Your browser doesn't support javascript.
loading
Porous Organic Polymer-Derived Nanopalladium Catalysts for Chemoselective Synthesis of Antitumor Benzofuro[2,3- b]pyrazine from 2-Bromophenol and Isonitriles.
Wang, Mao-Rui; Deng, Li; Liu, Guo-Chen; Wen, Ling; Wang, Jin-Ge; Huang, Ke-Bin; Tang, Hai-Tao; Pan, Ying-Ming.
Afiliación
  • Wang MR; State Key Laboratory for Chemistry and Molecular Engineering of Medicinal Resources , School of Chemistry and Pharmaceutical Sciences of Guangxi Normal University , Guilin 541004 , People's Republic of China.
  • Deng L; State Key Laboratory for Chemistry and Molecular Engineering of Medicinal Resources , School of Chemistry and Pharmaceutical Sciences of Guangxi Normal University , Guilin 541004 , People's Republic of China.
  • Liu GC; State Key Laboratory for Chemistry and Molecular Engineering of Medicinal Resources , School of Chemistry and Pharmaceutical Sciences of Guangxi Normal University , Guilin 541004 , People's Republic of China.
  • Wen L; State Key Laboratory for Chemistry and Molecular Engineering of Medicinal Resources , School of Chemistry and Pharmaceutical Sciences of Guangxi Normal University , Guilin 541004 , People's Republic of China.
  • Wang JG; State Key Laboratory for Chemistry and Molecular Engineering of Medicinal Resources , School of Chemistry and Pharmaceutical Sciences of Guangxi Normal University , Guilin 541004 , People's Republic of China.
  • Huang KB; State Key Laboratory for Chemistry and Molecular Engineering of Medicinal Resources , School of Chemistry and Pharmaceutical Sciences of Guangxi Normal University , Guilin 541004 , People's Republic of China.
  • Tang HT; State Key Laboratory for Chemistry and Molecular Engineering of Medicinal Resources , School of Chemistry and Pharmaceutical Sciences of Guangxi Normal University , Guilin 541004 , People's Republic of China.
  • Pan YM; State Key Laboratory for Chemistry and Molecular Engineering of Medicinal Resources , School of Chemistry and Pharmaceutical Sciences of Guangxi Normal University , Guilin 541004 , People's Republic of China.
Org Lett ; 21(13): 4929-4932, 2019 07 05.
Article en En | MEDLINE | ID: mdl-31082239
ABSTRACT
An efficient strategy for the synthesis of benzofuro[2,3- b]pyrazines was developed. These tricyclic scaffolds were formed through a multistep cascade sequence, which includes double insertion of isonitriles and chemoselective bicyclization. In this reaction, a nanopalladium was used as a recyclable catalyst. Product 3w exhibited excellent anticancer activity toward T-24 (IC50 = 12.5 ± 0.9 µM) and HeLa (IC50 = 14.7 ± 1.6 µM) cells. We also explored the action mechanism of 3w on T-24 cells.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Fenoles / Pirazinas / Nitrilos Idioma: En Revista: Org Lett Asunto de la revista: BIOQUIMICA Año: 2019 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Fenoles / Pirazinas / Nitrilos Idioma: En Revista: Org Lett Asunto de la revista: BIOQUIMICA Año: 2019 Tipo del documento: Article