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Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/123456789/28759
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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.authorAksenov, D. A.-
dc.contributor.authorАксенов, Д. А.-
dc.contributor.authorGrishin, Y. I.-
dc.contributor.authorГришин, Ю. И.-
dc.contributor.authorAksenova, I. V.-
dc.contributor.authorАксенова, И. В.-
dc.contributor.authorAksenov, N. A.-
dc.contributor.authorАксенов, Н. А.-
dc.date.accessioned2024-08-14T14:35:23Z-
dc.date.available2024-08-14T14:35:23Z-
dc.date.issued2024-
dc.identifier.citationAksenov, A.V., Grishin, I.Y., Aksenov, D.A., Grishin, Y.I., Aksenova, I.V., Aksenov, N.A. Effects of the structure of primary nitroalkanes and reaction conditions on the selectivity of acylamination of arenes in polyphosphoric acid // Russian Chemical Bulletin. - 2024. - 73 (6). - pp. 1612-1622. - DOI: 10.1007/s11172-024-4277-8ru
dc.identifier.urihttps://dspace.ncfu.ru/handle/123456789/28759-
dc.description.abstractThe mechanism of acylamination of arenes with nitroalkanes in polyphosphoric acid has been clarified. The influence of the concentration of polyphosphoric acid, the structure of the starting compounds, and temperature on the result of the Beckmann rearrangement, which makes it possible to shift the reaction towards either benzamides or anilides, has been assessed.ru
dc.language.isoenru
dc.publisherSpringerru
dc.relation.ispartofseriesRussian Chemical Bulletin-
dc.subjectAcylaminationru
dc.subjectPolyphosphoric acidru
dc.subjectAliphatic nitro compoundsru
dc.subjectAnilidesru
dc.subjectBeckmann rearrangementru
dc.subjectBenzamidesru
dc.titleEffects of the structure of primary nitroalkanes and reaction conditions on the selectivity of acylamination of arenes in polyphosphoric acidru
dc.typeСтатьяru
vkr.instХимический факультетru
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