Please use this identifier to cite or link to this item: https://open.uns.ac.rs/handle/123456789/14354
Title: A novel and efficient 4-oxothiazolidine-1,2-dithiole rearrangement induced by Lawesson's reagent
Authors: Marković, Rade
Baranac, Marija
Jovetić, Stanka
Issue Date: 8-Sep-2003
Journal: Tetrahedron Letters
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.
URI: https://open.uns.ac.rs/handle/123456789/14354
ISSN: 00404039
DOI: 10.1016/S0040-4039(03)01721-0
Appears in Collections:PMF Publikacije/Publications

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