An unexpected inversion of CAL-B enantiopreference based on substrate engineering of 2-bromoesters: Effect of (R)-1-phenylethyl moiety-Reference-Cited by-同舟云学术

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An unexpected inversion of CAL-B enantiopreference based on substrate engineering of 2-bromoesters: Effect of (R)-1-phenylethyl moiety

Published:2016-11 Issue: Volume:133 Page:S317-S323
ISSN:1381-1177
Container-title:Journal of Molecular Catalysis B: Enzymatic
language:en
Short-container-title:Journal of Molecular Catalysis B: Enzymatic

Author:

da Silva Thiago Sabino,Campos Suelem Kluconski,de Oliveira Alfredo R.M.,Piovan Leandro

Funder

National Council for Scientific and Technological Development

Office to Improve University Personnel

Araucária Foundation

Publisher

Elsevier BV

Subject

Process Chemistry and Technology,Biochemistry,Bioengineering,Catalysis

Reference50 articles.

1. The production of fine chemicals by biotransformations

2. Biocatalysis in development of green pharmaceutical processes

3. Lipases: Useful biocatalysts for the preparation of pharmaceuticals

4. Industrial Enzymes: Structure, Function and Applications;Polaina,2007

5. Hydrolases in Organic Synthesis: Regio- and Stereoselective Biotransformations;Bornscheuer,2006

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Substituent Position‐Controlled Stereoselectivity in Enzymatic Reduction of Diaryl‐ and Aryl(heteroaryl)methanones;Advanced Synthesis & Catalysis;2019-02-28

2. Substrate engineering: Effects of different N-protecting groups in the CAL-B-catalysed asymmetric O-acylation of 1-hydroxymethyl-tetrahydro-β-carbolines;Tetrahedron;2018-05

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