Stereocontrolled Total Synthesis of (±)-Catharanthine via Radical-Mediated Indole Formation
- 8 September 1999
- journal article
- research article
- Published by American Chemical Society (ACS) in Organic Letters
- Vol. 1 (7) , 973-976
- https://doi.org/10.1021/ol990749i
Abstract
No abstract availableKeywords
This publication has 11 references indexed in Scilit:
- Radical Cyclization of 2-Alkenylthioanilides: A Novel Synthesis of 2,3-Disubstituted IndolesJournal of the American Chemical Society, 1999
- Syntheses and reactions of silyl carbamates. 1. Chemoselective transformation of amino protecting groups via tert-butyldimethylsilyl carbamatesThe Journal of Organic Chemistry, 1990
- One-pot conversion of N-benzyloxycarbonyl group into N-tert-butoxycarbonyl groupTetrahedron Letters, 1988
- Synthesis of (.+-.)-catharanthine via organopalladium chemistryThe Journal of Organic Chemistry, 1979
- Syntheses of velbanamine and catharanthineJournal of the American Chemical Society, 1970
- The Total Synthesis of Iboga Alkaloids1Journal of the American Chemical Society, 1966
- Vinca Alkaloids. XVII.1 Chemistry of Catharanthine2,3Journal of the American Chemical Society, 1965
- The structure of catharanthine, a novel variant of the iboga alkaloidsTetrahedron Letters, 1961
- Alkaloids of Vinca rosea Linn. (Catharanthus roseus G. Don.) V.**Organic Chemical Development and Lilly Research Laboratories, Eli Lilly and Co., Indianapolis, Ind.Journal of the American Pharmaceutical Association (Scientific ed.), 1959
- A Note on the Alkaloids of Vinca rosea Linn. (Catharanthus roseus G. Don.) II.**Lilly Research Laboratories and Organic Chemical Development, Eli Lilly and Co., Indianapolis, Ind.Journal of the American Pharmaceutical Association (Scientific ed.), 1959