Enantioselectivity of Pseudomonas cepacia and Candida rugosa lipases for the resolution of secondary alcohols: The effect of Candida rugosa isoenzymes-Reference-Cited by-同舟云学术

Enantioselectivity of Pseudomonas cepacia and Candida rugosa lipases for the resolution of secondary alcohols: The effect of Candida rugosa isoenzymes

Published:1998-02 Issue:2 Volume:22 Page:86-93
ISSN:0141-0229
Container-title:Enzyme and Microbial Technology
language:en
Short-container-title:Enzyme and Microbial Technology

Author:

Lundell Katri,Raijola Timo,Kanerva Liisa T.

Publisher

Elsevier BV

Subject

Applied Microbiology and Biotechnology,Biochemistry,Biotechnology,Bioengineering

Reference30 articles.

1. A rule to predict which enantiomer of a secondary alcohol reacts faster in reactions catalyzed by cholesterol esterase, lipase from Pseudomonas cepacia and lipase from Candida rugosa;Kazlauskas;J. Org. Chem.,1991

2. Lipase-catalyzed enantioselective transesterification of O-trityl 1, 2-diols. Practical synthesis of (R)-tritylglycidol;Kim;J. Org. Chem.,1992

3. A structural basis for the chiral preference of lipases;Cygler;J. Am. Chem. Soc.,1994

4. Alcohol induced reversal of enantioselectivity in a lipase catalyzed resolution of 2-chloropropionic acid;Holmberg;Biocatalysis,1992

5. Enantioselectivity of Candida rugosa lipase toward carboxylic acids: A predictive rule from substrate mapping and X-ray crystallography;Ahmed;Biocatalysis,1994

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