Application of ring-closing metathesis reactions in the synthesis of epothilones

J Nat Prod. 2004 Feb;67(2):139-43. doi: 10.1021/np030540k.

Abstract

There is wide interest in the epothilones, which like the taxoids initiate cytotoxicity through microtubule stabilization. Briefly described is an application of a ring-closing metathesis reaction toward the synthesis of epothilones as carried out in our laboratory. This has led to the discovery of the (E)-9,10-dehydroepothilones as second-generation anticancer drug candidates.

Publication types

  • Review

MeSH terms

  • Antineoplastic Agents / chemical synthesis*
  • Antineoplastic Agents / chemistry*
  • Drug Screening Assays, Antitumor
  • Epothilones / chemical synthesis*
  • Epothilones / chemistry*
  • Molecular Structure
  • Stereoisomerism
  • Structure-Activity Relationship
  • Taxoids

Substances

  • Antineoplastic Agents
  • Epothilones
  • Taxoids