Issue 9, 2011
From the journal:

Chemical Communications

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

Hui Lin,ab   Yan Liua  and  Zhong-Liu Wu*a  

* Corresponding authors

a Chengdu Institute of Biology, Chinese Academy of Sciences, P.O. Box 416, Chengdu, Sichuan 610041, China
E-mail: wuzhl@cib.ac.cn
Fax: +8628-8523-8385
Tel: +86 28-8523-8385

b Graduate University of the Chinese Academy of Sciences, Beijing, China

Abstract

Enantiomerically enriched glycidol derivatives with contiguous stereogenic centers were obtained in a highly diastereo- and enantio-selective epoxidation catalyzed with the styrene monooxygenase StyAB2.

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

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Article information

DOI
https://doi.org/10.1039/C0CC04360E
Article type
Communication
Submitted
12 Oct 2010
Accepted
16 Dec 2010
First published
13 Jan 2011

Chem. Commun., 2011,47, 2610-2612

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

H. Lin, Y. Liu and Z. Wu, Chem. Commun., 2011, 47, 2610 DOI: 10.1039/C0CC04360E

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