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Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/20.500.12258/3682
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dc.contributor.authorAksenov, A. V.-
dc.contributor.authorАксенов, А. В.-
dc.contributor.authorAksenov, N. A.-
dc.contributor.authorАксенов, Н. А.-
dc.contributor.authorDzhandigova, Z. V.-
dc.contributor.authorДжандигова, З. В.-
dc.contributor.authorAksenov, D. A.-
dc.contributor.authorАксенов, Д. А.-
dc.contributor.authorRubin, M. A.-
dc.contributor.authorРубин, М. А.-
dc.date.accessioned2018-12-14T14:17:33Z-
dc.date.available2018-12-14T14:17:33Z-
dc.date.issued2015-
dc.identifier.citationAksenov, A.V., Aksenov, N.A., Dzhandigova, Z.V., Aksenov, D.A., Rubin, M. Nitroalkenes as surrogates for cyanomethylium species in a one-pot synthesis of non-symmetric diarylacetonitriles // RSC Advances. - 2015. - Volume 5. - Issue 129. - Pages 106492-106497ru
dc.identifier.urihttp://hdl.handle.net/20.500.12258/3682-
dc.description.abstractNitroalkenes were used as synthetic equivalents of the cyanomethylium cation in a modular, one-pot synthesis of 2-(3-indolyl)acetonitriles and 2,2-diarylacetonitriles involving electrophilic functionalization of aromatic and heteroaromatic C-H bondru
dc.language.isoenru
dc.publisherRoyal Society of Chemistryru
dc.relation.ispartofseriesRSC Advances-
dc.subjectSynthesis (chemical)ru
dc.subjectOne-pot synthesisru
dc.subjectNitroalkenesru
dc.subjectSynthetic equivalentsru
dc.subjectElectrophilic functionalizationru
dc.titleNitroalkenes as surrogates for cyanomethylium species in a one-pot synthesis of non-symmetric diarylacetonitrilesru
dc.typeСтатьяru
vkr.amountPages 106492-106497ru
vkr.instИнститут математики и естественных наук-
Appears in Collections:Статьи, проиндексированные в SCOPUS, WOS

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