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Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/20.500.12258/14565
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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.authorSkomorokhov, A. A.-
dc.contributor.authorСкоморохов, А. А.-
dc.contributor.authorPrityko, L. A.-
dc.contributor.authorПритыко, Л. А.-
dc.contributor.authorAksenov, A. V.-
dc.contributor.authorАксенов, А. В.-
dc.contributor.authorGriaznov, G. D.-
dc.contributor.authorГрязнов, Г. Д.-
dc.contributor.authorRubin, M. A.-
dc.contributor.authorРубин, М. А.-
dc.date.accessioned2020-10-29T14:36:52Z-
dc.date.available2020-10-29T14:36:52Z-
dc.date.issued2020-
dc.identifier.citationAksenov, NA; Aksenov, DA; Skomorokhov, AA; Prityko, LA; Aksenov, AV; Griaznov, GD; Rubin, M. Synthesis of 2-(1H-Indol-2-yl)acetamides via bronsted acid-assisted cyclization cascade // JOURNAL OF ORGANIC CHEMISTRY. - 2020. - Том: 85. - Выпуск: 19. - Стр.: 12128-12146ru
dc.identifier.urihttp://hdl.handle.net/20.500.12258/14565-
dc.description.abstractAn efficient and straightforward Bronsted-acid mediated cascade process was developed, involving cyclization of readily available beta-ketonitriles into 2-aminofurans, and their subsequent recyclization into 2-(1H-indol-2-yl)acetamides is developed. This synthetic route opens a new avenue for an expeditious assembly ofru
dc.language.isoenru
dc.publisherAMER CHEMICAL SOCru
dc.relation.ispartofseriesJournal of Organic Chemistry-
dc.subject2'-aminochalconesru
dc.subjectEfficientru
dc.subjectMichael additionru
dc.subjectHistoneru
dc.subjectDiscoveryru
dc.subjectIndolesru
dc.subjectReductionru
dc.subjectInhibitory-activityru
dc.subjectNitrostyrenesru
dc.subjectRouteru
dc.titleSynthesis of 2-(1H-Indol-2-yl)acetamides via bronsted acid-assisted cyclization cascaderu
dc.typeСтатьяru
vkr.instИнститут математики и естественных наукru
Appears in Collections:Статьи, проиндексированные в SCOPUS, WOS

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