Convenient and efficient Suzuki-Miyaura cross-coupling catalyzed by a palladium/diazabutadiene system
G A Grasa1, A C Hillier, S P Nolan
1Department of Chemistry, University of New Orleans, New Orleans, Louisiana 70148, USA.
Abstract:
[structure: see text]. A Pd(OAc)2/diazabutadiene system has been developed for the catalytic cross-coupling of aryl halides with arylboronic acids. A combination of the diazabutadiene DAB-Cy (1, N,N'-dicyclohexyl-1,4-dizabutadiene) and Pd(OAc)2 was found to form an excellent catalyst for the Suzuki-Miyaura cross-coupling of various aryl bromides and activated aryl chlorides with arylboronic acids.
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