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Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/20.500.12258/2446
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dc.contributor.authorAksenov, A. V.-
dc.contributor.authorАксенов, А. В.-
dc.contributor.authorAksenov, D. A.-
dc.contributor.authorАксенов, Д. А.-
dc.contributor.authorGriaznov, G. D.-
dc.contributor.authorГрязнов, Г. Д.-
dc.contributor.authorAksenov, N. A.-
dc.contributor.authorАксенов, Н. А.-
dc.contributor.authorRubin, M. A.-
dc.contributor.authorРубин, М. А.-
dc.date.accessioned2018-07-25T14:32:00Z-
dc.date.available2018-07-25T14:32:00Z-
dc.date.issued2018-
dc.identifier.citationAksenov, A.V., Aksenov, D.A., Griaznov, G.D., Aksenov, N.A., Voskressensky, L.G., Rubin, M. Unexpected cyclization of 2-(2-aminophenyl)indoles with nitroalkenes to furnish indolo[3,2-: C] quinolines // Organic and Biomolecular Chemistry. - 2018. - Volume 16. - Issue 23. - Pages 4325-4332ru
dc.identifier.urihttps://dspace.ncfu.ru:443/handle/20.500.12258/2446-
dc.description.abstractThe polyphosphoric acid-mediated reaction of 2-(2-aminophenyl)indenes with nitroalkenes was tested in the frame of synthetic studies towards CDK inhibitors with the paullone core. Unexpectedly, this reaction proceeded via a different mechanistic pathway affording derivatives of the natural alkaloid isocryptolepine. The scope of this unusual transformation was investigated and a mechanistic rationale explaining this outcome is offeredru
dc.language.isoenru
dc.publisherRoyal Society of Chemistryru
dc.relation.ispartofseriesOrganic and Biomolecular Chemistry-
dc.subjectPositive ionsru
dc.subjectCDK inhibitorsru
dc.subjectMechanistic pathwaysru
dc.subjectMediated reactionsru
dc.subjectNitroalkenesru
dc.subjectPolyphosphoric acidsru
dc.subjectSynthetic studyru
dc.subjectChemistryru
dc.titleUnexpected cyclization of 2-(2-aminophenyl)indoles with nitroalkenes to furnish indolo[3,2-: C] quinolinesru
dc.typeСтатьяru
vkr.amountPages 4325-4332ru
vkr.instИнститут математики и естественных наук-
Appears in Collections:Статьи, проиндексированные в SCOPUS, WOS

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