Electrochemical Oxidation of 3-Aryl-2-cyanothioacrylamides
Electrochemical oxidation of (Е)-3-aryl-2-cyanoprop-2-enethioamides in a undivided cell in the presence of KBr in an aqueous or aqueous-organic medium has led to the formation of (2Е,2′E)-2,2′-(1,2,4-thiadiazole-3,5-diyl)bis[3-arylacrylonitriles] in 37–76% yield. A plausible reaction mechanism has b...
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2023
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ir-20.500.12258-222772025-02-12T14:52:49Z Electrochemical Oxidation of 3-Aryl-2-cyanothioacrylamides Dotsenko, V. V. Доценко, В. В. Strelkov, V. D. Стрелков, В. Д. Aksenov, N. A. Аксенов, Н. А. Aksenova, I. V. Аксенова, И. В. Growth-regulating activity Antidote activity against 2,4-D Thioamides Oxidative dimerization Electrochemical synthesis 1,2,4-thiadiazoles Electrochemical oxidation of (Е)-3-aryl-2-cyanoprop-2-enethioamides in a undivided cell in the presence of KBr in an aqueous or aqueous-organic medium has led to the formation of (2Е,2′E)-2,2′-(1,2,4-thiadiazole-3,5-diyl)bis[3-arylacrylonitriles] in 37–76% yield. A plausible reaction mechanism has been discussed. In laboratory experiments, (2E,2′E)-2,2′-(1,2,4-thiadiazol-3,5-diyl)bis[3-(4-methoxyphenyl)acrylonitrile] has revealed pronounced antidote effect against herbicide 2,4-D on sunflower seedlings and no pronounced growth-regulating properties. 2023-01-27T12:05:40Z 2023-01-27T12:05:40Z 2022 Статья Osminin, V.I., Mironenko, A.A., Dahno, P.G., Nazarenko, M.A., Oflidi, A.I., Dotsenko, V.V., Strelkov, V.D., Aksenov, N.A., Aksenova, I.V. Electrochemical Oxidation of 3-Aryl-2-cyanothioacrylamides // Russian Journal of General Chemistry. - 2022. - 92 (11), pp. 2235-2245. - DOI: 10.1134/S1070363222110068 http://hdl.handle.net/20.500.12258/22277 ru Russian Journal of General Chemistry application/pdf application/pdf |
| institution |
СКФУ |
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Репозиторий |
| language |
Russian |
| topic |
Growth-regulating activity Antidote activity against 2,4-D Thioamides Oxidative dimerization Electrochemical synthesis 1,2,4-thiadiazoles |
| spellingShingle |
Growth-regulating activity Antidote activity against 2,4-D Thioamides Oxidative dimerization Electrochemical synthesis 1,2,4-thiadiazoles Dotsenko, V. V. Доценко, В. В. Strelkov, V. D. Стрелков, В. Д. Aksenov, N. A. Аксенов, Н. А. Aksenova, I. V. Аксенова, И. В. Electrochemical Oxidation of 3-Aryl-2-cyanothioacrylamides |
| description |
Electrochemical oxidation of (Е)-3-aryl-2-cyanoprop-2-enethioamides in a undivided cell in the presence of KBr in an aqueous or aqueous-organic medium has led to the formation of (2Е,2′E)-2,2′-(1,2,4-thiadiazole-3,5-diyl)bis[3-arylacrylonitriles] in 37–76% yield. A plausible reaction mechanism has been discussed. In laboratory experiments, (2E,2′E)-2,2′-(1,2,4-thiadiazol-3,5-diyl)bis[3-(4-methoxyphenyl)acrylonitrile] has revealed pronounced antidote effect against herbicide 2,4-D on sunflower seedlings and no pronounced growth-regulating properties. |
| format |
Статья |
| author |
Dotsenko, V. V. Доценко, В. В. Strelkov, V. D. Стрелков, В. Д. Aksenov, N. A. Аксенов, Н. А. Aksenova, I. V. Аксенова, И. В. |
| author_facet |
Dotsenko, V. V. Доценко, В. В. Strelkov, V. D. Стрелков, В. Д. Aksenov, N. A. Аксенов, Н. А. Aksenova, I. V. Аксенова, И. В. |
| author_sort |
Dotsenko, V. V. |
| title |
Electrochemical Oxidation of 3-Aryl-2-cyanothioacrylamides |
| title_short |
Electrochemical Oxidation of 3-Aryl-2-cyanothioacrylamides |
| title_full |
Electrochemical Oxidation of 3-Aryl-2-cyanothioacrylamides |
| title_fullStr |
Electrochemical Oxidation of 3-Aryl-2-cyanothioacrylamides |
| title_full_unstemmed |
Electrochemical Oxidation of 3-Aryl-2-cyanothioacrylamides |
| title_sort |
electrochemical oxidation of 3-aryl-2-cyanothioacrylamides |
| publishDate |
2023 |
| url |
https://dspace.ncfu.ru/handle/20.500.12258/22277 |
| work_keys_str_mv |
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