derivatives of thiazolidinone ring systems are known to act as anti-hiv infections , analgesic, anti-bacterial, anti-convulsant, anti parasitic, potential anti-inflammatory and herbicidal agents. due biological activities of thiazolidinones ring, several methods for their synthesis have been illustrated in literature. imidazolidine-2-thiones were synthesized by the oxidative cyclization of 1-be...

some chromeno[4,3-b]quinoline derivatives were synthesized in a tricomponents one-pot reaction of 1,3-cyclohexadione arylaldehydes and 4-aminocoumarin under microwave irradiation in the solventless system by using a heteropolyacid catalyst ,h3[pw12o40] in 80-95% yields and high rates. the shorter reaction times, one-pot, good yields, simple work-up procedure and environmentally friendly conditi...

we have reported the fabrication of boric acid incorporated into surface of magnetite nanoparticles. the catalyst was characterized using spectroscopic, magnetic and thermal techniques (ft-ir, sem, xrd, icp, vsm and tga). it catalyzed mukaiyama aldol reaction of a ketene silyl acetal type nucleophile ((1-methoxy-2-methylprop-1-enyloxy) trimethylsilane), and various aldehydes (aromatic, aliphati...

3,4-dihydropyrimidinones and their derivatives are synthesized via biginelli routes involving an aromatic aldehydes, ethylacetoacetates and urea in one-pot procedure by using cds nanoparticles as efficient heterogeneous catalyst in solvent-free conditions. compared with classical biginelli reaction reported in 1893, this new method provides much improved modification in terms of simplicity. the...