Abstract
It was established that polymethyl-substituted 2-azafluorences obtained by catalytic dehydrocyclization of pyridine- and benzene-ring-substituted γ-arylpyridines have different structures depending on the position of the methyl groups in the starting compound and which methyl group participates in the cyclization reaction. The 1,4, 7-trimethyl-2-azafluorene synthesized by this method was used for the preparation of new condensed heterocyclic systems of the 3-azafluoranthene and cyclohexano-8-azafluoranthene type.
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 6, pp. 814–818, June, 1977.
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Prostakov, N.S., Obynochnyi, A.A., Dorogov, V.V. et al. Polymethyl-substituted 2-azafluorenes and synthesis of azafluoranthene derivatives from them. Chem Heterocycl Compd 13, 663–667 (1977). https://doi.org/10.1007/BF00480676
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DOI: https://doi.org/10.1007/BF00480676