4.6 Article

Evaluation of P-bridged biaryl phosphine ligands in palladium-catalysed Suzuki-Miyaura cross-coupling reactions

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RSC ADVANCES
卷 11, 期 43, 页码 26883-26891

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ROYAL SOC CHEMISTRY
DOI: 10.1039/d1ra04947j

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  1. Research Centre for Synthesis and Catalysis (University of Johannesburg)
  2. Sasol (Pty) Ltd.

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A new family of biaryl phosphacyclic ligands have been developed for efficient Suzuki-Miyaura cross-coupling of aryl bromides and chlorides, with successful coupling of sterically hindered and heterocyclic substrates at room temperature.
A family of biaryl phosphacyclic ligands derived from phobane and phosphatrioxa-adamantane frameworks is described. The rigid biaryl phosphacycles are efficient for Suzuki-Miyaura cross-coupling of aryl bromides and chlorides. In particular, coupling reactions of the challenging sterically hindered and heterocyclic substrates were viable at room temperature.

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