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Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/20.500.12258/8015
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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.authorAksenov, N. A.-
dc.contributor.authorАксенов, Н. А.-
dc.contributor.authorAleksandrova, E. V.-
dc.contributor.authorАлександрова, Е. В.-
dc.contributor.authorRubin, M. A.-
dc.contributor.authorРубин, М. А.-
dc.date.accessioned2019-10-23T14:16:56Z-
dc.date.available2019-10-23T14:16:56Z-
dc.date.issued2019-
dc.identifier.citationAksenov, A.V., Aksenov, D.A., Aksenov, N.A., Aleksandrova, E.V., Rubin, M. Preparation of Stereodefined 2-(3-Oxoindolin-2-yl)-2-Arylacetonitriles via One-Pot Reaction of Indoles with Nitroalkenes // Journal of Organic Chemistry. - 2019. - Volume 84. - Issue 19. - Pages 12420-12429ru
dc.identifier.urihttp://hdl.handle.net/20.500.12258/8015-
dc.description.abstractRecently discovered reactivity of nitrostyrenes in phosphorous acid to facilitate the diastereoselective [4 + 1]-cycloaddition of indoles in combination with unusual oxazoline ring cleavage and subsequent 1,2-alkyl shift afforded stereochemically defined 2-(3-oxoindolin-2-yl)-2-arylacetonitriles as sole productsru
dc.language.isoenru
dc.publisherAmerican Chemical Societyru
dc.relation.ispartofseriesJournal of Organic Chemistry-
dc.subjectChemistryru
dc.subjectDiastereoselectiveru
dc.subjectNitroalkenesru
dc.subjectOne-pot reactionru
dc.subjectOxazoline ringru
dc.subjectPhosphorous acidru
dc.subjectOrganic compoundsru
dc.titlePreparation of stereodefined 2-(3-Oxoindolin-2-yl)-2-arylacetonitriles via one-pot reaction of indoles with nitroalkenesru
dc.typeСтатьяru
vkr.amountPages 12420-12429ru
vkr.instИнститут математики и естественных наук-
Appears in Collections:Статьи, проиндексированные в SCOPUS, WOS

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