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Article: N-HETEROCYCLIC ANALOGS OF INDENOCORANNULENE

TitleN-HETEROCYCLIC ANALOGS OF INDENOCORANNULENE
Authors
Issue Date2022
Citation
Heterocycles, 2022, v. 105, n. 1, p. 477-486 How to Cite?
AbstractFour chiral N-heterocyclic monoindenocorannulenes were prepared by fusing pyridine, quinoline, and indole across the peri-positions of corannulene via tandem Suzuki-aryl-aryl coupling and C-Cl activated ring closure reactions. The UV-Vis, fluorescence, and CV properties of these N-doped polynuclear aromatics are discussed. Resolution of enantiomers is performed on chiral stationary phase HPLC and the absolute configurations are assigned by comparison of experimental and quantum mechanically predicted ECD spectra.
Persistent Identifierhttp://hdl.handle.net/10722/341365
ISSN
2023 Impact Factor: 0.8
2023 SCImago Journal Rankings: 0.172
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorLi, Ansu-
dc.contributor.authorXu, Jun-
dc.contributor.authorBaldridge, Kim K.-
dc.contributor.authorSiegel, Jay S.-
dc.date.accessioned2024-03-13T08:42:15Z-
dc.date.available2024-03-13T08:42:15Z-
dc.date.issued2022-
dc.identifier.citationHeterocycles, 2022, v. 105, n. 1, p. 477-486-
dc.identifier.issn0385-5414-
dc.identifier.urihttp://hdl.handle.net/10722/341365-
dc.description.abstractFour chiral N-heterocyclic monoindenocorannulenes were prepared by fusing pyridine, quinoline, and indole across the peri-positions of corannulene via tandem Suzuki-aryl-aryl coupling and C-Cl activated ring closure reactions. The UV-Vis, fluorescence, and CV properties of these N-doped polynuclear aromatics are discussed. Resolution of enantiomers is performed on chiral stationary phase HPLC and the absolute configurations are assigned by comparison of experimental and quantum mechanically predicted ECD spectra.-
dc.languageeng-
dc.relation.ispartofHeterocycles-
dc.titleN-HETEROCYCLIC ANALOGS OF INDENOCORANNULENE-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.3987/COM-22-S(R)19-
dc.identifier.scopuseid_2-s2.0-85133853797-
dc.identifier.volume105-
dc.identifier.issue1-
dc.identifier.spage477-
dc.identifier.epage486-
dc.identifier.eissn1881-0942-
dc.identifier.isiWOS:000829667500017-

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