Enantiomeric selectivity of a lipase from Penicillium simplicissimum in the esterification of menthol in microemulsions
- 1 May 1993
- journal article
- Published by Springer Nature in Biotechnology Letters
- Vol. 15 (5) , 471-476
- https://doi.org/10.1007/bf00129321
Abstract
No abstract availableKeywords
This publication has 20 references indexed in Scilit:
- Chemoenzymatic preparation of optically active hydroxy azido butyric acidsBiotechnology Letters, 1992
- Lipase-catalysed reactions of chiral hydroxyacid esters: competition of esterification and transesterificationEnzyme and Microbial Technology, 1991
- Lipase-catalyzed resolution of chiral 2-amino 1-alcoholsThe Journal of Organic Chemistry, 1987
- Rules for optimization of biocatalysis in organic solventsBiotechnology & Bioengineering, 1987
- Quantitative analyses of biochemical kinetic resolution of enantiomers. 2. Enzyme-catalyzed esterifications in water-organic solvent biphasic systemsJournal of the American Chemical Society, 1987
- Lipase catalyzed reactions and strategy for alcohol resolutionTetrahedron Letters, 1986
- Characteristics of lipase‐catalyzed hydrolysis of olive oil in AOT–isooctane reversed micellesBiotechnology & Bioengineering, 1986
- Comparison of different strategies for the lipase‐catalyzed preparative resolution of racemic acids and alcohols: Asymmetric hydrolysis, esterification, and transesterificationBiotechnology & Bioengineering, 1984
- Lipase-catalyzed hydrolysis as a route to esters of chiral epoxy alcoholsJournal of the American Chemical Society, 1984
- Preparative production of optically active esters and alcohols using esterase-catalyzed stereospecific transesterification in organic mediaJournal of the American Chemical Society, 1984