Please use this identifier to cite or link to this item: https://open.uns.ac.rs/handle/123456789/14354
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dc.contributor.authorMarković, Radeen_US
dc.contributor.authorBaranac, Marijaen_US
dc.contributor.authorJovetić, Stankaen_US
dc.date.accessioned2020-03-03T14:55:52Z-
dc.date.available2020-03-03T14:55:52Z-
dc.date.issued2003-09-08-
dc.identifier.issn00404039en_US
dc.identifier.urihttps://open.uns.ac.rs/handle/123456789/14354-
dc.description.abstractFunctionalized 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 13C NMR data confirmed the meso-ionic structure of these aromatic-type 1,2-dithioles. © 2003 Elsevier Ltd. All rights reserved.en
dc.relation.ispartofTetrahedron Lettersen
dc.titleA novel and efficient 4-oxothiazolidine-1,2-dithiole rearrangement induced by Lawesson's reagenten_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.doi10.1016/S0040-4039(03)01721-0-
dc.identifier.scopus2-s2.0-0042659138-
dc.identifier.urlhttps://api.elsevier.com/content/abstract/scopus_id/0042659138-
dc.description.versionUnknownen_US
dc.relation.lastpage7090en
dc.relation.firstpage7087en
dc.relation.issue37en
dc.relation.volume44en
item.grantfulltextnone-
item.fulltextNo Fulltext-
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