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Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/123456789/29345
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dc.contributor.authorDotsenko, V. V.-
dc.contributor.authorДоценко, В. В.-
dc.contributor.authorAksenov, N. A.-
dc.contributor.authorАксенов, Н. А.-
dc.contributor.authorAksenova, I. V.-
dc.contributor.authorАксенова, И. В.-
dc.date.accessioned2024-12-10T08:28:25Z-
dc.date.available2024-12-10T08:28:25Z-
dc.date.issued2024-
dc.identifier.citationPakholka, 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/S1070363224100025ru
dc.identifier.urihttps://dspace.ncfu.ru/handle/123456789/29345-
dc.description.abstractThe 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.ru
dc.language.isoenru
dc.publisherPleiades Publishingru
dc.relation.ispartofseriesRussian Journal of General Chemistry-
dc.subject1,3-thiazolesru
dc.subjectα-bromoketonesru
dc.subject2-cyanothioacrylamidesru
dc.subject5-nitro-1,3-thiazolesru
dc.subjectHantzsch reactionru
dc.subjectNitrationru
dc.titleRegioselective Nitration of (2E)-3-Aryl-2-(4-arylthiazol-2-yl)acrylonitrilesru
dc.typeСтатьяru
vkr.instХимический факультетru
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