TY  - JOUR
AU  - Rašović, Aleksandar
AU  - Koch, Andreas
AU  - Kleinpeter, Erich
AU  - Marković, Rade
PY  - 2013
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/1227
AB  - Trithiaazapentalene derivatives were prepared by the reaction of 2-alkylidene-4-oxothiazolidines with Lawesson's reagent. They are classified as two structurally different trithiaazapentalene compounds that have different contributions of monocyclic 1,2-dithiole and 1,2,4-dithiazole structures and degrees of aromaticity of the bicyclic trithiaazapentalene system. The electron-donating ability of substituents at the C(5) position of the trithiaazapentalene system is recognized as the main cause for changes in pi-Celectron distribution. This is the first complete study of substituent effects on the structure of trithiapentalenes.
PB  - Oxford : Pergamon-Elsevier Science Ltd
T2  - Tetrahedron
T1  - Studies of the regioselective ring-opening closing mode of functionally different thiazolidine type enaminones: en route to the synthesis of trithiaazapentalene derivatives
VL  - 69
IS  - 51
SP  - 10849
EP  - 10857
DO  - 10.1016/j.tet.2013.10.088
ER  - 

@article{
author = "Rašović, Aleksandar and Koch, Andreas and Kleinpeter, Erich and Marković, Rade",
year = "2013",
abstract = "Trithiaazapentalene derivatives were prepared by the reaction of 2-alkylidene-4-oxothiazolidines with Lawesson's reagent. They are classified as two structurally different trithiaazapentalene compounds that have different contributions of monocyclic 1,2-dithiole and 1,2,4-dithiazole structures and degrees of aromaticity of the bicyclic trithiaazapentalene system. The electron-donating ability of substituents at the C(5) position of the trithiaazapentalene system is recognized as the main cause for changes in pi-Celectron distribution. This is the first complete study of substituent effects on the structure of trithiapentalenes.",
publisher = "Oxford : Pergamon-Elsevier Science Ltd",
journal = "Tetrahedron",
title = "Studies of the regioselective ring-opening closing mode of functionally different thiazolidine type enaminones: en route to the synthesis of trithiaazapentalene derivatives",
volume = "69",
number = "51",
pages = "10849-10857",
doi = "10.1016/j.tet.2013.10.088"
}

Rašović, A., Koch, A., Kleinpeter, E.,& Marković, R.. (2013). Studies of the regioselective ring-opening closing mode of functionally different thiazolidine type enaminones: en route to the synthesis of trithiaazapentalene derivatives. in Tetrahedron
Oxford : Pergamon-Elsevier Science Ltd., 69(51), 10849-10857.
https://doi.org/10.1016/j.tet.2013.10.088

Rašović A, Koch A, Kleinpeter E, Marković R. Studies of the regioselective ring-opening closing mode of functionally different thiazolidine type enaminones: en route to the synthesis of trithiaazapentalene derivatives. in Tetrahedron. 2013;69(51):10849-10857.
doi:10.1016/j.tet.2013.10.088 .

Rašović, Aleksandar, Koch, Andreas, Kleinpeter, Erich, Marković, Rade, "Studies of the regioselective ring-opening closing mode of functionally different thiazolidine type enaminones: en route to the synthesis of trithiaazapentalene derivatives" in Tetrahedron, 69, no. 51 (2013):10849-10857,
https://doi.org/10.1016/j.tet.2013.10.088 . .