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dc.contributor.authorAksenov, Nicolai A.
dc.contributor.authorAksenov, Alexander V.
dc.contributor.authorKornienko, Alexander
dc.contributor.authorDe Carvalho, Annelise
dc.contributor.authorMathieu, Véronique
dc.contributor.authorAksenov, Dmitrii A.
dc.contributor.authorOvcharov, Sergei N.
dc.contributor.authorGriaznov, Georgii D.
dc.contributor.authorRubin, Michael
dc.date.accessioned2022-07-12T18:21:28Z
dc.date.available2022-07-12T18:21:28Z
dc.date.issued2018-11-01
dc.identifier.citationAksenov NA, Aksenov AV, Kornienko A, De Carvalho A, Mathieu V, Aksenov DA, Ovcharov SN, Griaznov GD, Rubin M. A nitroalkane-based approach to one-pot three-component synthesis of isocryptolepine and its analogs with potent anti-cancer activities. RSC Adv. 2018 Nov 1;8(64):36980-36986. doi: 10.1039/c8ra08155g. PMID: 35558925; PMCID: PMC9089289.en_US
dc.identifier.urihttp://hdl.handle.net/1808/32831
dc.description.abstractA second generation polyphosphoric acid-mediated one-pot three-component synthesis of indoloquinoline scaffold is developed. This improved version of the process involves electrophilically activated nitroalkanes for the installation of strategic C–C and C–N bonds and ring C assembly. This modification allows the elimination of unnecessary solvent change operations and all steps are carried out in a true, uninterrupted one-pot manner. A further improvement involves the possibility to install an ortho-amino group in situ. A synthetic application of this method is showcased by the concise synthesis of an isocryptolepine alkaloid and its synthetic analogs with potent anticancer activities.en_US
dc.publisherRoyal Society of Chemistryen_US
dc.rightsThis article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. © The Royal Society of Chemistry 2018.en_US
dc.rights.urihttps://creativecommons.org/licenses/by-nc/4.0/en_US
dc.titleA nitroalkane-based approach to one-pot three-component synthesis of isocryptolepine and its analogs with potent anti-cancer activitiesen_US
dc.typeArticleen_US
kusw.kuauthorRubin, Michael
kusw.kudepartmentChemistryen_US
dc.identifier.doi10.1039/c8ra08155gen_US
dc.identifier.orcidhttps://orcid.org/ 0000-0002-7125-9066en_US
dc.identifier.orcidhttps://orcid.org/ 0000-0002-6644-9949en_US
dc.identifier.orcidhttps://orcid.org/ 0000-0003-2041-7367en_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.pmidPMC35558925en_US
dc.rights.accessrightsopenAccessen_US


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This article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. © The Royal Society of Chemistry 2018.
Except where otherwise noted, this item's license is described as: This article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. © The Royal Society of Chemistry 2018.