Key points are not available for this paper at this time.
A straightforward, one-pot, solvent-free, and environmentally friendly method for synthesizing 4,6-Diarylpyrimidin-2(1H)-ones through a Biginelli-type reaction is presented, utilizing sulfated tungstate as a catalyst. This approach offers enhanced product yields while employing a cost-effective and easily accessible catalyst. The simplicity of the experimental setup makes it an effective and stress-free strategy for producing 4,6-diarylpyrimidin-2-(1H)-ones. The catalyst demonstrates remarkable activity and can be reused, further contributing to the method’s efficiency.
SHELAR et al. (Thu,) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: