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dc.creatorMaslak, Veselin
dc.creatorMatovic, R
dc.creatorSaičić, Radomir
dc.date.accessioned2018-11-22T00:07:21Z
dc.date.available2018-11-22T00:07:21Z
dc.date.issued2004
dc.identifier.issn0040-4020
dc.identifier.urihttp://cherry.chem.bg.ac.rs/handle/123456789/660
dc.description.abstractTitanium tetrachloride promoted reaction of silyl ketene acetals with epoxides, followed by acidic work-up, affords butanolides in moderate/good yields. With epihalohydrins the reaction is regioselective and occurs at the less substituted end of the epoxide; the gamma-haloalkyl-gamma-butanolides thus obtained can be further transformed into various products. (C) 2004 Elsevier Ltd. All rights reserved.en
dc.publisherPergamon-Elsevier Science Ltd, Oxford
dc.rightsrestrictedAccess
dc.sourceTetrahedron
dc.subjectepoxidesen
dc.subjectketene acetalsen
dc.subjectlactonesen
dc.subjecttitanium and compoundsen
dc.subjectalkylationen
dc.titleReaction of silyl ketene acetals with epoxides: a new method for the synthesis of gamma-butanolidesen
dc.typearticle
dc.rights.licenseARR
dcterms.abstractМаслак, Веселин; Саичић, Радомир; Матовиц, Р;
dc.citation.volume60
dc.citation.issue40
dc.citation.spage8957
dc.citation.epage8966
dc.identifier.wos000223935100021
dc.identifier.doi10.1016/j.tet.2004.07.007
dc.citation.other60(40): 8957-8966
dc.citation.rankM21
dc.type.versionpublishedVersionen
dc.identifier.scopus2-s2.0-4444296427
dc.identifier.rcubKon_1612


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