Enhancing the biocatalytic synthesis of chiral drug intermediate by rational design an aldo-keto reductase from Bacillus megaterium YC4-R4
Author:
Publisher
Elsevier BV
Subject
Applied Microbiology and Biotechnology,Biochemistry,Biotechnology,Bioengineering
Reference29 articles.
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3. Bioreductive production of enantiopure (S)-duloxetine intermediates catalyzed with ketoreductase ChKRED15;Ren;J. Mol. Catal. B-Enzym.,2015
4. A chemoenzymatic dynamic kinetic resolution approach to enantiomerically pure (R)- and (s)-duloxetine;Traff;J. Org. Chem.,2011
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1. Multi-strategy orthogonal enhancement and analysis of aldo-keto reductase thermal stability;International Journal of Biological Macromolecules;2024-04
2. Specific coenzyme preference switching for an aldo-keto reductase that synthesizes the chiral intermediate of duloxetine;Enzyme and Microbial Technology;2023-12
3. Mining of a novel reductase and its application for asymmetric reduction of p-methoxyacetophenone;Letters in Applied Microbiology;2023-08
4. Ketoreductase-assisted synthesis of chiral selective tert-butyl{5-[(4-cyanophenyl)(hydroxy)methyl]-2-fluorophenyl}carbamate: process minutiae, optimization and characterization;Chemical Papers;2023-02-06
5. Engineering ketoreductases for the enantioselective synthesis of chiral alcohols;Chemical Communications;2023
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