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Synthesis, S-alkylation, and fungicidal activity of 4-(benzylideneamino)thioglycolurils Научная публикация

Журнал Russian Chemical Bulletin
ISSN: 1573-9171 , E-ISSN: 1066-5285
Вых. Данные Год: 2018, Том: 67, Номер: 6, Страницы: 1059-1064 Страниц : 6 DOI: 10.1007/s11172-018-2180-x
Авторы Gazieva G.A. 1 , Nechaeva T.V. 2 , Kostikova N.N. 1 , Sigay N.V. 1 , Serkov S.A. 1 , Popkov S.V. 3
Организации
1 N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
2 The State Scientific-Research Institute of Chemical Reagents and High Purity Chemical Substances, National Research Center “Kurchatov Institute”, Moscow, Russian Federation
3 D. I. Mendeleev University of Chemical Technology of Russia, Moscow, Russian Federation

Реферат: A series of 1,3-disubstituted 4-benzylideneamino-5-thioxohexahydroimidazo[4,5-d]imidazol-2(1H)-ones (thioglycolurils) was synthesized via the reaction of 5,7-disubstituted 3-thioxoperhydroimidazo[4,5-e]-1,2,4-triazin-6-ones with hydroxy-, alkoxy-, and fluorocontaining benzaldehyde derivatives. An alkylation of the obtained thioglycolurils with methyl iodide or 4-bromobenzyl bromide provided the corresponding 6-benzylideneamino-5-alkylsulfanyl-3,3a,6,6a-tetrahydroimidazo[4,5-d]imidazol-2(1H)-ones. The fungicidal activity of some synthesized compounds against pathogens causing diseases of agricultural crops was studied.
Библиографическая ссылка: Gazieva G.A. , Nechaeva T.V. , Kostikova N.N. , Sigay N.V. , Serkov S.A. , Popkov S.V.
Synthesis, S-alkylation, and fungicidal activity of 4-(benzylideneamino)thioglycolurils
Russian Chemical Bulletin. 2018. V.67. N6. P.1059-1064. DOI: 10.1007/s11172-018-2180-x WOS Scopus OpenAlex
Идентификаторы БД:
≡ Web of science: WOS:000445942700019
≡ Scopus: 2-s2.0-85053883148
≡ OpenAlex: W2892872968
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