Schotten-Baumann acylation of N-debenzoyltaxol; an efficient route to N-acyl taxol analogues and their biological evaluation
- 20 January 1994
- journal article
- Published by Elsevier in Bioorganic & Medicinal Chemistry Letters
- Vol. 4 (2) , 335-338
- https://doi.org/10.1016/s0960-894x(01)80139-6
Abstract
No abstract availableKeywords
This publication has 7 references indexed in Scilit:
- A highly efficient route to taxotere by the β-Lactam Synthon MethodTetrahedron Letters, 1993
- Synthesis of biologically active taxol analogs with modified phenylisoserine side chainsJournal of Medicinal Chemistry, 1992
- Taxol Photoaffinity Label: 7-(p-Azidobenzoyl)taxol Synthesis and Biological EvaluationBioorganic & Medicinal Chemistry Letters, 1992
- The clinical pharmacology and use of antimicrotubule agents in cancer chemotherapeuticsPharmacology & Therapeutics, 1991
- Efficient and practical asymmetric synthesis of the taxol C-13 side chain, N-benzoyl-(2R,3S)-3-phenylisoserine, and its analogs via chiral 3-hydroxy-4-aryl-.beta.-lactams through chiral ester enolate-imine cyclocondensationThe Journal of Organic Chemistry, 1991
- Taxol: an antimitotic agent with a new mechanism of actionPharmacology & Therapeutics, 1984
- Plant antitumor agents. VI. Isolation and structure of taxol, a novel antileukemic and antitumor agent from Taxus brevifoliaJournal of the American Chemical Society, 1971