J. W. Labadie, D. Tueting and S. K. Stille, “Synthetic Utility of the Palladium-Catalyzed Coupling Reaction of Acid Chlorides with Organotins,” The Journal of Organic Chemistry, Vol. 48, No. 24, 1983, pp. 4634-4642. doi:10.1021/jo00172a038

has been cited by the following article:

• TITLE: Recent Advances of Modern Protocol for C-C Bonds—The Suzuki Cross-Coupling

  AUTHORS: Jadwiga Sołoducho, Kamila Olech, Agnieszka Świst, Dorota Zając, Joanna Cabaj

  KEYWORDS: C-C Bond Formation; Coupling Reactions; Palladium Catalysts; Suzuki Coupling; Heterocyclic Copolymers

  JOURNAL NAME: Advances in Chemical Engineering and Science, Vol.3 No.3A1, July 15, 2013

  ABSTRACT: Over the past 20 years, small molecule solid phase synthesis has become a powerful tool in the discovery of novel molecular materials. In the development of organic chemistry, the carbon-carbon bond formation has always been one of the most useful and fundamental reaction. The current review summarizes recent developments in metal-catalyzed coupling reactions. The following method is discussed in detail—the cross-coupling of aryl halides with aryl boronic acids (the Suzuki coupling), and the others C-C bond formation reactions as the palladium-catalyzed reaction between an aryl and (or) alkyl halide and a vinyl functionality (the Heck reaction); and the palladium-catalyzed cross-coupling reaction of organostannyl reagents with a variety of organic electrophiles (the Stille reaction)—are mentioned.