Studies on the identification and syntheses of insect pheromones XXI stereoselective synthesis of all the possible optical isomers of the mosquito oviposition attractant pheromone
- 31 December 1985
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 26 (9) , 1233-1236
- https://doi.org/10.1016/s0040-4039(00)98441-7
Abstract
No abstract availableKeywords
This publication has 11 references indexed in Scilit:
- Total synthesis of leukotriene B5Tetrahedron Letters, 1983
- Synthesis of both the enantiomers of erythro-6-acetoxy-5-hexadecanolideTetrahedron, 1983
- Synthese von Hydroxy‐γ‐lactonen aus α,β‐ungesättigten AldehydenEuropean Journal of Organic Chemistry, 1982
- erythro-6-Acetoxy-5-hexadecanolide, the major component of a mosquito oviposition attractant pheromoneJournal of the Chemical Society, Chemical Communications, 1982
- 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
- Palladium(0) catalyzed reaction of 1,3-diene epoxides. A useful method for the site-specific oxygenation of 1,3-dienesJournal of the American Chemical Society, 1979
- Syntheses of macrolide antibiotics. I. MethymycinJournal of the American Chemical Society, 1975
- The Wittig Reaction. I. Synthesis of β,γ-Unsaturated AcidsJournal of the American Chemical Society, 1964
- 1121. Syntheses of long-chain acids. Part V. Synthesis of some ω-hydroxy-acetylenic acidsJournal of the Chemical Society, 1963