dc.contributor.author | Matheny, Jonathon P. | |
dc.contributor.author | Yamanushkin, Pavel M. | |
dc.contributor.author | Petillo, Peter A. | |
dc.contributor.author | Rubin, Michael | |
dc.date.accessioned | 2022-07-11T20:59:41Z | |
dc.date.available | 2022-07-11T20:59:41Z | |
dc.date.issued | 2020-12-15 | |
dc.identifier.citation | Matheny 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.uri | http://hdl.handle.net/1808/32829 | |
dc.description.abstract | The 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.publisher | Royal Society of Chemistry | en_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.uri | https://creativecommons.org/licenses/by-nc/4.0/ | en_US |
dc.title | Facile assembly of 1,5-diazocan-2-ones via cyclization of tethered sulfonamides to cyclopropenes | en_US |
dc.type | Article | en_US |
kusw.kuauthor | Matheny, Jonathon P. | |
kusw.kuauthor | Yamanushkin, Pavel M. | |
kusw.kuauthor | Petillo, Peter A. | |
kusw.kuauthor | Rubin, Michael | |
kusw.kudepartment | Chemistry | en_US |
dc.identifier.doi | 10.1039/d0ra09014j | en_US |
dc.identifier.orcid | https://orcid.org/ 0000-0002-1668-9311 | en_US |
kusw.oaversion | Scholarly/refereed, publisher version | en_US |
kusw.oapolicy | This item meets KU Open Access policy criteria. | en_US |
dc.identifier.pmid | PMC35517142 | en_US |
dc.rights.accessrights | openAccess | en_US |