Your browser doesn't support javascript.
loading
Synthesis of Coumestrol and Aureol.
Sheng, Jianfei; Xu, Tianlong; Zhang, Ensheng; Zhang, Xuejing; Wei, Wentao; Zou, Yong.
Afiliación
  • Sheng J; School of Pharmaceutical Sciences, Sun Yat-sen University , Guangzhou, 510006, People's Republic of China.
  • Xu T; Zhongshan WanYuan New Drug R&D Co., Ltd. , Zhongshan City, 528451, People's Republic of China.
  • Zhang E; Guangzhou Institute of Chemistry, Chinese Academy of Sciences , Guangzhou, 510650, People's Republic of China.
  • Zhang X; Zhongshan WanYuan New Drug R&D Co., Ltd. , Zhongshan City, 528451, People's Republic of China.
  • Wei W; Guangzhou Institute of Chemistry, Chinese Academy of Sciences , Guangzhou, 510650, People's Republic of China.
  • Zou Y; Zhongshan WanYuan New Drug R&D Co., Ltd. , Zhongshan City, 528451, People's Republic of China.
J Nat Prod ; 79(10): 2749-2753, 2016 10 28.
Article en En | MEDLINE | ID: mdl-27704859
ABSTRACT
A total synthesis of coumestrol (1) and aureol (2) is described. The Perkin condensation of 2-bromo-4-hydroxylphenylacetic acid (6) and o-hydroxybenzaldehydes (7) gave the corresponding 2'-bromo-3-arylcoumarins (9). A copper-catalyzed consecutive hydroxylation and aerobic oxidative coupling of 9 under microwave conditions facilitated the total synthesis of 1 and 2, respectively, with spectroscopic data highly similar to those of natural products.
Asunto(s)
Buscar en Google
Bases de datos: MEDLINE Asunto principal: Sesquiterpenos / Cumestrol Idioma: En Revista: J Nat Prod Año: 2016 Tipo del documento: Article
Buscar en Google
Bases de datos: MEDLINE Asunto principal: Sesquiterpenos / Cumestrol Idioma: En Revista: J Nat Prod Año: 2016 Tipo del documento: Article