Synthesis of optically active pheromones with an epoxy ring, (+)-disparlure and the saltmarsh caterpillar moth pheromone [(Z,Z)-3,6-cis-1-9,10-epoxyheneicosadiene]
- 31 December 1981
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 22 (43) , 4281-4282
- https://doi.org/10.1016/s0040-4039(01)82934-8
Abstract
No abstract availableThis publication has 2 references indexed in Scilit:
- 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