Stereoselective ionic hydrogenation of Vinca alkaloids and vinorelbine in superacids: an access to 4′R-reduced analogs
- 1 November 1998
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 39 (45), 8281-8282
- https://doi.org/10.1016/s0040-4039(98)01889-9
Abstract
No abstract availableKeywords
This publication has 7 references indexed in Scilit:
- Antimitotic and tubulin-interacting properties of vinflunine, a novel fluorinated Vinca alkaloidBiochemical Pharmacology, 1998
- Preclinical in vivo antitumor activity of vinflunine, a novel fluorinated Vinca alkaloidCancer Chemotherapy and Pharmacology, 1998
- Vinca Alkaloids in Superacidic Media: A Method for Creating a New Family of Antitumor DerivativesJournal of the American Chemical Society, 1997
- Total Synthesis of Indole and Dihydroindole Alkaloids. XVIII. Isomers and analogues of vinblastineHelvetica Chimica Acta, 1980
- 5'-Nor anhydrovinblastineTetrahedron, 1979
- Application of a modification of the Polonovski reaction to the synthesis of vinblastine-type alkaloidsJournal of the American Chemical Society, 1976
- Vinca alkaloids. XXX. Chemistry of the deoxyvinblastines (deoxy-vlb), leurosine (vlr), and pleurosine, dimeric alkaloids fromTetrahedron Letters, 1968