Please use this identifier to cite or link to this item:
https://open.uns.ac.rs/handle/123456789/14354
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Marković, Rade | en_US |
dc.contributor.author | Baranac, Marija | en_US |
dc.contributor.author | Jovetić, Stanka | en_US |
dc.date.accessioned | 2020-03-03T14:55:52Z | - |
dc.date.available | 2020-03-03T14:55:52Z | - |
dc.date.issued | 2003-09-08 | - |
dc.identifier.issn | 00404039 | en_US |
dc.identifier.uri | https://open.uns.ac.rs/handle/123456789/14354 | - |
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 13C NMR data confirmed the meso-ionic structure of these aromatic-type 1,2-dithioles. © 2003 Elsevier Ltd. All rights reserved. | en |
dc.relation.ispartof | Tetrahedron Letters | en |
dc.title | A novel and efficient 4-oxothiazolidine-1,2-dithiole rearrangement induced by Lawesson's reagent | en_US |
dc.type | Journal/Magazine Article | en_US |
dc.identifier.doi | 10.1016/S0040-4039(03)01721-0 | - |
dc.identifier.scopus | 2-s2.0-0042659138 | - |
dc.identifier.url | https://api.elsevier.com/content/abstract/scopus_id/0042659138 | - |
dc.description.version | Unknown | en_US |
dc.relation.lastpage | 7090 | en |
dc.relation.firstpage | 7087 | en |
dc.relation.issue | 37 | en |
dc.relation.volume | 44 | en |
item.grantfulltext | none | - |
item.fulltext | No Fulltext | - |
Appears in Collections: | PMF Publikacije/Publications |
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