Abstract

A new bis(carbene) ligand architecture has been developed and was evaluated in the Suzuki-Miyaura cross-coupling reaction of various aryl halides with phenylboronic acid. Several new bis(carbene) ligands were tested in different carbene:Pd ratios. Pd(OAc)(2) and Pd(2)(dba)(3) were compared for efficiency as a Pd source. It was found that the Pd(OAc)(2)/bis(carbene) system formed a catalyst for the activation of chlorobenzene. [reaction: see text]

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