Progress toward the total synthesis of maytansinoids. An efficient route to two major precursors (western-southern zone)
- 31 December 1978
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 19 (16) , 1375-1378
- https://doi.org/10.1016/s0040-4039(01)94549-6
Abstract
No abstract availableThis publication has 10 references indexed in Scilit:
- Tumor inhibitors. 124. Structural requirements for antileukemic activity among the naturally occurring and semisynthetic maytansinoidsJournal of Medicinal Chemistry, 1978
- Preparation of a benzenoid intermediate For use in the synthesis of MaytansineTetrahedron Letters, 1977
- Ansa macrolide synthesis preoaration of the aromatic portion of maytansineTetrahedron Letters, 1977
- The cyclic carbamate unit of maytansineCanadian Journal of Chemistry, 1977
- Maytansinoids. Synthesis of a fragment of known absolute configuration involving chiral centers C-6 and C-7The Journal of Organic Chemistry, 1976
- 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
- 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
- Facile and specific conversion of allylic alcohols to allylic chlorides without rearrangementThe Journal of Organic Chemistry, 1971