Enantioselectivity in microbial reduction of prochiral carbonyl groups: A wide screening toward R and S isomers-Reference-Cited by-同舟云学术

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Enantioselectivity in microbial reduction of prochiral carbonyl groups: A wide screening toward R and S isomers

Published:1991-01 Issue:4 Volume:2 Page:243-246
ISSN:0957-4166
Container-title:Tetrahedron: Asymmetry
language:en
Short-container-title:Tetrahedron: Asymmetry

Author:

Fantin Giancarlo,Fogagnolo Marco,Medici Alessandro,Pedrini Paola,Poli Silvia,Gardini Fausto,Guerzoni M.Elisabetta

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis

Reference15 articles.

1. Tetrahedron report number 203

2. Baker's Yeast as a Reagent in Organic Synthesis

3. Microbial Asymmetric Catalysis?Enantioselective Reduction of Ketones [New Synthetic Methods (45)]

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1. Fluorogenic kinetic assay for high-throughput discovery of stereoselective ketoreductases relevant to pharmaceutical synthesis;Bioorganic & Medicinal Chemistry;2018-04

2. Synthesis of both enantiomers of ethyl-4-chloro-3-hydroxbutanoate from a prochiral ketone using Candida parapsilosis ATCC 7330;Tetrahedron: Asymmetry;2011-07

3. ChemInform Abstract: Enantioselectivity in Microbial Reduction of Prochiral Carbonyl Groups: A Wide Screening Toward R and S Isomers.;ChemInform;2010-08-22

4. Reduction screening with endophytic fungi: Synthesis of homochiral secondary alcohols;Journal of Molecular Catalysis B: Enzymatic;2009-10

5. Kinetic Resolution and Chemoenzymatic Dynamic Kinetic Resolution of Functionalized γ-Hydroxy Amides;The Journal of Organic Chemistry;2005-03-02

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