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.
*‹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.
*ˆÀ“cC; ‹ß“¡Œ’; ‘êàV”E; ùˆäG–¾ “ú–{‰»Šw‰ï ‘æ102”N‰ïi2022jyƒIƒ“ƒ‰ƒCƒ“ŠJÃz, 3ŒŽ26“ú, 2022”N.
*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.
*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 applicationiΞһӥ\j
*Chandu G. Krishnan; ‹ß“¡Œ’; ’†‘ºŒ°⽃; ‘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 HydroxycarbazolesiΞһӥ\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 DONAC²ŒÃ^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 (Ξһ)
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. WathsalaAŠÝ“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
CompoundsiΞһj
*–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 SenA’|’†˜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. ChakiAJianfei 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
PhenolsiΞһj
*™›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 HydroxycarbazolesiΞһj
*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
PhenolsiΞһj
*–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. WathsalaA‘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. WathsalaAŠÝ“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‹@•ªŽq−ƒpƒ‰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
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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.
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*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.
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*“Œ“cŒbŒÞA²ŒÃ^A‘êàV”EAùˆäG–¾C‘æ38‰ñ—L‹@‡¬ŽáŽèƒZƒ~ƒi[CŠÖ¼Šw‰@‘åŠw@¼‹{ブŒ´ƒLƒƒƒ“ƒpƒXi•ºŒÉjC8ŒŽ7“úC2018”ND
31.
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*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.
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*“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
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35.
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*‘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.
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*‰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.
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 SenA’|’†˜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. AbozeidA‘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. ChakiAJianfei 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 UmpolungiΞһj
*–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 EsteriΞһj
*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)iΞһj
*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)iΞһj
*–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 iΞһj
–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 SenA’|’†˜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 AbhijitA*•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 DerivativesiΞһj
*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 AbhijitA’|’†˜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.
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. ChakiA˜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. AbozeidA‘êàV”EAùˆäG–¾C“ú–{‰»Šw‰ï‘æ96t‹G”N‰ïC“¯ŽuŽÐ‘åŠwi‹ž“sjC3ŒŽ24`27“úC2016”ND
10.
Catalytic and
Enantioselective Synthesis of Heterohelicene
DerivativesiΞһj
*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 WateriΞһj
*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) ComplexiΞһj
*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 CatalystsiΞһj
*‘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. AbozeidA‘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 CyclohexadienonesiΞһj
*’|’†˜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.
<Domestic>
1. ƒpƒ‰ƒWƒEƒ€G”}‚ð—p‚¢‚éƒAƒ‹ƒPƒjƒ‹ƒIƒLƒVƒ€‚̃Gƒiƒ“ƒ`ƒI‘I‘ð“IŠÂ‰»\ŠÂ‰»•t‰Á”½‰žiŒû“ªj
*Mohamed A. AbozeidA‘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 OrganocatalystiΞһj
*•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 OrganocatalysisiΞһj
*•“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 FunctionalitiesiΞһj
*—ÑŒ«¡A’|’†˜a_AùˆäG–¾C“ú–{‰»Šw‰ï‘æ95t‹G”N‰ïC“ú–{‘åŠwiç—tjC3ŒŽ26`29“úC2015”ND
12.
Ir-Catalyzed
Asymmetric Tishchenko Type ReactioniΞһj
—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. MohantaAàV“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 UmpolungiΞһj
*’|’†˜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
*–kìŽÑ‰›‡A‹gì—tA—é–Ø—œŽÑA‘êàV”EA‹ËŒ´³”VC‘æ41‰ñ”½‰ž‚Ƈ¬‚Ìi•àƒVƒ“ƒ|ƒWƒEƒ€C‹ß‹E‘åŠw“Œ‘åãƒLƒƒƒ“ƒpƒXi‘åãjC10ŒŽ26`27“úC2015”N.
26.
ƒoƒiƒWƒEƒ€G”}‚ðŠˆ—p‚·‚éƒwƒeƒƒwƒŠƒZƒ“—U“±‘̂̃Gƒiƒ“ƒ`ƒI‘I‘ð“I‡¬–@‚ÌŠJ”iƒ|ƒXƒ^[j
*ˆê”V£˜a–íA²ŒÃ^A•“à–FŽ÷A‘êàV”EA’ÒŒ´“N–çA¬Ž›ƒ•½A‰Í–ì•xˆêAùˆäG–¾C‘æ41‰ñ”½‰ž‚Ƈ¬‚Ìi•àƒVƒ“ƒ|ƒWƒEƒ€C‹ß‹E‘åŠw“Œ‘åãƒLƒƒƒ“ƒpƒXi‘åãjC10ŒŽ26`27“úC2015”N.
<International>
1. Palladium-Catalyzed Direct C5 Arylation of Isoxazoles:
Mechanistic Study and Application (Oral)
*Shigenobu, M.; Takenaka, K.; Sasai, H. Biotechnology and Chemistry for Green Growth (Aachen-Osaka Joint Symposium), Osaka, Japan, March
10-11, 2015.
2. Palladium-Catalyzed Direct 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.
<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
*‹g“c‘׎uA‘êàV”EAùˆäG–¾C“ú–{‰»Šw‰ï‘æ94t‹G”N‰ïC–¼ŒÃ‰®‘åŠwiˆ¤’mjC3ŒŽ27`30“úC2014”ND
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 DasA’|’†˜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
*‘êàV”EA’ÒŒ´“N–çA¬Ž›ƒ•½AH“cŽOrA‹g“c‘׎uA²ŒÃ^A“yˆä‹M—TA”©’†–«AùˆäG–¾C“ú–{‰»Šw‰ï‘æ94t‹G”N‰ïC–¼ŒÃ‰®‘åŠwiˆ¤’mjC3ŒŽ27`30“úC2014”ND
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] CycloadditioniΞһj
*Fernando Arteaga-ArteagaA‘êàV”EAùˆäG–¾C“ú–{‰»Šw‰ï‘æ94t‹G”N‰ïC–¼ŒÃ‰®‘åŠwiˆ¤’mjC3ŒŽ27`30“úC2014”ND
12.
Enantioselective
Palladium(II) Catalyzed Cyclization-Cycloaddition Cascade ReactionsiΞһj
*Abozeid Mohamed AhmedA‘êàV”EAùˆäG–¾C“ú–{‰»Šw‰ï‘æ94t‹G”N‰ïC–¼ŒÃ‰®‘åŠwiˆ¤’mjC3ŒŽ27`30“úC2014”ND
13.
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‘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
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*‘êàV”ECu—L‹@•ªŽqG”}‚É‚æ‚é–¢—ˆŒ^•ªŽq•ÏŠ·v‘æ4‰ñŒöŠJƒVƒ“ƒ|ƒWƒEƒ€(•ªŽqŠˆ«‰»|—L‹@•ªŽqG”}‡“¯ƒVƒ“ƒ|ƒWƒEƒ€)A–kŠC“¹‘åŠwi–kŠC“¹jC6ŒŽ20`21“úC2014”ND
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*‘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.
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*àV“c˜a–íA‚’JC•½A’|’†˜a_AùˆäG–¾C‘æ34‰ñ—L‹@‡¬ŽáŽèƒZƒ~ƒi[C‘åã‘åŠwi‘åãjC8ŒŽ5“úC2014”ND
19.
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<—DGŒ¤‹†”•\ÜŽóÜ>
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.
<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. DhageA’|’†˜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. MohantaA’|’†˜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 FanA‘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-ArteagaA‘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 FanA‘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 FanA*•“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. DhageA’|’†˜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 FanA•“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-ArteagaA‘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 FanA*•“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.
<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. NguyenAAndré 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. MohantaA’|’†˜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 DhageA’|’†˜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. MohantaA’|’†˜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. DhageA’|’†˜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 OrganocatalysisiΞһj
*‘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-SPRIXiΞһj
*’|’†˜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.
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-NhatAæâ“~—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 ChandraA’|’†˜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 MohamedABajracharya, 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.
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.
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 Buchwald–Hartwig 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.
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.
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.
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.
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-NanoscienceÓ 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-NanoscienceÓ 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-NanoscienceÓ 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-NanoscienceÓ 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-NanoscienceÓ 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-NanoscienceÓ 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-NanoscienceÓ 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-NanoscienceÓ 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-NanoscienceÓ 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-NanoscienceÓ 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.
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), MŽrida 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-NanoscienceÓ 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-NanoscienceÓ 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-NanoscienceÓ 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-NanoscienceÓ 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-NanoscienceÓ 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-NanoscienceÓ 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-NanoscienceÓ 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-NanoscienceÓ 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.
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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