Synthesis of 2,4,6-trisubstituted pyridines via an olefin cross-metathesis/Heck-cyclisation-elimination sequence

Chem Commun (Camb). 2011 Oct 14;47(38):10611-3. doi: 10.1039/c1cc14257g. Epub 2011 Aug 25.

Abstract

Heck reactions were performed on α,β-unsaturated-δ-sulfonamido intermediates, derived from cross metathesis, to allow the instalment of substituents at the β position. Subsequent one-pot cyclisation/elimination provides an operationally simple, catalytic and convergent synthesis of 2,4,6-trisubstituted pyridines.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alkenes / chemistry*
  • Catalysis
  • Cyclization
  • Pyridines / chemical synthesis
  • Pyridines / chemistry*
  • Transition Elements / chemistry

Substances

  • Alkenes
  • Pyridines
  • Transition Elements