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Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/20.500.12258/14853
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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.authorSkomorokhov, A. A.-
dc.contributor.authorСкоморохов, А. А.-
dc.contributor.authorAleksandrova, E. V.-
dc.contributor.authorАлександрова, Е. В.-
dc.contributor.authorRubin, M. A.-
dc.contributor.authorРубин, М. А.-
dc.date.accessioned2021-02-02T13:43:48Z-
dc.date.available2021-02-02T13:43:48Z-
dc.date.issued2021-
dc.identifier.citationAksenov, A.V., Aksenov, D.A., Aksenov, N.A., Skomorokhov, A.A., Aleksandrova, E.V., Rubin, M. Preparation of spiro[indole-3,5′-isoxazoles] via Grignard conjugate addition/spirocyclization sequence // RSC Advances. - 2021. - Volume 11. - Issue 3. - Pages 1783-1793ru
dc.identifier.urihttp://hdl.handle.net/20.500.12258/14853-
dc.description.abstractA highly efficient one-pot procedure combining conjugate addition of Grignard reagents to (2-nitroalkenyl)indoles and sub-sequent Brønsted acid-assisted spirocyclization allowed for preparation of 4′H-spiro[indole-3,5′-isoxazoles] in a diastereomerically selective fashion. Utilization of alkyl Grignard reagents provided an easy access to 4′-alkylsubstituted derivatives hardly available by other meansru
dc.language.isoenru
dc.publisherRoyal Society of Chemistryru
dc.relation.ispartofseriesRSC Advances-
dc.subjectAddition reactionsru
dc.subjectReagentsru
dc.subjectAlkyl-substituted derivativesru
dc.subjectPolycyclic aromatic hydrocarbonsru
dc.titlePreparation of spiro[indole-3,5′-isoxazoles] via Grignard conjugate addition/spirocyclization sequenceru
dc.typeСтатьяru
vkr.instХимико-фармацевтический факультетru
Appears in Collections:Статьи, проиндексированные в SCOPUS, WOS

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