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Al-Masum, M. and Wai, E.Ng. (2011) Palladium-Catalyzed Direct Cross-Coupling of Potassium Styryltri-fluuoroborates and Benzoyl Chlorides—A One Step Method for Chalcone Synthesis. Tetrahedron Letters, 52, 1008-1010.
https://doi.org/10.1016/j.tetlet.2010.12.085

has been cited by the following article:

• TITLE: Efficient Cross-Coupling Reaction of Aryltrifluoroborates and Aroyl Chlorides for the Synthesis of Fluorine Substituted Aromatic Ketones

  AUTHORS: Mohammed Al-Masum, Tasfia Islam, Grady Clopton

  KEYWORDS: ArBF3K, Aroyl Chlorides, Direct Aroylation to Ketones, Minute Reaction

  JOURNAL NAME: International Journal of Organic Chemistry, Vol.9 No.1, March 18, 2019

  ABSTRACT: The direct aroylation of ArCOPdCl with potassium aryltrifluoroborates establishes a new cross-coupling synthetic tool for the synthesis of various fluorine substituted benzophenones. The new microwave irradiated process is very efficient and produce high yield benzophenone products within minutes.