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MARIA LUISA SALADINO

Suzuki-Miyaura cross-coupling of arenediazonium salts catalyzed by alginate/gellan-stabilized palladium nanoparticles under aerobic conditions in water

  • Autori: Cacchi, S; Caponetti, E.; Casadei, MA; Di Giulio, A; Fabrizi, G.; Forte, G; Goggiamani,A; Moreno, S.; Paolicelli,P; Petrucci, F; Prastaro,A; Saladino ML
  • Anno di pubblicazione: 2012
  • Tipologia: Articolo in rivista (Articolo in rivista)
  • OA Link: http://hdl.handle.net/10447/62332

Abstract

The use of palladium nanoparticles stabilized by natural beads made of an alginate/gellan mixture in the Suzuki-Miyaura cross-coupling reaction of arenediazonium tetrafluoroborates with potassium aryltrifluoroborates (1 : 1 molar ratio) with loading as low as 0.01–0.002 mol% under aerobic, phosphine-, and base-free conditions in water is described. The catalyst system can be reused several times without significant loss of activity.