A simple method for calculating enantiomer ratio and equilibrium constants in biocatalytic resolutions
- 31 December 1995
- journal article
- Published by Elsevier in Tetrahedron: Asymmetry
- Vol. 6 (12) , 3015-3022
- https://doi.org/10.1016/0957-4166(95)00398-3
Abstract
No abstract availableKeywords
This publication has 7 references indexed in Scilit:
- Co-solvent enhancement of enantioselectivity in lipase-catalysed hydrolysis of racemic esters. A process for production of homochiral C-3 building blocks using lipase B from Candida antarcticaTetrahedron: Asymmetry, 1995
- Stereoselectivity of Baker's Yeast Reduction of 2-Propanones: Influence of Substituents.Acta Chemica Scandinavica, 1994
- Water activity influences enantioselectivity in a lipase-catalysed resolution by esterification in an organic solventTetrahedron: Asymmetry, 1993
- Water activity does not influence the enantioselectivity of Lipase PS and lipoprotein lipase in organic solventsBiotechnology Letters, 1993
- Use of salt hydrates to buffer optimal water level during lipase catalysed in synthesis in organic media: a practical procedure for organic chemistsTetrahedron, 1992
- Quantitative analyses of biochemical kinetic resolution of enantiomers. 2. Enzyme-catalyzed esterifications in water-organic solvent biphasic systemsJournal of the American Chemical Society, 1987
- Quantitative analyses of biochemical kinetic resolutions of enantiomersJournal of the American Chemical Society, 1982