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Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/20.500.12258/19633
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dc.contributor.authorShcherbakov, S. V.-
dc.contributor.authorЩербаков, С. В.-
dc.contributor.authorMagometov, A. Y.-
dc.contributor.authorМагометов, А. Ю.-
dc.contributor.authorVendin, M. V.-
dc.contributor.authorВендин, М. В.-
dc.contributor.authorShcherbakova, V. Y.-
dc.contributor.authorЩербакова, В. Ю.-
dc.contributor.authorAksenov, N. A.-
dc.contributor.authorАксенов, Н. А.-
dc.contributor.authorAksenov, A. V.-
dc.contributor.authorАксенов, А. В.-
dc.contributor.authorRubin, M. A.-
dc.contributor.authorРубин, М. А.-
dc.date.accessioned2022-05-27T11:54:53Z-
dc.date.available2022-05-27T11:54:53Z-
dc.date.issued2022-
dc.identifier.citationShcherbakov, S. V., Magometov, A. Y., Vendin, M. V., Shcherbakova, V. Y., Aksenov, N. A., Aksenov, A. V., Naji, O., Rubin, M. Investigation of cationic transformations involving 5-ethynyl-4-arylpyrimidines // Tetrahedron. - 2022. - Номер статьи 132796. - DOI10.1016/j.tet.2022.132796ru
dc.identifier.urihttp://hdl.handle.net/20.500.12258/19633-
dc.description.abstractAn innovative synthetic approach towards 5-ethynyl-4-arylpyrimidines was developed involving acid-catalyzed electrophilic alkylation of phenols with 5-bromopyrimidine, followed by oxidation and palladium-catalyzed Sonogashira cross-coupling reaction. Reactions of these compounds in the presence of trifluoromethanesulfonic acid were investigated. It was discovered these reactions take a different route for precursors with a different position of phenol group in an arene substituent.ru
dc.language.isoenru
dc.publisherElsevier Ltdru
dc.relation.ispartofseriesTetrahedron-
dc.subjectAcetylenesru
dc.subjectCationic rearrangementsru
dc.subjectHeterocyclic chemistryru
dc.subjectReaction mechanismsru
dc.subjectSynthetic methodologyru
dc.titleInvestigation of cationic transformations involving 5-ethynyl-4-arylpyrimidinesru
dc.typeСтатьяru
vkr.instХимико-фармацевтический факультетru
Appears in Collections:Статьи, проиндексированные в SCOPUS, WOS

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