articleJournal of the American Chemical SocietyDec 16, 2005Closed access

Catalytic Direct Arylation with Aryl Chlorides, Bromides, and Iodides:  Intramolecular Studies Leading to New Intermolecular Reactions

University of Ottawa

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Abstract

A catalyst for the intramolecular direct arylation of a broad range of simple and heterocyclic arenes with aryl iodides, bromides, and chlorides has been developed. These reactions occur in excellent yield and are highly selective. Studies with aryl iodides substrates revealed that catalyst poisoning occurs due to the accumulation of iodide in the reaction media. This can be overcome by the addition of silver salts which also permits these reactions to occur at lower temperature. The utility of the methodology is illustrated by a rapid synthesis of a carbazole natural product and by the synthesis of sterically encumbered tetra-ortho-substituted biaryls via ring-opening reactions of the direct arylation…

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676
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Authors

4

Topics & keywords

Keywords
  • Chemistry
  • Aryl
  • Intramolecular force
  • Catalysis
  • Steric effects
  • Intermolecular force
  • Iodide
  • Palladium
UN Sustainable Development Goals
  • Clean water and sanitation
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