Asymmetric synthesis III. Enantiospecific synthesis of the natural 3r, 5r, 9r (−) gephyrotoxin-223 AB
- 31 December 1985
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 26 (12), 1515-1518
- https://doi.org/10.1016/s0040-4039(00)98540-x
Abstract
No abstract availableKeywords
This publication has 7 references indexed in Scilit:
- High diastereoselectivity in the reaction of α-aminonitriles bearing an (S)-(+)-2-methoxymethylpyrrolidine group with Grignard reagentsJournal of the Chemical Society, Chemical Communications, 1984
- Chiral 1,4-dihydropyridine equivalents: a new approach to the asymmetric synthesis of alkaloids. The enantiospecific synthesis of (+)- and (-)-coniine and dihydropinidineJournal of the American Chemical Society, 1983
- Stereoselective indolizidine synthesis: preparation of stereoisomers of gephyrotoxin-223ABThe Journal of Organic Chemistry, 1982
- Studies on the stereochemistry of nucleophilic additions to tetrahydropyridinium salts. A stereospecific total synthesis of one of the stereoisomers of gephyrotoxin 223Journal of the Chemical Society, Chemical Communications, 1982
- The structure of gephyrotoxin (GTX) 223ABCellular and Molecular Life Sciences, 1981
- Indolizidine alkaloid synthesis. Preparation of the pharaoh ant trail pheromone and gephyrotoxin 223 stereoisomersThe Journal of Organic Chemistry, 1980
- Classification of skin alkaloids from neotropical poison-dart frogs (dendrobatidae)Toxicon, 1978