Please use this identifier to cite or link to this item: https://scidar.kg.ac.rs/handle/123456789/12541
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dc.rights.licenserestrictedAccess-
dc.contributor.authorPejović, Anka-
dc.contributor.authorDamljanović, Ivan-
dc.contributor.authorStevanović, Dragana-
dc.contributor.authorIlić Komatina D.-
dc.contributor.authorVukićević, Miomir-
dc.contributor.authorBogdanovic, Goran A.-
dc.contributor.authorVukicevic R.-
dc.date.accessioned2021-04-20T21:05:55Z-
dc.date.available2021-04-20T21:05:55Z-
dc.date.issued2013-
dc.identifier.issn0040-4039-
dc.identifier.urihttps://scidar.kg.ac.rs/handle/123456789/12541-
dc.description.abstractDimethyl(2-ferrocenoylethyl)sulfonium iodide was synthesized by reacting 1-ferrocenyl-4-thiapentan-1-one with iodomethane and characterized from spectral data and single crystal X-ray structure analysis. This compound was capable of reacting with different N-, S-, and O-nucleophiles giving the corresponding β-functionalized ferrocene-containing ketones. Furthermore, dimethyl sulfide can be displaced from the dimethyl(2-ferrocenoylethyl)sulfonium ion with cyanide or carbanions derived from 1,3-bifunctional compounds and nitropropane, leading to products with a new carbon-carbon bond. © 2013 Elsevier Ltd. All rights reserved.-
dc.rightsinfo:eu-repo/semantics/restrictedAccess-
dc.sourceTetrahedron Letters-
dc.titleSynthesis, characterization, and nucleophilic substitutions of dimethyl(2-ferrocenoylethyl)sulfonium iodide-
dc.typearticle-
dc.identifier.doi10.1016/j.tetlet.2013.06.130-
dc.identifier.scopus2-s2.0-84880839901-
Appears in Collections:Faculty of Science, Kragujevac

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