Syntheses of novel C-9 and C-10 modified bioactive taxanes
- 20 March 1995
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 36 (12) , 1985-1988
- https://doi.org/10.1016/0040-4039(95)00208-t
Abstract
No abstract availableKeywords
This publication has 7 references indexed in Scilit:
- Selective C-2 and C-4 deacylation and acylation of taxol: The first synthesis of a C-4 substituted taxol analogueTetrahedron Letters, 1994
- The first synthesis of a C-9 carbonyl modified baccatin III derivative and its conversion to novel taxol® and taxotere® analoguesBioorganic & Medicinal Chemistry Letters, 1994
- Electrochemical reduction of taxoids: Selective preparation of 9-dihydro-, 10-deoxy- and 10-deacetoxy-taxoidsTetrahedron Letters, 1994
- Samarium Diiodide-Mediated Deoxygenation of Taxol: A One-Step Synthesis of 10-DeacetoxytaxolThe Journal of Organic Chemistry, 1994
- Cleavage reactions of 10-deacetylbaccatin III. Retrosynthetic approach to the total synthesis of taxol derivatives.Tetrahedron, 1994
- Synthesis of biologically active taxol analogs with modified phenylisoserine side chainsJournal of Medicinal Chemistry, 1992
- Plant antitumor agents. VI. Isolation and structure of taxol, a novel antileukemic and antitumor agent from Taxus brevifoliaJournal of the American Chemical Society, 1971