Study on Sharpless Kinetic Resol Ution of Racemic Allyl Propargyl Alcohols
- 1 December 1988
- journal article
- research article
- Published by Taylor & Francis in Synthetic Communications
- Vol. 18 (18) , 2325-2330
- https://doi.org/10.1080/00397918808082377
Abstract
A kinetic resolution of racemic allyl propargyl alcohols by enantioselective epoxidation is described.Keywords
This publication has 8 references indexed in Scilit:
- Asymmetric Epoxidation of Allylic Alcohols: The Sharpless EpoxidationSynthesis, 1986
- On the Mechanism of Asymmetric Epoxidation with Titanium—Tartrate CatalystsPublished by Elsevier ,1985
- On the mechanism of titanium-tartrate catalyzed asymmetric epoxidationPure and Applied Chemistry, 1983
- Kinetic resolution of racemic allylic alcohols by enantioselective epoxidation. A route to substances of absolute enantiomeric purity?Journal of the American Chemical Society, 1981
- Synthesis of optically active forms of methyl (E)-2,4,5-tetradecatrienoate, the pheromone of the male dried bean beetleTetrahedron, 1981
- The first practical method for asymmetric epoxidationJournal of the American Chemical Society, 1980
- Vanadium-catalyzed epoxidations. I. A new selectivity pattern for acyclic allylic alcohols.Tetrahedron Letters, 1979
- Correlation of configuration and fluorine-19 chemical shifts of .alpha.-methoxy-.alpha.-trifluoromethylphenyl acetate derivativesThe Journal of Organic Chemistry, 1973