Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/20.500.12258/4247
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dc.contributor.authorAksenov, A. V.-
dc.contributor.authorАксенов, А. В.-
dc.contributor.authorSmirnov, A. N.-
dc.contributor.authorСмирнов, А. Н.-
dc.contributor.authorAksenov, N. A.-
dc.contributor.authorАксенов, Н. А.-
dc.contributor.authorAksenova, I. V.-
dc.contributor.authorАксенова, И. В.-
dc.contributor.authorRubin, M. A.-
dc.contributor.authorРубин, М. А.-
dc.date.accessioned2019-02-11T12:23:38Z-
dc.date.available2019-02-11T12:23:38Z-
dc.date.issued2015-
dc.identifier.citationAksenov, A.V., Smirnov, A.N., Aksenov, N.A., Aksenova, I.V., Matheny, J.P., Rubin, M. Metal-free ring expansion of indoles with nitroalkenes: A simple, modular approach to 3-substituted 2-quinolones // RSC Advances. - 2015. - Volume 5. - Issue 12. - Pages 8647-8656ru
dc.identifier.urihttp://hdl.handle.net/20.500.12258/4247-
dc.description.abstract3-Substituted 2-quinolones are obtained via a novel metal-free transannulation reaction of 2-nitroolefins with 2-substituted indoles in polyphosphoric acid. This acid-mediated cascade transformation operates via the ANRORC (Addition of Nucleophile, Ring Opening, and Ring Closure) mechanism and can be used in combination with the Fisher indole synthesis to offer a practical three-component hetero-annulation approach to 2-quinolones from arylhydrazines, 2-nitroalkenes, and acetophenone. An alternative entry to this chemistry employing the alkylation of electron-rich arenes and hetarenes with 1-(2-indolyl)-2-nitroalkene has also been demonstratedru
dc.language.isoenru
dc.publisherRoyal Society of Chemistryru
dc.relation.ispartofseriesRSC Advances-
dc.subjectKetonesru
dc.subjectArylhydrazinesru
dc.subjectCascade transformationsru
dc.subjectElectron-rich arenesru
dc.subjectModular approachru
dc.subjectPolyphosphoric acidsru
dc.subjectRing expansionru
dc.subjectSynthesis (chemical)ru
dc.titleMetal-free ring expansion of indoles with nitroalkenes: A simple, modular approach to 3-substituted 2-quinolonesru
dc.typeСтатьяru
vkr.amountPages 8647-8656ru
vkr.instИнститут математики и естественных наук-
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