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Efficient Synthesis of 5(4H)-Imidazolones and in vitro Antifungal Activity Studies Against Selected Phytopathogens

机译:5(4H)-咪唑酮的有效合成和对某些植物病原菌的体外抗真菌活性研究

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摘要

A series of five new 1-(substituted phenyl)-2-phenyl-4-(substituted benzylidine)imidazole-5-one derivatives (or) 5(4H)-imidazolones have been synthesized adopting SiO2, Al2O3-90 and Y-faujasite (Y-H type) zeolite as catalysts. These compounds were assayed for their antifungal activity on three different selected phytopathogens which disparately affects the Jowar crop (Sorghum vulgare) of poaceae family. Among the screened target molecules, compound 18 exhibited potent inhibitory activity compared to the standard drug bavistine, which is worth for further investigation.
机译:利用SiO2,Al2O3-90和Y-八面沸石合成了一系列五个新的1-(取代的苯基)-2-苯基-4-(取代的苄基)咪唑-5-酮衍生物(或)5(4H)-咪唑啉酮(YH型)沸石作为催化剂。分析了这些化合物对三种不同选择的植物病原体的抗真菌活性,这些植物病原体分别影响禾本科的Jowar作物(高粱)。在筛选的目标分子中,与标准药物巴维斯汀相比,化合物18表现出有效的抑制活性,值得进一步研究。

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