Synthesis and Bioevaluation of Novel Thiazolidinones from Aromatic Azo-Aldehydes
Abstract: Some novel substituted 4-Thiazolidinones (azo-dispersive dyes) were synthesized from azo-incorporated aromatic aldehydes (1a-1c) and heteryl hydrazides (2a-2b) in zinc chloride and DMF via synthesis of azomethines (Schiff bases) (4a-4e) conventionally by using mercaptoacetic acid, a very important precursor responsible for cyclization of azomethines.
Keywords: 4-Thiazolidinones, azo-incorporated aromatic aldehydes, heteryl hydrazides, azomethines, mercaptoacetic acid
How to Cite?: Shivani D. Kawale, Dr. Gayatri Phadnaik, "Synthesis and Bioevaluation of Novel Thiazolidinones from Aromatic Azo-Aldehydes", Volume 13 Issue 1, January 2024, International Journal of Science and Research (IJSR), Pages: 419-422, https://www.ijsr.net/getabstract.php?paperid=SR231228124802, DOI: https://dx.doi.org/10.21275/SR231228124802