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Electrophilically activated nitroalkanes in reaction with aliphatic diamines en route to imidazolines

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.date.accessioned2021-02-09T22:51:12Z
dc.date.available2021-02-09T22:51:12Z
dc.date.issued2019-11-29
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.identifier.urihttp://hdl.handle.net/1808/31410
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.rights.urihttps://creativecommons.org/licenses/by-nc/3.0/en_US
dc.titleElectrophilically activated nitroalkanes in reaction with aliphatic diamines en route to imidazolinesen_US
dc.typeArticleen_US
kusw.kuauthorRubin, Michael
kusw.kudepartmentChemistryen_US
kusw.oanotesPer Sherpa Romeo 02/09/2021:

RSC Advances [Open panel below]Publication Information TitleRSC Advances [English] ISSNsElectronic: 2046-2069 URLhttp://pubs.rsc.org/en/journals/journalissues/ra PublishersRoyal Society of Chemistry [Society Publisher] DOAJ Listinghttps://doaj.org/toc/2046-2069 Requires APCYes [Data provided by DOAJ] [Open panel below]Publisher Policy Open Access pathways permitted by this journal's policy are listed below by article version. Click on a pathway for a more detailed view.

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NoneCC BY Any Website, Journal Website, +4 OA PublishingThis pathway includes Open Access publishing EmbargoNo Embargo Licence CC BY CC BY-NC Copyright OwnerAuthors Location Academic Social Network Any Website Author's Homepage Non-Commercial Institutional Repository Non-Commercial Subject Repository Journal Website ConditionsPublished source must be acknowledged with citation		en_US
dc.identifier.doi10.1039/c9ra08630gen_US
dc.identifier.orcidhttps://orcid.org/0000-0002-6644-9949en_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
kusw.proidID198090633216en_US
dc.rights.accessrightsopenAccessen_US


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© The Royal Society of Chemistry 2019.
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