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Synthesis of imidazo[1,5-a]pyridines via cyclocondensation of 2-(aminomethyl)pyridines with electrophilically activated nitroalkanes

dc.contributor.authorAksenov, Dmitrii A.
dc.contributor.authorArutiunov, Nikolai A.
dc.contributor.authorMaliuga, Vladimir V.
dc.contributor.authorAksenov, Alexander V.
dc.contributor.authorRubin, Michael
dc.date.accessioned2022-01-17T18:50:42Z
dc.date.available2022-01-17T18:50:42Z
dc.date.issued2020-11-26
dc.identifier.citationAksenov, D. A.; Arutiunov, N. A.; Maliuga, V. V.; Aksenov, A. V.; Rubin, M. Beilstein J. Org. Chem. 2020, 16, 2903–2910. doi:10.3762/bjoc.16.239en_US
dc.identifier.urihttp://hdl.handle.net/1808/32407
dc.description.abstractImidazo[1,5-a]pyridines were efficiently prepared via the cyclization of 2-picolylamines with nitroalkanes electrophilically activated in the presence of phosphorous acid in polyphosphoric acid (PPA) medium.en_US
dc.publisherBeilstein-Instituten_US
dc.rights© 2020 Aksenov et al.; licensee Beilstein-Institut. This is an Open Access article under the terms of the Creative Commons Attribution License. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc)en_US
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en_US
dc.subjectCyclizationen_US
dc.subjectHeterocyclesen_US
dc.subjectImidazo[1,5-a]pyridinesen_US
dc.subjectNitroalkanesen_US
dc.subjectPolyphosphoric aciden_US
dc.titleSynthesis of imidazo[1,5-a]pyridines via cyclocondensation of 2-(aminomethyl)pyridines with electrophilically activated nitroalkanesen_US
dc.typeArticleen_US
kusw.kuauthorRubin, Michael
kusw.kudepartmentChemistryen_US
dc.identifier.doi10.3762/bjoc.16.239en_US
dc.identifier.orcidhttps://orcid.org/ 0000-0002-0727-9652en_US
dc.identifier.orcidhttps://orcid.org/ 0000-0003-2675-9093en_US
dc.identifier.orcidhttps://orcid.org/ 0000-0002-2702-5684en_US
dc.identifier.orcidhttps://orcid.org/ 0000-0002-6644-9949en_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.pmidPMC7705866en_US
dc.rights.accessrightsopenAccessen_US


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© 2020 Aksenov et al.; licensee Beilstein-Institut. This is an Open Access article under the terms of the Creative Commons Attribution License. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc)
Except where otherwise noted, this item's license is described as: © 2020 Aksenov et al.; licensee Beilstein-Institut. This is an Open Access article under the terms of the Creative Commons Attribution License. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc)