1-Ethoxyvinyl acetate as a novel, highly reactive, and reliable acyl donor for enzymatic resolution of alcohols
- 7 October 1996
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 37 (41) , 7369-7372
- https://doi.org/10.1016/0040-4039(96)01658-9
Abstract
No abstract availableKeywords
This publication has 27 references indexed in Scilit:
- Enantioselective synthesis through enzymatic asymmetrizationTetrahedron, 1996
- Fitness of Lipases and Substrates in Lipase-catalyzed Resolution.Journal of Synthetic Organic Chemistry, Japan, 1995
- Enzyme-Catalyzed Irreversible Acyl TransferSynthesis, 1992
- Enzymatic regioselective acylation of hexoses and pentoses using oxime estersJournal of the Chemical Society, Perkin Transactions 1, 1992
- Regioselective Acylation of 2′-Deoxynucleosides Through an Enzymatic Reaction with Oxime EstersSynthesis, 1992
- Limitations of enzymatic acylation using oxime esters: Cosubstrate inhibition and the reversibility of the reactionBiotechnology Letters, 1991
- 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
- Oxime esters as novel irreversible acyl transfer agents for lipase catalysis in organic mediaJournal of the Chemical Society, Chemical Communications, 1989
- Modification of proteases to esterases for peptide synthesis: methylchymotrypsinJournal of the American Chemical Society, 1988
- Resolution of racemic mixtures via lipase catalysis in organic solventsJournal of the American Chemical Society, 1985