Aminoborylation/Suzuki-Miyaura tandem cross coupling of aryl iodides as efficient and selective synthesis of unsymmetrical biaryls

Chem Commun (Camb). 2012 Feb 1;48(10):1553-5. doi: 10.1039/c1cc14605j. Epub 2011 Sep 30.

Abstract

Sequential borylation of a first aryl iodide using a dialkylaminoborane followed by a Suzuki-Miyaura cross coupling of second aryl iodide ended up with an efficient, selective and practical synthesis of unsymmetrical biaryls. This tandem coupling shows a wide range of applicability.

MeSH terms

  • Biphenyl Compounds / chemical synthesis*
  • Biphenyl Compounds / chemistry
  • Boranes / chemistry*
  • Hydrocarbons, Iodinated / chemistry*
  • Molecular Structure

Substances

  • Biphenyl Compounds
  • Boranes
  • Hydrocarbons, Iodinated