| Literature DB >> 31082239 |
Mao-Rui Wang1, Li Deng1, Guo-Chen Liu1, Ling Wen1, Jin-Ge Wang1, Ke-Bin Huang1, Hai-Tao Tang1, Ying-Ming Pan1.
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.Entities:
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Year: 2019 PMID: 31082239 DOI: 10.1021/acs.orglett.9b01230
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005