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Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/123456789/32959
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dc.contributor.authorAksenov, A. V.-
dc.contributor.authorАксенов, А. В.-
dc.contributor.authorGrishin, I. Y.-
dc.contributor.authorГришин, И. Ю.-
dc.contributor.authorMalyuga, V. V.-
dc.contributor.authorМалюга, В. В.-
dc.contributor.authorAksenov, D. A.-
dc.contributor.authorАксенов, Д. А.-
dc.contributor.authorDzhioeva, R. G.-
dc.contributor.authorДжиоева, Р. Г.-
dc.contributor.authorAksenov, N. A.-
dc.contributor.authorАксенов, Н. А.-
dc.date.accessioned2026-04-29T12:11:03Z-
dc.date.available2026-04-29T12:11:03Z-
dc.date.issued2026-
dc.identifier.citationAksenov A. V., Grishin I. Y., Malyuga V. V., Aksenov D. A., Dzhioeva R. G., Aksenov N. A. Synthesis of Acylaminoperimidines by the Reaction of 1,8-Naphthylenediamine with Nitroketones // Russian Journal of General Chemistry. - 2026. - 96 (2). - art. no. 12. - DOI: 10.1134/S1070363225606957ru
dc.identifier.urihttps://dspace.ncfu.ru/handle/123456789/32959-
dc.description.abstractThe reaction of 1,8-naphthylenediamine with α-nitoketones yielded 9-acetyl- and 6(7)-acetamidoperimidines. The reaction exhibits high atom economy and is based on a tandem of benzoylation reactions of the diamine involving nitoketones, and an acylation-amination of arenes in polyphosphoric acid (PPA) medium, using the acyl forms of nitroalkanes liberated in the first stage. The dependence of the transformation’s course on the concentration of polyphosphoric acid has been investigated.ru
dc.language.isoenru
dc.publisherPleiades Publishingru
dc.relation.ispartofseriesRussian Journal of General Chemistry-
dc.subjectAcylaminationru
dc.subjectAcylationru
dc.subjectHeterocyclizationru
dc.subjectNitroalkanesru
dc.subjectNitroketonesru
dc.subjectPolyphosphoric acidru
dc.titleSynthesis of Acylaminoperimidines by the Reaction of 1,8-Naphthylenediamine with Nitroketonesru
dc.typeСтатьяru
vkr.instХимический факультетru
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