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Quantum-chemical study of the mechanism of aminomethylation of tetrazoles according to the elimination–addition scheme without preliminary formation of N-protonated azolium salts Научная публикация

Журнал Mendeleev Communications
ISSN: 1364-551X , E-ISSN: 0959-9436
Вых. Данные Год: 2018, Том: 28, Номер: 5, Страницы: 548-550 Страниц : 3 DOI: 10.1016/j.mencom.2018.09.034
Авторы Belen’kii Leonid I. 1 , Radzhabov Maxim R. 1 , Pivina Tatyana S. 1
Организации
1 N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 119991 Moscow, Russian Federation

Реферат: Based on analysis of quantum chemical DFT/B3LYP/6-31G(d) calculations results, thermodynamic characteristics of electrophilic dimethylaminomethylation of 1H-tetrazole and 1-methyl-tetrazole according to addition–elimination and elimination–addition schemes were correlated. The possibility of the dimethylaminomethylation without the preliminary formation of N-protonated azolium salts was demonstrated.
Библиографическая ссылка: Belen’kii L.I. , Radzhabov M.R. , Pivina T.S.
Quantum-chemical study of the mechanism of aminomethylation of tetrazoles according to the elimination–addition scheme without preliminary formation of N-protonated azolium salts
Mendeleev Communications. 2018. V.28. N5. P.548-550. DOI: 10.1016/j.mencom.2018.09.034 WOS Scopus OpenAlex
Идентификаторы БД:
Web of science: WOS:000448100900034
Scopus: 2-s2.0-85054335300
OpenAlex: W2894760985
Цитирование в БД:
БД Цитирований
OpenAlex 2
Scopus 2
Web of science 1
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