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  3. Institute for Information Technologies, Kragujevac
Please use this identifier to cite or link to this item: https://scidar.kg.ac.rs/handle/123456789/9903
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dc.contributor.authorKostic, Marina-
dc.contributor.authorDivac, Vera-
dc.contributor.authorRadenković N.-
dc.contributor.authorBugarčić Z.-
dc.date.accessioned2021-04-20T14:21:34Z-
dc.date.available2021-04-20T14:21:34Z-
dc.date.issued2011-
dc.identifier.issn0932-0776-
dc.identifier.urihttps://scidar.kg.ac.rs/handle/123456789/9903-
dc.description.abstractAn innovative route for intramolecular cyclization of pent-4-en-1-ol has been delineated through a ring closing reaction with phenylselenyl halides, in good yield. Several catalysts (triethylamine, quinoline, 2,2′-bipyridine, pyridine, CoCl2 and SnCl2) enable fast, facile and efficient cyclization. © 2011 Verlag der Zeitschrift für Naturforschung, Tübingen.-
dc.rightsrestrictedAccess-
dc.sourceZeitschrift fur Naturforschung - Section B Journal of Chemical Sciences-
dc.titleCyclization of unsaturated alcohols. Mild and efficient selenocyclization of pent-4-en-1-ol-
dc.typearticle-
dc.identifier.doi10.1515/znb-2011-1213-
dc.identifier.scopus2-s2.0-84855266611-
Appears in Collections:Faculty of Science, Kragujevac
Institute for Information Technologies, Kragujevac

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