Highly diastereo- and enantio-selective epoxidation of secondary allylic alcohols catalyzed by styrene monooxygenase

被引：39
|
作者：
Lin, Hui [1 ,2 ]
Liu, Yan [1 ]
Wu, Zhong-Liu [1 ]
机构：
[1] Chinese Acad Sci, Chengdu Inst Biol, Chengdu 610041, Sichuan, Peoples R China
[2] Chinese Acad Sci, Grad Univ, Beijing 100049, Peoples R China
来源：
CHEMICAL COMMUNICATIONS | 2011年 / 47卷 / 09期
基金：
中国国家自然科学基金;
关键词：
ASYMMETRIC EPOXIDATION; VANADIUM; STRAIN; OXIDE;
D O I：
10.1039/c0cc04360e
中图分类号：
O6 [化学];
学科分类号：
0703 ;
摘要：
Enantiomerically enriched glycidol derivatives with contiguous stereogenic centers were obtained in a highly diastereo- and enantio-selective epoxidation catalyzed with the styrene monooxygenase StyAB2.
引用
收藏
页码：2610 / 2612
页数：3
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