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A bioinspired catalytic aerobic oxidative C-H functionalization of primary aliphatic amines: synthesis of 1,2-disubstituted benzimidazoles.
Nguyen, Khac Minh Huy; Largeron, Martine.
Afiliação
  • Nguyen KM; UMR 8638 CNRS-Université Paris Descartes (Paris 5), Sorbonne Paris Cité, Faculté de Pharmacie de Paris, 4 avenue de l'Observatoire, 75270 Paris cedex 06 (France).
  • Largeron M; UMR 8638 CNRS-Université Paris Descartes (Paris 5), Sorbonne Paris Cité, Faculté de Pharmacie de Paris, 4 avenue de l'Observatoire, 75270 Paris cedex 06 (France). martine.largeron@parisdescartes.fr.
Chemistry ; 21(36): 12606-10, 2015 Sep 01.
Article em En | MEDLINE | ID: mdl-26206475
ABSTRACT
Aerobic oxidative CH functionalization of primary aliphatic amines has been accomplished with a biomimetic cooperative catalytic system to furnish 1,2-disubstituted benzimidazoles that play an important role as drug discovery targets. This one-pot atom-economical multistep process, which proceeds under mild conditions, with ambient air and equimolar amounts of each coupling partner, constitutes a convenient environmentally friendly strategy to functionalize non-activated aliphatic amines that remain challenging substrates for non-enzymatic catalytic aerobic systems.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Benzimidazóis / Aminas Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Benzimidazóis / Aminas Idioma: En Ano de publicação: 2015 Tipo de documento: Article