期刊文献+

新型芳氧苯胺类化合物的合成及除草活性研究

Synthesis and Herbicidal Activity of Novel Aryloxyaniline Analogues
在线阅读 下载PDF
导出
摘要 以芳氧苯氧丙酸酯类除草剂-异噁草醚为先导,通过生物电子等排、骨架跃迁等方法,设计合成了一系列含有芳氧苯胺结构的化合物,对所合成的目标化合物进行了NMR表征,确定了目标化合物的结构,并进行了除草活性,测试结果表明,大部分化合物对稗草、狗尾草、苘麻和百日草均具有一定的除草活性。其中,化合物Ⅰ-4(4-((4-硝基吡啶-2-基)氧基、苯基)氨基甲酸4-氯-2甲基苯酯)表现出广谱的除草活性,500 g/hm^(2)含量下,对稗草和狗尾草的除草活性大于90%,对苘麻和百日草的除草活性大于40%,优于对照药剂异噁草醚,作为除草剂具有进一步研究的潜力。 With aryloxyphenoxypropionate herbicide clomazone as the lead compound,a series of compounds containing aryloxy aniline structures were designed and synthesized by bioisosterism and scaffold hopping method.The NMR characterization was carried out to determine the structures of the target compounds,and their herbicidal activities were tested.The test results indicated that that most of the compo unds had certain herbicidal activity against Echinochloa crusgalli,Setaria viridis,Abutilon theophrasti and Zinnia elegans.Among them,compound I-4 showed broad-spectrum herbicidal activity.At a concentration of 500 g/hm^(2),compound I-4 exhibited more than 90%herbicidal activity against Echinochloa crusgalli,Setaria viridis,which was comparable to acetochlor;more than 40%herbicidal activity against Abutilon theophrasti and Zinnia elegans,which was significantly better than that of acetochlor,and it has the potential for further research as a herbicide.
作者 郝泽生 王滢秀 王海利 张晓慷 张新刚 江忠萍 韩金涛 HAO Zesheng;WANG Yingxiu;WANG Haili;ZHANG Xiaokang;ZHANG Xingang;JIANG Zhongping;HAN Jintao(Shandong Academy of Pesticide Sciences,Jinan 250100,China)
出处 《山东化工》 2025年第6期1-3,8,共4页 Shandong Chemical Industry
基金 山东省自然科学基金(ZR^(2)022QC224) 山东省农业科学院农业科技创新工程(CXGC2024F18) 山东省技术创新引导计划(中央引导地方科技发展资金)(YDZX2023051)。
关键词 芳氧苯胺 合成 除草活性 构效关系 aryloxyaniline synthesis herbicidal activity structure-activity relationship
  • 相关文献

参考文献12

二级参考文献102

  • 1中国农药工业六十年回顾[J].中国农药,2009,0(8):1-6. 被引量:1
  • 2尹仪民.现代农药工业的起步和发展的几个关键时期——庆祝建国六十周年[J].中国农药,2009,0(8):7-15. 被引量:1
  • 3黄文耀,李钟华,王龙根.农药自主创新成绩显著,硕果累累[J].农药研究与应用,2006,10(4):7-9. 被引量:2
  • 4Marshall L C,Somers D A,Dotray P D,et al.Allelic mutations in acetyl-coenzyme A carboxylase confer herbicide tolerance in maize[J].Theor Appl Genet,1992,83:435-442.
  • 5Egli M A,Gengenbach B G.,Gronwald J W,et al.Characterization of maize acetyl-coenzyme A carboxylase[J].Plant Physiol,1993,101:499-506.
  • 6Sasaki Y,Nagano Y.Plant acetyl-CoA carboxylase:structure,biosynthesis,regulation and gene manipulation for plant breeding[J].Biosci Biotechnol Biochem,2004,68:1175-1184.
  • 7Kozaki A,Ayuoi M K,Sasaki Y.Thiol-disulfide exchange between nuclear-encode and chloroplasten-coded subunit of pea caetyl-CoA carboxylase[J].J Biol Chem,2001,276:39919-39925.
  • 8Nikolau B J,Ohlrogge J B,Wurtele E S.Plant biotin-containing carboxylases[J].Arch Biochem Biophys,2003,414:211-222.
  • 9Schuhe W,Topfer R,Stracke R,et al.Multi-functional acetyl-CoA carboxylase from brassica napus encode by a multigene family:indication for plastidic calization of at least one isoform[J].Proc Natl Acad Sci USA,1997,94:3465-3470.
  • 10Diacovich L,Peirú S,Kurth D,et ai.Kinetic and structural analysis of a new group of acyl-CoA carboxylases found in streptomyces coelicolor A3 (2)[J].J Bio Chem,2002,277:31228-31236.

共引文献75

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部