A novel and efficient 4-oxothiazolidine-1,2-dithiole rearrangement induced by Lawesson's reagent
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.
Keywords:
thiazolidines / rearrangements / dithiolesSource:
Tetrahedron Letters, 2003, 44, 37, 7087-7090Publisher:
- Pergamon-Elsevier Science Ltd, Oxford
DOI: 10.1016/S0040-4039(03)01721-0
ISSN: 0040-4039
WoS: 000185151400026
Scopus: 2-s2.0-0042659138
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Institution/Community
Hemijski fakultet / Faculty of ChemistryTY - JOUR AU - Marković, R. AU - Baranac-Stojanović, Marija AU - Jovetic, S PY - 2003 UR - https://cherry.chem.bg.ac.rs/handle/123456789/146 AB - 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. PB - Pergamon-Elsevier Science Ltd, Oxford T2 - Tetrahedron Letters T1 - A novel and efficient 4-oxothiazolidine-1,2-dithiole rearrangement induced by Lawesson's reagent VL - 44 IS - 37 SP - 7087 EP - 7090 DO - 10.1016/S0040-4039(03)01721-0 ER -
@article{ author = "Marković, R. and Baranac-Stojanović, Marija and Jovetic, S", year = "2003", 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.", publisher = "Pergamon-Elsevier Science Ltd, Oxford", journal = "Tetrahedron Letters", title = "A novel and efficient 4-oxothiazolidine-1,2-dithiole rearrangement induced by Lawesson's reagent", volume = "44", number = "37", pages = "7087-7090", doi = "10.1016/S0040-4039(03)01721-0" }
Marković, R., Baranac-Stojanović, M.,& Jovetic, S.. (2003). A novel and efficient 4-oxothiazolidine-1,2-dithiole rearrangement induced by Lawesson's reagent. in Tetrahedron Letters Pergamon-Elsevier Science Ltd, Oxford., 44(37), 7087-7090. https://doi.org/10.1016/S0040-4039(03)01721-0
Marković R, Baranac-Stojanović M, Jovetic S. A novel and efficient 4-oxothiazolidine-1,2-dithiole rearrangement induced by Lawesson's reagent. in Tetrahedron Letters. 2003;44(37):7087-7090. doi:10.1016/S0040-4039(03)01721-0 .
Marković, R., Baranac-Stojanović, Marija, Jovetic, S, "A novel and efficient 4-oxothiazolidine-1,2-dithiole rearrangement induced by Lawesson's reagent" in Tetrahedron Letters, 44, no. 37 (2003):7087-7090, https://doi.org/10.1016/S0040-4039(03)01721-0 . .