Nucleophilic functionalization of 2-alkylidene-4-oxothiazolidines at C(5)-position induced by formation of novel pyridinium salt
Abstract
The synthesis of unsubstituted pyridinium salt containing the 4-oxothiazolidine moiety bonded via C(5) to the N position of the pyridine nucleus is reported. The nucleophilic displacement of pyridine from pyridinium salt by the selected nucleophiles leads to the formation of new 5-substituted 4-oxothiazolidines in good yields.
Keywords:
4-oxothiazolidine / methoxy group / neutral nucleophile / nucleophilic substitution / pyridinium saltSource:
Phosphorus Sulfur and Silicon and the Related Elements, 2005, 180, 5-6, 1411-1415Publisher:
- Taylor & Francis Ltd, Abingdon
DOI: 10.1080/10426500590912754
ISSN: 1042-6507
WoS: 000228669300044
Scopus: 2-s2.0-27244442066
Collections
Institution/Community
Hemijski fakultet / Faculty of ChemistryTY - JOUR AU - Marković, R. AU - Pavlovich, JG AU - Baranac-Stojanović, Marija PY - 2005 UR - https://cherry.chem.bg.ac.rs/handle/123456789/696 AB - The synthesis of unsubstituted pyridinium salt containing the 4-oxothiazolidine moiety bonded via C(5) to the N position of the pyridine nucleus is reported. The nucleophilic displacement of pyridine from pyridinium salt by the selected nucleophiles leads to the formation of new 5-substituted 4-oxothiazolidines in good yields. PB - Taylor & Francis Ltd, Abingdon T2 - Phosphorus Sulfur and Silicon and the Related Elements T1 - Nucleophilic functionalization of 2-alkylidene-4-oxothiazolidines at C(5)-position induced by formation of novel pyridinium salt VL - 180 IS - 5-6 SP - 1411 EP - 1415 DO - 10.1080/10426500590912754 ER -
@article{ author = "Marković, R. and Pavlovich, JG and Baranac-Stojanović, Marija", year = "2005", abstract = "The synthesis of unsubstituted pyridinium salt containing the 4-oxothiazolidine moiety bonded via C(5) to the N position of the pyridine nucleus is reported. The nucleophilic displacement of pyridine from pyridinium salt by the selected nucleophiles leads to the formation of new 5-substituted 4-oxothiazolidines in good yields.", publisher = "Taylor & Francis Ltd, Abingdon", journal = "Phosphorus Sulfur and Silicon and the Related Elements", title = "Nucleophilic functionalization of 2-alkylidene-4-oxothiazolidines at C(5)-position induced by formation of novel pyridinium salt", volume = "180", number = "5-6", pages = "1411-1415", doi = "10.1080/10426500590912754" }
Marković, R., Pavlovich, J.,& Baranac-Stojanović, M.. (2005). Nucleophilic functionalization of 2-alkylidene-4-oxothiazolidines at C(5)-position induced by formation of novel pyridinium salt. in Phosphorus Sulfur and Silicon and the Related Elements Taylor & Francis Ltd, Abingdon., 180(5-6), 1411-1415. https://doi.org/10.1080/10426500590912754
Marković R, Pavlovich J, Baranac-Stojanović M. Nucleophilic functionalization of 2-alkylidene-4-oxothiazolidines at C(5)-position induced by formation of novel pyridinium salt. in Phosphorus Sulfur and Silicon and the Related Elements. 2005;180(5-6):1411-1415. doi:10.1080/10426500590912754 .
Marković, R., Pavlovich, JG, Baranac-Stojanović, Marija, "Nucleophilic functionalization of 2-alkylidene-4-oxothiazolidines at C(5)-position induced by formation of novel pyridinium salt" in Phosphorus Sulfur and Silicon and the Related Elements, 180, no. 5-6 (2005):1411-1415, https://doi.org/10.1080/10426500590912754 . .