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dc.creatorKonstantinović, Stanimir
dc.creatorBugarčić, Zorica
dc.creatorMilosavljević, Slobodan
dc.creatorSchroth, Gerhard
dc.creatorMihailovíć, Mihailo Lj.
dc.date.accessioned2021-07-08T12:10:48Z
dc.date.available2021-07-08T12:10:48Z
dc.date.issued1992
dc.identifier.issn0170-2041
dc.identifier.urihttps://cer.ihtm.bg.ac.rs/handle/123456789/4742
dc.description.abstractThe regioselectivity in cyclofunctionalization of some acyclic olefinic alcohols with benzeneselenenyl halides (PhSeCl and PhSeBr) at different temperatures (−78°C, 0°C and room temperature) is investigated. It has been found that Δ4‐ and Δ5‐ alkenols are converted into five‐ and/or six‐membered cyclic phenyl selenoethers, the yield of which decreases with increasing reaction temperature. PhSeCl has been found to be more efficient than PhSeBr in the cyclization reactions.sr
dc.language.isoensr
dc.publisherWileysr
dc.rightsrestrictedAccesssr
dc.sourceLiebigs Annalen der Chemiesr
dc.subjectBenzeneselenenyl halidessr
dc.subjectCyclofunctionalizationsr
dc.subjectOlefinic alcoholssr
dc.subjectRegioselectivitysr
dc.titleRegioselectivity in Cyclofunctionalization of Olefinic Alcohols with Benzeneselenenyl Halides at Different Temperaturessr
dc.typearticlesr
dc.rights.licenseARRsr
dcterms.abstractМилосављевић, Слободан; Бугарчић, Зорица; Сцхротх, Герхард; Константиновић, Станимир; Михаиловíћ, Михаило Љ.;
dc.citation.volume1992
dc.citation.issue3
dc.citation.spage261
dc.citation.epage268
dc.identifier.doi10.1002/jlac.199219920145
dc.identifier.scopus2-s2.0-84986674880
dc.type.versionpublishedVersionsr


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