Quantitative Structure−Activity Relationships for the Enantioselectivity of Oxirane Ring-Opening Catalyzed by Epoxide Hydrolases-Reference-Cited by-同舟云学术

Quantitative Structure−Activity Relationships for the Enantioselectivity of Oxirane Ring-Opening Catalyzed by Epoxide Hydrolases

Published:2003-04-26 Issue:3 Volume:43 Page:934-940
ISSN:0095-2338
Container-title:Journal of Chemical Information and Computer Sciences
language:en
Short-container-title:J. Chem. Inf. Comput. Sci.

Author:

Funar-Timofei Simona¹,Suzuki Takahiro¹,Paier Joachim A.¹,Steinreiber Andreas¹,Faber Kurt¹,Fabian Walter M. F.¹

Affiliation:

1. Institute of Chemistry, Romanian Academy, Bul. Mihai Viteazul 24, 1900 Timisoara, Romania, Faculty of Economics, Toyo University, 2-11-10 Oka, Asaka, Saitama 351-8510, Japan, and Institut für Chemie (IfC), Karl-Franzens Universität Graz, Heinrichstrasse 28, A-8010 Graz, Austria

Publisher

American Chemical Society (ACS)

Subject

Computational Theory and Mathematics,Computer Science Applications,Information Systems,General Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ci020047z

Reference45 articles.

1. Highly Selective Hydrolytic Kinetic Resolution of Terminal Epoxides Catalyzed by Chiral (salen)CoIII Complexes. Practical Synthesis of Enantioenriched Terminal Epoxides and 1,2-Diols

2. Fungal epoxide hydrolases: new tools for the synthesis of enantiopure epoxides and diols

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