Collect. Czech. Chem. Commun.
1981, 46, 3097-3103
https://doi.org/10.1135/cccc19813097
Solvolysis kinetics and mechanism of 3-methyl-1,3-thiazolidine-2,4-dione
Vladimír Macháček, Vojeslav Štěrba and Helena Zahradníčková
Department of Organic Chemistry, Institute of Chemical Technology, 532 10 Pardubice
Crossref Cited-by Linking
- Rančić Milica P., Stojiljković Ivana, Milošević Milena, Prlainović Nevena, Jovanović Maja, Milčić Miloš K., Marinković Aleksandar D.: Solvent and substituent effect on intramolecular charge transfer in 5-arylidene-3-substituted-2,4-thiazolidinediones: Experimental and theoretical study. Arabian Journal of Chemistry 2019, 12, 5142. <https://doi.org/10.1016/j.arabjc.2016.12.013>
- Keil Alyssa M., Frederick Douglas M., Jacinto Erina Y., Kennedy Erica L., Zauhar Randy J., West Nathan M., Tchao Ruy, Harvison Peter J.: Cytotoxicity of thiazolidinedione-, oxazolidinedione- and pyrrolidinedione-ring containing compounds in HepG2 cells. Toxicology in Vitro 2015, 29, 1887. <https://doi.org/10.1016/j.tiv.2015.07.015>
- Patel Niti N., Crincoli Christine M., Frederick Douglas M., Tchao Ruy, Harvison Peter J.: Effect of structural modifications on 3‐(3,5‐dichlorophenyl)‐2,4‐thiazolidinedione‐induced hepatotoxicity in Fischer 344 rats. J of Applied Toxicology 2012, 32, 108. <https://doi.org/10.1002/jat.1639>
- Frederick Douglas M., Jacinto Erina Y., Patel Niti N., Rushmore Thomas H., Tchao Ruy, Harvison Peter J.: Cytotoxicity of 3-(3,5-dichlorophenyl)-2,4-thiazolidinedione (DCPT) and analogues in wild type and CYP3A4 stably transfected HepG2 cells. Toxicology in Vitro 2011, 25, 2113. <https://doi.org/10.1016/j.tiv.2011.09.015>
- Bowden Keith, Chana Ravinder S.: Structure–activity relations. Part 6. The alkaline hydrolysis of 3-methyl-5-methylidene- and 3,5-dimethylthiazolidine-2,4-diones. The addition of thiols to 3-methyl-5-methylidenethiazolidine-2,4-dione. J. Chem. Soc., Perkin Trans. 2 1990, 2163. <https://doi.org/10.1039/P29900002163>
