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dc.contributor.authorAksenov, Alexander V.
dc.contributor.authorKirilov, Nikita K.
dc.contributor.authorAksenov, Nicolai A.
dc.contributor.authorAksenov, Dmitrii A.
dc.contributor.authorSorokina, Elena A.
dc.contributor.authorLower, Carolyn
dc.contributor.authorRubin, Michael
dc.date.accessioned2021-12-03T18:24:00Z
dc.date.available2021-12-03T18:24:00Z
dc.date.issued2021-09-20
dc.identifier.citationAksenov, A.V.; Kirilov, N.K.; Aksenov, N.A.; Aksenov, D.A.; Sorokina, E.A.; Lower, C.; Rubin, M. Electrophilically Activated Nitroalkanes in Double Annulation of [1,2,4]Triazolo[4,3-a]quinolines and 1,3,4-Oxadiazole Rings. Molecules 2021, 26, 5692. https://doi.org/10.3390/molecules26185692en_US
dc.identifier.urihttp://hdl.handle.net/1808/32239
dc.description.abstractNitroalkanes activated with polyphosphoric acid could serve as efficient electrophiles in reactions with amines and hydrazines, enabling various cascade transformations toward heterocyclic systems. This strategy was developed for an innovative synthetic protocol employing simultaneous or sequential annulation of two different heterocyclic cores, affording [1,2,4]triazolo[4,3-a]quinolines with 1,3,4-oxadiazole substituents.en_US
dc.publisherMDPIen_US
dc.rights© 2021 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.subjectNitroalkanesen_US
dc.subjectHeterocyclesen_US
dc.subjectAnnulationen_US
dc.subjectCascade transformationsen_US
dc.titleElectrophilically Activated Nitroalkanes in Double Annulation of [1,2,4]Triazolo[4,3-a]quinolines and 1,3,4-Oxadiazole Ringsen_US
dc.typeArticleen_US
kusw.kuauthorLower, Carolyn
kusw.kuauthorRubin, Michael
kusw.kudepartmentChemistryen_US
dc.identifier.doi10.3390/molecules26185692en_US
dc.identifier.orcidhttps://orcid.org/ 0000-0002-6644-9949en_US
dc.identifier.orcidhttps://orcid.org/ 0000-0001-8688-7201en_US
dc.identifier.orcidhttps://orcid.org/ 0000-0001-8867-7988en_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.pmidPMC8464891en_US
dc.rights.accessrightsopenAccessen_US


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© 2021 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: © 2021 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.