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.
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CITATION STYLE
Wang, M. R., Deng, L., Liu, G. C., Wen, L., Wang, J. G., Huang, K. B., … Pan, Y. M. (2019). Porous organic polymer-derived nanopalladium catalysts for chemoselective synthesis of antitumor benzofuro[2,3-b]pyrazine from 2-Bromophenol and Isonitriles. Organic Letters, 21(13), 4929–4932. https://doi.org/10.1021/acs.orglett.9b01230
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