Pheromone Synthesis, CXIII. Synthesis of the Enantiomers of (3Z,6Z)-cis-9,10-Epoxy-1,3,6-henicosatriene and (3Z,6Z)-cis-9,10-Epoxy-1,3,6-icosatriene, the New Pheromone Components ofHyphantria cunea
- 19 May 1989
- journal article
- research article
- Published by Wiley in European Journal of Organic Chemistry
- Vol. 1989 (5) , 453-457
- https://doi.org/10.1002/jlac.198919890180
Abstract
No abstract availableKeywords
This publication has 6 references indexed in Scilit:
- Synthesis of both the enantiomers of (Z)-cis-9,10-epoxy-6-heneicosene.Agricultural and Biological Chemistry, 1989
- Syntheses of optically active pheromones with an epoxy ring, (+)-disparlure and both the enantiomers of (3z,6z)--9,10-epoxy-3,6-heneicosadieneTetrahedron, 1986
- Synthesis of highly unsaturated insect pheromones: (Z,Z,Z)-1,3,6,9-heneicosatetraene and (Z,Z,Z)-1,3,6,9-nonadecatetraeneThe Journal of Organic Chemistry, 1983
- Sex pheromone of the fall webworm moth,Hyphantria cuneaJournal of Chemical Ecology, 1982
- Synthesis of optically active pheromones with an epoxy ring, (+)-disparlure and the saltmarsh caterpillar moth pheromone [()-3,6--1-9,10-epoxyheneicosadiene]Tetrahedron Letters, 1981
- The first practical method for asymmetric epoxidationJournal of the American Chemical Society, 1980