A key intermediate for the synthesis of maytansine and related antitumor agents
- 31 December 1978
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 19 (12) , 1051-1054
- https://doi.org/10.1016/s0040-4039(01)85449-6
Abstract
No abstract availableFunding Information
- National Institutes of Health
This publication has 10 references indexed in Scilit:
- Preparation of a benzenoid intermediate For use in the synthesis of MaytansineTetrahedron Letters, 1977
- Progress toward the total synthesis of maytansinoids. A facile route to the aromatic moiety (western zone)Tetrahedron Letters, 1977
- Ansa macrolide synthesis preoaration of the aromatic portion of maytansineTetrahedron Letters, 1977
- Tumor inhibitors. 122. The maytansinoids. Isolation, structural elucidation, and chemical interrelation of novel ansa macrolidesThe Journal of Organic Chemistry, 1977
- A simple and highly effective route to α,β-unsaturated aldehydesTetrahedron Letters, 1976
- Selektive Synthesen mit Organometallen III. (Z)‐Crotylalkoholate mit metalltragenden olefinischen KohlenstoffatomenHelvetica Chimica Acta, 1974
- Mixed cuprate reagents of type R1R2CuLi which allow selective group transferJournal of the American Chemical Society, 1972
- Tumor inhibitors. LXXIII. Maytansine, a novel antileukemic ansa macrolide from Maytenus ovatusJournal of the American Chemical Society, 1972
- Carbon-carbon bond formation by selective coupling of n-alkylcopper reagents with organic halidesJournal of the American Chemical Society, 1968
- Selective formation of carbon-carbon bonds between unlike groups using organocopper reagentsJournal of the American Chemical Society, 1967