Enantioselective total synthesis of (+)-monomorine I
- 31 December 1988
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 29 (45) , 5767-5768
- https://doi.org/10.1016/s0040-4039(00)82186-3
Abstract
No abstract availableKeywords
This publication has 15 references indexed in Scilit:
- An efficient regio- and stereoselective synthesis of (.+-.)-monomorine I via the highly regioselective .alpha.-alkynylation of a 1-acylpyridinium saltThe Journal of Organic Chemistry, 1987
- A stereoselective synthesis of the ant trail pheromone (±)-monomorine ITetrahedron Letters, 1986
- Asymmetric synthesis. 2. Practical method for the asymmetric synthesis of indolizidine alkaloids: total synthesis of (-)-monomorine IThe Journal of Organic Chemistry, 1985
- Indolizidine alkaloid synthesis. Preparation of the pharaoh ant trail pheromone and gephyrotoxin 223 stereoisomersThe Journal of Organic Chemistry, 1980
- 13C nmr assignments of selected octahydroindolizinesJournal of Heterocyclic Chemistry, 1979
- Evalutiaon of four isomers of 3‐butyl‐5‐methloctahydroindoliz, a component of the trail pheromone of pharaoh's ant, Monomorium pharaonisAnnals of Applied Biology, 1978
- Synthesis of insect trail pheromones: The isomeric 3‐butyl‐5‐methyloctahydroindolizinesJournal of Heterocyclic Chemistry, 1975
- Synthesis of the isomers of 3-butyl-5-methyloctahydroindolizine, a trail pheromone of Pharaoh antThe Journal of Organic Chemistry, 1974
- Recent Development in Insect Pheromone Research, in Particular in the NetherlandsNetherlands Journal of Zoology, 1974
- 5-methyl-3-butyl-octahydroindolizine, a novel type of pheromone attractive to Pharaoh's ants (Monomorium pharaonis (L.)Cellular and Molecular Life Sciences, 1973