Abstract
The reaction of di(3-benzylidene-2-oxocyclohexyl)methane and its p-methoxy analog with primary amines results in the formation of derivatives of 4,5-diarylidenehydroacridines, whereas the reaction with o-phenylenediamine is accompanied by the elimination of one arylidene group and gives derivatives of 4-arylidenehydroacridines.
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 10, pp. 1393–1395, October, 1984.
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Minaeva, N.N., Kaminskii, V.A. & Tilichenko, M.N. Arylidenehydroacridines from di(3-arylidene-2-oxocyclohexyl)-methanes. Chem Heterocycl Compd 20, 1149–1151 (1984). https://doi.org/10.1007/BF00503609
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DOI: https://doi.org/10.1007/BF00503609