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W. J. Tang, A. G. Capacci, X. D. Wei, W. J. Li, A. White, N. D. Patel, J. Savoie, J. J. Gao, S. Rodriguez, B. Qu, N. Haddad, B. Z. Lu, D. Krishnamurthy, N. K. Yee and C. H. Senanayake, “A General and Special Catalyst for Suzuki-Miyaura Coupling Processes,” Angewandte Chemie, Vol. 122, No. 34, 2010, pp. 6015-6019.

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.