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Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/20.500.12258/19711
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dc.contributor.authorBorovleva, A. A.-
dc.contributor.authorБоровлева, А. А.-
dc.contributor.authorAvakyan, E. K.-
dc.contributor.authorАвакян, Е. К.-
dc.contributor.authorAmangasieva, G. A.-
dc.contributor.authorАмангазиева, Г. А.-
dc.contributor.authorDemidov, O. P.-
dc.contributor.authorДемидов, О. П.-
dc.contributor.authorPobedinskaya, D. Y.-
dc.contributor.authorПобединская, Д. Ю.-
dc.contributor.authorErmolenko, A. P.-
dc.contributor.authorЕрмоленко, А. П.-
dc.contributor.authorLarin, A. N.-
dc.contributor.authorЛарин, А. Н.-
dc.contributor.authorBorovlev, I. V.-
dc.contributor.authorБоровлев, И. В.-
dc.date.accessioned2022-06-21T09:49:06Z-
dc.date.available2022-06-21T09:49:06Z-
dc.date.issued2022-
dc.identifier.citationBorovleva, A. A., Avakyan, E. K., Amangasieva, G. A., Demidov, O. P., Pobedinskaya, D. Y., Ermolenko, A. P., Larin, A. N., Borovlev, I. V. SNH Amidation of 5(6,7,8)-nitroquinoline N-oxides // Chemistry of Heterocyclic Compounds. - 2022. - DOI10.1007/s10593-022-03077-8ru
dc.identifier.urihttp://hdl.handle.net/20.500.12258/19711-
dc.description.abstractDirect SNH amidation of 6- and 7-nitroquinoline N-oxides in anhydrous DMSO allowed to obtain N-oxides of 2- and 8-aroylaminonitroquinolines, respectively. 5-Nitroquinoline N-oxide was transformed into a mixture of amides derived from the N-oxides of 5-nitroand 5-nitrosoquinolines. 8-Nitroquinoline N-oxide underwent destruction under the same conditions.ru
dc.language.isoenru
dc.publisherSpringerru
dc.relation.ispartofseriesChemistry of Heterocyclic Compounds-
dc.subject5(6,7,8)-nitroquinoline N-oxidesru
dc.subjectDisproportionationru
dc.subjectN-(nitro(nitroso)-1-oxidoquinolinyl)benzamidesru
dc.subjectSNH amidationru
dc.titleSNH Amidation of 5(6,7,8)-nitroquinoline N-oxidesru
dc.typeСтатьяru
vkr.instХимико-фармацевтический факультетru
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