Palladium nanoparticles catalyzed Suzuki cross-coupling reactions in ambient conditions

An efficient pathway to synthesize biaryls and terphenyls through ligand-free palladium nanoparticles (PdNPs) catalyzed Suzuki cross-coupling reactions has been developed. Mild reaction conditions, high yields of desired products, absence of inert atmosphere and short reaction times are the notable...

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Bibliographic Details
Published in:Catalysis communications 2013-01, Vol.31, p.16-20
Main Authors: Mandali, Pavan Kumar, Chand, Dillip Kumar
Format: Article
Language:English
Subjects:
Ambient conditions
Heterocyclic ligands
Palladium nanoparticles
Suzuki cross-coupling
Terphenyl derivatives
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Summary:An efficient pathway to synthesize biaryls and terphenyls through ligand-free palladium nanoparticles (PdNPs) catalyzed Suzuki cross-coupling reactions has been developed. Mild reaction conditions, high yields of desired products, absence of inert atmosphere and short reaction times are the notable features of this method. [Display omitted] ► Suzuki cross-coupling reactions using ligand-free palladium nanoparticles (PdNPs). ► Reusable property of the catalyst without any significant loss of the activity. ► Synthesis of a variety of biaryls and terphenyls in ambient conditions. ► Precipitation of terphenyls from the reaction mixtures.
ISSN:1566-7367
1873-3905
DOI:10.1016/j.catcom.2012.10.020