Suzuki-Miyaura cross-coupling of aryl chlorides in water using ligandless palladium on activated carbon

Morten Lysén, Klaus Köhler

Research output: Contribution to journalArticlepeer-review

74 Scopus citations

Abstract

Aqueous reaction conditions that activate various aryl chlorides in Suzuki-Miyaura cross-coupling have been developed. These environment friendly conditions utilize ligandless Pd/C (Pd concentrations 0.2-2 mol%) that allow easy separation of the catalyst at the end of the reaction.

Original languageEnglish
Pages (from-to)1671-1674
Number of pages4
JournalSynlett
Issue number11
DOIs
StatePublished - 7 Jul 2005

Keywords

  • Aryl chlorides
  • Biaryls
  • Cross-coupling
  • Palladium
  • Water

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