Direct metal-catalyzed regioselective functionalization of enamides

Chemistry. 2014 Jun 16;20(25):7548-64. doi: 10.1002/chem.201402070. Epub 2014 May 26.

Abstract

Enamides are stable enamine surrogates and provide key intermediates for the synthesis of small but complex nitrogen-containing compounds. Metal-catalyzed regioselective functionalization of enamides provides a rapid method to synthesize useful nitrogen containing heterocycles. This review discloses the recent progress made in the development of the C-H functionalization of enamides involving efficient and atom-economical routes. Syntheses of different heterocycles are classified based on the site reactivity of enamides and key mechanistic insights are given for each transformation.

Keywords: CH functionalization; atom economy; enamides; heterocycles; metal catalysis.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Amides / chemistry*
  • Catalysis
  • Molecular Structure
  • Nitrogen
  • Stereoisomerism

Substances

  • Amides
  • Nitrogen