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Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/20.500.12258/3298
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dc.contributor.authorBorovlev, I. V.-
dc.contributor.authorБоровлев, И. В.-
dc.contributor.authorDemidov, O. P.-
dc.contributor.authorДемидов, О. П.-
dc.contributor.authorAmangasieva, G. A.-
dc.contributor.authorАмангазиева, Г. А.-
dc.contributor.authorAvakyan, E. K.-
dc.contributor.authorАвакян, Е. К.-
dc.contributor.authorKurnosova, N. A.-
dc.contributor.authorКурносова, Н. А.-
dc.date.accessioned2018-10-19T13:02:25Z-
dc.date.available2018-10-19T13:02:25Z-
dc.date.issued2016-
dc.identifier.citationBorovlev, I.V., Demidov, O.P., Amangasieva, G.A., Avakyan, E.K., Kurnosova, N.A. Ureas as new nucleophilic reagents for SN H amination and carbamoyl amination reactions in the 1,3,7-triazapyrene series // Arkivoc. - 2016. - Volume 2016. - Issue 3. - Pages 58-70ru
dc.identifier.urihttps://www.scopus.com/record/display.uri?eid=2-s2.0-84960124757&origin=resultslist&sort=plf-f&src=s&nlo=1&nlr=20&nls=afprfnm-t&affilName=north+caucasus+federal+university&sid=b34ee1a283c2e8415711b601b248f06f&sot=afnl&sdt=cl&cluster=scopubyr%2c%222016%22%2ct&sl=53&s=%28AF-ID%28%22North+Caucasus+Federal+University%22+60070541%29%29&relpos=81&citeCnt=6&searchTerm=-
dc.identifier.urihttp://hdl.handle.net/20.500.12258/3298-
dc.description.abstractThe ability of urea anions to react as nucleophiles with 1,3,7-triazapyrenes has been investigated. It was found that, against all expectations, the products of the substitution of hydrogen (SN H) by an amino group were isolated in good yields. The reactions proceed in anhydrous DMSO solution at room temperature. However, when anions of mono substituted ureas containing bulky substituents were used, the products of previously unknown SN H reactions of alkyl carbamoyl amination were obtainedru
dc.language.isoenru
dc.publisherArkatru
dc.relation.ispartofseriesArkivoc-
dc.subject1,3,7-triazapyren-6-aminesru
dc.subjectAminationru
dc.subjectCarbamoyl aminationru
dc.subjectNucleophilic aromatic substitution of hydrogenru
dc.titleUreas as new nucleophilic reagents for SN H amination and carbamoyl amination reactions in the 1,3,7-triazapyrene seriesru
dc.typeСтатьяru
vkr.amountPages 58-70ru
vkr.instИнститут математики и естественных наук-
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