Facile optical resolution of amino acid esters via hydrolysis by an industrial enzyme in organic solvents
- 1 January 1994
- journal article
- Published by Wiley in Journal of Chemical Technology & Biotechnology
- Vol. 59 (1) , 61-65
- https://doi.org/10.1002/jctb.280590110
Abstract
No abstract availableKeywords
This publication has 16 references indexed in Scilit:
- Peptide synthesis by proteases in organic solvents: Medium effect on substrate specificityEnzyme and Microbial Technology, 1992
- Inversion of enzyme enantioselectivity mediated by the solventJournal of the American Chemical Society, 1992
- Kinetic resolution of N-protected amino acid esters in organic solvents catalyzed by a stable industrial alkaline proteaseBiotechnology Letters, 1991
- How can the solvent affect enzyme enantioselectivity?Journal of the American Chemical Society, 1991
- Substrate structure and solvent hydrophobicity control lipase catalysis and enantioselectivity in organic mediaJournal of the American Chemical Society, 1991
- Solvent Effects in Lipase-Catalysed Transesterification Reactions.Acta Chemica Scandinavica, 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
- Enzymic resolution of racemic amines: crucial role of the solventJournal of the American Chemical Society, 1989
- Substrate specificity of enzymes in organic solvents vs. water is reversedJournal of the American Chemical Society, 1986
- Synthesis of Phenylalanines in High Enantiomeric Excess via Enzymatic ResolutionSynthesis, 1983