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Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/20.500.12258/22264
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dc.contributor.authorAvakyan, E. K.-
dc.contributor.authorАвакян, Е. К.-
dc.contributor.authorBorovleva, A. A.-
dc.contributor.authorБоровлева, А. А.-
dc.contributor.authorPobedinskaya, D. Y.-
dc.contributor.authorПобединская, Д. Ю.-
dc.contributor.authorDemidov, O. P.-
dc.contributor.authorДемидов, О. П.-
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.accessioned2023-01-26T14:52:14Z-
dc.date.available2023-01-26T14:52:14Z-
dc.date.issued2022-
dc.identifier.citationAvakyan, E.K., Borovleva, A.A., Pobedinskaya, D.Y., Demidov, O.P., Ermolenko, A.P., Larin, A.N., Borovlev, I.V. SNH Amidation of 5-Nitroisoquinoline: Access to Nitro- and Nitroso Derivatives of Amides and Ureas on the Basis of Isoquinoline // Molecules. - 2022. - 27 (22), статья № 7862. - DOI: 10.3390/molecules27227862ru
dc.identifier.urihttp://hdl.handle.net/20.500.12258/22264-
dc.description.abstractFor the first time, amides and ureas based on both 5-nitroisoquinoline and 5-nitrosoisoquinoline were obtained by direct nucleophilic substitution of hydrogen in the 5-nitroisoquinoline molecule. In the case of urea and monosubstituted ureas, only 5-nitrosoisoquinoline-6-amine is formed under anhy- drous conditions.ru
dc.language.isoenru
dc.relation.ispartofseriesMolecules-
dc.subjectHeterocyclesru
dc.subjectSNH methodologyru
dc.subjectMetal-free C–N bond formationru
dc.subject5-nitroisoquinolineru
dc.subjectRedox processru
dc.subjectOxidative SNH amidationru
dc.subjectSNH dialkylcarbamoylaminationru
dc.subjectRegioselectivityru
dc.titleSNH Amidation of 5-Nitroisoquinoline: Access to Nitro- and Nitroso Derivatives of Amides and Ureas on the Basis of Isoquinolineru
dc.typeСтатьяru
vkr.instХимико-фармацевтический факультетru
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