首页|Synthesis and in vitro evaluation of the antifungal activities of dihydropyrimidinones.
Synthesis and in vitro evaluation of the antifungal activities of dihydropyrimidinones.
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Copper (II) chloride in the absence of any solvent, efficiently catalyses the synthesis of dihydropyrimidinones (80-96% yields) by the Biginelli reaction. Six compounds were selected and examined their antifungal activities against the radial growth of three fungal species viz., Trichoderma hammatum, Trichoderma koningii and Aspergillus niger.