Domino reaction of 3-nitro-2-(trifluoromethyl)-2H-chromenes with 2-(1-phenylalkylidene)malononitriles: synthesis of functionalized 6-(trifluoromethyl)-6H-dibenzo[b,d]pyrans and a rare case of [1,5] sigmatropic shift of the nitro group |
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Authors: | Vladislav Yu. Korotaev Alexey Yu. BarkovVyacheslav Ya. Sosnovskikh |
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Affiliation: | Department of Chemistry, Ural Federal University, pr. Lenina 51, 620000 Ekaterinburg, Russian Federation |
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Abstract: | ![]() A variety of functionalized 6-(trifluoromethyl)-6H-dibenzo[b,d]pyrans were easily synthesized in good yields under mild conditions by a domino reaction of 3-nitro-2-(trifluoromethyl)-2H-chromenes with 2-(1-phenylethylidene)- and 2-(1-phenylpropylidene)malononitriles. In the latter case, intermediate 7-amino-10-methyl-10-nitro-9-phenyl-6-(trifluoromethyl)-10,10a-dihydro-6H-benzo[c]chromene-8-carbonitriles were isolated as a result of a rare [1,5] sigmatropic shift of the nitro group. |
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Keywords: | 3-Nitro-2-(trifluoromethyl)-2H-chromenes 1,1-Dicyanoolefins 6-(Trifluoromethyl)-6H-dibenzo[b,d]pyrans Domino reaction [1,5] Sigmatropic nitro-shift |
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