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Oxamic acids: useful precursors of carbamoyl radicals.
Ogbu, Ikechukwu Martin; Kurtay, Gülbin; Robert, Frédéric; Landais, Yannick.
Afiliação
  • Ogbu IM; University of Bordeaux, Institute of Molecular Sciences (ISM), UMR-CNRS 5255, 351, Cours de la Libération, 33405 Talence, Cedex, France. yannick.landais@u-bordeaux.fr.
  • Kurtay G; Alex Ekwueme Federal University, Department of Chemistry, Faculty of Sciences, Ndufu-Alike Ikwo, Abakaliki, Ebonyi State, Nigeria.
  • Robert F; University of Bordeaux, Institute of Molecular Sciences (ISM), UMR-CNRS 5255, 351, Cours de la Libération, 33405 Talence, Cedex, France. yannick.landais@u-bordeaux.fr.
  • Landais Y; University of Ankara, Department of Chemistry, Faculty of Science, Ankara, Turkey.
Chem Commun (Camb) ; 58(55): 7593-7607, 2022 Jul 07.
Article em En | MEDLINE | ID: mdl-35735051
This review article describes the recent development in the chemistry of carbamoyl radicals generated from oxamic acids. This mild and efficient method compares well with previous methods of generation of these nucleophilic radicals. The oxidative decarboxylation of oxamic acids can be mediated through thermal, photochemical, electrochemical or photoelectrochemical means, generating carbamoyl radicals, which may further add to unsaturated systems to provide a broad range of important amides. Oxidative decarboxylation of oxamic acids also offers a straightforward entry for the preparation of urethanes, ureas, and thioureas.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ácido Oxâmico / Amidas Idioma: En Revista: Chem Commun (Camb) Assunto da revista: QUIMICA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: França

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ácido Oxâmico / Amidas Idioma: En Revista: Chem Commun (Camb) Assunto da revista: QUIMICA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: França