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Novel 4-Methylumbelliferone Amide Derivatives: Synthesis, Characterization and Pesticidal Activities

机译:新型4-甲基纤维酮酰胺衍生物:合成,表征和杀虫活性

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摘要

A series of novel 4-methylumbelliferone amide derivatives were designed, synthesized and characterized by 1H NMR, 13C NMR and HR-ESI-MS. The structures of compounds 4bd and 4be (compounds named by authors) were further confirmed by X-ray single crystal diffraction. The acaricidal, herbicidal and antifungal activities of the synthesized compounds were assayed for their potential use as pesticide. The results indicated that compounds 4bi, 4ac and 4bd were strong acaricidals against Tetranychus cinnabarinus, with 72h corrected mortalities of greater than 80% at 1000 mg/L. Meanwhile, compounds 4bh and 4bf exhibit the strongest inhibition against the taproot development of Digitaria sanguinalis and Chenopodium glaucum, and were even more potent than the commercial herbicide Acetochlor against D. sanguinalis. In addition, compounds 4bk, 4bh and 4bp showed the highest antifungal activity against the mycelium growth of Valsa mali, which makes them more effective than commercial fungicide Carbendazim.
机译:设计了一系列新的4-甲基纤维素酰胺衍生物,合成和以1H NMR,13C NMR和HR-ESI-MS为特征。通过X射线单晶衍射进一步证实化合物4BD和4Be的结构(由作者命名的化合物)。将合成化合物的杀螨剂,除草和抗真菌活性进行测定,潜在用作农药。结果表明,化合物4BI,4AC和4BD对Tetranychus Cinnnabarinus的强酰胺,72h校正的死亡率大于80%,1000mg / L.同时,4BH和4BF的化合物对Digitaria sanguinalis和Chenopopodium肺糖蛋白的Taproot发育表现出最强的抑制作用,并且比对D. sanguinalis的商业除草剂乙酰乙酰乙酰氯更有效。此外,化合物4BK,4BH和4BP显示出抗缬沙马利菌丝菌丝体生长的最高抗真菌活性,这使得它们比商业杀菌剂碳化物更有效。

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