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Annulation of Perimidines with 5-Alkynylpyrimidines en Route to 7-Formyl-1,3-Diazopyrenes

dc.contributor.authorShcherbakov, Stanislav V.
dc.contributor.authorAksenov, Alexander V.
dc.contributor.authorVendin, Maksim V.
dc.contributor.authorShcherbakova, Viktoria Yu.
dc.contributor.authorIvanova, Anna Yu.
dc.contributor.authorShcheglov, Maksim O.
dc.contributor.authorOvcharov, Sergei N.
dc.contributor.authorRubin, Michael
dc.date.accessioned2023-02-03T19:10:21Z
dc.date.available2023-02-03T19:10:21Z
dc.date.issued2022-12-10
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. Int. J. Mol. Sci. 2022, 23, 15657. https://doi.org/10.3390/ijms232415657en_US
dc.identifier.urihttp://hdl.handle.net/1808/33733
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.en_US
dc.publisherMDPIen_US
dc.rights© 2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license.en_US
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en_US
dc.subjectAnnulationsen_US
dc.subjectAcetylenesen_US
dc.subjectNitrogen heterocyclesen_US
dc.subjectBrønsted acid catalysisen_US
dc.subjectRearrangementsen_US
dc.titleAnnulation of Perimidines with 5-Alkynylpyrimidines en Route to 7-Formyl-1,3-Diazopyrenesen_US
dc.typeArticleen_US
kusw.kuauthorRubin, Michael
kusw.kudepartmentChemistryen_US
dc.identifier.doi10.3390/ijms232415657en_US
dc.identifier.orcidhttps://orcid.org/0000-0002-6644-9949en_US
dc.identifier.orcidhttps://orcid.org/0000-0003-3788-1350en_US
dc.identifier.orcidhttps://orcid.org/0000-0002-1668-9311en_US
kusw.oaversionScholarly/refereed, publisher versionen_US
kusw.oapolicyThis item meets KU Open Access policy criteria.en_US
dc.identifier.pmidPMC9778996en_US
dc.rights.accessrightsopenAccessen_US


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© 2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license.
Except where otherwise noted, this item's license is described as: © 2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license.