Enzymatic optical resolution of a synthetic pyrethroid alcohol. Enantioselective transesterification by lipase in organic solvent
- 1 January 1991
- journal article
- research article
- Published by Wiley in Recueil des Travaux Chimiques des Pays-Bas
- Vol. 110 (5) , 151-154
- https://doi.org/10.1002/recl.19911100503
Abstract
No abstract availableKeywords
This publication has 21 references indexed in Scilit:
- Irreversible and highly enantioselective acylation of 2-halo-1-arylethanols in organic solvents catalyzed by a lipase from Pseudomonas fluorescensThe Journal of Organic Chemistry, 1988
- Aspects Of Biocatalyst Stability In Organic SolventsBiocatalysis, 1987
- Enzymes as Catalysts in Synthetic Organic Chemistry [New Synthetic Methods (53)]Angewandte Chemie International Edition in English, 1985
- Comparison of different strategies for the lipase‐catalyzed preparative resolution of racemic acids and alcohols: Asymmetric hydrolysis, esterification, and transesterificationBiotechnology & Bioengineering, 1984
- Quantitative analyses of biochemical kinetic resolutions of enantiomersJournal of the American Chemical Society, 1982
- Stereospecific hydrolysis by soluble and immobilized lipasesBiotechnology & Bioengineering, 1982
- Absolute configuration of synthetic pyrethroids containing .ALPHA.-ethynyl alcohol moiety.Agricultural and Biological Chemistry, 1981
- Recent topics in the chemistry of synthetic pyrethroids containing certain secondary alcohol moietiesPesticide Science, 1980
- Enzymic and chemical resolution of 1-octyn-4-olThe Journal of Organic Chemistry, 1977
- Biochemical resolution of racemic terpenes. VII. Microbial resolution of some racemic monocyclic alcohols.Agricultural and Biological Chemistry, 1975