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dc.contributor.authorAksenov, Alexander V.
dc.contributor.authorAksenov, Nicolai A.
dc.contributor.authorArutiunov, Nikolai A.
dc.contributor.authorMalyuga, Vladimir V.
dc.contributor.authorOvcharov, Sergey N.
dc.contributor.authorRubin, Michael
dc.identifier.citationA. V. Aksenov, N. A. Aksenov, N. A. Arutiunov, V. V. Malyuga, S. N. Ovcharov and M. Rubin, "Electrophilically activated nitroalkanes in reaction with aliphatic diamines en route to imidazolines", RSC Adv., 2019, 9, 39458, DOI: 10.1039/C9RA08630Gen_US
dc.descriptionThis article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence. Material from this article can be used in other publications provided that the correct acknowledgement is given with the reproduced material and it is not used for commercial purposes.en_US
dc.description.abstractA novel synthetic methodology for the assembly of imidazolines via an unusual reaction between nitroalkanes and aliphatic 1,2-diamines in the presence of phosphorous acid is described. In contrast to the related highly efficient preparation of benzimidazoles from aromatic amines, this process represents a major synthetic challenge and for a long time was elusive. Analysis of the method limitations is provided.en_US
dc.publisherRoyal Society of Chemistryen_US
dc.rights© The Royal Society of Chemistry 2019.en_US
dc.titleElectrophilically activated nitroalkanes in reaction with aliphatic diamines en route to imidazolinesen_US
kusw.kuauthorRubin, Michael
kusw.oaversionScholarly/refereed, publisher versionen_US
kusw.oapolicyThis item meets KU Open Access policy criteria.en_US

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© The Royal Society of Chemistry 2019.
Except where otherwise noted, this item's license is described as: © The Royal Society of Chemistry 2019.