A novel and efficient 4-oxothiazolidine-1,2-dithiole rearrangement induced by Lawesson's reagent

dc.creator	Marković, R.
dc.creator	Baranac-Stojanović, Marija
dc.creator	Jovetic, S
dc.date.accessioned	2018-11-22T00:05:28Z
dc.date.available	2018-11-22T00:05:28Z
dc.date.issued	2003
dc.identifier.issn	0040-4039
dc.identifier.uri	https://cherry.chem.bg.ac.rs/handle/123456789/146
dc.description.abstract	Functionalized 1,2-dithioles have been synthesized by a ring opening-closing process of 5-substituted- and 5-unsubstituted-2-alkylidene-4-oxothiazolidines with Lawesson's reagent. The C-13 NMR data confirmed the meso-ionic structure of these aromatic-type 1,2-dithioles. (C) 2003 Elsevier Ltd. All rights reserved.	en
dc.publisher	Pergamon-Elsevier Science Ltd, Oxford
dc.rights	restrictedAccess
dc.source	Tetrahedron Letters
dc.subject	thiazolidines	en
dc.subject	rearrangements	en
dc.subject	dithioles	en
dc.title	A novel and efficient 4-oxothiazolidine-1,2-dithiole rearrangement induced by Lawesson's reagent	en
dc.type	article
dc.rights.license	ARR
dc.citation.volume	44
dc.citation.issue	37
dc.citation.spage	7087
dc.citation.epage	7090
dc.identifier.wos	000185151400026
dc.identifier.doi	10.1016/S0040-4039(03)01721-0
dc.citation.other	44(37): 7087-7090
dc.citation.rank	M21
dc.type.version	publishedVersion	en
dc.identifier.scopus	2-s2.0-0042659138