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
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.
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页码：43 / 45
页数：3
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