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Please use this identifier to cite or link to this item: https://scidar.kg.ac.rs/handle/123456789/19411
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dc.contributor.authorMihajlović, Kristina-
dc.contributor.authorMarjanović, Jovana S-
dc.contributor.authorDivac, Vera-
dc.contributor.authorKostic, Marina-
dc.contributor.authorMilović, Emilija-
dc.contributor.authorBugarčić, Zorica-
dc.date.accessioned2023-11-14T13:03:15Z-
dc.date.available2023-11-14T13:03:15Z-
dc.date.issued2020-
dc.identifier.citationKristina Mihajlović, Jovana Marjanović, Vera Divac, Marina Kostić, Emilija Milović, Zorica Bugarčić Kinetic and Mehanistic Studies of Pyridine-Catalyzed Selenolaktonization of 2-cyclopentene-1-acetic acid IV. International Congress on New Trends in Science, Engineering and Technology (ICONTRENDS), Book of Abstracts P22, ISBN: 978-625-400-393-6 St. Petersburg 7-9 July 2020.en_US
dc.identifier.isbn978-625-400-393-6en_US
dc.identifier.urihttps://scidar.kg.ac.rs/handle/123456789/19411-
dc.description.abstractIn addition to the wide range of reagents that can be used in intramolecular cyclization reactions of unsaturated substrates like alcohols, acids and amines, phenylselenyl halides represent very useful reagents due to the high regioselectivity of these reactions as well as mild reaction conditions. (Denmark, 2006:71). The purpose of this research was to obtain synthetically very useful bicyclic lactone by intramolecular cyclization of 2-cyclopentene-1-acetic acid by PhSeCl and PhSeBr as reagents. Also, the aim of this study was to improve the reaction yields and selectivity through the optimization of reaction conditions and investigation of kinetic and mechanism of these reactions.en_US
dc.language.isoenen_US
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/us/*
dc.subjectkineticsen_US
dc.subjectcyclizationen_US
dc.subjectorganoseleniumen_US
dc.subjectpyridineen_US
dc.subjectunsaturated acidsen_US
dc.subjectlactonesen_US
dc.titleKinetic and mechanistic studies of pyridine-catalyzed selenolactonization of 2-cyclopentene-1-acetic aciden_US
dc.typeconferenceObjecten_US
dc.description.versionPublisheden_US
dc.relation.conferenceIV International Congress on New Trends in Science, Engineering and Technology (ICONTRENDS)en_US
dc.type.versionPublishedVersionen_US
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