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Synthesis and Activity of Novel Acylthiourea with Hydantoin

机译:乙内酰脲与新型酰基硫脲的合成及活性

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The 41 novel acylthiourea derivatives with hydantoin were synthesized in moderate to excellent yields by using 5-(4-aminophenyl)- and 5-(4-aminobenzyl)- hydantoin or 5-(4-aminobenzyl)-thiohydantoin as raw materials and characterized by IR, 1H NMR spectra and elementary analysis. The preliminary bioassay showed that these compounds exhibit certain selectively herbicidal activities with the 91%, 94% and 87% inhibition rates of 7l, 8o and 8p against B. campestris, 100%, 100% and 95% efficacy against B. campestris in a greenhouse test, respectively. 7a, 7b, 7c and 7d exhibited 74%, 79%, 79% and 71% inhibition rates against F. oxysporum, respectively.
机译:以5-(4-氨基苯基)-和5-(4-氨基苄基)-乙内酰脲或5-(4-氨基苄基)-硫代乙内酰脲为原料,以中等至优异的收率合成了41种具有乙内酰脲的新酰基硫脲衍生物,并对其进行了表征。 IR, 1 H NMR光谱和元素分析。初步的生物测定表明,这些化合物表现出一定的选择性除草活性,对菜豆中的油菜双歧杆菌的抑制率分别为91、94和87%,分别为7l,8o和8p,对菜豆中的油菜的抑制率分别为100%,100%和95%。温室测试。图7a,7b,7c和7d分别显示出针对尖孢镰刀菌的74%,79%,79%和71%的抑制率。

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