Kinetic resolution of sulfoxides with high enantioselectivity using a new homologue of methionine sulfoxide reductase B
Author:
Affiliation:
1. Department of Biochemistry, School of Preclinical Medicine, Zunyi Medical University, China
2. Key Laboratory of Biocatalysis & Chiral Drug Synthesis of Guizhou Province, School of Pharmacy, Zunyi Medical University, China
Abstract
Funder
National Natural Science Foundation of China
Guizhou Science and Technology Department
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2023/OB/D3OB00402C
Reference36 articles.
1. Chiral Sulfoxide Ligands in Asymmetric Catalysis
2. Chiral sulfoxides: advances in asymmetric synthesis and problems with the accurate determination of the stereochemical outcome
3. Development of Chiral Sulfoxide Ligands for Asymmetric Catalysis
4. Sulfoxide Reductases and Applications in Biocatalytic Preparation of Chiral Sulfoxides: A Mini-Review
5. Modern Stereoselective Synthesis of Chiral Sulfinyl Compounds
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1. Engineering of methionine sulfoxide reductase A with simultaneously improved stability and activity for kinetic resolution of chiral sulfoxides;International Journal of Biological Macromolecules;2024-03
2. Catalytic Mechanism of Mycobacterium tuberculosis Methionine Sulfoxide Reductase A;Biochemistry;2024-01-29
3. Peroxygenase‐Catalysed Sulfoxidations in Non‐Aqueous Media;ChemSusChem;2023-11-22
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