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Article: Cyclobis(paraquat-p-phenylene)-based [2]catenanes prepared by kinetically controlled reactions involving alkynes

TitleCyclobis(paraquat-p-phenylene)-based [2]catenanes prepared by kinetically controlled reactions involving alkynes
Authors
Issue Date2006
Citation
Organic Letters, 2006, v. 8, n. 21, p. 4835-4838 How to Cite?
Abstract(Chemical Equation Presented) Charged donor-acceptor [2]catenanes, in which the π-accepting cyclobis(paraquat-p-phenylene) acts as a tetracationic template for the threading-followed-by-clipping of acyclic oligoethers, incorporating centrally a π-donating 1,5-dioxynaphthalene ring system and terminated either by acetylene units or by acetylene and azide functions, are the products of copper-mediated Eglinton coupling and Huisgen 1,3-dipolar cycloaddition, respectively. © 2006 American Chemical Society.
Persistent Identifierhttp://hdl.handle.net/10722/332710
ISSN
2023 Impact Factor: 4.9
2023 SCImago Journal Rankings: 1.245
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorMiljanić, Ognjen Š-
dc.contributor.authorDichtel, William R.-
dc.contributor.authorMortezaei, Shahab-
dc.contributor.authorStoddart, J. Fraser-
dc.date.accessioned2023-10-06T05:13:40Z-
dc.date.available2023-10-06T05:13:40Z-
dc.date.issued2006-
dc.identifier.citationOrganic Letters, 2006, v. 8, n. 21, p. 4835-4838-
dc.identifier.issn1523-7060-
dc.identifier.urihttp://hdl.handle.net/10722/332710-
dc.description.abstract(Chemical Equation Presented) Charged donor-acceptor [2]catenanes, in which the π-accepting cyclobis(paraquat-p-phenylene) acts as a tetracationic template for the threading-followed-by-clipping of acyclic oligoethers, incorporating centrally a π-donating 1,5-dioxynaphthalene ring system and terminated either by acetylene units or by acetylene and azide functions, are the products of copper-mediated Eglinton coupling and Huisgen 1,3-dipolar cycloaddition, respectively. © 2006 American Chemical Society.-
dc.languageeng-
dc.relation.ispartofOrganic Letters-
dc.titleCyclobis(paraquat-p-phenylene)-based [2]catenanes prepared by kinetically controlled reactions involving alkynes-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1021/ol061864d-
dc.identifier.scopuseid_2-s2.0-33750325605-
dc.identifier.volume8-
dc.identifier.issue21-
dc.identifier.spage4835-
dc.identifier.epage4838-
dc.identifier.isiWOS:000241030900042-

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