Aspidosperma alkaloids. Conversion of tabersonine into vindoline
- 1 January 1987
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Journal of the Chemical Society, Perkin Transactions 1
- No. 1,p. 155-161
- https://doi.org/10.1039/p19870000155
Abstract
An efficient synthesis of vindoline, the indoline portion of the clinically useful antitumour agent vinblastine, starting from tabersonine is described.This publication has 4 references indexed in Scilit:
- A new efficient total synthesis of vindorosine and vindolineThe Journal of Organic Chemistry, 1985
- An efficient and short degradation of the cholic acid side chain: a new method for the preparation and dehydrogenation of 4,5-dihydro-oxazolesJournal of the Chemical Society, Perkin Transactions 1, 1985
- Derives 14-hydroxyles de la vincadifformine et de la vincamineTetrahedron, 1979
- Total synthesis of indole and dihydroindole alkaloids. 14. A total synthesis of vindolineJournal of the American Chemical Society, 1978