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dc.contributor.authorLarin, A. N.-
dc.contributor.authorЛарин, А. Н.-
dc.contributor.authorBorovleva, A. A.-
dc.contributor.authorБоровлева, А. А.-
dc.contributor.authorDemidov, O. P.-
dc.contributor.authorДемидов, О. П.-
dc.contributor.authorAvakyan, E. K.-
dc.contributor.authorАвакян, Е. К.-
dc.contributor.authorPobedinskaya, D. Y.-
dc.contributor.authorПобединская, Д. Ю.-
dc.contributor.authorErmolenko, A. P.-
dc.contributor.authorЕрмоленко, А. П.-
dc.contributor.authorKolosov, S. E.-
dc.contributor.authorКолосов, С. Е.-
dc.contributor.authorBorovlev, I. V.-
dc.contributor.authorБоровлев, И. В.-
dc.date.accessioned2025-03-03T10:17:08Z-
dc.date.available2025-03-03T10:17:08Z-
dc.date.issued2025-
dc.identifier.citationLarin 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.202400490ru
dc.identifier.urihttps://dspace.ncfu.ru/handle/123456789/29837-
dc.description.abstractDirect 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.ru
dc.language.isoenru
dc.publisherJohn Wiley and Sons Incru
dc.relation.ispartofseriesAsian Journal of Organic Chemistry-
dc.subjectC−H activationru
dc.subjectIsoquinolineru
dc.subjectNucleophilic substitution of hydrogenru
dc.subjectQuinolineru
dc.titleSelective SNH Alkylamination of 3(5,6,7,8)-Nitroquinoline and 5-Nitroisoquinoline in an Aqueous Mediumru
dc.typeСтатьяru
vkr.instХимический факультетru
Appears in Collections:Статьи, проиндексированные в SCOPUS, WOS

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