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Efficient and Mild Ullmann-Type N-Arylation of Amides, Carbamates, and Azoles in Water.
Bollenbach, Maud; Aquino, Pedro G V; de Araújo-Júnior, João Xavier; Bourguignon, Jean-Jacques; Bihel, Frédéric; Salomé, Christophe; Wagner, Patrick; Schmitt, Martine.
Afiliação
  • Bollenbach M; Université de Strasbourg, CNRS, LIT UMR 7200, 67000, Strasbourg, France.
  • Aquino PGV; Université de Strasbourg, CNRS, LIT UMR 7200, 67000, Strasbourg, France.
  • de Araújo-Júnior JX; Laboratório de Pesquisa em Recursos Naturais, UFAL, Maceió, Brazil.
  • Bourguignon JJ; Laboratório de Pesquisa em Recursos Naturais, UFAL, Maceió, Brazil.
  • Bihel F; Université de Strasbourg, CNRS, LIT UMR 7200, 67000, Strasbourg, France.
  • Salomé C; Université de Strasbourg, CNRS, LIT UMR 7200, 67000, Strasbourg, France.
  • Wagner P; Université de Strasbourg, CNRS, LIT UMR 7200, 67000, Strasbourg, France.
  • Schmitt M; SpiroChem AG, c/o, ETH-Zürich, Vladimir-Prelog-Weg 3, 8093, Zürich, Switzerland.
Chemistry ; 23(55): 13676-13683, 2017 Oct 04.
Article em En | MEDLINE | ID: mdl-28696045
ABSTRACT
A simple, sustainable, efficient, mild, and low-cost protocol was developed for d-glucose-assisted Cu-catalyzed Ullmann reactions in water for amides, carbamates, and nitrogen-containing heterocycles. The reaction was compatible with diverse aryl/heteroaryl iodides, giving highly substituted pyridine, indole, or indazole rings. This method offers an attractive alternative to existing protocols, because the reaction proceeds in aqueous media, occurs at or near ambient temperature, and provides the N-arylated products in good to high yields.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: Chemistry Assunto da revista: QUIMICA Ano de publicação: 2017 Tipo de documento: Article País de afiliação: França

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: Chemistry Assunto da revista: QUIMICA Ano de publicação: 2017 Tipo de documento: Article País de afiliação: França