Stereocontrolled route to a key intermediate for the synthesis of maytansine
- 31 December 1975
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 16 (31), 2643-2646
- https://doi.org/10.1016/s0040-4039(00)75203-8
Abstract
No abstract availableThis publication has 7 references indexed in Scilit:
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- Progress toward the total synthesis of maytansine. A model system containing the C-7 to C-16 moiety (southern and eastern zone)Tetrahedron Letters, 1975
- Generation and synthetic applications of 2-lithio-1,3-dithianesThe Journal of Organic Chemistry, 1975
- Studies directed toward the total synthesis of maytansine. The preparation and properties of the carbinolamide moiety.Tetrahedron Letters, 1974
- Plant antitumour agents: colubrinol acetate and colubrinol, antileukaemic ansa macrolides from Colubrina texensisJournal of the Chemical Society, Chemical Communications, 1973
- Protection of hydroxyl groups as tert-butyldimethylsilyl derivativesJournal of the American Chemical Society, 1972
- Tumor inhibitors. LXXIII. Maytansine, a novel antileukemic ansa macrolide from Maytenus ovatusJournal of the American Chemical Society, 1972