2-Methylalkanoic acids resolved by esterification catalysed by lipase from Candida rugosa: Alcohol chain length and enantioselectivity
- 1 August 1993
- journal article
- Published by Elsevier in Tetrahedron: Asymmetry
- Vol. 4 (8) , 1869-1878
- https://doi.org/10.1016/s0957-4166(00)80427-9
Abstract
No abstract availableKeywords
This publication has 34 references indexed in Scilit:
- Displacement of the equilibrium in lipase catalysed transesterification in ethyl octanoate by continous evaporation of ethanolBiotechnology Letters, 1992
- Bakers' yeast reduction of thiophenepropaenals. Enantioselective synthesis of (S)-2-methyl-1-alkanols via bakers' yeast mediated reduction of 2-methyl-3-(2-thiophene)propenalsThe Journal of Organic Chemistry, 1992
- Studies of the Heterogeneity of aCandida cylindracea(rugosa) Lipase: Monitoring of Esterolytic Activity and Enantioselectivity by Chiral Liquid ChromatographyBiocatalysis, 1992
- Enantioselective enzymatic catalysis.:2. Applicability of methods for enantiomeric ratio determinationsRecueil des Travaux Chimiques des Pays-Bas, 1991
- ASYMMETRIC SYNTHESIS OF 2-,3-, AND 4-METHYLOCTANOIC ACIDSOrganic Preparations and Procedures International, 1990
- Characterization of three distinct forms of lipolytic enzyme in a commercialCandida lipase preparationBiotechnology Letters, 1989
- Centenary Lecture. Chemical multiplication of chirality: science and applicationsChemical Society Reviews, 1989
- Kinetic resolutions of aliphatic alcohols with a fungal lipase from Mucor mieheiThe Journal of Organic Chemistry, 1987
- Kinetic resolution of racemic allylic alcohols by enantioselective epoxidation. A route to substances of absolute enantiomeric purity?Journal of the American Chemical Society, 1981
- Steric Effects and Stereochemistry of Lithium Aluminum Hydride ReductionJournal of the American Chemical Society, 1950