”}‚É‚æ‚é–Ē—ˆŒ^•ŠŽq•ÏŠ·v‘æ4‰ņŒöŠJƒVƒ“ƒ|ƒWƒEƒ€(•ŠŽqŠˆŦ‰ŧ|—L‹@•ŠŽqG”}‡“ŊƒVƒ“ƒ|ƒWƒEƒ€)A–kŠC“đ‘åŠwi–kŠC“đjC6ŒŽ20`21“úC2014”ND

15.              G”}“I•sÄ˜A‘ą”―‰ž‚É‚æ‚éƒLƒ‰ƒ‹ƒrƒ‹ƒfƒBƒ“ƒOƒuƒƒbƒN‚Ė‘noiŒû“Šj
*‘ęāV”EC‘æ27‰ņƒCƒ“ƒ^[ƒtƒFƒbƒNƒXƒWƒƒƒpƒ“C“Œ‹žƒrƒbƒNƒTƒCƒgi“Œ‹žjC7ŒŽ2`4“úC2014”ND

16.              •sÄ—L‹@•ŠŽqG”}‚ð—p‚Ē‚éƒGƒiƒ“ƒ`ƒI‘I‘ð“Iaza-MBHŒ^ƒhƒ~ƒm”―‰ž‚ĖŠJ”­iƒ|ƒXƒ^[j
*•―“cCˆęA‘ęāV”EAˆäã’žlAFernando Arteaga-ArteagaA‹g“c‘ŨŽuA—é–Ø’Ę‹ąAųˆäG–ūC“ú–{ƒvƒƒZƒX‰ŧŠw‰ï2014ƒTƒ}[ƒVƒ“ƒ|ƒWƒEƒ€Cƒ^ƒ[ƒz[ƒ‹‘D–xi“Œ‹žjC7ŒŽ31`8ŒŽ1“úC2014”ND

17.              5‰ŋ‚ĖƒoƒiƒWƒEƒ€G”}‚ð—p‚Ē‚éƒGƒiƒ“ƒ`ƒI‘I‘ð“IC-CŒ‹‡Œ`Ž”―‰ž‚ĖŠJ”­‚Ɖž—piƒ|ƒXƒ^[j
âˆä’qOA
*‘ęāV”EAŽŽ›ƒ•―A‹g“c‘ŨŽuAēŒÃ^AųˆäG–ūC‘æ34‰ņ—L‹@‡ŽŽáŽčƒZƒ~ƒi[C‘åã‘åŠwi‘åãjC8ŒŽ5“úC2014”ND

18.              ƒCƒ~ƒ_ƒ][ƒ‹‚ð”zˆĘ•”ˆĘ‚Æ‚·‚éV‹KƒLƒ‰ƒ‹ƒXƒsƒŒ^”zˆĘŽq‚ĖŠJ”­iƒ|ƒXƒ^[j
*āV“c˜a–íA‚’JC•―A’|’†˜a_AųˆäG–ūC‘æ34‰ņ—L‹@‡ŽŽáŽčƒZƒ~ƒi[C‘åã‘åŠwi‘åãjC8ŒŽ5“úC2014”ND

19.              Žl’uŠ·ƒIƒŒƒtƒBƒ“‚ĖŠČ•Ö‚Đ‚Âƒƒ^ƒ‹ƒtƒŠ[‚Č—§‘Ė‘I‘ð“I‡Ž–@‚ĖŠJ”­iƒ|ƒXƒ^[j
*ŠÝ“S”nAFernando Arteaga-ArteagaA•―“cCˆęA‘ęāV”EAųˆäG–ūC‘æ34‰ņ—L‹@‡ŽŽáŽčƒZƒ~ƒi[C‘åã‘åŠwi‘åãjC8ŒŽ5“úC2014”ND
<—DGŒĪ‹†”­•\ÜŽóÜ>

20.              —L‹@G”}‚ð—p‚Ē‚éŒ`ŽŪ“IŠÂ‰ŧ•t‰Á”―‰ž‚ƃLƒ‰ƒ‹Žl’uŠ·’Y‘f‚ð—L‚·‚é•Ą‘fŠÂ‡Ž‚Ö‚Ė“WŠJiŒû“Šj
*
‘ęāV”EAFernando Arteaga-ArteagaA‹g“c‘ŨŽuA—é–Ø’Ę‹ąATue
M.-N. NguyenAųˆäG–ūC‘æ44‰ņ•Ą‘fŠÂ‰ŧŠw“Ē˜_‰ïCŽD–yŽs–Ŋƒz[ƒ‹i–kŠC“đjC9ŒŽ10`12“úC2014”ND

21.              Enantioselective CC Bond Forming Reactions Using Vanadium(V) Catalystsiƒ|ƒXƒ^[j
*
‘ęāV”EA’ŌŒī“N–įAŽŽ›ƒ•―A‹g“c‘ŨŽuAēŒÃ^A‰Í–ė•xˆęAųˆäG–ūC‘æ61‰ņ—L‹@‹ā‘Ū‰ŧŠw“Ē˜_‰ïC‹ãB‘åŠwi•Ÿ‰ŠjC9ŒŽ23`25“úC2014”ND

22.              Enantioselective Pd(II)/Pd(IV) Catalysis Utilizing a SPRIX Ligand: Efficient Construction of Chiral 3-Oxy-tetrahydrofuransiƒ|ƒXƒ^[j
*
’|’†˜a_AYogesh D. DhageAųˆäG–ūC‘æ61‰ņ—L‹@‹ā‘Ū‰ŧŠw“Ē˜_‰ïC‹ãB‘åŠwi•Ÿ‰ŠjC9ŒŽ23`25“úC2014”ND

23.              —L‹@•ŠŽqG”}‚ð—p‚Ē‚éƒGƒiƒ“ƒ`ƒI‘I‘ð“I•ŠŽq“āRauhut-Currier”―‰ž‚É‚æ‚éƒŋ-ƒƒ`ƒŠƒfƒ“-ƒÁ-ƒuƒ`ƒƒ‰ƒNƒ^ƒ€‚ĖŒø—Ķ“I‡ŽiŒû“Šj
‘ęāV”EA*ŠÝ“S”nAFernando Arteaga-ArteagaAųˆäG–ūC‘æ64‰ņ“ú–{–ōŠw‰ï‹ß‹EŽx•”‘‰ïE‘å‰ïC‹ž“s–ō‰Č‘åŠwi‹ž“sjC10ŒŽ11“úC2014”ND

24.              ƒwƒŠƒZƒ“‹y‚ŅƒwƒŠƒZƒ“—l‰ŧ‡•Ļ‚ĖƒGƒiƒ“ƒ`ƒI‘I‘ð“IŒø—Ķ‡Ž–@‚ĖŠJ”­iƒ|ƒXƒ^[j
‘ęāV”EA’ŌŒī“N–įA*‹g“c‘ŨŽuAŽŽ›ƒ•―AēŒÃ^A“yˆä‹M—TAųˆäG–ūC‘æ40‰ņ”―‰ž‚ƍ‡Ž‚Ėi•āƒVƒ“ƒ|ƒWƒEƒ€C“Œ–k‘åŠwi‹{éjC11ŒŽ10`11“úC2014”ND

25.              ‘―’uŠ·ŦŽl’uŠ·ƒIƒŒƒtƒBƒ“‚Ė—§‘Ė‘I‘ð“I‡Ž‚Æ‚ŧ‚Ė‰ž—piƒ|ƒXƒ^[j
*
‘ęāV”EAŠÝ“S”nAFernando Arteaga-ArteagaA•―“cCˆęAųˆäG–ūC‘æ40‰ņ”―‰ž‚ƍ‡Ž‚Ėi•āƒVƒ“ƒ|ƒWƒEƒ€C“Œ–k‘åŠwi‹{éjC11ŒŽ10`11“úC2014”ND

<International>

1.  Facile Synthesis of Tetrasubstituted Olefins Bearing Four Different Functional Units (Poster)
*Kishi, K.; Takizawa, S.; Arteaga, F. A.;
Sasai, H. The 17th SANKEN International Symposium, Osaka, Japan, January 21-22, 2014.

2.  Enantioselective Pd(II)/Pd(IV) Catalysis Utilizing SPRIX Ligand: Effective Construction of Chiral Acetoxylated Tetrahydrofurans (Poster)
*Dhage, Y. D.; Takenaka, K.;
Sasai, H. The 17th SANKEN International Symposium, Osaka, Japan, January 21-22, 2014.

3.  Enantioselective Palladium(II) Catalyzed Cyclization-Cycloaddition Cascade Reactions of Alkenyl Oximes (Poster)
*Abozeid, M. A.; Takizawa, S.;
Sasai, H. The 17th SANKEN International Symposium, Osaka, Japan, January 21-22, 2014.

4.  Development of Ni-SPRIX Catalysts toward Enantioselective Michael-type Reaction of Indoles with Nitroolefins (Poster)
*Das, P.; Takenaka, K.;
Sasai, H. The 17th SANKEN International Symposium, Osaka, Japan, January 21-22, 2014.

5.  Umpolung Reactivity of Pd Enolate: Cyclative Diacetoxylation of Alkynyl Cyclohexadienones Catalyzed by Pd-SPRIX (Poster)
*Mohanta, S. C.; Takenaka, K.;
Sasai, H. The 17th SANKEN International Symposium, Osaka, Japan, January 21-22, 2014.

6.  Ir Catalyzed Asymmetric Tandem Reaction of meso-Diols and Aldehydes (Poster)
Suzuki, T.; Ishizaka, Y.; Ghozati, K.; *Ismiyarto; Zhou, D.; Asano, K.;
Sasai, H. The 17th SANKEN International Symposium, Osaka, Japan, January 21-22, 2014.

7.  Catalytic Enantioselective Synthesis of Spiro Compounds and Their Applications to Asymmetric Catalysis (Poster)
*Fan, L.; Takeuchi, Y.; Takizawa, S.;
Sasai, H. The 17th SANKEN International Symposium, Osaka, Japan, January 21-22, 2014.

8.  Chiral Trisimidazole-Catalyzed Friedel-Crafts (FC)-type Reaction (Poster)
*Hirata, S.; Takizawa, S.; Murai, K.; Fujioka, H.;
Sasai, H. The 17th SANKEN International Symposium, Osaka, Japan, January 21-22, 2014.

9.  Development of Artificial Enzyme as Luminescence Probe (Poster)
*Nguyen, T. M.-N.; Nagata, Y.;
Sasai, H. The 17th SANKEN International Symposium, Osaka, Japan, January 21-22, 2014.

10.              Palladium-Catalyzed Direct C5 Arylation of Isoxazoles (Poster)
*Shigenobu, M.; Takenaka, K.;
Sasai, H. The 17th SANKEN International Symposium, Osaka, Japan, January 21-22, 2014.

11.              Dual Activation in Homo-Couplings Catalyzed by a Chiral Dinuclear Vanadium(V) Complex (Poster)
Takizawa, S.; Tsujihara, T.; Kodera, J.; *Sako, M.; Akita, M.; Doi, T.; Hatanaka, M.;
Sasai, H. The 17th SANKEN International Symposium, Osaka, Japan, January 21-22, 2014.

12.              Development of New SPRIX Ligands Having an Effective Asymmetric Environment (Poster)
*Lin, X.; Takenaka, K.; Takizawa, S.;
Sasai, H. The 17th SANKEN International Symposium, Osaka, Japan, January 21-22, 2014.
<Poster AwardŽóÜ>

13.              Enantioselective Organocatalyzed Formal [n+2] Cycloaddition Using Ketimines and Allenoates (Poster)
*Arteaga, F. A.; Takizawa, S.; Yoshida, Y.; Suzuki, M.; Sasai, H. The 17th SANKEN International Symposium, Osaka, Japan, January 21-22, 2014.

14.              Development of Chiral Catalyst Based on Functionalization of 1,2,3-Triazoles (Poster)
*Yoshida, Y.; Takizawa, S.; Sasai, H. The 17th SANKEN International Symposium, Osaka, Japan, January 21-22, 2014.

15.              Enantioselective Synthesis of ƒŋ-Methylidene-ƒÁ-Butyrolactones and ƒÁ-Butyrolactams: Intramolecular Rauhut-Currier Reaction Promoted by Bifunctional Organocatalysts (Poster)
Takizawa, S.; Nguyen, T. M.-N.; Kishi, K.; *Arteaga, F. A.; Suzuki, M.; Sasai, H. 15th Tetrahedron Symposium, London, UK, June 24-27, 2014.
<Elsevier Best Poster PrizeŽóÜ>

16.              Enantioselective Organocatalyzed Formal [n+2] Cycloaddition Using Allenoates (Poster)
Takizawa, S.; Arteaga, F. A.; *Yoshida, Y.; Suzuki, M.; Nguyen, T. M.-N.; Sasai, H. 15th Tetrahedron Symposium, London, UK, June 24-27, 2014.


17.              Catalytic Enantioselective Pd(II)/Pd(IV) Reactions Using SPRIX Ligand (Oral)
*Sasai, H. 20th International Conference on Organic Synthesis, Budapest, Hungary, June 29-July 4, 2014.


18.              Ir Catalyzed Asymmetric Tandem Reaction of meso-Diols and Aldehydes (Poster)
*Suzuki, T.; Ishizaka, Y.; Ghozati, K.; Zhou, D.; Asano, K.;
Sasai, H. 2nd International Symposium on C-H Activation, Rennes, France, June 30-July 3, 2014.

19.              Ir Catalyzed Asymmetric Tandem Reaction of meso-Diols and Aldehydes (Oral)
*Suzuki, T.; Ishizaka, Y.; Ghozati, K.; Zhou, D.; Asano, K.;
Sasai, H. The XXVI International Conference on Organometallic Chemistry, Sapporo, Japan, July 13-18, 2014.

20.              Recent Progress in Enantioselective Reactions Catalyzed by Pd-SPRIX: Pd Enolate Umpolung and Pd(II)/Pd(IV) Catalysis (Oral)
*Takenaka, K.; Mohanta, S. C.; Dhage, Y. D.;
Sasai, H. The XXVI International Conference on Organometallic Chemistry, Sapporo, Japan, July 13-18, 2014.

21.              Enantioselective Synthesis of Chiral Spiro Compounds and Their Applications to Organocatalysis (Poster)
*Takeuchi, Y.; Fan, L.; Takizawa, S.;
Sasai, H. The XXVI International Conference on Organometallic Chemistry, Sapporo, Japan, July 13-18, 2014.

22.              Recent Progress in Enantioselective Reactions Catalyzed by Pd-SPRIX: Pd Enolate Umpolung and Pd(II)/Pd(IV) Catalysis (Invite)
*Takenaka, K.
ICOMC-2014 Post-Symposium, Osaka, Japan, July 19, 2014.

23.              Enantioselective C-C Bond Forming Reactions Catalyzed by Vanadium(V) complex (Poster)
*Sako, M.; Takizawa, S.; Yoshida, Y.; Kodera, J.; Doi, T.;
Sasai, H. ICOMC-2014 Post-Symposium, Osaka, Japan, July 19, 2014.

24.              Development of Novel Chiral Spiro Ligands Bearing Imidazole Coordination Sites (Poster)
*Takatani, S.; Sawada, K.; Takenaka, K.;
Sasai, H. ICOMC-2014 Post-Symposium, Osaka, Japan, July 19, 2014.

25.              Palladium-Catalyzed Direct C-H Arylation of Isoxazoles at Their 5-Position (Poster)
*Shigenobu, M.; Takenaka, K.;
Sasai, H. ICOMC-2014 Post-Symposium, Osaka, Japan, July 19, 2014.

26.              Recent Progress of Enantioselective Catalysis Promoted by Pd-SPRIX (Poster)
*Mohanta, S. C.; Dhage, Y. D.; Takenaka, K.;
Sasai, H. 248th ACS National Meeting & Exposition, San Francisco, USA, August 10-14, 2014.

27.              Enantioselective Organocatalyzed Domino Process Based on aza-Morita-Baylis-Hillman-type (aza-MBH) Reaction (Poster)
*Hirata, S.; Takizawa, S.; Inoue, N.; Arteaga, F. A.; Yoshida, Y.; Suzuki, M.; Sasai, H.
248th ACS National Meeting & Exposition, San Francisco, USA, August 10-14, 2014.

28.              Enantioselective Palladium(II) Catalyzed Cyclization-Cycloaddition Cascade Reactions of Alkenyl Oximes (Poster)
*Abozeid, M. A.; Takizawa, S.;
Sasai, H. 248th ACS National Meeting & Exposition, San Francisco, USA, August 10-14, 2014.

29.              Organocatalyzed Enantioselective Reactions of Ketimines with Allenoates (Oral)
Takizawa, S.; Arteaga, F. A.; Yoshida, Y.; Suzuki, M.; *
Sasai, H. Aachen-Osaka Joint Symposium, Aachen, Germany, September 3-5, 2014.

30.              Palladium-Catalyzed Direct CH Arylation of Isoxazoles at Their 5-Position (Oral)
*Shigenobu, M.; Takenaka, K.;
Sasai, H. Aachen-Osaka Joint Symposium, Aachen, Germany, September 3-5, 2014.

31.              Enantioselective CC Bond Forming Reactions Catalyzed by Vanadium(V) Complex (Oral)
*Sako, M.; Takizawa, S.; Yoshida, Y.; Kodera, J.;
Sasai, H. Aachen-Osaka Joint Symposium, Aachen, Germany, September 3-5, 2014.

32.              Recent Progress of Enantioselective Catalysis Promoted by Pd-SPRIX (Poster)
Mohanta, S. C.; *Lin, X.; Takenaka, K.;
Sasai, H. ETH Zürich-Osaka Univ. Joint Symposium, Osaka, Japan, October 9-10, 2014.

33.              Enantioselective CC Bonf Forming Reactions Catalyzed by Vanadium(V) Complex (Poster)
*Sako, M.; Takizawa, S.; Tsujihara, T.; Yoshida, Y.; Kodera, J.; Kawano, T.;
Sasai, H. ETH Zürich-Osaka Univ. Joint Symposium, Osaka, Japan, October 9-10, 2014.

34.              Recent Progress in Enantioselective Reactions Catalyzed by Pd-SPRIX: Pd Enolate Umpolung and Pd(II)/Pd(IV) Catalysis (Poster)
*Mohanta, S. C.; Dhage, Y. D.; Takenaka, K.;
Sasai, H. The 2nd International Conference on Organometallics and Catalysis, Nara, Japan, October 26-29, 2014.

35.              Development of Novel Chiral Spiro Ligands Bearing Imidazole Coordination Sites (Poster)
*Sawada, K.; Takatani, S.; Takenaka, K.;
Sasai, H. The 2nd International Conference on Organometallics and Catalysis, Nara, Japan, October 26-29, 2014.

36.              Palladium-Catalyzed Direct CH Arylation of Isoxazoles at Their 5-Position (Poster)
Shigenobu, M.; *Takenaka, K.;
Sasai, H. The 2nd International Conference on Organometallics and Catalysis, Nara, Japan, October 26-29, 2014.

37.              Novel Enantioselective Reactions Promoted by Pd-SPRIX; Pd(II)/Pd(IV) Catalyses and Umpolung of Pd-Enolates (Invite)
*
Sasai, H. Molecular Chirality Asia 2014, Beijing, China, October 29-31, 2014.

38.              Enantioselective Palladium(II) Catalyzed Cyclization-Cycloaddition Cascade Reactions of Alkenyl Oximes (Poster)
*Abozeid, M. A.; Takizawa, S.;
Sasai, H. Molecular Chirality Asia 2014, Beijing, China, October 29-31, 2014.

39.              Development of New SPRIX Ligands Having an effective Asymmetric Environment (Poster)
*Lin, X.; Takenaka, K.;
Sasai, H. Molecular Chirality Asia 2014, Beijing, China, October 29-31, 2014.
<Poster AwardŽóÜ>

40.              Enantioselective CC Bond Forming Reactions Catalyzed by Vanadium(V) Complex (Poster)
Takizawa, S.; Yoshida, Y.; Sako, M.; Kodera, J.; *Sakai, T.;
Sasai, H. Molecular Chirality Asia 2014, Beijing, China, October 29-31, 2014.

41.              Enantioselective Organocatalyzed Formal [n+2] Cycloaddition Using Allenoates (Poster)
*Takizawa, S.; Arteaga, F. A.; Yoshida, Y.; Suzuki, M.; Kishi, K.; Nguyen, T. M.-N.;
Sasai, H. Molecular Chirality Asia 2014, Beijing, China, October 29-31, 2014.

42.              Enantio- and Diastereoselective Rauhut-Currier Reaction: Facile Synthesis of ƒŋ-Methylidene-ƒÁ-Butyrolactones and ƒÁ-Butyrolactams (Poster)
*Takizawa, S.; Kishi, K.; Nguyen, T. M.-N.; Arteaga, F. A.; Suzuki, M.;
Sasai, H. Advanced Molecular Transformations by Organocatalysts 2nd International Conference & 7th Symposium on Organocatalysis, Tokyo, Japan, November 21-22, 2014.

43.              Ir Catalyzed Asymmetric Tandem Reaction of meso-Diols and Aldehydes (Poster)
Suzuki, T.; *Ismiyarto; Ishizaka, Y.; Ghozati, K.; Zhou, D.-Y.; Asano, K.;
Sasai, H. The 18th SANKEN and The 13th SANKEN Nanotechnology Symposium, Osaka, Japan, December 10-11, 2014.

44.              Carbon Nanotubes(CNTs)-Supported Vanadium(V) Catalyst (Poster)
*Sako, M.; Takizawa, S.; Tsujihara, T.; Yoshida, Y.; Kodera, J.; Kawano, T.;
Sasai, H. The 18th SANKEN and The 13th SANKEN Nanotechnology Symposium, Osaka, Japan, December 10-11, 2014.

45.              Organocatalyzed Enantioselective Reactions of Ketimines with Allenoates (Invite)
*
Sasai, H. 8th Singapore International Chemistry Conference 2014, Singapore, December 14-17, 2014.

 

TopŠ

 

2013

<Domestic>

1.  Œø‰Ę“I‚Č•sÄŠÂ‹Ŧ‚ðŽ‚ÂSPRIX”zˆĘŽq‚ĖŠJ”­iŒû“Šj
*
—ŅŒŦĄA’|’†˜a_A‘ęāV”EAųˆäG–ūC“ú–{‰ŧŠw‰ï‘æ93t‹G”N‰ïC—§–―ŠŲ‘åŠwiŽ ‰ęjC3ŒŽ22`25“úC2013”ND

2.  SPRIX”zˆĘŽq‚ðŠˆ—p‚·‚éƒGƒiƒ“ƒ`ƒI‘I‘ð“IPd(II)/Pd(IV)G”}”―‰žFƒLƒ‰ƒ‹‚Čƒeƒgƒ‰ƒqƒhƒƒtƒ‰ƒ“—U“ą‘Ė‚ĖŒø—Ķ“I‡ŽiŒû“Šj
*Yogesh D. Dhage
A’|’†˜a_A‘ęāV”EAųˆäG–ūC“ú–{‰ŧŠw‰ï‘æ93t‹G”N‰ïC—§–―ŠŲ‘åŠwiŽ ‰ęjC3ŒŽ22`25“úC2013”ND

3.  PdƒGƒmƒ‰[ƒg‚Ė‹ÉŦ“]Š·FPd-SPRIXG”}‚É‚æ‚éƒAƒ‹ƒLƒjƒ‹ƒVƒNƒƒwƒLƒTƒWƒGƒmƒ“‚ĖŠÂ‰ŧ“IƒnƒƒAƒZƒgƒLƒV‰ŧ”―‰žiŒû“Šj
*Suman C. Mohanta
A’|’†˜a_A‘ęāV”EAųˆäG–ūC“ú–{‰ŧŠw‰ï‘æ93t‹G”N‰ïC—§–―ŠŲ‘åŠwiŽ ‰ęjC3ŒŽ22`25“úC2013”ND

4.  ƒpƒ‰ƒWƒEƒ€G”}‚É‚æ‚éƒCƒ\ƒIƒLƒTƒ][ƒ‹ŠÂ5ˆĘ‚Ė’žÚ“IC-HŒ‹‡ƒAƒŠ[ƒ‹‰ŧiŒû“Šj
*
dM‹§ŽuA’|’†˜a_AųˆäG–ūC“ú–{‰ŧŠw‰ï‘æ93t‹G”N‰ïC—§–―ŠŲ‘åŠwiŽ ‰ęjC3ŒŽ22`25“úC2013”ND

5.  “šG”}‚ðŠˆ—p‚·‚éƒXƒsƒƒrƒLƒmƒŠƒ“œŠi‚ĖƒGƒiƒ“ƒ`ƒI‘I‘ð“I\’ziŒû“Šj
*
ēŒÃ^A’|’†˜a_AųˆäG–ūC“ú–{‰ŧŠw‰ï‘æ93t‹G”N‰ïC—§–―ŠŲ‘åŠwiŽ ‰ęjC3ŒŽ22`25“úC2013”ND

6.  ŒõŠwŠˆŦƒXƒsƒ[4.4]ƒmƒiƒ“œŠi‚ĖG”}“I‡Ž‚ðŠî”Õ‚Æ‚·‚é•sÄ—L‹@•ŠŽqG”}‚ĖŠJ”­‚Ɖž—piŒû“Šj
*Lulu Fan
A‘ęāV”EAųˆäG–ūC“ú–{‰ŧŠw‰ï‘æ93t‹G”N‰ïC—§–―ŠŲ‘åŠwiŽ ‰ęjC3ŒŽ22`25“úC2013”ND

7.  ‹@”\Ŧ1,2,3-ƒgƒŠƒAƒ][ƒ‹‚ĖŠJ”­‚Æ•sÄ”―‰ž‚Ö‚Ė“WŠJiŒû“Šj
*
‹g“c‘ŨŽuA‘ęāV”EAųˆäG–ūC“ú–{‰ŧŠw‰ï‘æ93t‹G”N‰ïC—§–―ŠŲ‘åŠwiŽ ‰ęjC3ŒŽ22`25“úC2013”ND

8.  —L‹@•ŠŽqG”}‚ð—p‚Ē‚éƒGƒiƒ“ƒ`ƒI‘I‘ð“I•ŠŽq“āRauhut-Currier”―‰ž‚É‚æ‚éƒŋ-ƒƒ`ƒŠƒfƒ“-ƒÁ-ƒuƒ`ƒƒ‰ƒNƒgƒ“—Þ‚ĖŒø—Ķ‡ŽiŒû“Šj
*Tue
M.-N. NguyenAAndré GrossmannA—é–Ø’Ę‹ąA‘ęāV”EADieter EndersAųˆäG–ūC“ú–{‰ŧŠw‰ï‘æ93t‹G”N‰ïC—§–―ŠŲ‘åŠwiŽ ‰ęjC3ŒŽ22`25“úC2013”ND

9.  —L‹@•ŠŽqG”}‚É‚æ‚éƒPƒ`ƒ~ƒ“‚ðŠîŽŋ‚Æ‚·‚éƒGƒiƒ“ƒ`ƒI‘I‘ð“Iaza-MBH”―‰ž‚ĖŠJ”­iŒû“Šj
*Fernando Arteaga-Arteaga
A
‘ęāV”EAEmmanuelle RémondAJérôme BayardonA‹g“c‘ŨŽuASridharan VellaisamyASylvain JugéAųˆäG–ūC“ú–{‰ŧŠw‰ï‘æ93t‹G”N‰ïC—§–―ŠŲ‘åŠwiŽ ‰ęjC3ŒŽ22`25“úC2013”ND

10.              5‰ŋ‚ĖƒoƒiƒWƒEƒ€G”}‚ð—p‚Ē‚éƒGƒiƒ“ƒ`ƒI‘I‘ð“I’Y‘f|’Y‘fŒ‹‡Œ`Ž”―‰ž‚ĖŠJ”­‚Ɖž—piŒû“Šj
*
‘ęāV”EAŽŽ›ƒ•―AFernando Arteaga-ArteagaA‹g“c‘ŨŽuA‰i“c‰Ā‘åAųˆäG–ūC“ú–{‰ŧŠw‰ï‘æ93t‹G”N‰ïC—§–―ŠŲ‘åŠwiŽ ‰ęjC3ŒŽ22`25“úC2013”ND

11.              ƒLƒ‰ƒ‹ƒXƒsƒ[4.4]ƒmƒiƒ“œŠi‚ĖƒGƒiƒ“ƒ`ƒI‘I‘ð“I‡Ž–@‚ĖŠJ”­‚Æ•sÄG”}”―‰ž‚Ö‚Ė‰ž—piƒ|ƒXƒ^[j
*Lulu Fan
A‘ęāV”EAųˆäG–ūCSymposium on Molecular Chirality 2013C‹ž“s‘åŠw‹g“cƒLƒƒƒ“ƒpƒXi‹ž“sjC5ŒŽ10`11“úC2013”ND

12.              5‰ŋ‚Ė“ņŠjƒoƒiƒWƒEƒ€G”}‚ð—p‚Ē‚é•sÄ’Y‘f|’Y‘fŒ‹‡Œ`Ž”―‰ž‚ĖŠJ”­iƒ|ƒXƒ^[j
*
‘ęāV”EA’ŌŒī“N–įAŽŽ›ƒ•―AFernando Arteaga-ArteagaA‹g“c‘ŨŽuA‰i“c‰Ā‘åA”Đ’†–ŦAųˆäG–ūCSymposium on Molecular Chirality 2013C‹ž“s‘åŠw‹g“cƒLƒƒƒ“ƒpƒXi‹ž“sjC5ŒŽ10`11“úC2013”ND

13.              ƒpƒ‰ƒWƒEƒ€G”}‚É‚æ‚éƒCƒ\ƒIƒLƒTƒ][ƒ‹ŠÂ5ˆĘ‚Ė’žÚ“IC|HŒ‹‡ƒAƒŠ[ƒ‹‰ŧiƒ|ƒXƒ^[j
*
dM‹§ŽuA’|’†˜a_AųˆäG–ūC‘æ33‰ņ—L‹@‡ŽŽáŽčƒZƒ~ƒi[C_ŒË‘åŠw˜Zb‘äƒLƒƒƒ“ƒpƒXi•šŒÉjC8ŒŽ2“úC2013”ND

14.              ƒLƒ‰ƒ‹ƒXƒsƒ[4.4]ƒmƒiƒ“œŠi‚ĖƒGƒiƒ“ƒ`ƒI‘I‘ð“I‡Ž–@‚ĖŠJ”­‚Æ‚ŧ‚Ė‰ž—piƒ|ƒXƒ^[j
Lulu Fan
A*•“ā–FŽũA‘ęāV”EAųˆäG–ūC‘æ33‰ņ—L‹@‡ŽŽáŽčƒZƒ~ƒi[C_ŒË‘åŠw˜Zb‘äƒLƒƒƒ“ƒpƒXi•šŒÉjC8ŒŽ2“úC2013”ND

15.              —L‹@•ŠŽqG”}‚É‚æ‚éƒPƒ`ƒ~ƒ“‚ƃAƒŒƒmƒA[ƒg‚Æ‚ðŠîŽŋ‚Æ‚·‚éƒGƒiƒ“ƒ`ƒI‘I‘ð“Iaza-MBHŒ^ŠÂ‰ŧ”―‰ž‚ĖŠJ”­iƒ|ƒXƒ^[j
*
—é–Ø’Ę‹ąA‘ęāV”EAFernando Arteaga-ArteagaA‹g“c‘ŨŽuAųˆäG–ūC‘æ33‰ņ—L‹@‡ŽŽáŽčƒZƒ~ƒi[C_ŒË‘åŠw˜Zb‘äƒLƒƒƒ“ƒpƒXi•šŒÉjC8ŒŽ2“úC2013”ND

16.              Palladium-Catalyzed Direct C5 Arylation of Isoxazolesiƒ|ƒXƒ^[j
*
dM‹§ŽuA’|’†˜a_AųˆäG–ūC‘æ60‰ņ—L‹@‹ā‘Ū‰ŧŠw“Ē˜_‰ïCŠwK‰@‘åŠwi“Œ‹žjC9ŒŽ12`14“úC2013”ND

17.              SPRIX”zˆĘŽq‚ĖŠJ”­‚Ɖž—pi“Á•Ęu‰‰j
*
ųˆäG–ūC•―Ž25”N“x—L‹@‡Ž‰ŧŠw–k—ĪƒZƒ~ƒi[CÎėŒ§Â­”N‘‡ŒĪCƒZƒ“ƒ^[i‹ž“sjC10ŒŽ4`5“úC2013”ND

18.              —L‹@•ŠŽqG”}‚É‚æ‚éƒGƒiƒ“ƒ`ƒI‘I‘ð“I[n+2]ŠÂ‰ŧ•t‰Á”―‰žiƒ|ƒXƒ^[j
*
—é–Ø’Ę‹ąA‘ęāV”EAFernando Arteaga-ArteagaA‹g“c‘ŨŽuAųˆäG–ūC•―Ž25”N“x—L‹@‡Ž‰ŧŠw–k—ĪƒZƒ~ƒi[CÎėŒ§Â­”N‘‡ŒĪCƒZƒ“ƒ^[i‹ž“sjC10ŒŽ4`5“úC2013”ND

19.              Enantioselective Pd(II)/Pd(IV) Catalysis Utilizing SPRIX Ligand: Effective Construction of Chiral Acetoxylated Tetrahydrofuransiƒ|ƒXƒ^[j
*Yogesh D. Dhage
A’|’†˜a_A‘ęāV”EAųˆäG–ūC•―Ž25”N“x—L‹@‡Ž‰ŧŠw–k—ĪƒZƒ~ƒi[CÎėŒ§Â­”N‘‡ŒĪCƒZƒ“ƒ^[i‹ž“sjC10ŒŽ4`5“úC2013”ND

20.              Catalytic Enantioselective Synthesis of Spiro Compounds and Their Applications to Asymmetric Catalysisiƒ|ƒXƒ^[j
*Lulu Fan
A•“ā–FŽũA‘ęāV”EAųˆäG–ūC•―Ž25”N“x—L‹@‡Ž‰ŧŠw–k—ĪƒZƒ~ƒi[CÎėŒ§Â­”N‘‡ŒĪCƒZƒ“ƒ^[i‹ž“sjC10ŒŽ4`5“úC2013”ND

21.              ’žÚ“IC-HŒ‹‡ŠˆŦ‰ŧ‚É‚æ‚éƒCƒ\ƒIƒLƒTƒ][ƒ‹ŠÂ5ˆĘ‚ĖƒAƒŠ[ƒ‹‰ŧ”―‰ž‚ĖŠJ”­iƒ|ƒXƒ^[j
*
dM‹§ŽuA’|’†˜a_AųˆäG–ūC•―Ž25”N“x—L‹@‡Ž‰ŧŠw–k—ĪƒZƒ~ƒi[CÎėŒ§Â­”N‘‡ŒĪCƒZƒ“ƒ^[i‹ž“sjC10ŒŽ4`5“úC2013”ND

22.              ƒXƒsƒƒrƒ‰ƒNƒ^ƒ€‚ðŠî”Õ‚Æ‚ĩ‚―V‹KƒLƒ‰ƒ‹”zˆĘŽq‚ĖŠJ”­iƒ|ƒXƒ^[j
*
‚’JC•―Aúá–{Œ[•ãA’|’†˜a_AųˆäG–ūC•―Ž25”N“x—L‹@‡Ž‰ŧŠw–k—ĪƒZƒ~ƒi[CÎėŒ§Â­”N‘‡ŒĪCƒZƒ“ƒ^[i‹ž“sjC10ŒŽ4`5“úC2013”ND

23.              ƒLƒ‰ƒ‹”zˆĘŽqSPRIX‚Ė•sÄŠÂ‹Ŧ‚ÉŠÖ‚·‚éŒĪ‹†iƒ|ƒXƒ^[j
*
—ŅŒŦĄA’|’†˜a_A‘ęāV”EAųˆäG–ūC•―Ž25”N“x—L‹@‡Ž‰ŧŠw–k—ĪƒZƒ~ƒi[CÎėŒ§Â­”N‘‡ŒĪCƒZƒ“ƒ^[i‹ž“sjC10ŒŽ4`5“úC2013”ND

24.              P]ƒLƒ‰ƒ‹—L‹@•ŠŽqG”}‚ð—p‚Ē‚éŒõŠwŠˆŦ4’uŠ·’Y‘f‚Ė‡Ž‚Ɖž—piƒ|ƒXƒ^[j
*Fernando Arteaga-Arteaga
A
‘ęāV”EAEmmanuelle RémondA‹g“c‘ŨŽuAJérôme BayardonASridharan VellaisamyASylvain JugéAųˆäG–ūC•―Ž25”N“x—L‹@‡Ž‰ŧŠw–k—ĪƒZƒ~ƒi[CÎėŒ§Â­”N‘‡ŒĪCƒZƒ“ƒ^[i‹ž“sjC10ŒŽ4`5“úC2013”ND
<—DG”­•\ÜŽóÜ>

25.              ƒgƒŠƒAƒ][ƒ‹‚Ė‹@”\‰ŧ‚ðŠî”Õ‚Æ‚·‚é•sÄG”}‚ĖŠJ”­iƒ|ƒXƒ^[j
*
‹g“c‘ŨŽuA
‘ęāV”EAųˆäG–ūC•―Ž25”N“x—L‹@‡Ž‰ŧŠw–k—ĪƒZƒ~ƒi[CÎėŒ§Â­”N‘‡ŒĪCƒZƒ“ƒ^[i‹ž“sjC10ŒŽ4`5“úC2013”ND

26.              1,3]ƒvƒƒpƒ“ƒWƒAƒ~ƒ“•”ˆĘ‚ðŒŪƒ†ƒjƒbƒg‚Æ‚·‚éƒLƒ‰ƒ‹“ņdŠˆŦ‰ŧŒ^—L‹@•ŠŽqG”}‚ĖŠJ”­iƒ|ƒXƒ^[j
*
•―“cCˆęA“c’†_ˆęAžˆä‰Ã’ÖįAFernando Arteaga-ArteagaA‹g“c‘ŨŽuA
‘ęāV”EAųˆäG–ūC•―Ž25”N“x—L‹@‡Ž‰ŧŠw–k—ĪƒZƒ~ƒi[CÎėŒ§Â­”N‘‡ŒĪCƒZƒ“ƒ^[i‹ž“sjC10ŒŽ4`5“úC2013”ND

27.              ŒõŠwŠˆŦ‘JˆÚ‹ā‘ŪG”}‚ð—p‚Ē‚éƒGƒiƒ“ƒ`ƒI‘I‘ð“I‚Č2]ƒiƒtƒg[ƒ‹—Þ‚ĖŽ_‰ŧ“IƒJƒbƒvƒŠƒ“ƒO”―‰ž‚ĖŠJ”­iƒ|ƒXƒ^[j
‘ęāV”EA’ŌŒī“N–įAŽŽ›ƒ•―A*H“cŽOrAēŒÃ^A“yˆä‹M—TA”Đ’†–ŦAųˆäG–ūC•―Ž25”N“x—L‹@‡Ž‰ŧŠw–k—ĪƒZƒ~ƒi[CÎėŒ§Â­”N‘‡ŒĪCƒZƒ“ƒ^[i‹ž“sjC10ŒŽ4`5“úC2013”ND

28.              ƒGƒiƒ“ƒ`ƒI‘I‘ð“IRauhut-Currier”―‰ž‚ð—p‚Ē‚éƒŋ-ƒƒ`ƒŠƒfƒ“-ƒÁ-ƒuƒ`ƒƒ‰ƒNƒgƒ“‚Ė‡ŽiŒû“Šj
*
‘ęāV”EATue
M.-N. NguyenAAndré GrossmannA—é–Ø’Ę‹ąADieter EndersAųˆäG–ūC•―Ž25”N“x—L‹@‡Ž‰ŧŠw–k—ĪƒZƒ~ƒi[CÎėŒ§Â­”N‘‡ŒĪCƒZƒ“ƒ^[i‹ž“sjC10ŒŽ4`5“úC2013”ND

29.              ƒLƒ‰ƒ‹ƒXƒsƒ‰ŧ‡•Ļ‚ĖƒGƒiƒ“ƒ`ƒI‘I‘ð“I‡Ž–@‚ĖŠJ”­‚Ɖž—piŒû“Šj
Lulu Fan
A*•“ā–FŽũA‘ęāV”EAųˆäG–ūC‘æ63‰ņ“ú–{–ōŠw‰ï‹ß‹EŽx•”‘‰ïE‘å‰ïC“ŊŽxŽÐ—Žq‘åŠw‹ž“c•ÓƒLƒƒƒ“ƒpƒXi‹ž“sjC10ŒŽ12“úC2013”ND

30.              IrG”}‚ð—p‚Ē‚郁ƒ\ƒWƒI[ƒ‹‚ƃAƒ‹ƒfƒqƒh‚Ė˜A‘ąŒ^•sÄƒJƒbƒvƒŠƒ“ƒO”―‰ž‚ĖŠJ”­iŒû“Šj
*
—é–ØŒ’”VAÎâ—FAŽü‘å—gA’Đ–ė–FDAųˆäG–ūC‘æ63‰ņ“ú–{–ōŠw‰ï‹ß‹EŽx•”‘‰ïE‘å‰ïC“ŊŽxŽÐ—Žq‘åŠw‹ž“c•ÓƒLƒƒƒ“ƒpƒXi‹ž“sjC10ŒŽ12“úC2013”ND

31.              —L‹@•ŠŽqG”}‚É‚æ‚éƒPƒ`ƒ~ƒ“‚Æ2,3|ƒuƒ^ƒWƒGƒ“Ž_ƒGƒXƒeƒ‹‚Æ‚ðŠîŽŋ‚Æ‚·‚éƒGƒiƒ“ƒ`ƒI‘I‘ð“Iaza-MBHŒ^ŠÂ‰ŧ”―‰ž‚ĖŠJ”­iŒû“Šj
*
—é–Ø’Ę‹ąA‘ęāV”EAFernando Arteaga-ArteagaA‹g“c‘ŨŽuAųˆäG–ūC‘æ63‰ņ“ú–{–ōŠw‰ï‹ß‹EŽx•”‘‰ïE‘å‰ïC“ŊŽxŽÐ—Žq‘åŠw‹ž“c•ÓƒLƒƒƒ“ƒpƒXi‹ž“sjC10ŒŽ12“úC2013”ND

32.              Pd-SPRIXG”}‚ðŠˆ—p‚·‚éƒtƒ‰ƒ“—U“ą‘Ė‚ĖƒGƒiƒ“ƒ`ƒI‘I‘ð“I‡ŽiŒû“Šj
*
’|’†˜a_ASuman C. MohantaAYogesh D. DhageAųˆäG–ūC‘æ43‰ņ•Ą‘fŠÂ‰ŧŠw“Ē˜_‰ïC’·—Įė‘Û‰ï‹cęiŠō•ŒjC10ŒŽ17`19“úC2013”ND

33.              —L‹@•ŠŽqG”}‚É‚æ‚éƒPƒ`ƒ~ƒ“‚Æ2,3|ƒuƒ^ƒWƒGƒ“Ž_ƒGƒXƒeƒ‹‚Æ‚ðŠîŽŋ‚Æ‚·‚éƒGƒiƒ“ƒ`ƒI‘I‘ð“Iaza-MBHŒ^ŠÂ‰ŧ”―‰ž‚ĖŠJ”­iƒ|ƒXƒ^[j
*
—é–Ø’Ę‹ąA‘ęāV”EAFernando Arteaga-ArteagaA‹g“c‘ŨŽuAųˆäG–ūC‘æ39‰ņ”―‰ž‚ƍ‡Ž‚Ėi•āƒVƒ“ƒ|ƒWƒEƒ€C‹ãB‘åŠw•a‰@ƒLƒƒƒ“ƒpƒXi•Ÿ‰ŠjC11ŒŽ5`6“úC2013”ND

34.              “ņŠjƒoƒiƒWƒEƒ€G”}‚ð—p‚Ē‚é•sÄ’Y‘f|’Y‘fŒ‹‡Œ`Ž”―‰ž‚ĖŠJ”­iŒû“Šj
*
‘ęāV”EA’ŌŒī“N–įAŽŽ›ƒ•―AFernando Arteaga-ArteagaA‹g“c‘ŨŽuA‰i“c‰Ā‘åA”Đ’†–ŦAųˆäG–ūC‘æ39‰ņ”―‰ž‚ƍ‡Ž‚Ėi•āƒVƒ“ƒ|ƒWƒEƒ€C‹ãB‘åŠw•a‰@ƒLƒƒƒ“ƒpƒXi•Ÿ‰ŠjC11ŒŽ5`6“úC2013”ND

<International>

1.  Recent Progress of Enantioselective Catalysis Promoted by Pd-SPRIX (Poster)
*Mohanta, S. C.; Dhage, Y. D.; Takenaka, K.; Takizawa, S.;
Sasai, H. The 16th SANKEN International and The 11th SANKEN Nanotechnology Symposium, Osaka, Japan, January 22-23, 2013.

2.  Enantioselective Cyclization of 4-Alkenoic Acids via an Oxidative Allylic C-H Esterification (Poster)
*Akita, M.; Tanigaki, Y.; Takenaka, K.; Takizawa, S.;
Sasai, H. The 16th SANKEN International and The 11th SANKEN Nanotechnology Symposium, Osaka, Japan, January 22-23, 2013.

3.  Study on Asymmetric Environment of SPRIX Ligand (Poster)
*Lin, X.; Takenaka, K.; Takizawa, S.;
Sasai, H. The 16th SANKEN International and The 11th SANKEN Nanotechnology Symposium, Osaka, Japan, January 22-23, 2013.

4.  Pd-catalyzed Direct C-H Arylation of 5-Position of Isoxazole Ring (Poster)
*Shigenobu, M.; Takenaka, K.;
Sasai, H. The 16th SANKEN International and The 11th SANKEN Nanotechnology Symposium, Osaka, Japan, January 22-23, 2013.

5.  Copper-catalyzed Enantioselective Construction of Spirobiquinoline Skeleton (Poster)
*Sako, M.; Takenaka, K.;
Sasai, H. The 16th SANKEN International and The 11th SANKEN Nanotechnology Symposium, Osaka, Japan, January 22-23, 2013.

6.  Design and Synthesis of Organocatalysts Bearing Spiro Backbone (Poster)
*Fan, L.; Takizawa, S.;
Sasai, H. The 16th SANKEN International and The 11th SANKEN Nanotechnology Symposium, Osaka, Japan, January 22-23, 2013.

7.  Development of New Efficient Synthesis Method of Spiro Bis(1,2,3-triazole)s and Their Applications (Poster)
*Yoshida, Y.; Takizawa, S.;
Sasai, H. The 16th SANKEN International and The 11th SANKEN Nanotechnology Symposium, Osaka, Japan, January 22-23, 2013.

8.  Enantioselective Synthesis of a-Methylidene-g-Butyrolactones: Intramolecular Rauhut-Currier Reaction Promoted by Acid/Base Organocatalysts (Poster)
*
Nguyen, T. M.-N.; Takizawa, S.; Grossmann, A.; Suzuki, M.; Enders, D.; Sasai, H. The 16th SANKEN International and The 11th SANKEN Nanotechnology Symposium, Osaka, Japan, January 22-23, 2013.

9.  Organocatalyzed Enantioselective Aza-MBH Reaction of Ketimines (Poster)
Takizawa, S.;
Rémond, E.; *Arteaga-Arteaga, F.; Bayardon, J.; Yoshida, Y.; Vellaisamy, S.; Jugé, S.; Sasai, H. The 16th SANKEN International and The 11th SANKEN Nanotechnology Symposium, Osaka, Japan, January 22-23, 2013.

10.              Ir Catalyzed Asymmetric Tandem Reaction of meso-Diols and Aldehydes (Poster)
*Suzuki, T.; Ishizaka Y.; Ghozati, K.; Zhou, D.-Y.; Asano, K.;
Sasai, H. The 16th SANKEN International and The 11th SANKEN Nanotechnology Symposium, Osaka, Japan, January 22-23, 2013.

11.              Enantioselective Pd(II)/Pd(IV) Catalysis Using SPRIX Ligand: Efficient Synthesis of Chiral Tetrahydrofuran Derivatives (Oral)
*Takenaka, K.; Dhage, Y. D.; Takizawa, S.;
Sasai, H. Aachen-Osaka Symposium gBiological and Chemical Methods for Selective Catalysish, Osaka, Japan, March 11-13, 2013.

12.              Development of New Efficient Synthesis Method of Spiro Bis(1,2,3-triazole)s and Their Applications (Oral)
*Yoshida, Y.; Takizawa, S.;
Sasai, H. Aachen-Osaka Symposium gBiological and Chemical Methods for Selective Catalysish, Osaka, Japan, March 11-13, 2013.

13.              Umpolung Reactivity of Pd Enolate: Cyclative Diacetoxylation of Alkynyl Cyclohexadienones Catalyzed by Pd-SPRIX (Oral)
*Takenaka, K.; Mohanta, S. C.; Takizawa, S.;
Sasai, H. 245th ACS National Meeting, New Orleans, USA, April 7-11, 2013.

14.              Enantioselective cyclization of 4-alkenoic acids via an oxidative allylic CH esterification (Poster)
*Akita, M.; Tanigaki, Y.; Takenaka, K.; Takizawa, S.;
Sasai, H. 245th ACS National Meeting, New Orleans, USA, April 7-11, 2013.

15.              Copper-catalyzed Enantioselective Construction of Chiral Spirobi(tetrahydroquinoline) Scaffold (Poster)
*Sako, M.; Takenaka, K.;
Sasai, H. 245th ACS National Meeting, New Orleans, USA, April 7-11, 2013.

16.              Dual Activation in Homo- and Hetero-couplings Promoted by a Chiral Dinuclear Vanadium(V) Catalyst (Poster)
*Takizawa, S.; Tsujihara, T.; Kodera, J.; Arteaga-Arteaga, F.; Yoshida, Y.; Nagata, Y.; Sasai, H. The 4th UK/Japan Conference in Catalytic Asymmetric Synthesis, Sendai, Japan, April 19-20, 2013.

17.              Recent Progress of Enantioselective Catalysis Promoted by Pd-SPRIX (Poster)
*Takenaka, K.; Mohanta, S. C.; Dhage, Y. D.; Akita, M.; Sasai, H. The 4th UK/Japan Conference in Catalytic Asymmetric Synthesis, Sendai, Japan, April 19-20, 2013.

18.              Enantioselective Synthesis of Multifunctional Heterocyclic Compounds via Acid-Base Organocatalysis (Poster)
*Takizawa, S.; Nguyen, T. M.-N.; Inoue, N.; Hirata, S.; Sasai, H. 7th International Symposium on Acid-Base Catalysis, Tokyo, Japan, May 12-15, 2013.

19.              Enantioselective C-C Bond Forming Reactions Using Multi-Functional Organocatalysts: aza-Morita-Baylis-Hillman (aza-MBH) Reaction of Ketimines (Invited)
*Takizawa, S. Advanced Molecular Transformations by Organocatalysts 1st International Conference & 6th Symposium on Organocatalysis, Shiga, Japan, May 27-28, 2013.

20.              Catalytic Enantioselective Synthesis of Chiral Spiro[4.4]nonane Derivatives and Their Applications to Asymmetric Catalysis (Poster)
*Fan, L.; Takizawa, S.; Sasai, H. 25th International Symposium on Chirality (ISCD-25), Shanghai, China, July 7-10, 2013.
<Poster AwardŽóÜ>

21.              Recent Progress in Pd-SPRIX Catalyzed Enantioselective Reactions (Poster)
Takenaka, K.; Mohanta, S. C.; Dhage, Y. D.; Takizawa, S.; *Sasai, H. 17th IUPAC International Symposium on Organometallic Chemistry Directed toward Organic Synthesis (OMCOS 17), Fort Collins, USA, July 28-August 1, 2013.

22.              Dual Activation in Homo- and Hetero-Couplings Promoted by a Chiral Dinuclear Vanadium(V) Catalyst (Poster)
*Takizawa, S.; Kodera, J.; Arteaga, F. A.; Yoshida, Y.; Nagata, Y.; Sasai, H. The 16th International Symposium on Relations between Homogeneous and Heterogeneous Catalysis, Sapporo, Japan, August 4-9, 2013.

23.              Enantioselective Organocatalyzed aza-MBH Domino Reactions of Ketimines (Poster)
Takizawa, S.; Arteaga, F. A.; *Yoshida, Y.; Sasai, H. The 16th International Symposium on Relations between Homogeneous and Heterogeneous Catalysis, Sapporo, Japan, August 4-9, 2013.

24.              Ir Catalyzed Asymmetric Tandem Reaction of meso-Diols and Aldehydes (Poster)
*Suzuki, T.; Ishizaka, Y.; Ghozati, K.; Zhou, D.-Y.; Asano, K.; Sasai, H. The 16th International Symposium on Relations between Homogeneous and Heterogeneous Catalysis, Sapporo, Japan, August 4-9, 2013.

25.              Enantioselective Organocatalyzed Aza-Morita-Baylis-Hillman (aza-MBH) Reraction of Ketimines (Poster)
Takizawa, S.; Rémond, E.; *Arteaga, F. A.; Yoshida, Y.; Vellaisamy, S.; Bayardon, J.; Jugé, S.; Sasai, H. 15th Asian Chemical Congress, Resorts World Sentosoa, Singapore, August 19-23, 2013.

26.              Dual Activation in Homo- and Hetero-Couplings Promoted by A Chiral Dinuclear Vanadium(V) Catalyst (Poster)
*Takizawa, S.; Tsujihara, T.; Kodera, J.; Arteaga, F. A.; Yoshida, Y.; Nagata, Y.; Sasai, H. 15th Asian Chemical Congress, Resorts World Sentosoa, Singapore, August 19-23, 2013.

27.              Enantioselective Organocatalyzed Formal [n+2] Cycloaddition of Ketimines (Poster)
*Arteaga, F. A.; Takizawa, S.; Yoshida, Y.; Suzuki, M.; Sasai, H. 10th International Symposium on Carbanion Chemistry, Kyoto, Japan, September 23-26, 2013.

28.              Acid-Base Organocatalyzed Enantioselective Synthesis of Highly Functionalized Heterocyclic Compounds (Poster)
*Takizawa, S.; Nguyen, T. M.-N.; Inoue, N.; Hirata, S.; Sasai, H. 10th International Symposium on Carbanion Chemistry, Kyoto, Japan, September 23-26, 2013.

29.              Exploring a Novel Carbon-carbon Bond Forming Reaction Using a Bifunctional Asymmetric Catalyst (Invited)
Sasai, H. Univ. of Bourgogne, France, October 15, 2013.

30.              Recent Progress in Pd-SPRIX Catalyzed Reactions (Invited)
Sasai, H. Gif s/Yvette Centre de Recherches de Gif, France, October 17, 2013.

31.              Recent Progress in Pd-SPRIX Catalyzed Reactions (Invited)
Sasai, H. Univ. of Bourgogne,, France, October 25, 2013.

32.              Exploring a Novel Carbon-carbon Bond Forming Reaction Using a Bifunctional Asymmetric Catalyst (Invited)
Sasai, H. University of Bologna, Italy, October 28, 2013.

33.              Exploring a Novel Carbon-carbon Bond Forming Reaction Using a Bifunctional Asymmetric Catalyst (Invited)
Sasai, H. The University of Parma, Italy, October 31, 2013.

34.              Enantioselective Organocatalyzed Cycloadditions Based on the aza-Morita-Baylis-Hillman-type (aza-MBH) and Rauhut-Currier (RC) Process (Poster)
*Takizawa, S.; Sasai, H. The 8th International Conference on Cutting-Edge Organic Chemistry in Asia (ICCEOCA-8) and The 4th New Phase International Conference on S Cutting-Edge Organic Chemistry in Asia (NICCEOCA-4), Osaka, Japan, November 25-28, 2013.

35.              Recent Progress in Pd-SPRIX Catalyses (Poster)
Takenaka, K.; Mohanta, S. C.; Dhage, Y. D.; Takizawa, S.; *Sasai, H. The 8th International Conference on Cutting-Edge Organic Chemistry in Asia (ICCEOCA-8) and The 4th New Phase International Conference on S Cutting-Edge Organic Chemistry in Asia (NICCEOCA-4), Osaka, Japan, November 25-28, 2013.

36.              Enantioselective Organocatalyzed Formal [n+2] Cycloaddition of Ketimines with Allenoates (Poster)
*Arteaga, F. A.; Takizawa, S.; Yoshida, Y.; Suzuki, M.; Sasai, H. The 8th International Symposium on Integrated Synthesis (ISIS-8), Nara, Japan, November 29-December 1, 2013.

37.              Recent Progress in Pd-SPRIX Catalyzed Enantioselective Reactions (Poster)
Takenaka, K.; *Dhage, Y. D.; Mohanta, S. C.; Takizawa, S.; Sasai, H. The 8th International Symposium on Integrated Synthesis (ISIS-8), Nara, Japan, November 29-December 1, 2013.

38.              Ir Catalyzed Asymmetric Tandem Reaction of meso-Diols and Aldehydes (Poster)
Suzuki, T.; *Ismiyarto; Ishizaka, Y.; Ghozati, K.; Zhou, D.-Y.; Asano, K.; Sasai, H. The 8th International Symposium on Integrated Synthesis (ISIS-8), Nara, Japan, November 29-December 1, 2013.

39.              Novel Catalytic Reaction Promoted by Pd-SPRIX Complex (Oral)
Takenaka, K.; Mohanta, S. C.; Dhage, Y. D.; Takizawa, S.; *Sasai, H. First Osaka University-EPFL International Symposium, Osaka, Japan, December 2-4, 2013.

40.              Enantioselective Organocatalyzed Formal [n+2] Cycloaddition of Ketimines (Poster)
*Arteaga, F. A.; Takizawa, S.; Yoshida, Y.; Suzuki, M.; Sasai, H. First Osaka University-EPFL International Symposium, Osaka, Japan, December 2-4, 2013.

41.              Enantioselective Synthesis of a-Methylidene-g-Butyrolactones: Intramolecular Rauhut-Currier Reaction Promoted by Acid/Base Organocatalysts (Poster)
*
Nguyen, T. M.-N.; Grossmann, A.; Takizawa, S.; Suzuki, M.; Enders, D.; Sasai, H. First Osaka University-EPFL International Symposium, Osaka, Japan, December 2-4, 2013.

 

TopŠ

 

2012

<Domestic>

1.  V‹K“ņdŠˆŦ‰ŧŒ^—L‹@•ŠŽqG”}‚ĖŠJ”­‚Æ•sÄFriedel-Crafts”―‰ž‚Ö‚Ė‰ž—piŒû“Šj
*
‰i“c‰Ā‘åA‘ęāV”EAųˆäG–ūC“ú–{‰ŧŠw‰ï‘æ92t‹G”N‰ïCŒcœä‹`m‘åŠwi_“ސėjC3ŒŽ25`28“úC2012”ND

2.  ƒXƒsƒœŠi‚ð—L‚·‚éŽ_-‰–ŠîŒ^—L‹@•ŠŽqG”}‚ð—p‚Ē‚―ƒGƒiƒ“ƒ`ƒI‘I‘ð“Iaza-MBH”―‰ž‚ĖŠJ”­iŒû“Šj
*
‰ÆŠėŒ’‘ūA‹ËŽR‹M”üŽqA‘ęāV”EAųˆäG–ūC“ú–{‰ŧŠw‰ï‘æ92t‹G”N‰ïCŒcœä‹`m‘åŠwi_“ސėjC3ŒŽ25`28“úC2012”ND

3.  —L‹@G”}‚ð—p‚Ē‚éƒGƒiƒ“ƒ`ƒI‘I‘ð“I•ŠŽq“āRauhut-Currier”―‰žiŒû“Šj
*Tue M.-N. Nguyen
AAndré GrossmannA‘ęāV”EAųˆäG–ūC“ú–{‰ŧŠw‰ï‘æ92t‹G”N‰ïCŒcœä‹`m‘åŠwi_“ސėjC3ŒŽ25`28“úC2012”ND

4.  ŒõŠwŠˆŦ1,2,3-ƒgƒŠƒAƒ][ƒ‹—U“ą‘Ė‚Ė‡Ž‚Æ•sÄ”―‰ž‚Ö‚Ė‰ž—piŒû“Šj
*
‹g“c‘ŨŽuA‘ęāV”EAųˆäG–ūC“ú–{‰ŧŠw‰ï‘æ92t‹G”N‰ïCŒcœä‹`m‘åŠwi_“ސėjC3ŒŽ25`28“úC2012”ND

5.  Pd-SPRIXG”}‚ð—p‚Ē‚é4]ƒAƒ‹ƒPƒ“Ž_‚ĖƒGƒiƒ“ƒ`ƒI‘I‘ð“I‚Č•ŠŽq“āŽ_‰ŧ“IƒAƒŠƒ‹ˆĘCHŒ‹‡ƒGƒXƒeƒ‹‰ŧ”―‰žiŒû“Šj
*
H“cŽOrA’JŠ_—E„A’|’†˜a_A‘ęāV”EAųˆäG–ūC“ú–{‰ŧŠw‰ï‘æ92t‹G”N‰ïCŒcœä‹`m‘åŠwi_“ސėjC3ŒŽ25`28“úC2012”ND

6.  Pd-SPRIXG”}‚É‚æ‚éƒGƒiƒ“ƒ`ƒI‘I‘ð“I‚ČŽ_‰ŧ“IŠÂ‰ŧ]ƒJƒ‹ƒ{ƒLƒVƒ‹‰ŧ˜A‘ą”―‰žFPd|ƒGƒmƒ‰[ƒg’†ŠÔ‘Ė‚ĖƒJƒ‹ƒ{ƒLƒVƒ‹‰ŧiŒû“Šj
* S. C. Mohanta
A’|’†˜a_A‘ęāV”EAųˆäG–ūC“ú–{‰ŧŠw‰ï‘æ92t‹G”N‰ïCŒcœä‹`m‘åŠwi_“ސėjC3ŒŽ25`28“úC2012”ND

7.  ƒLƒ‰ƒ‹ƒXƒsƒƒrƒ‰ƒNƒ^ƒ€‚ðŠî”Õ‚Æ‚·‚éV‹Kƒ`ƒIƒAƒ~ƒhŒ^”zˆĘŽq‚ĖŠJ”­iŒû“Šj
*
‚’JC•―A’|’†˜a_AųˆäG–ūC“ú–{‰ŧŠw‰ï‘æ92t‹G”N‰ïCŒcœä‹`m‘åŠwi_“ސėjC3ŒŽ25`28“úC2012”ND

8.  ƒLƒ‰ƒ‹”zˆĘŽqSPRIX ‚Ė•sÄŠÂ‹Ŧ‚ÉŠÖ‚·‚éŒĪ‹†iŒû“Šj
*
—ŅŒŦĄA’|’†˜a_A‘ęāV”EAųˆäG–ūC“ú–{‰ŧŠw‰ï‘æ92t‹G”N‰ïCŒcœä‹`m‘åŠwi_“ސėjC3ŒŽ25`28“úC2012”ND

9.  ƒGƒiƒ“ƒ`ƒI‘I‘ð“IPd(II)/Pd(IV)G”}‚É‚æ‚éƒAƒ‹ƒPƒjƒ‹ƒAƒ‹ƒR[ƒ‹‚ĖŽ_‰ŧ“I•ŠŽq“āŠÂ‰ŧ”―‰žiŒû“Šj
*Yogesh Daulat Dhage
A’|’†˜a_A‘ęāV”EAųˆäG–ūC“ú–{‰ŧŠw‰ï‘æ92t‹G”N‰ïCŒcœä‹`m‘åŠwi_“ސėjC3ŒŽ25`28“úC2012”ND

10.              IrG”}‚ð—p‚Ē‚郁ƒ\ƒWƒI[ƒ‹‚ƃAƒ‹ƒfƒqƒh‚Ė˜A‘ąŒ^•sÄƒJƒbƒvƒŠƒ“ƒO”―‰ž‚ĖŠJ”­iŒû“Šj
—é–ØŒ’”VA*Îâ—FAŽü‘å—gA’Đ–ė–FDAųˆäG–ūC“ú–{‰ŧŠw‰ï‘æ92t‹G”N‰ïCŒcœä‹`m‘åŠwi_“ސėjC3ŒŽ25`28“úC2012”ND

11.              “šG”}‚ðŠˆ—p‚·‚éƒLƒ‰ƒ‹ƒXƒsƒœŠi‚ĖŠČ•Ö\’ziŒû“Šj
*
’|’†˜a_AųˆäG–ūC“ú–{‰ŧŠw‰ï‘æ92t‹G”N‰ïCŒcœä‹`m‘åŠwi_“ސėjC3ŒŽ25`28“úC2012”ND

12.              Pd-SPRIXG”}‚É‚æ‚éƒGƒiƒ“ƒ`ƒI‘I‘ð“I‚ČŽ_‰ŧ“IŠÂ‰ŧ]ƒJƒ‹ƒ{ƒLƒVƒ‹‰ŧ˜A‘ą”―‰žFPd|ƒGƒmƒ‰[ƒg’†ŠÔ‘Ė‚ĖƒJƒ‹ƒ{ƒLƒVƒ‹‰ŧiŒû“Šj
*Suman C. Mohanta
A’|’†˜a_A‘ęāV”EAųˆäG–ūCSymposium on Molecular Chirality ASIA 2012C‹ãB‘åŠwi•Ÿ‰ŠjC5ŒŽ17`18“úC2012”ND

13.              ƒGƒiƒ“ƒ`ƒI‘I‘ð“IPd(II)/Pd(IV)G”}‚É‚æ‚éƒAƒ‹ƒPƒjƒ‹ƒAƒ‹ƒR[ƒ‹‚ĖŽ_‰ŧ“I•ŠŽq“āŠÂ‰ŧ”―‰žiƒ|ƒXƒ^[j
*Yogesh D. Dhage
A’|’†˜a_A‘ęāV”EAųˆäG–ūCSymposium on Molecular Chirality ASIA 2012C‹ãB‘åŠwi•Ÿ‰ŠjC5ŒŽ17`18“úC2012”ND

14.              —L‹@•ŠŽqG”}‚É‚æ‚éƒPƒ`ƒ~ƒ“‚ðŠîŽŋ‚Æ‚·‚éaza-MBH”―‰žiƒ|ƒXƒ^[j
‘ęāV”EAEmmanuelle
RémondA*Fernando Arteaga-ArteagaAJérôme BayardonA‹g“c‘ŨŽuASylvain JugéAųˆäG–ūCSymposium on Molecular Chirality ASIA 2012C‹ãB‘åŠwi•Ÿ‰ŠjC5ŒŽ17`18“úC2012”ND

15.              Enantioselective Synthesis of Multifunctional Compounds via Bifunctional OrganocatalysisiŒû“Šj
*‘ęāV”EC•ķ•”‰ČŠwČ‰ČŠwŒĪ‹†”ï•â•‹āuVŠwp—ĖˆæŒĪ‹†iŒĪ‹†—Ėˆæ’ņˆÄŒ^jE—L‹@•ŠŽqG”}v‘æ1‰ņ‘S‘Ė‰ï‹cC‹ž“s‘åŠwi‹ž“sjC6ŒŽ8`9“úC2012”ND

16.              Pd-SPRIXG”}‚É‚æ‚é4|ƒAƒ‹ƒPƒ“Ž_‚ĖŽ_‰ŧ“IƒAƒŠƒ‹ˆĘC-HŒ‹‡ŠˆŦ‰ŧ‚ðŒo‚éƒGƒiƒ“ƒ`ƒI‘I‘ð“IŠÂ‰ŧ”―‰žiƒ|ƒXƒ^[j
*H“cŽOrA’JŠ_—E„A’|’†˜a_A‘ęāV”EAųˆäG–ūC‘æ39‰ņ—L‹@”―‰ž§’k‰ïCŠÖž‘åŠwi‘åãjC8ŒŽ3“úC2012”ND

17.              “šG”}‚ðŠˆ—p‚·‚éƒXƒsƒƒrƒLƒmƒŠƒ“œŠi‚ĖƒGƒiƒ“ƒ`ƒI‘I‘ð“I\’ziƒ|ƒXƒ^[j
*ēŒÃ^A’|’†˜a_AųˆäG–ūC‘æ39‰ņ—L‹@”―‰ž§’k‰ïCŠÖž‘åŠwi‘åãjC8ŒŽ3“úC2012”ND

18.              ƒLƒ‰ƒ‹ƒXƒsƒƒrƒ‰ƒNƒ^ƒ€‚ðŠî”Õ‚Æ‚·‚éV‹Kƒ`ƒIƒAƒ~ƒhŒ^”zˆĘŽq‚ĖŠJ”­iƒ|ƒXƒ^[j
*‚’JC•―A’|’†˜a_AųˆäG–ūC‘æ39‰ņ—L‹@”―‰ž§’k‰ïCŠÖž‘åŠwi‘åãjC8ŒŽ3“úC2012”ND

19.              “ņdŠˆŦ‰ŧŒ^—L‹@•ŠŽqG”}‚ð—p‚Ē‚éƒLƒ‰ƒ‹‘―ŠŊ”\Ŧ‰ŧ‡•Ļ‚Ė‡Ž‚Ɖž—piŒû“Šj
*‘ęāV”EC•ķ•”‰ČŠwČ‰ČŠwŒĪ‹†”ï•â•‹āuVŠwp—ĖˆæŒĪ‹†iŒĪ‹†—Ėˆæ’ņˆÄŒ^jE—L‹@•ŠŽqG”}v‘æ1‰ņ—L‹@•ŠŽqG”}@ŽáŽčƒZƒ~ƒi[Cƒ‰ƒtƒH[ƒŒ“ߐ{i“Č–ØjC9ŒŽ8`9“úC2012”ND

20.              Umpolung Reactivity of Pd Enolate: Cyclative Diacetoxylation of Alkynyl Cyclohexadienones Catalyzed by Pd-SPRIXiŒû“Šj
*’|’†˜a_ASuman C. MohantaA‘ęāV”EAųˆäG–ūC‘æ59‰ņ—L‹@‹ā‘Ū‰ŧŠw“Ē˜_‰ïC‘åã‘åŠwi‘åãjC9ŒŽ13`15“úC2012”ND

21.              Study on Asymmetric Environment of SPRIX Ligandiƒ|ƒXƒ^[j
*—ŅŒŦĄA’|’†˜a_A‘ęāV”EAųˆäG–ūC‘æ59‰ņ—L‹@‹ā‘Ū‰ŧŠw“Ē˜_‰ïC‘åã‘åŠwi‘åãjC9ŒŽ13`15“úC2012”ND

22.              Enantioselective Coupling of Phenanthrols Using Vanadium Catalystsiƒ|ƒXƒ^[j
*
ŽŽ›ƒ•―A‘ęāV”EAųˆäG–ūC‘æ59‰ņ—L‹@‹ā‘Ū‰ŧŠw“Ē˜_‰ïC‘åã‘åŠwi‘åãjC9ŒŽ13`15“úC2012”ND

23.              Ir Catalyzed Asymmetric Tandem Reaction of meso-Diols and Aldehydesiƒ|ƒXƒ^[j
*—é–ØŒ’”VAÎâ—FAŽü‘å—gA’Đ–ė–FDAųˆäG–ūC‘æ59‰ņ—L‹@‹ā‘Ū‰ŧŠw“Ē˜_‰ïC‘åã‘åŠwi‘åãjC9ŒŽ13`15“úC2012”ND

24.              ƒLƒ‰ƒ‹ƒXƒsƒƒrƒ‰ƒNƒ^ƒ€‚ðŠî”Õ‚Æ‚·‚éV‹Kƒ`ƒIƒAƒ~ƒhŒ^”zˆĘŽq‚ĖŠJ”­iƒ|ƒXƒ^[j
*‚’JC•―A’|’†˜a_AųˆäG–ūC‘æ42‰ņ•Ą‘fŠÂ‰ŧŠw“Ē˜_‰ïC‹ž“sƒeƒ‹ƒTi‹ž“sjC10ŒŽ11`13“úC2012”ND

25.              —L‹@•ŠŽqG”}‚É‚æ‚éƒPƒ`ƒ~ƒ“‚ðŠîŽŋ‚Æ‚·‚é•sÄaza-MBH”―‰žiŒû“Šj
‘ęāV”EAEmmanuelle RémondA*Fernando Arteaga ArteagaAJérôme BayardonA‹g“c‘ŨŽuASylvain JugéAųˆäG–ūC‘æ62‰ņ“ú–{–ōŠw‰ï‹ß‹EŽx•”‘‰ïE‘å‰ïC•ŒÉė—Žq‘åŠwi•šŒÉjC10ŒŽ20“úC2012”ND

26.              ƒoƒiƒWƒEƒ€G”}‚ð—p‚Ē‚éƒGƒiƒ“ƒ`ƒI‘I‘ð“I’Y‘f|’Y‘fŒ‹‡Œ`Ž”―‰ž‚ĖŠJ”­‚Ɖž—piŒû“Šj
*
‘ęāV”EAFernando Arteaga-ArteagaA‹g“c‘ŨŽuAŽŽ›ƒ•―A‰i“c‰Ā‘åAųˆäG–ūC‘æ62‰ņ“ú–{–ōŠw‰ï‹ß‹EŽx•”‘‰ïE‘å‰ïC•ŒÉė—Žq‘åŠwi•šŒÉjC10ŒŽ20“úC2012”ND

27.              —L‹@•ŠŽqG”}‚É‚æ‚éƒPƒ`ƒ~ƒ“‚ðŠîŽŋ‚Æ‚·‚é•sÄaza-MBH”―‰žiƒ|ƒXƒ^[j
‘ęāV”EAEmmanuelle RémondA*Fernando Arteaga-ArteagaAJérôme BayardonA‹g“c‘ŨŽuASridharan VellaisamyASylvain JugéAųˆäG–ūC‘æ5‰ņ—L‹@G”}ƒVƒ“ƒ|ƒWƒEƒ€CŠwK‰@‘åŠwi“Œ‹žjC10ŒŽ26`27“úC2012”ND

<International>

1.  Catalytic Enantioselective Coupling of Phenanthrols (Poster)
*Kodera, J.; Takizawa, S.; Sasai, H. The 15th SANKEN International Symposium and The 10th SANKEN Nanotechnology Symposium, Osaka, Japan, January 12-13, 2012.

2.  Enantioselective Rauhut-Currier Reaction (Oral)
Takizawa, S.; *Nguyen, T. M.-N.; Grossmann, A.; Enders, D.; Sasai, H. Osaka-Aachen Mini-symposium, Osaka, Japan, March 12, 2012.

3.  Enantioselective C-C Bond-Forming Reactions Using Vanadium(V) Complexes (Poster)
*Takizawa, S.; Kodera, J.; Rajesh, D.; Katayama, T.; Sasai, H. 243rd ACS National Meeting, San Diego, USA, March 25-29, 2012.

4.  Development of Chiral Spiro Bis(isoxazoline) Ligand gSPRIXh (Invited)
*
Sasai, H. BITfs 3rd Annual World Congress of Catalytic Asymmetric Synthesis-2012, Beijin, China, May 12-14, 2012.

5.  Exploring Novel Enantioselective Domino Reactions Promoted by Bifunctional Organocatalysts (Invited)
*
Sasai, H. 3rd International Symposium on Organic Synthesis and Drug Development (ISOSDD2012), Changzhou, China, May 20-23, 2012.

6.  Enantioselective Intramolecular Rauhut-Currier Reaction (Poster)
*
Nguyen, T. M.-N.; Grossmann, A.; Takizawa, S.; Enders, D.; Sasai, H. 3rd International Symposium on Organic Synthesis and Drug Development (ISOSDD2012), Changzhou, China, May 20-23, 2012.

7.  Development of BINOL-Derived Organocatalysts with Dual Activation Mechanism and Their Applications to Enantioselective Friedel-Crafts Type Reaction (Poster)
*Nagata
, Y.; Takizawa, S.; Sasai, H. 3rd International Symposium on Organic Synthesis and Drug Development (ISOSDD2012), Changzhou, China, May 20-23, 2012.

8.  Development of Enantioselective Carbon-Carbon Bond Forming Reactions Using Multi-functional Organocatalyst (Invited)
*
Sasai, H. International Conference on Functional Organic Materials and Related Devices, Hsinchu, Taiwan, June 16-17, 2012.

9.  Enantioselective Coupling of Phenanthrols Using Vanadium Catalysts (Poster)
*Kodera, J.; Takizawa, S.;
Sasai, H. International Conference on Functional Organic Materials and Related Devices, Hsinchu, Taiwan, June 16-17, 2012.

10.              Enantioselective Carboxylation via a p-Allyl Pd Intermediate Promoted by Pd-SPRIX Catalyst (Poster)
*Takenaka, K.; Akita, M.; Mohanta, S. C.; Takizawa, S.;
Sasai, H. International Conference on Functional Organic Materials and Related Devices, Hsinchu, Taiwan, June 16-17, 2012.

11.              Several Catalytic Enantioselective Reactions Promoted by Vanadium Complexes (Oral)
*Takizawa, S.;
Sasai, H. Osaka-Bielefeld Symposium on Chiral Synthetic Chemistry, Bielefeld, Germany, July 11, 2012.

12.              Enantioselective C-C Bond-forming Reactions Catalyzed by Vanadium(V) Complexes (Invited)
*
Sasai, H; Takizawa, S.; Kodera, J. 8th International Vanadium Symposium Chemistry, Biological Chemistry, & Toxicology (V8), Washington DC, USA, August 15-18, 2012.

13.              Enantioselective Synthesis of a-Alkylidene-g-Butyrolactones: Intramolecular Rauhut-Currier Reaction Promoted by Acid/Base Organocatalysts (Poster)
*
Nguyen, T. M.-N.; Takizawa, S.; Grossmann, A.; Enders, D.; Sasai, H. The 6th Takeda Science Foundation Symposium on PharmaSciences, Osaka, Japan, September 13-14, 2012.

14.              Recent Application of Spiro Bis(isoxazoline) Ligand (SPRIX) for Asymmetric Catalysis (Poster)
*Mohanta, S. C.; Tsujihara, T.; Akita, M.; Takenaka, K.; Takizawa, S.;
Sasai, H. The 6th Takeda Science Foundation Symposium on PharmaSciences, Osaka, Japan, September 13-14, 2012.

15.              Ir Catalyzed Asymmetric Tandem Reaction of meso-Diols and Aldehydes (Poster)
*Suzuki, T.; Ishizaka Y.; Ghozati, K.; Zhou, D.-Y.; Asano, K.;
Sasai, H. The 6th Takeda Science Foundation Symposium on PharmaSciences, Osaka, Japan, September 13-14, 2012.

16.              Umpolung Reactivity of Pd Enolate: Cyclative Diacetoxylation of Alkynyl Cyclohexadienones Catalyzed by Pd-SPRIX (Invited)
Takenaka, K.; Mohanta, S. C.; Takizawa, S.; *
Sasai, H. The 6th Kansai-CMDS Meeting on OMCOS, 2012, Gangwon-do, Korea, September 21-23, 2012.

17.              Dual Activation In Asymmetric Organocatalyses (Keynote)
*Sasai, H. 17th Malaysian Chemical Congress (17MCC) 2012, Kuala Lumpur, Malaysia, October 15-17, 2012.

18.              Development of Chiral Spiro Bis(isoxazoline) Ligand gSPRIXh (Invited)
*
Sasai, H. Cambodian Malaysian Chemical Conference (CMCC) 2012, Siem Reap, Cambodia, October 19-21, 2012.

19.              Development of Chiral Spiro Bis(isoxazoline) Ligand gSPRIXh (Oral)
*
Sasai, H. Cambodian Malaysian Chemical Conference, Siem Reap, Cambodia, October 19-21, 2012.

20.              Enantioselective C-C Bond Forming Reactions Using Multi-Functional Organocatalysts (Poster)
*Takizawa, S.; Matsui, K.; Inoue, N.;
Nguyen, T. M.-N.; Sasai, H. The 12th International Kyoto Conference on New Aspects of Organic Chemistry, Kyoto, Japan, November 12-16, 2012.

21.              Recent Progress of Enantioselective Catalysis Promoted by Pd-SPRIX (Poster)
*Takenaka, K.; Mohanta, S. C.; Akita, M.; Takizawa, S.;
Sasai, H. The 12th International Kyoto Conference on New Aspects of Organic Chemistry, Kyoto, Japan, November 12-16, 2012.

22.              Ir Catalyzed Asymmetric Tandem Reaction of meso-Diols and Aldehydes (Poster)
*Suzuki, T.; Ishizaka Y.; Ghozati, K.; Zhou, D.-Y.; Asano, K.;
Sasai, H. The 12th International Kyoto Conference on New Aspects of Organic Chemistry, Kyoto, Japan, November 12-16, 2012.

23.              Organocatalyzed Enantioselective Aza-MBH Reaction of Ketimines (Poster)
Takizawa, S.;
Rémond, E.; *Arteaga-Arteaga, F.; Bayardon, J.; Yoshida, Y.; Jugé, S.; Sasai, H. The 12th International Kyoto Conference on New Aspects of Organic Chemistry, Kyoto, Japan, November 12-16, 2012.

24.              Umpolung Reactivity of Pd Enolate (Oral)
Takenaka, K.; Mohanta, S. C.; Takizawa, S.; *
Sasai, H. Aachen-Osaka Symposium gBiological and Chemical Methods for Selective Catalysish, Aachen, Germany, December 3-5, 2012.

25.              Enantioselective Organocatalyzed Aza-Morita-Baylis-Hillman (Aza-MBH) Reaction of Ketimines (Oral)
*Takizawa, S.;
Arteaga-Arteaga, F.; Yoshida, Y.; Vellaisamy, S.; Rémond, E.; Bayardon, J.; Jugé, S.; Sasai, H. Aachen-Osaka Symposium gBiological and Chemical Methods for Selective Catalysish, Aachen, Germany, December 3-5, 2012.

26.              Design and Synthesis of Organocatalysts Bearing Spiro Backbone (Oral)
*Fan, L.; Takizawa, S.;
Sasai, H. Aachen-Osaka Symposium gBiological and Chemical Methods for Selective Catalysish, Aachen, Germany, December 3-5, 2012.

27.              Study on Asymmetric Environment of SPRIX Ligand (Oral)
*Lin, X.; Takenaka, K.; Takizawa, S.;
Sasai, H. Aachen-Osaka Symposium gBiological and Chemical Methods for Selective Catalysish, Aachen, Germany, December 3-5, 2012.

28.              Enantioselective Organocatalyzed Aza-Morita-Baylis-Hillman (Aza-MBH) Reaction of Ketimines (Invited)
*Takizawa, S.;
Arteaga-Arteaga, F.; Yoshida, Y.; Vellaisamy, S.; Rémond, E.; Bayardon, J.; Jugé, S.; Sasai, H. First Japan-USA Organocatalytic Symposium, Hawaii, USA, December 15-18, 2012.

 

TopŠ

 

2011

<Domestic>

1.  V‹KƒXƒsƒƒrƒXƒgƒŠƒAƒ][ƒ‹—U“ą‘Ė‚ĖŒø—Ķ‡Ž–@‚ĖŠJ”­‚Æ•sÄ”―‰ž‚Ö‚Ė‰ž—piŒû“Šj
*
‹g“c‘ŨŽuA‘ęāV”EAųˆäG–ūC“ú–{‰ŧŠw‰ï‘æ91t‹G”N‰ïC_“ސė‘åŠwi_“ސėjC3ŒŽ26`29“úC2011”ND

2.  —L‹@•ŠŽqG”}‚É‚æ‚éƒGƒiƒ“ƒ`ƒI‘I‘ð“I•ŠŽq“āƒNƒƒXƒ}ƒCƒPƒ‹”―‰ž‚ĖŠJ”­‚Ɖž—piŒû“Šj
*Nguyen, Tue Minh-Nhat
Aæâ“~—ŅA‘ęāV”EAųˆäG–ūC“ú–{‰ŧŠw‰ï‘æ91t‹G”N‰ïC_“ސė‘åŠwi_“ސėjC3ŒŽ26`29“úC2011”ND

3.  Ž_‰–ŠîŒ^—L‹@•ŠŽqG”}‚ð—p‚Ē‚éƒGƒiƒ“ƒ`ƒI‘I‘ð“IMBH”―‰ž‚ĖŠJ”­iŒû“Šj
*
‘šã^–ëA‘ęāV”EAųˆäG–ūC“ú–{‰ŧŠw‰ï‘æ91t‹G”N‰ïC_“ސė‘åŠwi_“ސėjC3ŒŽ26`29“úC2011”ND

4.  ƒXƒsƒœŠi‚ð—L‚·‚éŽ_-‰–ŠîŒ^•sÄ—L‹@•ŠŽqG”}‚ĖŠJ”­iŒû“Šj
*
‹ËŽR‹M”üŽqA‰ÆŠėŒ’‘ūA‘ęāV”EAųˆäG–ūC“ú–{‰ŧŠw‰ï‘æ91t‹G”N‰ïC_“ސė‘åŠwi_“ސėjC3ŒŽ26`29“úC2011”ND

5.  Ž_-‰–ŠîŒ^ŒÅ’č‰ŧ—L‹@•ŠŽqG”}‚ĖŠJ”­iŒû“Šj
*
•―“cCˆęAˆäã’žlA‘ęāV”EAųˆäG–ūC“ú–{‰ŧŠw‰ï‘æ91t‹G”N‰ïC_“ސė‘åŠwi_“ސėjC3ŒŽ26`29“úC2011”ND

6.  Pd-SPRIXG”}‚É‚æ‚éŠÂ‰ŧ‚𔚂ĪƒAƒ‹ƒLƒjƒ‹ƒVƒNƒƒwƒLƒTƒWƒGƒmƒ“‚ĖƒGƒiƒ“ƒ`ƒI‘I‘ð“IƒWƒAƒZƒgƒLƒV‰ŧ”―‰žiŒû“Šj
*Mohanta, Suman Chandra
A’|’†˜a_A‘ęāV”EA—é–ØŒ’”VAųˆäG–ūC“ú–{‰ŧŠw‰ï‘æ91t‹G”N‰ïC_“ސė‘åŠwi_“ސėjC3ŒŽ26`29“úC2011”ND

7.  Pd-SPRIXG”}‚Å‘Ģi‚ģ‚ę‚éƒĀ,ƒÁ-•s–O˜aƒJƒ‹ƒ{ƒ“Ž_—Þ‚Ė5-endo-trigŒ^ŠÂ‰ŧ”―‰ž‹@\‚ĖDFTŒvŽZ‚É‚æ‚élŽ@iŒû“Šj
Gabr, Randa Kasem Mohamed
ABajracharya, Gan B.A—ŅŒŦĄA’|’†˜a_A‘ęāV”EA‰Š“c‹gOA”ĐŽR‘ôŽŸA’†‘šģŽĄAųˆäG–ūC“ú–{‰ŧŠw‰ï‘æ91t‹G”N‰ïC_“ސė‘åŠwi_“ސėjC3ŒŽ26`29“úC2011”ND

8.  —°‰Đ‚ðƒhƒi[ŒīŽq‚Æ‚·‚éV‹KƒLƒ‰ƒ‹ƒXƒsƒŒ^”zˆĘŽq‚ĖŠJ”­iŒû“Šj
‚’JC•―A’|’†˜a_AųˆäG–ūC“ú–{‰ŧŠw‰ï‘æ91t‹G”N‰ïC_“ސė‘åŠwi_“ސėjC3ŒŽ26`29“úC2011”ND

9.  ‘―‹@”\•sÄG”}‚ĖŠJ”­‚ƐG”}“I•sÄ”―‰ž‚Ö‚Ė‰ž—piŽóÜu‰‰j
*ųˆäG–ūCSymposium on Molecular Chirality 2011C“Œ‹žH‹Æ‘åŠwi“Œ‹žjC5ŒŽ20`21“úC2011”ND

10.              PdSPRIXG”}‚É‚æ‚é4−ƒAƒ‹ƒPƒ“Ž_‚ĖŽ_‰ŧ“IƒAƒŠƒ‹ˆĘCHŒ‹‡ƒGƒXƒeƒ‹‰ŧ‚ðŒo‚éƒGƒiƒ“ƒ`ƒI‘I‘ð“IŠÂ‰ŧ”―‰žiƒ|ƒXƒ^[j
*H“cŽOrA’JŠ_—E„A’|’†˜a_A‘ęāV”EAųˆäG–ūCSymposium on Molecular Chirality 2011C“Œ‹žH‹Æ‘åŠwi“Œ‹žjC5ŒŽ20`21“úC2011”ND

11.              Ž_−‰–ŠîŒ^—L‹@•ŠŽqG”}‚ð—p‚Ē‚éƒGƒiƒ“ƒ`ƒI‘I‘ð“I”―‰ž‚ĖŠJ”­iƒ|ƒXƒ^[j
*‰ÆŠėŒ’‘ūA‹ËŽR‹M”üŽqA‘ęāV”EAųˆäG–ūCSymposium on Molecular Chirality 2011C“Œ‹žH‹Æ‘åŠwi“Œ‹žjC5ŒŽ20`21“úC2011”ND

12.              V‹KƒXƒsƒƒgƒŠƒAƒ][ƒ‹—U“ą‘Ė‚ĖŒø—Ķ“I‡Ž–@‚ĖŠJ”­‚Æ•sÄ”―‰ž‚Ö‚Ė‰ž—piƒ|ƒXƒ^[j
*‹g“c‘ŨŽuA‘ęāV”EAųˆäG–ūCSymposium on Molecular Chirality 2011C“Œ‹žH‹Æ‘åŠwi“Œ‹žjC5ŒŽ20`21“úC2011”ND

13.              ƒoƒiƒWƒEƒ€G”}‚ð—p‚Ē‚é9−ƒtƒFƒiƒ“ƒgƒ[ƒ‹—Þ‚Ė•sÄŽ_‰ŧƒJƒbƒvƒŠƒ“ƒO”―‰žiƒ|ƒXƒ^[j
*ŽŽ›ƒ•―ADoss RajeshA•ÐŽR’q”üA‘ęāV”EAųˆäG–ūCSymposium on Molecular Chirality 2011C“Œ‹žH‹Æ‘åŠwi“Œ‹žjC5ŒŽ20`21“úC2011”ND

14.              Ž_‰–ŠîŒ^—L‹@•ŠŽqG”}‚ð—p‚Ē‚éƒGƒiƒ“ƒ`ƒI‘I‘ð“I”―‰ž‚ĖŠJ”­iƒ|ƒXƒ^[j
*‰ÆŠėŒ’‘ūA‹ËŽR‹M”üŽqA‘ęāV”EAųˆäG–ūC‘æ38‰ņ—L‹@”―‰ž§’k‰ïC‘åã•{—§‘åŠwi‘åãjC8ŒŽ3“úC2011”ND

15.              Enantioselective Cyclization of 4-Alkenoic Acids via an Oxidative Allylic CH Esterification Promoted by PdSPRIX Catalystiƒ|ƒXƒ^[j
*H“cŽOrA’JŠ_—E„A’|’†˜a_A‘ęāV”EAųˆäG–ūC‘æ38‰ņ—L‹@”―‰ž§’k‰ïC‘åã•{—§‘åŠwi‘åãjC8ŒŽ3“úC2011”ND

16.              5‰ŋ‚ĖƒoƒiƒWƒEƒ€G”}‚ð—p‚Ē‚éƒGƒiƒ“ƒ`ƒI‘I‘ð“I’Y‘f|’Y‘fŒ‹‡Œ`Ž”―‰ž‚ĖŠJ”­‚Ɖž—piƒ|ƒXƒ^[j
*ŽŽ›ƒ•―ADoss RajeshA•ÐŽR’q”üA‘ęāV”EAųˆäG–ūC‘æ38‰ņ—L‹@”―‰ž§’k‰ïC‘åã•{—§‘åŠwi‘åãjC8ŒŽ3“úC2011”ND

17.              Enantioselective Cyclization of 4-Alkenoic Acids via an Oxidative Allylic CH Esterification Promoted by PdSPRIX Catalystiƒ|ƒXƒ^[j
*H“cŽOrA’JŠ_—E„A’|’†˜a_A‘ęāV”EAųˆäG–ūC‘æ58‰ņ—L‹@‹ā‘Ū‰ŧŠw“Ē˜_‰ïC–žŒÃ‰Ū‘åŠwi–žŒÃ‰ŪjC9ŒŽ7`9“úC2011”ND

18.              Development of Chiral Thioamide Ligands Based on a Spirobilactamiƒ|ƒXƒ^[j
*‚’JC•―Aúá–{Œ[•ãA’|’†˜a_AųˆäG–ūC‘æ58‰ņ—L‹@‹ā‘Ū‰ŧŠw“Ē˜_‰ïC–žŒÃ‰Ū‘åŠwi–žŒÃ‰ŪjC9ŒŽ7`9“úC2011”ND

19.              V‹KƒXƒsƒƒgƒŠƒAƒ][ƒ‹—U“ą‘Ė‚ĖŒø—Ķ“I‡Ž–@‚ĖŠJ”­‚Ɖž—piƒ|ƒXƒ^[j
*‹g“c‘ŨŽuA‘ęāV”EAųˆäG–ūC‘æ41‰ņ•Ą‘fŠÂ‰ŧŠw“Ē˜_‰ïC’é‘åŠwiŒF–{jC10ŒŽ20`22“úC2011”ND

20.              5‰ŋ‚ĖƒoƒiƒWƒEƒ€G”}‚ð—p‚Ē‚éƒGƒiƒ“ƒ`ƒI‘I‘ð“I’Y‘f|’Y‘fŒ‹‡Œ`Ž”―‰ž‚ĖŠJ”­‚Ɖž—piƒ|ƒXƒ^[j
*ŽŽ›ƒ•―ADoss RajeshA•ÐŽR’q”üA‘ęāV”EAųˆäG–ūC‘æ37‰ņ”―‰ž‚ƍ‡Ž‚Ėi•āƒVƒ“ƒ|ƒWƒEƒ€C‚ ‚í‚Ž‚ņƒz[ƒ‹i“ŋ“‡jC11ŒŽ7`8“úC2011”ND

21.              V‹KƒGƒiƒ“ƒ`ƒI‘I‘ð“IG”}”―‰žŒn‚ĖŠJ‘ņiĩ‘Ōu‰‰j
*ųˆäG–ūC–kŠC“đ‘åŠwGCOE‘æ‚P‚V‰ņļ–§‡Ž‰ŧŠwƒZƒ~ƒi[ ƒWƒ‡ƒCƒ“ƒgƒVƒ“ƒ|ƒWƒEƒ€C–kŠC“đ‘åŠwi–kŠC“đjC12ŒŽ19“úC2011”ND

<International>

1.  Enantioselective Organocatalyzed aza-MBH Domino Process: Application to the Facile Synthesis of Tetrahydropyridines and Isoindolines (Oral)
S. Takizawa, N. Inoue, S. Hirata, *H. Sasai, 241st ACS National Meeting, Anaheim, USA, March 27-31, 2011.

2.  Exploring a New Asymmetric Reaction Using Chiral Spiro Bis(isoxazoline) Ligand gSPRIXh (Invited)
*H. Sasai, The International Symposium on Physical Organic Chemistry and Synthetic Materials, Tianjin, China, July 2, 2011.

3.  Development of Enantioselective Catalyses Using Chiral Spiro Compounds (Invited)
*H. Sasai, Chirality 2011, Liverpool, UK, July 10-13, 2011.

4.  Development of Novel Chiral Spiro Ligands Bearing Sulfur Donor (Poster)
*S. Takatani, K. Sugimoto, K. Takenaka, H. Sasai, The 16th IUPAC International Symposium on Organometallic Chemistry Directed Towards Organic Synthesis (OMCOS 16), Shanghai, China, July 24-28, 2011.

5.  Development of New Method for an Efficient Synthesis of Spiro Bis(triazole) Derivatives and Their Applications to Asymmetric Catalysis (Poster)
*Y. Yoshida, S. Takizawa, H. Sasai, The 2nd International Symposium on Process Chemistry (ISPC 2011), Kyoto, Japan, August 10-12, 2011.

6.  Enantioselective Carbon-Carbon Bond-Forming Reactions Using Vanadium(V) Complexes (Oral)
*S. Takizawa, J. Kodera, D. Rajesh, T. Katayama, H. Sasai, 4th Aachen-Osaka Joint Symposium, Aachen, German, September 1, 2011.

7.  Development of Novel Chiral Spiro Ligands Bearing Sulfur Donor (Oral)
*S. Takatani, K. Sugimoto, K. Takenaka, H. Sasai, 4th Aachen-Osaka Joint Symposium, Aachen, German, September 1-2, 2011.

8.  Catalytic Enantioselective Reactions via Pd(II/IV) Catalysis (Invited)
*H. Sasai, 14th Asian Chemical Congress 2011, Bangkok, Thailand, September 5-8, 2011.

9.  Organocatalyzed Domino Process Based on the Aza-Morita-Baylis-Hillman (Aza-MBH) Reaction (Poster)
*S. Takizawa, N. Inoue, S. Hirata, H. Sasai, The 7th International Symposium on Integrated Synthesis (ISIS-7), Kobe, Japan, October 9-10, 2011.

10.              Intramolecular Enantioselective Rauhut-Currier Reaction (Poster)
*T. M.-N. Nguyen, S. Takizawa, H. Sasai, The 7th International Symposium on Integrated Synthesis (ISIS-7), Kobe, Japan, October 9-10, 2011.

11.              Oxidative Desymmetrization of Diols by Iridium Catalysts (Poster)
*T. Suzuki, K. Ghozati, S. Takatani, D. Zhou, K. Asano, T. Katoh, H. Sasai, 8th AFMC International Medicinal Chemistry Symposium (AIMECS 11), Tokyo, Japan, November 29-December 2, 2011.

12.              Enantioselective Cyclization/Diacetoxylation of Alkynyl Cyclohexadienones Catalyzed by Palladium-Spiro Bis(isoxazoline) Complex (Poster)
*S. C. Mohanta, K. Takenaka, S. Takizawa, T. Suzuki, H. Sasai, 8th AFMC International Medicinal Chemistry Symposium (AIMECS 11), Tokyo, Japan, November 29-December 2, 2011.

13.              Organocatalyzed Domino Process Based on the Aza-Morita-Baylis-Hillman (Aza-MBH) Reaction (Oral)
*S. Hirata, S. Takizawa, N. Inoue, H. Sasai, The 1st Junior International Conference on Cutting-Edge Organic Chemistry in Asia, Xiamen, China, December 9-11, 2011.

14.              Organocatalyzed Domino Process Based on the Aza-Morita-Baylis-Hillman (Aza-MBH) Reaction (Oral)
S. Hirata, *S. Takizawa, N. Inoue, H. Sasai, The 6th International Conference on Cutting-Edge Organic Chemistry in Asia and The 2nd New Phase International Conference on the Cutting-Edge Organic Chemistry in Asia, Hong Kong, China, December 11-15, 2011.

15.              Enantioselective Cyclization of 4-Alkenoic Acids via an Oxidative Allylic CH Esterification (Oral)
*M. Akita, Y. Tanigaki, K. Takenaka, S. Takizawa, H. Sasai, The 2nd Seleca Minisymposium, Aachen, German, December 13, 2011.

 

TopŠ

 

2010

1.  Oxidative Desymmetrization of Diols by Iridium Catalyst
*T. Suzuki, K. Ghozati, K. Katoh, H. Sasai, The 13th SANKEN International Symposium, Osaka, Japan, January 18-19, 2010.

2.  Novel Enantioselective Domino Reactions Promoted by Acid-Base Organocatalysts
*S. Takizawa, N. Inoue, S. Hirata, H. Sasai,
The 13th SANKEN International Symposium, Osaka, Japan, January 18-19, 2010.

3.  Enantioselective PdII/PdIV Catalysis Using Spiro Bis(isoxazoline) Ligand
*K. Takenaka, T. Tsujihara, K. Onitsuka, M. Hatanaka, H. Sasai,
The 13th SANKEN International Symposium, Osaka, Japan, January 18-19, 2010.

4.  Exploring a New Paradigm in Immobilization of Asymmetric Catalysts
*H. Sasai, S. Takizawa, D Rajesh, 239th ACS National Meeting & Exposition, San Francisco, USA, March 21-25, 2010.

5.  Enantioselective Domino Reactions Promoted by Acid-Base Organocatalysts
*S. Takizawa, N. Inoue, S. Hirata, H. Sasai, 22nd
International Symposium on Chirality (ISCD-22), Sapporo, Japan, July 12-15, 2010.

6.  Enantioselective Pd(II)/Pd(IV) Catalysis Using Spiro Bis(isoxazoline) Ligand
K. Takenaka, T. Tsujihara, K. Onitsuka, M. Hatanaka, *H. Sasai,
The 6th Tokyo Conference on Advanced Catalytic Science and Technology & The 5th Asia Pacific Congress on Catalysis (TOCAT6/APCAT5), Sapporo, Japan, July 18-23, 2010.

7.  Novel Asymmetric Domino Reactions Promoted by Acid-Base Organocatalysts
*H. Sasai, 3rd Aachen-Osaka Joint Symposium, Aachen, Germany, September 6-7, 2010.

8.  Novel Catalytic Enantioselective Reactions Promoted by a Pd-SPRIX Complex
*H. Sasai, Japan-Korea Symposium on Organometallic Chemistry, Nara, Japan, October 1-3, 2010.

9.  One-Pot Preparation of Chiral Dinuclear Vanadium(V) Complex
S. Takizawa, D. Rajesh, T. Katayama, *H. Sasai, 7th International Symposium on Chemistry and Biological Chemistry of Vanadium, Toyama, Japan, October 6-9, 2010.

10.              Novel Oxidative Asymmetric Cyclizations Promoted by Pd-SPRIX Catalyst
*H. Sasai, The International Chemical Congress of Pacific Basin Societies (PACIFICHEM 2010), Honolulu, USA, December 15-20, 2010.

11.              Development of Chiral Bifunctional Organocatalysts
*H. Sasai, The
International Chemical Congress of Pacific Basin Societies (PACIFICHEM 2010), Honolulu, USA, December 15-20, 2010.

12.              Enantioselective Oxidative Coupling of 2-Naphthols Using Dinuclear Vanadium Complex
*S. Takizawa, T. Katayama, R. Doss, H. Sasai, The
International Chemical Congress of Pacific Basin Societies (PACIFICHEM 2010), Honolulu, USA, December 15-20, 2010.

13.              Oxidative Desymmetrization of Diols by Iridium Catalyst
*T. Suzuki, K. Ghozati, S. Takatani, T. Katoh, H. Sasai, The
International Chemical Congress of Pacific Basin Societies (PACIFICHEM 2010), Honolulu, USA, December 15-20, 2010.

14.              Enantioselective Synthesis of ƒÁ-Lactones via Intramolecular Wacker-type Cyclization Catalyzed by Pd-SPRIX
*M. Akita, Y. Tanigaki, K. Takenaka, S. Takizawa, H. Sasai, The International Chemical Congress of Pacific Basin Societies (PACIFICHEM 2010), Honolulu, USA, December 15-20, 2010.

15.              DFT Study on 5-Endo-Trig Type Cyclization of ƒĀ,ƒÁ-Unsaturated Carboxylic Acids Using Pd-SPRIX Catalyst
*R. K. M. Gabr, G. B. Bajracharya, X. Lin, K. Takenaka, S. Takizawa, Y. Okada, T. Hatakeyama, M. Nakamura, H. Sasai, The International Chemical Congress of Pacific Basin Societies (PACIFICHEM 2010), Honolulu, USA, December 15-20, 2010.

16.              Enantioselective Aza-Morita-Baylis-Hillman (Aza-MBH) Domino Reactions Promoted by Acid-Base Organocatalyst
*N. Inoue, S. Takizawa, S. Hirata, T. M.-N. Nguyen, H. Sasai, The
International Chemical Congress of Pacific Basin Societies (PACIFICHEM 2010), Honolulu, USA, December 15-20, 2010.

17.              Bifunctional Organocatalyst Bearing (S)-1,1f-Spirobiindane As Chiral Backbone
*K. Kiriyama, S. Takizawa, H. Sasai, The
International Chemical Congress of Pacific Basin Societies (PACIFICHEM 2010), Honolulu, USA, December 15-20, 2010.

18.              Development of Bifunctional Organocatalysts for Enantioselective Morita-Baylis-Hillman Reaction
*S. Murakami, S. Takizawa, H. Sasai, The
International Chemical Congress of Pacific Basin Societies (PACIFICHEM 2010), Honolulu, USA, December 15-20, 2010.

 

TopŠ

 

2009

1.  Iridium-catalyzed Oxidative Dimerization, Tishchenko Reaction and Oxidative Desymmetrization
*T. Suzuki, K. Ghozati, N. K. Mangu, H. Sasai, The 12th SANKEN International Symposium, Osaka, Japan, January 22, 2009.

2.  Novel Enantioselective Reactions Catalyzed by Palladium(II)-Spiro Bis(isoxazoline) Complex
T. Tsujihara, G. B. Bajracharya, P. S. Koranne, R. N. Nadaf, *K. Takenaka, S. Takizawa, K. Onitsuka, H. Sasai, The 12th SANKEN International Symposium, Osaka, Japan, January 22, 2009.

3.  Enantioselective Synthesis of Spirobilactams via the Intramolecular Double BuchwaldHartwig Reaction
*K. Takenaka, N. Itoh, K. Sugimoto, H. Sasai, The 12th SANKEN International Symposium, Osaka, Japan, January 22, 2009.

4.  Development of Dinuclear Vanadium Catalysts and Acid-Base Organocatalysts for Enantioselective Reactions via Dual Activation Mechanism
*S. Takizawa, K. Matsui, T. Katayama, N. Inoue, D. Rajesh, S. Hirata, K. Kiriyama, T. Suzuki, H. Sasai, The 12th SANKEN International Symposium, Osaka, Japan, January 22, 2009.

5.  Oxidative Desymmetrization of Diols by Iridium Catalyst
*T. Suzuki, K. Ghozati, K. Suzuki, T. Kato, H. Sasai, 15th IUPAC
International Symposium on Organometallic Chemistry Directed toward Organic Synthesis (OMCOS 15), Glasgow, UK, July 26-30, 2009.

6.  Enantioselective PdII/PdIV Catalysis Using Spiro Bis(isoxazoline) Ligand
*K. Takenaka, T. Tsujihara, K. Onitsuka, M. Hatanaka, H. Sasai, 15th IUPAC
International Symposium on Organometallic Chemistry Directed toward Organic Synthesis (OMCOS 15), Glasgow, UK, July 26-30, 2009.

7.  Exploring a New Paradigm in Immobilization of Multicomponent Asymmetric Catalyst
* H. Sasai, S. Takizawa, M. L. Patil, K. Marubayashi, The 14th International Symposium on Relations between Homogeneous and Heterogeneous Catalysis, Stockholm, Sweden, September 13-18, 2009.

8.  Enantioselective Oxidative Coupling Reaction of 2-Naphthol Derivatives Using Dinuclear Vanadium Complexes
*R. Doss, S. Takizawa, H. Sasai, 5th Spanish-Portuguese-Japanese Organic Chemistry Symposium
(5th SPJ-OCS), Osaka, Japan, November 6-8, 2009.

9.  Iridium-Catalyzed Oxidative Desymmetrization of meso-Diols
*K. Ghozati, S. Takatani, T. Kato, T. Suzuki, H. Sasai, 5th Spanish-Portuguese-Japanese Organic Chemistry Symposium
(5th SPJ-OCS), Osaka, Japan, November 6-8, 2009.

10.              Enantioselective Oxidative 6-Endo-Trig Cyclizations Catalyzed by Palladium(II)-Spiro Bis(isoxazoline) Complex
*S. C. Mohanta, Y. Tanigaki, M. L. Patil, C. V. L. Rao, K. Takenaka, S. Takizawa, T. Suzuki, H. Sasai, 5th Spanish-Portuguese-Japanese Organic Chemistry Symposium
(5th SPJ-OCS), Osaka, Japan, November 6-8, 2009.

11.              Enantioselective PdII/PdIV Catalysis Using Spiro Bis(isoxazoline) Ligand
*K. Takenaka, T. Tsujihara, K. Onitsuka, M. Hatanaka, H. Sasai, The 11th
International Kyoto Conference on New Aspects of Organic Chemistry (IKCOC-11), Kyoto, Japan, November 9-13, 2009.

12.              Enantioselective Oxidative Coupling of 2-Naphthols Using Dinuclear Vanadium(V) Catalysts
*R. Doss, S. Takizawa, H. Sasai, The 11th
International Kyoto Conference on New Aspects of Organic Chemistry (IKCOC-11), Kyoto, Japan, November 9-13, 2009.

13.              Iridium-Catalyzed Oxidative Desymmetrization of meso-Diols
*K. Ghozati, S. Takatani, T. Kato, H. Sasai, T. Suzuki, The 11th
International Kyoto Conference on New Aspects of Organic Chemistry (IKCOC-11), Kyoto, Japan, November 9-13, 2009.

14.              Enantioselective Oxidative 6-Endo-Trig Cyclizations Catalyzed by Palladium(II)-Spiro Bis(isoxazoline) Complex
*S. C. Mohanta, Y. Tanigaki, M. L. Patil, C. V. L. Rao, K. Takenaka, S. Takizawa, T. Suzuki, H. Sasai, The 11th
International Kyoto Conference on New Aspects of Organic Chemistry (IKCOC-11), Kyoto, Japan, November 9-13, 2009.

15.              Development of Enantioselective Organocatalyzed Domino Reactions
*S. Takizawa, N. Inoue, K. Kiriyama, S. Hirata, S. Murakami, T. Nguyen, T. Suzuki, H. Sasai, The 11th
International Kyoto Conference on New Aspects of Organic Chemistry (IKCOC-11), Kyoto, Japan, November 9-13, 2009.

 

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2008

1.  Design of Novel Helical Polymer Ligands and Their Application to Asymmetric Diels-Alder Reaction
*K. Onitsuka, Y. Itano, H. Sasai, 11th Sanken, 6th Nanotechnology Center, 1st MSTEC International Symposium, Hyogo, Japan, February 4-5, 2008.

2.  Asymmetric Catalysis of Planar-chiral Cyclopentadienyl-ruthenium Complexes: Regio- and Enantioselective Allylic Substitutions
*K. Onitsuka, H. Okuda, C. Kameyama, H. Sasai, 11th Sanken, 6th Nanotechnology Center, 1st MSTEC International Symposium, Hyogo, Japan, February 4-5, 2008.

3.  Synthesis of Optically Active Spiro Compounds via Palladium-catalyzed Asymmetric Amidation
*N. Itoh, K. Takenaka, H. Sasai, 11th Sanken, 6th Nanotechnology Center, 1st MSTEC International Symposium, Hyogo, Japan, February 4-5, 2008.

4.  Development of Dendritic Artificial Enzymes with Catechol Oxidase Activity
*S. Hashimoto, R. N. Nadaf, D. Jayaprakash, T. Kawase, G. R. K. Mohamed, M. Mikami, T. Suzuki, H. Sasai, 11th Sanken, 6th Nanotechnology Center, 1st MSTEC International Symposium, Hyogo, Japan, February 4-5, 2008.

5.  Catalytic Enantioselective Synthesis of Spirobilactams via an Intramolecular Double Buchwald-Hartwig Reaction
*K. Takenaka, N. Itoh, H. Sasai,
Third International Conference on Advanced Organic Synthesis Directed toward the Ultimate Efficiency and Practicability, Shiga, Japan, May 26-27, 2008.

6.  Novel Enantioselective Reactions Catalyzed by Palladium(II)-Spiro Bis(isoxazoline) Complex
*H. Sasai, S. Takizawa, K. Takenaka, T. Tsujihara, R. N. Nadaf, G. B. Bajracharya, P. S. Koranne, K. Onitsuka,
International Symposium on Homogeneous Catalysis 16 (ISHC-16), Florence, Italy, July 6-11, 2008.

7.  Chiral Dinuclear Vanadium(V) Catalyst for Dual Activation of 2-Naphthols in Oxidative Couplings
*H. Sasai, S. Takizawa, T. Katayama,
6th International Vanadium Symposium, Lisbon, Portugal, July 17-19, 2008.

8.  Enantioselective Synthesis of Spirobilactams via the Intramolecular Double BuchwaldHartwig Reaction
*K. Takenaka, N. Itoh, H. Sasai, The First International Symposium on Process Chemistry (ISPC 08), Kyoto, Japan, July 28-30, 2008.

9.  Novel Catalytic Enantioselective Reactions Promoted by a Pd-SPRIX Complex
*H. Sasai, 3rd International Conference on Cutting-Edge Organic Chemistry in Asia, Hangzhou, China, October 19-23, 2008.

10.              Novel Catalytic Enantioselective Reactions Promoted by Palladium(II)-Spiro Bis(isoxazoline) Complex
*H. Sasai, 11th International Symposium on Natural Product Chemistry, Karachi, Pakistan, October 29-November 1, 2008.

11.              Enantioselective Synthesis of Spirobilactams via the Intramolecular Double BuchwaldHartwig Reaction
*K. Takenaka, N. Itoh, K. Sugimoto, H. Sasai, UK/Japan Joint Symposium on Asymmetric Catalysis (2008), Kyoto, Japan, December 8-9, 2008.

12.              Novel Catalytic Enantioselective Reactions Promoted by Pd-SPRIX Complexes
*H. Sasai, UK/Japan Joint Symposium on Asymmetric Catalysis (2008), Kyoto, Japan, December 8-9, 2008.

 

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2007

1.  Living Polymerization of Bulky Aryl Isocyanide with Arylrhodium Complexes and Application to Precise Synthesis of Helical Polymers
*K. Onitsuka, M. Yamamoto, T. Mori, F. Takei, S. Takahashi, Osaka University Macromolecular Symposium on Chemistry, Physics, and Biology in Macromolecular Science, Osaka, Japan, Feb. 19-21, 2007.

2.  Development of New Catalytic Enantioselective Reactions Promoted by Pd(II)-Spiro Bis(isoxazoline) Complexes
*G. B. Bajracharya, P. S. Koranne, M. L. Patil, C. V. L. Rao, T. Tsujihara, S. Takizawa, T. Suzuki, H. Sasai, 19th French-Japanese Symposium on Medicinal and Fine Chemistry (FJS-2007), Toyama, Japan, May 13-16, 2007.

3.  Development of Bifunctional Organocatalysts for Enantioselective Aza-Morita-Baylis-Hillman Reaction
*H. Sasai,
First International Conference on Advanced Organic Synthesis Directed toward the Ultimate Efficiency and Practicability, International Conference on Asymmetric Organocatalysis, Otsu, Japan, May 28-29, 2007.

4.  Bifunctional Chiral Organocatalysts for the Enantioselective aza-Morita-Baylis-Hillman Reaction
*H. Sasai, 21st International Congress for Heterocyclic Chemistry, Sydney, Australia, July 15-20, 2007.

5.  Pd(II)-SPRIX-Catalyzed Enantioselective Intramolecular Cyclizations
*G. B. Bajracharya, M. L. Patil, P. S. Koranne, C. V. L. Rao, T. Tsujihara, T. Suzuki, H. Sasai, 14th IUPAC Symposium on Organometallic Chemistry Directed towards Organic Synthesis (OMCOS 14), Nara, Japan, August 2-6, 2007.

6.  Regio- and Enantioselective O-Allylation of Phenol and Alcohol Catalyzed by Planar-Chiral Cyclopentadienyl-Ruthenium Complex
*K. Onitsuka, H. Okuda, C. Kameyama, H. Sasai, 14th IUPAC Symposium on Organometallic Chemistry Directed towards Organic Synthesis, Nara, Japan, Aug. 2-6, 2007.

7.  Development of Dendritic Artificial Enzymes with Catechol Oxidase Activity
D. Jayaprakash, *R. N. Nadaf, T. Kawase, T. Suzuki, H. Sasai, 12th Asian Chemical Congress, Kuala Lumpur, Malaysia, August 22-25, 2007.

8.  Organoruthenium Dendrimers Possessing Tri(4-Ethynylphenyl)Amine Bridges
*K. Onitsuka, S. Takahashi, 12th IUPAC International Symposium on MacroMolecular Complexes, Fukuoka, Japan, August. 27-31, 2007.

9.  Development of Dendritic Artificial Enzymes with Caetchol Oxidase Activity
*D. Jayaprakash, R. N. Nadaf, T. Kawase, T. Suzuki, H. Sasai, Chirality at the Nanoscale, Barcelona,
Spain, September 17-21, 2007.

10.              Development of New Catalytic Enantioselective Reactions Promoted by Pd(II)-Spiro Bis(isoxazoline) Complex
G. B. Bajracharya, P. S. Koranne, M. L. Patil, C. V. L. Rao, T. Tsujihara, S. Takizawa, T. Suzuki, *H. Sasai, Chirality at the Nanoscale, Barcelona,
Spain, September 17-21, 2007.

11.              Dual Activation Catalysis
*H.
Sasai, Green Sustainable Biological and Chemical Processes, Osaka, Japan, November 15-17, 2007.

12.              Development of New Catalytic Enantioselective Reactions Promoted by Pd(II)-Spiro Bis(isoxazoline) Complexes
*Y. Tanigaki, G. B. Bajracharya, P. S. Koranne, C. V. L. Rao, M. L. Patil, T. Tsujihara, K. Takenaka, S. Takizawa, K. Onitsuka, H. Sasai, Green Sustainable Biological and Chemical Processes, Osaka, Japan, November 15-17, 2007.

13.              Development of Novel Chiral Spiro-type Ligands
*S. Nakatsuka, T. Nagano, P. S. Koranne, K. Takenaka, S. Takizawa, T. Suzuki, K. Onitsuka, H. Sasai, Green Sustainable Biological and Chemical Processes, Osaka, Japan, November 15-17, 2007.

14.              Synthesis of Optically Active Spiro Compounds via Palladium-catalyzed Asymmetric Amidation
*N. Itoh, K. Takenaka, H. Sasai, Green Sustainable Biological and Chemical Processes, Osaka, Japan, November 15-17, 2007.

15.              Development of Dendritic Artificial Enzymes with Catechol Oxidase Activity
*R. N. Nadaf, D. Jayaprakash, T. Kawase, R. K. M. Gabr, S. Hashimoto, M. Mikami, T. Suzuki, H. Sasai, Green Sustainable Biological and Chemical Processes, Osaka, Japan, November 15-17, 2007.

16.              Development of New Catalytic Asymmetric Reaction Using Helical Polymer
*Y. Itano, K. Onitsuka, H. Sasai, Green Sustainable Biological and Chemical Processes, Osaka, Japan, November 15-17, 2007.

17.              Novel Enantioselective Reactions Promoted by Pd(II)-SPRIX Catalyst
*H. Sasai, International Chemical Conference (ICCT-2007), Hsinchu, Taipei, December 13-16, 2007
.

18.              Dual Activation in Oxidative Coupling of 2-Naphthols Catalyzed by Chiral Dinuclear Vanadium Complexes
*H. Sasai, Post-symposium of ICCT-2007, Hsinchu, Taipei, December 17, 2007
.

 

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2006

1.  New Concepts for Immobilization of Asymmetric Catalysts
*H. Sasai, Handai Nanoscience and Nanotechnology International Symposium, Osaka, Japan, January 30-February 1, 2006.

2.  Development and Applications of Metal-Bridged Polymers as Asymmetric Catalysts
S. Takizawa, *N. Inoue, H. Sasai, Handai Nanoscience and Nanotechnology International Symposium, Osaka, Japan, January 30-February 1, 2006.

3.  Development of Effective Enzyme Mimics Utilizing Dendrimers
*D. Jayaprakash, R. N. Nadaf, H. Sasai, Handai Nanoscience and Nanotechnology International Symposium, Osaka, Japan, January 30-February 1, 2006.

4.  Trinuclear Ruthenium-Acetylide Complexes with Tri(ethynylphenyl)amine-Bridge: A New Building Block for Multi-Step Redox Active Organometallic Macromolecules
*K. Onitsuka, Handai Nanoscience and Nanotechnology International Symposium, Osaka, Japan, January 30-February 1, 2006.

5.  Green Solid-Phase Epoxidation System: Participation of New Peroxo-Nanocluster of Polyoxometalte Catalyst
*J. Ichihara, K. Iteya, S. Hoshi, K. Momoi, Y. Sasaki, Sanken International Symposium 2006 on Advanced Science and Technology for Materials, Biology, and Information by Quantum Beams (SIS-2006), Osaka, Japan, February 8-9, 2006.

6.  Design and Synthesis of Novel Chiral Spiro Ionic Liquids
*M. L. Patil, C. V. L. Rao, K. Yonezawa, S. Takizawa, K. Onitsuka, H. Sasai, 8th International Symposium on Organic Reactions, Kobe, Japan, April 23-26, 2006.

7.  Development of Effective Enzyme Mimic for Urease
*D. Jayaprakash, R. N. Nadaf, H. Sasai, 8th International Symposium on Organic Reactions, Kobe, Japan, April 23-26, 2006.

8.  Development and Applications of Novel Spiro-type Ligands
*P. S. Koranne, T. Tsujihara, K. Takenaka, K. Onitsuka, H. Sasai, 8th International Symposium on Organic Reactions, Kobe, Japan, April 23-26, 2006.

9.  Design of New Building Block for Multi-Step Redox Active Organometallic Dendrimers
*K. Onitsuka, S. Takahashi, 8th International Symposium on Organic Reactions, Kobe, Japan, April 23-26, 2006.

10.              Development of Catalytic Enantioselective Reaction utilizing Chiral Spiro-type ligands
*T. Tsujihara, P. S. Koranne, J. Yogo, K. Wakita, T. Shinohara, S. Takizawa, K. Onitsuka, H. Sasai, International Molecular Chirality Conference (IMCT, MC2006), Toyama, Japan,
May 18-19, 2006.

11.              Design and Synthesis of Novel Chiral Ionic Liquids Bearing Spiro Skeleton
*
M. L. Patil, C. V. L. Rao, K. Yonezawa, S. Takizawa, K. Onitsuka, H. Sasai, International Molecular Chirality Conference (IMCT, MC2006), Toyama, Japan, May 18-19, 2006.

12.              A Novel Bifunctional Asymmetric Organocatalysts for aza-Morita-Baylis-Hillman (aza-MBH) Reaction
*K. Matsui, S. Takizawa, H. Sasai, 7th Tetrahedron Symposium Challenges in Organic Chemistry, Kyoto, Japan,
May 25-26, 2006.

13.              Enantioselective Catalysis Using Novel Spiro-type Ligands
*P. S. Koranne, T. Tsujihara, S. Takizawa, K. Onitsuka, H. Sasai,
7th Tetrahedron Symposium Challenges in Organic Chemistry, Kyoto, Japan, May 25-26, 2006.

14.              Development of Novel Chiral Isoxazoline/Isoxazole Hybrid-type Ligands
P. S. Koranne, T. Tsujihara, S. Takizawa, K. Onitsuka, *H. Sasai, 18th International Symposium on Chirality (Chirality-2006), Busan, Korea, June 25-28, 2006.

15.              Development of New Methods towards the Synthesis of Novel Chiral Spiro Ionic Liquids
M. L. Patil, C. V. L. Rao, K. Yonezawa, S. Takizawa, K. Onitsuka, H. Sasai, 18th International Symposium on Chirality (Chirality-2006), Busan, Korea, June 25-28, 2006.

16.              Bifunctional Organocatalysts for enantioselective aza-Morita-Baylis-Hillman Reaction
*S. Takizawa, K. Matsui, K. Tanaka, A. Horii, H. Sasai,
18th International Symposium on Chirality (Chirality-2006), Busan, Korea, June 25-28, 2006.

17.              Bifunctional Organocatalysts for Enantioselective aza-Morita-Baylis-Hillman Reaction
K. Matsui, K. Tanaka, A. Horii, S. Takizawa, *H. Sasai, International Symposium on Organocatalysis in Organic Synthesis, Glasgow, UK, July 5-7, 2006.

18.              Development of Metal-bridged Polymers as Enantioselective Catalysts
S. Takizawa, *N. Inoue, H. Sasai, XXII International Conference on Organometallic Chemistry, Zaragoza, Spain, July 23-28, 2006.

19.              Precise Synthesis and Properties of Helical Polyisocyanides
*K. Onitsuka, S. Takahashi, 16th
International Symposium on Fine Chemistry and Functional Polymers (FCFP-XVI) & IUPAC 2nd International Symposium on Novel Materials and Synthesis (NMS-II), Lanzhou, China, July 24-27, 2006.

20.              Enantioselective Catalysis Using Novel Spiro-type Ligands and Novel Spiro Isoxazoline-Isoxazole Hybrid Ligands
*P. S. Koranne, T. Tsujihara, S. Takizawa, K. Onitsuka, H. Sasai, 232nd ACS National Meeting, San Francisco, USA, September 10-14, 2006.

21.              Asymmetric Catalysis of Planar-Chiral Cyclopentadienyl-Ruthenium Complexes in Allylic Substitutions
*K. Onitsuka, H. Okuda, H. Sasai, 1st International Conference of Cutting-Edge Organic Chemistry in Asia, Naha, Okinawa, Japan, October 16-20, 2006.

22.              Bifunctional Organocatalysts for Enantioselective aza-Morita-Baylis-Hillman (aza-MBH) Reaction
*K. Matsui, K. Tanaka, A. Horii, S. Takizawa, H. Sasai, 1st International Conference of Cutting-Edge Organic Chemistry in Asia, Naha, Okinawa, Japan, October 16-20, 2006.

23.              Asymmetric Allylation Catalyzed by Planar-Chiral Cyclopentadienyl-Ruthenium Complexes
*K. Onitsuka, H. Okuda, H. Sasai, 10th International Kyoto Conference on New Aspects of Organic Chemistry, Kyoto, Japan, November 13-17, 2006.

24.              Bifunctional Organocatalysts for Enantioselective Aza-Morita-Baylis-Hillman (Aza-MBH) Reaction
*K. Matsui, K. Tanaka, A. Horii, S. Takizawa, H. Sasai, 10th International Kyoto Conference on New Aspects of Organic Chemistry, Kyoto, Japan, November 13-17, 2006.

25.              Dual Activation in an Enantioselective Homolytic Coupling Reaction
*T. Katayama, C. Kameyama, S. Takizawa, K, Onitsuka, H, Sasai, 10th International Kyoto Conference on New Aspects of Organic Chemistry, Kyoto, Japan, November 13-17, 2006.

26.              Enantioselective Synthesis of Heterocyclic Compounds Utilizing Pd(II)-SPRIX Catalyst
*G. B. Bajracharya, P. Koranne, T. Tsujihara, K. Takenaka, S. Takizawa, K. Onitsuka, H, Sasai, 10th International Kyoto Conference on New Aspects of Organic Chemistry, Kyoto, Japan, November 13-17, 2006.

27.              Development of Oxidative Reactions Catalyzed by Ir Complex
*T. Suzuki, N. K. Mangu, T. Yamada, T. Matsuo, K. Watanabe, T. Katoh, H, Sasai, 10th International Kyoto Conference on New Aspects of Organic Chemistry, Kyoto, Japan, November 13-17, 2006.

28.              Applications of Novel Chiral Spiro Isoxazoline/Isoxazole
P. S. Koranne, G. B. Bajracharya, K. Onitsuka, *H, Sasai, 5th 21st Century COE towards Creating New Industries Based on Inter-Nanosience International Symposium, Awaji, Japan, December 8-9, 2006.

29.              Development of Chiral Isoxazoline/Isoxazole Ligands and Their Application in Enantioselective Catalysis
*P. S. Koranne, G. B. Bajracharya, M. L. Patil, T. Tsujihara, C. V. L. Rao, S. Takizawa, K. Onitsuka, H, Sasai, 5th 21st Century COE towards Creating New Industries Based on Inter-Nanosience International Symposium, Awaji, Japan, December 8-9, 2006.

30.              Development of Novel Asymmetric Cascade Reaction Catalyzed by Pd-SPRIX
*T. Tsujihara, K. Takenaka, S. Takizawa, K. Onitsuka, H, Sasai, 5th 21st Century COE towards Creating New Industries Based on Inter-Nanosience International Symposium, Awaji, Japan, December 8-9, 2006.

31.              Development of Artificial Enzyme Utilizing Multiple Interactions in Catalytic Site
*T. Kawase, R. N. Nadaf. G. R. Kassem, D. Jayaprakash, S. Takizawa, H, Sasai, 5th 21st Century COE towards Creating New Industries Based on Inter-Nanosience International Symposium, Awaji, Japan, December 8-9, 2006.

 

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2005

1.  Dual Activation in a Homolytic Coupling Reaction Promoted by an Enantioselective Dinuclear Vanadium Catalyst
T. Yoshida, *T. Katayama, H. Somei, Y. Asano, S. Takizawa, H. Sasai, THE INTERNATIONAL SYMPOSIUM ON DYNAMIC COMPLEX (ISDC-2005), Nagoya, Japan, January 9-10, 2005.

2.  Development of Novel Spiro-type Ligands
T. Tsujihara, P. S. Koranne, C. Muthiah, K. Wakita, J. Yogo, S. Takizawa, *H. Sasai, THE INTERNATIONAL SYMPOSIUM ON DYNAMIC COMPLEX (ISDC-2005), Nagoya, Japan, January 9-10, 2005.

3.  Synthesis and Electrochemical Behavior of Organo-Ruthenium Dendrimers with Tri(4-ethynylphenyl)amine Bridges
*K. Onitsuka, N. Ohara, F. Takei, S. Takahashi, 21st Century COE towards Creating New Industries Based on Inter-Nanoscience
Ó Third International Symposium 2005, Shiga, Japan, March 9-10, 2005.

4.  Development and Application of a Novel Method for the Immobilization of Multicomponent Asymmetric Catalysts
*K. Marubayashi, S. Takizawa, H. Sasai, 21st Century COE towards Creating New Industries Based on Inter-Nanoscience
Ó Third International Symposium 2005, Shiga, Japan, March 9-10, 2005.

5.  Development of Artificial Enzymes with Relevance to Bioluminescence
*T. Kawase, D. Jayaprakash, S. Takizawa, H. Sasai, 21st Century COE towards Creating New Industries Based on Inter-Nanoscience
Ó Third International Symposium 2005, Shiga, Japan, March 9-10, 2005.

6.  Design and Synthesis of Novel Chiral Spiro Ligands and Ionic Liquids
*C. V. L. Rao, M. L. Patil, S. Takizawa, H. Sasai, 21st Century COE towards Creating New Industries Based on Inter-Nanoscience
Ó Third International Symposium 2005, Shiga, Japan, March 9-10, 2005.

7.  Study of Novel Chiral Ligands Bearing Spiro Skeleton and their Applications to Asymmetric Cyclizations
*C. V. L. Rao, M. L. Patil, S. Takizawa, H. Sasai, 21st Century COE towards Creating New Industries Based on Inter-Nanoscience
Ó Third International Symposium 2005, Shiga, Japan, March 9-10, 2005.

8.  Development of Novel Chiral Spiro-type Ligands
*T. Tsujihara, P. S. Koranne, K. Wakita, C. Muthiah, J. Yogo, S. Takizawa, H. Sasai, 229th ACS National Meeting, San Diego, CA, USA, March 13-17, 2005

9.  Phosphovanadomolybdate/Fluorapatite Solid-Phase System for Aerobic Oxidative Dehydrogenation (Poster),
K. Iteya, Y. Sasaki, S. Itoh, J. Ichihara, The 10th Japan-Korea Symposium on Catalysis, Matsue, Japan, May 10-13, 2005.

10.              High Efficiency of Hydrogen Peroxide in Fluorapatite Solid-Phase Epoxidation System
K. Sato, Y. Sasaki, J. Ichihara, The 10th Japan-Korea Symposium on Catalysis, Matsue, Japan, May 10-13, 2005.

11.              Solvent-Free H2O2-Epoxidation in Ttungstate/Hydrotalcite Solid-Phase System
S. Hoshi, Y. Sasaki, S. Yamaguchi, T. Nosu, J. Ichihara, The 10th Japan-Korea Symposium on Catalysis, Matsue, Japan, May 10-13, 2005.

12.              Metal-Bridged Polymers as Highly Enantioselective Catalysts
*S. Takizawa, H. Sasai, N. Inoue, D. Jayaprakash, The 13th IUPAC International Symposium on Organometallic Chemistry Directed towards Organic Synthesis (OMCOS13), Geneva, Switzerland, July 17-21, 2005.

13.              Dinuclear Vanadium Complexes with Dual Activation: Enantioselective Homolytic Coupling Reaction of 2-Naphthols
*H. Sasai, H. Somei, Y. Asano, T. Yoshida, T. Katayama, S. Takizawa, The 13th IUPAC International Symposium on Organometallic Chemistry Directed towards Organic Synthesis (OMCOS13), Geneva, Switzerland, July 17-21, 2005.

14.              Development of Novel Chiral Ligands Bearing Spiro Skeleton
P. S. Koranne, T. Tsujihara, T. Shinohara, S. Takizawa, *H. Sasai, Palermo, Italy, the 20th International Congress of Heterocyclic Chemistry, July 31-Aug. 5, 2005.

15.              Synthesis and Stereoselective Reactions of Planar-Chiral Cyclopentadienyl-Ruthenium Complexes
*K. Onitsuka, S. Tanakahashi, 7th International Symposium on Biotechnology, Metal Complexes and Catalysis (BMC-VII), Beijing, China, August 17-20, 2005.

16.              Effective Forms of Hydroxyapatite Disperse Phase in Solvent-Free Epoxidation System
K. Iteya, Y. Sasaki, S. Itoh, J. Ichihara, 5th International Symposium on Inorganic Phosphate Materials
Ô05, Kasugai, Japan, September 6-8, 2005.

17.              Participation of New Active Species in Epoxidation with Cetylpyridinium Dodecatungstate /FAp /Urea-H2O2 System
*J. Ichihara, Y. Sasaki, 5th World Congress on Oxidation Catalysis, Sapporo, Japan, September 25-30, 2005.

18.              Novel Bifunctional Organocatalysts for Enantioselective aza-Morita-Baylis-Hillman (aza-MBH) Reaction
*K. Matsui, S. Takizawa, H. Sasai, The 3rd International Symposium on Integrated Synthesis 2005 (ISIS-3), Osaka, Japan, September 30-October 1, 2005.

19.              Rational Design and Syntesis of Novel Chiral Spiro Type Ligands
*S. P. Koranne, T. Tsujihara, J. Yogo, S. Takizawa, H. Sasai, The 3rd International Symposium on Integrated Synthesis 2005 (ISIS-3), Osaka, Japan, September 30-October 1, 2005.

20.              Precise Synthesis of Organometallic Dendrimers
*K. Onitsuka, S. Tanakahashi, 15th International Symposium on Fine Chemistry and Functional Polymers (FCFP-XV), Shanghai, China, October 17-20, 2005.

21.              Multifunctional Asymmetric Organocatalyst
*H. Sasai,The 10th International Chemical Conference in Taipei (ICCT10), Hsinchu, Taiwan. October 28-30, 2005.

22.              Development of Enantioselective Intramolecular Aminocarbonylation Catalyzed by Pd-SPRIX
*T. Tsujihara, P. S. Koranne, J. Yogo, K. Wakita, T. Shinohara, M. A. Arai, T. Arai, S. Takizawa, K. Onitsuka, H. Sasai, 4th 21st Century COE towards Creating New Industries Based on Inter-Nanoscience
Ó International Symposium 2005, Mie, Japan, November 18-19, 2005.

23.              Design and Synthesis of Novel Chiral Ionic Liquids with Spiro Skeleton
*C. V. L. Rao, M. L. Patil, K. Yonezawa, S. Takizawa, K. Onitsuka, H. Sasai, 4th 21st Century COE towards Creating New Industries Based on Inter-Nanoscience
Ó International Symposium 2005, Mie, Japan, November 18-19, 2005.

24.              Synthesis of Dendric Copper(I) Complex and its Reactivity Towards Dioxygen
*.R N. Nadaf, D. Jayaprakash, H. Sasai, 4th 21st Century COE towards Creating New Industries Based on Inter-Nanoscience
Ó International Symposium 2005, Mie, Japan, November 18-19, 2005.

25.              A Rational Approach Toward the Development of Spiro Ligands
*P. S. Koranne, T. Tsujihara, J. Yogo, S. Takizawa, H. Sasai, 4th 21st Century COE towards Creating New Industries Based on Inter-Nanoscience
Ó International Symposium 2005, Mie, Japan, November 18-19, 2005.

26.              Development of Functionalized Nanoparticles Towards Targeted Drug Delivery Systems
*S. Takizawa, K. Tatematsu, 4th 21st Century COE towards Creating New Industries Based on Inter-Nanoscience
Ó International Symposium 2005, Mie, Japan, November 18-19, 2005.

27.              Bifunctional Organocatalysts for enantioselective aza-Morita-Baylis-Hillman (aza-MBH) Reaction
K. Matsui, K. Tanaka, S. Takizawa, *H. Sasai, PACIFICHEM 2005, Hawaii, USA, December 15-20, 2005.

28.              Development of Novel Chiral Spiro-Type Ligands Bearing Isoxazoline/Isoxazole Rings
P. S. Koranne, T. Tsujihara, J. Yogo, M. A. Arai, S. Takizawa, *H. Sasai, PACIFICHEM 2005, Hawaii, USA, December 15-20, 2005.

29.              Syntheses and Properties of Transition-Metal Acetylide Dendrimers
*K. Onitsuka, PACIFICHEM 2005, Hawaii, USA, December 15-20, 2005.

 

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2004

1.  Effect of fluorapatite as a solid-disperse-phase on solvent-free catalytic epoxidation
*J. Ichihara, K. Iteya, K. Ushimaru, Y. Sasaki, International Conference in Fluorine Chemistry (ICFC
Õ04) Kyoto, Japan, May 9-11, 2004.

2.  Design and Synthesis of Novel Spiro-type Ligands
*T. Tsujihara, K. Wakita, T. Kato, A. Shimomoto, M. L. Patil, C. V. L. Rao, T. Shinohara, M. A. Arai, S. Takizawa, H. Sasai, 17th French-Japanese Symposium on Medicinal and Fine Chemistry (FJS-2004), Miyagi, Japan, May 17-20, 2004.

3.  Dual Activation in a Homolytic Coupling Reaction Promoted by an Enantioselective Dinuclear Vanadium(IV) Catalyst
H. Somei, Y. Asano, *T. Yoshida, S. Takizawa, H. Yamataka, H. Sasai, 17th French-Japanese Symposium on Medicinal and Fine Chemistry (FJS-2004), Miyagi, Japan, May 17-20, 2004.

4.  The aza-Morita-Baylis-Hillman Reaction Catalyzed by Chiral Phosphine-Binol as an Organocatalyst
*K. Matsui, S. Takizawa, H. Sasai, 16th International Symposium on Chirality (ISCD 16), New York, USA, July 11-14, 2004.

5.  Development of Novel Chiral Spiro-type Ligands
*H. Sasai, K. Wakita, T. Kato, Y. Honda, M. A. Arai, T. Shinohara, C. Muthiah, T. Tsujihara, S. Takizawa, The 36th International Conference on Coordination Chemistry (ICCC-36), M
Žrida Yucat‡n, MŽxico, July 18-23, 2004.

6.  Dual Activation in a Homolytic Coupling Reaction Promoted by an Enantioselective Dinuclear Vanadium(IV) Catalyst
H. Somei, Y. Asano, *T. Yoshida, S. Takizawa, H. Yamataka, H. Sasai, 15th International Conference on Organic Synthesis (ICOS-15), Aichi, Japan, Aug. 2-6, 2004.

7.  The aza-Morita-Baylis-Hillman (aza-MBH) Reaction Promoted by Chiral Phosphine-BINOL as an Organocatalyst
*K. Matsui, S. Takizawa, H. Sasai, 15th International Conference on Organic Synthesis (ICOS-15), Aichi, Japan, Aug. 2-6, 2004.

8.  Novel Bifunctional Asymmetric Organocatalysts for aza-Morita-Baylis-Hillman (aza-MBH) Reaction
*K. Matsui, S. Takizawa, H. Sasai, The 7th IUPAC International Conference on Heteroatom Chemistry (ICHAC-7), Shanghai, China, Aug. 20-25, 2004.

9.  Catalytic Enantioselective Direct Henry Reaction
S. Takizawa, K. Murai, K. Wataguchi, T. Hara, *H. Sasai, Rare Earths
Õ04 in Nara, Nara, Japan, Nov. 7-12, 2004.

10.              Novel Bifunctional Organocatalysts for Enantioselective aza-Morita-Baylis-Hillman (aza-MBH) Reaction
*K. Matsui, S. Takizawa, H. Sasai, International Symposium on Scientific and Industrial Nanotechnology 2004 (SISSIN-2004)-Advanced Characterization for Nanomaterials, Nanodevices and Nanoprocessing-, Osaka, Japan, Dec. 6-7, 2004.

11.              Development and Application of Novel Immobilization Method for Multicomponent Asymmetric Catalysts
S. Takizawa, K. Marubayashi, *N. Inoue, H. Sasai, International Symposium on Scientific and Industrial Nanotechnology 2004 (SISSIN-2004)-Advanced Characterization for Nanomaterials, Nanodevices and Nanoprocessing-, Osaka, Japan, Dec. 6-7, 2004.

12.              Environmentally benign solid-phase-reaction-system for aerobic oxidative dehydrogenation
*J. Ichihara, K. Iteya, Y. Sasaki, International Symposium on Scientific and Industrial Nanotechnology 2004 (SISSIN-2004)-Advanced Characterization for Nanomaterials, Nanodevices and Nanoprocessing-, Osaka, Japan, Dec. 6-7, 2004.

13.              Stereoselective Reactions of Planar-Chiral CyclopentadienylÐRuthenium Complexes
*K. Onitsuka, S. Takahashi, XXIst International Conference on Organometallic Chemistry, The University of British Columbia, Vancouver, Canada, July 25-30, 2004.

14.              Novel Redox-Active Organometallic Dendrimers Composed of Ruthenium-Acetylide Units
*K. Onitsuka, N. Ohara, F. Takei, S. Takahashi, International Symposium on Scientific and Industrial Nanotechnology 2004 (SISSIN-2004) -Advanced Characterization for Nanomaterials, Nanodevices and Nanoprocessing-, Osaka, Japan, Dec. 6-7, 2004.

15.              Cyclic Aminocarbonylation of Alkynylimines with Cobalt-Catalyst
*D.-Y. Zhou, S. Suetsugu, K. Onitsuka and S. Takahashi, International Symposium on Scientific and Industrial Nanotechnology 2004 (SISSIN-2004) -Advanced Characterization for Nanomaterials, Nanodevices and Nanoprocessing-, Osaka, Japan, Dec. 6-7, 2004.

16.              Immobilization of Enantioselective Catalysts onto the Surface of Spherical Nanoparticles
*K. Marubayashi, S. Takizawa, F. Yonezawa, T. Kawakusu, D. Jayaprakash, M. L. Patil, T. Arai, T. Hanada, H. Sasai, Second 21st Century COE towards Creating New Industries Based on Inter-Nanoscience
Ó 7th SANKEN International Symposium on Hybridization of Chemistry, Biology, and Material Science -Perspectives in Nanoscience-, Osaka, Japan, January 13-14, 2004.

17.              The aza-Morita-Baylis-Hillman (aza-MBH) Reaction Promoted by Chiral Phosphine-BINOL as an Organocatalyst
*K. Matsui, S. Takizawa, H. Sasai, Second 21st Century COE towards Creating New Industries Based on Inter-Nanoscience
Ó 7th SANKEN International Symposium on Hybridization of Chemistry, Biology, and Material Science -Perspectives in Nanoscience-, Osaka, Japan, January 13-14, 2004.

18.              Design and Synthesis of Novel Spiro Chiral Phase Transfer Catalysts
*M. L. Patil, C. V. L. Rao, S. Takizawa, H. Sasai, Second 21st Century COE towards Creating New Industries Based on Inter-Nanoscience
Ó 7th SANKEN International Symposium on Hybridization of Chemistry, Biology, and Material Science -Perspectives in Nanoscience-, Osaka, Japan, January 13-14, 2004.

19.              Enantioselective Reactions Promoted by Pd(II)-SPRIX Catalysts
*C. Muthiah M. A. Arai, T. Shinohara, T. Arai, S. Takizawa,H. Sasai, Second 21st Century COE towards Creating New Industries Based on Inter-Nanoscience
Ó 7th SANKEN International Symposium on Hybridization of Chemistry, Biology, and Material Science -Perspectives in Nanoscience-, Osaka, Japan, January 13-14, 2004.

20.              New Approach for the Immobilization of Multicomponent Asymmetric Catalysts with High Enantiocontrol
*S. Takizawa, D. Jayaprakash, H. Somei, T. Sekiguti, K. Otsuki, T. Arai, H. Sasai, Second 21st Century COE towards Creating New Industries Based on Inter-Nanoscience
Ó 7th SANKEN International Symposium on Hybridization of Chemistry, Biology, and Material Science -Perspectives in Nanoscience-, Osaka, Japan, January 13-14, 2004.

21.              Effective Immobilization of Multifunctional Asymmetric Catalysts
*D. Jayaprakash, T. Sekiguti, Y. Iizuka, T. Arai, H. Sasai, Second 21st Century COE towards Creating New Industries Based on Inter-Nanoscience
Ó 7th SANKEN International Symposium on Hybridization of Chemistry, Biology, and Material Science -Perspectives in Nanoscience-, Osaka, Japan, January 13-14, 2004.

22.              Dual Activation in a Homolytic Coupling Reaction Promoted by an Enantioselective Dinuclear Vanadium(IV) Catalyst
H. Somei, Y. Asano, *T. Yoshida, S. Takizawa, H. Sasai, Second 21st Century COE towards Creating New Industries Based on Inter-Nanoscience
Ó 7th SANKEN International Symposium on Hybridization of Chemistry, Biology, and Material Science -Perspectives in Nanoscience-, Osaka, Japan, January 13-14, 2004.

23.              Design and Synthesis of Novel Spiro-Type Ligands
*T. Tsujihara, K. Wakita, T. Kato, T. Shinohara, M. A. Arai, S. Takizawa, T. Arai, H. Sasai, Second 21st Century COE towards Creating New Industries Based on Inter-Nanoscience
Ó 7th SANKEN International Symposium on Hybridization of Chemistry, Biology, and Material Science -Perspectives in Nanoscience-, Osaka, Japan, January 13-14, 2004.

24.              Immobilization of Multicomponent Asymmetric Catalysts
*S. Takizawa and H. Sasai, International Workshop on Recent Progress in Organic Chemistry, Osaka, Japan, March 1-3, 2004.

25.              Some Enantioselective Reactions Using Spiro Chiral Compounds
*H. Sasai, International Workshop on Recent Progress in Organic Chemistry (Oral), Osaka, Japan, March 1-3, 2004.

26.              Immobilization of Multifunctional Asymmetric Catalysts (MACs)
D. Jayaprakash, S. Takizawa, T. Arai, and *H. Sasai, 227th ACS National Meeting, California, USA, March 28 - April 1, 2004.

27.              Enantioselective Catalysis Using Novel Spiro-type Ligands
*H. Sasai, 227th ACS National Meeting, California, USA, March 28 - April 1, 2004.

28.              Clean Polyoxometalate/Apatite Solid-Phase-System for Oxidation of Sulfides to Sulfoxides and Sulfones
*J. Ichihara, K. Ushimaru, and Y. Sasaki, 7th SANKEN International Symposium on Hybridization of Chemistry, Biology, and Material Science, Osaka, Japan, January 13-14, 2004.

 

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2003

1.  Development of Multifunctional Asymmetric Catalysts (MAC) for Morita-Baylis-Hillman (MBH) Reaction
*K. Matsui, S. Takizawa, H. Sasai, 12th Symposium on Organo-metallic Chemistry Directed toward Organic Synthesis (OMCOS 12), Toronto, Canada, July 6-10, 2003.

2.  Design and Synthesis of Novel Spiro-Type Ligands
*T. Kato, K. Wakita, T. Shinohara, C. Muthiah, M. A. Arai, S. Takizawa, H. Sasai, 12th Symposium on Organo-metallic Chemistry Directed toward Organic Synthesis (OMCOS 12), Toronto, Canada, July 6-10, 2003.

3.  Development of Novel Multifunctional Asymmetric Catalysts
*S. Takizawa, H. Somei, K. Murai, T. Arai, D. Jayaprakash, H. Sasai, The International Symposium on Dynamic Complexes (ISDC 2003), Tokyo, Japan, August 4, 2003.

4.  Enantioselective Catalysis Using Novel Spiro-type Ligands
*K. Wakita, M. A. Arai, T. Shinohara, T. Kato, C. Muthiah, S. Takizawa, T. Arai, H. Sasai, The 15th International Symposium on Chirality (Chirality 2003), Shizuoka, Japan, October 20-23, 2003.

5.  Enantioselective Catalysis Using Novel Spiro-type Ligands
*K. Wakita, T. Kato, T. Shinohara, C. Muthiah, M. A. Arai, S. Takizawa, T. Arai, H. Sasai, The 9th International Kyoto Conference on New Aspects of Organic Chemistry (IKCOC-9), Kyoto, Japan, November 10-14, 2003.

6.  Effective Immobilization of Mulitifunctional Asymmetric Catalysts
*D. Jayaprakash, T. Sekiguti, Y. Iizuka, S. Takizawa, T. Arai, H. Sasai, The 9th International Kyoto Conference on New Aspects of Organic Chemistry (IKCOC-9), Kyoto, Japan, November 10-14, 2003.

7.  Dual Activation in a Homolytic Coupling Reaction Promoted by an Enantioselective Dinuclear Vanadium(IV) Catalyst
H. Somei, Y. Asano, T. Yoshida, *S. Takizawa, H. Yamataka, H. Sasai, The 9th International Kyoto Conference on New Aspects of Organic Chemistry (IKCOC-9), Kyoto, Japan, November 10-14, 2003.

8.  Metal-bridged Polymers as Insoluble Multicomponent Asymmetric Catalysts (MACs) with High Enantiocontrol: An Approach for the Immobilization of Catalysts without Using any Support
*S. Takizawa, H. Somei, D. Jayaprakash, H. Sasai, International Symposium on Scientific and Industrial Nanotechnology 2003 (ISSIN-2003), Osaka, Japan, December 8-9, 2003.

9.  Monolayer-protected Au Cluster (MPC)-supported Ti-BINOLate Complex
*T. Kawakusu, K. Marubayashi, S. Takizawa, T. Arai, H. Sasai, International Symposium on Scientific and Industrial Nanotechnology 2003 (ISSIN-2003), Osaka, Japan, December 8-9, 2003.

10.              Metal-bridged Polymers as Insoluble Multicomponent Asymmetric Catalysts (MACs) with High Enantiocontrol: An Approach for the Immobilization of Catalysts without Using any Support
*S. Takizawa, H. Somei, D. Jayaprakash, H. Sasai, International Symposium on Organic Reactions 2003 (ISOR-2003), Kaohsiung, Taiwan, December 19-21, 2003.

11.              Dynamics-driven Reaction Pathway: In What Case Is a Reaction Controlled by Dynamics?
*H. Yamataka, S. C. Ammal, 9th European Symposium on Organic Reactivity, Oslo, Norway, July12-17, 2003.

12.              Can Enol of Carboxylic Acid Halides Be Prepared?
Z. Rappoport, S. C. Ammal, *H. Yamataka, 10th Kyushu International Symposium on Physical Organic Chemistry, Fukuoka, Japan, September 30 - October 3, 2003.

13.              Theoretical Study on the Mechanism of Halogen Exchange Reaction of Alkyl Halide in Aqueous Solution
M. Ohisa, M. Aida, *H. Yamataka, 10th Kyushu International Symposium on Physical Organic Chemistry, Fukuoka, Japan, September 30 - October 3, 2003.

14.              Cetylpyridinium Dodecatungstate Dispersed on Apatite: A Reusable, Efficient Solid-catalyst-phase in the H2O2-epoxidations
Y. Sasaki, *A. Kanbara, K. Iteya, J. Ichihara, S. Yamaguchi, The 9th Korea-Japan Symposium on Catalysis, Pohang, Korea, May 20-21, 2003.

15.              Catalytic Activities and Active Species in Phosphomolybdate/Urea-H2O2/Apatite Solid-phase System
J. Ichihara, *K. Iteya, K. Ushimaru, H. Kawaguchi, Y. Sasaki, S. Yamaguchi, and H. Nakayama, The 9th Korea-Japan Symposium on Catalysis, Pohang, Korea, May 20-21, 2003.

 

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