Enantioselective hydrolysis of hydrophobic amino acid derivatives by lipases
- 1 June 1992
- journal article
- research article
- Published by Springer Nature in Biotechnology Letters
- Vol. 14 (6) , 461-464
- https://doi.org/10.1007/bf01023167
Abstract
No abstract availableKeywords
This publication has 10 references indexed in Scilit:
- Ser-His-Glu triad forms the catalytic site of the lipase from Geotrichum candidumNature, 1991
- A serine protease triad forms the catalytic centre of a triacylglycerol lipaseNature, 1990
- Enzymatic Catalysts in Organic SynthesisScience, 1989
- Resolution of Enantiomers via BiocatalysisTopics in Stereochemistry, 1989
- Kinetic resolutions of aliphatic alcohols with a fungal lipase from Mucor mieheiThe Journal of Organic Chemistry, 1987
- Lipase-catalyzed ester formation in organic solvents an easy preparative resolution α-substituted cyclohexanolsTetrahedron Letters, 1985
- Resolution of racemic mixtures via lipase catalysis in organic solventsJournal of the American Chemical Society, 1985
- Stereoselective esterification of dl-menthol by polyurethane-entrapped lipase in organic solventJournal of Biotechnology, 1985
- Lipase-catalyzed hydrolysis as a route to esters of chiral epoxy alcoholsJournal of the American Chemical Society, 1984
- Quantitative analyses of biochemical kinetic resolutions of enantiomersJournal of the American Chemical Society, 1982