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Mizoroki-Heck Cross-coupling Reactions Catalyzed by Dichloro{bis[1,1',1''-(phosphinetriyl)tripiperidine]}palladium Under Mild Reaction Conditions
Published on: March 20, 2014
Well-defined Ir/Pd complexes with a triazolyl-diylidene bridge as catalysts for multiple tandem reactions
Alessandro Zanardi1, José A Mata, Eduardo Peris
1Departamento de Química Inorgánica y Orgánica, Universitat Jaume I, Avda. Vicente Sos Baynat s/n, Castellón, E-12071 Spain.
Abstract:
The ligand 1,2,4-trimethyl-triazolyl-diylidene has been used for the preparation of a series of three iridium/palladium heterometallic complexes that have been fully characterized. The presence of the two different metals allows tandem processes to be designed by combining reactions that are typically catalyzed by Ir and Pd. Three tandem reactions have been studied: dehalogenation/transfer hydrogenation of haloacetophenones, Suzuki-coupling/transfer hydrogenation of p-bromoacetophenone, and Suzuki-coupling/alpha-alkylation of p-bromoacetophenone. All three reactions yielded excellent outcomes to the corresponding final products, with the relevant feature that the heterodimetallic complexes are more active than the sum of the corresponding homodimetallic species. All three catalytic reactions reported here constitute unprecedented examples of tandem approaches to complex organic molecules.
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