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首页> 外文期刊>Bulletin of the Korean Chemical Society >Spirodiclofen Analogues as Potential Lipid Biosynthesis Inhibitors: A Convenient Synthesis, Biological Evaluation, and Structure-Activity Relationship
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Spirodiclofen Analogues as Potential Lipid Biosynthesis Inhibitors: A Convenient Synthesis, Biological Evaluation, and Structure-Activity Relationship

机译:Spirodiclofen类似物作为潜在的脂质生物合成抑制剂:方便的合成,生物学评估和结构活性关系。

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Twenty spirodiclofen analogues have been designed and conveniently synthesized via three steps including esterification, one-pot heterocyclization, and acylation reactions. The target molecules have been identified on the basis of analytical spectra (1H NMR, 13C NMR and ESI-MS) data. All newly synthesized compounds have been screened for their potential insecticidal and herbicidal activity by standard method. The preliminary assays indicated that some of analogues displayed moderate to good insecticidal activity against Plutella xylostella compared with spirodiclofen, and some compounds showed obvious activity against Brassica chinensis. Structure-activity relationship (SAR) is also discussed based on the experimental data.
机译:已经设计并通过三个步骤方便地合成了二十种螺二氯苯酚类似物,包括酯化,一锅杂环和酰化反应三个步骤。根据分析光谱(1 H NMR,13 C NMR和ESI-MS)数据确定了目标分子。已通过标准方法筛选了所有新合成的化合物的潜在杀虫和除草活性。初步分析表明,与螺二氯芬相比,一些类似物对小菜蛾具有中等至良好的杀虫活性,而某些化合物对小白菜具有明显的杀虫活性。还基于实验数据讨论了结构-活性关系(SAR)。

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