Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/20.500.12258/5582
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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.authorArutiunov, N. A.-
dc.contributor.authorАрутюнов, Н. 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.accessioned2019-06-25T12:20:31Z-
dc.date.available2019-06-25T12:20:31Z-
dc.date.issued2019-
dc.identifier.citationAksenov, A.V., Aksenov, D.A., Arutiunov, N.A., Aksenov, N.A., Aleksandrova, E.V., Zhao, Z., Du, L., Kornienko, A., Rubin, M. Synthesis of Spiro[indole-3,5′-isoxazoles] with Anticancer Activity via a Formal [4 + 1]-Spirocyclization of Nitroalkenes to Indoles // Journal of Organic Chemistry. - 2019. - Volume 84. - Issue 11. - Pages 7123-7137ru
dc.identifier.urihttp://hdl.handle.net/20.500.12258/5582-
dc.description.abstractAn acid-assisted [4 + 1]-cycloaddition of indoles with nitrostyrenes affords 4′H-spiro[indole-3,5′-isoxazoles] in a diastereomerically pure form. Several of these spirocyclic molecules exhibit promising anticancer activity by reducing viability and inducing differentiation of neuroblastoma cellsru
dc.language.isoenru
dc.publisherAmerican Chemical Societyru
dc.relation.ispartofseriesJournal of Organic Chemistry-
dc.subjectAnticancer activityru
dc.subjectIndolesru
dc.subjectNitroalkenesru
dc.subjectSpirocyclizationru
dc.titleSynthesis of spiro[indole-3,5′-isoxazoles] with anticancer activity via a formal [4 + 1]-spirocyclization of nitroalkenes to indolesru
dc.typeСтатьяru
vkr.amountPages 7123-7137ru
vkr.instИнститут математики и естественных наук-
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