An environmentally friendly and economically favorable approach to the formation of C-N bonds is presented. The methodology is particularly interesting in that the reaction is realized under both solvent- and ligand-free conditions and involves the use of a low loading of a palladium catalyst dispersed with the reactants on a suitable solid support. The reaction proceeds rapidly under microwave irradiation.

Solvent- and Ligand-Free Palladium-Catalyzed Amination of Aryl Halides / E. Beccalli, L. Basolo, A. Bernasconi, G. Broggini, S. Gazzola. - In: SYNTHESIS. - ISSN 0039-7881. - 45:22(2013), pp. 3151-3156.

Solvent- and Ligand-Free Palladium-Catalyzed Amination of Aryl Halides

E. Beccalli
Primo
;
L. Basolo
Secondo
;
A. Bernasconi;
2013

Abstract

An environmentally friendly and economically favorable approach to the formation of C-N bonds is presented. The methodology is particularly interesting in that the reaction is realized under both solvent- and ligand-free conditions and involves the use of a low loading of a palladium catalyst dispersed with the reactants on a suitable solid support. The reaction proceeds rapidly under microwave irradiation.
amination; arylation; catalysis; green-chemistry; microwave; solid-phase synthesis
Settore CHIM/06 - Chimica Organica
2013
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/226431
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