biginelli-type pyrimidines contain an interesting moiety which has attracted considerable attention of medicinal chemists in the last few decades. despite the very diverse pharmacologic effects ascribed to this kind of pyrimidines, there are few reports on the antioxidant evaluation of biginelli pyrimidines. in this study synthesis of some novel biginelli-type pyrimidines is reported. the prepa...

TiO2 nanoparticles/melamine Tri sulfonic acid (MTSA) supported on silica gel as an efficient catalytic system for simple, one pot, solvent-free and environmentally benign process for synthesis of dihydropyrimidines via Biginelli reaction at 110 °C is described. It was found that the catalyst is reusable and exhibited remarkable activity. The catalyst can be easily separated and reused several t...

TiO2 nanoparticles/melamine Tri sulfonic acid (MTSA) supported on silica gel as an efficient catalytic system for simple, one pot, solvent-free and environmentally benign process for synthesis of dihydropyrimidines via Biginelli reaction at 110 °C is described. It was found that the catalyst is reusable and exhibited remarkable activity. The catalyst can be easily separated and reuse...

A one-pot three-component synthesis of dihydropyrimidinones via a molecular iodine-catalyzed tandem reaction of simple readily available mono-substituted urea, alkylaldehyde, and arylaldehyde has been developed. The reaction proceeds with high chemo- and regioselectivity to give highly diverse dihydropyrimidinones in reasonable yields under mild reaction conditions. Moreover, the first catalyti...

The search for renewable monomers radical polymerization techniques is of current interest due to the awareness sustainability requirements in chemical sciences. Herein, synthesis and reversible addition-fragmentation chain-transfer (RAFT) a methacrylate monomer based on ricinoleic acid as sustainable starting material presented. In addition, hydroxy moiety converted an acetoacetate order allow...

Four series of N-Mannich bases of 3,4-dihydropyrimidine-2(1H)-thiones 7a-g, 8a-g, 9a-g and 10a-g (DHPMs) have been prepared by Mannich reaction with seven different heterocyclic secondary amino compounds 6a-g and formaldehyde 5. In this reaction, four different derivatives of 3,4-dihydropyrimidine-2(1H)-thiones 4a-d have been used as hydrogen active compound. These precursors have been derived ...

5-acetyl-6-methyl-4-aryl-3,4-dihydropyrimidin-2(1H)-ones were synthesized in good to excellent by one-pot three-component Biginelli condensation in the presence of ammonium salt [Et3NH][HSO4] as an inexpensive and green catalyst under solvent-free conditions. High yields, short reaction time, easy work-up, a green environment which requires no toxic o...