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A Convenient Way to Quinoxaline Derivatives through the Reaction of 2-(3-Oxoindolin-2-yl)-2-phenylacetonitriles with Benzene-1,2-diamines

dc.contributor.authorAksenov, Alexander V.
dc.contributor.authorArutiunov, Nikolai A.
dc.contributor.authorAksenov, Dmitrii A.
dc.contributor.authorSamovolov, Artem V.
dc.contributor.authorKurenkov, Igor A.
dc.contributor.authorAksenov, Nicolai A.
dc.contributor.authorAleksandrova, Elena A.
dc.contributor.authorMomotova, Daria S.
dc.contributor.authorRubin, Michael
dc.date.accessioned2023-02-14T16:05:12Z
dc.date.available2023-02-14T16:05:12Z
dc.date.issued2022-09-22
dc.identifier.citationAksenov, A.V.; Arutiunov, N.A.; Aksenov, D.A.; Samovolov, A.V.; Kurenkov, I.A.; Aksenov, N.A.; Aleksandrova, E.A.; Momotova, D.S.; Rubin, M. A Convenient Way to Quinoxaline Derivatives through the Reaction of 2-(3-Oxoindolin-2-yl)-2-phenylacetonitriles with Benzene-1,2-diamines. Int. J. Mol. Sci. 2022, 23, 11120. https://doi.org/10.3390/ijms231911120en_US
dc.identifier.urihttp://hdl.handle.net/1808/33791
dc.description.abstractMicrowave-assisted reaction between 2-(3-oxoindolin-2-yl)-2-phenylacetonitriles andbenzene-1,2-diamines leads to the high-yielding formation of the corresponding quinoxalines as sole, easily isolaable products. The featured transformation involves unusual extrusion of phenylacetonitrile molecule and could be performed in a short sequence starting from commonly available indoles and nitroolefins.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.subjectCyclizationen_US
dc.subjectQuinoxalinesen_US
dc.subjectMicrowave synthesisen_US
dc.titleA Convenient Way to Quinoxaline Derivatives through the Reaction of 2-(3-Oxoindolin-2-yl)-2-phenylacetonitriles with Benzene-1,2-diaminesen_US
dc.typeArticleen_US
kusw.kuauthorRubin, Michael
kusw.kudepartmentChemistryen_US
dc.identifier.doi10.3390/ijms231911120en_US
dc.identifier.orcidhttps://orcid.org/0000-0002-0911-4093en_US
dc.identifier.orcidhttps://orcid.org/0000-0002-7125-9066en_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.pmidPMC9570350en_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.