Iron-catalyzed Suzuki-Miyaura coupling of alkyl halides

J Am Chem Soc. 2010 Aug 11;132(31):10674-6. doi: 10.1021/ja103973a.

Abstract

In the presence of novel iron(II) chloride-diphosphine complexes and magnesium bromide, lithium arylborates react with primary and secondary alkyl halides to give the corresponding coupling products in good to excellent yields. High functional group compatibility is also demonstrated in the reactions of substrates possessing reactive substituents, such as alkoxycarbonyl, cyano, and carbonyl groups.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Catalysis
  • Crystallography, X-Ray
  • Ferrous Compounds / chemistry*
  • Hydrocarbons, Halogenated / chemistry*
  • Models, Molecular
  • Molecular Structure
  • Phosphines / chemical synthesis*
  • Phosphines / chemistry

Substances

  • Ferrous Compounds
  • Hydrocarbons, Halogenated
  • Phosphines
  • ferrous chloride