CuI/1,10-phen/PEG promoted decarboxylation of 2,3-diarylacrylic acids: synthesis of stilbenes under neutral and microwave conditions with an in situ generated recyclable catalyst

Org Biomol Chem. 2013 Sep 25;11(40):6967-74. doi: 10.1039/c3ob41588k.

Abstract

A series of trans- or cis-stilbenes have been synthesized in good to excellent yields via a functional group-dependent decarboxylation process from the corresponding 2,3-diaryl acrylic acids in a neutral CuI/1,10-phen/PEG-400 system under microwave conditions. The in situ generation of the recyclable catalytic complex, the use of environmentally benign solvent PEG-400, the operational simplicity, the short reaction times, as well as the functional group-dependent chemo- and stereo-selectivity have made the decarboxylation process a highly efficient and applicable protocol.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acrylates / chemistry*
  • Catalysis
  • Copper / chemistry*
  • Decarboxylation
  • Iodides / chemistry*
  • Microwaves*
  • Molecular Structure
  • Organometallic Compounds / chemistry
  • Phenanthrolines / chemistry*
  • Polyethylene Glycols / chemistry*
  • Stereoisomerism
  • Stilbenes / chemical synthesis*
  • Stilbenes / chemistry

Substances

  • Acrylates
  • Iodides
  • Organometallic Compounds
  • Phenanthrolines
  • Stilbenes
  • Polyethylene Glycols
  • Copper
  • cuprous iodide
  • acrylic acid
  • 1,10-phenanthroline