A Bioinspired Catalytic Aerobic Oxidative C-H Functionalization of Primary Aliphatic Amines: Synthesis of 1,2-Disubstituted Benzimidazoles - Archive ouverte HAL Accéder directement au contenu
Article Dans Une Revue Chemistry - A European Journal Année : 2015

A Bioinspired Catalytic Aerobic Oxidative C-H Functionalization of Primary Aliphatic Amines: Synthesis of 1,2-Disubstituted Benzimidazoles

Résumé

Aerobic oxidative C-H functionalization of primary aliphatic amines has been accomplished with ab iomimetic cooperative catalytic system to furnish1 ,2-disubstituted benzimidazoles that play an important role as drug discovery targets.T his one-pot atom-economical multistep process, which proceeds under mild conditions, with ambient air and equimolar amounts of each coupling partner,c onstitutes ac onvenient environmentally friendly strategy to functionalize non-activated aliphatic amines that remain challenging substrates for non-enzymatic catalytic aerobic systems.
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hal-02384771 , version 1 (21-11-2020)

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Khac Minh Huy Nguyen, Martine Largeron. A Bioinspired Catalytic Aerobic Oxidative C-H Functionalization of Primary Aliphatic Amines: Synthesis of 1,2-Disubstituted Benzimidazoles. Chemistry - A European Journal, 2015, 21 (36), pp.12606-12610. ⟨10.1002/chem.201502487⟩. ⟨hal-02384771⟩
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