Highly Enantioselective Conversion of Racemic 1-Phenyl-1,2-ethanediol by Stereoinversion Involving a Novel Cofactor-Dependent Oxidoreduction System of Candida parapsilosis CCTCC M203011
Author:
Affiliation:
1. Key Laboratory of Industrial Biotechnology of Ministry of Education and School of Biotechnology, Southern Yangtze University, Wuxi 214036, P. R. China
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/op0341519
Reference22 articles.
1. Nonenzymatic Kinetic Resolution of 1,2-Diols Catalyzed by an Organotin Compound
2. Stereospecific dihydroxylation of the styrene vinyl group by purified naphthalene dioxygenase from Pseudomonas sp. strain NCIB 9816-4
3. Enzymatic resolution of 1,2-diols: comparison between hydrolysis and transesterification reactions
4. Enzymatic resolution of 1-phenyl-1,2-ethanediol by enantioselective oxidation: Overcoming product inhibition by continuous extraction
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