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Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/20.500.12258/3723
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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.authorKurnosova, N. A.-
dc.contributor.authorКурносова, Н. А.-
dc.contributor.authorAmangasieva, G. A.-
dc.contributor.authorАмангазиева, Г. А.-
dc.contributor.authorAvakyan, E. K.-
dc.contributor.authorАвакян, Е. К.-
dc.date.accessioned2018-12-19T14:27:30Z-
dc.date.available2018-12-19T14:27:30Z-
dc.date.issued2015-
dc.identifier.citationBorovlev, I.V., Demidov, O.P., Kurnosova, N.A., Amangazieva, G.A., Avakyan, E.K. Amides of 1,3,7-triazapyrene series: Synthesis by nucleophilic substitution of alkoxy groups // Chemistry of Heterocyclic Compounds. - 2015. - Volume 51. - Issue 4. - Pages 334-339ru
dc.identifier.urihttps://www.scopus.com/record/display.uri?eid=2-s2.0-84938963778&origin=resultslist&sort=plf-f&src=s&nlo=1&nlr=20&nls=afprfnm-t&affilName=north+caucasus+federal+university&sid=fe656e0c7517dbc25228b3d577bd000c&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=36&citeCnt=3&searchTerm=-
dc.identifier.urihttp://hdl.handle.net/20.500.12258/3723-
dc.description.abstractThe treatment of 6,8-dialkoxy-1,3,7-triazapyrenes with sodium acylamides in DMSO at room temperature resulted in ipso substitution of one alkoxy group with amide group, giving 8-acylamino-6-alkoxy-1,3,7-triazapyrenes. The reaction at 65-70°C proceeded as a tandem SNAr ipso -SN2 process, leading to the formation of 8-acylamino-6-oxo-6,7-dihydro-1,3,7-triazapyrenesru
dc.language.isoenru
dc.publisherSpringer New York LLCru
dc.relation.ispartofseriesChemistry of Heterocyclic Compounds-
dc.subject6,8-dialkoxy-1,3,7-triazapyrenesru
dc.subjectIpso substitution of alkoxy groupsru
dc.subjectNucleophilic amidationru
dc.subjectTandem SNAr ipso -SN2 reactionsru
dc.titleAmides of 1,3,7-triazapyrene series: synthesis by nucleophilic substitution of alkoxy groupsru
dc.typeСтатьяru
vkr.amountPages 334-339ru
vkr.instИнститут математики и естественных наук-
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