A practical and convenient palladium-catalyzed carbonylative Suzuki coupling of aryl halides under CO gas-free conditions has been developed. For the first time, formic acid has been employed as the CO source with acetic anhydride as the activator. In their Full Paper on page 17650 ff., X.-F. Wu and co-workers describe the preparation of a variety of diarylketones in moderate to excellent yields from the corresponding aryl halides and arylboronic acids.

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已经开发了在无CO气体条件下实用且方便的钯催化的芳基卤化物的羰基Suzuki偶合反应。第一次，甲酸被用作CO源，乙酸酐作为活化剂。X.-F.在其第17650页及其后的全文中。Wu和同事描述了从相应的芳基卤化物和芳基硼​​酸以中等到极好的收率制备各种二芳基酮的方法。