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Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/20.500.12258/19606
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dc.contributor.authorAksenov, N. A.-
dc.contributor.authorАксенов, Н. А.-
dc.contributor.authorAksenov, A. V.-
dc.contributor.authorАксенов, А. В.-
dc.contributor.authorKurenkov, I. A.-
dc.contributor.authorКуренков, И. А.-
dc.contributor.authorKirilov, N. K.-
dc.contributor.authorКирилов, Н. К.-
dc.contributor.authorAksenov, D. A.-
dc.contributor.authorАксенов, Д. А.-
dc.contributor.authorArutiunov, N. A.-
dc.contributor.authorАрутюнов, Н. А.-
dc.contributor.authorAksenova, D. S.-
dc.contributor.authorАксенова, Д. С.-
dc.contributor.authorRubin, M. A.-
dc.contributor.authorРубин, М. А.-
dc.date.accessioned2022-05-25T07:08:58Z-
dc.date.available2022-05-25T07:08:58Z-
dc.date.issued2022-
dc.identifier.citationAksenov, N. A., Aksenov, A. V., Kurenkov, I. A., Kirillov, N. K., Aksenov, D. A., Arutiunov, N. A., Aksenova, D. S., Rubin, M. One-Pot Synthesis of (E)-2-(3-Oxoindolin-2-Ylidene)-2-Arylacetonitriles // Molecules. - 2022. - Том 27. - Выпуск 9. - Номер статьи 2808. - DOI10.3390/molecules27092808ru
dc.identifier.urihttp://hdl.handle.net/20.500.12258/19606-
dc.description.abstractA highly efficient and expeditious one-pot approach towards 2-(3-oxoindolin-2-yl)acetonitriles was designed, which involves a base-assisted aldol reaction of ortho-nitroacetophenones, followed by hydrocyanation, triggering an unusual reductive cyclization reaction.ru
dc.language.isoenru
dc.publisherMDPIru
dc.relation.ispartofseriesMolecules-
dc.subjectBrønsted acid catalysisru
dc.subjectCascade transformationsru
dc.subjectIndolesru
dc.subjectNitroalkanesru
dc.subjectRearrangementsru
dc.titleOne-Pot Synthesis of (E)-2-(3-Oxoindolin-2-Ylidene)-2-Arylacetonitrilesru
dc.typeСтатьяru
vkr.instХимико-фармацевтический факультетru
Appears in Collections:Статьи, проиндексированные в SCOPUS, WOS

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