Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/123456789/29345
Title: Regioselective Nitration of (2E)-3-Aryl-2-(4-arylthiazol-2-yl)acrylonitriles
Authors: Dotsenko, V. V.
Доценко, В. В.
Aksenov, N. A.
Аксенов, Н. А.
Aksenova, I. V.
Аксенова, И. В.
Keywords: 1,3-thiazoles;α-bromoketones;2-cyanothioacrylamides;5-nitro-1,3-thiazoles;Hantzsch reaction;Nitration
Issue Date: 2024
Publisher: Pleiades Publishing
Citation: Pakholka, N.A., Dotsenko, V.V., Aksenov, N., Aksenova, I.V., Krivokolysko, S.G. Regioselective Nitration of (2E)-3-Aryl-2-(4-arylthiazol-2-yl)acrylonitriles // Russian Journal of General Chemistry. - 2024. - 94 (10). - pp. 2578-2585. - DOI: 10.1134/S1070363224100025
Series/Report no.: Russian Journal of General Chemistry
Abstract: The reaction of (2E)-3-aryl-2-(4-aryl-1,3-thiazol-2-yl)acrylonitriles with an excess of nitric acid in AcOH proceeds regioselectively to afford previously unknown (2E)-3-aryl-2-(4-aryl-5-nitro-1,3-thiazol-2-yl)acrylonitriles in 82–96% yields.
URI: https://dspace.ncfu.ru/handle/123456789/29345
Appears in Collections:Статьи, проиндексированные в SCOPUS, WOS

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