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dc.creatorBaranac-Stojanović, Marija
dc.creatorMarkovic, Rade
dc.date.accessioned2018-11-22T00:10:42Z
dc.date.available2018-11-22T00:10:42Z
dc.date.issued2007
dc.identifier.issn0040-4039
dc.identifier.urihttp://cherry.chem.bg.ac.rs/handle/123456789/823
dc.description.abstractPush-pull 2-alkylidene-4-oxothiazolidine vinyl bromides undergo efficient C(5) functionalization through DMSO-assisted carbon-bromine cleavage, followed by a bromine transfer-substitution (or elimination) sequence. A mechanism for this novel transformation is proposed. (c) 2007 Elsevier Ltd. All rights reserved.en
dc.publisherPergamon-Elsevier Science Ltd, Oxford
dc.rightsrestrictedAccess
dc.sourceTetrahedron Letters
dc.subjectpush-pull 2-alkylidene-4-oxothiazolidinesen
dc.subjectvinyl bromidesen
dc.subjectdimethyl sulfoxideen
dc.subjectC(5) functionalizationen
dc.titleCarbon-bromine cleavage by dimethyl sulfoxide: the key step of C(5) functionalization of push-pull 2-alkylidene-4-oxothiazolidine vinyl bromidesen
dc.typearticle
dc.rights.licenseARR
dcterms.abstractМарковиц, Раде; Баранац-Стојановић, Марија;
dc.citation.volume48
dc.citation.issue10
dc.citation.spage1695
dc.citation.epage1698
dc.identifier.wos000244643800005
dc.identifier.doi10.1016/j.tetlet.2007.01.051
dc.citation.other48(10): 1695-1698
dc.citation.rankM22
dc.identifier.scopus2-s2.0-33846785296
dc.identifier.rcubKon_1776


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