Thiazolyl Phosphine Ligands for Copper-Catalyzed Arylation and Vinylation of Nucleophiles in Organic and Aqueous Media - Université Toulouse III - Paul Sabatier - Toulouse INP Accéder directement au contenu
Article Dans Une Revue Organometallics Année : 2008

Thiazolyl Phosphine Ligands for Copper-Catalyzed Arylation and Vinylation of Nucleophiles in Organic and Aqueous Media

Résumé

A straightforward and efficient synthetic route to thiazolyl phosphines is reported. Moreover, the first application of these molecules in catalysis is described. These phosphines are excellent ligands in the copper-catalyzed arylation and Vinylation of nucleophiles. The reactions could be performed in acetonitrile and Various mixed aqueous/organic solvents and even in pure water in the presence of a phase transfer catalyst. In each case, coupling products are obtained with high yields at very mild temperatures.

Domaines

Chimie organique

Dates et versions

hal-00356546 , version 1 (27-01-2009)

Identifiants

Citer

Gennady V. Oshovsky, Armelle Ouali, Ning Xia, Maria Zablocka, René T. Boeré, et al.. Thiazolyl Phosphine Ligands for Copper-Catalyzed Arylation and Vinylation of Nucleophiles in Organic and Aqueous Media. Organometallics, 2008, 27 (21), pp.5733-5736. ⟨10.1021/om800728m⟩. ⟨hal-00356546⟩
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