4.6 Article

A Convenient Palladium-Catalyzed Carbonylative Suzuki Coupling of Aryl Halides with Formic Acid as the Carbon Monoxide Source

Journal

CHEMISTRY-A EUROPEAN JOURNAL
Volume 21, Issue 49, Pages 17650-17656

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/chem.201502943

Keywords

carbonylation; cross-coupling; heterogeneous catalysis; palladium; synthesis design

Funding

  1. NSFC [21472174]
  2. Education Department of Zhejiang Province [Y201432060]
  3. Zhejiang Sci-Tech University [1206838-Y, 14062015-Y]
  4. Matthias Beller in LIKAT

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A practical palladium-catalyzed carbonylative Suzuki coupling of aryl halides under carbon monoxide gas-free conditions has been developed. Here, formic acid was utilized as the carbon monoxide source for the first time with acetic anhydride as the additive. A variety of diaryl-ketones were produced in moderate to excellent yields from the corresponding aryl halides and arylboronic acids.

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