Efficient Synthesis of Optically Pure 1,1,1-Trifluoro-2-alkanols through Lipase-Catalyzed Acylation in Organic Media
- 1 January 1996
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 61 (7) , 2332-2336
- https://doi.org/10.1021/jo951976a
Abstract
No abstract availableKeywords
This publication has 16 references indexed in Scilit:
- Effects of Substrate Structure on Lipase-Catalyzed Transesterification of ω-Substituted 1-Alkanols in Organic SolventsBulletin of the Chemical Society of Japan, 1994
- A Structural Basis for the Chiral Preferences of LipasesJournal of the American Chemical Society, 1994
- Biotransformation of 1,1,1-trifluoroheptane-2-one and octane-2-one by the cell suspension culture of Nicotiana tabacum-acceleration by fluorine substitutionJournal of Biotechnology, 1994
- Pseudomonas lipases as catalysts in organic synthesis: specificity of lipoprotein lipaseJournal of the Chemical Society, Chemical Communications, 1992
- Synthesis and Properties of Ferroelectric Liquid Crystals with a Fluorinated Asymmetric Frame.Journal of Synthetic Organic Chemistry, Japan, 1991
- Enzymatic optical resolution of a synthetic pyrethroid alcohol. Enantioselective transesterification by lipase in organic solventRecueil des Travaux Chimiques des Pays-Bas, 1991
- Control of enzyme enantioselectivity by the reaction mediumJournal of the American Chemical Society, 1988
- A microbially based approach for the preparation of chiral molecules possessing the trifluoromethyl groupThe Journal of Organic Chemistry, 1987
- ASYMMETRICAL REDUCTION OF PERFLUOROALKYLATED KETONES, KETOESTERS AND VINYL COMPOUNDS WITH BAKER’S YEASTChemistry Letters, 1983
- Quantitative analyses of biochemical kinetic resolutions of enantiomersJournal of the American Chemical Society, 1982