Abstract
In our effort to obtain biologically active compounds, new 3,5-disubstituted 1,3-thiazolidine-2,4- diones (5a - r) were synthesized. A series of 5-arylmethylidene-1,3-thiazolidine-2,4-diones (3a - r) were prepared by Knoevenagel reaction from 1,3-thiazolidine-2,4-dione (2) and appropriate aromatic aldehydes. Condensation of 3a - r with 7-hydroxy-4-bromomethyl-2-oxo- 2H-chromene (1) afforded novel 3-(7-hydroxy-2-oxo-2H-chromen-4-ylmethyl)-5- arylidene-1,3-thiazolidine-2,4-diones 5a - r. Compounds 3a - r and 5a - r were evaluated for their antioxidant activity (DPPH free radical scavenging activity). © 2011 Verlag der Zeitschrift für Naturforschung, Tübingen.
Author supplied keywords
Cite
CITATION STYLE
Čačić, M., & Molnar, M. (2011). Design, synthesis and characterization of some novel 3-coumarinyl- 5-aryliden-1,3-thiazolidine-2,4-diones and their antioxidant activity. Zeitschrift Fur Naturforschung - Section B Journal of Chemical Sciences, 66(2), 177–183. https://doi.org/10.1515/znb-2011-0210
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.