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Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/20.500.12258/3709
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dc.contributor.authorAmangasieva, G. A.-
dc.contributor.authorАмангазиева, Г. А.-
dc.contributor.authorBorovlev, I. V.-
dc.contributor.authorБоровлев, И. В.-
dc.contributor.authorDemidov, O. P.-
dc.contributor.authorДемидов, О. П.-
dc.contributor.authorKurnosova, N. A.-
dc.contributor.authorКурносова, Н. А.-
dc.contributor.authorAvakyan, E. K.-
dc.contributor.authorАвакян, Е. К.-
dc.date.accessioned2018-12-18T12:43:05Z-
dc.date.available2018-12-18T12:43:05Z-
dc.date.issued2015-
dc.identifier.citationAmangasieva, G.A., Borovlev, I.V., Demidov, O.P., Kurnosova, N.A., Avakyan, E.K. Urea in an aminodemethoxylation reaction of 6-methoxy-1,3,7-triazapyrenes // Chemistry of Heterocyclic Compounds. - 2015. - Volume 51. - Issue 6. - Pages 586-588ru
dc.identifier.urihttps://www.scopus.com/record/display.uri?eid=2-s2.0-84938974457&origin=resultslist&sort=plf-f&src=s&nlo=1&nlr=20&nls=afprfnm-t&affilName=north+caucasus+federal+university&sid=c73d1c358909356c25b8ba1aa4ce585d&sot=afnl&sdt=cl&cluster=scopubyr%2c%222015%22%2ct&sl=53&s=%28AF-ID%28%22North+Caucasus+Federal+University%22+60070541%29%29&relpos=23&citeCnt=2&searchTerm=-
dc.identifier.urihttp://hdl.handle.net/20.500.12258/3709-
dc.description.abstractUpon reaction of N-anion of urea with 6-methoxy-1,3,7-triazapyrenes in DMSO at room temperature the products of nucleophilic ipso substitution of methoxy group with amino group form in high yieldsru
dc.language.isoenru
dc.publisherSpringer New York LLCru
dc.relation.ispartofseriesChemistry of Heterocyclic Compounds-
dc.subject6-methoxy-1,3,7-triazapyrenesru
dc.subjectNucleophilic ipso substitution of methoxy groupru
dc.subjectUrearu
dc.titleUrea in an aminodemethoxylation reaction of 6-methoxy-1,3,7-triazapyrenesru
dc.typeСтатьяru
vkr.amountPages 586-588ru
vkr.instИнститут математики и естественных наук-
Appears in Collections:Статьи, проиндексированные в SCOPUS, WOS

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