Microbiological Transformations. 33. Fungal Epoxide Hydrolases Applied to the Synthesis of Enantiopure Para-Substituted Styrene Oxides. A Mechanistic Approach-Reference-Cited by-同舟云学术

Microbiological Transformations. 33. Fungal Epoxide Hydrolases Applied to the Synthesis of Enantiopure Para-Substituted Styrene Oxides. A Mechanistic Approach

Published:1996-01-01 Issue:21 Volume:61 Page:7402-7407
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Pedragosa-Moreau S.¹,Morisseau C.¹,Zylber J.¹,Archelas A.¹,Baratti J.¹,Furstoss R.¹

Affiliation:

1. Groupe Biocatalyse et Chimie Fine, ERS 157 associée au CNRS, Faculté des Sciences de Luminy, Case 901, 163 avenue de Luminy, 13288 Marseille Cedex 9, France

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo960558i

Reference32 articles.

1. Isolation and characterization of a cDNA encoding rat liver cytosolic epoxide hydrolase and its functional expression in Escherichia coli

2. The rabbit liver microsomal biotransformation of 1,1-dialkylethylenes: Enantioface selection of epoxidation and enantioselectivity of epoxide hydrolysis

3. Kinetics and stereochemistry of the microsomal epoxide hydrolase-catalyzed hydrolysis ofcis-stilbene oxides

4. Stereocontrolled Hydrolysis of the Linoleic Acid Monoepoxide Regioisomers Catalyzed by Soybean Epoxide Hydrolase

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