Introduction of hydroxyl group at C-14 of indole alkaloids: the partial synthesis of 14α-hydroxyrauniticine
- 31 December 1983
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 24 (36) , 3861-3864
- https://doi.org/10.1016/s0040-4039(00)94296-5
Abstract
No abstract availableKeywords
This publication has 7 references indexed in Scilit:
- A 400 mhz 1H NMR study of the eight basic heteroyohimbine alkaloidsTetrahedron, 1980
- Alkaloids of Uncaria attenuata from ThailandPhytochemistry, 1980
- Alcaloides indoliques CVI (1) Identité de la mayumbine et de l'épi-19 ajmalicine. L'iso-3 rauniticine, un nouvel alcaloïde extrait du (R. Good) N. Hallé.Tetrahedron Letters, 1977
- 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
- Carbon-13 Fourier transform nuclear magnetic resonance spectroscopy of indolo[2,3-a]quinolizidines. Specific deuteration and relaxation methods in structure assignmentsThe Journal of Organic Chemistry, 1975
- The Conversion of Tetrahydro-β-carbolines into 2-AcylindolesThe Journal of Organic Chemistry, 1967
- Dehydrogenation of Alkaloids of the Yohimbine Type with tert.-Butyl Hypochlorite. Conversion of Yohimbine to Pseudoyohimbine.Acta Chemica Scandinavica, 1956