Synthetic Studies in the Alkaloid Field. Part VIII. The Sodium Borohydride Reduction of 3-Acetyl-1-[2-(3-indolyl)-ethyl]pyridinium Bromide.
- 1 January 1978
- journal article
- research article
- Published by Danish Chemical Society in Acta Chemica Scandinavica
- Vol. 32b (3) , 216-220
- https://doi.org/10.3891/acta.chem.scand.32b-0216
Abstract
The preparation of 3 isomeric acetylhexahydroindolo[2,3-a]-quinolizines by the sodium borohydride reduction of 3-acetyl-1-[2-(3-indolyl)ethyl]pyridinium bromide, followed by acid-induced cyclization, is described.This publication has 4 references indexed in Scilit:
- Synthetic studies in the alkaloid field—VTetrahedron, 1978
- Reaktionen an Indolderivaten, XXX Die stereoselektive und stereospezifische Totalsynthese der Geissoschizin‐IsomerenEuropean Journal of Inorganic Chemistry, 1976
- General methods of synthesis of indole alkaloids. 14. Short routes of construction of yohimboid and ajmalicinoid alkaloid systems and their carbon-13 nuclear magnetic resonance spectral analysisJournal of the American Chemical Society, 1976
- Synthetic Studies in the Alkaloid Field. Part III. Selective Alkaline Decarboalkoxylative Cyclization of Some N-Alkyldihydro- and N-Alkyltetrahydropyridines.Acta Chemica Scandinavica, 1976