Complete asymmetric induction in heteroconjugate addition on an acyclic system a new synthetic approach directed toward ansamacrolide maytansine
- 31 December 1979
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 20 (36) , 3465-3468
- https://doi.org/10.1016/s0040-4039(01)95436-x
Abstract
No abstract availableThis publication has 9 references indexed in Scilit:
- Total synthesis of vernolepin—ITetrahedron, 1979
- Dithiane chemistry. III. The addition of Grignard reagents to substituted ketene dithioacetals.Tetrahedron Letters, 1978
- Vinylsilanes as substrates for the synthesis of sulfinesTetrahedron Letters, 1978
- Vinyl phenyl selenide: a +CH:CH- synthonThe Journal of Organic Chemistry, 1978
- Asymmetric synthesis of (+)- or (-)-2-methyloctanal via the metalloenamines of chiral alkoxy aminesThe Journal of Organic Chemistry, 1978
- Synthesis of sesquiterpene antitumor lactones I a facile synthesis of -fused-a-ring in vernolepin and vernomeninTetrahedron Letters, 1977
- Tumor inhibitors. 122. The maytansinoids. Isolation, structural elucidation, and chemical interrelation of novel ansa macrolidesThe Journal of Organic Chemistry, 1977
- Erzeugung von und Olefinierung mit α‐S‐, ‐Se‐, ‐Si‐ und ‐Sn‐perheterosubstituierten (Trimethylsilyl)methyllithium‐VerbindungenEuropean Journal of Inorganic Chemistry, 1977
- Tumor inhibitors. LXXIII. Maytansine, a novel antileukemic ansa macrolide from Maytenus ovatusJournal of the American Chemical Society, 1972