Conversion of a pentane-1,3,5-triol derivative using lipases as chiral catalysts and possible function of the lid for the regulation of substrate selectivity and enantioselectivity-Reference-Cited by-同舟云学术

Conversion of a pentane-1,3,5-triol derivative using lipases as chiral catalysts and possible function of the lid for the regulation of substrate selectivity and enantioselectivity

Published:2012-03 Issue:2 Volume:30 Page:217-225
ISSN:1024-2422
Container-title:Biocatalysis and Biotransformation
language:en
Short-container-title:Biocatalysis and Biotransformation

Author:

Köhler Jens,Wünsch Bernhard

Publisher

Informa UK Limited

Subject

Biochemistry,Catalysis,Biotechnology

Link

http://www.tandfonline.com/doi/pdf/10.3109/10242422.2012.661726

Reference30 articles.

1. Berglund P, Vallikivi I, Fransson L, Dannacher H, Holmquist M, Martinelle M, Björkling F, Parve O, Hult K. 1999. Switched enantiopreference of Humicola lipase for 2-phenoxyalkanoic acid ester homologs can be rationalized by different substrate binding modes. Tetrahedron: Asymmetr 10:4191–4202.

2. Bornscheuer UT, Kazlauskas RJ. 2005. Hydrolases in organic synthesis: regio- and stereoselective biotransformations. Weinheim, Germany: Wiley-VCH.

3. A serine protease triad forms the catalytic centre of a triacylglycerol lipase

4. Design, total synthesis, and functional overexpression of the Candida rugosa lipl gene coding for a major industrial lipase

5. Switching from S- to R-Selectivity in the Candida antarctica Lipase B-Catalyzed Ring-Opening of ω-Methylated Lactones: Tuning Polymerizations by Ring Size

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