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Electrophilic Intermediates in the Nef and Meyer Reactions: A Computational Study Научная публикация

Журнал Journal of Organic Chemistry
ISSN: 1520-6904 , E-ISSN: 0022-3263
Вых. Данные Год: 2024, Том: 89, Номер: 24, Страницы: 18109–18121 Страниц : DOI: 10.1021/acs.joc.4c01933
Авторы Malykhin Roman S. 1 , Sukhorukov Alexey Yu. 1
Организации
1 Laboratory of organic and metal−organic nitrogen−oxygen systems, N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Leninsky prospect, 47, Moscow 119991, Russian Federation

Реферат: The generation, interconversion, and reactivity of electrophilic species generated upon activation of nitroalkanes with protic acids (the Nef and Meyer reactions) were investigated by quantum-chemical calculations. N,N-Bis(hydroxy)iminium (R2C═N+(OH)2) and N-oxoiminium (R2C═N+═O) cations were shown to be produced independently from aci-nitroalkanes, while N-hydroxynitrilium cations (RC≡N+–OH) were formed via nearly barrierless C–H bond cleavage in N-oxoiminium cations. The N-oxoiminium and N-hydroxynitrilium cations whose formation is favored under highly acidic anhydrous conditions are strong electrophiles capable of reacting even with nonactivated arenes under ambient conditions. The N-oxoiminium cations R2C═N+═O are highly unusual ambident species containing three contiguous electrophilic centers (C, N, and O atoms). Nucleophilic addition at the oxygen atom is less preferred than the C- and N-attack yet possible in an intramolecular variant. These computational results shed light on some key aspects of the mechanisms of the Nef and Meyer reactions and predict the possibility of numerous interrupted versions of these reactions.
Библиографическая ссылка: Malykhin R.S. , Sukhorukov A.Y.
Electrophilic Intermediates in the Nef and Meyer Reactions: A Computational Study
Journal of Organic Chemistry. 2024. V.89. N24. P.18109–18121. DOI: 10.1021/acs.joc.4c01933 WOS Scopus OpenAlex
Идентификаторы БД:
Web of science: WOS:001372148400001
Scopus: 2-s2.0-85211384841
OpenAlex: W4405137684
Цитирование в БД:
БД Цитирований
OpenAlex 3
Web of science 3
Scopus 3
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