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Please use this identifier to cite or link to this item: https://scidar.kg.ac.rs/handle/123456789/13538
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dc.rights.licenseBY-NC-ND-
dc.contributor.authorŠmit, Biljana-
dc.contributor.authorStanić, Petar-
dc.contributor.authorJoksović, Ljubinka-
dc.contributor.authorAšanin, Darko-
dc.contributor.authorSimic, Zoran-
dc.date.accessioned2021-09-24T22:53:08Z-
dc.date.available2021-09-24T22:53:08Z-
dc.date.issued2021-
dc.identifier.issn0352-5139-
dc.identifier.urihttps://scidar.kg.ac.rs/handle/123456789/13538-
dc.description.abstract5-Alkenyl hydantoins and alkenyl spirohydantoins are converted into bicyclic and tricyclic hydantoins, under indirect electrochemical conditions, generating the phenylselenyl cation in situ. The reactions proceeded in good to exelent yields. The influence of electrochemical conditions on regio- and diastereoselectivity of the selenocyclization reactions is investigated.-
dc.rightsopenAccess-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/-
dc.sourceJournal of the Serbian Chemical Society-
dc.titleInfluence of electrochemical conditions on the regio- And stereoselectivity of selenocyclization of alkenyl hydantoins-
dc.typearticle-
dc.identifier.doi10.2298/JSC201022023S-
dc.identifier.scopus2-s2.0-85111165708-
Appears in Collections:Faculty of Science, Kragujevac
Institute for Information Technologies, Kragujevac

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