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Carbonates: Ecofriendly Solvents for Palladium-Catalyzed Direct 2-Arylation of Oxazole Derivatives

Authors

  • Julien Roger,

    1. Institut Sciences Chimiques de Rennes, UMR 6226 CNRS-Université de Rennes 1, “Catalyse et Organometalliques“, Campus de Beaulieu, 35042 Rennes (France), Fax: (+33) 0223236939
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  • Cécile Verrier,

    1. Institut de Chimie Organique Fine (IRCOF) associée au CNRS (UMR 6014), INSA et Université de Rouen, BP08, 76131 Mont Saint Aignan (France), Fax: (+33) 0235522462
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  • Ronan Le Goff,

    1. Institut Sciences Chimiques de Rennes, UMR 6226 CNRS-Université de Rennes 1, “Catalyse et Organometalliques“, Campus de Beaulieu, 35042 Rennes (France), Fax: (+33) 0223236939
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  • Christophe Hoarau Dr.,

    1. Institut de Chimie Organique Fine (IRCOF) associée au CNRS (UMR 6014), INSA et Université de Rouen, BP08, 76131 Mont Saint Aignan (France), Fax: (+33) 0235522462
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  • Henri Doucet Dr.

    1. Institut Sciences Chimiques de Rennes, UMR 6226 CNRS-Université de Rennes 1, “Catalyse et Organometalliques“, Campus de Beaulieu, 35042 Rennes (France), Fax: (+33) 0223236939
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Abstract

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Bien-bon-ates. Carbonates offer an environmentally friendly alternative to standard polar solvents. Since a few years, carbonates have been employed successfully for some classical metal-catalyzed reactions. Here, the palladium-catalyzed direct 2-arylation of oxazole derivatives in carbonate solvents is reported.

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