Pd-catalyzed reaction of sterically hindered hydrazones with aryl halides: synthesis of tetra-substituted olefins related to iso-combretastatin A4

Org Lett. 2010 Sep 17;12(18):4042-5. doi: 10.1021/ol101639g.

Abstract

PdCl(2)(MeCN)(2) in combination with dppp proved to be a powerful and efficient catalyst for the coupling of sterically hindered N-arylsulfonylhydrazones with aryl halides, thus providing a flexible and convergent access to tetrasubstituted olefins related to iso-combretastatin A4 in good yields. This new protocol has been applied successfully to the formal synthesis of biphenylisopropylidene 4-pyridine CYP17 inhibitor, 12b, of biological interest.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alkenes / chemical synthesis*
  • Alkenes / pharmacology
  • Catalysis
  • Halogens / chemistry*
  • Hydrazones / chemistry*
  • Molecular Structure
  • Palladium / chemistry*
  • Stereoisomerism
  • Steroid 17-alpha-Hydroxylase / antagonists & inhibitors
  • Stilbenes / chemistry*
  • Stilbenes / pharmacology
  • Tubulin / chemistry

Substances

  • Alkenes
  • Halogens
  • Hydrazones
  • Stilbenes
  • Tubulin
  • Palladium
  • Steroid 17-alpha-Hydroxylase
  • fosbretabulin