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The features of the Michael reaction in ([1,2,4]triazolo[4,3-a][1,3,5]triazin-5-yl)dinitromethanides Научная публикация

Журнал Chemistry of Heterocyclic Compounds
ISSN: 1573-8353 , E-ISSN: 0009-3122
Вых. Данные Год: 2022, Том: 58, Номер: 10, Страницы: 506-513 Страниц : 8 DOI: 10.1007/s10593-022-03120-8
Авторы Golovina Olga V. 1 , Parfenov Victor E. 1 , Slepukhin Pavel А. 2 , Khakimov Dmitry V. 3 , Sheremetev Aleksei B. 3 , Bakharev Vladimir V. 1
Организации
1 Samara State Technical University, 244 Molodogvardeyskaya St., Samara 443100, Russia
2 Postovsky Institute of Organic Synthesis, Ural Branch of the Russian Academy of Sciences, 22/20 Sofyi Kovalevskoi St., Yekaterinburg 620219, Russia
3 N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky Ave., Moscow 119991, Russi

Реферат: The Michael addition of activated alkenes to ([1,2,4]triazolo[4,3-a][1,3,5]triazin-5-yl)dinitromethanides in the presence of K2HPO4 leads regioselectively to N1-alkylation products. The structure of [7-(dimethylamino)-1-(3-oxobutyl)[1,2,4]triazolo[4,3-a][1,3,5]triazin-5-yl]- dinitromethanide was established by X-ray structural analysis. The features of the reactivity of dinitromethanides are explained with quantum-chemical methods.
Библиографическая ссылка: Golovina O.V. , Parfenov V.E. , Slepukhin P.А. , Khakimov D.V. , Sheremetev A.B. , Bakharev V.V.
The features of the Michael reaction in ([1,2,4]triazolo[4,3-a][1,3,5]triazin-5-yl)dinitromethanides
Chemistry of Heterocyclic Compounds. 2022. V.58. N10. P.506-513. DOI: 10.1007/s10593-022-03120-8 WOS Scopus OpenAlex
Идентификаторы БД:
≡ Web of science: WOS:000878486700001
≡ Scopus: 2-s2.0-85146402302
≡ OpenAlex: W4308494698
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