首页> 外文期刊>Journal of Heterocyclic Chemistry: The International Journal of Heterocyclic Chemistry >Synthesis and Biological Activity of 1-(Substituted phenoxyacetoxy)1-(pyridin-2-yl or thien-2-yl) methylphosphonates
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Synthesis and Biological Activity of 1-(Substituted phenoxyacetoxy)1-(pyridin-2-yl or thien-2-yl) methylphosphonates

机译:1-(取代的苯氧基乙酰氧基)1-(吡啶-2-基或噻吩-2-基)甲基膦酸酯的合成及生物活性

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摘要

A series of novel O,O-dimethyl 1-(substituted phenoxyacetoxy)-1-(pyridin-2-yl or thien-2-yl)methylphosphonates 6a, 6b, 6c, 6d, 6e, 6f, 6g, 6h, 6i, 6j, 6k, 6l, 6m, 6n and 7a, 7b, 7c, 7d were synthesized. Their structures were confirmed by IR, H-1 NMR, mass spectroscopy, and elemental analyses. The results of preliminary bioassays show that some of the title compounds exhibit moderate to good herbicidal and fungicidal activities. For example, the title compounds 6a, 6c, 6l, 6m, and 7d possess 90-100% inhibition against most of the tested plants at the dosage of 1500gai/ha, whereas the title compounds 6b, 6g, 6h and 6n possess 92-100% inhibition against Fusarium oxysporum, Phyricularia grisea, Botrytis cinereapers, Gibberella zeae, Sclerotinia sclerotiorum, and Cercospora beticola at the concentration of 50mg/L.
机译:一系列新颖的O,O-二甲基1-(取代的苯氧基乙酰氧基)-1-(吡啶-2-基或噻吩-2-基)甲基膦酸酯6a,6b,6c,6d,6e,6f,6g,6h,6i,合成了6j,6k,6l,6m,6n和7a,7b,7c,7d。通过IR,H-1 NMR,质谱和元素分析证实了它们的结构。初步生物测定的结果表明,某些标题化合物具有中等至良好的除草和杀真菌活性。例如,标题化合物6a,6c,6l,6m和7d在1500gai / ha的剂量下对大多数受试植物具有90-100%的抑制作用,而标题化合物6b,6g,6h和6n具有92-浓度为50mg / L的100%的抗尖孢镰刀菌,稻瘟病菌,灰葡萄孢,灰霉菌,菌核盘菌和番茄斜纹夜蛾的100%抑制作用。

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