Syntheses of optically active pheromones with an epoxy ring, (+)-disparlure and both the enantiomers of (3z,6z)--9,10-epoxy-3,6-heneicosadiene
- 1 January 1986
- journal article
- research article
- Published by Elsevier in Tetrahedron
- Vol. 42 (13) , 3471-3478
- https://doi.org/10.1016/s0040-4020(01)87314-2
Abstract
No abstract availableThis publication has 23 references indexed in Scilit:
- Synthesis of chiral 1,2-diols and related compounds of biological activities via stepwise ring fission of 5-alkyl-6,8-dioxabicyclo[3.2.1]octane skeletonTetrahedron Letters, 1986
- Stereo and regioselective openings of chiral 2,3-epoxy alcohols. Versatile routes to optically pure natural products and drugs. Unusual kinetic resolutionsPure and Applied Chemistry, 1983
- Asymmetric epoxidation provides shortest routes to four chiral epoxy alcohols which are key intermediates in syntheses of methymycin, erythromycin, leukotriene C-1, and disparlureJournal of the American Chemical Society, 1981
- The first practical method for asymmetric epoxidationJournal of the American Chemical Society, 1980
- Synthesis and enantiomeric purity determination of the optically active epoxide disparlure, sex pheromone of the gypsy mothThe Journal of Organic Chemistry, 1979
- Stereoselective synthesis of the both enantiomers of disparlure, the pheromone of the gypsy mothTetrahedron, 1979
- A stereospecific synthesis of (+)-disparlure, sex attractant of the gypsy mothTetrahedron Letters, 1977
- Stereoselective synthesis of optically active disparlure, the pheromone of the gypsy moth (Tetrahedron Letters, 1976
- Synthesis and activity of optically active disparlureJournal of the American Chemical Society, 1974
- Potent Sex Attractant of the Gypsy Moth: Its Isolation, Identification, and SynthesisScience, 1970