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Total Synthesis of Tedarene A.
Maurent, Kelly; Vanucci-Bacqué, Corinne; Saffon-Merceron, Nathalie; Baltas, Michel; Bedos-Belval, Florence.
Afiliación
  • Maurent K; UMR CNRS 5068, LSPCMIB, Université Paul Sabatier , 118 Route de Narbonne, Toulouse, 31062 Cedex 9, France.
  • Vanucci-Bacqué C; UMR CNRS 5068, LSPCMIB, Université Paul Sabatier , 118 Route de Narbonne, Toulouse, 31062 Cedex 9, France.
  • Saffon-Merceron N; Institut de Chimie de Toulouse, ICT FR 2599, Université Paul Sabatier , Toulouse III, Toulouse 31062 Cedex 9, France.
  • Baltas M; UMR CNRS 5068, LSPCMIB, Université Paul Sabatier , 118 Route de Narbonne, Toulouse, 31062 Cedex 9, France.
  • Bedos-Belval F; UMR CNRS 5068, LSPCMIB, Université Paul Sabatier , 118 Route de Narbonne, Toulouse, 31062 Cedex 9, France.
J Nat Prod ; 80(5): 1623-1630, 2017 05 26.
Article en En | MEDLINE | ID: mdl-28463511
ABSTRACT
Tedarene A is a macrocyclic diaryl ether heptanoid isolated from the marine sponge Tedania ignis showing an inhibitory effect against nitric oxide production. The first total synthesis of tedarene A was achieved starting from the commercially available 3-(4-methoxyphenyl)propan-1-ol in nine steps and 15.3% overall yield. The synthetic sequence featured an E,Z-dienic bond introduction and a macrocyclization under Ullman conditions. During the synthesis, the E,E-isomer of tedarene A was also obtained and fully characterized.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Poríferos / Propanoles / Diarilheptanoides / Éteres Límite: Animals Idioma: En Revista: J Nat Prod Año: 2017 Tipo del documento: Article País de afiliación: Francia

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Poríferos / Propanoles / Diarilheptanoides / Éteres Límite: Animals Idioma: En Revista: J Nat Prod Año: 2017 Tipo del documento: Article País de afiliación: Francia