Absolute stereochemistry of serricornin, the sex pheromone of cigarette beetle, as determined by the synthesis of its (4S,6R,7R)-isomer
- 31 December 1982
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 23 (6), 667-670
- https://doi.org/10.1016/s0040-4039(00)86917-8
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
- Determination of the absolute configuration at C-6 and C-7 of serricornin (4,6-dimethyl-7-hydroxy-3-nonanone), the sex pheromone of the cigarette beetleTetrahedron Letters, 1981
- Pheromone synthesis. Stereoselective synthesis of erythro-serricornin,(4R,6R,7S)-,and (4S,6R,7S)-4,6-dimethyl-7-hydroxynonan-3-one,stereoisomers of the sex pheromone of cigarette beetle.Agricultural and Biological Chemistry, 1981
- 4.6-dimethyl-7-hydroxy-nonan-3-one, a sex pheromone of the cigarette beetle (Lasioderma serricorne F.)Tetrahedron Letters, 1979
- Ciral synthons for the multistriatinsTetrahedron Letters, 1979
- Synthesis of (±)-Serricornin, 4, 6-Dimethyl-7-hydroxy-nonan-3-one, A Sex Pheromone of Cigarette Beetle (Lasioderma serricorne F.)Agricultural and Biological Chemistry, 1979
- Stereospecific synthesis of (−)-α-multistriatin from D-glucoseCanadian Journal of Chemistry, 1978
- Generation and synthetic applications of 2-lithio-1,3-dithianesThe Journal of Organic Chemistry, 1975
- Studies in asymmetric synthesis. Highly stereoselective reactions of organosulfur compoundsTetrahedron, 1974
- Reactions of lithium diorganocuprates(I) with tosylates. I. Synthetic aspectsJournal of the American Chemical Society, 1973