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- Publisher Website: 10.1021/ol061864d
- Scopus: eid_2-s2.0-33750325605
- WOS: WOS:000241030900042
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Article: Cyclobis(paraquat-p-phenylene)-based [2]catenanes prepared by kinetically controlled reactions involving alkynes
Title | Cyclobis(paraquat-p-phenylene)-based [2]catenanes prepared by kinetically controlled reactions involving alkynes |
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Authors | |
Issue Date | 2006 |
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 Identifier | http://hdl.handle.net/10722/332710 |
ISSN | 2023 Impact Factor: 4.9 2023 SCImago Journal Rankings: 1.245 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Miljanić, Ognjen Š | - |
dc.contributor.author | Dichtel, William R. | - |
dc.contributor.author | Mortezaei, Shahab | - |
dc.contributor.author | Stoddart, J. Fraser | - |
dc.date.accessioned | 2023-10-06T05:13:40Z | - |
dc.date.available | 2023-10-06T05:13:40Z | - |
dc.date.issued | 2006 | - |
dc.identifier.citation | Organic Letters, 2006, v. 8, n. 21, p. 4835-4838 | - |
dc.identifier.issn | 1523-7060 | - |
dc.identifier.uri | http://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.language | eng | - |
dc.relation.ispartof | Organic Letters | - |
dc.title | Cyclobis(paraquat-p-phenylene)-based [2]catenanes prepared by kinetically controlled reactions involving alkynes | - |
dc.type | Article | - |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1021/ol061864d | - |
dc.identifier.scopus | eid_2-s2.0-33750325605 | - |
dc.identifier.volume | 8 | - |
dc.identifier.issue | 21 | - |
dc.identifier.spage | 4835 | - |
dc.identifier.epage | 4838 | - |
dc.identifier.isi | WOS:000241030900042 | - |