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首页> 外文期刊>Journal of the Serbian Chemical Society >Facile synthesis and antifungal activity of dithiocarbamate derivatives bearing an amide moiety
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Facile synthesis and antifungal activity of dithiocarbamate derivatives bearing an amide moiety

机译:带有酰胺部分的二硫代氨基甲酸酯衍生物的简便合成和抗真菌活性

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A series of novel dithiocarbamate derivatives bearing amide moiety 3a-3i and 4a-4i were synthesized by a facile method, and the structures of these derivatives were confirmed by 1H NMR, 13C NMR, elemental analysis and high-resolution mass spectrometry (HRMS). Their antifungal activity against five phytopathogenic fungi were evaluated, and the results showed that most of the target compounds displayed low antifungal activity in vitro against Gibberella zeae, Cytospora sp., Collectotrichum gloeosporioides, Alternaria solani, and Fusarium solani at concentration of 100 mg/L. Compound 4f and 4g exhibited significant activity against Alternaria solani and Collectotrichum gloeosporioides, respectively.
机译:通过简便的方法合成了一系列具有酰胺部分3a-3i和4a-4i的新型二硫代氨基甲酸酯衍生物,并通过1H NMR,13C NMR,元素分析和高分辨率质谱(HRMS)证实了这些衍生物的结构。评估了它们对五种植物病原真菌的抗真菌活性,结果表明,大多数目标化合物在100 mg / L的浓度下对玉米赤霉菌,Cytospora sp。,Collectotrichum gloeosporioides,链格孢和链霉镰刀菌均表现出较低的抗真菌活性。 。化合物4f和4g分别显示出对茄格链格孢(Alternaria solani)和Collectotrichum gloeosporioides的显着活性。

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