Ruthenium-catalyzed direct arylations through C-H bond cleavages

Top Curr Chem. 2010:292:211-29. doi: 10.1007/128_2009_9.

Abstract

Stoichiometric cycloruthenation reactions of substrates containing Lewis-basic functionalities set the stage for efficient ruthenium-catalyzed C-H bond functionalization reactions. Thereby, selective addition reactions of C-H bonds across alkenes or alkynes enabled atom-economical synthesis of substituted arenes. More recently, ruthenium-catalyzed direct arylation reactions were examined, which display an unparalleled scope and, hence, represent economically and environmentally benign alternatives to traditional cross-coupling chemistry.

Publication types

  • Review

MeSH terms

  • Alkenes / chemistry
  • Alkylation
  • Catalysis
  • Chelating Agents / chemistry
  • Chemistry, Organic / methods
  • Chlorides
  • Hydrocarbons, Aromatic / chemical synthesis*
  • Hydrogen / chemistry*
  • Organometallic Compounds / chemistry
  • Ruthenium / chemistry*

Substances

  • Alkenes
  • Chelating Agents
  • Chlorides
  • Hydrocarbons, Aromatic
  • Organometallic Compounds
  • Ruthenium
  • Hydrogen