首页> 外文期刊>Bulletin of the Korean Chemical Society >Synthesis of 4H,6H-Furo[3,4-c]isoxazole Derivatives as New Potent Fungicides and Their Structure Activity Relationship
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Synthesis of 4H,6H-Furo[3,4-c]isoxazole Derivatives as New Potent Fungicides and Their Structure Activity Relationship

机译:4H,6H-呋喃并[3,4-c]异恶唑衍生物作为新型强效杀菌剂的合成及其结构活性关系

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4H,6H-Furo[3,4-c]isoxazoles (グ-コ), potential fungicides, have been designed and synthesized via intramolecular [2+3] cycloaddition of nitroalkyne 3 as a key step. The broad spectrum of fungicidal activities of furoisoxazoles (グ-コ) were observed on plant pathogens at 250 ppm. Furoisoxazoles ケ, ゲ with chlorophenyl at 6-position and methyl or alkylated oxime group at 3-position gave effective control of plant diseases. The furoisoxazole コ with a chlorophenyl group at 4-position also resulted in high fungicidal activities.
机译:作为关键步骤,已经通过硝基炔3的分子内[2 + 3]环加成设计并合成了潜在的杀真菌剂4H,6H-呋喃[3,4-c]异恶唑(グ-コ)。在250 ppm的植物病原体上观察到了呋喃恶唑(グ-グ)的广谱杀真菌活性。呋喃并恶唑ケ,ゲ在6-位带有氯苯基,在3-位带有甲基或烷基化的肟基,可以有效地控制植物病害。在4-位具有氯苯基的呋喃恶唑azole也具有很高的杀真菌活性。

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