Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/123456789/28759
Title: Effects of the structure of primary nitroalkanes and reaction conditions on the selectivity of acylamination of arenes in polyphosphoric acid
Authors: Aksenov, A. V.
Аксенов, А. В.
Grishin, I. Y.
Гришин, И. Ю.
Aksenov, D. A.
Аксенов, Д. А.
Grishin, Y. I.
Гришин, Ю. И.
Aksenova, I. V.
Аксенова, И. В.
Aksenov, N. A.
Аксенов, Н. А.
Keywords: Acylamination;Polyphosphoric acid;Aliphatic nitro compounds;Anilides;Beckmann rearrangement;Benzamides
Issue Date: 2024
Publisher: Springer
Citation: Aksenov, 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/s11172-024-4277-8
Series/Report no.: Russian Chemical Bulletin
Abstract: The 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.
URI: https://dspace.ncfu.ru/handle/123456789/28759
Appears in Collections:Статьи, проиндексированные в SCOPUS, WOS

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