A short enantioselective route to corynanthe alkaloid precursors
- 1 January 1990
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 31 (5) , 739-742
- https://doi.org/10.1016/s0040-4039(00)94617-3
Abstract
No abstract availableKeywords
This publication has 6 references indexed in Scilit:
- A concise strategy for the syntheses of indole alkaloids of the heteroyohimboid and corynantheioid families. Total syntheses of (.+-.)-tetrahydroalstonine, (.+-.)-cathenamine and (.+-.)-geissoschizineJournal of the American Chemical Society, 1988
- Enantioselective deprotonation by chiral lithium amide bases: asymmetric synthesis of trimethylsilyl enol ethers from 4-alkylcyclohexanonesJournal of the American Chemical Society, 1986
- Design and reactivity of topologically unique, chiral phosphonamides. Remarkable diastereofacial selectivity in asymmetric olefination and alkylationJournal of the American Chemical Society, 1984
- Regioselective synthesis of β-ketoesters from lithium enolates and methyl cyanoformateTetrahedron Letters, 1983
- Conversion of secologanin into elenolic acid and 18-oxayohimban alkaloidsJournal of the Chemical Society, Perkin Transactions 1, 1976
- Total syntheses of dl-ajmalicine and emetineJournal of the American Chemical Society, 1969