Your browser doesn't support javascript.
loading
Cp*Co(III)-Catalyzed Dearomative [3 + 2] Spiroannulation of 2-Alkenylphenols with Ynamides via C-H Activation.
Lin, Peng-Peng; Han, Xiang-Lei; Ye, Guo-Hua; Li, Ji-Lin; Li, Qingjiang; Wang, Honggen.
Afiliación
  • Lin PP; School of Pharmaceutical Sciences , Sun Yat-sen University , Guangzhou 510006 , China.
  • Han XL; School of Pharmaceutical Sciences , Sun Yat-sen University , Guangzhou 510006 , China.
  • Ye GH; School of Chinese Medicine , Shandong College of Traditional Chinese Medicine , Yantai 264199 , China.
  • Li JL; School of Pharmaceutical Sciences , Sun Yat-sen University , Guangzhou 510006 , China.
  • Li Q; School of Pharmaceutical Sciences , Sun Yat-sen University , Guangzhou 510006 , China.
  • Wang H; State Key Laboratory of Natural and Biomimetic Drugs , Peking University , Beijing 100191 , China.
J Org Chem ; 84(20): 12966-12974, 2019 10 18.
Article en En | MEDLINE | ID: mdl-31490696
ABSTRACT
An oxidative [3 + 2] C-H spiroannulation reaction of 2-alkenylphenols with ynamides has been developed toward the synthesis of spiro[4,5]decane derivatives. This dearomative reaction employs earth-abundant cobalt as the metal catalyst and occurs under rather mild reaction conditions (room temperature). The use of ynamides confers unique reactivity and exclusive regioselectivity. The products bearing an all-carbon quaternary stereogenic center were constructed in generally good yields with good functional group tolerance being observed. Experimental mechanistic studies were conducted, and a possible reaction mechanism is proposed.

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: J Org Chem Año: 2019 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: J Org Chem Año: 2019 Tipo del documento: Article País de afiliación: China