Studies on the enzymatic resolution of chiral tricarbonyl(benzaldehyde oxime)chromium complexes
- 1 May 1993
- journal article
- Published by Elsevier in Tetrahedron: Asymmetry
- Vol. 4 (5) , 767-772
- https://doi.org/10.1016/s0957-4166(00)80113-5
Abstract
No abstract availableKeywords
This publication has 15 references indexed in Scilit:
- Inversion of enzyme enantioselectivity mediated by the solventJournal of the American Chemical Society, 1992
- Effects of medium and of reaction conditions on the enantioselectivity of lipases in organic solvents and possible rationalesTetrahedron: Asymmetry, 1992
- Microbial resolution of organometallic planar chirality. Enantioselective reduction of orto- and meta-substituted tricarbonylchromium benzaldehydes by bakers' yeastJournal of Organometallic Chemistry, 1991
- A rule to predict which enantiomer of a secondary alcohol reacts faster in reactions catalyzed by cholesterol esterase, lipase from Pseudomonas cepacia, and lipase from Candida rugosaThe Journal of Organic Chemistry, 1991
- Lipase-mediated homotopic and heterotopic double resolutions of a planar chiral organometallic alcoholBiotechnology Letters, 1991
- Stereoselectivity of the enzymatic reduction of aldehydic and ketonic carbonyl groups in planar chiral organomanganese complexes.Agricultural and Biological Chemistry, 1990
- Synthesis of Oxime Esters Through an Enzymatic Oximolysis ReactionSynlett, 1990
- Chemoenzymic synthesis of chiral furan derivatives: useful building blocks for optically active structuresThe 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
- Quantitative analyses of biochemical kinetic resolutions of enantiomersJournal of the American Chemical Society, 1982