English

• 

• 1. [1] WANG Mingqi,YE Fei.Study and Application of Phenoxycarboxylic Acid Herbicides[J].New Pestic,2005,39(1):20-22(in Chinese).王铭琦,叶非.苯氧羧酸类除草剂的研究与应用进展[J].新农药,2005,39(1):20-22.[1] WANG Mingqi,YE Fei.Study and Application of Phenoxycarboxylic Acid Herbicides[J].New Pestic,2005,39(1):20-22(in Chinese).王铭琦,叶非.苯氧羧酸类除草剂的研究与应用进展[J].新农药,2005,39(1):20-22.

  2. [2] ZHANG Yuju,LI Jide,ZHANG Desheng,et al.Diagnose of Phytotoxicity and Technology of Safe Application of Phenoxycarboxylic Acid and Benzoic Acid Herbicides[J].J He'nan Agric Sci,2001,30(11):13-15(in Chinese).张玉聚,李继德,张德胜,等.苯氧羧酸类和苯甲酸类除草剂药害诊断与安全应用技术[J].河南农业科学,2001,30(11):13-15.[2] ZHANG Yuju,LI Jide,ZHANG Desheng,et al.Diagnose of Phytotoxicity and Technology of Safe Application of Phenoxycarboxylic Acid and Benzoic Acid Herbicides[J].J He'nan Agric Sci,2001,30(11):13-15(in Chinese).张玉聚,李继德,张德胜,等.苯氧羧酸类和苯甲酸类除草剂药害诊断与安全应用技术[J].河南农业科学,2001,30(11):13-15.

  3. [3] Sandmann G,B ger P.In Herbicide Activity:Toxicology,Biochemistry,and Molecular Biology[M].Roe R M,Burton J D,Kuhr R J.Eds.Amsterdam:IOS Press,1997:1-10.[3] Sandmann G,B ger P.In Herbicide Activity:Toxicology,Biochemistry,and Molecular Biology[M].Roe R M,Burton J D,Kuhr R J.Eds.Amsterdam:IOS Press,1997:1-10.

  4. [4] Sandmann G.In Herbicidal Classes in Development:Mode of Action,Targets,Genetic Engineering,Chemistry[M].B ger P,Wakabayashi K,Hirai K,Eds.Berlin:Springer,2002:43-55.[4] Sandmann G.In Herbicidal Classes in Development:Mode of Action,Targets,Genetic Engineering,Chemistry[M].B ger P,Wakabayashi K,Hirai K,Eds.Berlin:Springer,2002:43-55.

  5. [5] Mitchell G.In Synthesis and Chemistry of Agrochemicals IV,ACS Symposium Series[M].Baker D A,Fenyes J G,Moberg W K,et al.Ed.Washington DC:American Chemical Society,1995,584:161-170.[5] Mitchell G.In Synthesis and Chemistry of Agrochemicals IV,ACS Symposium Series[M].Baker D A,Fenyes J G,Moberg W K,et al.Ed.Washington DC:American Chemical Society,1995,584:161-170.

  6. [6] Sandmann G,Kowalczyk-Schroder S,Taylor H M.Quantitative Structure-Activity Relationship of Fluridone Derivatives with Phytoene Desaturase[J].Pestic Biochem Physiol,1992,42(1):1-6.[6] Sandmann G,Kowalczyk-Schroder S,Taylor H M.Quantitative Structure-Activity Relationship of Fluridone Derivatives with Phytoene Desaturase[J].Pestic Biochem Physiol,1992,42(1):1-6.

  7. [7] Sandmann G,Bramley P M,B ger P.New Herbicidal Inhibitors of Carotene Biosynthesis[J].Pestic Sci,1985,10(1):19-24.[7] Sandmann G,Bramley P M,B ger P.New Herbicidal Inhibitors of Carotene Biosynthesis[J].Pestic Sci,1985,10(1):19-24.

  8. [8] Heap I.International survey of herbicide resistance weeds,http://weedscience.com.[8] Heap I.International survey of herbicide resistance weeds,http://weedscience.com.

  9. [9] Ohno R,Nagaoka M,Hirai K,et al.Synthesis and Insecticidal Activity of Novel 1-Alkyl-3-Sulfonyloxypyrazole-4-Carboxamide Derivatives[J].J Pestic Sci,2010,35(1):15-22.[9] Ohno R,Nagaoka M,Hirai K,et al.Synthesis and Insecticidal Activity of Novel 1-Alkyl-3-Sulfonyloxypyrazole-4-Carboxamide Derivatives[J].J Pestic Sci,2010,35(1):15-22.

  10. [10] Omura S,Tanaka T.Pesticide Chemistry[M].Ohkawa H,Miyagawa H,Lee P W.Ed.Weinheim:Wiley-VCH,1991,7:87.[10] Omura S,Tanaka T.Pesticide Chemistry[M].Ohkawa H,Miyagawa H,Lee P W.Ed.Weinheim:Wiley-VCH,1991,7:87.

  11. [11] Guan A,Liu C,Yang X,et al.Application of the Intermediate Derivatization Approach in Agrochemical Discovery[J].Chem Rev,2014,114(14):7079-7107.[11] Guan A,Liu C,Yang X,et al.Application of the Intermediate Derivatization Approach in Agrochemical Discovery[J].Chem Rev,2014,114(14):7079-7107.

  12. [12] D mling A,Wang W,Wang K.Chemistry and Biology of Multicomponent Reactions[J].Chem Rev,2012,112(6):3083-3155.[12] D mling A,Wang W,Wang K.Chemistry and Biology of Multicomponent Reactions[J].Chem Rev,2012,112(6):3083-3155.

  13. [13] Marcaccini S,Torroba T.The Use of the Ugi Four-component Condensation[J].Nat Protoc,2007,2(3):632-639.[13] Marcaccini S,Torroba T.The Use of the Ugi Four-component Condensation[J].Nat Protoc,2007,2(3):632-639.

  14. [14] Ugi I,Werner B,D mling A.The Chemistry of Isocyanides,Their MultiComponent Reactions and Their Libraries[J].Molecules,2003,8(1):53-66.[14] Ugi I,Werner B,D mling A.The Chemistry of Isocyanides,Their MultiComponent Reactions and Their Libraries[J].Molecules,2003,8(1):53-66.

  15. [15] Zuo X,Mi N,Fan Z,et al.Synthesis of 4-Methyl-1,2,3-thiadiazole Derivatives via Ugi Reaction and Their Biological Activities[J].J Agric Food Chem,2010,58(5):2755-2762.[15] Zuo X,Mi N,Fan Z,et al.Synthesis of 4-Methyl-1,2,3-thiadiazole Derivatives via Ugi Reaction and Their Biological Activities[J].J Agric Food Chem,2010,58(5):2755-2762.

  16. [16] HU Hanning,LI Anling,ZHANG Hanyun,et al.Synthesis of N-Cyclohexyl 2-{N-(3-Trifluoromethylphenyl)-[3-(trifluo-romethyl) benzoyl,2-(substitutedphenoxy) propionyl,2-(4,6-dime-thoxypyrimidinyl-2-oxy) benzoyl-]-amino}-substituted-phenyl-acetamides via Ugi Reaction and Their Herbicidal Activity Evaluation[J].Chinese J Org Chem,2015,35:2162-2167(in Chinese).胡汉宁,黎安玲,张瀚匀,等.利用Ugi反应合成2-{N-(3-三氟甲基苯基)-[3-(三氟甲基)苯甲酰、2-(取代苯氧)丙酰、2-(4,6-二甲氧基-嘧啶-2-氧基)苯甲酰]-氨基}-取代苯乙酰环己胺及其除草活性评价[J].有机化学,2015,35:2162-2167.[16] HU Hanning,LI Anling,ZHANG Hanyun,et al.Synthesis of N-Cyclohexyl 2-{N-(3-Trifluoromethylphenyl)-[3-(trifluo-romethyl) benzoyl,2-(substitutedphenoxy) propionyl,2-(4,6-dime-thoxypyrimidinyl-2-oxy) benzoyl-]-amino}-substituted-phenyl-acetamides via Ugi Reaction and Their Herbicidal Activity Evaluation[J].Chinese J Org Chem,2015,35:2162-2167(in Chinese).胡汉宁,黎安玲,张瀚匀,等.利用Ugi反应合成2-{N-(3-三氟甲基苯基)-[3-(三氟甲基)苯甲酰、2-(取代苯氧)丙酰、2-(4,6-二甲氧基-嘧啶-2-氧基)苯甲酰]-氨基}-取代苯乙酰环己胺及其除草活性评价[J].有机化学,2015,35:2162-2167.

  17. [17] HE Hongwu,WANG Jun,LIU Zhaojie,et al.Study on Biologically Active Organophosphorus Compounds V.Syntheses and Properties of α-(Sunstituted Phenoxy-acetoxy) Alkyl Phosphonates[J].Chinese J Appl Chem,1994,11(4):21-26(in Chinese).贺红武,汪军,刘钊杰,等.具有生物活性的有机磷化合物的研究V.α-[(取代)芳氧基乙酰氧基]烷基膦酸酯的合成和性质[J].应用化学,1994,11(4):21-26.[17] HE Hongwu,WANG Jun,LIU Zhaojie,et al.Study on Biologically Active Organophosphorus Compounds V.Syntheses and Properties of α-(Sunstituted Phenoxy-acetoxy) Alkyl Phosphonates[J].Chinese J Appl Chem,1994,11(4):21-26(in Chinese).贺红武,汪军,刘钊杰,等.具有生物活性的有机磷化合物的研究V.α-[(取代)芳氧基乙酰氧基]烷基膦酸酯的合成和性质[J].应用化学,1994,11(4):21-26.

  18. [18] Ugi I,Meyr R,Lipinski M,et al.Cyclohexyl Isocyanide[J].Org Synth,1961,41:13.[18] Ugi I,Meyr R,Lipinski M,et al.Cyclohexyl Isocyanide[J].Org Synth,1961,41:13.

  19. [19] Chen X B,Shi D Q,Zhu X F.Synthesis,Crystal Structure and Biological Activities of O,O-Dialkyl α-[1-(2-Chlorothiazol-5-ylmethyl)-5-methyl-1H-1,2,3-triazol-4-ylcarbonyloxy]alkylphosphonates[J].Chinese J Chem,2007,25(12):1854-1858.[19] Chen X B,Shi D Q,Zhu X F.Synthesis,Crystal Structure and Biological Activities of O,O-Dialkyl α-[1-(2-Chlorothiazol-5-ylmethyl)-5-methyl-1H-1,2,3-triazol-4-ylcarbonyloxy]alkylphosphonates[J].Chinese J Chem,2007,25(12):1854-1858.

  20. [20] Liu Y X,Wei D G,Zhu Y R,et al.Synthesis,Herbicidal Activities,and 3D-QSAR of 2-Cyanoacrylates Containing Aromatic Methylamine Moieties[J].J Agric Food Chem,2008,56(1):204-212.[20] Liu Y X,Wei D G,Zhu Y R,et al.Synthesis,Herbicidal Activities,and 3D-QSAR of 2-Cyanoacrylates Containing Aromatic Methylamine Moieties[J].J Agric Food Chem,2008,56(1):204-212.

•