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dc.contributor.authorAksenov, Alexander V.
dc.contributor.authorOvcharov, Dmitrii S.
dc.contributor.authorAksenov, Nicolai A.
dc.contributor.authorAksenov, Dmitrii A.
dc.contributor.authorNadein, Oleg N.
dc.contributor.authorRubin, Michael
dc.date.accessioned2018-11-12T20:29:33Z
dc.date.available2018-11-12T20:29:33Z
dc.date.issued2017-06-08
dc.identifier.citationAksenov, A. V., Ovcharov, D. S., Aksenov, N. A., Aksenov, D. A., Nadein, O. N., & Rubin, M. (2017). Dual role of polyphosphoric acid-activated nitroalkanes in oxidative peri-annulations: efficient synthesis of 1, 3, 6, 8-tetraazapyrenes. RSC Advances, 7(48), 29927-29932.en_US
dc.identifier.urihttp://hdl.handle.net/1808/27300
dc.description.abstractA highly efficient synthetic method for expeditious and selective assembly of tetraazopyrenes (TAPy) is reported, based on the novel reaction of electrophilically activated nitroalkanes with aromatic amines. Remarkably, the nitroalkanes play a dual role in this process, also serving as mild and efficient oxidants promoting aromatization of the final product and allowing for the exclusion of a poorly controllable aerobic treatment.en_US
dc.publisherRoyal Society of Chemistryen_US
dc.rights© The Royal Society of Chemistry 2017. This article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence.en_US
dc.rights.urihttps://creativecommons.org/licenses/by-nc/3.0/us/en_US
dc.titleDual role of polyphosphoric acid-activated nitroalkanes in oxidative peri-annulations: efficient synthesis of 1,3,6,8-tetraazapyrenesen_US
dc.typeArticleen_US
kusw.kuauthorRubin, Michael
kusw.kudepartmentChemistryen_US
dc.identifier.doi10.1039/C7RA04751Gen_US
kusw.oaversionScholarly/refereed, publisher versionen_US
kusw.oapolicyThis item meets KU Open Access policy criteria.en_US
dc.rights.accessrightsopenAccessen_US


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© The Royal Society of Chemistry 2017. This article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence.
Except where otherwise noted, this item's license is described as: © The Royal Society of Chemistry 2017. This article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence.