ES2656676T3 - Combinaciones de principios activos con propiedades insecticidas y acaricidas - Google Patents
Combinaciones de principios activos con propiedades insecticidas y acaricidas Download PDFInfo
- Publication number
- ES2656676T3 ES2656676T3 ES15184181.4T ES15184181T ES2656676T3 ES 2656676 T3 ES2656676 T3 ES 2656676T3 ES 15184181 T ES15184181 T ES 15184181T ES 2656676 T3 ES2656676 T3 ES 2656676T3
- Authority
- ES
- Spain
- Prior art keywords
- insecticidal
- combinations
- active ingredients
- acaricidal properties
- weight
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Active
Links
- 239000004480 active ingredient Substances 0.000 title description 7
- 230000000895 acaricidal effect Effects 0.000 title 1
- 230000000749 insecticidal effect Effects 0.000 title 1
- 230000009286 beneficial effect Effects 0.000 abstract description 5
- 241001465754 Metazoa Species 0.000 abstract description 3
- 241000607479 Yersinia pestis Species 0.000 abstract description 3
- 241000238876 Acari Species 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 238000011282 treatment Methods 0.000 description 8
- 230000000694 effects Effects 0.000 description 7
- 239000013543 active substance Substances 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 241000238631 Hexapoda Species 0.000 description 5
- 238000002360 preparation method Methods 0.000 description 5
- 239000002689 soil Substances 0.000 description 5
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- 241000196324 Embryophyta Species 0.000 description 4
- 239000003995 emulsifying agent Substances 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 244000141359 Malus pumila Species 0.000 description 3
- 235000011430 Malus pumila Nutrition 0.000 description 3
- 235000015103 Malus silvestris Nutrition 0.000 description 3
- PGOOBECODWQEAB-UHFFFAOYSA-N (E)-clothianidin Chemical compound [O-][N+](=O)\N=C(/NC)NCC1=CN=C(Cl)S1 PGOOBECODWQEAB-UHFFFAOYSA-N 0.000 description 2
- 241001425394 Anthocoris nemoralis Species 0.000 description 2
- 241001192596 Aphelinus mali Species 0.000 description 2
- 241001124076 Aphididae Species 0.000 description 2
- 241000131068 Coccinella septempunctata Species 0.000 description 2
- 241000917107 Eriosoma lanigerum Species 0.000 description 2
- 241000256244 Heliothis virescens Species 0.000 description 2
- 241000526145 Psylla Species 0.000 description 2
- 125000002877 alkyl aryl group Chemical group 0.000 description 2
- QXAITBQSYVNQDR-ZIOPAAQOSA-N amitraz Chemical compound C=1C=C(C)C=C(C)C=1/N=C/N(C)\C=N\C1=CC=C(C)C=C1C QXAITBQSYVNQDR-ZIOPAAQOSA-N 0.000 description 2
- 229960002587 amitraz Drugs 0.000 description 2
- 239000012141 concentrate Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 230000003071 parasitic effect Effects 0.000 description 2
- 229920000151 polyglycol Polymers 0.000 description 2
- 239000010695 polyglycol Substances 0.000 description 2
- 241000894007 species Species 0.000 description 2
- 230000009261 transgenic effect Effects 0.000 description 2
- 241001529600 Diabrotica balteata Species 0.000 description 1
- 241001057636 Dracaena deremensis Species 0.000 description 1
- 244000068988 Glycine max Species 0.000 description 1
- 235000010469 Glycine max Nutrition 0.000 description 1
- 241000721621 Myzus persicae Species 0.000 description 1
- 244000046052 Phaseolus vulgaris Species 0.000 description 1
- 235000010627 Phaseolus vulgaris Nutrition 0.000 description 1
- 240000001987 Pyrus communis Species 0.000 description 1
- 235000014443 Pyrus communis Nutrition 0.000 description 1
- 241000985245 Spodoptera litura Species 0.000 description 1
- 240000008042 Zea mays Species 0.000 description 1
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 1
- 235000005822 corn Nutrition 0.000 description 1
- 101150038956 cup-4 gene Proteins 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- XDDAORKBJWWYJS-UHFFFAOYSA-N glyphosate Chemical compound OC(=O)CNCP(O)(O)=O XDDAORKBJWWYJS-UHFFFAOYSA-N 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 230000024241 parasitism Effects 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N63/00—Biocides, pest repellants or attractants, or plant growth regulators containing microorganisms, viruses, microbial fungi, animals or substances produced by, or obtained from, microorganisms, viruses, microbial fungi or animals, e.g. enzymes or fermentates
- A01N63/10—Animals; Substances produced thereby or obtained therefrom
- A01N63/14—Insects
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
- A01N43/36—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom five-membered rings
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/90—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/02—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having no bond to a nitrogen atom
- A01N47/06—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having no bond to a nitrogen atom containing —O—CO—O— groups; Thio analogues thereof
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Zoology (AREA)
- General Health & Medical Sciences (AREA)
- Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Dentistry (AREA)
- Plant Pathology (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Environmental Sciences (AREA)
- Insects & Arthropods (AREA)
- Biotechnology (AREA)
- Microbiology (AREA)
- Virology (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Uso del compuesto de fórmula (1-4)**Fórmula** en combinación con organismos beneficiosos de la familia de los ácaros depredadores (Phytoseidae) para combatir plagas animales.
Description
- Tabla B Insectos dañinos para las plantas Ensayo de Myzus persicae
- Principio activo Ej. 1-4’
- 4 Concentración en ppm o en % Número de animales Mortalidad después de 7d 10
- Coccinella septempunctata
- 1
- 10
Ej. I-4’ + Coccinella septempunctata enc.* calc..** 4 + 1 animal 70 19
* enc. = efecto encontrado ** calc. = efecto calculado según la fórmula de Colby
Se tratan cada tres manzanos de aproximadamente 25 años (aprox. 2 m de altura de copa) de la variedad "Elan" en tres repeticiones contra pulgones del manzano, Eriosoma lanigerum. A este respecto, se ensayan comparativamente el principio activo (1-4’) (150OD) y el patrón comercial clotianidina (WG 50) en las cantidades de aplicación dadas en presencia de avispa parásita de pulgones del manzano (organismo beneficioso) Aphelinus mali. Se realiza la
10 aplicación con un aparato atomizador (Atomizer) con una cantidad de aplicación de agua de 500 l/Ha. Se llevan a cabo tanto solo una como dos aplicaciones en el intervalo de 34 días.
Se realiza la valoración 7, 30, 44, 52, 59, 66 y 73 días después del primer tratamiento, valorando la mortalidad de las plagas adultas y el número de plagas parásitas cada 10 colonias según Abbott. A este respecto, se compara el principio activo (I-4’) después de solo un tratamiento con el patrón después de dos tratamientos, ya que el principio
15 activo (I-4’) muestra un efecto de un 100% después de dos tratamientos y por tanto no se proporcionaría alimento (presas) para el organismo beneficioso.
- Cantidades de aplicación
- Efecto (% Abbott) Eriosoma lanigerum
- g/Ha/m de altura de copa
- 7 d 30 d 44 d 52 d 59 d 66 d 73 d
- Clotianidina 37,5
- 71 76 85 [81,8] [81,8] 80 80
- (I-4´) 75
- 48 95 99 99,4 98,2 98 98
- Agua de control
- 0 0 0 0 0 0 0
- Cantidades de aplicación
- Parasitismo por los organismos beneficiosos (%) Aphelinus mali
- g/Ha/m de altura de copa
- 7 d 30 d 44 d 52 d 59 d 66 d 73 d
- Clotianidina 37,5
- 0 0 0 [1] 10 24 50
- (I-4´) 75
- 0 0 0 - 35 54 90
- Agua de control
- 0 0 [1] 3 51 75 97
20 Se tratan perales de aprox 3 m de altura de la variedad "Conference" con 4 repeticiones contra sila, Psylla piri. A este respecto, se emplean el principio activo (I-4’) (100OD) y el patrón comercial Amitraz (UL 400) en las cantidades de aplicación dadas. Se realiza la aplicación con una mochila de pulverización con la que se han aplicado 1000 l/ha de agua. El organismo beneficioso Anthocoris nemoralis apareció 14 días después del tratamiento
Se realiza la valoración 4, 8 y 14 días después del tratamiento, valorando la mortalidad de las ninfas L-1 y las ninfas 25 L-4 sobre las ramas.
9
- Cantidad de aplicación
- Efecto (% Abbott) Psylla piri Número Anthocoris nemoralis
- g/Ha/m altura de
- L-1 L-4 L-1 L-4 L-1 L-4
- copa
- 4 d 4 d 8 d 8 d 14 d 14 d 4 d 8 d 14 d
- Amitraz 400
- 23,6 0,0 41,0 44,6 41,8 44,4 5
- (I-4’) 75
- 62,7 91,4 69,5 98,4 76,6 99,3 12
- Controles
- 0 0 15
Ensayo de concentración límite/insectos de suelo -Tratamiento de plantas transgénicas
5 Insecto de ensayo: Diabrotica balteata -Larvas en suelo
Disolvente: 7 partes en peso de acetona
Emulsionante: 1 parte en peso de alquilarilpoliglicoléter
Para la fabricación de un preparado de principio activo conveniente, se mezcla 1 parte en peso de principio activo con la cantidad dada de disolvente, se añade la cantidad dada de emulsionante y se diluye el concentrado con agua 10 a la concentración deseada.
Se vierte el preparado de principio activo en el suelo. A este respecto, la concentración del principio activo en el preparado no desempeña prácticamente ningún papel, solo es decisiva la cantidad de principio activo en peso por unidad de volumen de suelo, que se da en ppm (mg/l). Se rellenan con el suelo macetas de 0,25 l y se dejan reposar éstas a 20 ºC.
15 Inmediatamente después de la mezcla de reacción, se disponen en cada maceta 5 granos de maíz pregerminados de la especie YIELD GUARD (marca comercial de Monsanto Comp., EE.UU.). Después de 2 días, se disponen en los suelos tratados los correspondientes insectos de prueba. Después de otros 7 días, se determina el grado de efecto del principio activo mediante recuento de las plantas de maíz crecidas (1 planta = 20% de efecto).
Ejemplo E (no de acuerdo con la invención) 20 Ensayo de Heliothis virescens -Tratamiento de plantas transgénicas
Disolvente: 7 partes en peso de acetona Emulsionante: 1 parte en peso de alquilarilpoliglicoléter Para la fabricación de un preparado de principio activo conveniente, se mezcla 1 parte en peso de principio activo
con la cantidad dada de disolvente, se añade la cantidad dada de emulsionante y se diluye el concentrado con agua 25 a la concentración deseada. Se tratan brotes de soja (Glycine max) de la especie Roundup Ready (marca comercial de Monsanto Comp. EE.UU.)
mediante inmersión en el preparado de principio activo de la concentración deseada, y se aplica la oruga del tabaco Heliothis virescens mientras las hojas sigan húmedas. Después del tiempo deseado, se determina la mortalidad de los insectos.
30
10
Claims (1)
-
imagen1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102006027731A DE102006027731A1 (de) | 2006-06-16 | 2006-06-16 | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| DE102006027731 | 2006-06-16 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2656676T3 true ES2656676T3 (es) | 2018-02-28 |
Family
ID=38608409
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES07725831.7T Active ES2560090T3 (es) | 2006-06-16 | 2007-06-05 | Combinaciones de principios activos con propiedades insecticidas y acaricidas |
| ES15184181.4T Active ES2656676T3 (es) | 2006-06-16 | 2007-06-05 | Combinaciones de principios activos con propiedades insecticidas y acaricidas |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES07725831.7T Active ES2560090T3 (es) | 2006-06-16 | 2007-06-05 | Combinaciones de principios activos con propiedades insecticidas y acaricidas |
Country Status (17)
| Country | Link |
|---|---|
| US (2) | US8211931B2 (es) |
| EP (2) | EP2040553B1 (es) |
| JP (1) | JP5220735B2 (es) |
| KR (1) | KR101395725B1 (es) |
| CN (1) | CN101466268B (es) |
| AU (1) | AU2007260347C1 (es) |
| BR (1) | BRPI0712970A2 (es) |
| DE (1) | DE102006027731A1 (es) |
| ES (2) | ES2560090T3 (es) |
| IL (2) | IL195498A (es) |
| MA (1) | MA30572B1 (es) |
| MX (1) | MX2008015839A (es) |
| PL (2) | PL3001905T3 (es) |
| PT (2) | PT3001905T (es) |
| TW (1) | TW200814926A (es) |
| WO (1) | WO2007144086A1 (es) |
| ZA (1) | ZA200810455B (es) |
Families Citing this family (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102004053192A1 (de) * | 2004-11-04 | 2006-05-11 | Bayer Cropscience Ag | 2-Alkoxy-6-alkyl-phenyl substituierte spirocyclische Tetramsäure-Derivate |
| DE102006027730A1 (de) * | 2006-06-16 | 2007-12-20 | Bayer Cropscience Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| DE102006027731A1 (de) | 2006-06-16 | 2007-12-20 | Bayer Cropscience Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| DE102006027732A1 (de) * | 2006-06-16 | 2008-01-10 | Bayer Cropscience Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| DE102006031978A1 (de) * | 2006-07-11 | 2008-01-17 | Bayer Cropscience Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| DE102006033154A1 (de) | 2006-07-18 | 2008-01-24 | Bayer Cropscience Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| DE102006057037A1 (de) * | 2006-12-04 | 2008-06-05 | Bayer Cropscience Ag | cis-Alkoxyspirocyclische biphenylsubstituierte Tetramsäure-Derivate |
| EP2011394A1 (de) * | 2007-07-03 | 2009-01-07 | Bayer CropScience AG | Verwendung von Tetramsäure - Derivaten zur Bekämpfung von virusübertragenden Vektoren |
| US8389443B2 (en) * | 2008-12-02 | 2013-03-05 | Bayer Cropscience Ag | Geminal alkoxy/alkylspirocyclic substituted tetramate derivatives |
| US8846946B2 (en) | 2008-12-02 | 2014-09-30 | Bayer Cropscience Ag | Germinal alkoxy/alkylspirocyclic substituted tetramate derivatives |
| US20100243524A1 (en) * | 2009-03-31 | 2010-09-30 | Powers Donald H | Processing of acid containing hydrocarbons |
| US20100243523A1 (en) * | 2009-03-31 | 2010-09-30 | Powers Donald H | Processing of acid containing hydrocarbons |
| WO2010127787A2 (de) * | 2009-05-07 | 2010-11-11 | Bayer Cropscience Ag | Wirkstoffkombinationen mit insektiziden und akariziden eigenschaften |
| CN102480946A (zh) * | 2009-06-03 | 2012-05-30 | 拜尔农作物科学股份公司 | 氟虫双酰胺和有益生物的结合物 |
| KR20120099396A (ko) * | 2009-09-09 | 2012-09-10 | 바이엘 크롭사이언스 아게 | 식물병원성 박테리아를 구제하기 위한 사이클릭 케토에놀의 용도 |
Family Cites Families (73)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1147374A (en) | 1914-05-11 | 1915-07-20 | Wash Coe | Chimney-lining apparatus. |
| US4985063A (en) | 1988-08-20 | 1991-01-15 | Bayer Aktiengesellschaft | 3-aryl-pyrrolidine-2,4-diones |
| ES2063108T3 (es) | 1989-01-07 | 1995-01-01 | Bayer Ag | Derivados de 3-aril-pirrolidin-2,4-diona. |
| DE3929087A1 (de) | 1989-09-01 | 1991-03-07 | Bayer Ag | 3-aryl-pyrrolidin-2,4-dion-derivate |
| DE4032090A1 (de) | 1990-02-13 | 1991-08-14 | Bayer Ag | Polycyclische 3-aryl-pyrrolidin-2,4-dion-derivate |
| DE4004496A1 (de) | 1990-02-14 | 1991-08-22 | Bayer Ag | 3-aryl-pyrrolidin-2,4-dion-derivate |
| DE4107394A1 (de) | 1990-05-10 | 1991-11-14 | Bayer Ag | 1-h-3-aryl-pyrrolidin-2,4-dion-derivate |
| US5107046A (en) | 1990-05-23 | 1992-04-21 | Mallinckrodt Specialty Chemicals Co., Inc. | Process for preparing aromatic fluorides |
| US5811374A (en) | 1991-02-07 | 1998-09-22 | Bayer Aktiengesellschaft | 3-aryl-pyrrolidine-2,4-dione derivatives |
| DE4121365A1 (de) | 1991-06-28 | 1993-01-14 | Bayer Ag | Substituierte 1-h-3-aryl-pyrrolidin-2,4-dion-derivate |
| DE4216814A1 (de) | 1991-07-16 | 1993-01-21 | Bayer Ag | 3-aryl-4-hydroxy-(delta)(pfeil hoch)3(pfeil hoch)-dihydrofuranon- und 3-aryl-4-hydroxy-(delta)(pfeil hoch)3(pfeil hoch)-dihydrothiophenon-derivate |
| US5504913A (en) * | 1992-05-14 | 1996-04-02 | Apple Computer, Inc. | Queue memory with self-handling addressing and underflow |
| AU666040B2 (en) | 1992-10-28 | 1996-01-25 | Bayer Aktiengesellschaft | Substituted 1-H-3-aryl-pyrrolidine-2,4-dione derivatives |
| DE4306259A1 (de) | 1993-03-01 | 1994-09-08 | Bayer Ag | Dialkyl-1-H-3-(2,4-dimethylphenyl)-pyrrolidin-2,4-dione, ihre Herstellung und ihre Verwendung |
| WO1995001971A1 (de) | 1993-07-05 | 1995-01-19 | Bayer Aktiengesellschaft | Substituierte aryl-ketoenolheterocyclen |
| WO1995001997A1 (en) | 1993-07-09 | 1995-01-19 | Smithkline Beecham Corporation | RECOMBINANT AND HUMANIZED IL-1β ANTIBODIES FOR TREATMENT OF IL-1 MEDIATED INFLAMMATORY DISORDERS IN MAN |
| DE4425617A1 (de) | 1994-01-28 | 1995-08-03 | Bayer Ag | 1-H-3-Aryl-pyrrolidin-2,4-dion-Derivate |
| DE4431730A1 (de) | 1994-02-09 | 1995-08-10 | Bayer Ag | Substituierte 1H-3-Aryl-pyrrolidin-2,4-dion-Derivate |
| AU2072695A (en) | 1994-04-05 | 1995-10-23 | Bayer Aktiengesellschaft | Alkoxy-alkyl-substituted 1-h-3-aryl-pyrrolidine-2,4-diones used as herbicides and pesticides |
| AU4715896A (en) | 1995-02-13 | 1996-09-04 | Bayer Aktiengesellschaft | 2-phenyl-substituted heterocyclic 1,3-ketonols as herbicides and pesticides |
| AU5762696A (en) | 1995-05-09 | 1996-11-29 | Bayer Aktiengesellschaft | Alkyl dihalogenated phenyl-substituted ketoenols useful as p esticides and herbicides |
| JP4082724B2 (ja) | 1995-06-28 | 2008-04-30 | バイエル・アクチエンゲゼルシヤフト | 有害生物防除剤及び除草剤として使用される２，４，５−三置換されたフェニルケト−エノール |
| EP0835243B1 (de) | 1995-06-30 | 2003-01-29 | Bayer CropScience AG | Dialkyl-halogenphenylsubstituierte ketoenole zur verwendung als herbizide und pestizide |
| BR9708425B1 (pt) | 1996-04-02 | 2012-02-22 | fenilcetoenóis substituìdos, processo para preparação e uso dos mesmos, bem como pesticidas ou herbicidas e método para controle de pragas e ervas daninhas. | |
| JP4306799B2 (ja) | 1996-05-10 | 2009-08-05 | バイエル アクチェンゲゼルシャフト | 新規な置換ピリジルケトエノール |
| JP4202423B2 (ja) | 1996-08-05 | 2008-12-24 | バイエル・アクチエンゲゼルシヤフト | ２―および２，５―置換フェニルケトエノール |
| DE19632126A1 (de) | 1996-08-09 | 1998-02-12 | Bayer Ag | Phenylsubstituierte cyclische Ketoenole |
| DE19651686A1 (de) | 1996-12-12 | 1998-06-18 | Bayer Ag | Neue substituierte Phenylketoenole |
| DE19742492A1 (de) | 1997-09-26 | 1999-04-01 | Bayer Ag | Spirocyclische Phenylketoenole |
| DE19749720A1 (de) | 1997-11-11 | 1999-05-12 | Bayer Ag | Neue substituierte Phenylketoenole |
| DE19808261A1 (de) | 1998-02-27 | 1999-10-28 | Bayer Ag | Arylphenylsubstituierte cyclische Ketoenole |
| DE19813354A1 (de) | 1998-03-26 | 1999-09-30 | Bayer Ag | Arylphenylsubstituierte cyclische Ketoenole |
| DE19818732A1 (de) | 1998-04-27 | 1999-10-28 | Bayer Ag | Arylphenylsubstituierte cyclische Ketoenole |
| CZ299375B6 (cs) | 1998-11-30 | 2008-07-09 | Nihon Nohyaku Co., Ltd. | Ftalamidové deriváty nebo jejich soli, zemedelsko-zahradnický insekticid je obsahující a jeho použití |
| JP4122475B2 (ja) * | 1998-11-30 | 2008-07-23 | 日本農薬株式会社 | フタラミド誘導体又はその塩類及び農園芸用殺虫剤並びにその使用方法 |
| DE19935963A1 (de) | 1999-07-30 | 2001-02-01 | Bayer Ag | Biphenylsubstituierte cyclische Ketoenole |
| CN1272324C (zh) | 1999-09-07 | 2006-08-30 | 辛根塔参与股份公司 | 新颖的除草剂 |
| DE19946625A1 (de) | 1999-09-29 | 2001-04-05 | Bayer Ag | Trifluormethylsubstituierte spirocyclische Ketoenole |
| DE10016544A1 (de) | 2000-04-03 | 2001-10-11 | Bayer Ag | C2-phenylsubstituierte Ketoenole |
| DE10139465A1 (de) | 2001-08-10 | 2003-02-20 | Bayer Cropscience Ag | Selektive Herbizide auf Basis von substituierten, cayclischen Ketoenolen und Safenern |
| DE10231333A1 (de) | 2002-07-11 | 2004-01-22 | Bayer Cropscience Ag | Cis-Alkoxysubstituierte spirocyclische 1-H-Pyrrolidin-2,4-dion-Derivate |
| KR20050018961A (ko) * | 2002-07-11 | 2005-02-28 | 바이엘 크롭사이언스 아게 | 살해충제로 작용하는 시스-알콕시-치환된 스피로사이클릭1-ｈ-피롤리딘-2,4-디온-유도체 |
| DE10239479A1 (de) | 2002-08-28 | 2004-03-04 | Bayer Cropscience Ag | Substituierte spirocyclische Ketoenole |
| DE10301804A1 (de) | 2003-01-20 | 2004-07-29 | Bayer Cropscience Ag | 2,4-Dihalogen-6-(C2-C3-alkyl)-phenyl substituierte Tetramsäure-Derivate |
| DE10311300A1 (de) | 2003-03-14 | 2004-09-23 | Bayer Cropscience Ag | 2,4,6-Phenylsubstituierte cyclische Ketoenole |
| DE10326386A1 (de) | 2003-06-12 | 2004-12-30 | Bayer Cropscience Ag | N-Heterocyclyl-phenylsubstituierte cyclische Ketoenole |
| DE10330723A1 (de) | 2003-07-08 | 2005-02-03 | Bayer Cropscience Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| DE10330724A1 (de) | 2003-07-08 | 2005-01-27 | Bayer Cropscience Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| DE10351646A1 (de) | 2003-11-05 | 2005-06-09 | Bayer Cropscience Ag | 2-Halogen-6-alkyl-phenyl substituierte spirocyclische Tetramsäure-Derivate |
| DE10351647A1 (de) | 2003-11-05 | 2005-06-09 | Bayer Cropscience Ag | 2-Halogen-6-alkyl-phenyl substituierte Tetramsäure-Derivate |
| WO2005049596A1 (en) | 2003-11-20 | 2005-06-02 | Natco Pharma Limited | A process for the preparation of high purity escitalopram |
| DE10354628A1 (de) | 2003-11-22 | 2005-06-16 | Bayer Cropscience Ag | 2-Ethyl-4,6-dimethyl-phenyl-substituierte Tetramsäure-Derivate |
| DE10354629A1 (de) | 2003-11-22 | 2005-06-30 | Bayer Cropscience Ag | 2-Ethyl-4,6-dimethyl-phenyl substituierte spirocyclische Tetramsäure-Derivate |
| US8821898B2 (en) | 2003-12-04 | 2014-09-02 | Bayer Cropscience Ag | Active compound combinations having insecticidal and acaricidal properties |
| DE102004001433A1 (de) | 2004-01-09 | 2005-08-18 | Bayer Cropscience Ag | cis-Alkoxyspiro-substituierte Tetramsäure-Derivate |
| DE102004011006A1 (de) | 2004-03-06 | 2005-09-22 | Bayer Cropscience Ag | Suspensionskonzentrate auf Ölbasis |
| DE102004014620A1 (de) | 2004-03-25 | 2005-10-06 | Bayer Cropscience Ag | 2,4,6-phenylsubstituierte cyclische Ketoenole |
| DE102004030753A1 (de) | 2004-06-25 | 2006-01-19 | Bayer Cropscience Ag | 3'-Alkoxy spirocyclische Tetram- und Tretronsäuren |
| DE102004035133A1 (de) | 2004-07-20 | 2006-02-16 | Bayer Cropscience Ag | Selektive Insektizide auf Basis von substituierten, cyclischen Ketoenolen und Safenern |
| DE102004041529A1 (de) | 2004-08-27 | 2006-03-02 | Bayer Cropscience Gmbh | Herbizid-Kombinationen mit speziellen Ketoenolen |
| DE102004044827A1 (de) | 2004-09-16 | 2006-03-23 | Bayer Cropscience Ag | Jod-phenylsubstituierte cyclische Ketoenole |
| DE102004053191A1 (de) | 2004-11-04 | 2006-05-11 | Bayer Cropscience Ag | 2,6-Diethyl-4-methyl-phenyl substituierte Tetramsäure-Derivate |
| DE102004053192A1 (de) | 2004-11-04 | 2006-05-11 | Bayer Cropscience Ag | 2-Alkoxy-6-alkyl-phenyl substituierte spirocyclische Tetramsäure-Derivate |
| DE102005003076A1 (de) | 2005-01-22 | 2006-07-27 | Bayer Cropscience Ag | Verwendung von Tetramsäurederivaten zur Bekämpfung von Insekten aus der Gattung der Pflanzenläuse (Sternorrhyncha) |
| DE102005008033A1 (de) | 2005-02-22 | 2006-08-24 | Bayer Cropscience Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| DE102005008021A1 (de) | 2005-02-22 | 2006-08-24 | Bayer Cropscience Ag | Spiroketal-substituierte cyclische Ketoenole |
| US20070029252A1 (en) * | 2005-04-12 | 2007-02-08 | Dunson James B Jr | System and process for biomass treatment |
| DE102005051325A1 (de) | 2005-10-27 | 2007-05-03 | Bayer Cropscience Ag | Alkoxyalkyl spirocyclische Tetram- und Tetronsäuren |
| DE102006007882A1 (de) | 2006-02-21 | 2007-08-30 | Bayer Cropscience Ag | Cycloalkyl-phenylsubstituierte cyclische Ketoenole |
| DE102006025874A1 (de) | 2006-06-02 | 2007-12-06 | Bayer Cropscience Ag | Alkoxyalkyl-substituierte cyclische Ketoenole |
| DE102006027731A1 (de) | 2006-06-16 | 2007-12-20 | Bayer Cropscience Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| DE102006027732A1 (de) | 2006-06-16 | 2008-01-10 | Bayer Cropscience Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| DE102006027730A1 (de) | 2006-06-16 | 2007-12-20 | Bayer Cropscience Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
-
2006
- 2006-06-16 DE DE102006027731A patent/DE102006027731A1/de not_active Withdrawn
-
2007
- 2007-06-05 EP EP07725831.7A patent/EP2040553B1/de active Active
- 2007-06-05 CN CN2007800222861A patent/CN101466268B/zh not_active Expired - Fee Related
- 2007-06-05 PL PL15184181T patent/PL3001905T3/pl unknown
- 2007-06-05 KR KR1020097000776A patent/KR101395725B1/ko not_active Expired - Fee Related
- 2007-06-05 WO PCT/EP2007/004963 patent/WO2007144086A1/de not_active Ceased
- 2007-06-05 PL PL07725831T patent/PL2040553T3/pl unknown
- 2007-06-05 MX MX2008015839A patent/MX2008015839A/es active IP Right Grant
- 2007-06-05 ES ES07725831.7T patent/ES2560090T3/es active Active
- 2007-06-05 BR BRPI0712970-0A patent/BRPI0712970A2/pt not_active Application Discontinuation
- 2007-06-05 EP EP15184181.4A patent/EP3001905B1/de active Active
- 2007-06-05 US US12/304,904 patent/US8211931B2/en not_active Expired - Fee Related
- 2007-06-05 AU AU2007260347A patent/AU2007260347C1/en not_active Ceased
- 2007-06-05 ES ES15184181.4T patent/ES2656676T3/es active Active
- 2007-06-05 JP JP2009514667A patent/JP5220735B2/ja not_active Expired - Fee Related
- 2007-06-05 PT PT151841814T patent/PT3001905T/pt unknown
- 2007-06-05 PT PT77258317T patent/PT2040553E/pt unknown
- 2007-06-15 TW TW096121632A patent/TW200814926A/zh unknown
-
2008
- 2008-11-25 IL IL195498A patent/IL195498A/en active IP Right Grant
- 2008-12-10 ZA ZA2008/10455A patent/ZA200810455B/en unknown
-
2009
- 2009-01-06 MA MA31547A patent/MA30572B1/fr unknown
-
2012
- 2012-05-30 US US13/483,134 patent/US8658688B2/en not_active Expired - Fee Related
- 2012-12-09 IL IL223507A patent/IL223507A/en active IP Right Grant
Also Published As
| Publication number | Publication date |
|---|---|
| US20100048661A1 (en) | 2010-02-25 |
| KR101395725B1 (ko) | 2014-05-21 |
| IL195498A0 (en) | 2009-09-01 |
| EP3001905B1 (de) | 2017-11-01 |
| BRPI0712970A2 (pt) | 2013-04-02 |
| US8211931B2 (en) | 2012-07-03 |
| US20120237609A1 (en) | 2012-09-20 |
| PL2040553T3 (pl) | 2016-03-31 |
| CN101466268B (zh) | 2013-03-13 |
| MA30572B1 (fr) | 2009-07-01 |
| EP2040553B1 (de) | 2015-10-28 |
| PL3001905T3 (pl) | 2018-03-30 |
| JP2009539898A (ja) | 2009-11-19 |
| AU2007260347A1 (en) | 2007-12-21 |
| JP5220735B2 (ja) | 2013-06-26 |
| US8658688B2 (en) | 2014-02-25 |
| EP2040553A1 (de) | 2009-04-01 |
| MX2008015839A (es) | 2009-01-09 |
| IL223507A0 (en) | 2013-02-03 |
| AU2007260347B2 (en) | 2013-09-12 |
| AU2007260347C1 (en) | 2014-04-03 |
| KR20090023484A (ko) | 2009-03-04 |
| ZA200810455B (en) | 2010-02-24 |
| IL195498A (en) | 2013-07-31 |
| EP3001905A1 (de) | 2016-04-06 |
| PT3001905T (pt) | 2018-01-25 |
| IL223507A (en) | 2015-11-30 |
| CN101466268A (zh) | 2009-06-24 |
| PT2040553E (pt) | 2016-02-25 |
| DE102006027731A1 (de) | 2007-12-20 |
| TW200814926A (en) | 2008-04-01 |
| ES2560090T3 (es) | 2016-02-17 |
| WO2007144086A1 (de) | 2007-12-21 |
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