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49 条记录 (耗时 0.032 秒)

    Method for Controlling Harmful Fungi
    31.
    发明申请
    Method for Controlling Harmful Fungi 审中-公开
    控制有害真菌的方法

    公开(公告)号：US20100099774A1

    公开(公告)日：2010-04-22

    申请号：US12523804

    申请日：2008-01-28

    申请人： Henry Van Tuyl Cotter ,  David Allen Hunt ,  David G. Kuhn

    发明人： Henry Van Tuyl Cotter ,  David Allen Hunt ,  David G. Kuhn

    IPC分类号： A01N33/02 ,  A01P3/00

    CPC分类号： A01N37/52

    摘要： The present invention relates to a method for controlling phytopathogenic fungior harmful fungi in the protection of materials, wherein the fungi or the materials, plants, soil or seed to be protected against fungal attack are treated with a fungicidally effective amount of an amidrazone of the formula (I) wherein R, R1, R2, R3, A, B, W, Y and n have the meanings as defined in the description.

    摘要翻译： 本发明涉及一种在保护材料中控制植物病原性真菌有害真菌的方法，其中用杀真菌有效量的式（Ⅰ）的莠去津处理待真菌侵害的真菌或材料，植物，土壤或种子， （I）其中R，R1，R2，R3，A，B，W，Y和n具有如说明书中定义的含义。

    Fungicidal mixtures
    35.
    发明授权
    Fungicidal mixtures 失效
    杀菌混合物

    公开(公告)号：US06518275B1

    公开(公告)日：2003-02-11

    申请号：US09809512

    申请日：2001-03-15

    申请人： Henry Van Tuyl Cotter ,  Leslie May ,  Gunter Reichert ,  Ewald Sieverding

    发明人： Henry Van Tuyl Cotter ,  Leslie May ,  Gunter Reichert ,  Ewald Sieverding

    IPC分类号： A01N3744

    CPC分类号： A01N43/90 ,  A01N61/00 ,  A01N59/20 ,  A01N59/02 ,  A01N47/44 ,  A01N47/38 ,  A01N47/40 ,  A01N47/04 ,  A01N43/84 ,  A01N43/76 ,  A01N43/653 ,  A01N43/60 ,  A01N43/54 ,  A01N43/32 ,  A01N43/42 ,  A01N43/40 ,  A01N37/50 ,  A01N37/46 ,  A01N37/38 ,  A01N37/34 ,  A01N2300/00

    摘要： Fungicidal compositions comprising an acceptable carrier and/or surface active agent and synergistically effective amounts of (a) at least one azolopyrimidine of formula I  in which R1, R2, L1, L2 and L3 have the meaning given in claim 1; and (b) at least one fungicidal active ingredient selected from benomyl, carboxin, captan, chlorothalonil, copper oxychloride, cyprodinil, dimethomorph, dithianon, dodine, famoxadone, fenhexamid, fenpiclonil, fenpropimorph, fluazinam, mancozeb, metalaxyl, pyrimethanil, quinoxifen, sulfur, triforine, vinclozolin, a fungicidal triazole derivative, and a synthetic strobilurine derivative. The invention also provides a method of controlling the growth of phytopathogenic fungi at a locus by applying synergistically effective amounts of at least one azolopyrimidine of formula I and at least one fungicidal active ingredient (b) to the locus.

    摘要翻译： 包含可接受的载体和/或表面活性剂的杀真菌组合物和协同有效量的（a）至少一种式I的偶氮嘧啶，其中R 1，R 2，L 1，L 2和L 3具有权利要求1中给出的含义; 和（b）至少一种杀真菌活性成分，其选自苯菌灵，呋喃丹，克拉曼，百菌清，氯氧化铜，西酞替尼，烯酰吗啉，二噻吩，十二烷，恶唑酮，芬己酰，芬替尼，芬卡芬，氟啶胺，代森锰锌，甲霜灵，嘧霉胺，喹喔啉， ，triperine，长春菌素，杀真菌三唑衍生物和合成次溴酸衍生物。 本发明还提供了一种通过将协同有效量的至少一种式I的偶氮嘧啶和至少一种杀真菌活性成分（b）施用于该基因座来控制植物病原真菌在一个场所生长的方法。

    Azoline Compounds for Combating Arthropod Pests
    36.
    发明申请
    Azoline Compounds for Combating Arthropod Pests 审中-公开
    用于防治节肢动物害虫的唑啉化合物

    公开(公告)号：US20100010058A1

    公开(公告)日：2010-01-14

    申请号：US12305267

    申请日：2007-05-25

    申请人： Christopher Koradin ,  Markus Kordes ,  Ronan Le Vezouet ,  Deborah L. Culbertson ,  Douglas D. Anspaugh ,  Henry Van Tuyl Cotter

    发明人： Christopher Koradin ,  Markus Kordes ,  Ronan Le Vezouet ,  Deborah L. Culbertson ,  Douglas D. Anspaugh ,  Henry Van Tuyl Cotter

    IPC分类号： A01N43/78 ,  C07D277/18 ,  A01P5/00 ,  A01P7/00

    CPC分类号： C07D277/18

    摘要： The present invention relates to azoline compounds and their salts which are useful for combating arthropod pests. The present invention also relates to a method for combating arthropod pests and to agricultural compositions for combating said pests. It has been found that these objectives can be achieved by azoline compounds of the general formulae Ia or Ib, wherein X is S, O or NR4; Ar is phenyl or a 5 or 6 membered heteroaromatic ring; R1 is H, C1-C6-alkyl, C2-C6-alkenyl, phenyl, a heteroaromatic ring etc.; R2a, R2b are H, CN, C1-C6-alkyl etc.; R1 together with R2a may also form a linear C2-C4-alkandiyl; R3a-d are H, halogen, C1-C6-alkyl etc.

    摘要翻译： 本发明涉及可用于防治节肢动物害虫的唑啉化合物及其盐。 本发明还涉及一种防治节肢动物害虫的方法和用于对抗所述害虫的农业组合物。 已经发现，这些目的可以通过通式Ia或Ib的唑啉化合物来实现，其中X是S，O或NR 4; Ar是苯基或5或6元杂芳环; R1是H，C1-C6-烷基，C2-C6-烯基，苯基，杂芳环等; R2a，R2b是H，CN，C1-C6-烷基等; R1与R2a一起也可以形成直链C 2 -C 4 - 烷二基; R3a-d为H，卤素，C1-C6烷基等。

    Quinoline Derivatives and Their Use as Pesticides
    37.
    发明申请
    Quinoline Derivatives and Their Use as Pesticides 审中-公开
    喹啉衍生物及其作为农药的用途

    公开(公告)号：US20090029855A1

    公开(公告)日：2009-01-29

    申请号：US12282608

    申请日：2007-03-12

    申请人： Michael Puhl ,  Wassilios Grammenos ,  Joachim Rheinheimer ,  Jan Klaas Lohmann ,  Michael Rack ,  Liliana Parra Rapado ,  Christopher Koradin ,  Jurgen Langewald ,  Deborah L. Culbertson ,  Douglas D. Anspaugh ,  Hassan Oloumi-Sadeghi ,  Henry Van Tuyl Cotter ,  David G. Kuhn

    发明人： Michael Puhl ,  Wassilios Grammenos ,  Joachim Rheinheimer ,  Jan Klaas Lohmann ,  Michael Rack ,  Liliana Parra Rapado ,  Christopher Koradin ,  Jurgen Langewald ,  Deborah L. Culbertson ,  Douglas D. Anspaugh ,  Hassan Oloumi-Sadeghi ,  Henry Van Tuyl Cotter ,  David G. Kuhn

    IPC分类号： A01N25/26 ,  C07D215/14 ,  A01N43/42 ,  A01N59/26 ,  A01P5/00 ,  A01P7/04

    CPC分类号： C07D215/12 ,  C07D215/60

    摘要： This invention relates to quinoline derivatives of formula I wherein R1, R2, R3 are each independently halogen, hydroxy, cyano, amino, nitro, C1-C6-alkyl, C2-C6-alkenyl, C2-C6-alkynyl, C3-C7-cycloalkyl, C3-C7-cycloalkyl-C1-C4-alkyl, C1-C6-alkoxy, C2-C6-alkenyloxy, C2-C6-alkynyloxy, C1-C4-alkoxy-C1-C4-alkoxy, C3-C7-cycloalkyl-C1-C4-alkoxy, C(OH)(CF3)2, C1-C6-haloalkyl, C1-C6-haloalkoxy, C1-C6-alkylthio, C1-C6-haloalkylthio, C1-C6-alkylsulfinyl, C1-C6-haloalkylsulfinyl, C1-C6-alkylsulfonyl, C1-C6-haloalkylsulfonyl, C(Ra)═O, C(Ra)═NORb, C(═O)ORx, or C(═O)NRxRy; Ra is hydrogen or C1-C4-alkyl; Rb is hydrogen, C1-C4-alkyl, C2-C4-alkenyl, C2-C4-alkynyl, C1-C4-haloalkyl, or C2-C4-haloalkenyl; Rx, Ry are each independently hydrogen, C1-C4-alkyl, C1-C4-haloalkyl, C1-C4-alkoxy-C1-C4-alkyl, C1-C4-thioalkyl-C1-C4-alkyl, C1-C4-alkyl-S(═O)C1-C4-alkyl, C1-C4-alkyl-S(═O)2C1-C4-alkyl, C3-C6-cyloalkyl, C1-C4-alkyl-C3-C6-cycloalkyl, C3-C6-alkenyl, C3-C6-alkinyl; R4, R5, R6, R7 are each independently hydrogen, halogen, cyano, amino, nitro, hydroxy, C1-C6-alkyl, C1-C6-alkoxy, C1-C6-haloalkyl, C1-C6-haloalkoxy, C1-C6-alkylthio, C1-C6-haloalkylthio, C1-C6-alkylsulfinyl, C1-C6-haloalkylsulfinyl, C1-C6-alkylsulfonyl, C1-C6-haloalkylsulfonyl, or C(═O)ORc; Rc is hydrogen, C1-C6-alkyl, C2-C6-alkenyl, or C2-C6-alkinyl; m and n are each independently 1, 2, 3, 4, or 5; p is 0, 1, 2, 3, 4, or 5; and the N-oxides, enantiomers, diastereomers and salts thereof, processes and intermediates for the preparation of compounds I, use of compounds I for combating insects, acarids, or nematodes and a method for treating, controlling, preventing or protecting animals against infestation or infection by parasites using compounds I.

    摘要翻译： 本发明涉及式I的喹啉衍生物，其中R 1，R 2，R 3各自独立地为卤素，羟基，氰基，氨基，硝基，C 1 -C 6烷基，C 2 -C 6 - 烯基，C 2 -C 6炔基，C 3 -C 7 - 环烷基，C 3 -C 7 - 环烷基-C 1 -C 4 - 烷基，C 1 -C 6 - 烷氧基，C 2 -C 6 - 烯氧基，C 2 -C 6 - 炔氧基，C 1 -C 4烷氧基-C 1 -C 4烷氧基，C 3 -C 7 - 环烷基 - C 1 -C 6烷氧基，C（OH）（CF 3）2，C 1 -C 6卤代烷基，C 1 -C 6卤代烷氧基，C 1 -C 6烷硫基，C 1 -C 6卤代烷硫基，C 1 -C 6烷基亚磺酰基， C 1 -C 6烷基磺酰基，C 1 -C 6卤代烷基磺酰基，C（R a）-O，C（R a）-NOR b，C（-O）OR x或C（-O）NR x R y; R a是氢或C 1 -C 4 - 烷基; R b是氢，C 1 -C 4 - 烷基，C 2 -C 4 - 烯基，C 2 -C 4 - 炔基，C 1 -C 4卤代烷基或C 2 -C 4 - 卤代烯基; R x，R y各自独立地为氢，C 1 -C 4 - 烷基，C 1 -C 4 - 卤代烷基，C 1 -C 4 - 烷氧基-C 1 -C 4烷基，C 1 -C 4 - 硫代烷基-C 1 -C 4烷基，C 1 -C 4烷基 - S（-O）C 1 -C 4 - 烷基，C 1 -C 4烷基-S（-O）2 C 1 -C 4烷基，C 3 -C 6 - 环烷基，C 1 -C 4烷基-C 3 -C 6环烷基，C 3 -C 6 - 烯基，C 3 -C 6 - 炔基; R4，R5，R6，R7各自独立地为氢，卤素，氰基，氨基，硝基，羟基，C1-C6-烷基，C1-C6-烷氧基，C1-C6-卤代烷基，C1-C6-卤代烷氧基，C1-C6- C 1 -C 6烷基亚磺酰基，C 1 -C 6烷基磺酰基，C 1 -C 6卤代烷基磺酰基或C（-O）OR c; R c是氢，C 1 -C 6 - 烷基，C 2 -C 6 - 烯基或C 2 -C 6 - 炔基; m和n各自独立地为1,2,3,4或5; p是0，1，2，3，4或5; 及其N-氧化物，对映异构体，非对映异构体及其盐，制备化合物I的方法和中间体，化合物I用于防治昆虫，螨虫或线虫的用途，以及用于治疗，控制，预防或保护动物免受感染或 使用化合物I的寄生虫感染

    Fungicidal mixtures
    40.
    发明授权
    Fungicidal mixtures 失效
    杀菌混合物

    公开(公告)号：US06699874B2

    公开(公告)日：2004-03-02

    申请号：US10314594

    申请日：2002-12-10

    申请人： Henry Van Tuyl Cotter ,  Leslie May ,  Gunter Reichert ,  Ewald Sieverding

    发明人： Henry Van Tuyl Cotter ,  Leslie May ,  Gunter Reichert ,  Ewald Sieverding

    IPC分类号： A01N4354

    CPC分类号： A01N43/90 ,  A01N2300/00

    摘要： Fungicidal compositions comprising an acceptable carrier and/or surface active agent and synergistically effective amounts of (a) at least one azolopyrimidine of formula I  in which R1, R2, L1, L2 and L3 have the meaning given in claim 1; and (b) at least one fungicidal active ingredient selected from benomyl, carboxin, captan, chlorothalonil, copper oxychloride, cyprodinil, dimethomorph, dithianon, dodine, famoxadone, fenhexamid, fenpiclonil, fenpropimorph, fluazinam, mancozeb, metalaxyl, pyrimethanil, quinoxifen, sulfur, triforine, vinclozolin, a fungicidal triazole derivative, and a synthetic strobilurine derivative. The invention also provides a method of controlling the growth of phytopathogenic fungi at a locus by applying synergistically effective amounts of at least one azolopyrimidine of formula I and at least one fungicidal active ingredient (b) to the locus.

    摘要翻译： 包含可接受的载体和/或表面活性剂和协同有效量的（a）至少一种R 1，R 2，L 1，L 2和L 3的式Iin的偶氮嘧啶的杀真菌组合物 >具有权利要求1中给出的含义; 和（b）至少一种杀真菌活性成分，其选自苯菌灵，呋喃丹，克拉曼，百菌清，氯氧化铜，西酞替尼，烯酰吗啉，二噻吩，十二烷，恶唑酮，芬己酰，芬替尼，芬卡芬，氟啶胺，代森锰锌，甲霜灵，嘧霉胺，喹喔啉， ，triperine，长春菌素，杀真菌三唑衍生物和合成次溴酸衍生物。 本发明还提供了一种通过将协同有效量的至少一种式I的偶氮嘧啶和至少一种杀真菌活性成分（b）施用于该基因座来控制植物病原真菌在一个场所生长的方法。