Pressure-dependent enantio selectivity in the organozinc addition to aldehydes in supercritical fluids

被引：16

作者：

Jessop, PG ^{[1
]}

Brown, RA

Yamakawa, M

Xiao, JL

Ikariya, T

Kitamura, M

Tucker, SC

Noyori, R

机构：

[1] Univ Calif Davis, Dept Chem, Davis, CA 95616 USA

[2] Kinjo Gakuin Univ, Nagoya, Aichi 4638521, Japan

[3] Univ Liverpool, Dept Chem, Leverhulme Ctr Innovat Catalysis, Liverpool L69 7ZD, Merseyside, England

[4] Tokyo Inst Technol, Dept Chem Technol, Meguro Ku, Tokyo 1528552, Japan

[5] Nagoya Univ, Dept Chem, Nagoya, Aichi 4648602, Japan

来源：

JOURNAL OF SUPERCRITICAL FLUIDS | 2002年 / 24卷 / 02期

基金：

美国国家科学基金会;

关键词：

alkylation; enantioselectivity; ethane; fluoroform; homogeneous catalysis; pressure effect; solvent effect;

D O I：

10.1016/S0896-8446(02)00030-X

中图分类号：

O64 [物理化学（理论化学）、化学物理学];

学科分类号：

070304 ; 081704 ;

摘要：

Amino alcohol-catalyzed asymmetric alkylation of benzaldehydes by dialkylzines can be achieved in supercritical fluoroform (scCH(3)) and supercritical ethane (SCC2H6) with high conversion and enantio selectivity. The higher enantioselectivity in ethane compared to CHF3 suggests that solvent polarity affects the reaction. The enantioselectivity in scCHF(3) is strongly pressure dependent. (C) 2002 Elsevier Science B.V. All rights reserved.

引用

页码：161 / 172

页数：12

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