Synthesis of 2-trifluoromethylpyrazolo[5,1-a]isoquinolines via silver triflate-catalyzed or electrophile-mediated one-pot tandem reaction

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Abstract

An efficient one-pot tandem cyclization/[3 + 2] cycloaddition reaction of N '-(2-alkynylbenzylidene)hydrazides with ethyl 4,4,4- trifluorobut-2-ynoate under silver triflate-catalyzed or electrophile-mediated conditions is described. Various trifluoromethylated pyrazolo[5,1-a]isoquinolines were afforded in moderate to excellent yield by this developed method.

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Zhou, X., Liu, M., Luo, P., Lai, Y., Yan, T., & Ding, Q. (2014). Synthesis of 2-trifluoromethylpyrazolo[5,1-a]isoquinolines via silver triflate-catalyzed or electrophile-mediated one-pot tandem reaction. Beilstein Journal of Organic Chemistry, 10, 2286–2292. https://doi.org/10.3762/bjoc.10.238

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