Synthesis of (+)-vinblastine and its analogues

Org Lett. 2007 Nov 8;9(23):4737-40. doi: 10.1021/ol702040y. Epub 2007 Oct 13.

Abstract

A synthetic route to vinblastine and its analogues with an ethynyl group, which features a stereoselective coupling of an 11-membered key intermediate with vindoline, is described. Transformations of the alkynyl moiety including a partial reduction as well as a Sonogashira coupling furnished a variety of analogues.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Proliferation / drug effects
  • Humans
  • K562 Cells
  • Molecular Structure
  • Vinblastine / analogs & derivatives*
  • Vinblastine / chemical synthesis*
  • Vinblastine / chemistry
  • Vinblastine / toxicity

Substances

  • Vinblastine