A new synthesis of both the enantiomers of grandisol, the boll weevil pheromon
- 1 January 1987
- journal article
- Published by Elsevier in Tetrahedron
- Vol. 43 (10) , 2229-2239
- https://doi.org/10.1016/s0040-4020(01)86806-x
Abstract
No abstract availableKeywords
This publication has 23 references indexed in Scilit:
- Synthesis of optically pure enantiomers of grandisolThe Journal of Organic Chemistry, 1986
- Efficient asymmetric (2 + 2) photocycloaddition leading to chiral cyclobutanes. Application to the total synthesis of (-)-grandisolJournal of the American Chemical Society, 1986
- Intramolecular [2 + 2] cycloadditions of ketenesJournal of the American Chemical Society, 1985
- Novel silicon-promoted cycloalkylation of alkenylmetal derivativesJournal of the American Chemical Society, 1983
- Enzymes in organic synthesis. 26.Synthesis of enantiomerically pure grandisol from an enzyme-generated chiral synthonCanadian Journal of Chemistry, 1982
- A New, Convenient Preparation ofcis-(±)2-Acetyl-1-methylcyclobutaneacetic Acid, a Key Intermediate in the Synthesis of (±)GrandisolSynthesis, 1979
- Studies on terpenes. 4. Synthesis of optically active grandisol, the boll weevil pheromoneJournal of the American Chemical Society, 1976
- Neopentyl displacement without rearrangementJournal of the American Chemical Society, 1972
- Identification and synthesis of the four compounds comprising the boll weevil sex attractantThe Journal of Organic Chemistry, 1971
- Synthesis of d- and 1-sirenin and their absolute configurationsJournal of the American Chemical Society, 1971