首页> 外文期刊>Synthesis: International Journal of Methods in Synthetic Organic Chemistry >Synthesis and Fungicidal Activity of (E)-5-[1-(4-Phenyl-2-oxo-1-oxaspiro[4.5]dec-3-en-3-yl)ethylidene]-2-aminoimidazolin-4-one Derivatives
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Synthesis and Fungicidal Activity of (E)-5-[1-(4-Phenyl-2-oxo-1-oxaspiro[4.5]dec-3-en-3-yl)ethylidene]-2-aminoimidazolin-4-one Derivatives

机译:(e)-5- [1-(4-苯基-2-氧代-1-牛水唑啉-3-烯-3-氧化硅唑啉-4-一种衍生物(E)-5- [1-(4-苯基-2-氧代-1-氧化硅[4.5] -Aminoimidazolin-4-一种衍生物的合成和杀真菌活性

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摘要

(E)-5-[1-(4-Phenyl-2-oxo-1-oxaspiro[4.5]dec-3-en-3-yl)ethylidene]-2-aminoimidazolin-4-one derivatives, as novel fungicidal agents, are designed and synthesized in moderate to excellent yields in four steps from (1-hydroxycyclohexyl)(phenyl)methanone and diketene as the starting materials. The products are characterized by H-1 NMR and HRMS (ESI) analysis. An in vivo bioassay shows that some of the products exhibit good to excellent inhibition against P. cubensis and C. lagenarium, whilst up to 94.7% inhibition against P. capsici and up to 78.1% inhibition against B. cinerea is demonstrated in the in vitro bioassay. EC50 values of 3.40 and 5.86 mu g/mL are demonstrated against P. capsici and B. cinerea.
机译:(e)-5- [1-(4-苯基-2-氧代-1-氧化氢[4.5-34-烯-3-基)乙基] -2-氨基咪唑林-4-一种衍生物,作为新型杀菌剂 ,在从(1-羟基环己基)(苯基)甲基酮和二酮作为原料中,以中等至优异的产率设计和合成优异的产率。 该产品的特征在于H-1 NMR和HRMS(ESI)分析。 体内生物测定表明,一些产品表现出对P.立方体和C.Lagenarium的优异抑制作用,而在体外,在体外证明了高达94.7%的抑制作用,高达78.1%的抑制作用。 生物测定。 EC50值为3.40和5.86μg/ ml,对P. Capsici和B. Cinerea进行了证明。

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