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Direct Access to 2,3-Disubstituted Amido-Indenones through Annulation of 2-Iodobenzaldehydes with Ynamides.
Golling, Stéphane; Hansjacob, Pierre; Bami, Nassim; Leroux, Frédéric R; Donnard, Morgan.
Afiliação
  • Golling S; CNRS, UMR 7042-LIMA, ECPM, Université de Strasbourg, Université de Haute-Alsace, F-67000 Strasbourg, France.
  • Hansjacob P; CNRS, UMR 7042-LIMA, ECPM, Université de Strasbourg, Université de Haute-Alsace, F-67000 Strasbourg, France.
  • Bami N; CNRS, UMR 7042-LIMA, ECPM, Université de Strasbourg, Université de Haute-Alsace, F-67000 Strasbourg, France.
  • Leroux FR; CNRS, UMR 7042-LIMA, ECPM, Université de Strasbourg, Université de Haute-Alsace, F-67000 Strasbourg, France.
  • Donnard M; CNRS, UMR 7042-LIMA, ECPM, Université de Strasbourg, Université de Haute-Alsace, F-67000 Strasbourg, France.
J Org Chem ; 87(24): 16860-16866, 2022 12 16.
Article em En | MEDLINE | ID: mdl-36472915
ABSTRACT
In this paper we report the annulation reaction between 2-iodobenzaldehyde derivatives and various ynamides. This palladium-catalyzed reaction leads to rare polysubstituted amino-indenones in good yields with a regioselectivity up to complete. Remarkably, a regiodivergent selectivity has been identified between aryl and alkyl or silyl ynamides, with the first leading mainly to 2-amido-indenones and the second to 3-amido-indenones.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Paládio Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Paládio Idioma: En Ano de publicação: 2022 Tipo de documento: Article