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dc.creatorLalic, G
dc.creatorPetrovski, Z
dc.creatorGalonic, D
dc.creatorMatović, Radomir
dc.creatorSaičić, Radomir N.
dc.date.accessioned2019-04-28T16:26:34Z
dc.date.available2019-04-28T16:26:34Z
dc.date.issued2001
dc.identifier.issn0040-4020
dc.identifier.urihttp://cer.ihtm.bg.ac.rs/handle/123456789/2765
dc.description.abstractTitanium tetrachloride promoted reaction of trimethylsilyl enol ethers with ethylene oxide affords homoaldol type products in moderate/good yields. Monosubstituted epoxides react regioselectively: the nucleophilic attack of the enolate occurs at the more substituted position of propene oxide whereas epichlorohydrin reacts at the less substituted end. (C) 2001 Elsevier Science Ltd. All rights reserved.en
dc.publisherPergamon-Elsevier Science Ltd, Oxford
dc.rightsrestrictedAccess
dc.sourceTetrahedron
dc.subjectalkylationen
dc.subjectepoxidesen
dc.subjectenol ethersen
dc.subjectMukaiyama reactionsen
dc.subjecttitanium and compoundsen
dc.titleAlkylation of carbonyl compounds in the TiCl4-promoted reaction of trimethylsilyl enol ethers with epoxidesen
dc.typearticle
dc.rights.licenseARR
dcterms.abstractГалониц, Д; Матовић, Радомир; Саичић, Радомир Н.; Лалиц, Г; Петровски, З;
dc.citation.volume57
dc.citation.issue3
dc.citation.spage583
dc.citation.epage591
dc.citation.other57(3): 583-591
dc.citation.rankM21
dc.identifier.doi10.1016/S0040-4020(00)01028-0
dc.identifier.rcubKon_1420
dc.identifier.scopus2-s2.0-0035857271
dc.identifier.wos000166391800019
dc.type.versionpublishedVersionen


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