Separation and characterization of all configurational isomers by enzymatic discrimination of each chiral function
- 1 October 1992
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 33 (42) , 6335-6338
- https://doi.org/10.1016/s0040-4039(00)60967-x
Abstract
No abstract availableThis publication has 13 references indexed in Scilit:
- 2,2‐Dimethyl‐α,α,α′,α′‐tetrakis(β‐naphthyl)‐1,3‐dioxolan‐4,5‐dimethanol (DINOL) for the Titanate‐Mediated Enantioselective Addition of Diethylzinc to AldehydesAngewandte Chemie International Edition in English, 1991
- Asymmetric transformations catalyzed by enzymes in organic solventsAccounts of Chemical Research, 1990
- Application of Pig Liver Esterases (PLE) in Asymetric SynthesisTetrahedron, 1990
- Baker's Yeast as a Reagent in Organic SynthesisSynthesis, 1990
- Enzymatic Catalysts in Organic SynthesisScience, 1989
- Enzyme-catalyzed synthesis of carbohydratesTetrahedron, 1989
- A highly selective ester hydrolase from Pseudomonas sp. for the enzymatic preparation of enantiomerically pure secondary alcohols; chiral auxiliaries in organic synthesisJournal of the Chemical Society, Chemical Communications, 1988
- Tetrahedron report number 203Tetrahedron, 1986
- Microbial oxygenation of dialkylbenzenes (I)Bioorganic Chemistry, 1973
- Vinyl Aromatic Compounds. I. The Vapor Phase Dehydration of ArylmethylcarbinolsJournal of the American Chemical Society, 1946