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Article: Synthesis of oligopyridines and their metal complexes as precursors to topological stereoisomers

TitleSynthesis of oligopyridines and their metal complexes as precursors to topological stereoisomers
Authors
Issue Date2001
Citation
Organic Letters, 2001, v. 3, n. 7, p. 967-969 How to Cite?
Abstract(Matrix Presented) Palladium-based carbon-carbon coupling reactions in sequence with halogen-exchange chemistry on a series of heterocycles lead to an effecient synthetic strategy for oligopyridines that bind metal ions such as ruthenium to form coordination racks. The particular structures are designed to form tepyridine subunits for octahedral binding. Reactions of 4,6-diiodopyrimide produces a "duoble-bay" terpyridine from which binuclear coordination complexes have been formed.
Persistent Identifierhttp://hdl.handle.net/10722/341000
ISSN
2023 Impact Factor: 4.9
2023 SCImago Journal Rankings: 1.245

 

DC FieldValueLanguage
dc.contributor.authorBenaglia, Maurizio-
dc.contributor.authorPonzini, Francesco-
dc.contributor.authorWoods, Craig R.-
dc.contributor.authorSiegel, Jay S.-
dc.date.accessioned2024-03-13T08:39:21Z-
dc.date.available2024-03-13T08:39:21Z-
dc.date.issued2001-
dc.identifier.citationOrganic Letters, 2001, v. 3, n. 7, p. 967-969-
dc.identifier.issn1523-7060-
dc.identifier.urihttp://hdl.handle.net/10722/341000-
dc.description.abstract(Matrix Presented) Palladium-based carbon-carbon coupling reactions in sequence with halogen-exchange chemistry on a series of heterocycles lead to an effecient synthetic strategy for oligopyridines that bind metal ions such as ruthenium to form coordination racks. The particular structures are designed to form tepyridine subunits for octahedral binding. Reactions of 4,6-diiodopyrimide produces a "duoble-bay" terpyridine from which binuclear coordination complexes have been formed.-
dc.languageeng-
dc.relation.ispartofOrganic Letters-
dc.titleSynthesis of oligopyridines and their metal complexes as precursors to topological stereoisomers-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.5555/ol007052d-
dc.identifier.pmid11277771-
dc.identifier.scopuseid_2-s2.0-0011776201-
dc.identifier.volume3-
dc.identifier.issue7-
dc.identifier.spage967-
dc.identifier.epage969-

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