Presentations

2024 🐉

<Domestic>

1.    Å­ŠwKƒf[ƒ^‚É‚æ‚éƒf[ƒ^‹ì“®Œ^¸–§—L‹@‡¬”½‰ž‚ÌŠJ”­iµ‘Òu‰‰j*‘êàV”E; ‚•ªŽqu‰‰‰ïi“ŒŠCj, ˆ¤’m 19th January 2024.

 

2.    Kinetically Guided Photo-Induced Autooxidation of Aldehydes (Poster) *Muthu Karuppasamy, Mohamed S. H. Salem, Carla Dubois, Yuya Takamura, Atsuhito Kitajima, Takuma Kawai, Shinobu Takizawa, Masayuki Kirihara; The 50th Symposium on Progress in Reactions and Syntheses (The Pharmaceutical Society of Japan), Kobe, 27th-28th October 2024.

 

<International>

1.    Electrochemical Synthesis of Oxaza[9]-,[12]-, and [15]Helicenes (Poster) *Ahmed Sabri Gabr, Hiroaki Sasai, Mohamed S. H. Salem, Shinobu Takizawa; The 34th Chirality, Kyoto, 26th-29th August 2024.

 

2.    Sequential Electrochemical Synthesis of Hetero[7]dehydrohelicene and Double Hetero[7] dehydrohelicene (Poster) *Rubal Sharma, Mohamed S.H. Salem, Md. Imrul Khalid, Mitsuhiro Arisawa,  Shinobu Takizawa; The 34th Chirality, Kyoto, 26th-29th August 2024.

 

3.    Diastereoselective synthesis and applications of cobalt(III) complexes in catalysis and medicinal chemistry (Poster). *Mohamed S. H. Salem, Yasmine M. Abdel Aziz, Marwa Elewa, Shinobu Takizawa; The 6th Annual Conference of Graduate Researchers in Pharmaceutical Sciences, Suez Canal University, 9th December 2024.

 

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 Synthesish, 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.      ƒxƒCƒYÅ“K‰»‚É‚æ‚鸖§—L‹@‡¬”½‰žðŒ‚Ì’Tõiµ‘Òu‰‰j*‘êàV”E; The 103rd CSJ Annual Meeting, Chiba, 22nd-25th March 2023.

 

5.      Electrochemical Synthesis of [7]helicenes, dehydro[7]helicenes and [8]circulenes iOralj *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.      Å­ŠwKƒf[ƒ^‚É‚æ‚éƒf[ƒ^‹ì“®Œ^¸–§—L‹@‡¬”½‰ž‚ÌŠJ”­@`ƒxƒCƒYÅ“K‰»‚É‚æ‚锽‰žðŒ‚Ìv‘¬Å“K‰»`iµ‘Òu‰‰j*‘êàV”E; 142nd Annual Meeting the Pharmaceutical Society of Japan (PSJ), Hokkaido, 25th-28th March 2023.

 

7.      Auto-Organocatalytic Ring Expansion via Chiral Self-Recognition of N-Tosyl-tetrahydrocarbolines (Oral) *Tin Zar Aye, Mohamed S. H. Salem, Masaru Kondo, Hiroaki Sasai, Shinobu Takizawa; Molecular Chirality 2023, Hokkaido, 15th-16th June 2023.

 

8.      Electrochemical One-pot Synthesis of Oxaza[7]helicenes, Dehydro-oxaza[7]helicenes and Oxaza[8]circulenes (Poster) *Mohamed S. H. Salem, Md. Imrul Khalid, Ahmed Sabri, Hiroaki Sasai, Shinobu Takizawa; Molecular Chirality 2023, Hokkaido, 15th-16th June 2023.

 

9.      Bayesian Optimization-assisted Multi-parameter Screening: Towards Hundred-gram Scale Process (Poster) *Shinobu Takizawa, Masaru Kondo, H. D. P. Wathsala, Mohamed S. H. Salem, Daisuke Yamashita, Takeshi Miyazaki, Yoji Ohno, Hiroaki Sasai, Takashi Washio; “ú–{ƒvƒƒZƒX‰»Šw‰ï2023ƒTƒ}[ƒVƒ“ƒ|ƒWƒEƒ€, Tokyo August 3rd-4th 2023.

 

10.  Electrochemical one-pot synthesis of hetero[8]circulenes and their application in photocatalysisiPosterj*Ahmed S. Gabr, Mohamed S. H. Salem, Md. Imrul Khalid, Hiroaki Sasai, Shinobu Takizawa; ‘æ39‰ñ—L‹@‡¬‰»ŠwƒZƒ~ƒi[ Hyogo 20th-22nd September 2023.

 

11.  Chiral vanadium(V) complex-catalyzed oxidative hetero-coupling of 2-naphthylamines via photoactivationiOralj Duona Fan, Ganesh T. Kamble, ùˆä G–¾,‘êàV ”E; ‘æ123‰ñ—L‹@‡¬ƒVƒ“ƒ|ƒWƒEƒ€ Tokyo 6th-7th November 2023.

 

12.  ƒwƒeƒ[8]ƒT[ƒLƒ…ƒŒƒ“‚Ì“d‰ð‡¬‚ÆŒõG”}‚Æ‚µ‚Ẳž—piOralj*²ŒÃ^, Ahmed S. Gabr, Mohamed S. H. Salem, Md. Imrul Khalid, ‘êàV ”E; ‘æ16‰ñ—L‹@•ªŽqG”}ƒVƒ“ƒ|ƒWƒEƒ€ Miyagi 27th-28th November 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.

 

3.      Electrochemical and flow syntheses of polycyclic aromatics (Invited) *Shinobu Takizawa; Trilateral Japan-Canada-Germany mini-symposium -Smart molecules design and practical applications in chemical and biochemical process-, Hokkaido 28th July 2023.

 

4.      Enantioselective Synthesis of a Triply-twisted Möbius Molecules (Poster) *Mohamed S. H. Salem, Akimasa Sugizaki, Md. Imrul Khalid, Hiroaki Sasai, Shinobu Takizawa; CD2023, Hiroshima 17th-21st September 2023.

 

5.      Vanadium(V) Complex-catalyzed Oxidative Hetero-coupling of Arenols and/or Aryl Amines (Poster) *Duona Fan, Ganesh T. Kamble, Hiroaki Sasai, Shinobu Takizawa; IKCOC-15, Kyoto 20th-23rd November 2023.

 

6.      Bayesian Optimization (BO)-driven Screening of Multiple Parameters: Towards Efficient Electrochemical       and     Flow      Synthesis                  (Poster)* Mohamed S. H. Salem, Masaru Kondo, H. D. P. Wathsala, Akimasa Sugizaki, Md. Imrul Khalid, Hiroaki Sasai, Takashi Washio, Shinobu Takizawa; IKCOC-15, Kyoto 20th-23rd November 2023.

 

7.      Data-driven Multi-parameter Screening of Electrochemical and Flow Reaction Conditions Using Bayesian Optimization (Invited) *Shinobu Takizawa; International Joint Symposium 2023 on Synthetic Organic Chemistry, Hyogo 5th-8th December 2023.

 

8.      Data-driven Electrochemical One-pot Synthesis of Double Hetero[7]dehydrohelicene *Rubal Sharma, Mohamed S. H. Salem, Mitsuhiro Arisawa, Shinobu Takizawa; International Joint Symposium 2023 on Synthetic Organic Chemistry, Hyogo 5th-8th December 2023.

 

2022 🐯

<Domestic>

1.    “ñdŠˆ«‰»Œ^•sÄG”}‚Ì‘n»iµ‘Òu‰‰j

*ùˆäG–¾ —L‹@‡¬Vtu‰‰‰ïyƒIƒ“ƒ‰ƒCƒ“ŠJÃz, 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–{‰»Šw‰ï ‘æ102”N‰ïi2022jyƒIƒ“ƒ‰ƒCƒ“ŠJÃz, 3ŒŽ23“ú, 2022”N.

 

3.    ŒõŠwŠˆ«‚ÈŠÂóBINOLŽO—ʑ̂̑I‘ð“I‡¬iŒû“ª”­•\j

*™›½W«; ‘êàV”E; ùˆäG–¾ “ú–{‰»Šw‰ï ‘æ102”N‰ïi2022jyƒIƒ“ƒ‰ƒCƒ“ŠJÃz, 3ŒŽ24“ú, 2022”N.

 

4.   ‹@ŠBŠwK‹ì“®Œ^ƒ}ƒ‹ƒ`ƒpƒ‰ƒ[ƒ^ƒXƒNƒŠ[ƒjƒ“ƒO‚É‚æ‚éƒPƒ`ƒ~ƒ“‚Ì“d‰ð‡¬‚Ì”½‰žðŒÅ“K‰»iŒû“ª”­•\j

*‹ß“¡Œ’; ™›½W«; Khalid Md Imrul; H. D. P. Wathsala; Îìˆêé; Œ´‘; ‘é‡F”V; ˜h”ö—²; ‘êàV”E; ùˆäG–¾ “ú–{‰»Šw‰ï ‘æ102”N‰ïi2022jyƒIƒ“ƒ‰ƒCƒ“ŠJÃz, 3ŒŽ24“ú, 2022”N.

 

5.   Œõ‰ž“šŒ^ƒuƒŒƒ“ƒXƒeƒbƒhŽ_•sÄG”}‚Ì‘n»Œ¤‹†iŒû“ª”­•\j

*ˆÀ“cC; ‹ß“¡Œ’; ‘êàV”E; ùˆäG–¾ “ú–{‰»Šw‰ï ‘æ102”N‰ïi2022jyƒIƒ“ƒ‰ƒCƒ“ŠJÃz, 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–{‰»Šw‰ï ‘æ102”N‰ïi2022jyƒIƒ“ƒ‰ƒCƒ“ŠJÃz, 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–{‰»Šw‰ï ‘æ102”N‰ïi2022jyƒIƒ“ƒ‰ƒCƒ“ŠJÃz, 3ŒŽ26“ú, 2022”N.

 

8.    Ž_‰»“IƒwƒeƒƒJƒbƒvƒŠƒ“ƒOE’E…ŠÂ‰»E’E…‘fŠÂ‰»”½‰ž‚É‚æ‚éŒõŠwŠˆ«ƒAƒUƒIƒLƒTƒfƒqƒhƒ[7]ƒwƒŠƒZƒ“—ނ̃hƒ~ƒm‡¬Œ¤‹†iŒû“ª”­•\j

*‘êàV”E; Khalid Md. Imrul ; Salem H. Mohamed; ‹ß“¡Œ’; ²ŒÃ^; ùˆäG–¾ “ú–{–òŠw‰ï ‘æ142”N‰ïi2022jyƒIƒ“ƒ‰ƒCƒ“ŠJÃz, 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–{–òŠw‰ï ‘æ142”N‰ïi2022jyƒIƒ“ƒ‰ƒCƒ“ŠJÃz, 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), yOnlinez, 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–{ƒvƒƒZƒX‰»Šw‰ï2022ƒTƒ}[ƒVƒ“ƒ|ƒWƒEƒ€, Toyama, 30th Jun-1st July 2022.

 

12. ‹@ŠBŠwKƒxƒCƒYÅ“K‰»‚ðŠˆ—p‚·‚éƒPƒ`ƒ~ƒ“‚Ì“d‰ð‡¬”½‰žðŒÅ“K‰» (Poster)

*Md. Imrul Khalid, Masaru Kondo, ™›½¸«CH. D. P. Wathsala, ÎìˆêéCŒ´‘C‘éF”VC˜h”ö—²CHiroaki Sasai, Shinobu Takizawa; “ú–{ƒvƒƒZƒX‰»Šw‰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–{ƒvƒƒZƒX‰»Šw‰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. ’‚‘fEŽ_‘fE—°‰©Œ´Žq‚ðŠÜ‚Þƒwƒeƒ[9]ƒwƒŠƒZƒ“‚̃Gƒiƒ“ƒ`ƒI‘I‘ð“I‡¬(Poster)

*Ankit Kumar, ²ŒÃ ^, ùˆäG–¾, ‘êàV ”E; 51st Congress of Heterocyclic Chemistry, Osaka University, 15th-17th September 2022.

 

16. •sÄ‘•‚𔺂¤ŒõŠwŠˆ«ŠÜ’‚‘f‚WˆõŠÂ‚̇¬Œ¤‹†(Poster)

*‘êàV ”E, Tin Zar Aye, ‹ß“¡ Œ’, ùˆäG–¾; 51st Congress of Heterocyclic Chemistry, Osaka University, 15th-17th September 2022.

 

17. Å­ŠwKƒf[ƒ^‚É‚æ‚éƒf[ƒ^‹ì“®Œ^¸–§—L‹@‡¬”½‰ž‚ÌŠJ”­iµ‘Òu‰‰j

*‘êàV”E; ŽYŒ¤ŽŸ¢‘ã—L‹@‰»ŠwƒZƒ~ƒi[, ‘åã‘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‚¨‚æ‚Ñ“ñŠjƒoƒiƒWƒEƒ€G”}”½‰ž‚É‚æ‚鎲•sĉ»‡•¨‚̃Gƒiƒ“ƒ`ƒI‘I‘ð“I‡¬(Poster)

*Ankit KumarAùˆäG–¾A‘êàV”E; The 38th Seminar on Synthetic Organic Chemistry, Fukuoka, 28th-30th September 2022.

 

20. Å­ŠwKƒf[ƒ^‚É‚æ‚éƒf[ƒ^‹ì“®Œ^¸–§—L‹@‡¬”½‰ž‚ÌŠJ”­iµ‘Òu‰‰j

*‘êàV”E; ‹ß‹E‰»Šw‹¦‰ï ‡¬•”‰ï ƒtƒ[Eƒ}ƒCƒNƒ‡¬Œ¤‹†‰ï ‘æ96‰ñŒ¤‹†‰ï, ‘åã‰ÈŠw‹ZpƒZƒ“ƒ^[, 2022”N11ŒŽ18“ú

 

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

*Duona Fan, Ganesh T. Kamble, Hiroaki Sasai, Shinobu Takizawa; ‘æ48‰ñ”½‰ž‚Ƈ¬‚Ìi•àƒVƒ“ƒ|ƒWƒEƒ€CChiba, 28th-29th November 2022.

 

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

*‘êàV ”E, Tin Zar Aye, ‹ß“¡ Œ’, ùˆäG–¾; ‘æ48‰ñ”½‰ž‚Ƈ¬‚Ìi•àƒVƒ“ƒ|ƒWƒEƒ€CChiba, 28th-29th November 2022.

 

23. ‹@ŠBŠwK‚ðŠˆ—p‚·‚鸖§—L‹@‡¬”½‰žðŒ‚ÌÅ“K‰»(µ‘Òu‰‰)

*‘êàV”E; ‘æ105‰ñŽYŒ¤ƒeƒNƒmƒTƒƒ“, ‘åã‘åŠw, 2022”N12ŒŽ19“ú

 

24. Å­ŠwKƒf[ƒ^‚É‚æ‚éƒf[ƒ^‹ì“®Œ^¸–§—L‹@‡¬F”½‰žŠJ”­‚ð‰Á‘¬‚·‚é‹@ŠBŠwKƒxƒCƒYÅ“K‰»‚É‚æ‚锽‰žðŒÅ—lj»(µ‘Òu‰‰)

*‘êàV”E; uAI‚Æ—L‹@‡¬‰»Šwv‘æ10‰ñ•׋­‰ï, ‚¨’ƒ‚Ì…ƒ†ƒjƒIƒ“ƒrƒ‹, 2022”N12ŒŽ22“úu‰‰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“ŠJÃz, 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“ŠJÃz, 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. ‹@ŠBŠwK‚Æ—L‹@‡¬‰»Šwiµ‘Òu‰‰j

*ùˆäG–¾@—L‹@‡¬2ŒŽƒZƒ~ƒi[u—L‹@‡¬‚̃jƒ…[ƒgƒŒƒ“ƒh2021vyWEB”zMz, 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–{‰»Šw‰ï@‘æ101t‹G”N‰ïi2021jyƒIƒ“ƒ‰ƒCƒ“ŠJÃz, 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–{‰»Šw‰ï@‘æ101t‹G”N‰ïi2021jyƒIƒ“ƒ‰ƒCƒ“ŠJÃz, 3ŒŽ19“ú, 2021”N.

 

4. Œõ‰ž“šŒ^•sÄ‘ŠŠÔˆÚ“®G”}‚ÌŠJ”­iŒû“ª”­•\j

*’†‘ºŒ°“l; ‹ß“¡Œ’; Krishnan, C.; ‘êàV”E; ùˆäG–¾ “ú–{‰»Šw‰ï@‘æ101t‹G”N‰ïi2021jyƒIƒ“ƒ‰ƒCƒ“ŠJÃz, 3ŒŽ19“ú, 2021”N.

 

5. Enantioselective Synthesis of Spirooxindoles via Sequential ReactionsiOralj

*Aye, T. Z.; Matsuyama, N.; Mattan, I.; Kondo, M.; Takizawa, S.; Sasai, H. “ú–{‰»Šw‰ï@‘æ101t‹G”N‰ïi2021jyƒIƒ“ƒ‰ƒCƒ“ŠJÃz, 3ŒŽ21“ú, 2021”N.

 

6. Electrochemical Synthesis of Azaoxa[7]helicenes via Oxidative Hetero-coupling/Dehydrative Cyclization Sequence of ArenolsiOralj

*Salem, M. S. H.; Khalid, Md. I.; Sako, M.; Takizawa, S.; Sasai, H. “ú–{‰»Šw‰ï@‘æ101t‹G”N‰ïi2021jyƒIƒ“ƒ‰ƒCƒ“ŠJÃz, 3ŒŽ21“ú, 2021”N.

 

7. ŒÅ’艻ƒoƒiƒWƒEƒ€G”}V-MPS4‚É‚æ‚éC-HН”\‰»ƒwƒeƒƒrƒAƒŠ[ƒ‹ƒJƒbƒvƒŠƒ“ƒO–@‚ÌŠJ”­‚Æ‚»‚̉ž—piŒû“ª”­•\j*Š}ŠÔŒšŒá; “ú“ì—D–ç; Gamal. A. I. M.; ²ŒÃ^; ‘êàV”E; ùˆäG–¾; ÔˆäŽüŽi “ú–{–òŠw‰ï@‘æ141”N‰ïiL“‡jyƒIƒ“ƒ‰ƒCƒ“ŠJÃz, 3ŒŽ28“ú, 2021”N.

 

8. ‹@ŠBŠwK‚ðŠˆ—p‚·‚éƒtƒ[‡¬‚̉•σpƒ‰ƒ[ƒ^[Å“K‰»iµ‘Òu‰‰j*ùˆäG–¾ ‹ß‹E‰»Šw‹¦‰ï‡¬•”‰ïƒtƒ[Eƒ}ƒCƒNƒ‡¬Œ¤‹†‰ï ‘æ35‰ñŒöŠJu‰‰‰ïi‘æ91‰ñŒ¤‹†‰ïjyƒIƒ“ƒ‰ƒCƒ“ŠJÃz, 8ŒŽ6“ú 2021”N

 

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

*Tin Zar Aye; ‹ß“¡Œ’; ¼ŽR®Ž÷; Irshad Mattan; ‘êàV”E; ùˆäG–¾ ‘æ47‰ñ”½‰ž‚Ƈ¬‚Ìi•àƒVƒ“ƒ|ƒWƒEƒ€yƒIƒ“ƒ‰ƒCƒ“ŠJÃz, 10ŒŽ2“ú, 4“ú 2021”N

 

10. “d‰ð˜A‘±”½‰ž‚É‚æ‚éŠÂóƒfƒqƒhƒƒIƒLƒTƒwƒŠƒZƒ“‚̇¬iŒû“ª”­•\j

*Mohamed S. H. Salem; Md. Imrul Khalid; ²ŒÃ^; ‹ß“¡Œ’; ‘êàV”E; ùˆäG–¾ ‘æ50‰ñ•¡‘fŠÂ‰»Šw“¢˜_‰ïyƒIƒ“ƒ‰ƒCƒ“ŠJÃz, 10ŒŽ9“ú 2021”N

 

11. Photoswitchable chiral phase transfer catalyst: Design and applicationiŒû“ª”­•\j

*Chandu G. Krishnan; ‹ß“¡Œ’; ’†‘ºŒ°; ‘êàV”E; ùˆäG–¾ ‘æ14‰ñ—L‹@G”}ƒVƒ“ƒ|ƒWƒEƒ€ yƒIƒ“ƒ‰ƒCƒ“ŠJÃz, 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), yƒnƒCƒuƒŠƒbƒhŠJÃz, 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–{‰»Šw‰ï‘æ100t‹G”N‰ïC“Œ‹ž—‰È‘åŠw@–ì“cƒLƒƒƒ“ƒpƒXiç—tjC3ŒŽ22“ú`3ŒŽ25“úC2020”ND

2. Chiral Vanadium Complex-catalyzed Enantioselective Oxidative Coupling of 4-Hydroxycarbazoles (Oral)
*Park, H.; Sako, M.; Takizawa, S.; Sasai, H.
“ú–{‰»Šw‰ï‘æ100t‹G”N‰ïC“Œ‹ž—‰È‘åŠw@–ì“cƒLƒƒƒ“ƒpƒXiç—tjC3ŒŽ22“ú`3ŒŽ25“úC2020”ND

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–{‰»Šw‰ï‘æ100t‹G”N‰ïC“Œ‹ž—‰È‘åŠw@–ì“cƒLƒƒƒ“ƒpƒXiç—tjC3ŒŽ22“ú`3ŒŽ25“úC2020”ND

4. Vanadium Complex-catalyzed Enantioselective Synthesis of Hetero[9]helicenes and Their Physical Properties (Oral)
*Sako, M.; Kumar, A.; Takizawa, S.; Sasai, H.
“ú–{‰»Šw‰ï‘æ100t‹G”N‰ïC“Œ‹ž—‰È‘åŠw@–ì“cƒLƒƒƒ“ƒpƒXiç—tjC3ŒŽ22“ú`3ŒŽ25“úC2020”ND

5. Development of Asymmetric Catalyst Bearing Dithienylethene and Application (Oral)
*Wakabayashi, Y.; Nakamura, K.; Kondo, M.; Sasai, H.
“ú–{‰»Šw‰ï‘æ100t‹G”N‰ïC“Œ‹ž—‰È‘åŠw@–ì“cƒLƒƒƒ“ƒpƒXiç—tjC3ŒŽ22“ú`3ŒŽ25“úC2020”N

6. Development of Photoresponsive Chiral Pyridine-Oxazoline Ligand (Oral)
*Nakamura, K.; Wakabayashi, Y.; Kondo, M.; Sasai, H.
“ú–{‰»Šw‰ï‘æ100t‹G”N‰ïC“Œ‹ž—‰È‘åŠw@–ì“cƒLƒƒƒ“ƒpƒXiç—tjC3ŒŽ22“ú`3ŒŽ25“úC2020”N

7. Development of a Novel Photoisomerizable Organocatalyst (Oral)
*Kondo, M.; Nakamura, K.; Wakabayashi, Y.; Sasai, H.
“ú–{‰»Šw‰ï‘æ100t‹G”N‰ïC“Œ‹ž—‰È‘åŠw@–ì“cƒLƒƒƒ“ƒpƒXiç—tjC3ŒŽ22“ú`3ŒŽ25“úC2020”N

8. Electrochemical Synthesis of Heterohelicenes via Oxidative Hetero-coupling/Intramolecular Cyclization Sequence (Oral)
*Khalid, M. I.; Sako, M.; Takizawa, S.; Sasai H.
“ú–{‰»Šw‰ï‘æ100t‹G”N‰ïC“Œ‹ž—‰È‘åŠw@–ì“cƒLƒƒƒ“ƒpƒXiç—tjC3ŒŽ22“ú`3ŒŽ25“úC2020”ND

9. ƒLƒ‰ƒ‹ƒoƒiƒWƒEƒ€G”}‚ð—p‚¢‚éƒAƒŒƒm[ƒ‹—Þ‚ÌŽ_‰»“IƒwƒeƒƒJƒbƒvƒŠƒ“ƒO”½‰žiŒû“ªj
*
“Œ“cŒbŒÞA²ŒÃ^A‘êàV”EAùˆäG–¾C“ú–{–òŠw‰ï‘æ140”N‰ïC‘—§‹ž“s‘Û‰ïŠÙ@‘¼i‹ž“sjC3ŒŽ25“ú`3ŒŽ28“úC2020”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–{–òŠw‰ï‘æ140”N‰ïC‘—§‹ž“s‘Û‰ïŠÙ@‘¼i‹ž“sjC3ŒŽ25“ú`3ŒŽ28“úC2020”N.

11. Development of Anionic Octahedral Salicylimine-based Cobalt(III) Catalysts for Enantioselective Reactions (Oral)
*Salem, M.; Takizawa, S.; Sasai, H.
“ú–{–òŠw‰ï‘æ140”N‰ïC‘—§‹ž“s‘Û‰ïŠÙ@‘¼i‹ž“sjC3ŒŽ25“ú`3ŒŽ28“úC2020”N.

 

12. ƒvƒƒpƒ‹ƒMƒ‹ƒAƒZƒe[ƒg‚Ì•sĊ‰»|ƒJƒ‹ƒ{ƒjƒ‹‰»”½‰ž‚ðŠî”Õ‚Æ‚µ‚½(|)-Graminin A‚Ì‘S‡¬iŒû“ª”­•\j

*“ú‰º•”‘¾ˆê; ˆÉ“¡—zˆê; ‚‹´Œ\‰î; Dhage, T. D.; â“cŒ’; ùˆäG–¾; ‰Á“¡Œb‰î@‘æ117‰ñ—L‹@‡¬ƒVƒ“ƒ|ƒWƒEƒ€2020”NyƒIƒ“ƒ‰ƒCƒ“z, 10ŒŽ29“ú`10ŒŽ30“ú, 2020”N.

 

13. ‹@ŠBŠwK‚ðŠˆ—p‚·‚鸖§ƒtƒ[•s欂ÌÅ“KðŒ’TõiŒû“ª”­•\j

*‹ß“¡Œ’; Wathsala, H. D. P.; ²ŒÃ^; ‰Ô’J—D‘¾˜N; Îìˆêé;Œ´‘; ‘é‡F”V; ˜h”ö—²; ‘êàV”E; ùˆäG–¾@‘æ117‰ñ—L‹@‡¬ƒVƒ“ƒ|ƒWƒEƒ€2020”NyƒIƒ“ƒ‰ƒCƒ“z, 10ŒŽ29“ú`10ŒŽ30“ú, 2020”N.

 

14. Vanadium Complex-catalyzed Enantioselective Oxidative Coupling of HydroxycarbazolesiŒû“ª”­•\j

–pŠØúÙ; ²ŒÃ^; ‘êàV”E; ùˆäG–¾@@‘æ117‰ñ—L‹@‡¬ƒVƒ“ƒ|ƒWƒEƒ€2020”NyƒIƒ“ƒ‰ƒCƒ“z, 10ŒŽ29“ú`10ŒŽ30“ú, 2020”N.


<International>

1. Efficient Synthesis of Hetero-helicenes and Their Chiroptical PropertiesiKeynote Lecturej

*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–{‰»Šw‰ï‘æ99t‹G”N‰ïCb“ì‘åŠwi•ºŒÉjC3ŒŽ16“ú`3ŒŽ19“úC2019”ND

2. Development of New Chiral Ligands Based on a Tetraphenylene Backbone (Oral)
*Kataoka, K.; Takenaka, K.; Sasai, H.
“ú–{‰»Šw‰ï‘æ99t‹G”N‰ïCb“ì‘åŠwi•ºŒÉjC3ŒŽ16“ú`3ŒŽ19“úC2019”ND

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–{‰»Šw‰ï‘æ99t‹G”N‰ïCb“ì‘åŠwi•ºŒÉjC3ŒŽ16“ú`3ŒŽ19“úC2019”ND

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–{‰»Šw‰ï‘æ99t‹G”N‰ïCb“ì‘åŠwi•ºŒÉjC3ŒŽ16“ú`3ŒŽ19“úC2019”ND

5. Effect of Phosphine Ligands on Pd-catalyzed Cyclative Hydroamination (Oral)
*Kusaba, M.; Takenaka, K.; Sasai, H.
“ú–{‰»Šw‰ï‘æ99t‹G”N‰ïCb“ì‘åŠwi•ºŒÉjC3ŒŽ16“ú`3ŒŽ19“úC2019”ND

6. Synthetic Study of Bismurayaquinone-A Using Chiral Vanadium Catalyst (Oral)
*Park, H.; Sako, M.; Takizawa, S.; Sasai, H.
“ú–{‰»Šw‰ï‘æ99t‹G”N‰ïCb“ì‘åŠwi•ºŒÉjC3ŒŽ16“ú`3ŒŽ19“úC2019”ND

7. Chiral Vanadium Complex-catalyzed Enantioselective Oxidative Hetero-coupling Reactions of Phenols (Oral)
*Higashida, K.; Sako, M.; Takizawa, S.; Sasai, H.
“ú–{‰»Šw‰ï‘æ99t‹G”N‰ïCb“ì‘åŠwi•ºŒÉjC3ŒŽ16“ú`3ŒŽ19“úC2019”ND

8. Chiral Vanadium Complex-Catalyzed Efficient Synthesis of Heterohelicenes (Oral)
*Tamori, Y.; Sako, M.; Takizawa, S.; Sasai, H.
“ú–{‰»Šw‰ï‘æ99t‹G”N‰ïCb“ì‘åŠwi•ºŒÉjC3ŒŽ16“ú`3ŒŽ19“úC2019”ND

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–{‰»Šw‰ï‘æ99t‹G”N‰ïCb“ì‘åŠwi•ºŒÉjC3ŒŽ16“ú`3ŒŽ19“úC2019”ND

10.                Vanadium Complex-catalyzed Enantioselective oxa-Piancatelli Rearrangement Reaction (Oral)
*Sako, M.; Schober, L.; Takizawa, S.; Gröger, H.; Sasai, H.
“ú–{‰»Šw‰ï‘æ99t‹G”N‰ïCb“ì‘åŠwi•ºŒÉjC3ŒŽ16“ú`3ŒŽ19“úC2019”ND

11.                Development of Novel Photoswitchable Chiral Catalyst (Oral)
*Kondo, M.; Nakamura K.; Sasai, H.
“ú–{‰»Šw‰ï‘æ99t‹G”N‰ïCb“ì‘åŠwi•ºŒÉjC3ŒŽ16“ú`3ŒŽ19“úC2019”ND

12.                Development of Novel Photoswitchable Chiral Oxazoline Catalyst (Oral)
*Nakamura K.; Kondo, M.; Sasai, H.
“ú–{‰»Šw‰ï‘æ99t‹G”N‰ïCb“ì‘åŠwi•ºŒÉjC3ŒŽ16“ú`3ŒŽ19“úC2019”ND

13.                ƒOƒŠ[ƒ“ƒPƒ~ƒXƒgƒŠ[ŽuŒüŒ^•s欔½‰ž‚ÌŠJ”­‚Æ‘½Š¯”\«•¡‘fŠÂœŠi\’z‚ւ̉ž—pi“ú–{–òŠw‰ï@ŠwpU‹»ÜŽóÜu‰‰jiŒû“ªj
*
‘êàV”EC“ú–{–òŠw‰ï‘æ139”N‰ïC–‹’£ƒƒbƒZ@‘¼iç—tjC3ŒŽ20“ú`3ŒŽ23“úC2019”ND

14.                ƒLƒ‰ƒ‹ƒoƒiƒWƒEƒ€G”}‚ð—p‚¢‚éƒGƒiƒ“ƒ`ƒI‘I‘ð“IŽ_‰»ƒJƒbƒvƒŠƒ“ƒO‚ÌŠJ”­‚Ɖž—piŒû“ªj
*
²ŒÃ^C–ØFŒ›C‘êàV”ECùˆäG–¾C“ú–{–òŠw‰ï‘æ139”N‰ïC–‹’£ƒƒbƒZ@‘¼iç—tjC3ŒŽ20“ú`3ŒŽ23“úC2019”ND

15.                ƒtƒ[ƒVƒXƒeƒ€‚ð—p‚¢‚éG”}“I•sĘA‘±”½‰ž‚ÌŠJ”­iŒû“ªj
*Piyumi HETTIARACHCHIGE DONA
C²ŒÃ^CŠÝ“S”nC‘êàV”ECùˆäG–¾C“ú–{–òŠw‰ï‘æ139”N‰ïC–‹’£ƒƒbƒZ@‘¼iç—tjC3ŒŽ20“ú`3ŒŽ23“úC2019”ND

16.                ƒoƒiƒWƒEƒ€G”}‚ðŠˆ—p‚·‚éŠÜ’‚‘f–F‘°‰»‡•¨‚̃ƒ“ƒ|ƒbƒg‡¬iŒû“ªj
*
‘ëΕü‘åC²ŒÃ^C‘êàV”ECNadine ZUMBRAEGELCHarald GROEGERCùˆäG–¾C“ú–{–òŠw‰ï‘æ139”N‰ïC–‹’£ƒƒbƒZ@‘¼iç—tjC3ŒŽ20“ú`3ŒŽ23“úC2019”ND

17.                ‹@ŠBŠwK‚É‚æ‚锽‰žðŒÅ“K‰»‚ðŠˆ—p‚·‚éƒXƒsƒƒIƒLƒVƒCƒ“ƒh[ƒ‹—Þ‰‘̸̂–§ƒtƒ[•sć¬iƒ|ƒXƒ^[j
*
‹ß“¡Œ’A²ŒÃ^AùˆäG–¾A‘êàV”ECVŠwp—̈挤‹†u”½‰žWω»‚ª“±‚­’†•ªŽqí—ª:‚ŽŸ¶•¨‹@”\•ªŽq‚Ì‘n»v‘æ8‰ñ¬‰Ê•ñ‰ïC‹ž“s‘åŠwŒjƒLƒƒƒ“ƒpƒX‘Dˆäï—Ç‹L”Ou“°i‹ž“sjC5ŒŽ31`6ŒŽ1“úC2019”ND

18.                ƒLƒ‰ƒ‹ƒoƒiƒWƒEƒ€G”}‚ð—p‚¢‚éƒtƒFƒm[ƒ‹—Þ‚ÌŽ_‰»“IƒwƒeƒƒJƒbƒvƒŠƒ“ƒO”½‰žiŒû“ªj
*
“Œ“cŒbŒÞA²ŒÃ^A‘êàV”EAùˆäG–¾C‘æ115‰ñ—L‹@‡¬ƒVƒ“ƒ|ƒWƒEƒ€C“Œ–k‘åŠw—tŽRƒRƒ‚ƒ“ƒYi‹{éjC6ŒŽ3“ú`4“úC2019”ND

19.                ˜A‘±”½‰ž‚ð—˜—p‚·‚éƒXƒsƒƒIƒLƒVƒCƒ“ƒh[ƒ‹—Þ‚Ì’ZH’ö•sć¬iƒ|ƒXƒ^[j
*
¼ŽR®Ž÷A‹ß“¡Œ’A‘êàV”EAùˆäG–¾C‘æ115‰ñ—L‹@‡¬ƒVƒ“ƒ|ƒWƒEƒ€C“Œ–k‘åŠw —tŽRƒRƒ‚ƒ“ƒYi‹{éjC6ŒŽ3“ú`4“úC2019”ND

20.                ƒLƒ‰ƒ‹ƒoƒiƒWƒEƒ€ö‘̂̎_G”}”\‚ðŠˆ—p‚·‚é•sÄ”½‰ž‚ÌŠJ”­iŒû“ªj
*
²ŒÃ^A‘ëΕü‘åALukas SchoberAHarald GrögerA‘êàV”EAùˆäG–¾CƒVƒ“ƒ|ƒWƒEƒ€ ƒ‚ƒŒƒLƒ…ƒ‰[EƒLƒ‰ƒŠƒeƒB[2019C‹à‘ò¤H‰ï‹cŠiÎìjC6ŒŽ14“ú`15“úC2019”ND

21.                AIŠˆ—p‚É‚æ‚鸖§ƒtƒ[•sć¬‚Ì”½‰žÅ“K‰»iƒ|ƒXƒ^[j
*
‹ß“¡Œ’AH. D. P. WathsalaA²ŒÃ^A‰Ô’J—D‘¾˜NAÎìˆêéAŒ´‘A‘é‡F”VA˜h”ö—²A‘êàV”EAùˆäG–¾C‘æ8‰ñJACI/GSCƒVƒ“ƒ|ƒWƒEƒ€C“Œ‹ž‘ÛƒtƒH[ƒ‰ƒ€i“Œ‹žjC6ŒŽ24“ú`6ŒŽ25“úC2019”ND

22.                ƒpƒ‰ƒWƒEƒ€ƒGƒmƒ‰[ƒg‚̋ɫ“]Š·Œ^‹Šj“IƒAƒ~ƒm‰»”½‰ž‚ÌŠJ”­iƒ|ƒXƒ^[j
*
‘ê–¢—ˆA–ì–{—T–çA’|’†˜a_AùˆäG–¾C‘æ52‰ñ—L‹@‹à‘®ŽáŽè‚̉ï‰Ä‚ÌŠwZA‘q•~‚¹‚Æ‚¤‚¿Ž™“‡ƒzƒeƒ‹i‰ªŽRjA6ŒŽ24“ú`26“úA2019”ND

23.                ‹@ŠBŠwK‚ð—p‚¢‚鸖§ƒtƒ[•s欂ÌÅ“KðŒ—\‘ªiŒû“ªj
*
‹ß“¡Œ’CŽY‹Æ‰ÈŠwAIƒZƒ“ƒ^[”­‘«‹L”OƒLƒbƒNƒIƒtu‰‰‰ïAŽY‹Æ‰ÈŠwŒ¤‹†Šu“°i‘åãjA7ŒŽ6“úA2019”ND

24.                Œõ‰ž“š«•sÄG”}‚ÌŠJ”­‚Ɖž—p (ƒ|ƒXƒ^[)
*
Žá—Ñ—Ç’mA‹ß“¡Œ’AùˆäG–¾C‘æ39‰ñ—L‹@‡¬ŽáŽèƒZƒ~ƒi[C‘åã•{—§‘åŠw@’†•Sã’¹ƒLƒƒƒ“ƒpƒXi‘åãjC8ŒŽ8“úC2019”ND

25.                •ªŽqŠÔ‹É«“]Š·Œ^•săhƒ~ƒm”½‰ž‚ÌŠJ”­Œ¤‹†iƒ|ƒXƒ^[j
*
ŒÃì’q‘åA²ŒÃ^A‰Ô’J—D‘¾˜NA‹ß“¡Œ’A‘êàV”EAùˆäG–¾C‘æ39‰ñ—L‹@‡¬ŽáŽèƒZƒ~ƒi[C‘åã•{—§‘åŠw@’†•Sã’¹ƒLƒƒƒ“ƒpƒXi‘åãjC8ŒŽ8“úC2019”ND

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‰ñ—L‹@‡¬ŽáŽèƒZƒ~ƒi[C‘åã•{—§‘åŠw@’†•Sã’¹ƒLƒƒƒ“ƒpƒXi‘åãjC8ŒŽ8“úC2019”ND

27.                ƒLƒ‰ƒ‹ƒoƒiƒWƒEƒ€G”}‚ð—p‚¢‚éƒtƒFƒm[ƒ‹—Þ‚ÌŽ_‰»“IƒwƒeƒƒJƒbƒvƒŠƒ“ƒO”½‰žiŒû“ªj
*
²ŒÃ^A“Œ“cŒbŒÞA‘êàV”EAùˆäG–¾C‘æ66‰ñ—L‹@‹à‘®‰»Šw“¢˜_‰ïCŽñ“s‘åŠw“Œ‹ž@“ì‘å‘òƒLƒƒƒ“ƒpƒXi“Œ‹žjC9ŒŽ14“ú`9ŒŽ16“úC2019”ND

28.                ‹É«“]Š·Œ^ƒGƒiƒ“ƒ`ƒI‘I‘ð“Iƒhƒ~ƒm”½‰ž‚ÌŠJ”­‚ƃLƒ‰ƒ‹‘æŽl‹‰’Y‘f\’z‚ւ̉ž—piƒ|ƒXƒ^[j
*
‰Ô’J—D‘¾˜NA‹ß“¡Œ’AŒÃì’q‘åA²ŒÃ^A‘êàV”EAùˆäG–¾C‘æ45‰ñ”½‰ž‚Ƈ¬‚Ìi•àƒVƒ“ƒ|ƒWƒEƒ€-ƒ‰ƒCƒtƒTƒCƒGƒ“ƒX‚ðŽuŒü‚µ‚½—˜_C”½‰ž‚¨‚æ‚ч¬-C‘q•~ŽsŒ|•¶ŠÙi‰ªŽRjC10ŒŽ28“ú`10ŒŽ29“úC2019”ND

29.                V‹KŒõ‰ž“šŒ^•sÄ”zˆÊŽq‚ÌŠJ”­iƒ|ƒXƒ^[j
*
’†‘ºŒ°“lA‹ß“¡Œ’AùˆäG–¾C‘æ45‰ñ”½‰ž‚Ƈ¬‚Ìi•àƒVƒ“ƒ|ƒWƒEƒ€-ƒ‰ƒCƒtƒTƒCƒGƒ“ƒX‚ðŽuŒü‚µ‚½—˜_C”½‰ž‚¨‚æ‚ч¬-C‘q•~ŽsŒ|•¶ŠÙi‰ªŽRjC10ŒŽ28“ú`10ŒŽ29“úC2019”ND

30.                ˜A‘±”½‰ž‚ð—˜—p‚·‚éƒXƒsƒƒIƒLƒVƒCƒ“ƒh[ƒ‹—Þ‚Ì’ZH’ö•sć¬iƒ|ƒXƒ^[j
*
¼ŽR®Ž÷A‹ß“¡Œ’ATin Zar AyeA‘êàV”EAùˆäG–¾C‘æ45‰ñ”½‰ž‚Ƈ¬‚Ìi•àƒVƒ“ƒ|ƒWƒEƒ€-ƒ‰ƒCƒtƒTƒCƒGƒ“ƒX‚ðŽuŒü‚µ‚½—˜_C”½‰ž‚¨‚æ‚ч¬-C‘q•~ŽsŒ|•¶ŠÙi‰ªŽRjC10ŒŽ28“ú`10ŒŽ29“úC2019”ND

31.                ƒLƒ‰ƒ‹ƒoƒiƒWƒEƒ€ö‘Ì‚ð—p‚¢‚é•sÄG”}”½‰ž‚ÌŠJ”­iƒ|ƒXƒ^[j
*
²ŒÃ^A‘êàV”EAùˆäG–¾C‘æ7‰ñƒAƒ‰ƒCƒAƒ“ƒXŽáŽèŒ¤‹†Œð—¬‰ïC‘åã‘åŠwŽY‹Æ‰ÈŠwŒ¤‹†Ši‘åãjC11ŒŽ12“ú`13“úC2019”ND

32.                Exploration of Flow Reaction Conditions Using Machine-learning for Enantioselective Organocatalyzed Rauhut-Currier/[3+2] Annulation Sequence (Œû“ª)
Kondo, M.; Wathsala, H. D. P.; Sako, M.; Hanatani, Y.; Ishikawa, K.; Hara, S.; Takaai, T.; Washio, T.; *Takizawa, S.; Sasai, H.
‘æ12‰ñ—L‹@G”}ƒVƒ“ƒ|ƒWƒEƒ€C‹ž“s‘åŠw–òŠwŒ¤‹†‰È@ˆã–òŒn‘‡Œ¤‹†“@“¡‘½‹L”Oƒz[ƒ‹EƒAƒEƒgƒŠ[ƒ`ƒGƒŠƒAi‹ž“sjC12ŒŽ4“ú~12ŒŽ5“úC2019”ND

33.                Development of Enantioselective Umpolung Domino Reaction (ƒ|ƒXƒ^[)
*Furukawa, T.; Sako, M.; Hanatani, Y.; Kondo, M.; Takizawa, S.; Sasai, H.
‘æ12‰ñ—L‹@G”}ƒVƒ“ƒ|ƒWƒEƒ€C‹ž“s‘åŠw–òŠwŒ¤‹†‰È@ˆã–òŒn‘‡Œ¤‹†“@“¡‘½‹L”Oƒz[ƒ‹EƒAƒEƒgƒŠ[ƒ`ƒGƒŠƒAi‹ž“sjC12ŒŽ4“ú~12ŒŽ5“úC2019”ND

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‰ñ—L‹@G”}ƒVƒ“ƒ|ƒWƒEƒ€C‹ž“s‘åŠw–òŠwŒ¤‹†‰È@ˆã–òŒn‘‡Œ¤‹†“@“¡‘½‹L”Oƒz[ƒ‹EƒAƒEƒgƒŠ[ƒ`ƒGƒŠƒAi‹ž“sjC12ŒŽ4“ú~12ŒŽ5“úC2019”ND

<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 AwardŽóÜ>

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 Pictet–Spengler 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. ‘½‹@”\G”}‚ðŠˆ—p‚·‚éŽÀ—p“I•sÄ•ªŽq•ÏŠ·iƒ|ƒXƒ^[j
*
‘êàV”ECVŠwp—̈挤‹†@”½‰žWω»‚ª“±‚­’†•ªŽqí—ª@‚ŽŸ¶•¨‹@”\•ªŽq‚Ì‘n»@‘æ‚T‰ñŒöŠJ¬‰Ê•ñ‰ïC‘åã‘åŠw–L’†ƒLƒƒƒ“ƒpƒX“ì•”—zˆê˜Yƒz[ƒ‹i‘åãjC1ŒŽ26“ú`27“úC2018”ND

2. Organocatalytic Enantioselective Sequential C-C Bond Forming Reaction in Flow SystemiΞһj
*H. D. P. Wathsala
AŠÝ“S”nAQingwen ChenA‘êàV”EAùˆäG–¾C“ú–{‰»Šw‰ï‘æ98t‹G”N‰ïC“ú–{‘åŠwiç—tjC3ŒŽ20`23“úC2018”ND

3. Development of New Spiro-type Chiral Ligands Bearing a Functional Side ArmiΞһj
*
V‹“c‹±ÍA’|’†˜a_AùˆäG–¾C“ú–{‰»Šw‰ï‘æ98t‹G”N‰ïC“ú–{‘åŠwiç—tjC3ŒŽ20`23“úC2018”ND

4. Palladium Enolate Umpolung: Approach to ƒ¿-Aminocarbonyl CompoundsiŒû“ªj
*
–ì–{—T–çA’|’†˜a_AùˆäG–¾C“ú–{‰»Šw‰ï‘æ98t‹G”N‰ïC“ú–{‘åŠwiç—tjC3ŒŽ20`23“úC2018”ND

5. Enantioselective Synthesis of Nitrogen Heterocycles via aza-Wacker-type Reaction Catalyzed by Pd-SPRIX ComplexiΞһj
*Abhijit Sen
A’|’†˜a_AùˆäG–¾C“ú–{‰»Šw‰ï‘æ98t‹G”N‰ïC“ú–{‘åŠwiç—tjC3ŒŽ20`23“úC2018”ND

6. Enantioselective Synthesis of Bicyclic Pyrrolidine Derivatives via One-Pot Organo and Palladium Catalysis RelayiΞһj
*Bijan M. Chaki
AJianfei BaiA’|’†˜a_A‘êàV”EAùˆäG–¾C“ú–{‰»Šw‰ï‘æ98t‹G”N‰ïC“ú–{‘åŠwiç—tjC3ŒŽ20`23“úC2018”ND

7. Facile synthesis of spirooxindoles via an enantioselective organocatalyzed sequential reactioniΞһj
*
‘ê–¢—ˆAŠÝ“S”nA‘êàV”EAJianfei BaiAùˆäG–¾C“ú–{‰»Šw‰ï‘æ98t‹G”N‰ïC“ú–{‘åŠwiç—tjC3ŒŽ20`23“úC2018”ND

8. Irö‘Ì‚ðG”}‚Æ‚µ‚½ƒeƒBƒVƒ…ƒ`ƒFƒ“ƒRŒ^”½‰ž‚É‚æ‚éƒGƒ“ƒeƒƒ‰ƒNƒgƒ“‚ÌG”}“I•sć¬iƒ|ƒXƒ^[j
—é–ØŒ’”VA*‘«—§—S‹MAŠÝMŠóAŽü‘å—gA’©–ì–FDAùˆäG–¾C“ú–{‰»Šw‰ï‘æ98t‹G”N‰ïC“ú–{‘åŠwiç—tjC3ŒŽ20`23“úC2018”ND

9. Development and Application of Organocatalyzed Stereoselective Umpolung Double Michael ReactioniΞһj
*
ŠÝ“S”nA‘êàV”EAùˆäG–¾C“ú–{‰»Šw‰ï‘æ98t‹G”N‰ïC“ú–{‘åŠwiç—tjC3ŒŽ20`23“úC2018”ND

10.                Chiral Vanadium Complex-catalyzed Enantioselective Oxidative Coupling Reactions of Polycyclic PhenolsiŒû“ªj
*
™›½W«A²ŒÃ^A‘êàV”EAùˆäG–¾C“ú–{‰»Šw‰ï‘æ98t‹G”N‰ïC“ú–{‘åŠwiç—tjC3ŒŽ20`23“úC2018”ND

11.                Chiral Vanadium Complex-catalyzed Enantioselective Oxidative Coupling Reactions of HydroxycarbazolesiŒû“ªj
*
²ŒÃ^A‘êàV”EAùˆäG–¾C“ú–{‰»Šw‰ï‘æ98t‹G”N‰ïC“ú–{‘åŠwiç—tjC3ŒŽ20`23“úC2018”ND

12.                Chiral Vanadium Complex-catalyzed Enantioselective Oxidative Coupling Reactions of Monocyclic PhenolsiŒû“ªj
*
–ØFŒ›A²ŒÃ^A‘êàV”EAùˆäG–¾C“ú–{‰»Šw‰ï‘æ98t‹G”N‰ïC“ú–{‘åŠwiç—tjC3ŒŽ20`23“úC2018”ND
 

13.                —L‹@•ªŽqG”}‚ð—p‚¢‚éƒXƒsƒƒIƒLƒVƒCƒ“ƒh[ƒ‹—Þ‰‘̂̒ZH’ö•sć¬iŒû“ªj
*
‘ê–¢—ˆAŠÝ“S”nA‘êàV”EAJianfei BaiAùˆäG–¾C“ú–{–òŠw‰ï‘æ138”N‰ïCÎ쌧—§‰¹Šy“°@‘¼iÎìjC3ŒŽ25`28“úC2018”N.
 

14.                ƒAƒ~ƒh‰»/Rauhut-Currier˜A‘±”½‰ž‚É‚æ‚郿-ƒƒ`ƒŠƒfƒ“-ƒÁ-ƒ‰ƒNƒ^ƒ€‚ÌG”}“I•sć¬iŒû“ªj
*
ŠÝ“S”nAFernando Arteaga-ArteagaA‘êàV”EAJianfei BaiAùˆäG–¾C“ú–{–òŠw‰ï‘æ138”N‰ïCÎ쌧—§‰¹Šy“°@‘¼iÎìjC3ŒŽ25`28“úC2018”N.
<“ú–{–òŠw‰ï‘æ138”N‰ïŠw¶—DG”­•\ÜiŒû“ª”­•\‚Ì•”j>
 

15.                —L‹@•ªŽqG”}‚É‚æ‚é1,3-cis-ƒCƒ“ƒhƒŠƒ“‰»‡•¨‚̃Gƒiƒ“ƒ`ƒI‘I‘ð“Iƒƒ“ƒ|ƒbƒg‡¬iŒû“ªj
*H. D. P. Wathsala
A‘êàV”EA²ŒÃ^AŠÝ“S”nA•½“cCˆêA‘ºˆäŒ’ˆêA“¡‰ªO“¹AùˆäG–¾C“ú–{–òŠw‰ï‘æ138”N‰ïCÎ쌧—§‰¹Šy“°@‘¼iÎìjC3ŒŽ25`28“úC2018”N.

16.                ƒoƒiƒWƒEƒ€G”}‚ð—p‚¢‚éƒJƒ‹ƒoƒ][ƒ‹—U“±‘̂̃Gƒiƒ“ƒ`ƒI‘I‘ð“IŽ_‰»ƒJƒbƒvƒŠƒ“ƒO”½‰ž‚ÌŠJ”­iŒû“ªj
*
‘êàV”EA²ŒÃ^Aˆê”V£˜a–íAùˆäG–¾C“ú–{–òŠw‰ï‘æ138”N‰ïCÎ쌧—§‰¹Šy“°@‘¼iÎìjC3ŒŽ25`28“úC2018”N.

17.                ƒIƒLƒ\ƒƒ^ƒ‹’†S‚̃Lƒ‰ƒŠƒeƒB[§Œä‚ðŠî”Õ‚Æ‚·‚鑽‹@”\•sÄG”}‚Ì‘n»iƒ|ƒXƒ^[j
*
‘êàV”ECVŠwp—̈挤‹†u”zˆÊƒAƒVƒ“ƒƒgƒŠ[v‘æ‚R‰ñ—̈æ‘S‘̉ï‹cC‹ãB‘åŠw•a‰@’n‹æ•S”Nu“°i•Ÿ‰ªjC5ŒŽ8“ú`9“úC2018”N.

18.                ŠÂóƒWƒGƒmƒ“‚Ì”ñ‘Î̉»‚ðŒ®H’ö‚Æ‚·‚éƒGƒiƒ“ƒ`ƒI‘I‘ð“I Rauhut–Currier ˜A‘±”½‰ž‚ÌŠJ”­‚Ɖž—piŒû“ªj
*
‘êàV”EA‹g“c‘׎uAFernando Arteaga ArteagaAŠÝ“S”nAùˆä G–¾CSymposium on Molecular Chirality 2018Cç—t‘åŠw¼ç—tƒLƒƒƒ“ƒpƒX‚¯‚â‚«‰ïŠÙiç—tjC5ŒŽ11“ú`12“úC2018”N.

19.                ƒtƒ[ƒVƒXƒeƒ€‚ð—p‚¢‚éG”}“I•sĘA‘±”½‰ž‚ÌŠJ”­iƒ|ƒXƒ^[j
*H. D. P. Wathsala
AŠÝ“S”nA²ŒÃ^A‘êàV”EAùˆä G–¾CSymposium on Molecular Chirality 2018Cç—t‘åŠw¼ç—tƒLƒƒƒ“ƒpƒX‚¯‚â‚«‰ïŠÙiç—tjC5ŒŽ11“ú`12“úC2018”N.

20.                ƒoƒiƒWƒEƒ€G”}‚ðŠˆ—p‚·‚éƒwƒeƒƒwƒŠƒZƒ“‚̃Gƒiƒ“ƒ`ƒI‘I‘ð“I‡¬iƒ|ƒXƒ^[j
*
“cX—T‹MA™›½W«A²ŒÃ^A‘êàV”EAùˆä G–¾CSymposium on Molecular Chirality 2018Cç—t‘åŠw¼ç—tƒLƒƒƒ“ƒpƒX‚¯‚â‚«‰ïŠÙiç—tjC5ŒŽ11“ú`12“úC2018”N.

21.                —L‹@•ªŽqƒpƒ‰ƒWƒEƒ€˜A‘±G”}”½‰ž‚ðŠˆ—p‚·‚é“ñŠÂŽ®ƒsƒƒŠƒWƒ“—U“±‘̂̃Gƒiƒ“ƒ`ƒI‘I‘ð“Iƒƒ“ƒ|ƒbƒg‡¬iƒ|ƒXƒ^[j
*
’|’†˜a_ABijan Mohon ChakiAJianfei BaiA‘êàV”EAùˆäG–¾CSymposium on Molecular Chirality 2018Cç—t‘åŠw¼ç—tƒLƒƒƒ“ƒpƒX‚¯‚â‚«‰ïŠÙiç—tjC5ŒŽ11“ú`12“úC2018”N.

22.                ‹É«“]Š·Œ^ƒ_ƒuƒ‹ƒ}ƒCƒPƒ‹•t‰Á”½‰ž‚É‚æ‚éƒqƒhƒƒCƒ“ƒh[ƒ‹‹y‚уqƒhƒƒxƒ“ƒ[ƒ“ƒtƒ‰ƒ“-2-ƒJƒ‹ƒ{ƒ“Ž_ƒGƒXƒeƒ‹‚̇¬iƒ|ƒXƒ^[j
*
‘êàV”ECVŠwp—̈挤‹†@”½‰žWω»‚ª“±‚­’†•ªŽqí—ª@‚ŽŸ¶•¨‹@”\•ªŽq‚Ì‘n»@‘æ6‰ñŒöŠJ¬‰Ê•ñ‰ïC‘ˆî“c‘åŠw‘Û‰ï‹cêi“Œ‹žjC6ŒŽ1“ú`6ŒŽ2“úC2018”N.

23.                —L‹@•ªŽq•sÄG”}‚ð—p‚¢‚éƒXƒsƒƒIƒLƒVƒCƒ“ƒh[ƒ‹œŠi‚̃Gƒiƒ“ƒ`ƒI‘I‘ð“I\’ziƒ|ƒXƒ^[j
*
‘ê–¢—ˆAŠÝ“S”nA‘êàV”EAùˆäG–¾C‘æ 7 ‰ñ JACI/GSC ƒVƒ“ƒ|ƒWƒEƒ€CANAƒNƒ‰ƒEƒ“ƒvƒ‰ƒUƒzƒeƒ‹_ŒËi•ºŒÉjC6ŒŽ14“ú`6ŒŽ15“úC2018”N.
<—DGƒ|ƒXƒ^[ÜŽóÜ>

24.                ƒoƒiƒWƒEƒ€G”}‚ðŠˆ—p‚·‚é’PŠÂŽ®ƒtƒFƒm[ƒ‹‚Ì•săJƒbƒvƒŠƒ“ƒO”½‰ž‚ÌŠJ”­iƒ|ƒXƒ^[j
*
²ŒÃ^A–ØFŒ›A‘êàV”EAùˆäG–¾C‘æ 7 ‰ñ JACI/GSC ƒVƒ“ƒ|ƒWƒEƒ€CANAƒNƒ‰ƒEƒ“ƒvƒ‰ƒUƒzƒeƒ‹_ŒËi•ºŒÉjC6ŒŽ14“ú`6ŒŽ15“úC2018”N.

25.                ƒtƒ[ƒVƒXƒeƒ€‚ð—p‚¢‚éG”}“I•sĘA‘±”½‰ž‚ÌŠJ”­iƒ|ƒXƒ^[j
*
‘êàV”EAH. D. P. WathsalaA²ŒÃ^AŠÝ“S”nAùˆäG–¾C“ú–{ƒvƒƒZƒX‰»Šw‰ï2018ƒTƒ}[ƒVƒ“ƒ|ƒWƒEƒ€Cƒ^ƒ[ƒz[ƒ‹‘D–xi“Œ‹žjC7ŒŽ26“ú`7ŒŽ27“úC2018”ND

26.                ˜A‘±G”}ƒvƒƒZƒX‚É‚æ‚é“ñŠÂŽ®ƒsƒƒŠƒWƒ“—U“±‘̂̃Gƒiƒ“ƒ`ƒI‘I‘ð“Iƒƒ“ƒ|ƒbƒg‡¬iƒ|ƒXƒ^[j
–’|’†˜a_ABijan Mohon ChakiAJianfei BaiA‘êàV”EAùˆäG–¾C“ú–{ƒvƒƒZƒX‰»Šw‰ï2018ƒTƒ}[ƒVƒ“ƒ|ƒWƒEƒ€Cƒ^ƒ[ƒz[ƒ‹‘D–xi“Œ‹žjC7ŒŽ26“ú`7ŒŽ27“úC2018”ND

27.                ƒtƒ[ƒŠƒAƒNƒ^[‚ðŠˆ—p‚·‚éG”}“I•săhƒ~ƒm”½‰ž‚ÌŠJ”­iƒ|ƒXƒ^[j
*
‘ê–¢—ˆAH. D. P. WathsalaA²ŒÃ^AŠÝ“S”nA‘êàV”EAùˆäG–¾C‘æ38‰ñ—L‹@‡¬ŽáŽèƒZƒ~ƒi[CŠÖ¼Šw‰@‘åŠw@¼‹{ブŒ´ƒLƒƒƒ“ƒpƒXi•ºŒÉjC8ŒŽ7“úC2018”ND

28.                V‹KŒõ‰ž“šŒ^ƒrƒXƒIƒLƒTƒ]ƒŠƒ“”zˆÊŽq‚ÌŠJ”­iƒ|ƒXƒ^[j
*
’†‘ºŒ°“lA‹ß“¡ŸAùˆäG–¾C‘æ38‰ñ—L‹@‡¬ŽáŽèƒZƒ~ƒi[CŠÖ¼Šw‰@‘åŠw@¼‹{ブŒ´ƒLƒƒƒ“ƒpƒXi•ºŒÉjC8ŒŽ7“úC2018”ND

29.                ƒoƒiƒWƒEƒ€G”}‚ðŠˆ—p‚·‚éƒwƒeƒƒwƒŠƒZƒ“‚ÌŒø—¦“I‡¬iƒ|ƒXƒ^[j
*
“cX—T‹MA²ŒÃ^A‘êàV”EAùˆäG–¾C‘æ38‰ñ—L‹@‡¬ŽáŽèƒZƒ~ƒi[CŠÖ¼Šw‰@‘åŠw@¼‹{ブŒ´ƒLƒƒƒ“ƒpƒXi•ºŒÉjC8ŒŽ7“úC2018”ND

30.                ƒLƒ‰ƒ‹ƒoƒiƒWƒEƒ€G”}‚ð—p‚¢‚éŽ_‰»“IƒwƒeƒƒJƒbƒvƒŠƒ“ƒO”½‰ž‚ÌŠJ”­iƒ|ƒXƒ^[j
*
“Œ“cŒbŒÞA²ŒÃ^A‘êàV”EAùˆäG–¾C‘æ38‰ñ—L‹@‡¬ŽáŽèƒZƒ~ƒi[CŠÖ¼Šw‰@‘åŠw@¼‹{ブŒ´ƒLƒƒƒ“ƒpƒXi•ºŒÉjC8ŒŽ7“úC2018”ND

31.                ƒoƒiƒWƒEƒ€G”}‚ðŠˆ—p‚·‚é’PŠÂŽ®ƒtƒFƒm[ƒ‹‚Ì•săJƒbƒvƒŠƒ“ƒO”½‰ž‚ÌŠJ”­iŒû“ªj
*
²ŒÃ^A–ØFŒ›A‘êàV”EAùˆäG–¾C‘æ‚T‰ñ VŠwp—̈挤‹†u”½‰žWω»‚ª“±‚­’†•ªŽqí—ªF‚ŽŸ¶•¨‹@”\•ªŽq‚Ì‘n»vŽáŽèƒVƒ“ƒ|ƒWƒEƒ€CƒV[ƒpƒ‹{–i•ºŒÉjC8ŒŽ17“úC2018”ND

32.                ƒLƒ‰ƒ‹ƒoƒiƒWƒEƒ€G”}‚ð—p‚¢‚éƒwƒeƒƒwƒŠƒZƒ“‚ÌŒø—¦“I‡¬iƒ|ƒXƒ^[j
*
“cX—T‹MA²ŒÃ^A‘êàV”EAùˆäG–¾C‘æ48‰ñ@•¡‘fŠÂ‰»Šw“¢˜_‰ïC’·èƒuƒŠƒbƒNƒz[ƒ‹@‘Û‰ï‹cêi’·èjC9ŒŽ3“ú`9ŒŽ5“úC2018”ND

33.                ƒGƒiƒ“ƒ`ƒI‘I‘ð“Iƒpƒ‰ƒWƒEƒ€2‰¿–4‰¿G”}”½‰ž‚ðŠî”Õ‚Æ‚·‚é“ñŠÂŽ®ƒsƒƒŠƒWƒ“—U“±‘̂̃ƒ“ƒ|ƒbƒg‡¬iƒ|ƒXƒ^[j
*
’|’†˜a_ABijan Mohon ChakiALinpeng ZHUAJianfei BaiA‘êàV”EAùˆäG–¾C‘æ65‰ñ—L‹@‹à‘®‰»Šw“¢˜_‰ïC“¯ŽuŽÐ‘åŠw¡oìZ’n@Žº’¬ƒLƒƒƒ“ƒpƒXi‹ž“sjC9ŒŽ19“ú`9ŒŽ21“úC2018”ND

34.                Pd-SPRIXG”}‚ð—p‚¢‚éaza-WackerŒ^”½‰ž‚ÌŠJ”­iƒ|ƒXƒ^[j
*Abhijit Sen
A’|’†˜a_AùˆäG–¾C‘æ65‰ñ—L‹@‹à‘®‰»Šw“¢˜_‰ïC“¯ŽuŽÐ‘åŠw¡oìZ’n@Žº’¬ƒLƒƒƒ“ƒpƒXi‹ž“sjC9ŒŽ19“ú`9ŒŽ21“úC2018”ND

35.                ‹É«“]Š·Œ^ƒ_ƒuƒ‹ƒ}ƒCƒPƒ‹•t‰Á”½‰ž‚É‚æ‚éƒqƒhƒƒCƒ“ƒh[ƒ‹‹y‚уqƒhƒ•Ù‚¼ƒtƒ‰ƒ“-2-ƒJƒ‹ƒ{ƒ“Ž_ƒGƒXƒeƒ‹‚̇¬iŒû“ªj
*
‘êàV”EAŠÝ“S”nAùˆäG–¾C‘æ44‰ñ”½‰ž‚Ƈ¬‚Ìi•àƒVƒ“ƒ|ƒWƒEƒ€|ƒ‰ƒCƒtƒTƒCƒGƒ“ƒX‚ðŽuŒü‚µ‚½—˜_A”½‰ž‚¨‚æ‚ч¬|CŽs–¯‰ïŠÙƒVƒA[ƒYƒz[ƒ€–²ƒz[ƒ‹iŒF–{jC11ŒŽ5“ú`6“úC2018”ND

36.                ƒIƒLƒ\ƒƒ^ƒ‹’†S‚̃Lƒ‰ƒŠƒeƒB[§Œä‚ÆWω»‚ðŠî”Õ‚Æ‚·‚鑽‹@”\•sÄG”}‚Ì‘n»iŒû“ªj
*
‘êàV”ECVŠwp—̈挤‹†u”zˆÊƒAƒVƒ“ƒƒgƒŠ[v‘æ‚S‰ñ—̈æ‘S‘̉ï‹cC‹à‘ò¤H‰ï‹cЉïŠÙiÎìjC11ŒŽ29“ú`11ŒŽ30“úC2018”ND

37.                ‹É«“]Š·Œ^•sÄG”}”½‰ž‚É‚æ‚éƒLƒ‰ƒ‹‘æŽl‹‰’Y‘f‚Ì\’ziƒ|ƒXƒ^[j
*
‰Ô’J—D‘¾˜NA‹ß“¡Œ’A‘êàV”EAùˆäG–¾C‘æ11 ‰ñ—L‹@G”}ƒVƒ“ƒ|ƒWƒEƒ€CŠwK‰@‘n—§•SŽü”N‹L”O‰ïŠÙi“Œ‹žjC12ŒŽ3“ú`12ŒŽ4“úC2018”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 C–C 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 AwardŽóÜ>

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 BIOCATALYSISh FINAL AACHEM-OSAKA SYMPOSIUM, Aachen, Germany, November 26-27, 2018.

Topª

 

2017@🐓

<Domestic>

1. ‰EŽèŒn‚̉»‡•¨‚¾‚¯‚ð‡¬‚·‚é•û–@ `ŒõŠwŠˆ«‰»‡•¨‚Ì“­‚«`iµ‘Òj
*
ùˆäG–¾Cƒtƒ@ƒCƒ“ƒPƒ~ƒJƒ‹ƒYŒ¤‹†‰ïCKKRƒzƒeƒ‹‘åãi‘åãjC3ŒŽ2“úC2017”ND

2. Enantioselective aza-Wacker Reaction Promoted by Pd-SPRIXiΞһj
*Abhijit Sen
A’|’†˜a_AùˆäG–¾C“ú–{‰»Šw‰ï‘æ97t‹G”N‰ïCŒcœä‘åŠwi_“ÞìjC3ŒŽ16`19“úC2017”ND

3. Pd(II)-SPRIX Catalyzed Enantioselective Annulation of Alkenylindoles: Allyl Group Assisted Construction of Quaternary Carbon CenteriΞһj
*Mohamed A. Abozeid
A‘êàV”EA’|’†˜a_AùˆäG–¾C“ú–{‰»Šw‰ï‘æ97t‹G”N‰ïCŒcœä‘åŠwi_“ÞìjC3ŒŽ16`19“úC2017”ND

4. Development of Novel Spiro-type Chiral Ligands Bearing Pyrazole DonorsiΞһj
*
dM‹§ŽuA’|’†˜a_AùˆäG–¾C“ú–{‰»Šw‰ï‘æ97t‹G”N‰ïCŒcœä‘åŠwi_“ÞìjC3ŒŽ16`19“úC2017”ND

5. Synthetic Study of Sorazolon E2 Using Chiral Vanadium CatalystiΞһj
*
ˆê”V£˜a–íA²ŒÃ^A‘êàV”EAùˆäG–¾C“ú–{‰»Šw‰ï‘æ97t‹G”N‰ïCŒcœä‘åŠwi_“ÞìjC3ŒŽ16`19“úC2017”ND

6. Facile Synthesis of Spirooxindoles via an Enantioselective Organocatalyzed Sequential Reaction of Oxindole Derivatives with YnonesiΞһj
*
‘ê–¢—ˆAŠÝ“S”nAJianfei BaiA‘êàV”EAùˆäG–¾C“ú–{‰»Šw‰ï‘æ97t‹G”N‰ïCŒcœä‘åŠwi_“ÞìjC3ŒŽ16`19“úC2017”ND

7. Enantioselective Synthesis of Bicyclic Pyrrolidine Derivatives via Sequential Organo- and Pd-CatalysisiΞһj
*Bijan M. Chaki
AJianfei BaiA’|’†˜a_A‘êàV”EAùˆäG–¾C“ú–{‰»Šw‰ï‘æ97t‹G”N‰ïCŒcœä‘åŠwi_“ÞìjC3ŒŽ16`19“úC2017”ND

8. Development of Enantioselective Reactions Using Fe CatalystsiΞһj
*
•ÄŽRSAV‹“c‹±ÍA’|’†˜a_A‘êàV”EAùˆäG–¾C“ú–{‰»Šw‰ï‘æ97t‹G”N‰ïCŒcœä‘åŠwi_“ÞìjC3ŒŽ16`19“úC2017”ND

9. ƒ¿-Functionalization of Carbonyl Compounds Based on Palladium Enolate UmpolungiŒû“ªj
*
–ì–{—T–çAàV“c˜a–íA’|’†˜a_AùˆäG–¾C“ú–{‰»Šw‰ï‘æ97t‹G”N‰ïCŒcœä‘åŠwi_“ÞìjC3ŒŽ16`19“úC2017”ND

10.                Phosphine-Catalyzed Umpolung Tandem Michael Addition of Alkynyl EsteriŒû“ªj
*
ŠÝ“S”nA‘êàV”EA‘ê–¢—ˆAùˆäG–¾C“ú–{‰»Šw‰ï‘æ97t‹G”N‰ïCŒcœä‘åŠwi_“ÞìjC3ŒŽ16`19“úC2017”ND

11.                Chiral Vanadium (V) Complex-catalyzed Enantioselective C-C Bond Forming Reactions (1)iŒû“ªj
*
²ŒÃ^A™›½W«A‘êàV”EAùˆäG–¾C“ú–{‰»Šw‰ï‘æ97t‹G”N‰ïCŒcœä‘åŠwi_“ÞìjC3ŒŽ16`19“úC2017”ND

12.                Chiral Vanadium (V) Complex-catalyzed Enantioselective C-C Bond Forming Reactions (2)iŒû“ªj
*
–ØFŒ›A‘êàV”EA²ŒÃ^AùˆäG–¾C“ú–{‰»Šw‰ï‘æ97t‹G”N‰ïCŒcœä‘åŠwi_“ÞìjC3ŒŽ16`19“úC2017”ND

13.                ƒJƒ‹ƒoƒ][ƒ‹—U“±‘̂̃Gƒiƒ“ƒ`ƒI‘I‘ð“IŽ_‰»ƒJƒbƒvƒŠƒ“ƒO”½‰ž‚ÌŠJ”­‚Ɖž—piƒ|ƒXƒ^[j
*
²ŒÃ^Aˆê”V£˜a–íA‘êàV”EAùˆäG–¾C‘æ111‰ñ—L‹@‡¬ƒVƒ“ƒ|ƒWƒEƒ€C‰ªŽR‘åŠw‘n—§ŒÜ\Žü”N‹L”OŠÙi‰ªŽRjC6ŒŽ8`9“úC2017”ND

14.                ƒGƒiƒ“ƒ`ƒI‘I‘ð“Iƒhƒ~ƒm”½‰ž‚É‚æ‚éƒXƒsƒƒIƒLƒVƒCƒ“ƒh[ƒ‹—U“±‘̇¬iƒ|ƒXƒ^[j
*
‘ê–¢—ˆAŠÝ“S”nA‘êàV”EABai JianfeiAùˆäG–¾C‘æ111‰ñ—L‹@‡¬ƒVƒ“ƒ|ƒWƒEƒ€C‰ªŽR‘åŠw‘n—§ŒÜ\Žü”N‹L”OŠÙi‰ªŽRjC6ŒŽ8`9“úC2017”ND

15.                ƒpƒ‰ƒWƒEƒ€ƒGƒmƒ‰[ƒg‚̋ɫ“]Š·‚ð—˜—p‚·‚鑽Н”\«ƒJƒ‹ƒ{ƒjƒ‹‰»‡•¨‚ÌŒø—¦‡¬iƒ|ƒXƒ^[j
*
–ì–{—T–çA’|’†˜a_AàV“c˜a–íASuman C. MohantaAùˆäG–¾C‘æ111‰ñ—L‹@‡¬ƒVƒ“ƒ|ƒWƒEƒ€C‰ªŽR‘åŠw‘n—§ŒÜ\Žü”N‹L”OŠÙi‰ªŽRjC6ŒŽ8`9“úC2017”ND

16.                Ž_‘f‚ð‹¤Ž_‰»Ü‚Æ‚·‚éƒJƒ‹ƒoƒ][ƒ‹‚Ì•săJƒbƒvƒŠƒ“ƒO”½‰ž‚ÌŠJ”­iƒ|ƒXƒ^[j
*
²ŒÃ^A‘êàV”EAùˆäG–¾C‘æ6‰ñ JACI/GSCƒVƒ“ƒ|ƒWƒEƒ€C“Œ‹ž‘ÛƒtƒH[ƒ‰ƒ€i“Œ‹žjC7ŒŽ3`4“úC2017”ND
<—DGƒ|ƒXƒ^[ÜŽóÜ>

17.                ƒŒƒhƒbƒNƒXEŽ_‹¦“¯G”}‚ðŠˆ—p‚·‚éƒIƒLƒTƒwƒŠƒZƒ“‚ÌŒø—¦“I‚ȃGƒiƒ“ƒ`ƒI‘I‘ð“I‡¬iƒ|ƒXƒ^[j
²ŒÃ^A*‘êàV”EAùˆäG–¾C‘æ6‰ñ JACI/GSCƒVƒ“ƒ|ƒWƒEƒ€C“Œ‹ž‘ÛƒtƒH[ƒ‰ƒ€i“Œ‹žjC7ŒŽ3`4“úC2017”ND

18.                Development of Asymmetric Umpolung Tandem Michael Addition iŒû“ªj
–ŠÝ“S”nC‘æ3‰ñ–ìˆËƒtƒH[ƒ‰ƒ€ŽáŽèˆç¬mC–¼ŒÃ‰®‘åŠw@–ìˆË‹L”O•¨Ž¿‰»ŠwŒ¤‹†ŠÙiˆ¤’mjC7ŒŽ20`21“úC2017”ND

19.                ƒLƒ‰ƒ‹‚ȃoƒiƒWƒEƒ€G”}‚ð—p‚¢‚éƒqƒhƒƒLƒVƒJƒ‹ƒoƒ][ƒ‹—Þ‚Ì•sÄŽ_‰»ƒJƒbƒvƒŠƒ“ƒO”½‰ž‚ÌŠJ”­iƒ|ƒXƒ^[j
*
²ŒÃ^A‘êàV”EAùˆäG–¾C“ú–{ƒvƒƒZƒX‰»Šw‰ï2017ƒTƒ}[ƒVƒ“ƒ|ƒWƒEƒ€C‘åã‘ی𗬃Zƒ“ƒ^[i‘åãjC8ŒŽ3`4“úC2017”ND

20.                Enantioselective Aza-Wacker-Type Reaction Promoted by Pd-SPRIX Catalystiƒ|ƒXƒ^[j
*Abhijit Sen
A’|’†˜a_AùˆäG–¾C“ú–{ƒvƒƒZƒX‰»Šw‰ï2017ƒTƒ}[ƒVƒ“ƒ|ƒWƒEƒ€C‘åã‘ی𗬃Zƒ“ƒ^[i‘åãjC8ŒŽ3`4“úC2017”ND

21.                ƒoƒiƒWƒEƒ€G”}‚ð—p‚¢‚éƒtƒFƒm[ƒ‹—Þ‚ÌŽ_‰»“I•săJƒbƒvƒŠƒ“ƒO”½‰žiƒ|ƒXƒ^[j
*
–ØFŒ›A²ŒÃ^A‘êàV”EAùˆäG–¾C“ú–{ƒvƒƒZƒX‰»Šw‰ï2017ƒTƒ}[ƒVƒ“ƒ|ƒWƒEƒ€C‘åã‘ی𗬃Zƒ“ƒ^[i‘åãjC8ŒŽ3`4“úC2017”ND

22.                ƒ¿-ƒAƒ~ƒmƒJƒ‹ƒ{ƒjƒ‹‰»‡•¨‚ð—^‚¦‚éƒpƒ‰ƒWƒEƒ€ƒGƒmƒ‰[ƒg‚̋ɫ“]Š·Œ^‹Šj“IƒAƒ~ƒm‰»”½‰ž‚ÌŠJ”­iƒ|ƒXƒ^[j
*
–ì–{—T–çA’|’†˜a_AùˆäG–¾C“ú–{ƒvƒƒZƒX‰»Šw‰ï2017ƒTƒ}[ƒVƒ“ƒ|ƒWƒEƒ€C‘åã‘ی𗬃Zƒ“ƒ^[i‘åãjC8ŒŽ3`4“úC2017”ND

23.                ƒwƒŠƒZƒ“œŠi‚ðŽ‚Â—L‹@•ªŽqG”}‹y‚Ñ•sÄ”zˆÊŽq‚̇¬Œ¤‹†iƒ|ƒXƒ^[j
*
“cX—T‹MA²ŒÃ^A‘êàV”EAùˆäG–¾C‘æ37‰ñ—L‹@‡¬ŽáŽèƒZƒ~ƒi[C“¯ŽuŽÐ‘åŠwŽº’¬ƒLƒƒƒ“ƒpƒXi‹ž“sjC8ŒŽ9“úC2017”ND

24.                Pd-SPRIXG”}‚ð—p‚¢‚éƒGƒiƒ“ƒ`ƒI‘I‘ð“I•ªŽq“àaza-WackerŒ^ŠÂ‰»”½‰žiƒ|ƒXƒ^[j
Sen Abhijit
A*•Љªq—CA’|’†˜a_AùˆäG–¾C‘æ37‰ñ—L‹@‡¬ŽáŽèƒZƒ~ƒi[C“¯ŽuŽÐ‘åŠwŽº’¬ƒLƒƒƒ“ƒpƒXi‹ž“sjC8ŒŽ9“úC2017”ND

25.                “ñŠjƒoƒiƒWƒEƒ€G”}‚ð—p‚¢‚é’PŠÂŽ®ƒtƒFƒm[ƒ‹—U“±‘̂̎_‰»“I•săJƒbƒvƒŠƒ“ƒO”½‰žiƒ|ƒXƒ^[j
*
–ØFŒ›A²ŒÃ^A‘êàV”EAùˆäG–¾C‘æ37‰ñ—L‹@‡¬ŽáŽèƒZƒ~ƒi[C“¯ŽuŽÐ‘åŠwŽº’¬ƒLƒƒƒ“ƒpƒXi‹ž“sjC8ŒŽ9“úC2017”ND
<—DGƒ|ƒXƒ^[ÜŽóÜ>

26.                IrG”}‚ð—p‚¢‚郃\Œ^ƒWƒI[ƒ‹‚ƃAƒ‹ƒfƒqƒh‚Ì•să^ƒ“ƒfƒ€ƒJƒbƒvƒŠƒ“ƒO”½‰žiƒ|ƒXƒ^[j
—é–ØŒ’”VA*‘«—§—S‹MAùˆäG–¾C‘æ37‰ñ—L‹@‡¬ŽáŽèƒZƒ~ƒi[C“¯ŽuŽÐ‘åŠwŽº’¬ƒLƒƒƒ“ƒpƒXi‹ž“sjC8ŒŽ9“úC2017”ND

27.                ƒJƒ‹ƒoƒ][ƒ‹—U“±‘̂̃Gƒiƒ“ƒ`ƒI‘I‘ð“IƒJƒbƒvƒŠƒ“ƒO”½‰ž‚ÌŠJ”­‚Ɖž—piŒû“ªj
*
²ŒÃ^A‘êàV”EAùˆäG–¾C‘æŽl‰ñ@VŠwp—̈挤‹†u”½‰žWω»‚ª“±‚­’†•ªŽqí—ªF‚ŽŸ¶•¨‹@”\•ªŽq‚Ì‘n»vŽáŽèƒVƒ“ƒ|ƒWƒEƒ€CH•ÛƒŠƒ][ƒg@ƒzƒeƒ‹ƒNƒŒƒZƒ“ƒgi‹{éjC8ŒŽ18`19“úC2017”ND

28.                Development of Catalytic Synthetic Method for ƒ¿-Amino Carbonyl Compounds Based on Palladium Enolate Umpolungiƒ|ƒXƒ^[j
*
’|’†˜a_A–ì–{—T–çAùˆäG–¾C‘æ64‰ñ—L‹@‹à‘®‰»Šw“¢˜_‰ïC“Œ–k‘åŠwì“àƒLƒƒƒ“ƒpƒXi‹{éjC9ŒŽ7`9“úC2017”ND

29.                Chiral Vanadium(V) Complex-catalyzed Enantioselective Oxidative Coupling of Phenol DerivativesiŒû“ªj
*
²ŒÃ^A–ØFŒ›A‘êàV”EAùˆäG–¾C‘æ64‰ñ—L‹@‹à‘®‰»Šw“¢˜_‰ïC“Œ–k‘åŠwì“àƒLƒƒƒ“ƒpƒXi‹{éjC9ŒŽ7`9“úC2017”ND

30.                Enantioselective aza-Wacker-Type Reaction Promoted by Pd-SPRIX Catalystiƒ|ƒXƒ^[j
*Sen Abhijit
A’|’†˜a_AùˆäG–¾C‘æ34‰ñ—L‹@‡¬‰»ŠwƒZƒ~ƒi[C‹à‘òŽs•¶‰»ƒz[ƒ‹iÎìjC9ŒŽ12`14“úC2017”ND

31.                ƒLƒ‰ƒ‹‚ȃoƒiƒWƒEƒ€G”}‚ð—p‚¢‚é’PŠÂŽ®ƒtƒFƒm[ƒ‹—Þ‚ÌŽ_‰»“I•săJƒbƒvƒŠƒ“ƒO”½‰žiƒ|ƒXƒ^[j
*
–ØFŒ›A²ŒÃ^A‘êàV”EAùˆäG–¾C‘æ34‰ñ—L‹@‡¬‰»ŠwƒZƒ~ƒi[C‹à‘òŽs•¶‰»ƒz[ƒ‹iÎìjC9ŒŽ12`14“úC2017”ND

32.                ƒAƒ‹ƒLƒjƒ‹ƒGƒXƒeƒ‹‚̋ɫ“]Š·Œ^ƒ^ƒ“ƒfƒ€ƒ}ƒCƒPƒ‹•t‰Á‚É‚æ‚é•¡‘fŠÂ‰»‡•¨‚̇¬iƒ|ƒXƒ^[j
*
ŠÝ“S”nA‘êàV”EA‘ê–¢—ˆAùˆäG–¾C‘æ34‰ñ—L‹@‡¬‰»ŠwƒZƒ~ƒi[C‹à‘òŽs•¶‰»ƒz[ƒ‹iÎìjC9ŒŽ12`14“úC2017”ND

33.                “ñdŠˆ«‰»Œ^•sÄG”}‚Ì‘n»i“Á•Êu‰‰j
*
ùˆäG–¾C•½¬29”N“x—L‹@‡¬‰»Šw–k—¤ƒZƒ~ƒi[C‚܂‚âççi•ŸˆäjC10ŒŽ6`7“úC2017”ND

34.                ƒoƒiƒWƒEƒ€ö‘Ì‚ðG”}‚Æ‚·‚鑽ŠÂŽ®•¡‘fŠÂ‚ÌŽ_‰»“I•săJƒbƒvƒŠƒ“ƒO”½‰ž‚ÌŠJ”­iƒ|ƒXƒ^[j
*
™›½W«A²ŒÃ^A‘êàV”EAùˆäG–¾C•½¬29”N“x—L‹@‡¬‰»Šw–k—¤ƒZƒ~ƒi[C‚܂‚âççi•ŸˆäjC10ŒŽ6`7“úC2017”ND

35.                ‚P,3-ƒVƒX-ƒCƒ\ƒCƒ“ƒhƒŠƒ“‰»‡•¨‚̃Gƒiƒ“ƒ`ƒI‘I‘ð“Iƒƒ“ƒ|ƒbƒg‡¬iƒ|ƒXƒ^[j
*
‘ëΕü‘åAH. D. P. WathsalaAŠÝ“S”nAMohamed Ahmed AbozeidA•½“cCˆêA²ŒÃ^A‘ºˆäŒ’ˆêA“¡‰ªO“¹A‘êàV”EAùˆäG–¾C•½¬29”N“x—L‹@‡¬‰»Šw–k—¤ƒZƒ~ƒi[C‚܂‚âççi•ŸˆäjC10ŒŽ6`7“úC2017”ND

36.                ƒAƒ~ƒh‰»/Rauhut-Currier ˜A‘±”½‰ž‚É‚æ‚é ƒ¿-ƒƒ`ƒŠƒfƒ“-ƒÁ-ƒ‰ƒNƒ^ƒ€‚ÌG”}“I•sć¬iŒû“ªj
*
ŠÝ“S”nAFernando Arteaga-ArteagaA‘êàV”EAùˆäG–¾C‘æ67‰ñ“ú–{–òŠw‰ï‹ß‹EŽx•”‘‰ïE‘å‰ïC•ºŒÉˆã—ÑåŠwi•ºŒÉjC10ŒŽ14“úC2017”ND

37.                ’PŠÂŽ®ƒtƒFƒm[ƒ‹—U“±‘̂̎_‰»“I•săJƒbƒvƒŠƒ“ƒO”½‰ž\ƒLƒ‰ƒ‹ƒoƒiƒWƒEƒ€G”}‚ð—p‚¢‚éŠÂ‹«’ᕉ‰×Œ^‡¬–@\iŒû“ªj
*
‘êàV”EA–ØFŒ›A²ŒÃ^AùˆäG–¾C‘æ67‰ñ“ú–{–òŠw‰ï‹ß‹EŽx•”‘‰ïE‘å‰ïC•ºŒÉˆã—ÑåŠwi•ºŒÉjC10ŒŽ14“úC2017”ND

38.                ƒoƒiƒWƒEƒ€G”}‚ð—p‚¢‚é•sÄŽ_‰»“IƒJƒbƒvƒŠƒ“ƒO”½‰ž‚ÌŠJ”­‚Ɖž—piŒû“ªj
*
²ŒÃ^A‘êàV”EAùˆäG–¾C‘æ47‰ñ•¡‘fŠÂ‰»Šw“¢˜_‰ïC‚’mŒ§—§Œ§–¯•¶‰»ƒz[ƒ‹i‚’mjC10ŒŽ26`28“úC2017”ND

39.                ‘½ŠÂŽ®ƒtƒFƒm[ƒ‹‚ÌŽ_‰»ƒJƒbƒvƒŠƒ“ƒO”½‰ž‚ðŠî”Õ‚Æ‚·‚é–F‘°•¡‘fŠÂ‰»‡•¨‚ÌG”}“I•sć¬iƒ|ƒXƒ^[j
*
‘êàV”EA²ŒÃ^Aˆê”V£˜a–íA’ÒŒ´“N–çA‰Í–ì•xˆêAùˆäG–¾C‘æ43‰ñ”½‰ž‚Ƈ¬‚Ìi•àƒVƒ“ƒ|ƒWƒEƒ€\ƒ‰ƒCƒtƒTƒCƒGƒ“ƒX‚ðŽwŒü‚µ‚½—˜_C”½‰ž‹y‚ч¬\C•xŽR‘Û‰ï‹cêi•xŽRjC11ŒŽ6`7“úC2017”ND

40.                ƒGƒiƒ“ƒ`ƒI‹y‚уWƒAƒXƒeƒŒƒI‘I‘ð“IBetti/aza-Michael˜A‘±”½‰ž‚ÌŠJ”­‚Æ1,3-“ñ’uŠ·ƒCƒ\ƒCƒ“ƒhƒŠƒ“œŠi\’z‚ւ̉ž—piƒ|ƒXƒ^[j
‘êàV”EA‘ºˆäŒ’ˆêA*H. D. P. WathsalaA²ŒÃ^AŠÝ“S”nA•½“cCˆêA“¡‰ªO“¹AùˆäG–¾C‘æ43‰ñ”½‰ž‚Ƈ¬‚Ìi•àƒVƒ“ƒ|ƒWƒEƒ€\ƒ‰ƒCƒtƒTƒCƒGƒ“ƒX‚ðŽwŒü‚µ‚½—˜_C”½‰ž‹y‚ч¬\C•xŽR‘Û‰ï‹cêi•xŽRjC11ŒŽ6`7“úC2017”ND

41.                ƒzƒXƒtƒBƒ“G”}‚É‚æ‚é‹É«“]Š·Œ^ƒ_ƒuƒ‹ƒ}ƒCƒPƒ‹•t‰Á”½‰ž‚ðŠˆ—p‚·‚éƒqƒhƒƒCƒ“ƒh[ƒ‹‹y‚уqƒhƒƒxƒ“ƒ]ƒtƒ‰ƒ“-2-ƒJƒ‹ƒ{ƒ“Ž_ƒGƒXƒeƒ‹‚̇¬iƒ|ƒXƒ^[j
*
ŠÝ“S”nA‘êàV”EAùˆäG–¾C‘æ10‰ñ—L‹@G”}ƒVƒ“ƒ|ƒWƒEƒ€C“Œ–k‘åŠw‘åŠw‰@—ŠwŒ¤‹†‰È‘åu‹`Žºi‹{éjC11ŒŽ30“ú`12ŒŽ1“úC2017”ND

 

<International>

1. Vanadium(V) Complex-Catalyzed Enantioselective C–C 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 ƒ¿-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.

Topª

 

2016@🐵

<Domestic>

1. ƒGƒiƒ“ƒ`ƒI‘I‘ð“I”ñ‘Î̉»‚ðŠî”Õ‚Æ‚·‚é“ñ˜A‘±•sÄ’Y‘f‚ð—L‚·‚é•¡‘fŠÂ‰»‡•¨‚̇¬iƒ|ƒXƒ^[j
*
ŠÝ“S”nA‘êàV”EA‹g“c‘׎uAùˆäG–¾Cu—L‹@•ªŽqG”}‚É‚æ‚é–¢—ˆŒ^•ªŽq•ÏŠ·v‘æ6‰ñŒöŠJƒVƒ“ƒ|ƒWƒEƒ€C‘åã‰ÈŠw‹ZpƒZƒ“ƒ^[i‘åãjC1ŒŽ22`23“úC2016”N.
<—DGƒ|ƒXƒ^[ÜŽóÜ>

2. Palladium Enolate Umpolung: Cyclative Haloacetoxylation of Alkynyl CyclohexadienonesiΞһj
*
’|’†˜a_ASuman C. MohantaAùˆäG–¾C“ú–{‰»Šw‰ï‘æ96t‹G”N‰ïC“¯ŽuŽÐ‘åŠwi‹ž“sjC3ŒŽ24`27“úC2016”ND

3. Palladium Enolate Umpolung: Cyclative Hydroacyloxylation of Alkynyl CyclohexadienonesiΞһj
*
àV“c˜a–íASuman C. MohantaA’|’†˜a_AùˆäG–¾C“ú–{‰»Šw‰ï‘æ96t‹G”N‰ïC“¯ŽuŽÐ‘åŠwi‹ž“sjC3ŒŽ24`27“úC2016”ND

4. Efficient Synthesis of Spiro-type Chiral Ligands Based on Direct C5 Arylation of IsoxazolesiΞһj
*
dM‹§ŽuA’|’†˜a_AùˆäG–¾C“ú–{‰»Šw‰ï‘æ96t‹G”N‰ïC“¯ŽuŽÐ‘åŠwi‹ž“sjC3ŒŽ24`27“úC2016”ND

5. Catalytic Asymmetric Synthesis of Natural Products Using Ir Catalyzed Tishchenko-type ReactioniΞһj
—é–ØŒ’”VA*“yˆä‹M—TAIsmiyartoAŽü‘å—gA’©–ì–FDAùˆäG–¾C“ú–{‰»Šw‰ï‘æ96t‹G”N‰ïC“¯ŽuŽÐ‘åŠwi‹ž“sjC3ŒŽ24`27“úC2016”ND

6. Development of Enantioselective Reaction Using Abundant Transition MetalsiΞһj
*
•ÄŽRSA’|’†˜a_A‘êàV”EAùˆäG–¾C“ú–{‰»Šw‰ï‘æ96t‹G”N‰ïC“¯ŽuŽÐ‘åŠwi‹ž“sjC3ŒŽ24`27“úC2016”ND

7. Chiral Amine-Catalyzed Enantioselective Rauhut-Currier ReactioniΞһj
*
ŠÝ“S”nA‘êàV”EAFernando Arteaga-ArteagaAùˆäG–¾C“ú–{‰»Šw‰ï‘æ96t‹G”N‰ïC“¯ŽuŽÐ‘åŠwi‹ž“sjC3ŒŽ24`27“úC2016”ND

8. Asymmetric Synthesis of Spiro-type Chiral Ligands via Catalytic DesymmetrizationiΞһj
*Bijan M. Chaki
A˜e“c˜a•FA’|’†˜a_A‘êàV”EAùˆäG–¾C“ú–{‰»Šw‰ï‘æ96t‹G”N‰ïC“¯ŽuŽÐ‘åŠwi‹ž“sjC3ŒŽ24`27“úC2016”ND

9. Pd(II)-SPRIX Catalyzed Enantioselective Fujiwara-Moritani Annulation of AlkenylindolesiΞһj
*Mohamed A. Abozeid
A‘êàV”EAùˆäG–¾C“ú–{‰»Šw‰ï‘æ96t‹G”N‰ïC“¯ŽuŽÐ‘åŠwi‹ž“sjC3ŒŽ24`27“úC2016”ND

10.                Catalytic and Enantioselective Synthesis of Heterohelicene DerivativesiŒû“ªj
*
ˆê”V£˜a–íA²ŒÃ^A‘êàV”EAùˆäG–¾C“ú–{‰»Šw‰ï‘æ96t‹G”N‰ïC“¯ŽuŽÐ‘åŠwi‹ž“sjC3ŒŽ24`27“úC2016”ND

11.                Enantioselective and Aerobic Oxidative Coupling of 2-Naphthols Derivatives Using Chiral Dinuclear Vanadium(V) Complex in WateriŒû“ªj
*
²ŒÃ^A‘êàV”EA‹g“c‘׎uAùˆäG–¾C“ú–{‰»Šw‰ï‘æ96t‹G”N‰ïC“¯ŽuŽÐ‘åŠwi‹ž“sjC3ŒŽ24`27“úC2016”ND

12.                The Development of Enantioselective Oxidative Coupling Reactions of 1-Naphthol Derivatives Catalyzed by Vanadium(V) ComplexiŒû“ªj
*
âˆä’qOA¬Ž›ƒ•½A‘êàV”EAùˆäG–¾C“ú–{‰»Šw‰ï‘æ96t‹G”N‰ïC“¯ŽuŽÐ‘åŠwi‹ž“sjC3ŒŽ24`27“úC2016”ND

13.                Efficient Enantioselective Synthesis of Oxahelicenes Using Redox/Acid Cooperative CatalystsiŒû“ªj
*
‘êàV”EC‘æ‚Q‚S‰ñ•ªŽq‡¬‰»ŠwƒZƒ~ƒi[CےˬE‰Ô‚Ì—¢‰·òEŽR…ŠÙi‘åãjC6ŒŽ11`12“úC2016”ND

14.                “ñdŠˆ«‰»Œ^G”}‚Ì‘n»‚ðŠî”Õ‚Æ‚·‚éV‹K•ªŽqœŠi\’z”½‰ž‚ÌŠJ”­iµ‘Òj
*
ùˆäG–¾C‘n–òŒ¤‹†ƒZƒ“ƒ^[ƒVƒ“ƒ|ƒWƒEƒ€C“Œ–kˆã‰È–ò‰È‘åŠwi‹{éjC6ŒŽ18“úC2016”ND

15.                “ñdŠˆ«‰»Œ^•sÄG”}‚Ì‘n»‚Æ“WŠJiµ‘Òj
*
ùˆäG–¾C‘æ11‰ñ—L‹@‡¬‰»Šw‚̃tƒƒ“ƒeƒBƒAC—‰»ŠwŒ¤‹†Š—é–Ø”~‘¾˜Yƒz[ƒ‹ié‹ÊjC6ŒŽ24“úC2016”ND

16.                ƒpƒ‰ƒWƒEƒ€ƒGƒmƒ‰[ƒg‚̋ɫ“]Š·‚ðŠî޲‚Æ‚·‚鑽Н”\«ƒJƒ‹ƒ{ƒjƒ‹‰»‡•¨‚ÌŒø—¦“I‡¬iƒ|ƒXƒ^[jC
*
’|’†˜a_AàV“c˜a–íASuman C. MohantaAùˆäG–¾C“ú–{ƒvƒƒZƒX‰»Šw‰ï2016ƒTƒ}[ƒVƒ“ƒ|ƒWƒEƒ€C–¼ŒÃ‰®‘Û‰ï‹cêiˆ¤’mjC7ŒŽ28`29“úC2016”ND

17.                —L‹@•ªŽqG”}‚É‚æ‚éŠÜ’‚‘f•¡‘fŠÂ‚̃Gƒiƒ“ƒ`ƒI‘I‘ð“I\’ziƒ|ƒXƒ^[j
*
ŠÝ“S”nA‘êàV”EAFernando Arteaga-ArteagaAùˆäG–¾C“ú–{ƒvƒƒZƒX‰»Šw‰ï2016ƒTƒ}[ƒVƒ“ƒ|ƒWƒEƒ€C–¼ŒÃ‰®‘Û‰ï‹cêiˆ¤’mjC7ŒŽ28`29“úC2016”ND

18.                ƒoƒiƒWƒEƒ€G”}‚ðŠˆ—p‚·‚éƒGƒiƒ“ƒ`ƒI‘I‘ð“I’Y‘f|’Y‘fŒ‹‡Œ`¬”½‰ž‚ÌŠJ”­‚Ɖž—piƒ|ƒXƒ^[j
*
²ŒÃ^A‘êàV”EAùˆäG–¾C“ú–{ƒvƒƒZƒX‰»Šw‰ï2016ƒTƒ}[ƒVƒ“ƒ|ƒWƒEƒ€C–¼ŒÃ‰®‘Û‰ï‹cêiˆ¤’mjC7ŒŽ28`29“úC2016”ND

19.                ƒoƒiƒWƒEƒ€G”}‚ðŠˆ—p‚·‚éƒwƒeƒƒwƒŠƒZƒ“—U“±‘̂̌ø—¦“I‡¬iƒ|ƒXƒ^[j
²ŒÃ^A*ˆê”V£˜a–íA‘êàV”EAùˆäG–¾C‘æ36‰ñ—L‹@‡¬ŽáŽèƒZƒ~ƒi[C‹ž“s–ò‰È‘åŠwi‹ž“sjC8ŒŽ9“úC2016”ND
<ƒ|ƒXƒ^[ÜŽóÜ>

20.                ƒpƒ‰ƒWƒEƒ€ƒGƒmƒ‰[ƒg‚̋ɫ“]Š·‚ðŠî޲‚Æ‚·‚鑽Н”\«ƒJƒ‹ƒ{ƒjƒ‹‰»‡•¨‚ÌŒø—¦“I‡¬iƒ|ƒXƒ^[j
*
–ì–{—T–çA’|’†˜a_AàV“c˜a–íASuman C. MohantaAùˆäG–¾C‘æ36‰ñ—L‹@‡¬ŽáŽèƒZƒ~ƒi[C‹ž“s–ò‰È‘åŠwi‹ž“sjC8ŒŽ9“úC2016”ND

21.                •¡‘fŠÂ‚ð—L‚·‚鑽ŠÂŽ®ƒtƒFƒm[ƒ‹—Þ‚Ì•sÄŽ_‰»“IƒJƒbƒvƒŠƒ“ƒO”½‰ž‚ÌŠJ”­iƒ|ƒXƒ^[j
*
™›½W«A²ŒÃ^A‘êàV”EAùˆäG–¾C‘æ36‰ñ—L‹@‡¬ŽáŽèƒZƒ~ƒi[C‹ž“s–ò‰È‘åŠwi‹ž“sjC8ŒŽ9“úC2016”ND

22.                —L‹@G”}‚Ì‹¤–ðƒAƒ‹ƒLƒ“‚Ö‚Ì•t‰Á‚ðŒ®‚Æ‚·‚éƒhƒ~ƒm”½‰ž‚ÌŠJ”­iƒ|ƒXƒ^[j
*
‘ê–¢—ˆAŠÝ“S”nA‘êàV”EAJianfei BaiAùˆäG–¾C‘æ36‰ñ—L‹@‡¬ŽáŽèƒZƒ~ƒi[C‹ž“s–ò‰È‘åŠwi‹ž“sjC8ŒŽ9“úC2016”ND

23.                “ñdŠˆ«‰»Œ^•sÄG”}‚Ì‘noiµ‘Òj
*
ùˆäG–¾C•ªŽqŒ¤Œ¤‹†‰ï@—L‹@‹à‘®‰»Šw‚̑咪—¬C‰ªèƒRƒ“ƒtƒ@ƒŒƒ“ƒXƒZƒ“ƒ^[iˆ¤’mjC9ŒŽ2`3“úC2016”ND

24.                Pd(II)-SPRIX Catalyzed Enantioselective Annulation of Alkenylindolesiƒ|ƒXƒ^[j
*Mohamed A. Abozeid
A‘êàV”EAùˆäG–¾C‘æ63‰ñ—L‹@‹à‘®‰»Šw“¢˜_‰ïC‘ˆî“c‘åŠw¼‘ˆî“cƒLƒƒƒ“ƒpƒXi“Œ‹žjC9ŒŽ14`16“úC2016”ND

25.                Palladium Enolate Umpolung: Catalytic Cyclative Hydroacyloxylation of Alkynyl CyclohexadienonesiŒû“ªj
*
’|’†˜a_AàV“c˜a–íASuman C. MohantaAùˆäG–¾C‘æ63‰ñ—L‹@‹à‘®‰»Šw“¢˜_‰ïC‘ˆî“c‘åŠw¼‘ˆî“cƒLƒƒƒ“ƒpƒXi“Œ‹žjC9ŒŽ14`16“úC2016”ND

26.                ƒpƒ‰ƒWƒEƒ€ƒGƒmƒ‰[ƒg‚̋ɫ“]Š·‚ðŠˆ—p‚·‚éƒJƒ‹ƒ{ƒjƒ‹‰»‡•¨‚ÌG”}“IŠÂ‰»Š¯”\Šî‰»”½‰žiŒû“ªj
*
’|’†˜a_AàV“c˜a–íASuman C. MohantaAùˆäG–¾C‘æ46‰ñ•¡‘fŠÂ‰»Šw“¢˜_‰ïC‹à‘ò‰ÌŒ€ÀiÎìjC9ŒŽ26`28“úC2016”ND

27.                “ñdŠˆ«‰»Œ^•sÄG”}‚Ì‘no‚Ɖž—piµ‘Òj
*
ùˆäG–¾CiŒöj‰ÈŠw‹ZpŒð—¬à’c@ƒOƒŠ[ƒ“ƒPƒ~ƒXƒgƒŠ[‚ɪ·‚µ‚½—L‹@‡¬Žè–@Œ¤‹†‰ïC–¼ŒÃ‰®H‹Æ‘åŠwiˆ¤’mjC9ŒŽ30“úC2016”ND

28.                ƒAƒ~ƒh‰»ERauhut–Currier˜A‘±”½‰ž‚É‚æ‚郿]ƒƒ`ƒŠƒfƒ“]ƒÁ]ƒ‰ƒNƒ^ƒ€‚ÌG”}“I•sć¬iŒû“ªj
*
ŠÝ“S”nA‘êàV”EAùˆäG–¾C‘æ110‰ñ—L‹@‡¬ƒVƒ“ƒ|ƒWƒEƒ€C‘ˆî“c‘åŠw‘Û‰ï‹cêi“Œ‹žjC11ŒŽ10`11“úC2016”ND

29.                ƒAƒ~ƒh‰»^•ªŽq“àRauhut–Currier (RC) ˜A‘±”½‰ž‚É‚æ‚郿]ƒƒ`ƒŠƒfƒ“]ƒÁ]ƒ‰ƒNƒ^ƒ€œŠi‚̃Gƒiƒ“ƒ`ƒI‘I‘ð“IG”}‡¬iƒ|ƒXƒ^[j
*
‘êàV”EAŠÝ“S”nAùˆäG–¾C‘æ9‰ñ—L‹@G”}ƒVƒ“ƒ|ƒWƒEƒ€C–¼ŒÃ‰®‘åŠwiˆ¤’mjC12ŒŽ1`2“úC2016”ND

<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 Growthh, 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 Growthh, 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 AwardŽóÜ>

7. Facile Synthesis of ƒ¿-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 ƒ¿-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.

 

Topª

 

2015

<Domestic>

1. ƒpƒ‰ƒWƒEƒ€G”}‚ð—p‚¢‚éƒAƒ‹ƒPƒjƒ‹ƒIƒLƒVƒ€‚̃Gƒiƒ“ƒ`ƒI‘I‘ð“IŠÂ‰»\ŠÂ‰»•t‰Á”½‰žiŒû“ªj
*Mohamed A. Abozeid
A‘êàV”EAùˆäG–¾C“ú–{–òŠw‰ï‘æ135”N‰ïC_ŒËŠw‰@‘åŠwi•ºŒÉjC3ŒŽ25`28“úC2015”ND

2. V‹KƒXƒsƒŒ^ƒLƒ‰ƒ‹ƒCƒ~ƒ_ƒ][ƒ‹”zˆÊŽq‚ÌŠJ”­‚Ɖž—piŒû“ªj
*
àV“c˜a–íA‚’JC•½A’|’†˜a_AùˆäG–¾C“ú–{–òŠw‰ï‘æ135”N‰ïC_ŒËŠw‰@‘åŠwi•ºŒÉjC3ŒŽ25`28“úC2015”ND

3. Stereoselective Construction of Chiral Tetrasubstituted Carbon Stereogenic Centers Via Organocatalytic Rauhut–Currier Reactioni“Á•Êu‰‰j
*
‘êàV”EAùˆäG–¾C“ú–{‰»Šw‰ï‘æ95t‹G”N‰ïC“ú–{‘åŠwiç—tjC3ŒŽ26`29“úC2015”ND

4. Development of Enantioselective Organocatalyzed Formal [n+2] Cycloaddition of Allenic Ester with OlefinsiΞһj
*
‹g“c‘׎uA‘êàV”EAFernando Arteaga-ArteagaAŠÝ“S”nAùˆäG–¾C“ú–{‰»Šw‰ï‘æ95t‹G”N‰ïC“ú–{‘åŠwiç—tjC3ŒŽ26`29“úC2015”ND

5. Vanadium(V) Complex-Catalyzed Enantioselective Synthesis of Oxa[9]heliceneiΞһj
*
²ŒÃ^A‘êàV”EA’ÒŒ´“N–çA‹g“c‘׎uA¬Ž›ƒ•½A‰Í–ì•xˆêAùˆäG–¾C“ú–{‰»Šw‰ï‘æ95t‹G”N‰ïC“ú–{‘åŠwiç—tjC3ŒŽ26`29“úC2015”ND

6. Enantioselective Rauhut–Currier Reaction Promoted by an Immobilized OrganocatalystiŒû“ªj
*
•½“cCˆêAŠÝ“S”nA‘êàV”EAùˆäG–¾C“ú–{‰»Šw‰ï‘æ95t‹G”N‰ïC“ú–{‘åŠwiç—tjC3ŒŽ26`29“úC2015”ND

7. Enantioselective Synthesis of Hetero Helicenes Bearing 1,2,3-Triazole UnitsiΞһj
*
âˆä’qOA‹g“c‘׎uA‘êàV”EAùˆäG–¾C“ú–{‰»Šw‰ï‘æ95t‹G”N‰ïC“ú–{‘åŠwiç—tjC3ŒŽ26`29“úC2015”ND

8. Novel Chiral Benzimidazole Ligands Having a Spiro Skeleton: Design, Preparation and ApplicationiΞһj
*
‚’JC•½AàV“c˜a–íA’|’†˜a_AùˆäG–¾C“ú–{‰»Šw‰ï‘æ95t‹G”N‰ïC“ú–{‘åŠwiç—tjC3ŒŽ26`29“úC2015”ND

9. 2‰¿ƒpƒ‰ƒWƒEƒ€‚ðŠˆ«Ží‚Æ‚·‚é•sÄG”}”½‰ž‚ÌV“WŠJi“Á•Êu‰‰j
*
’|’†˜a_C“ú–{‰»Šw‰ï‘æ95t‹G”N‰ïC“ú–{‘åŠwiç—tjC3ŒŽ26`29“úC2015”ND
<Žá‚¢¢‘ã‚Ì“Á•Êu‰‰‰ï>

10.                Enantioselective Synthesis of Chiral Spiro Compounds and Their Applications to OrganocatalysisiŒû“ªj
*
•“à–FŽ÷ALulu FanA‘êàV”EAùˆäG–¾C“ú–{‰»Šw‰ï‘æ95t‹G”N‰ïC“ú–{‘åŠwiç—tjC3ŒŽ26`29“úC2015”ND

11.                Divergent Synthesis of SPRIX Ligands Having Oxygen FunctionalitiesiŒû“ªj
*
—ÑŒ«¡A’|’†˜a_AùˆäG–¾C“ú–{‰»Šw‰ï‘æ95t‹G”N‰ïC“ú–{‘åŠwiç—tjC3ŒŽ26`29“úC2015”ND

12.                Ir-Catalyzed Asymmetric Tishchenko Type ReactioniŒû“ªj
—é–ØŒ’”VA*IsmiyartoAŽü‘å—gA’©–ì–FDAùˆäG–¾C“ú–{‰»Šw‰ï‘æ95t‹G”N‰ïC“ú–{‘åŠwiç—tjC3ŒŽ26`29“úC2015”ND

13.                [n+2]•sĊ‰»”½‰ž‚É‚æ‚éƒLƒ‰ƒ‹Žl’uŠ·’Y‘f‚Ì\’ziƒ|ƒXƒ^[j
*
ŠÝ“S”nA‘êàV”EA‹g“c‘׎uAFernando Arteaga-ArteagaAùˆäG–¾C‘æ8‰ñ—L‹@G”}ƒVƒ“ƒ|ƒWƒEƒ€iu—L‹@•ªŽqG”}‚É‚æ‚é–¢—ˆŒ^•ªŽq•ÏŠ·v‘æ5‰ñŒöŠJƒVƒ“ƒ|ƒWƒEƒ€jC‰«“ꌧŽs’¬‘ºŽ©Ž¡‰ïŠÙi‰«“êjC5ŒŽ10`11“úC2015”ND

14.                ƒoƒiƒWƒEƒ€G”}‚ðŠˆ—p‚·‚éƒGƒiƒ“ƒ`ƒI‘I‘ð“I’Y‘f|’Y‘fŒ‹‡Œ`¬”½‰ž‚ÌŠJ”­‚Ɖž—piŒû“ªj
*
²ŒÃ^A•“à–FŽ÷A‘êàV”EA’ÒŒ´“N–çA‹g“c‘׎uA¬Ž›ƒ•½A‰Í–ì•xˆêAùˆäG–¾C‘æ107‰ñ—L‹@‡¬ƒVƒ“ƒ|ƒWƒEƒ€CŒc‰ž‹`m‘åŠw–òŠw•”ƒ}ƒ‹ƒ`ƒƒfƒBƒAu“°i“Œ‹žjC6ŒŽ9`10“úC2015”ND

15.                —L‹@•ªŽqG”}‚ð—p‚¢‚éƒGƒiƒ“ƒ`ƒI‘I‘ð“I[2+2]ŠÂ‰»”½‰ž‚É‚æ‚éŽlˆõŠÂ‚Ì\’ziƒ|ƒXƒ^[j
*
ŠÝ“S”nA‘êàV”EAFernando Arteaga-ArteagaA‹g“c‘׎uA—é–Ø’Ê‹±AùˆäG–¾CSymposium on Molecular Chirality 2015C‘ˆî“c‘åŠw¼‘ˆî“cƒLƒƒƒ“ƒpƒXi“Œ‹žjC6ŒŽ12`13“úC2015”ND

16.                “SG”}‚ð—p‚¢‚éƒtƒŠ[ƒfƒ‹EƒNƒ‰ƒtƒc”½‰ž‚ÌŠJ”­iƒ|ƒXƒ^[j
*
•ÄŽRSA‘êàV”EAùˆäG–¾C‘æ35‰ñ—L‹@‡¬ŽáŽèƒZƒ~ƒi[C‹ž“s•{—§‘åŠw‰ºŠ›ƒLƒƒƒ“ƒpƒXi‹ž“sjC8ŒŽ1“úC2015”ND

17.                ƒpƒ‰ƒWƒEƒ€ƒGƒmƒ‰[ƒg‚̋ɫ“]Š·‚ðŠî޲‚Æ‚·‚éŠÂ‰»“IН”\Šî‰»”½‰ž‚ÌŠJ”­iƒ|ƒXƒ^[j
Suman C. Mohanta
AàV“c˜a–íA*V‹“c‹±ÍA’|’†˜a_AùˆäG–¾C‘æ35‰ñ—L‹@‡¬ŽáŽèƒZƒ~ƒi[C‹ž“s•{—§‘åŠw‰ºŠ›ƒLƒƒƒ“ƒpƒXi‹ž“sjC8ŒŽ1“úC2015”ND

18.                Catalytic Cyclative Haloacetoxylation of Alkynyl Cyclohexadienones Based on Pd Enolate UmpolungiŒû“ªj
*
’|’†˜a_ASuman C. MohantaAùˆäG–¾C‘æ62‰ñ—L‹@‹à‘®‰»Šw“¢˜_‰ïCŠÖ¼‘åŠwç—¢ŽRƒLƒƒƒ“ƒpƒXi‘åãjC9ŒŽ7`9“úC2015”ND

19.                Ir Catalyzed Asymmetric Tandem Reaction of meso-Diolsiƒ|ƒXƒ^[j
—é–ØŒ’”VA*IsmiyartoAÎâ—FAŽü‘å—gA’©–ì–FDAùˆäG–¾C‘æ62‰ñ—L‹@‹à‘®‰»Šw“¢˜_‰ïCŠÖ¼‘åŠwç—¢ŽRƒLƒƒƒ“ƒpƒXi‘åãjC9ŒŽ7`9“úC2015”ND

20.                Carbon-Carbon Bonds Cleavage by Vanadium Catalyzed Aerobic Oxidationiƒ|ƒXƒ^[j
*
‹ËŒ´³”VAŠâˆä—˜–¾A¼“‡—È“ñA‘º¼—R—˜A‘å™—œ‰hA‹gì—tA—é–Ø—œŽÑA‘êàV”EC‘æ62‰ñ—L‹@‹à‘®‰»Šw“¢˜_‰ïCŠÖ¼‘åŠwç—¢ŽRƒLƒƒƒ“ƒpƒXi‘åãjC9ŒŽ7`9“úC2015”ND

21.                ƒoƒiƒWƒEƒ€G”}‚ðŠˆ—p‚·‚éƒIƒLƒTƒwƒŠƒZƒ“—ނ̃Gƒiƒ“ƒ`ƒI‘I‘ð“I‡¬iƒ|ƒXƒ^[j
*
‘êàV”EA²ŒÃ^A•“à–FŽ÷Aˆê”V£˜a–íA’ÒŒ´“N–çA¬Ž›ƒ•½A‰Í–ì•xˆêAùˆäG–¾C•½¬27”N“x—L‹@‡¬‰»Šw–k—¤ƒZƒ~ƒi[C•xŽRŠÏŒõƒzƒeƒ‹i•xŽRjC10ŒŽ2`3“úC2015”N.

22.                —L‹@•ªŽqG”}‚É‚æ‚é”ñ‘Î̉»‚ðŠî”Õ‚Æ‚·‚é“ñ˜A‘±•sÄ’Y‘f‚Ì\’ziƒ|ƒXƒ^[j
*
ŠÝ“S”nA‘êàV”EA‹g“c‘׎uASteffen MaderAMagnus RuepingAùˆäG–¾C•½¬27”N“x—L‹@‡¬‰»Šw–k—¤ƒZƒ~ƒi[C•xŽRŠÏŒõƒzƒeƒ‹i•xŽRjC10ŒŽ2`3“úC2015”ND

23.                ƒoƒiƒWƒEƒ€G”}‚ðŠˆ—p‚·‚éƒwƒeƒƒwƒŠƒZƒ“—U“±‘̂̃Gƒiƒ“ƒ`ƒI‘I‘ð“I‡¬–@‚ÌŠJ”­iƒ|ƒXƒ^[j
²ŒÃ^A•“à–FŽ÷A*ˆê”V£˜a–íA‘êàV”EA’ÒŒ´“N–çA¬Ž›ƒ•½A‰Í–ì•xˆêAùˆäG–¾C‘æ5‰ñCSJ‰»ŠwƒtƒFƒXƒ^Cƒ^ƒ[ƒz[ƒ‹‘D–xi“Œ‹žjC10ŒŽ13`15“úC2015”N.

24.                •sÄ—L‹@•ªŽqG”}‚ð—p‚¢‚é[n+2]ŠÂ‰»”½‰ž‚É‚æ‚éƒeƒgƒ‰ƒqƒhƒƒxƒ“ƒ]ƒtƒ‰ƒmƒ“—U“±‘̂̇¬iŒû“ªj
*
‘êàV”EAŠÝ“S”nA‹g“c‘׎uASteffen MaderAFernando Arteaga-ArteagaAMagnus RuepingAùˆäG–¾C‘æ41‰ñ”½‰ž‚Ƈ¬‚Ìi•àƒVƒ“ƒ|ƒWƒEƒ€C‹ß‹E‘åŠw“Œ‘åãƒLƒƒƒ“ƒpƒXi‘åãjC10ŒŽ26`27“úC2015”N.

25.                ŽŸˆŸ‰–‘fŽ_ƒiƒgƒŠƒEƒ€‚ð—p‚¢‚éƒCƒ~ƒ“Ž_‰»‚É‚æ‚éƒIƒLƒTƒWƒŠƒWƒ“‡¬iƒ|ƒXƒ^[j
*
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26.                ƒoƒiƒWƒEƒ€G”}‚ðŠˆ—p‚·‚éƒwƒeƒƒwƒŠƒZƒ“—U“±‘̂̃Gƒiƒ“ƒ`ƒI‘I‘ð“I‡¬–@‚ÌŠJ”­iƒ|ƒXƒ^[j
*
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<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 C–H 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 ƒ¿-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 Catalysish, Aachen, Germany, September 1-2, 2015.

10.                Vanadium(V)-Catalyzed Enantioselective C–C Bond Forming Reactions (Oral)
*Sako, M.; Takizawa, S.; Yoshida, Y.; Sasai, H.
Aachen-Osaka Joint Symposium gBiological and Chemical Methods for Selective Catalysish, 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.

 

Topª

 

2014

<Domestic>

1. ƒLƒ‰ƒ‹ƒ}ƒ“ƒKƒ“G”}‚ð—p‚¢‚é2|ƒiƒtƒg[ƒ‹—ނ̃Gƒiƒ“ƒ`ƒI‘I‘ð“I”½‰ž‚ÌŠJ”­iŒû“ªj
*
‘êàV”EAùˆäG–¾C“ú–{‰»Šw‰ï‘æ94t‹G”N‰ïC–¼ŒÃ‰®‘åŠwiˆ¤’mjC3ŒŽ27`30“úC2014”ND

2. ƒCƒ~ƒ_ƒ][ƒ‹‚ð”zˆÊ•”ˆÊ‚Æ‚µ‚Ä—L‚·‚éV‹KƒLƒ‰ƒ‹ƒXƒsƒŒ^”zˆÊŽq‚ÌŠJ”­iŒû“ªj
*
‚’JC•½A’|’†˜a_AùˆäG–¾C“ú–{‰»Šw‰ï‘æ94t‹G”N‰ïC–¼ŒÃ‰®‘åŠwiˆ¤’mjC3ŒŽ27`30“úC2014”ND

3. ƒrƒX1,2,3|ƒgƒŠƒAƒ][ƒ‹ƒ†ƒjƒbƒg‚ð—L‚·‚éƒwƒeƒƒwƒŠƒZƒ“‚̃Gƒiƒ“ƒ`ƒI‘I‘ð“I‡¬‚Æ•sÄG”}‚ւ̉ž—piŒû“ªj
*
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4. —L‹@•ªŽqG”}‚É‚æ‚éƒWƒGƒmƒ“‚Æ2,3|ƒuƒ^ƒWƒGƒ“Ž_ƒGƒXƒeƒ‹‚Æ‚ðŠîŽ¿‚Æ‚·‚éƒGƒiƒ“ƒ`ƒI‘I‘ð“IŒ`Ž®“I[3+2]ŠÂ‰»”½‰ž‚ÌŠJ”­iŒû“ªj
*
—é–Ø’Ê‹±AFernando Arteaga-ArteagaATue M.-N. NguyenA‘êàV”EAùˆäG–¾C“ú–{‰»Šw‰ï‘æ94t‹G”N‰ïC–¼ŒÃ‰®‘åŠwiˆ¤’mjC3ŒŽ27`30“úC2014”ND

5. ƒpƒ‰ƒWƒEƒ€G”}‚É‚æ‚éC-HŒ‹‡Šˆ«‰»‚ðŒo‚éƒCƒ\ƒIƒLƒTƒ][ƒ‹ŠÂ5ˆÊ‚ł̒¼Ú“IƒAƒŠ[ƒ‹‰»”½‰žiŒû“ªj
*
dM‹§ŽuA’|’†˜a_AùˆäG–¾C“ú–{‰»Šw‰ï‘æ94t‹G”N‰ïC–¼ŒÃ‰®‘åŠwiˆ¤’mjC3ŒŽ27`30“úC2014”ND

6. ‘æŽO‹‰ƒAƒŠƒ‹ƒAƒ‹ƒR[ƒ‹‚̃tƒb‘f‰»‚É‚æ‚鑽Н”\«Žl’uŠ·ƒIƒŒƒtƒBƒ“‚Ì—§‘Ì‘I‘ð“I‡¬iŒû“ªj
*
ŠÝ“S”nA‘êàV”EAFernando Arteaga-ArteagaAùˆäG–¾C“ú–{‰»Šw‰ï‘æ94t‹G”N‰ïC–¼ŒÃ‰®‘åŠwiˆ¤’mjC3ŒŽ27`30“úC2014”ND

7. Development of Ni-SPRIX Catalysts toward Enantioselective Michael-type Reaction of Indoles with NitroolefinsiΞһj
*Priyabrata Das
A’|’†˜a_AùˆäG–¾C“ú–{‰»Šw‰ï‘æ94t‹G”N‰ïC–¼ŒÃ‰®‘åŠwiˆ¤’mjC3ŒŽ27`30“úC2014”ND

8. 5‰¿‚̃oƒiƒWƒEƒ€G”}‚ð—p‚¢‚éƒGƒiƒ“ƒ`ƒI‘I‘ð“I’Y‘f|’Y‘fŒ‹‡Œ`¬”½‰ž‚ÌŠJ”­‚Ɖž—piŒû“ªj
*
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9. •sĊ‹«‚Ì‹y‚Ú‚·SPRIX”zˆÊŽq‚Ì’uŠ·ŠîŒø‰ÊiŒû“ªj
*
—ÑŒ«¡A’|’†˜a_AùˆäG–¾C“ú–{‰»Šw‰ï‘æ94t‹G”N‰ïC–¼ŒÃ‰®‘åŠwiˆ¤’mjC3ŒŽ27`30“úC2014”ND

10.                ƒXƒsƒ‰»‡•¨‚̃Gƒiƒ“ƒ`ƒI‘I‘ð“I‡¬–@‚ÌŠJ”­‚Æ—L‹@•ªŽqG”}‚Ö‚Ì“WŠJiŒû“ªj
*
•“à–FŽ÷ALulu FanA‘êàV”EAùˆäG–¾C“ú–{‰»Šw‰ï‘æ94t‹G”N‰ïC–¼ŒÃ‰®‘åŠwiˆ¤’mjC3ŒŽ27`30“úC2014”ND

11.                Enantioselective Organocatalyzed Synthesis of Cyclobutanes via Formal [2+2] CycloadditioniŒû“ªj
*Fernando Arteaga-Arteaga
A‘êàV”EAùˆäG–¾C“ú–{‰»Šw‰ï‘æ94t‹G”N‰ïC–¼ŒÃ‰®‘åŠwiˆ¤’mjC3ŒŽ27`30“úC2014”ND

12.                Enantioselective Palladium(II) Catalyzed Cyclization-Cycloaddition Cascade ReactionsiŒû“ªj
*Abozeid Mohamed Ahmed
A‘êàV”EAùˆäG–¾C“ú–{‰»Šw‰ï‘æ94t‹G”N‰ïC–¼ŒÃ‰®‘åŠwiˆ¤’mjC3ŒŽ27`30“úC2014”ND

13.                ƒwƒŠƒZƒ“‹y‚уwƒŠƒZƒ“—l‰»‡•¨‚ÌŒø—¦“I•s欖@‚ÌŠJ”­iƒ|ƒXƒ^[j
‘êàV”EA‹g“c‘׎uA¬Ž›ƒ•½A²ŒÃ^A*“yˆä‹M—TAùˆäG–¾CSymposium on Molecular Chirality 2014Aå‘ä‘ÛƒZƒ“ƒ^[i‹{éjC6ŒŽ6`7“úC2014”ND
<ƒ|ƒXƒ^[ÜŽóÜ>

14.                ‘½‹@”\—L‹@•ªŽqG”}‚ð—p‚¢‚éƒGƒiƒ“ƒ`ƒI‘I‘ð“Iƒhƒ~ƒm”½‰ž‚ÌŠJ”­iŒû“ªj
*
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15.                G”}“I•sĘA‘±”½‰ž‚É‚æ‚éƒLƒ‰ƒ‹ƒrƒ‹ƒfƒBƒ“ƒOƒuƒƒbƒN‚Ì‘noiŒû“ªj
*
‘êàV”EC‘æ27‰ñƒCƒ“ƒ^[ƒtƒFƒbƒNƒXƒWƒƒƒpƒ“C“Œ‹žƒrƒbƒNƒTƒCƒgi“Œ‹žjC7ŒŽ2`4“úC2014”ND

16.                •sÄ—L‹@•ªŽqG”}‚ð—p‚¢‚éƒGƒiƒ“ƒ`ƒI‘I‘ð“Iaza-MBHŒ^ƒhƒ~ƒm”½‰ž‚ÌŠJ”­iƒ|ƒXƒ^[j
*
•½“cCˆêA‘êàV”EAˆäã’¼lAFernando Arteaga-ArteagaA‹g“c‘׎uA—é–Ø’Ê‹±AùˆäG–¾C“ú–{ƒvƒƒZƒX‰»Šw‰ï2014ƒTƒ}[ƒVƒ“ƒ|ƒWƒEƒ€Cƒ^ƒ[ƒz[ƒ‹‘D–xi“Œ‹žjC7ŒŽ31`8ŒŽ1“úC2014”ND

17.                5‰¿‚̃oƒiƒWƒEƒ€G”}‚ð—p‚¢‚éƒGƒiƒ“ƒ`ƒI‘I‘ð“IC-CŒ‹‡Œ`¬”½‰ž‚ÌŠJ”­‚Ɖž—piƒ|ƒXƒ^[j
âˆä’qOA*‘êàV”EA¬Ž›ƒ•½A‹g“c‘׎uA²ŒÃ^AùˆäG–¾C‘æ34‰ñ—L‹@‡¬ŽáŽèƒZƒ~ƒi[C‘åã‘åŠwi‘åãjC8ŒŽ5“úC2014”ND

18.                ƒCƒ~ƒ_ƒ][ƒ‹‚ð”zˆÊ•”ˆÊ‚Æ‚·‚éV‹KƒLƒ‰ƒ‹ƒXƒsƒŒ^”zˆÊŽq‚ÌŠJ”­iƒ|ƒXƒ^[j
*
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19.                Žl’uŠ·ƒIƒŒƒtƒBƒ“‚̊ȕւ©‚ƒƒ^ƒ‹ƒtƒŠ[‚È—§‘Ì‘I‘ð“I‡¬–@‚ÌŠJ”­iƒ|ƒXƒ^[j
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20.                —L‹@G”}‚ð—p‚¢‚éŒ`Ž®“IŠÂ‰»•t‰Á”½‰ž‚ƃLƒ‰ƒ‹Žl’uŠ·’Y‘f‚ð—L‚·‚é•¡‘fŠÂ‡¬‚Ö‚Ì“WŠJiŒû“ªj
*
‘êàV”EAFernando Arteaga-ArteagaA‹g“c‘׎uA—é–Ø’Ê‹±ATue M.-N. NguyenAùˆäG–¾C‘æ44‰ñ•¡‘fŠÂ‰»Šw“¢˜_‰ïCŽD–yŽs–¯ƒz[ƒ‹i–kŠC“¹jC9ŒŽ10`12“úC2014”ND

21.                Enantioselective C–C Bond Forming Reactions Using Vanadium(V) Catalystsiƒ|ƒXƒ^[j
*
‘êàV”EA’ÒŒ´“N–çA¬Ž›ƒ•½A‹g“c‘׎uA²ŒÃ^A‰Í–ì•xˆêAùˆäG–¾C‘æ61‰ñ—L‹@‹à‘®‰»Šw“¢˜_‰ïC‹ãB‘åŠwi•Ÿ‰ªjC9ŒŽ23`25“úC2014”ND

22.                Enantioselective Pd(II)/Pd(IV) Catalysis Utilizing a SPRIX Ligand: Efficient Construction of Chiral 3-Oxy-tetrahydrofuransiƒ|ƒXƒ^[j
*
’|’†˜a_AYogesh D. DhageAùˆäG–¾C‘æ61‰ñ—L‹@‹à‘®‰»Šw“¢˜_‰ïC‹ãB‘åŠwi•Ÿ‰ªjC9ŒŽ23`25“úC2014”ND

23.                —L‹@•ªŽqG”}‚ð—p‚¢‚éƒGƒiƒ“ƒ`ƒI‘I‘ð“I•ªŽq“àRauhut-Currier”½‰ž‚É‚æ‚郿-ƒƒ`ƒŠƒfƒ“-ƒÁ-ƒuƒ`ƒƒ‰ƒNƒ^ƒ€‚ÌŒø—¦“I‡¬iŒû“ªj
‘êàV”EA*ŠÝ“S”nAFernando Arteaga-ArteagaAùˆäG–¾C‘æ64‰ñ“ú–{–òŠw‰ï‹ß‹EŽx•”‘‰ïE‘å‰ïC‹ž“s–ò‰È‘åŠwi‹ž“sjC10ŒŽ11“úC2014”ND

24.                ƒwƒŠƒZƒ“‹y‚уwƒŠƒZƒ“—l‰»‡•¨‚̃Gƒiƒ“ƒ`ƒI‘I‘ð“IŒø—¦‡¬–@‚ÌŠJ”­iƒ|ƒXƒ^[j
‘êàV”EA’ÒŒ´“N–çA*‹g“c‘׎uA¬Ž›ƒ•½A²ŒÃ^A“yˆä‹M—TAùˆäG–¾C‘æ40‰ñ”½‰ž‚Ƈ¬‚Ìi•àƒVƒ“ƒ|ƒWƒEƒ€C“Œ–k‘åŠwi‹{éjC11ŒŽ10`11“úC2014”ND

25.                ‘½’uŠ·«Žl’uŠ·ƒIƒŒƒtƒBƒ“‚Ì—§‘Ì‘I‘ð“I‡¬‚Æ‚»‚̉ž—piƒ|ƒXƒ^[j
*
‘êàV”EAŠÝ“S”nAFernando Arteaga-ArteagaA•½“cCˆêAùˆäG–¾C‘æ40‰ñ”½‰ž‚Ƈ¬‚Ìi•àƒVƒ“ƒ|ƒWƒEƒ€C“Œ–k‘åŠwi‹{éjC11ŒŽ10`11“úC2014”ND

<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 AwardŽóÜ>

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 ƒ¿-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 PrizeŽóÜ>

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 C–H 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 C–C 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 C–C 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 C–H 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 AwardŽóÜ>

40.                Enantioselective C–C 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 ƒ¿-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.

 

Topª

 

2013

<Domestic>

1. Œø‰Ê“I‚È•sĊ‹«‚ðŽ‚ÂSPRIX”zˆÊŽq‚ÌŠJ”­iŒû“ªj
*
—ÑŒ«¡A’|’†˜a_A‘êàV”EAùˆäG–¾C“ú–{‰»Šw‰ï‘æ93t‹G”N‰ïC—§–½ŠÙ‘åŠwiŽ ‰êjC3ŒŽ22`25“úC2013”ND

2. SPRIX”zˆÊŽq‚ðŠˆ—p‚·‚éƒGƒiƒ“ƒ`ƒI‘I‘ð“IPd(II)/Pd(IV)G”}”½‰žFƒLƒ‰ƒ‹‚ȃeƒgƒ‰ƒqƒhƒƒtƒ‰ƒ“—U“±‘̂̌ø—¦“I‡¬iŒû“ªj
*Yogesh D. Dhage
A’|’†˜a_A‘êàV”EAùˆäG–¾C“ú–{‰»Šw‰ï‘æ93t‹G”N‰ïC—§–½ŠÙ‘åŠwiŽ ‰êjC3ŒŽ22`25“úC2013”ND

3. PdƒGƒmƒ‰[ƒg‚̋ɫ“]Š·FPd-SPRIXG”}‚É‚æ‚éƒAƒ‹ƒLƒjƒ‹ƒVƒNƒƒwƒLƒTƒWƒGƒmƒ“‚̊‰»“IƒnƒƒAƒZƒgƒLƒV‰»”½‰žiŒû“ªj
*Suman C. Mohanta
A’|’†˜a_A‘êàV”EAùˆäG–¾C“ú–{‰»Šw‰ï‘æ93t‹G”N‰ïC—§–½ŠÙ‘åŠwiŽ ‰êjC3ŒŽ22`25“úC2013”ND

4. ƒpƒ‰ƒWƒEƒ€G”}‚É‚æ‚éƒCƒ\ƒIƒLƒTƒ][ƒ‹ŠÂ5ˆÊ‚Ì’¼Ú“IC-HŒ‹‡ƒAƒŠ[ƒ‹‰»iŒû“ªj
*
dM‹§ŽuA’|’†˜a_AùˆäG–¾C“ú–{‰»Šw‰ï‘æ93t‹G”N‰ïC—§–½ŠÙ‘åŠwiŽ ‰êjC3ŒŽ22`25“úC2013”ND

5. “ºG”}‚ðŠˆ—p‚·‚éƒXƒsƒƒrƒLƒmƒŠƒ“œŠi‚̃Gƒiƒ“ƒ`ƒI‘I‘ð“I\’ziŒû“ªj
*
²ŒÃ^A’|’†˜a_AùˆäG–¾C“ú–{‰»Šw‰ï‘æ93t‹G”N‰ïC—§–½ŠÙ‘åŠwiŽ ‰êjC3ŒŽ22`25“úC2013”ND

6. ŒõŠwŠˆ«ƒXƒsƒ[4.4]ƒmƒiƒ“œŠi‚ÌG”}“I‡¬‚ðŠî”Õ‚Æ‚·‚é•sÄ—L‹@•ªŽqG”}‚ÌŠJ”­‚Ɖž—piŒû“ªj
*Lulu Fan
A‘êàV”EAùˆäG–¾C“ú–{‰»Šw‰ï‘æ93t‹G”N‰ïC—§–½ŠÙ‘åŠwiŽ ‰êjC3ŒŽ22`25“úC2013”ND

7. ‹@”\«1,2,3-ƒgƒŠƒAƒ][ƒ‹‚ÌŠJ”­‚Æ•sÄ”½‰ž‚Ö‚Ì“WŠJiŒû“ªj
*
‹g“c‘׎uA‘êàV”EAùˆäG–¾C“ú–{‰»Šw‰ï‘æ93t‹G”N‰ïC—§–½ŠÙ‘åŠwiŽ ‰êjC3ŒŽ22`25“úC2013”ND

8. —L‹@•ªŽqG”}‚ð—p‚¢‚éƒGƒiƒ“ƒ`ƒI‘I‘ð“I•ªŽq“àRauhut-Currier”½‰ž‚É‚æ‚郿-ƒƒ`ƒŠƒfƒ“-ƒÁ-ƒuƒ`ƒƒ‰ƒNƒgƒ“—Þ‚ÌŒø—¦‡¬iŒû“ªj
*Tue M.-N.
NguyenAAndré GrossmannA—é–Ø’Ê‹±A‘êàV”EADieter EndersAùˆäG–¾C“ú–{‰»Šw‰ï‘æ93t‹G”N‰ïC—§–½ŠÙ‘åŠwiŽ ‰êjC3ŒŽ22`25“úC2013”ND

9. —L‹@•ªŽqG”}‚É‚æ‚éƒPƒ`ƒ~ƒ“‚ðŠîŽ¿‚Æ‚·‚éƒGƒiƒ“ƒ`ƒI‘I‘ð“Iaza-MBH”½‰ž‚ÌŠJ”­iŒû“ªj
*Fernando Arteaga-Arteaga
A‘êàV”EAEmmanuelle RémondAJérôme BayardonA‹g“c‘׎uASridharan VellaisamyASylvain JugéAùˆäG–¾C“ú–{‰»Šw‰ï‘æ93t‹G”N‰ïC—§–½ŠÙ‘åŠwiŽ ‰êjC3ŒŽ22`25“úC2013”ND

10.                5‰¿‚̃oƒiƒWƒEƒ€G”}‚ð—p‚¢‚éƒGƒiƒ“ƒ`ƒI‘I‘ð“I’Y‘f|’Y‘fŒ‹‡Œ`¬”½‰ž‚ÌŠJ”­‚Ɖž—piŒû“ªj
*
‘êàV”EA¬Ž›ƒ•½AFernando Arteaga-ArteagaA‹g“c‘׎uA‰i“c‰À‘åAùˆäG–¾C“ú–{‰»Šw‰ï‘æ93t‹G”N‰ïC—§–½ŠÙ‘åŠwiŽ ‰êjC3ŒŽ22`25“úC2013”ND

11.                ƒLƒ‰ƒ‹ƒXƒsƒ[4.4]ƒmƒiƒ“œŠi‚̃Gƒiƒ“ƒ`ƒI‘I‘ð“I‡¬–@‚ÌŠJ”­‚Æ•sÄG”}”½‰ž‚ւ̉ž—piƒ|ƒXƒ^[j
*Lulu Fan
A‘êàV”EAùˆäG–¾CSymposium on Molecular Chirality 2013C‹ž“s‘åŠw‹g“cƒLƒƒƒ“ƒpƒXi‹ž“sjC5ŒŽ10`11“úC2013”ND

12.                5‰¿‚Ì“ñŠjƒoƒiƒWƒEƒ€G”}‚ð—p‚¢‚é•sÄ’Y‘f|’Y‘fŒ‹‡Œ`¬”½‰ž‚ÌŠJ”­iƒ|ƒXƒ^[j
*
‘êàV”EA’ÒŒ´“N–çA¬Ž›ƒ•½AFernando Arteaga-ArteagaA‹g“c‘׎uA‰i“c‰À‘åA”©’†–«AùˆäG–¾CSymposium on Molecular Chirality 2013C‹ž“s‘åŠw‹g“cƒLƒƒƒ“ƒpƒXi‹ž“sjC5ŒŽ10`11“úC2013”ND

13.                ƒpƒ‰ƒWƒEƒ€G”}‚É‚æ‚éƒCƒ\ƒIƒLƒTƒ][ƒ‹ŠÂ5ˆÊ‚Ì’¼Ú“IC|HŒ‹‡ƒAƒŠ[ƒ‹‰»iƒ|ƒXƒ^[j
*
dM‹§ŽuA’|’†˜a_AùˆäG–¾C‘æ33‰ñ—L‹@‡¬ŽáŽèƒZƒ~ƒi[C_ŒË‘åŠw˜Zb‘äƒLƒƒƒ“ƒpƒXi•ºŒÉjC8ŒŽ2“úC2013”ND

14.                ƒLƒ‰ƒ‹ƒXƒsƒ[4.4]ƒmƒiƒ“œŠi‚̃Gƒiƒ“ƒ`ƒI‘I‘ð“I‡¬–@‚ÌŠJ”­‚Æ‚»‚̉ž—piƒ|ƒXƒ^[j
Lulu Fan
A*•“à–FŽ÷A‘êàV”EAùˆäG–¾C‘æ33‰ñ—L‹@‡¬ŽáŽèƒZƒ~ƒi[C_ŒË‘åŠw˜Zb‘äƒLƒƒƒ“ƒpƒXi•ºŒÉjC8ŒŽ2“úC2013”ND

15.                —L‹@•ªŽqG”}‚É‚æ‚éƒPƒ`ƒ~ƒ“‚ƃAƒŒƒmƒA[ƒg‚Æ‚ðŠîŽ¿‚Æ‚·‚éƒGƒiƒ“ƒ`ƒI‘I‘ð“Iaza-MBHŒ^ŠÂ‰»”½‰ž‚ÌŠJ”­iƒ|ƒXƒ^[j
*
—é–Ø’Ê‹±A‘êàV”EAFernando Arteaga-ArteagaA‹g“c‘׎uAùˆäG–¾C‘æ33‰ñ—L‹@‡¬ŽáŽèƒZƒ~ƒi[C_ŒË‘åŠw˜Zb‘äƒLƒƒƒ“ƒpƒXi•ºŒÉjC8ŒŽ2“úC2013”ND

16.                Palladium-Catalyzed Direct C5 Arylation of Isoxazolesiƒ|ƒXƒ^[j
*
dM‹§ŽuA’|’†˜a_AùˆäG–¾C‘æ60‰ñ—L‹@‹à‘®‰»Šw“¢˜_‰ïCŠwK‰@‘åŠwi“Œ‹žjC9ŒŽ12`14“úC2013”ND

17.                SPRIX”zˆÊŽq‚ÌŠJ”­‚Ɖž—pi“Á•Êu‰‰j
*
ùˆäG–¾C•½¬25”N“x—L‹@‡¬‰»Šw–k—¤ƒZƒ~ƒi[CÎ쌧­”N‘‡Œ¤CƒZƒ“ƒ^[i‹ž“sjC10ŒŽ4`5“úC2013”ND

18.                —L‹@•ªŽqG”}‚É‚æ‚éƒGƒiƒ“ƒ`ƒI‘I‘ð“I[n+2]ŠÂ‰»•t‰Á”½‰žiƒ|ƒXƒ^[j
*
—é–Ø’Ê‹±A‘êàV”EAFernando Arteaga-ArteagaA‹g“c‘׎uAùˆäG–¾C•½¬25”N“x—L‹@‡¬‰»Šw–k—¤ƒZƒ~ƒi[CÎ쌧­”N‘‡Œ¤CƒZƒ“ƒ^[i‹ž“sjC10ŒŽ4`5“úC2013”ND

19.                Enantioselective Pd(II)/Pd(IV) Catalysis Utilizing SPRIX Ligand: Effective Construction of Chiral Acetoxylated Tetrahydrofuransiƒ|ƒXƒ^[j
*Yogesh D. Dhage
A’|’†˜a_A‘êàV”EAùˆäG–¾C•½¬25”N“x—L‹@‡¬‰»Šw–k—¤ƒZƒ~ƒi[CÎ쌧­”N‘‡Œ¤CƒZƒ“ƒ^[i‹ž“sjC10ŒŽ4`5“úC2013”ND

20.                Catalytic Enantioselective Synthesis of Spiro Compounds and Their Applications to Asymmetric Catalysisiƒ|ƒXƒ^[j
*Lulu Fan
A•“à–FŽ÷A‘êàV”EAùˆäG–¾C•½¬25”N“x—L‹@‡¬‰»Šw–k—¤ƒZƒ~ƒi[CÎ쌧­”N‘‡Œ¤CƒZƒ“ƒ^[i‹ž“sjC10ŒŽ4`5“úC2013”ND

21.                ’¼Ú“IC-HŒ‹‡Šˆ«‰»‚É‚æ‚éƒCƒ\ƒIƒLƒTƒ][ƒ‹ŠÂ5ˆÊ‚̃AƒŠ[ƒ‹‰»”½‰ž‚ÌŠJ”­iƒ|ƒXƒ^[j
*
dM‹§ŽuA’|’†˜a_AùˆäG–¾C•½¬25”N“x—L‹@‡¬‰»Šw–k—¤ƒZƒ~ƒi[CÎ쌧­”N‘‡Œ¤CƒZƒ“ƒ^[i‹ž“sjC10ŒŽ4`5“úC2013”ND

22.                ƒXƒsƒƒrƒ‰ƒNƒ^ƒ€‚ðŠî”Õ‚Æ‚µ‚½V‹KƒLƒ‰ƒ‹”zˆÊŽq‚ÌŠJ”­iƒ|ƒXƒ^[j
*
‚’JC•½Aúá–{Œ[•ãA’|’†˜a_AùˆäG–¾C•½¬25”N“x—L‹@‡¬‰»Šw–k—¤ƒZƒ~ƒi[CÎ쌧­”N‘‡Œ¤CƒZƒ“ƒ^[i‹ž“sjC10ŒŽ4`5“úC2013”ND

23.                ƒLƒ‰ƒ‹”zˆÊŽqSPRIX‚Ì•sĊ‹«‚ÉŠÖ‚·‚錤‹†iƒ|ƒXƒ^[j
*
—ÑŒ«¡A’|’†˜a_A‘êàV”EAùˆäG–¾C•½¬25”N“x—L‹@‡¬‰»Šw–k—¤ƒZƒ~ƒi[CÎ쌧­”N‘‡Œ¤CƒZƒ“ƒ^[i‹ž“sjC10ŒŽ4`5“úC2013”ND

24.                P]ƒLƒ‰ƒ‹—L‹@•ªŽqG”}‚ð—p‚¢‚éŒõŠwŠˆ«4’uŠ·’Y‘f‚̇¬‚Ɖž—piƒ|ƒXƒ^[j
*Fernando Arteaga-Arteaga
A‘êàV”EAEmmanuelle RémondA‹g“c‘׎uAJérôme BayardonASridharan VellaisamyASylvain JugéAùˆäG–¾C•½¬25”N“x—L‹@‡¬‰»Šw–k—¤ƒZƒ~ƒi[CÎ쌧­”N‘‡Œ¤CƒZƒ“ƒ^[i‹ž“sjC10ŒŽ4`5“úC2013”ND
<—DG”­•\ÜŽóÜ>

25.                ƒgƒŠƒAƒ][ƒ‹‚Ì‹@”\‰»‚ðŠî”Õ‚Æ‚·‚é•sÄG”}‚ÌŠJ”­iƒ|ƒXƒ^[j
*
‹g“c‘׎uA‘êàV”EAùˆäG–¾C•½¬25”N“x—L‹@‡¬‰»Šw–k—¤ƒZƒ~ƒi[CÎ쌧­”N‘‡Œ¤CƒZƒ“ƒ^[i‹ž“sjC10ŒŽ4`5“úC2013”ND

26.                1,3]ƒvƒƒpƒ“ƒWƒAƒ~ƒ“•”ˆÊ‚ðŒ®ƒ†ƒjƒbƒg‚Æ‚·‚éƒLƒ‰ƒ‹“ñdŠˆ«‰»Œ^—L‹@•ªŽqG”}‚ÌŠJ”­iƒ|ƒXƒ^[j
*
•½“cCˆêA“c’†_ˆêA¼ˆä‰Ã’ÖçAFernando Arteaga-ArteagaA‹g“c‘׎uA‘êàV”EAùˆäG–¾C•½¬25”N“x—L‹@‡¬‰»Šw–k—¤ƒZƒ~ƒi[CÎ쌧­”N‘‡Œ¤CƒZƒ“ƒ^[i‹ž“sjC10ŒŽ4`5“úC2013”ND

27.                ŒõŠwŠˆ«‘JˆÚ‹à‘®G”}‚ð—p‚¢‚éƒGƒiƒ“ƒ`ƒI‘I‘ð“I‚È2]ƒiƒtƒg[ƒ‹—Þ‚ÌŽ_‰»“IƒJƒbƒvƒŠƒ“ƒO”½‰ž‚ÌŠJ”­iƒ|ƒXƒ^[j
‘êàV”EA’ÒŒ´“N–çA¬Ž›ƒ•½A*H“cŽOrA²ŒÃ^A“yˆä‹M—TA”©’†–«AùˆäG–¾C•½¬25”N“x—L‹@‡¬‰»Šw–k—¤ƒZƒ~ƒi[CÎ쌧­”N‘‡Œ¤CƒZƒ“ƒ^[i‹ž“sjC10ŒŽ4`5“úC2013”ND

28.                ƒGƒiƒ“ƒ`ƒI‘I‘ð“IRauhut-Currier”½‰ž‚ð—p‚¢‚郿-ƒƒ`ƒŠƒfƒ“-ƒÁ-ƒuƒ`ƒƒ‰ƒNƒgƒ“‚̇¬iŒû“ªj
*
‘êàV”EATue M.-N. NguyenAAndré GrossmannA—é–Ø’Ê‹±ADieter EndersAùˆäG–¾C•½¬25”N“x—L‹@‡¬‰»Šw–k—¤ƒZƒ~ƒi[CÎ쌧­”N‘‡Œ¤CƒZƒ“ƒ^[i‹ž“sjC10ŒŽ4`5“úC2013”ND

29.                ƒLƒ‰ƒ‹ƒXƒsƒ‰»‡•¨‚̃Gƒiƒ“ƒ`ƒI‘I‘ð“I‡¬–@‚ÌŠJ”­‚Ɖž—piŒû“ªj
Lulu Fan
A*•“à–FŽ÷A‘êàV”EAùˆäG–¾C‘æ63‰ñ“ú–{–òŠw‰ï‹ß‹EŽx•”‘‰ïE‘å‰ïC“¯ŽxŽÐ—Žq‘åŠw‹ž“c•ÓƒLƒƒƒ“ƒpƒXi‹ž“sjC10ŒŽ12“úC2013”ND

30.                IrG”}‚ð—p‚¢‚郃\ƒWƒI[ƒ‹‚ƃAƒ‹ƒfƒqƒh‚̘A‘±Œ^•săJƒbƒvƒŠƒ“ƒO”½‰ž‚ÌŠJ”­iŒû“ªj
*
—é–ØŒ’”VAÎâ—FAŽü‘å—gA’©–ì–FDAùˆäG–¾C‘æ63‰ñ“ú–{–òŠw‰ï‹ß‹EŽx•”‘‰ïE‘å‰ïC“¯ŽxŽÐ—Žq‘åŠw‹ž“c•ÓƒLƒƒƒ“ƒpƒXi‹ž“sjC10ŒŽ12“úC2013”ND

31.                —L‹@•ªŽqG”}‚É‚æ‚éƒPƒ`ƒ~ƒ“‚Æ2,3|ƒuƒ^ƒWƒGƒ“Ž_ƒGƒXƒeƒ‹‚Æ‚ðŠîŽ¿‚Æ‚·‚éƒGƒiƒ“ƒ`ƒI‘I‘ð“Iaza-MBHŒ^ŠÂ‰»”½‰ž‚ÌŠJ”­iŒû“ªj
*
—é–Ø’Ê‹±A‘êàV”EAFernando Arteaga-ArteagaA‹g“c‘׎uAùˆäG–¾C‘æ63‰ñ“ú–{–òŠw‰ï‹ß‹EŽx•”‘‰ïE‘å‰ïC“¯ŽxŽÐ—Žq‘åŠw‹ž“c•ÓƒLƒƒƒ“ƒpƒXi‹ž“sjC10ŒŽ12“úC2013”ND

32.                Pd-SPRIXG”}‚ðŠˆ—p‚·‚éƒtƒ‰ƒ“—U“±‘̂̃Gƒiƒ“ƒ`ƒI‘I‘ð“I‡¬iŒû“ªj
*
’|’†˜a_ASuman C. MohantaAYogesh D. DhageAùˆäG–¾C‘æ43‰ñ•¡‘fŠÂ‰»Šw“¢˜_‰ïC’·—Çì‘Û‰ï‹cêiŠò•ŒjC10ŒŽ17`19“úC2013”ND

33.                —L‹@•ªŽqG”}‚É‚æ‚éƒPƒ`ƒ~ƒ“‚Æ2,3|ƒuƒ^ƒWƒGƒ“Ž_ƒGƒXƒeƒ‹‚Æ‚ðŠîŽ¿‚Æ‚·‚éƒGƒiƒ“ƒ`ƒI‘I‘ð“Iaza-MBHŒ^ŠÂ‰»”½‰ž‚ÌŠJ”­iƒ|ƒXƒ^[j
*
—é–Ø’Ê‹±A‘êàV”EAFernando Arteaga-ArteagaA‹g“c‘׎uAùˆäG–¾C‘æ39‰ñ”½‰ž‚Ƈ¬‚Ìi•àƒVƒ“ƒ|ƒWƒEƒ€C‹ãB‘åŠw•a‰@ƒLƒƒƒ“ƒpƒXi•Ÿ‰ªjC11ŒŽ5`6“úC2013”ND

34.                “ñŠjƒoƒiƒWƒEƒ€G”}‚ð—p‚¢‚é•sÄ’Y‘f|’Y‘fŒ‹‡Œ`¬”½‰ž‚ÌŠJ”­iŒû“ªj
*
‘êàV”EA’ÒŒ´“N–çA¬Ž›ƒ•½AFernando Arteaga-ArteagaA‹g“c‘׎uA‰i“c‰À‘åA”©’†–«AùˆäG–¾C‘æ39‰ñ”½‰ž‚Ƈ¬‚Ìi•àƒVƒ“ƒ|ƒWƒEƒ€C‹ãB‘åŠw•a‰@ƒLƒƒƒ“ƒpƒXi•Ÿ‰ªjC11ŒŽ5`6“úC2013”ND

<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 Catalysish, 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 Catalysish, 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 C–H 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 AwardŽóÜ>

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.

 

Topª

 

2012

<Domestic>

1. V‹K“ñdŠˆ«‰»Œ^—L‹@•ªŽqG”}‚ÌŠJ”­‚Æ•sÄFriedel-Crafts”½‰ž‚ւ̉ž—piŒû“ªj
*
‰i“c‰À‘åA‘êàV”EAùˆäG–¾C“ú–{‰»Šw‰ï‘æ92t‹G”N‰ïCŒcœä‹`m‘åŠwi_“ÞìjC3ŒŽ25`28“úC2012”ND

2. ƒXƒsƒœŠi‚ð—L‚·‚éŽ_-‰–ŠîŒ^—L‹@•ªŽqG”}‚ð—p‚¢‚½ƒGƒiƒ“ƒ`ƒI‘I‘ð“Iaza-MBH”½‰ž‚ÌŠJ”­iŒû“ªj
*
‰ÆŠìŒ’‘¾A‹ËŽR‹M”üŽqA‘êàV”EAùˆäG–¾C“ú–{‰»Šw‰ï‘æ92t‹G”N‰ïCŒcœä‹`m‘åŠwi_“ÞìjC3ŒŽ25`28“úC2012”ND

3. —L‹@G”}‚ð—p‚¢‚éƒGƒiƒ“ƒ`ƒI‘I‘ð“I•ªŽq“àRauhut-Currier”½‰žiŒû“ªj
*Tue M.-N. Nguyen
AAndré GrossmannA‘êàV”EAùˆäG–¾C“ú–{‰»Šw‰ï‘æ92t‹G”N‰ïCŒcœä‹`m‘åŠwi_“ÞìjC3ŒŽ25`28“úC2012”ND

4. ŒõŠwŠˆ«1,2,3-ƒgƒŠƒAƒ][ƒ‹—U“±‘̂̇¬‚Æ•sÄ”½‰ž‚ւ̉ž—piŒû“ªj
*
‹g“c‘׎uA‘êàV”EAùˆäG–¾C“ú–{‰»Šw‰ï‘æ92t‹G”N‰ïCŒcœä‹`m‘åŠwi_“ÞìjC3ŒŽ25`28“úC2012”ND

5. Pd-SPRIXG”}‚ð—p‚¢‚é4]ƒAƒ‹ƒPƒ“Ž_‚̃Gƒiƒ“ƒ`ƒI‘I‘ð“I‚È•ªŽq“àŽ_‰»“IƒAƒŠƒ‹ˆÊC–HŒ‹‡ƒGƒXƒeƒ‹‰»”½‰žiŒû“ªj
*
H“cŽOrA’JŠ_—E„A’|’†˜a_A‘êàV”EAùˆäG–¾C“ú–{‰»Šw‰ï‘æ92t‹G”N‰ïCŒcœä‹`m‘åŠwi_“ÞìjC3ŒŽ25`28“úC2012”ND

6. Pd-SPRIXG”}‚É‚æ‚éƒGƒiƒ“ƒ`ƒI‘I‘ð“I‚ÈŽ_‰»“IŠÂ‰»]ƒJƒ‹ƒ{ƒLƒVƒ‹‰»˜A‘±”½‰žFPd|ƒGƒmƒ‰[ƒg’†ŠÔ‘̂̃Jƒ‹ƒ{ƒLƒVƒ‹‰»iŒû“ªj
* S. C. Mohanta
A’|’†˜a_A‘êàV”EAùˆäG–¾C“ú–{‰»Šw‰ï‘æ92t‹G”N‰ïCŒcœä‹`m‘åŠwi_“ÞìjC3ŒŽ25`28“úC2012”ND

7. ƒLƒ‰ƒ‹ƒXƒsƒƒrƒ‰ƒNƒ^ƒ€‚ðŠî”Õ‚Æ‚·‚éV‹Kƒ`ƒIƒAƒ~ƒhŒ^”zˆÊŽq‚ÌŠJ”­iŒû“ªj
*
‚’JC•½A’|’†˜a_AùˆäG–¾C“ú–{‰»Šw‰ï‘æ92t‹G”N‰ïCŒcœä‹`m‘åŠwi_“ÞìjC3ŒŽ25`28“úC2012”ND

8. ƒLƒ‰ƒ‹”zˆÊŽqSPRIX ‚Ì•sĊ‹«‚ÉŠÖ‚·‚錤‹†iŒû“ªj
*
—ÑŒ«¡A’|’†˜a_A‘êàV”EAùˆäG–¾C“ú–{‰»Šw‰ï‘æ92t‹G”N‰ïCŒcœä‹`m‘åŠwi_“ÞìjC3ŒŽ25`28“úC2012”ND

9. ƒGƒiƒ“ƒ`ƒI‘I‘ð“IPd(II)/Pd(IV)G”}‚É‚æ‚éƒAƒ‹ƒPƒjƒ‹ƒAƒ‹ƒR[ƒ‹‚ÌŽ_‰»“I•ªŽq“àŠÂ‰»”½‰žiŒû“ªj
*Yogesh Daulat Dhage
A’|’†˜a_A‘êàV”EAùˆäG–¾C“ú–{‰»Šw‰ï‘æ92t‹G”N‰ïCŒcœä‹`m‘åŠwi_“ÞìjC3ŒŽ25`28“úC2012”ND

10.                IrG”}‚ð—p‚¢‚郃\ƒWƒI[ƒ‹‚ƃAƒ‹ƒfƒqƒh‚̘A‘±Œ^•săJƒbƒvƒŠƒ“ƒO”½‰ž‚ÌŠJ”­iŒû“ªj
—é–ØŒ’”VA*Îâ—FAŽü‘å—gA’©–ì–FDAùˆäG–¾C“ú–{‰»Šw‰ï‘æ92t‹G”N‰ïCŒcœä‹`m‘åŠwi_“ÞìjC3ŒŽ25`28“úC2012”ND

11.                “ºG”}‚ðŠˆ—p‚·‚éƒLƒ‰ƒ‹ƒXƒsƒœŠi‚ÌŠÈ•Ö\’ziŒû“ªj
*
’|’†˜a_AùˆäG–¾C“ú–{‰»Šw‰ï‘æ92t‹G”N‰ïCŒcœä‹`m‘åŠwi_“ÞìjC3ŒŽ25`28“úC2012”ND

12.                Pd-SPRIXG”}‚É‚æ‚éƒGƒiƒ“ƒ`ƒI‘I‘ð“I‚ÈŽ_‰»“IŠÂ‰»]ƒJƒ‹ƒ{ƒLƒVƒ‹‰»˜A‘±”½‰žFPd|ƒGƒmƒ‰[ƒg’†ŠÔ‘̂̃Jƒ‹ƒ{ƒLƒVƒ‹‰»iŒû“ªj
*Suman C. Mohanta
A’|’†˜a_A‘êàV”EAùˆäG–¾CSymposium on Molecular Chirality ASIA 2012C‹ãB‘åŠwi•Ÿ‰ªjC5ŒŽ17`18“úC2012”ND

13.                ƒGƒiƒ“ƒ`ƒI‘I‘ð“IPd(II)/Pd(IV)G”}‚É‚æ‚éƒAƒ‹ƒPƒjƒ‹ƒAƒ‹ƒR[ƒ‹‚ÌŽ_‰»“I•ªŽq“àŠÂ‰»”½‰žiƒ|ƒXƒ^[j
*Yogesh D. Dhage
A’|’†˜a_A‘êàV”EAùˆäG–¾CSymposium on Molecular Chirality ASIA 2012C‹ãB‘åŠwi•Ÿ‰ªjC5ŒŽ17`18“úC2012”ND

14.                —L‹@•ªŽqG”}‚É‚æ‚éƒPƒ`ƒ~ƒ“‚ðŠîŽ¿‚Æ‚·‚éaza-MBH”½‰žiƒ|ƒXƒ^[j
‘êàV”EAEmmanuelle RémondA*Fernando Arteaga-ArteagaAJérôme BayardonA‹g“c‘׎uASylvain JugéAùˆäG–¾CSymposium on Molecular Chirality ASIA 2012C‹ãB‘åŠwi•Ÿ‰ªjC5ŒŽ17`18“úC2012”ND

15.                Enantioselective Synthesis of Multifunctional Compounds via Bifunctional OrganocatalysisiŒû“ªj
*‘êàV”EC•¶•”‰ÈŠwȉȊwŒ¤‹†”ï•â•‹àuVŠwp—̈挤‹†iŒ¤‹†—̈æ’ñˆÄŒ^jE—L‹@•ªŽqG”}v‘æ1‰ñ‘S‘̉ï‹cC‹ž“s‘åŠwi‹ž“sjC6ŒŽ8`9“úC2012”ND

16.                Pd-SPRIXG”}‚É‚æ‚é4|ƒAƒ‹ƒPƒ“Ž_‚ÌŽ_‰»“IƒAƒŠƒ‹ˆÊC-HŒ‹‡Šˆ«‰»‚ðŒo‚éƒGƒiƒ“ƒ`ƒI‘I‘ð“IŠÂ‰»”½‰žiƒ|ƒXƒ^[j
*H“cŽOrA’JŠ_—E„A’|’†˜a_A‘êàV”EAùˆäG–¾C‘æ39‰ñ—L‹@”½‰ž§’k‰ïCŠÖ¼‘åŠwi‘åãjC8ŒŽ3“úC2012”ND

17.                “ºG”}‚ðŠˆ—p‚·‚éƒXƒsƒƒrƒLƒmƒŠƒ“œŠi‚̃Gƒiƒ“ƒ`ƒI‘I‘ð“I\’ziƒ|ƒXƒ^[j
*²ŒÃ^A’|’†˜a_AùˆäG–¾C‘æ39‰ñ—L‹@”½‰ž§’k‰ïCŠÖ¼‘åŠwi‘åãjC8ŒŽ3“úC2012”ND

18.                ƒLƒ‰ƒ‹ƒXƒsƒƒrƒ‰ƒNƒ^ƒ€‚ðŠî”Õ‚Æ‚·‚éV‹Kƒ`ƒIƒAƒ~ƒhŒ^”zˆÊŽq‚ÌŠJ”­iƒ|ƒXƒ^[j
*‚’JC•½A’|’†˜a_AùˆäG–¾C‘æ39‰ñ—L‹@”½‰ž§’k‰ïCŠÖ¼‘åŠwi‘åãjC8ŒŽ3“úC2012”ND

19.                “ñdŠˆ«‰»Œ^—L‹@•ªŽqG”}‚ð—p‚¢‚éƒLƒ‰ƒ‹‘½Š¯”\«‰»‡•¨‚̇¬‚Ɖž—piŒû“ªj
*‘êàV”EC•¶•”‰ÈŠwȉȊwŒ¤‹†”ï•â•‹àuVŠwp—̈挤‹†iŒ¤‹†—̈æ’ñˆÄŒ^jE—L‹@•ªŽqG”}v‘æ1‰ñ—L‹@•ªŽqG”}@ŽáŽèƒZƒ~ƒi[Cƒ‰ƒtƒH[ƒŒ“ß{i“È–ØjC9ŒŽ8`9“úC2012”ND

20.                Umpolung Reactivity of Pd Enolate: Cyclative Diacetoxylation of Alkynyl Cyclohexadienones Catalyzed by Pd-SPRIXiŒû“ªj
*’|’†˜a_ASuman C. MohantaA‘êàV”EAùˆäG–¾C‘æ59‰ñ—L‹@‹à‘®‰»Šw“¢˜_‰ïC‘åã‘åŠwi‘åãjC9ŒŽ13`15“úC2012”ND

21.                Study on Asymmetric Environment of SPRIX Ligandiƒ|ƒXƒ^[j
*—ÑŒ«¡A’|’†˜a_A‘êàV”EAùˆäG–¾C‘æ59‰ñ—L‹@‹à‘®‰»Šw“¢˜_‰ïC‘åã‘åŠwi‘åãjC9ŒŽ13`15“úC2012”ND

22.                Enantioselective Coupling of Phenanthrols Using Vanadium Catalystsiƒ|ƒXƒ^[j
*
¬Ž›ƒ•½A‘êàV”EAùˆäG–¾C‘æ59‰ñ—L‹@‹à‘®‰»Šw“¢˜_‰ïC‘åã‘åŠwi‘åãjC9ŒŽ13`15“úC2012”ND

23.                Ir Catalyzed Asymmetric Tandem Reaction of meso-Diols and Aldehydesiƒ|ƒXƒ^[j
*—é–ØŒ’”VAÎâ—FAŽü‘å—gA’©–ì–FDAùˆäG–¾C‘æ59‰ñ—L‹@‹à‘®‰»Šw“¢˜_‰ïC‘åã‘åŠwi‘åãjC9ŒŽ13`15“úC2012”ND

24.                ƒLƒ‰ƒ‹ƒXƒsƒƒrƒ‰ƒNƒ^ƒ€‚ðŠî”Õ‚Æ‚·‚éV‹Kƒ`ƒIƒAƒ~ƒhŒ^”zˆÊŽq‚ÌŠJ”­iƒ|ƒXƒ^[j
*‚’JC•½A’|’†˜a_AùˆäG–¾C‘æ42‰ñ•¡‘fŠÂ‰»Šw“¢˜_‰ïC‹ž“sƒeƒ‹ƒTi‹ž“sjC10ŒŽ11`13“úC2012”ND

25.                —L‹@•ªŽqG”}‚É‚æ‚éƒPƒ`ƒ~ƒ“‚ðŠîŽ¿‚Æ‚·‚é•sÄaza-MBH”½‰žiŒû“ªj
‘êàV”EAEmmanuelle RémondA*Fernando Arteaga ArteagaAJérôme BayardonA‹g“c‘׎uASylvain JugéAùˆäG–¾C‘æ62‰ñ“ú–{–òŠw‰ï‹ß‹EŽx•”‘‰ïE‘å‰ïC•ŒÉì—Žq‘åŠwi•ºŒÉjC10ŒŽ20“úC2012”ND

26.                ƒoƒiƒWƒEƒ€G”}‚ð—p‚¢‚éƒGƒiƒ“ƒ`ƒI‘I‘ð“I’Y‘f|’Y‘fŒ‹‡Œ`¬”½‰ž‚ÌŠJ”­‚Ɖž—piŒû“ªj
*
‘êàV”EAFernando Arteaga-ArteagaA‹g“c‘׎uA¬Ž›ƒ•½A‰i“c‰À‘åAùˆäG–¾C‘æ62‰ñ“ú–{–òŠw‰ï‹ß‹EŽx•”‘‰ïE‘å‰ïC•ŒÉì—Žq‘åŠwi•ºŒÉjC10ŒŽ20“úC2012”ND

27.                —L‹@•ªŽqG”}‚É‚æ‚éƒPƒ`ƒ~ƒ“‚ðŠîŽ¿‚Æ‚·‚é•sÄaza-MBH”½‰žiƒ|ƒXƒ^[j
‘êàV”EAEmmanuelle RémondA*Fernando Arteaga-ArteagaAJérôme BayardonA‹g“c‘׎uASridharan VellaisamyASylvain JugéAùˆäG–¾C‘æ5‰ñ—L‹@G”}ƒVƒ“ƒ|ƒWƒEƒ€CŠwK‰@‘åŠwi“Œ‹žjC10ŒŽ26`27“úC2012”ND

<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 gSPRIXh (Invited)
*
Sasai, H. BITfs 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 gSPRIXh (Invited)
*
Sasai, H. Cambodian Malaysian Chemical Conference (CMCC) 2012, Siem Reap, Cambodia, October 19-21, 2012.

19.                Development of Chiral Spiro Bis(isoxazoline) Ligand gSPRIXh (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 Catalysish, 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 Catalysish, 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 Catalysish, 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 Catalysish, 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.

 

Topª

 

2011

<Domestic>

1. V‹KƒXƒsƒƒrƒXƒgƒŠƒAƒ][ƒ‹—U“±‘̂̌ø—¦‡¬–@‚ÌŠJ”­‚Æ•sÄ”½‰ž‚ւ̉ž—piŒû“ªj
*
‹g“c‘׎uA‘êàV”EAùˆäG–¾C“ú–{‰»Šw‰ï‘æ91t‹G”N‰ïC_“Þì‘åŠwi_“ÞìjC3ŒŽ26`29“úC2011”ND

2. —L‹@•ªŽqG”}‚É‚æ‚éƒGƒiƒ“ƒ`ƒI‘I‘ð“I•ªŽq“àƒNƒƒXƒ}ƒCƒPƒ‹”½‰ž‚ÌŠJ”­‚Ɖž—piŒû“ªj
*Nguyen, Tue Minh-Nhat
Aæâ“~—ÑA‘êàV”EAùˆäG–¾C“ú–{‰»Šw‰ï‘æ91t‹G”N‰ïC_“Þì‘åŠwi_“ÞìjC3ŒŽ26`29“úC2011”ND

3. Ž_‰–ŠîŒ^—L‹@•ªŽqG”}‚ð—p‚¢‚éƒGƒiƒ“ƒ`ƒI‘I‘ð“IMBH”½‰ž‚ÌŠJ”­iŒû“ªj
*
‘ºã^–ëA‘êàV”EAùˆäG–¾C“ú–{‰»Šw‰ï‘æ91t‹G”N‰ïC_“Þì‘åŠwi_“ÞìjC3ŒŽ26`29“úC2011”ND

4. ƒXƒsƒœŠi‚ð—L‚·‚éŽ_-‰–ŠîŒ^•sÄ—L‹@•ªŽqG”}‚ÌŠJ”­iŒû“ªj
*
‹ËŽR‹M”üŽqA‰ÆŠìŒ’‘¾A‘êàV”EAùˆäG–¾C“ú–{‰»Šw‰ï‘æ91t‹G”N‰ïC_“Þì‘åŠwi_“ÞìjC3ŒŽ26`29“úC2011”ND

5. Ž_-‰–ŠîŒ^ŒÅ’艻—L‹@•ªŽqG”}‚ÌŠJ”­iŒû“ªj
*
•½“cCˆêAˆäã’¼lA‘êàV”EAùˆäG–¾C“ú–{‰»Šw‰ï‘æ91t‹G”N‰ïC_“Þì‘åŠwi_“ÞìjC3ŒŽ26`29“úC2011”ND

6. Pd-SPRIXG”}‚É‚æ‚éŠÂ‰»‚𔺂¤ƒAƒ‹ƒLƒjƒ‹ƒVƒNƒƒwƒLƒTƒWƒGƒmƒ“‚̃Gƒiƒ“ƒ`ƒI‘I‘ð“IƒWƒAƒZƒgƒLƒV‰»”½‰žiŒû“ªj
*Mohanta, Suman Chandra
A’|’†˜a_A‘êàV”EA—é–ØŒ’”VAùˆäG–¾C“ú–{‰»Šw‰ï‘æ91t‹G”N‰ïC_“Þì‘åŠwi_“ÞìjC3ŒŽ26`29“úC2011”ND

7. Pd-SPRIXG”}‚Å‘£i‚³‚ê‚éƒÀ,ƒÁ-•s–O˜aƒJƒ‹ƒ{ƒ“Ž_—Þ‚Ì5-endo-trigŒ^ŠÂ‰»”½‰ž‹@\‚ÌDFTŒvŽZ‚É‚æ‚élŽ@iŒû“ªj
Gabr, Randa Kasem Mohamed
ABajracharya, Gan B.A—ÑŒ«¡A’|’†˜a_A‘êàV”EA‰ª“c‹gOA”©ŽR‘ôŽŸA’†‘º³Ž¡AùˆäG–¾C“ú–{‰»Šw‰ï‘æ91t‹G”N‰ïC_“Þì‘åŠwi_“ÞìjC3ŒŽ26`29“úC2011”ND

8. —°‰©‚ðƒhƒi[Œ´Žq‚Æ‚·‚éV‹KƒLƒ‰ƒ‹ƒXƒsƒŒ^”zˆÊŽq‚ÌŠJ”­iŒû“ªj
‚’JC•½A’|’†˜a_AùˆäG–¾C“ú–{‰»Šw‰ï‘æ91t‹G”N‰ïC_“Þì‘åŠwi_“ÞìjC3ŒŽ26`29“úC2011”ND

9. ‘½‹@”\•sÄG”}‚ÌŠJ”­‚ÆG”}“I•sÄ”½‰ž‚ւ̉ž—piŽóÜu‰‰j
*ùˆäG–¾CSymposium on Molecular Chirality 2011C“Œ‹žH‹Æ‘åŠwi“Œ‹žjC5ŒŽ20`21“úC2011”ND

10.                Pd−SPRIXG”}‚É‚æ‚é4−ƒAƒ‹ƒPƒ“Ž_‚ÌŽ_‰»“IƒAƒŠƒ‹ˆÊC−HŒ‹‡ƒGƒXƒeƒ‹‰»‚ðŒo‚éƒGƒiƒ“ƒ`ƒI‘I‘ð“IŠÂ‰»”½‰žiƒ|ƒXƒ^[j
*H“cŽOrA’JŠ_—E„A’|’†˜a_A‘êàV”EAùˆäG–¾CSymposium on Molecular Chirality 2011C“Œ‹žH‹Æ‘åŠwi“Œ‹žjC5ŒŽ20`21“úC2011”ND

11.                Ž_‰–ŠîŒ^—L‹@•ªŽqG”}‚ð—p‚¢‚éƒGƒiƒ“ƒ`ƒI‘I‘ð“I”½‰ž‚ÌŠJ”­iƒ|ƒXƒ^[j
*‰ÆŠìŒ’‘¾A‹ËŽR‹M”üŽqA‘êàV”EAùˆäG–¾CSymposium on Molecular Chirality 2011C“Œ‹žH‹Æ‘åŠwi“Œ‹žjC5ŒŽ20`21“úC2011”ND

12.                V‹KƒXƒsƒƒgƒŠƒAƒ][ƒ‹—U“±‘̂̌ø—¦“I‡¬–@‚ÌŠJ”­‚Æ•sÄ”½‰ž‚ւ̉ž—piƒ|ƒXƒ^[j
*‹g“c‘׎uA‘êàV”EAùˆäG–¾CSymposium on Molecular Chirality 2011C“Œ‹žH‹Æ‘åŠwi“Œ‹žjC5ŒŽ20`21“úC2011”ND

13.                ƒoƒiƒWƒEƒ€G”}‚ð—p‚¢‚é9−ƒtƒFƒiƒ“ƒgƒ[ƒ‹—Þ‚Ì•sÄŽ_‰»ƒJƒbƒvƒŠƒ“ƒO”½‰žiƒ|ƒXƒ^[j
*¬Ž›ƒ•½ADoss RajeshA•ÐŽR’q”üA‘êàV”EAùˆäG–¾CSymposium on Molecular Chirality 2011C“Œ‹žH‹Æ‘åŠwi“Œ‹žjC5ŒŽ20`21“úC2011”ND

14.                Ž_‰–ŠîŒ^—L‹@•ªŽqG”}‚ð—p‚¢‚éƒGƒiƒ“ƒ`ƒI‘I‘ð“I”½‰ž‚ÌŠJ”­iƒ|ƒXƒ^[j
*‰ÆŠìŒ’‘¾A‹ËŽR‹M”üŽqA‘êàV”EAùˆäG–¾C‘æ38‰ñ—L‹@”½‰ž§’k‰ïC‘åã•{—§‘åŠwi‘åãjC8ŒŽ3“úC2011”ND

15.                Enantioselective Cyclization of 4-Alkenoic Acids via an Oxidative Allylic C−H Esterification Promoted by Pd−SPRIX Catalystiƒ|ƒXƒ^[j
*H“cŽOrA’JŠ_—E„A’|’†˜a_A‘êàV”EAùˆäG–¾C‘æ38‰ñ—L‹@”½‰ž§’k‰ïC‘åã•{—§‘åŠwi‘åãjC8ŒŽ3“úC2011”ND

16.                5‰¿‚̃oƒiƒWƒEƒ€G”}‚ð—p‚¢‚éƒGƒiƒ“ƒ`ƒI‘I‘ð“I’Y‘f|’Y‘fŒ‹‡Œ`¬”½‰ž‚ÌŠJ”­‚Ɖž—piƒ|ƒXƒ^[j
*¬Ž›ƒ•½ADoss RajeshA•ÐŽR’q”üA‘êàV”EAùˆäG–¾C‘æ38‰ñ—L‹@”½‰ž§’k‰ïC‘åã•{—§‘åŠwi‘åãjC8ŒŽ3“úC2011”ND

17.                Enantioselective Cyclization of 4-Alkenoic Acids via an Oxidative Allylic C−H Esterification Promoted by Pd−SPRIX Catalystiƒ|ƒXƒ^[j
*H“cŽOrA’JŠ_—E„A’|’†˜a_A‘êàV”EAùˆäG–¾C‘æ58‰ñ—L‹@‹à‘®‰»Šw“¢˜_‰ïC–¼ŒÃ‰®‘åŠwi–¼ŒÃ‰®jC9ŒŽ7`9“úC2011”ND

18.                Development of Chiral Thioamide Ligands Based on a Spirobilactamiƒ|ƒXƒ^[j
*‚’JC•½Aúá–{Œ[•ãA’|’†˜a_AùˆäG–¾C‘æ58‰ñ—L‹@‹à‘®‰»Šw“¢˜_‰ïC–¼ŒÃ‰®‘åŠwi–¼ŒÃ‰®jC9ŒŽ7`9“úC2011”ND

19.                V‹KƒXƒsƒƒgƒŠƒAƒ][ƒ‹—U“±‘̂̌ø—¦“I‡¬–@‚ÌŠJ”­‚Ɖž—piƒ|ƒXƒ^[j
*‹g“c‘׎uA‘êàV”EAùˆäG–¾C‘æ41‰ñ•¡‘fŠÂ‰»Šw“¢˜_‰ïC’é‘åŠwiŒF–{jC10ŒŽ20`22“úC2011”ND

20.                5‰¿‚̃oƒiƒWƒEƒ€G”}‚ð—p‚¢‚éƒGƒiƒ“ƒ`ƒI‘I‘ð“I’Y‘f|’Y‘fŒ‹‡Œ`¬”½‰ž‚ÌŠJ”­‚Ɖž—piƒ|ƒXƒ^[j
*¬Ž›ƒ•½ADoss RajeshA•ÐŽR’q”üA‘êàV”EAùˆäG–¾C‘æ37‰ñ”½‰ž‚Ƈ¬‚Ìi•àƒVƒ“ƒ|ƒWƒEƒ€C‚ ‚킬‚ñƒz[ƒ‹i“¿“‡jC11ŒŽ7`8“úC2011”ND

21.                V‹KƒGƒiƒ“ƒ`ƒI‘I‘ð“IG”}”½‰žŒn‚ÌŠJ‘ñiµ‘Òu‰‰j
*ùˆäG–¾C–kŠC“¹‘åŠwGCOE‘æ‚P‚V‰ñ¸–§‡¬‰»ŠwƒZƒ~ƒi[ ƒWƒ‡ƒCƒ“ƒgƒVƒ“ƒ|ƒWƒEƒ€C–kŠC“¹‘åŠwi–kŠC“¹jC12ŒŽ19“úC2011”ND

<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 gSPRIXh (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 C−H Esterification (Oral)
*M. Akita, Y. Tanigaki, K. Takenaka, S. Takizawa, H. Sasai, The 2nd Seleca Minisymposium, Aachen, German, December 13, 2011.

 

Topª

 

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 ƒÀ,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)-1,1f-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.

 

Topª

 

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.

 

Topª

 

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 Buchwald–Hartwig 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 Buchwald–Hartwig 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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