Asymmetric reductions of ethyl 2-(benzamidomethyl)-3-oxobutanoate by yeasts-Reference-Cited by-同舟云学术

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Asymmetric reductions of ethyl 2-(benzamidomethyl)-3-oxobutanoate by yeasts

Published:2009-03 Issue:4 Volume:20 Page:411-414
ISSN:0957-4166
Container-title:Tetrahedron: Asymmetry
language:en
Short-container-title:Tetrahedron: Asymmetry

Author:

Gandolfi Raffaella,Cesarotti Edoardo,Molinari Francesco,Romano Diego,Rimoldi Isabella

Publisher

Elsevier BV

Subject

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

Reference32 articles.

1. Microbial/enzymatic synthesis of chiral intermediates for pharmaceuticals

2. Biocatalytic ketone reduction—a powerful tool for the production of chiral alcohols—part I: processes with isolated enzymes

3. Biocatalytic ketone reduction—a powerful tool for the production of chiral alcohols—part II: whole-cell reductions

4. Enantioselective hydrolysis of (RS)-isopropylideneglycerol acetate with Kluyveromyces marxianus

5. Application of α-keto acid decarboxylases in biotransformations

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3. Biocatalytic dynamic kinetic reductive resolution with ketoreductase from Klebsiella pneumoniae: the asymmetric synthesis of functionalized tetrahydropyrans;Organic & Biomolecular Chemistry;2019

4. Recent advances in biotechnological applications of alcohol dehydrogenases;Applied Microbiology and Biotechnology;2017-01-10

5. Preparation of enantiomerically enriched aromatic β-hydroxynitriles and halohydrins by ketone reduction with recombinant ketoreductase KRED1-Pglu;Tetrahedron;2016-07

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