Carbon-bromine cleavage by dimethyl sulfoxide: the key step of C(5) functionalization of push-pull 2-alkylidene-4-oxothiazolidine vinyl bromides

dc.creator	Baranac-Stojanović, Marija
dc.creator	Marković, Rade
dc.date.accessioned	2018-11-22T00:10:42Z
dc.date.available	2018-11-22T00:10:42Z
dc.date.issued	2007
dc.identifier.issn	0040-4039
dc.identifier.uri	https://cherry.chem.bg.ac.rs/handle/123456789/823
dc.description.abstract	Push-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.publisher	Pergamon-Elsevier Science Ltd, Oxford
dc.rights	restrictedAccess
dc.source	Tetrahedron Letters
dc.subject	push-pull 2-alkylidene-4-oxothiazolidines	en
dc.subject	vinyl bromides	en
dc.subject	dimethyl sulfoxide	en
dc.subject	C(5) functionalization	en
dc.title	Carbon-bromine cleavage by dimethyl sulfoxide: the key step of C(5) functionalization of push-pull 2-alkylidene-4-oxothiazolidine vinyl bromides	en
dc.type	article
dc.rights.license	ARR
dcterms.abstract	Марковиц, Раде; Баранац-Стојановић, Марија;
dc.citation.volume	48
dc.citation.issue	10
dc.citation.spage	1695
dc.citation.epage	1698
dc.identifier.wos	000244643800005
dc.identifier.doi	10.1016/j.tetlet.2007.01.051
dc.citation.other	48(10): 1695-1698
dc.citation.rank	M22
dc.type.version	publishedVersion	en
dc.identifier.scopus	2-s2.0-33846785296

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