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dc.contributor.authorMatheny, Jonathon P.
dc.contributor.authorYamanushkin, Pavel M.
dc.contributor.authorPetillo, Peter A.
dc.contributor.authorRubin, Michael
dc.date.accessioned2022-07-11T20:59:41Z
dc.date.available2022-07-11T20:59:41Z
dc.date.issued2020-12-15
dc.identifier.citationMatheny JP, Yamanushkin PM, Petillo PA, Rubin M. Facile assembly of 1,5-diazocan-2-ones via cyclization of tethered sulfonamides to cyclopropenes. RSC Adv. 2020 Dec 15;10(72):44183-44190. doi: 10.1039/d0ra09014j. PMID: 35517142; PMCID: PMC9058510.en_US
dc.identifier.urihttp://hdl.handle.net/1808/32829
dc.description.abstractThe sulfonamide moiety was evaluated as an activating and stabilizing functional group in the metal-templated strain release-driven intramolecular nucleophilic addition of amines to cyclopropenes to generate 1,5-diazocan-2-ones.en_US
dc.publisherRoyal Society of Chemistryen_US
dc.rights© The Royal Society of Chemistry 2020. This article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License.en_US
dc.rights.urihttps://creativecommons.org/licenses/by-nc/4.0/en_US
dc.titleFacile assembly of 1,5-diazocan-2-ones via cyclization of tethered sulfonamides to cyclopropenesen_US
dc.typeArticleen_US
kusw.kuauthorMatheny, Jonathon P.
kusw.kuauthorYamanushkin, Pavel M.
kusw.kuauthorPetillo, Peter A.
kusw.kuauthorRubin, Michael
kusw.kudepartmentChemistryen_US
dc.identifier.doi10.1039/d0ra09014jen_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.pmid35517142en_US
dc.rights.accessrightsopenAccessen_US


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© The Royal Society of Chemistry 2020. This article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License.
Except where otherwise noted, this item's license is described as: © The Royal Society of Chemistry 2020. This article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License.