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Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/20.500.12258/23806
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dc.contributor.authorAksenov, N. A.-
dc.contributor.authorАксенов, Н. А.-
dc.contributor.authorAksenov, D. A.-
dc.contributor.authorАксенов, Д. А.-
dc.contributor.authorGanusenko, D. D.-
dc.contributor.authorГанусенко, Д. Д.-
dc.contributor.authorKurenkov, I. A.-
dc.contributor.authorКуренков, И. А.-
dc.contributor.authorAksenov, A. V.-
dc.contributor.authorАксенов, А. В.-
dc.date.accessioned2023-06-30T12:23:59Z-
dc.date.available2023-06-30T12:23:59Z-
dc.date.issued2023-
dc.identifier.citationAksenov, N.A., Aksenov, D.A., Ganusenko, D.D., Kurenkov, I.A., Aksenov, A.V. A Diastereoselective Assembly of Tetralone Derivatives via a Tandem Michael Reaction and ipso-Substitution of the Nitro Group // Journal of Organic Chemistry. - 2023. - 88(9), pp, 5639–5651. - DOI: 10.1021/acs.joc.3c00134ru
dc.identifier.urihttp://hdl.handle.net/20.500.12258/23806-
dc.description.abstractA highly diastereoselective tandem reaction of 2'-nitrochalcones is reported, involving Michael addition and a subsequent ipso-substitution of the nitro group to produce 1-tetralones with two contiguous chiral centers. A related annulation reaction of 2'-nitrochalcones with potassium cyanide affording 1-indanones with a C3-quaternary chiral center is also demonstrated.ru
dc.language.isoenru
dc.relation.ispartofseriesJournal of Organic Chemistry-
dc.subjectTandem Michael reactionru
dc.subjectIpso-substitution of the nitro groupru
dc.subjectTetralone derivativesru
dc.titleA Diastereoselective Assembly of Tetralone Derivatives via a Tandem Michael Reaction and ipso-Substitution of the Nitro Groupru
dc.typeСтатьяru
vkr.instХимико-фармацевтический факультетru
Appears in Collections:Статьи, проиндексированные в SCOPUS, WOS

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