Labadie, J.W. and Stille, J.K. (1983) Mechanism of the Palladium-Catalyzed Couplings of Acid Chlorides with Organotin Reagents. Journal of the American Chemical Society, 105, 6129-6137.
https://doi.org/10.1021/ja00357a026

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.