Stereoselective hydrolysis of racemic ethyl 4-chloro-3-hydroxybutyrate by a lipase
Author:
Publisher
Informa UK Limited
Subject
Biochemistry,Catalysis,Biotechnology
Link
http://www.tandfonline.com/doi/pdf/10.1080/10242420801897585
Reference11 articles.
1. Lipase-catalyzed resolution of esters of 4-chloro-3-hydroxybutanoic acid: effects of the alkoxy group and solvent on the enantiomeric ratio
2. Stereoselective reduction of ethyl 4-chloro-3-oxobutanoate by Escherichia coli transformant cells coexpressing the aldehyde reductase and glucose dehydrogenase genes
3. A practical asymmetric synthesis of carnitine
4. Improvement on production of (R)-4-Chloro-3-hydroxybutyrate and (S)-3-hydroxy-γ-butyrolactone with recombinant Escherichia coli cells
5. (-)-β-Pinene as chiral promoter. Stereospecific access to (-)-γ-amino-β()-hydroxybutyric acid (gabob) and ()-carnitine.2
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3. A New Practical Synthesis of Ethyl (R)-(-)-4-Cyano-3-hydroxybutyrate From (S)-3-chloro-1,2-propanediol;Letters in Organic Chemistry;2012-07-01
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