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Selective Tsuji-Trost type C-allylation of hydrazones: a straightforward entry into 4,5-dihydropyrazoles.
El Mamouni, El Hachemia; Cattoen, Martin; Cordier, Marie; Cossy, Janine; Arseniyadis, Stellios; Ilitki, Hocine; El Kaïm, Laurent.
Afiliação
  • El Mamouni EH; Laboratoire de Synthèse Organique, CNRS, Ecole Polytechnique, ENSTA ParisTech-UMR 7652, Université Paris-Saclay, 828 Bd des Maréchaux, 91128, Palaiseau, France. laurent.elkaim@ensta-paristech.fr and Laboratoire de Chimie Organique, Institute of Chemistry, Biology and Innovation (CBI)-ESPCI Paris/CNR
  • Cattoen M; Queen Mary University of London, School of Biological and Chemical Sciences, Mile End Road, London, E1 4NS, UK.
  • Cordier M; Laboratoire de Chimie Moléculaire, UMR 9168, Department of Chemistry, Ecole Polytechnique, CNRS, 91128, Palaiseau Cedex, France.
  • Cossy J; Laboratoire de Chimie Organique, Institute of Chemistry, Biology and Innovation (CBI)-ESPCI Paris/CNRS (UMR8231)/PSL Research University, 10 rue Vauquelin, 75231 Paris Cedex 05, France.
  • Arseniyadis S; Laboratoire de Chimie Organique, Institute of Chemistry, Biology and Innovation (CBI)-ESPCI Paris/CNRS (UMR8231)/PSL Research University, 10 rue Vauquelin, 75231 Paris Cedex 05, France and Queen Mary University of London, School of Biological and Chemical Sciences, Mile End Road, London, E1 4NS, UK.
  • Ilitki H; Laboratory of the Chemistry and Electrochemistry of the Metallic Complexes, Department of Chemistry, Faculty of Sciences, University of Sciences and Technology of Oran Mohamed Boudiaf (U.S.T.O.M.B.), Algeria.
  • El Kaïm L; Laboratoire de Synthèse Organique, CNRS, Ecole Polytechnique, ENSTA ParisTech-UMR 7652, Université Paris-Saclay, 828 Bd des Maréchaux, 91128, Palaiseau, France. laurent.elkaim@ensta-paristech.fr.
Chem Commun (Camb) ; 52(100): 14490-14493, 2016 Dec 13.
Article em En | MEDLINE | ID: mdl-27905579
The 4,5-dihydropyrazole motif has drawn considerable attention over the years as it was shown to exhibit a plethora of biological and pharmacological properties, including anticancer, antibacterial, antifungal, antiviral, and anti-inflammatory properties. As such, it has been the target of a number of methods and drug discovery programs. We report here a straightforward and highly selective approach featuring a key palladium-catalysed Tsuji-Trost type C-allylation and subsequent intramolecular 1,4-addition of hydrazones.
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Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Chem Commun (Camb) Assunto da revista: QUIMICA Ano de publicação: 2016 Tipo de documento: Article País de publicação: Reino Unido
Buscar no Google
Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Chem Commun (Camb) Assunto da revista: QUIMICA Ano de publicação: 2016 Tipo de documento: Article País de publicação: Reino Unido