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Electrophilically Activated Nitroalkanes in Double Annulation of [1,2,4]Triazolo[4,3-a]quinolines and 1,3,4-Oxadiazole Rings
dc.contributor.author | Aksenov, Alexander V. | |
dc.contributor.author | Kirilov, Nikita K. | |
dc.contributor.author | Aksenov, Nicolai A. | |
dc.contributor.author | Aksenov, Dmitrii A. | |
dc.contributor.author | Sorokina, Elena A. | |
dc.contributor.author | Lower, Carolyn | |
dc.contributor.author | Rubin, Michael | |
dc.date.accessioned | 2021-12-03T18:24:00Z | |
dc.date.available | 2021-12-03T18:24:00Z | |
dc.date.issued | 2021-09-20 | |
dc.identifier.citation | Aksenov, 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/molecules26185692 | en_US |
dc.identifier.uri | http://hdl.handle.net/1808/32239 | |
dc.description.abstract | Nitroalkanes 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.publisher | MDPI | en_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.uri | http://creativecommons.org/licenses/by/4.0/ | en_US |
dc.subject | Nitroalkanes | en_US |
dc.subject | Heterocycles | en_US |
dc.subject | Annulation | en_US |
dc.subject | Cascade transformations | en_US |
dc.title | Electrophilically Activated Nitroalkanes in Double Annulation of [1,2,4]Triazolo[4,3-a]quinolines and 1,3,4-Oxadiazole Rings | en_US |
dc.type | Article | en_US |
kusw.kuauthor | Lower, Carolyn | |
kusw.kuauthor | Rubin, Michael | |
kusw.kudepartment | Chemistry | en_US |
dc.identifier.doi | 10.3390/molecules26185692 | en_US |
dc.identifier.orcid | https://orcid.org/ 0000-0002-6644-9949 | en_US |
dc.identifier.orcid | https://orcid.org/ 0000-0001-8688-7201 | en_US |
dc.identifier.orcid | https://orcid.org/ 0000-0001-8867-7988 | en_US |
dc.identifier.orcid | https://orcid.org/ 0000-0002-1668-9311 | en_US |
kusw.oaversion | Scholarly/refereed, publisher version | en_US |
kusw.oapolicy | This item meets KU Open Access policy criteria. | en_US |
dc.identifier.pmid | PMC8464891 | en_US |
dc.rights.accessrights | openAccess | en_US |