Abstract
The corresponding 2-(2-furyl)- and 2-[β-(2-furyl)vinyl] phenanthr[9,10]imidazoles were obtained by the condensation of 9,10 phenanthrenequinone with furfural, β-(2-furyl)acrolein, and their 5-bromo and 5-nitro derivatives in the presence of ammonium acetate in glacial acetic acid. Their metallation, acetylation, nitration, and replacement of halogen by a nitro group were studied.
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 8, pp. 1014–1016, August, 1971.
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Pozharskii, F.T., Oleinikova, L.Y. & Pupkova, L.G. Synthesis and transformations of 2-(2-furyl)- and 2-[β-(2-furyl)vinyl] phenanthr [9,10]imidazoles. Chem Heterocycl Compd 7, 950–952 (1971). https://doi.org/10.1007/BF00477367
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DOI: https://doi.org/10.1007/BF00477367