Abstract
With acid catalysts 2-(4′-acetylphenylamino)-3-piperidino-1,4-naphthoquinone reacts with hydroxylamine and aryl hydrazines exclusively at the carbonyl group of its side chain. The products corresponding to the condensation at the naphthoquinone C=O group could not be detected.
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Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 6, pp. 1086–1088, June, 1994.
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Rubashko, S.V., Mikhalina, T.V., Bagryanskaya, I.Y. et al. The interaction of 2-(4-acetylphenylamino)-3-piperidino-1,4-naphthoquinone with hydroxylamine and hydrazines. Russ Chem Bull 43, 1024–1026 (1994). https://doi.org/10.1007/BF01558071
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DOI: https://doi.org/10.1007/BF01558071