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Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/20.500.12258/22300
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dc.contributor.authorShcherbakov, S. V.-
dc.contributor.authorЩербаков, С. В.-
dc.contributor.authorAksenov, A. V.-
dc.contributor.authorАксенов, А. В.-
dc.contributor.authorVendin, M. V.-
dc.contributor.authorВендин, М. В.-
dc.contributor.authorShcherbakova, V. Y.-
dc.contributor.authorЩербакова, В. Ю.-
dc.contributor.authorIvanova, A. Y.-
dc.contributor.authorИванова, А. Ю.-
dc.contributor.authorShcheglov, M. O.-
dc.contributor.authorЩеглов, М. О.-
dc.contributor.authorOvcharov, S. N.-
dc.contributor.authorОвчаров, С. Н.-
dc.contributor.authorRubin, M. A.-
dc.contributor.authorРубин, М. А.-
dc.date.accessioned2023-02-03T08:16:05Z-
dc.date.available2023-02-03T08:16:05Z-
dc.date.issued2022-
dc.identifier.citationShcherbakov, S.V., Aksenov, A.V., Vendin, M.V., Shcherbakova, V.Y., Ivanova, A.Y., Shcheglov, M.O., Ovcharov, S.N., Rubin, M. Annulation of Perimidines with 5-Alkynylpyrimidines en Route to 7-Formyl-1,3-Diazopyrenes // International journal of molecular sciences. - 2022. - 23 (24), статья № 15657. - DOI: 10.3390/ijms232415657ru
dc.identifier.urihttp://hdl.handle.net/20.500.12258/22300-
dc.description.abstractUnusual rearrangements were shown to accompany Brønsted acid-assisted peri-annulations of 1H-perimidines with 5-alkynylpyrimidines. These transformations take different routes depending on the nature of acetylene precursor, and lead to the formation of 7-formyl-1,3-diazopyrenes.ru
dc.language.isoenru
dc.relation.ispartofseriesInternational Journal of Molecular Sciences-
dc.subjectBrønsted acid catalysisru
dc.subjectAcetylenesru
dc.subjectAnnulationsru
dc.subjectNitrogen heterocyclesru
dc.subjectRearrangementsru
dc.titleAnnulation of Perimidines with 5-Alkynylpyrimidines en Route to 7-Formyl-1,3-Diazopyrenesru
dc.typeСтатьяru
vkr.instХимико-фармацевтический факультетru
Appears in Collections:Статьи, проиндексированные в SCOPUS, WOS

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