Enzymatic recognition of diastereomeric esters
- 1 January 1990
- journal article
- research article
- Published by Elsevier in Tetrahedron
- Vol. 46 (12) , 4231-4240
- https://doi.org/10.1016/s0040-4020(01)86759-4
Abstract
No abstract availableThis publication has 28 references indexed in Scilit:
- Enantioselective inhibition: strategy for improving the enantioselectivity of biocatalytic systemsJournal of the American Chemical Society, 1989
- 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
- Enzymatic catalysis in monophasic organic solventsEnzyme and Microbial Technology, 1989
- Oxime esters as novel irreversible acyl transfer agents for lipase catalysis in organic mediaJournal of the Chemical Society, Chemical Communications, 1989
- Biocatalytic Preparation of Enantiomerically Pureendo-Bicyclo[3.3.0]oct-7-en-2-olSynthesis, 1989
- Anhydrides as acylating agents in lipase-catalyzed stereoselective esterification of racemic alcoholsThe Journal of Organic Chemistry, 1988
- Carbon tetrachloride-promoted stereo selective hydrolysis of methyl-2-chloropropionate by lipaseBiotechnology & Bioengineering, 1987
- Enzymatic resolution of norbornane-type estersTetrahedron, 1987
- Enzymatic reactions in organic synthesis: 2- ester interchange of vinyl estersTetrahedron Letters, 1987
- Tetrahedron report number 203Tetrahedron, 1986