Enhanced Heterogeneously Catalyzed Suzuki-Miyaura Reaction over SiliaCat Pd(0) (Articolo in rivista)

Type
Label
  • Enhanced Heterogeneously Catalyzed Suzuki-Miyaura Reaction over SiliaCat Pd(0) (Articolo in rivista) (literal)
Anno
  • 2013-01-01T00:00:00+01:00 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
  • 10.1016/j.tetlet.2013.06.099 (literal)
Alternative label
  • Valerica Pandarus, Delphine Desplantier-Giscard, Genevieve Gingras, Rosaria Ciriminna, Piera Demma Carà, François Béland, Mario Pagliaro (2013)
    Enhanced Heterogeneously Catalyzed Suzuki-Miyaura Reaction over SiliaCat Pd(0)
    in Tetrahedron letters; PERGAMON-ELSEVIER SCIENCE LTD, THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD (Regno Unito)
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • Valerica Pandarus, Delphine Desplantier-Giscard, Genevieve Gingras, Rosaria Ciriminna, Piera Demma Carà, François Béland, Mario Pagliaro (literal)
Pagina inizio
  • 4712 (literal)
Pagina fine
  • 4716 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#url
  • http://www.sciencedirect.com/science/article/pii/S0040403913010757 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
  • 54 (literal)
Rivista
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#pagineTotali
  • 5 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroFascicolo
  • 35 (literal)
Note
  • ISI Web of Science (WOS) (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
  • Valerica Pandarus, Delphine Desplantier-Giscard, Genevieve Gingras, François Béland: SiliCycle Inc, Quebec City, PQ G1P 4S6, Canada. Rosaria Ciriminna, Piera Demma Carà, Mario Pagliaro: CNR, Ist Studio Mat Nanostrutturati, I-90146 Palermo, Italy. (literal)
Titolo
  • Enhanced Heterogeneously Catalyzed Suzuki-Miyaura Reaction over SiliaCat Pd(0) (literal)
Abstract
  • The SiliaCat Pd(0) solid catalyst can be efficiently employed in the Suzuki-Miyaura cross-coupling of an ample variety of haloarenes, including economically viable chloroarenes. The catalyst can be extensively recycled without loss of activity and with low leaching of valued palladium, opening the route to widespread utilization of the method to afford high yields of biaryls devoid of contaminating by-products. (literal)
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