公开(公告)号：US5260315A

公开(公告)日：1993-11-09

申请号：US887933

申请日：1992-05-26

申请人： Gerhard Bringmann ,  Martin Ruebenacker ,  Eberhard Ammermann ,  Gisela Lorenz ,  Laurent A. Assi

发明人： Gerhard Bringmann ,  Martin Ruebenacker ,  Eberhard Ammermann ,  Gisela Lorenz ,  Laurent A. Assi

IPC分类号： A01N43/42 ,  C07D217/02

CPC分类号： A01N43/42

摘要： Methods for combating fungi using dioncophylline A or dioncophylline B.

摘要翻译： 使用Dioncophylline A或Dioncophylline B对抗真菌的方法

公开(公告)号：US08530380B2

公开(公告)日：2013-09-10

申请号：US11322211

申请日：2005-12-30

申请人： Klaus Schelberger ,  Maria Scherer ,  Karl Eicken ,  Manfred Hampel ,  Eberhard Ammermann ,  Gisela Lorenz ,  Siegfried Strathmann

发明人： Klaus Schelberger ,  Maria Scherer ,  Karl Eicken ,  Manfred Hampel ,  Eberhard Ammermann ,  Gisela Lorenz ,  Siegfried Strathmann

IPC分类号： A01N25/26 ,  A01N43/40

CPC分类号： A01N43/40 ,  A01N47/34 ,  A01N47/12 ,  A01N43/76 ,  A01N43/08 ,  A01N37/46 ,  A01N37/38 ,  A01N37/36 ,  A01N2300/00

摘要： Fungicidal mixtures comprise as active components a) an amide compound of the formula I A-CO—NR1R2  I in which A, R1 and R2 are as defined in the description, and b) dimethomorph or flumetover, and/or c) a valinamide of the formula III in which R13 is C3-C4-alkyl and R14 is naphthyl or phenyl, where the phenyl radical is substituted in the 4-position by a halogen atom, a C1-C4-alkyl or C1-C4-alkoxy group, and/or d) benalaxyl, ofurace, metalaxyl, furalaxyl or oxydixyl, and/or e) 1-(2-cyano-2-methoxyiminoacetyl)-3-ethylurea in a synergistically effective amount.

摘要翻译： 杀真菌混合物包含作为活性组分的a）式I A-CO-NR1R2I的酰胺化合物，其中A，R 1和R 2如说明书中所定义，和b）烯酰吗啉或灭火剂，和/或c）缬氨酰胺 式中R 13为C 3 -C 4 - 烷基，R 14为萘基或苯基，其中苯基在4-位被卤素原子取代，C 1 -C 4 - 烷基或C 1 -C 4 - 烷氧基，和/ 或d）苯菌灵，海藻，甲霜灵，furalaxyl或oxydixyl，和/或e）1-（2-氰基-2-甲氧基亚氨基乙酰基）-3-乙基脲以协同有效量。

公开(公告)号：US08188001B2

公开(公告)日：2012-05-29

申请号：US12640423

申请日：2009-12-17

申请人： Eberhard Ammermann ,  Reinhard Stierl ,  Gisela Lorenz ,  Ulrich Schöfl ,  Siegfried Strathmann ,  Klaus Schelberger ,  Thomas Christen

发明人： Eberhard Ammermann ,  Reinhard Stierl ,  Gisela Lorenz ,  Ulrich Schöfl ,  Siegfried Strathmann ,  Klaus Schelberger ,  Thomas Christen

IPC分类号： A01N25/26 ,  A01N43/00 ,  A01N43/64 ,  A01N25/00

CPC分类号： A01N43/653 ,  A01N37/46 ,  A01N2300/00

摘要： The invention relates to a fungicidal mixture comprising prothioconazole or a salt or adduct thereof with an inorganic acid an organic acid or a metal ion; and at least one further fungicidal compound, selected from the group consisting of thiram, fenoxanil, benthivalicarb, metalaxyl, fludioxonil and prochloraz, in a synergistically effective amount and to methods for controlling harmful fungi, comprising applying the fungicidal mixture.

摘要翻译： 本发明涉及杀真菌混合物，其包含丙硫菌唑或其盐或其与无机酸有机酸或金属离子的加合物; 和至少一种选自下组的至少一种杀真菌化合物，所述化合物选自由以下组成的组：组合有效量的西他郎，芬诺尼，苦参碱，甲霜灵

公开(公告)号：US07449471B2

公开(公告)日：2008-11-11

申请号：US11677862

申请日：2007-02-22

申请人： Andreas Gypser ,  Thomas Grote ,  Anja Schwögler ,  Joachim Rheinheimer ,  Frank Schieweck ,  Jordi Tormo i Blasco ,  Ingo Rose ,  Peter Schäfer ,  Markus Gewehr ,  Wassilios Grammenos ,  Bernd Müller ,  Eberhard Ammermann ,  Siegfried Strathmann ,  Gisela Lorenz ,  Reinhard Stierl

发明人： Andreas Gypser ,  Thomas Grote ,  Anja Schwögler ,  Joachim Rheinheimer ,  Frank Schieweck ,  Jordi Tormo i Blasco ,  Ingo Rose ,  Peter Schäfer ,  Markus Gewehr ,  Wassilios Grammenos ,  Bernd Müller ,  Eberhard Ammermann ,  Siegfried Strathmann ,  Gisela Lorenz ,  Reinhard Stierl

IPC分类号： C07D239/42 ,  C07D239/30 ,  A61K31/505 ,  A61K31/506 ,  A01N43/54

CPC分类号： C07D239/42 ,  C07D239/47 ,  C07D239/48 ,  C07D239/52 ,  C07D403/12

摘要： 5-Phenylpyrimidines of the formula I in which the substituents and the index are as defined below: R1,R2 are hydrogen, alkyl, haloalkyl, cycloalkyl, halocycloalkyl, alkenyl, haloalkenyl, alkynyl or haloalkynyl, and R1 and R2 together with the nitrogen atom to which they are attached may also form a saturated or unsaturated ring which may be interrupted by an ether, thio, sulfoxyl or sulfonyl group and may be substituted by one to four groups Ra and/or Rb; R3 is hydrogen, halogen, cyano, alkyl, haloalkyl, alkoxy, haloalkoxy or alkenyloxy; R4 is hydrogen, halogen, cyano, hydroxyl, mercapto, azido, alkyl, alkenyl, alkynyl, haloalkyl, alkoxy, alkenyloxy, alkynyloxy, haloalkoxy, alkylthio, alkenylthio, alkynylthio, haloalkylthio, —ON═CRaRb, —CRc═NORa, —NRcN═CRaRb, —NRaRb, —NRcNRaRb, —NORa, —NRcC(═NRc′)NRaRb, —NRcC(═O)NRaRb, —NRaC(═O)Rc, —NRaC(═NORc)Rc′, —OC(═O)Rc, —C(═NORc)NRaRb, —CRc(═NNRaRb), —C (═O)NRaRb or —C(═O)Rc; in which Ra, Rb and Rc are as defined in the description; X is halogen, alkyl, alkoxy or haloalkyl; and m is an integer from 1 to 5 ; processes for preparing these compounds, compositions comprising them and their use for controlling harmful fungi are described.

公开(公告)号：US20080269171A1

公开(公告)日：2008-10-30

申请号：US11778784

申请日：2007-07-17

申请人： Eberhard Ammermann ,  Reinhard Stierl ,  Gisela Lorenz ,  Siegfried Strathmann ,  Klaus Schelberger ,  V. James Spadafora ,  Thomas Christen

发明人： Eberhard Ammermann ,  Reinhard Stierl ,  Gisela Lorenz ,  Siegfried Strathmann ,  Klaus Schelberger ,  V. James Spadafora ,  Thomas Christen

IPC分类号： A01N57/16 ,  A01N43/653 ,  A01N43/88 ,  A01P3/00

CPC分类号： A01N43/653 ,  A01N57/16 ,  A01N51/00 ,  A01N47/02 ,  A01N2300/00

摘要： A fungicidal mixture, comprising (1) 2-[2-(1-chlorocyclopropyl)-3-(2-chlorophenyl)-2-hydroxypropyl]-2,4-dihydro-[1,2,4]-triazole-3-thione (prothioconazole) of the formula I or its salts or adducts and at least one insecticide selected from the group consisting of (2) fipronil of the formula II (3) chlorpyrifos of the formula III (4) thiamethoxam of the formula IV in a synergistically effective amount is described.

摘要翻译： 一种杀真菌混合物，其包含（1）2- [2-（1-氯环丙基）-3-（2-氯苯基）-2-羟丙基] -2,4-二氢 - [1,2,4] 式（I）的硫酮（丙硫菌唑）或其盐或加合物和至少一种杀虫剂，其选自（2）式II（3）的氟虫腈式（Ⅳ）式Ⅳ的毒死蜱将式Ⅳ的噻虫嗪 描述协同有效量。

公开(公告)号：US07186861B2

公开(公告)日：2007-03-06

申请号：US10507605

申请日：2003-03-12

申请人： Wassilios Grammenos ,  Thomas Grote ,  Carsten Blettner ,  Markus Gewehr ,  Andreas Gypser ,  Bernd Müller ,  Joachim Rheinheimer ,  Peter Schäfer ,  Anja Schwögler ,  Jordi Tormo i Blasco ,  Norbert Götz ,  Gisela Lorenz ,  Eberhard Ammermann ,  Siegfried Strathmann ,  Reinhard Stierl

发明人： Wassilios Grammenos ,  Thomas Grote ,  Carsten Blettner ,  Markus Gewehr ,  Andreas Gypser ,  Bernd Müller ,  Joachim Rheinheimer ,  Peter Schäfer ,  Anja Schwögler ,  Jordi Tormo i Blasco ,  Norbert Götz ,  Gisela Lorenz ,  Eberhard Ammermann ,  Siegfried Strathmann ,  Reinhard Stierl

IPC分类号： C07C233/09 ,  A01N37/18

CPC分类号： C07C235/34 ,  A01N37/18 ,  A01N37/36 ,  A01N37/38 ,  C07C233/22 ,  C07C2601/02 ,  C07C2601/08 ,  C07C2601/14

摘要： Z-substituted acrylamides of formula (I), where the substituents have the following meanings: X═H, halogen, alkyl, haloalkyl, alkoxy, haloalkoxy, with X in the 3- or 4-position, n=1 or 2, where X can be different if n=2, R1=alkyl, haloalkyl, cycloalkyl, alkoxy, haloalkoxy, aziridine and oxirane and R2═H, alkyl, haloalkyl, allyl, propargyl or CH2C≡C-alkyl. Methods for production thereof, agents comprising the above and the use thereof for the treatment of plant-pathogenic fungal pests.

摘要翻译： 式（I）的Z-取代的丙烯酰胺，其中取代基具有以下含义：XH，卤素，烷基，卤代烷基，烷氧基，卤代烷氧基，其中X为3-或4-位，n = 1或2，其中X可以 如果n = 2，R 1 =烷基，卤代烷基，环烷基，烷氧基，卤代烷氧基，氮丙啶和环氧乙烷和R 2 -H，烷基，卤代烷基，烯丙基，炔丙基 或CH 2C≡C-烷基。 其制备方法，包含上述物质及其用于治疗植物致病性真菌害虫的用途。

公开(公告)号：US07094894B2

公开(公告)日：2006-08-22

申请号：US10513030

申请日：2003-04-30

申请人： Jordi Tormo i Blasco ,  Carsten Blettner ,  Bernd Müller ,  Markus Gewehr ,  Wassilios Grammenos ,  Thomas Grote ,  Andreas Gypser ,  Joachim Rheinheimer ,  Peter Schäfer ,  Frank Schieweck ,  Anja Schwögler ,  Eberhard Ammermann ,  Siegfried Strathmann ,  Gisela Lorenz ,  Reinhard Stierl

发明人： Jordi Tormo i Blasco ,  Carsten Blettner ,  Bernd Müller ,  Markus Gewehr ,  Wassilios Grammenos ,  Thomas Grote ,  Andreas Gypser ,  Joachim Rheinheimer ,  Peter Schäfer ,  Frank Schieweck ,  Anja Schwögler ,  Eberhard Ammermann ,  Siegfried Strathmann ,  Gisela Lorenz ,  Reinhard Stierl

IPC分类号： C07D487/04 ,  A01N43/90 ,  C07C69/618

CPC分类号： C07D487/04 ,  A01N43/90 ,  C07C69/65

摘要： Disclosed are a method for producing fungicidal triazolopyrimidine compounds, agents containing said compounds, and the use thereof for controlling harmful fungi. Also disclosed are triazolopyrimidines of formula (I), in which the substituents have the following meaning: L1 represents alkyl; L2 represents halogen; L3represents hydrogen or halogen; X represents halogen, cyano, alkyl, alkoxy, or haloalkoxy; R1, R2 represent hydrogen, alkyl, haloalkyl, cycloalkyl, alkenyl, alkadienyl, alkinyl, or cycloalkinyl, phenyl, naphthyl, or a five-unit to ten-unit saturated, partially unsaturated, or aromatic heterocycle containing one to four heteroatoms from the group O, N, or S, R1 and R2 can also form a five-unit or six-unit ring along with the nitrogen atom to which they are linked. Said ring can be interrupted and/or substituted by an atom from the group O, N, and S while R1 and/or R2 can be substituted according to the description. The invention also relates to methods and intermediate products for producing said compounds, agents containing said compounds, and the use thereof for controlling harmful fungi

摘要翻译： 公开了生产杀真菌三唑并嘧啶化合物的方法，含有所述化合物的试剂及其用于控制​​有害真菌的用途。 还公开了式（I）的三唑并嘧啶，其中取代基具有以下含义：L 1表示烷基; L 2表示卤素; L 3表示氢或卤素; X表示卤素，氰基，烷基，烷氧基或卤代烷氧基; R 1，R 2代表氢，烷基，卤代烷基，环烷基，烯基，链二烯基，炔基或环炔基，苯基，萘基或五个单元至十个单元 饱和的，部分不饱和的或含有一至四个O，N或S杂原子的杂环，R 1和R 2也可以形成五单元或 六单元环与它们所连接的氮原子一起。 所述环可以被O，N和S基团的原子中断和/或取代，而R 1和/或R 2可以根据描述被取代 。 本发明还涉及用于生产所述化合物的方法和中间产物，含有所述化合物的试剂及其用于控制​​有害真菌的用途

公开(公告)号：US07026315B1

公开(公告)日：2006-04-11

申请号：US09868515

申请日：1999-12-11

申请人： Klaus Schelberger ,  Maria Scherer ,  Reinhold Saur ,  Karl Eicken ,  Egon Haden ,  Eberhard Ammermann ,  Thomas Grote ,  Gisela Lorenz ,  Siegfried Strathmann

发明人： Klaus Schelberger ,  Maria Scherer ,  Reinhold Saur ,  Karl Eicken ,  Egon Haden ,  Eberhard Ammermann ,  Thomas Grote ,  Gisela Lorenz ,  Siegfried Strathmann

IPC分类号： A61K31/535 ,  A61K31/15 ,  A61K31/165 ,  A61K31/435 ,  A61K31/335

CPC分类号： A01N43/40 ,  A01N43/84 ,  A01N43/56 ,  A01N43/10 ,  A01N37/52 ,  A01N2300/00

摘要： Fungicidal mixtures, comprising as active components a) a morpholine or piperidine derivative I selected from the group of the compounds Ia, Ib, Ic and Id and b) compounds of the formula II in a synergistically effective amount are described.

摘要翻译： 包含作为活性组分的杀真菌混合物a）描述了选自化合物Ia，Ib，Ic和Id的吗啉或哌啶衍生物I和b）协同有效量的式II化合物。

公开(公告)号：US20050256138A1

公开(公告)日：2005-11-17

申请号：US10513030

申请日：2003-04-30

申请人： Jordi Tormo i Blasco ,  Carsten Blettner ,  Bernd Muller ,  Markus Gewhr ,  Wassilios Grammenos ,  Thomas Grote ,  Andreas Gypser ,  Joachim Rheinheimer ,  Peter Schafer ,  Frank Schieweck ,  Anja Schwogler ,  Eberhard Ammermann ,  Siegfried Strathmann ,  Gisela Lorenz ,  Reinhard Stierl

发明人： Jordi Tormo i Blasco ,  Carsten Blettner ,  Bernd Muller ,  Markus Gewhr ,  Wassilios Grammenos ,  Thomas Grote ,  Andreas Gypser ,  Joachim Rheinheimer ,  Peter Schafer ,  Frank Schieweck ,  Anja Schwogler ,  Eberhard Ammermann ,  Siegfried Strathmann ,  Gisela Lorenz ,  Reinhard Stierl

IPC分类号： A01N43/90 ,  C07C69/65 ,  C07D487/04 ,  A61K31/519

CPC分类号： C07D487/04 ,  A01N43/90 ,  C07C69/65

摘要： Disclosed are a method for producing fungicidal triazolopyrimidine compounds, agents containing said compounds, and the use thereof for controlling harmful fungi. Also disclosed are triazolopyrimidines of formula (1), in which the substituents have the following meaning: L1 represents alkyl; L2 represents halogen; L3represents hydrogen or halogen; X represents halogen, cyano, alkyl, alkoxy, or haloalkoxy; R1, R2 represent hydrogen, alkyl, haloalkyl, cycloalkyl, alkenyl, alkadienyl, alkinyl, or cycloalkinyl, phenyl, naphthyl, or a five-unit to ten-unit saturated, partially unsaturated, or aromatic heterocycle containing one to four heteroatoms from the group O, N, or S. R1 and R2 can also form a five-unit or six-unit ring along with the nitrogen atom to which they are linked. Said ring can be interrupted and/or substituted by an atom from the group O, N, and S while R1 and/or R2 can be substituted according to the description. The invention also relates to methods and intermediate products for producing said compounds, agents containing said compounds, and the use thereof for controlling harmful fungi.

摘要翻译： 公开了生产杀真菌三唑并嘧啶化合物的方法，含有所述化合物的试剂及其用于控制​​有害真菌的用途。 还公开了式（1）的三唑并嘧啶，其中取代基具有以下含义：L 1表示烷基; L 2表示卤素; L 3表示氢或卤素; X表示卤素，氰基，烷基，烷氧基或卤代烷氧基; R 1，R 2代表氢，烷基，卤代烷基，环烷基，烯基，链二烯基，炔基或环炔基，苯基，萘基或五个单元至十个单元 饱和的，部分不饱和的或芳族杂环，其含有一至四个O，N或S的杂原子.R 1和R 2也可以形成五单元或 六单元环与它们所连接的氮原子一起。 所述环可以被O，N和S基团的原子中断和/或取代，而R 1和/或R 2可以根据描述被取代 。 本发明还涉及用于生产所述化合物的方法和中间产物，含有所述化合物的试剂及其用于控制​​有害真菌的用途。

公开(公告)号：US20050187265A1

公开(公告)日：2005-08-25

申请号：US11061470

申请日：2005-02-22

申请人： Joachim Rheinheimer ,  Karl Eicken ,  Ingo Rose ,  Thomas Grote ,  Eberhard Ammermann ,  John-Bryan Speakman ,  Siegfried Strathmann ,  Gisela Lorenz

发明人： Joachim Rheinheimer ,  Karl Eicken ,  Ingo Rose ,  Thomas Grote ,  Eberhard Ammermann ,  John-Bryan Speakman ,  Siegfried Strathmann ,  Gisela Lorenz

IPC分类号： A61P31/10 ,  A01N37/52 ,  A61K31/165 ,  C07C259/14 ,  C07D333/22 ,  A61K31/381 ,  A61K31/415 ,  A61K31/44 ,  C07C259/10

CPC分类号： C07C259/14 ,  A01N37/52 ,  C07C2601/02

摘要： Novel benzamidoxime derivatives, processes and intermediates for their preparation and their use as fungicides are described. In the context of the present invention, benzamidoxime derivatives are compounds of the formula I where: A is an aryl or hetaryl radical; Y is a straight-chain or branched C1-C4-alkylene group, where one carbon can be replaced by oxygen, nitrogen or sulfur or by a cyclopropyl group; Rn1 are one to five identical or different radicals from the group consisting of: hydrogen, halogen, C1-C6-alkyl, C1-C6-alkoxy, C1-C4-haloalkyl, C1-C4-haloalkoxy, C1-C4-alkylthio, C1-C4-alkoxyalkoxy; R2 is unsubstituted or substituted phenyl-C1-C6-alkyl, thienyl-C1-C4-alkyl, or pyrazolyl-C1-C4-alkyl, Rp3 are one to five identical or different radicals from the group consisting of: hydrogen, halogen, C1-C6-alkyl, C1-C6-alkoxy, C1-C4-haloalkyl, C1-C4-haloalkoxy, C1-C4-alkylthio, C1-C4-alkoxyalkoxy, C1-C6-alkylcarbonyl; n is 0-5; p is, depending on the number of free valencies, 0-4.

摘要翻译： 描述了新的苯甲酰胺肟衍生物，其制备方法和中间体及其作为杀真菌剂的用途。 在本发明的上下文中，苯甲酰胺肟衍生物是式I的化合物，其中：A是芳基或杂芳基; Y是直链或支链C 1 -C 4 - 亚烷基，其中一个碳可被氧，氮或硫取代或被环丙基取代; R 1是与以下组成的组中的一至五个相同或不同的基团：氢，卤素，C 1 -C 6 C 1 -C 6烷基，C 1 -C 6 - 烷氧基，C 1 -C 4 - 卤代烷基 ，C 1 -C 4 - 卤代烷氧基，C 1 -C 4 - 烷硫基，C 1 -C 4 - 烷氧基烷氧基; R 2是未取代或取代的苯基-C 1 -C 6 - 烷基，噻吩基-C 1 -C 或 - 吡唑基-C 1 -C 4 - C 1-4 - 烷基，R 3 - （CH 3）3 - / SUP>是与由以下组成的组中的一至五个相同或不同的基团：氢，卤素，C 1 -C 6 - 烷基，C 1 - C 1 -C 6 - 烷氧基，C 1 -C 4 - 卤代烷基，C 1 -C 4 - 卤代烷氧基 C 1 -C 4 - 烷硫基，C 1 -C 4 - 烷氧基烷氧基，C 1 -C 4烷基硫基，C 1 -C 4 - -C 6 - 烷基羰基; n为0-5; p取决于自由价格的数量，0-4。