Enzymatic ester hydrolysis and synthesis - two approaches to cycloalkane derivatives of high enantiomeric purity
- 31 December 1989
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 30 (14) , 1793-1796
- https://doi.org/10.1016/s0040-4039(00)99581-9
Abstract
No abstract availableThis publication has 11 references indexed in Scilit:
- Enzymic preparation of enantiomerically pure secondary alcohols. Ester synthesis by irreversible acyl transfer using a highly selective ester hydrolase from Pseudomonas sp.; an attractive alternative to ester hydrolysisJournal of the Chemical Society, Chemical Communications, 1988
- Enzymatic reactions in organic synthesis: 2- ester interchange of vinyl estersTetrahedron Letters, 1987
- Synthesis of both enantiomeric forms of 2-substituted 1,3-propanediol monoacetates starting from a common prochiral precursor, using enzymatic transformations in aqueous and in organic mediaTetrahedron Letters, 1986
- Enantioselective hydrolysis ofTetrahedron Letters, 1985
- Enzyme in der organischen SyntheseAngewandte Chemie, 1985
- Preparation of chiral hydroxyester synthons vis stereoselective porcine pancreatic lipase-catalysed hydrolyses of meso-diestersJournal of the Chemical Society, Chemical Communications, 1985
- Enzymatic Syntheses of Chiral Building Blocks from Prochiral meso‐Substrates: Preparation of Methyl(hydrogen)‐1,2‐cycloalkanedicarboxylatesAngewandte Chemie International Edition in English, 1984
- Enzymatische Synthesen chiraler Bausteine aus prochiralenmeso-Substraten: Herstellung von Methyl(hydrogen)-1,2-cycloalkandicarboxylatenAngewandte Chemie, 1984
- Enzymes in organic synthesis. 24. Preparations of enantiomerically pure chiral lactones via stereospecific horse liver alcohol dehydrogenase catalyzed oxidations of monocyclic meso diolsJournal of the American Chemical Society, 1982
- Preparation of useful chiral lactone synthons via stereospecific enzyme-catalysed oxidations of meso-diolsJournal of the Chemical Society, Chemical Communications, 1980