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Reversal of aryl bromide reactivity in Pd-catalysed aryl amination reactions promoted by a hemilabile aminophosphine ligand
Authors:Sebastien L Parisel  Adriana Amoedo Pereira  José M Vila
Institution:a Department of Chemistry, King's College London, Strand, London WC2R 2LS, UK
b Departamento de Química Inorgánica, Facultad de Química, Universidad de Santiago e Compostela, E-15782, Spain
c Department of Chemistry, Imperial College London, Exhibition Road, South Kensington, London SW7 2AZ, UK
Abstract:Incorporation of a hemilabile amino group with a bulky, electron-rich phosphorus ligand led to a reversal in the order of aryl bromide reactivity in Pd-catalysed aryl amination reactions.
Keywords:Palladium catalysis  PN ligands  Aryl amination  Aryl bromides
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