Enzyme-catalyzed asymmetric synthesis of optically active (R)- and (S)-ethyl -4-phenyl-4-hydroxybutyrate with microbial cells
Author:
Publisher
Informa UK Limited
Subject
Biochemistry,Catalysis,Biotechnology
Link
http://www.tandfonline.com/doi/pdf/10.3109/10242422.2012.758116
Reference12 articles.
1. Enantioselective Benzylic Hydroxylation withPseudomonas monteiliiTA-5: A Simple Method for the Syntheses of (R)-Benzylic Alcohols Containing Reactive Functional Groups
2. Preparation the Key Intermediate of Angiotensin-Converting Enzyme (ACE) Inhibitors: High Enantioselective Production of Ethyl (R)-2-Hydroxy-4-Phenylbutyrate withCandida boidinii CIOC21
3. High-Throughput Method for Determining the Enantioselectivity of Enzyme-Catalyzed Hydroxylations Based on Mass Spectrometry
4. Enantiocomplementary preparation of (S)- and (R)-mandelic acid derivatives via α-hydroxylation of 2-arylacetic acid derivatives and reduction of α-ketoester using microbial whole cells
5. A stable and easily prepared catalyst for the enantioselective reduction of ketones. Applications to multistep syntheses
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1. Biocatalytic Asymmetric Reduction of γ‐Keto Esters to Access Optically Active γ‐Aryl‐γ‐butyrolactones;Advanced Synthesis & Catalysis;2020-04-07
2. Synthesis of chiral γ-lactones via a RuPHOX-Ru catalyzed asymmetric hydrogenation of aroylacrylic acids;Tetrahedron;2019-06
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4. Asymmetric combinational “metal-biocatalytic system”: One approach to chiral 2-subsituted-tetrahydroquinoline-4-ols towards two-step one-pot processes in aqueous media;Tetrahedron Letters;2017-06
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