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含肟醚并取代异噁唑环的氨基甲酸酯类化合物的合成及生物活性(英文)
Synthesis and biological activity of novel carbamates containing methoxyimino-isoxazoline
【摘要】 为寻找具有优异生物活性的氨基甲酸酯类化合物,根据活性亚结构拼接原理,将取代异唑和肟醚基团引入多菌灵结构中,以取代苯甲醛(1)和2-氯苄胺(3)为起始原料,经多步反应设计合成了10个未见文献报道的含肟醚并取代异唑的氨基甲酸酯类化合物,其结构经1H NM R和MS确证。初步生物活性测定结果表明,部分目标化合物不仅具有一定的杀菌活性,同时还具有较好的除草活性。其中,活体盆栽试验结果表明,化合物11b对黄瓜霜霉病Pseudoperonospora cubensis的相对防效为90%,对黄瓜白粉病Sphaerotheca fuliginea的相对防效达95%,低于对照药剂多菌灵;除草活性皿测法表明,化合物11c和11j 200 mg/L下对靶标作物的根、茎抑制率均达80%以上,与对照药剂异丙酯草醚活性相当。盆栽法表明,150 g/hm2下,化合物11c和11j对繁缕Stellaria media苗前和苗后的抑制率均在70%以上,低于异丙酯草醚。此类化合物的构效关系有待进一步研究。
【Abstract】 To search for novel carbamates with unique biological activities,novel compounds were designed by splicing active groups oxime ether and isoxazoline into carbendazim.10 Novel title compounds were synthesized from substitutional benzaldehydes(1) and 2-chlorobenzylamine(3) in multiple steps.The structures of the compounds were confirmed by MS and ~1H NMR.The bioassays showed that the compounds exhibit both good fungicidal activity and herbicidal activity.Among them,with the small plant pot spray method,fungicidal efficacies of 11 b were 90%against Pseudoperonospora cubensis and 95%against Sphaerotheca fuliginea at200 mg/L,lower than carbendazim.The preliminary herbicidal screening showed that the inhibition rates of 11 c and 11 j were up to 80%against root and stem growth of all the target plants,nearly as good as pyribambenz isopropyl.However,the secondary herbicidal screening showed that the herbicidal efficacies of 11 c and 11 j against Stellaria media were up to 70%both by postmergence foliar spray and preemergence soil spray processing at 150 g/hm~2,lower than pyribambenz isopropyl.The relationship between structure and biological activity was also studied.
- 【文献出处】 农药学学报 ,Chinese Journal of Pesticide Science , 编辑部邮箱 ,2015年05期
- 【分类号】TQ25;TQ450.1
- 【被引频次】1
- 【下载频次】131