1. University of Kragujevac Digital Archive
  2. University of Kragujevac
  3. Faculty of Science, Kragujevac
Please use this identifier to cite or link to this item: https://scidar.kg.ac.rs/handle/123456789/10299
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dc.rights.licenserestrictedAccess-
dc.contributor.authorStevanović, Dragana-
dc.contributor.authorPejović, Anka-
dc.contributor.authorDamljanović, Ivan-
dc.contributor.authorVukićević, Miomir-
dc.contributor.authorDobrikov, Georgi-
dc.contributor.authorDimitrov, Vladimir-
dc.contributor.authorDenić M.-
dc.contributor.authorRadulovic, Niko-
dc.contributor.authorVukicevic R.-
dc.date.accessioned2021-04-20T15:23:36Z-
dc.date.available2021-04-20T15:23:36Z-
dc.date.issued2013-
dc.identifier.issn0018-019X-
dc.identifier.urihttps://scidar.kg.ac.rs/handle/123456789/10299-
dc.description.abstractTwo variants of a new pathway for the synthesis of (±)-curcumene ether are described. The key steps in these procedures are intramolecular cyclizations of 6-methyl-2-(4-methylphenyl)hept-6-en-2-ol and 2-methyl-6-(4-methylphenyl)hept-6-en-2-ol by means of an electrochemically generated phenylselenyl cation. This synthetic approach provides significantly better yields than the previously reported protocols. Copyright © 2013 Verlag Helvetica Chimica Acta AG, Zürich.-
dc.rightsinfo:eu-repo/semantics/restrictedAccess-
dc.sourceHelvetica Chimica Acta-
dc.titleElectrochemical phenylselenoetherification as a key step in the synthesis of (±)-curcumene ether-
dc.typearticle-
dc.identifier.doi10.1002/hlca.201200610-
dc.identifier.scopus2-s2.0-84879334997-
Appears in Collections:Faculty of Science, Kragujevac

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