Microbial deracemization of α-substituted carboxylic acids: control of the reaction path-Reference-Cited by-同舟云学术

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Microbial deracemization of α-substituted carboxylic acids: control of the reaction path

Published:2004-09 Issue:18 Volume:15 Page:2965-2973
ISSN:0957-4166
Container-title:Tetrahedron: Asymmetry
language:en
Short-container-title:Tetrahedron: Asymmetry

Author:

Kato Dai-ichiro,Miyamoto Kenji,Ohta Hiromichi

Publisher

Elsevier BV

Subject

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

Reference20 articles.

1. Microbial Deracemization of α-Substituted Carboxylic Acids

2. Microbial Deracemization of α-Substituted Carboxylic Acids: Substrate Specificity and Mechanistic Investigation

3. Chemoenzymatic dynamic kinetic resolution

4. Chiral inversion of 2-arylpropionic acid non-steroidal anti-inflammatory drugs—II Racemization and hydrolysis of (R)- and (S)-ibuprofen-CoA thioesters

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1. Catalytic Deracemization Reactions;Journal of the American Chemical Society;2023-05-13

2. Analysis, fate and toxicity of chiral non-steroidal anti-inflammatory drugs in wastewaters and the environment: a review;Environmental Chemistry Letters;2020-08-20

3. Enantioselective Synthesis of α‐Thiocarboxylic Acids by Nitrilase Biocatalysed Dynamic Kinetic Resolution of α‐Thionitriles;Chemistry – A European Journal;2020-07-16

4. Enantiospecific behaviour of chiral drugs in soil;Environmental Pollution;2020-07

5. Firefly Luciferase as Biocatalysts;Future Directions in Biocatalysis;2017

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