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dc.contributor.authorDotsenko, V. V.-
dc.contributor.authorДоценко, В. В.-
dc.contributor.authorStrelkov, V. D.-
dc.contributor.authorСтрелков, В. Д.-
dc.contributor.authorAksenov, N. A.-
dc.contributor.authorАксенов, Н. А.-
dc.contributor.authorAksenova, I. V.-
dc.contributor.authorАксенова, И. В.-
dc.date.accessioned2023-03-03T12:07:35Z-
dc.date.available2023-03-03T12:07:35Z-
dc.date.issued2022-
dc.identifier.citationDakhno, P.G., Dotsenko, V.V., Strelkov, V.D., Vasilin V. K., Aksenov, N.A., Aksenova, I.V. (2E,2′E)-2,2′-(1,2,4-Thiadiazole-3,5-diyl)bis[3-arylacrylonitriles]: Synthesis and Antidote Activity Towards 2,4-D Herbicide // Russian Journal of General Chemistry. - 2022. - 92(12), pp. 2822-2831. - DOI: 10.1134/S1070363222120337ru
dc.identifier.urihttp://hdl.handle.net/20.500.12258/22945-
dc.description.abstractOxidation of (Е)-3-aryl-2-cyanothioacrylamides under the action of the Et2S(O)–HCl system leads to the formation of (2Е,2′E)-2,2′-(1,2,4-thiadiazole-3,5-diyl)bis[3-arylacrylonitriles] in 54–91% yields. Structure of the obtained compounds was confirmed by the two-dimensional NMR spectroscopy data. A plausible reaction mechanism was discussed. Two compounds showed a pronounced antidote effect against 2,4-D herbicide in a laboratory experiment on sunflower seedlings in the absence of growth-stimulating activityru
dc.language.isoruru
dc.relation.ispartofseriesRussian Journal of General Chemistry-
dc.subjectCyanothioacetamideru
dc.subject2-cyanothioacrylamidesru
dc.subjectDiethyl sulfoxideru
dc.subjectOxidative dimerization of thioamidesru
dc.subject1,2,4-thiadiazolesru
dc.subjectHerbicide antidotesru
dc.title(2E,2′E)-2,2′-(1,2,4-Thiadiazole-3,5-diyl)bis[3-arylacrylonitriles]: Synthesis and Antidote Activity Towards 2,4-D Herbicideru
dc.typeСтатьяru
vkr.instХимико-фармацевтический факультетru
Appears in Collections:Статьи, проиндексированные в SCOPUS, WOS

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