Pd-catalyzed decarboxylative coupling of propiolic acids: one-pot synthesis of 1,4-disubstituted 1,3-diynes via Sonogashira-homocoupling sequence

J Org Chem. 2011 Apr 1;76(7):2214-9. doi: 10.1021/jo200096x. Epub 2011 Mar 4.

Abstract

One-pot synthesis of symmetric 1,4-disubstituted 1,3-diynes from iodoarenes and propiolic acid via Sonogashira reaction followed by Pd-catalyzed decarboxylative homocoupling is developed in high yields. Also, this system allows the one-pot synthesis of unsymmetric 1,4-disubstituted 1,3-diynes by cross-coupling of two different 3-substituted propiolic acids.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alkynes / chemistry*
  • Catalysis
  • Combinatorial Chemistry Techniques
  • Cross-Linking Reagents / chemistry
  • Diynes / chemical synthesis*
  • Diynes / chemistry*
  • Magnetic Resonance Spectroscopy
  • Molecular Structure
  • Palladium / chemistry*
  • Propionates / chemistry*

Substances

  • Alkynes
  • Cross-Linking Reagents
  • Diynes
  • Propionates
  • Palladium
  • propiolic acid