Rhodium-catalyzed C3-selective alkenylation of substituted thiophene-2-carboxylic acids and related compounds

J Org Chem. 2013 Jul 19;78(14):7216-22. doi: 10.1021/jo4011969. Epub 2013 Jul 8.

Abstract

The regioselective C3-alkenylation of thiophene-2-carboxylic acids can be achieved effectively via rhodium/silver-catalyzed oxidative coupling with alkenes, unaccompanied by decarboxylation. A wide range of substrates including brominated thiophenecarboxylic acids and furan-2-carboxylic acids can be employed together with styrenes as well as acrylates. The present catalyst system is also applicable to ortho-alkenylation of benzoic acids.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alkenes / chemical synthesis*
  • Alkenes / chemistry
  • Carboxylic Acids
  • Catalysis
  • Molecular Structure
  • Organometallic Compounds / chemistry*
  • Rhodium / chemistry*
  • Thiophenes / chemistry*

Substances

  • Alkenes
  • Carboxylic Acids
  • Organometallic Compounds
  • Thiophenes
  • 2-thiophene carboxylic acid
  • Rhodium