Репозиторий научных и учебно-методических публикаций
Северо-Кавказский федеральный университет
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https://dspace.ncfu.ru/handle/123456789/29837| Title: | Selective SNH Alkylamination of 3(5,6,7,8)-Nitroquinoline and 5-Nitroisoquinoline in an Aqueous Medium |
| Authors: | Larin, A. N. Ларин, А. Н. Borovleva, A. A. Боровлева, А. А. Demidov, O. P. Демидов, О. П. Avakyan, E. K. Авакян, Е. К. Pobedinskaya, D. Y. Побединская, Д. Ю. Ermolenko, A. P. Ермоленко, А. П. Kolosov, S. E. Колосов, С. Е. Borovlev, I. V. Боровлев, И. В. |
| Keywords: | C−H activation;Isoquinoline;Nucleophilic substitution of hydrogen;Quinoline |
| Issue Date: | 2025 |
| Publisher: | John Wiley and Sons Inc |
| Citation: | Larin A.N., Borovleva A.A., Demidov O.P., Avakyan E.K., Zubenko A.A., Pobedinskaya D.Y., Ermolenko A.P., Kolosov S.E., Borovlev I.V. Selective SNH Alkylamination of 3(5,6,7,8)-Nitroquinoline and 5-Nitroisoquinoline in an Aqueous Medium // Asian Journal of Organic Chemistry. - 2025. - 14 (2). - art. no. e202400490. - DOI: 10.1002/ajoc.202400490 |
| Series/Report no.: | Asian Journal of Organic Chemistry |
| Abstract: | Direct oxidative SNH alkylamination of 3-, 5-, 6-, 7-, 8-nitroquinolines and 5-nitroisoquinoline in an aqueous solution of an aliphatic amines gives rise to the corresponding alkylamino and dialkylamino derivatives of these nitrohetarenes. The nitro group solely dictates the regioselectivity of reactions. The antibacterial activity of some of them has been studied. |
| URI: | https://dspace.ncfu.ru/handle/123456789/29837 |
| Appears in Collections: | Статьи, проиндексированные в SCOPUS, WOS |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| WoS 2085.pdf Restricted Access | 115.5 kB | Adobe PDF | View/Open | |
| scopusresults 3499.pdf Restricted Access | 132.05 kB | Adobe PDF | View/Open |
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