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Activation of N−O σ Bonds with Transition Metals: A Versatile Platform for Organic Synthesis and C−N Bonds Formation**
Authors:Uroš Todorović  Dr R Martin Romero  Dr Lucile Anthore-Dalion
Institution:1. Université Paris-Saclay, CEA, CNRS NIMBE, 91191 Gif-sur-Yvette, France

These authors contributed equally to this work.;2. Université Paris-Saclay, CEA, CNRS NIMBE, 91191 Gif-sur-Yvette, France

Abstract:N−O σ bonds containing compounds are versatile substrates for organic synthesis under transition metal catalysis. Their ability to react through both polar (oxidative addition, formation of metallanitrene, nucleophilic substitution) and radical pathways (single electron transfer, homolytic bond scission) have triggered the development of various synthetic methodologies, particularly toward synthesizing nitrogen-containing compounds. In this review, we discuss the different modes of activation of N−O bonds in the presence of transition metal catalysts, emphasizing the experimental and computational mechanistic proofs in the literature to help to design new synthetic pathways toward the synthesis of C−N bonds.
Keywords:N−O bonds  electrophilic amination  hydroxylamines  mechanisms  metal catalysis
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