A highly stereoselective synthesis of the C18 cecropia juvenile hormone
- 31 December 1979
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 20 (7) , 593-594
- https://doi.org/10.1016/s0040-4039(01)86010-x
Abstract
No abstract availableThis publication has 8 references indexed in Scilit:
- Stannylation/destannylation. Preparation of .alpha.-alkoxy organolithium reagents and synthesis of dendrolasin via a carbinyl carbanion equivalentJournal of the American Chemical Society, 1978
- A highly stereoselective synthesis of Z-trisubstituted olefins via [2,3]-sigmatropic rearrangement. Preference for a pseudoaxially substituted transition stateJournal of the American Chemical Society, 1978
- O,2-Dilithio derivative of allyl alcohol, a useful synthetic reagentThe Journal of Organic Chemistry, 1975
- Sesterterpenes. I. Stereospecific total synthesis of moenocinolJournal of the American Chemical Society, 1975
- Stereoselective epoxidations of acyclic allylic alcohols by transition metal-hydroperoxide reagents. Synthesis of dl-C18 Cecropia juvenile hormone from farnesolJournal of the American Chemical Society, 1974
- Stereoselective synthesis of olefins. Reaction of dialkylcopper-lithium reagents with allylic acetatesJournal of the American Chemical Society, 1970
- Synthesis of Cecropia juvenile hormone from trans,trans-farnesolJournal of the American Chemical Society, 1970
- Stereospecific total synthesis of the dl-C18 Cecropia juvenile hormoneJournal of the American Chemical Society, 1968