Issue 2, 2012

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

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.

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

Supplementary files

Article information

Article type
Communication
Submitted
09 Jun 2011
Accepted
21 Nov 2011
First published
20 Dec 2011

Green Chem., 2012,14, 317-320

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

S. Cacchi, E. Caponetti, M. A. Casadei, A. Di Giulio, G. Fabrizi, G. Forte, A. Goggiamani, S. Moreno, P. Paolicelli, F. Petrucci, A. Prastaro and M. L. Saladino, Green Chem., 2012, 14, 317 DOI: 10.1039/C2GC15679B

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