Ansa macrolide synthesis preoaration of the aromatic portion of maytansine
- 31 December 1977
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 18 (9) , 775-776
- https://doi.org/10.1016/s0040-4039(01)92751-0
Abstract
No abstract availableThis publication has 6 references indexed in Scilit:
- Progress toward the total synthesis of maytansine. A stereoselective synthesis of the C-1 to C-7 moiety (northern zone)Tetrahedron Letters, 1975
- 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
- Tumor inhibitors. 107. Novel maytansinoids. Naturally occurring and synthetic antileukemic esters of maytansinolJournal of the American Chemical Society, 1975
- Stereocontrolled route to a key intermediate for the synthesis of maytansineTetrahedron Letters, 1975
- Studies directed toward the total synthesis of maytansine. The preparation and properties of the carbinolamide moiety.Tetrahedron Letters, 1974
- LXII.—Dihydric alcohols obtained by the reduction of substituted dihydroresorcinsJournal of the Chemical Society, Transactions, 1915