Highly efficient extractive biocatalysis in the asymmetric reduction of an acyclic enone by the yeast Pichia stipitis

被引：38

作者：

Conceiçao, GJA ^{[1
]}

Moran, PJS ^{[1
]}

Rodrigues, JAR ^{[1
]}

机构：

[1] Univ Estadual Campinas, Inst Quim, BR-13083970 Campinas, SP, Brazil

来源：

TETRAHEDRON-ASYMMETRY | 2003年 / 14卷 / 01期

基金：

巴西圣保罗研究基金会;

关键词：

D O I：

10.1016/S0957-4166(02)00798-X

中图分类号：

O61 [无机化学];

学科分类号：

070301 ; 081704 ;

摘要：

A concise highly chemo- and enantioselective preparation of (S)-2-ethyl-1-phenylprop-2-en-1-ol 6 (65% yield, >99% e.e.) via extractive biocatalysis by the yeast Pichia stipitis CCT 2617-mediated reduction of 2-ethyl-1-phenylprop-2-en-1-one 5 adsorbed on Amberlite(TM) XAD-7 is reported. (C) 2003 Published by Elsevier Science Ltd.

引用

页码：43 / 45

页数：3

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