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New opportunities with the Duff reaction.
Masurier, Nicolas; Moreau, Emmanuel; Lartigue, Claire; Gaumet, Vincent; Chezal, Jean-Michel; Heitz, Annie; Teulade, Jean-Claude; Chavignon, Olivier.
Afiliação
  • Masurier N; E.A.4231, Faculté de Pharmacie, 28 place Henri Dunant, B.P. 38, 63001 Clermont-Ferrand Cedex 1, France.
J Org Chem ; 73(15): 5989-92, 2008 Aug 01.
Article em En | MEDLINE | ID: mdl-18597528
ABSTRACT
The Duff reaction (HMTA, AcOH or TFA) was studied on substituted [6 + 5] heterocyclic compounds. This reaction provides a useful route to aldehydes for compounds bearing sensitive amide functions. It gives also access to tricyclic lactams of potential biological interest. The formation of an aminomethyl intermediate in the Duff reaction mechanism is unequivocally demonstrated.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Compostos Heterocíclicos Idioma: En Ano de publicação: 2008 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Compostos Heterocíclicos Idioma: En Ano de publicação: 2008 Tipo de documento: Article