以L-香芹酮(1)为原料，经盐酸羟胺肟化和O-磺酰化反应，合成得到23 个未见文献报道的L-香芹酮基磺酸肟酯类化合物3a～3w，并通过1 H NMR、13 C NMR、FT-IR和HRMS对目标化合物的结构进行了表征。采用琼脂稀释法测试了目标化合物对8 种植物病原菌的抑制活性。结果表明:在质量浓度50 mg/L时，目标化合物对所测试的8 种植物病原菌均有一定的抑菌活性，其中化合物3b(R =o-FPh)、3c(R =m-FPh)和3h(R =p-ClPh)对苹果轮纹病菌的抑制率分别为76。7%、75。9%和78。3%(均为B级活性水平)，均优于阳性对照百菌清;化合物3h对黄瓜枯萎病菌、苹果轮纹病菌、玉米小斑病菌和西瓜炭疽病菌的抑制率分别为78。4%、78。3%、82。2%和78。8%(均为B级活性水平)，具有一定的广谱抑菌活性;化合物3b对苹果轮纹病菌、玉米小斑病菌和西瓜炭疽病菌的抑制率分别为76。7%、77。5%和78。6%(均为B级活性水平)，也具有一定的广谱抑菌活性。
Synthesis and Antifungal Activity of L-Carvone-derived Oxime Sulfonate Compounds
23 novel L-carvone-derived oxime sulfonate compounds 3a-3w were synthesized through hydroxylamine hydrochloride oximation and o-sulfonylation reactions using L-carvone(1)as the starting material.The structures of the target compounds were characterized by 1 H NMR,13 C NMR,FT-IR and HRMS.The antifungal activities of the target compounds against 8 tested plant pathogens were evaluated by agar dilution method.The results showed that the target compounds exhibited certain antifungal activities against the tested plant pathogens at the mass concentration of 50 mg/L.Among them,compounds 3b(R =o-FPh),3c(R =m-FPh)and 3h(R = p-ClPh)had inhibition rates against Physalospora piricola of 76.7%,75.9%,and 78.3%(all in B-class activity level),which were better than that of the positive control chlorothalonil.Compound 3h displayed certain broad-spectrum antifungal activity owing to its good inhibition rates of 78.4%,78.3%,82.2%,and 78.8%,against Fusarium oxysporum f.sp.cucumerinum,Physalospora piricola,Bipolaris maydis,and Colleterichum orbicalare,respectively(all in B-class activity level).Compound 3b also displayed certain broad-spectrum antifungal activity owing to its good inhibition rates of 76.7%,77.5%,and 78.6%,against P.piricola,B.maydis,and C.orbicalare,respectively(all in B-class activity level).
万方数据
维普
