Limitations of enzymatic acylation using oxime esters: Cosubstrate inhibition and the reversibility of the reaction
- 1 September 1991
- journal article
- Published by Springer Nature in Biotechnology Letters
- Vol. 13 (9) , 653-656
- https://doi.org/10.1007/bf01086321
Abstract
No abstract availableKeywords
This publication has 14 references indexed in Scilit:
- An improved procedure for regioselective acylation of carbohydrates: novel enzymatic acylation of α-D-glucopyranose and methyl α-D-glucopyranosideJournal of the Chemical Society, Perkin Transactions 1, 1991
- Lipase-catalyzed irreversible transesterification using enol esters: XAD-8 immobilized lipoprotein lipase-catalyzed resolution of secondary alcoholsTetrahedron Letters, 1990
- Enzymatic acylation using acid anhydrides: Crucial removal of acidTetrahedron: Asymmetry, 1990
- General Aspects and Optimization of Enantioselective Biocatalysis in Organic Solvents: The Use of Lipases [New Synthetic Methods (76)]Angewandte Chemie International Edition in English, 1989
- Anhydrides as acylating agents in lipase-catalyzed stereoselective esterification of racemic alcoholsThe Journal of Organic Chemistry, 1988
- Quantitative analyses of biochemical kinetic resolution of enantiomers. 2. Enzyme-catalyzed esterifications in water-organic solvent biphasic systemsJournal of the American Chemical Society, 1987
- Enzymatic reactions in organic synthesis: 2- ester interchange of vinyl estersTetrahedron Letters, 1987
- Resolution of racemic mixtures via lipase catalysis in organic solventsJournal of the American Chemical Society, 1985
- Quantitative analyses of biochemical kinetic resolutions of enantiomersJournal of the American Chemical Society, 1982
- 4‐Dialkylaminopyridines as Highly Active Acylation Catalysts. [New synthetic method (25)]Angewandte Chemie International Edition in English, 1978