Stereoselective Hydrolysis of Epoxides by reVrEH3, a Novel Vigna radiata Epoxide Hydrolase with High Enantioselectivity or High and Complementary Regioselectivity
Author:
Affiliation:
1. Nanyang Provincial Engineering Laboratory of Insect Bio-reactor, Nanyang Normal University, Henan 473061, China
Funder
National Natural Science Foundation of China
Jiangsu Province
Publisher
American Chemical Society (ACS)
Subject
General Agricultural and Biological Sciences,General Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.jafc.7b03804
Reference48 articles.
1. Epoxide Hydrolases and their Application in Organic Synthesis
2. Nucleophilic addition of methyllithium to chiral oxime ethers: asymmetric preparation of 1-(aryl)ethylamines and application to a synthesis of calcimimetics (+)-NPS R-568 and its thio analogue
3. Synthesis, conformation and antiviral activity of nucleoside analogues with the (2-hydroxy-1-phenylethoxy)methyl glycone—a family of nucleoside analogues related to d4T and aciclovir
4. Recent developments in the asymmetric hydrolytic ring opening of epoxides catalysed by microbial epoxide hydrolase
5. Microbiological transformations. Part 45: A green chemistry preparative scale synthesis of enantiopure building blocks of Eliprodil: elaboration of a high substrate concentration epoxide hydrolase-catalyzed hydrolytic kinetic resolution process
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