| Project/Area Number |
05554016
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| Research Category |
Grant-in-Aid for Developmental Scientific Research (B)
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| Allocation Type | Single-year Grants |
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| Research Field |
Organic chemistry
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| Research Institution | Nagoya University |
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Principal Investigator |
NOYORI Ryoji Nagoya University Department of Chemistry Graduste School of Science Professor, 大学院・理学研究科, 教授 (50022554)
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| Co-Investigator(Kenkyū-buntansha) |
NAGAMURA Toshihiko Unisok Research Institute ; Director, 主任研究員
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| Project Period (FY) |
1993 – 1995
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| Project Status |
Completed (Fiscal Year 1995)
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| Budget Amount *help |
¥18,000,000 (Direct Cost: ¥18,000,000)
Fiscal Year 1995: ¥1,000,000 (Direct Cost: ¥1,000,000)
Fiscal Year 1994: ¥2,000,000 (Direct Cost: ¥2,000,000)
Fiscal Year 1993: ¥15,000,000 (Direct Cost: ¥15,000,000)
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| Keywords | Asymmetric Catalysis / Organozinc complexes / Alkylation / Chirality Multiplication / Chirality Amplification / Self Recognition / Nonself Recognition / Mechanism / 炭素-炭素結合形成 / 化学的不斉増殖 / DAIB |
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| Research Abstract |
In the presence of a catalytic amount of (-) -3-exo- (dimethylamino) isoborneol (DAIB), reaction of dialkylzincs and aldehydes is accelerated markedly to give, after hydrolysis, the corresponding S alcohols in high enantiomeric purity. In this enantioselective alkylation, nonlinear relationship between optical purities of the chiral source and products. For example, reaction of benzaldehyde and diethylzinc in the presence of 8 mol% of (-)-DAIB in 15% ee leads to (S)-1-phenyl-1-propanol in 95% ee. The mechanisms of chirality multiplication as well as amplification have been elucidated on the basis of the kinetic measurement, alkyl scrambling experiments, single crystal X-ray analysis, 1H-NMR study, molecular-weight determination of certain key intermediates, systematic investigation using DAIB and its stereoisomers. This unusual phenomenon has been understood as a result of a marked difference in chemical properties of the diastereomeric dinuclear complexes formed from dialkylzincs and the DAIB auxiliary, proposing importance of the self and nonself recognition of the asymmetric catalysts. This view is supported the ab initio molecular orbital calculations of the model systems.
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