AR051096A1 - Cetoenoles ciclicos substituidos por yodo-fenilo - Google Patents
Cetoenoles ciclicos substituidos por yodo-feniloInfo
- Publication number
- AR051096A1 AR051096A1 ARP050103913A ARP050103913A AR051096A1 AR 051096 A1 AR051096 A1 AR 051096A1 AR P050103913 A ARP050103913 A AR P050103913A AR P050103913 A ARP050103913 A AR P050103913A AR 051096 A1 AR051096 A1 AR 051096A1
- Authority
- AR
- Argentina
- Prior art keywords
- substituted
- appropriate
- alkyl
- halogen
- mean
- Prior art date
Links
- 125000000217 alkyl group Chemical group 0.000 abstract 15
- 229910052739 hydrogen Inorganic materials 0.000 abstract 11
- 239000001257 hydrogen Substances 0.000 abstract 11
- 229910052736 halogen Inorganic materials 0.000 abstract 9
- 150000002367 halogens Chemical class 0.000 abstract 9
- 125000004183 alkoxy alkyl group Chemical group 0.000 abstract 7
- 125000003545 alkoxy group Chemical group 0.000 abstract 7
- 125000005842 heteroatom Chemical group 0.000 abstract 7
- 150000002431 hydrogen Chemical class 0.000 abstract 6
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 6
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 5
- 125000003342 alkenyl group Chemical group 0.000 abstract 5
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 5
- 229920006395 saturated elastomer Polymers 0.000 abstract 5
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 4
- 229910052760 oxygen Inorganic materials 0.000 abstract 4
- 239000001301 oxygen Substances 0.000 abstract 4
- 229910052717 sulfur Inorganic materials 0.000 abstract 4
- 239000011593 sulfur Substances 0.000 abstract 4
- 125000006350 alkyl thio alkyl group Chemical group 0.000 abstract 3
- 125000003118 aryl group Chemical group 0.000 abstract 3
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 3
- 125000001072 heteroaryl group Chemical group 0.000 abstract 3
- 125000004414 alkyl thio group Chemical group 0.000 abstract 2
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 2
- 125000004429 atom Chemical group 0.000 abstract 2
- 229910052799 carbon Inorganic materials 0.000 abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 125000004438 haloalkoxy group Chemical group 0.000 abstract 2
- 125000001188 haloalkyl group Chemical group 0.000 abstract 2
- 239000004009 herbicide Substances 0.000 abstract 2
- 125000005346 substituted cycloalkyl group Chemical group 0.000 abstract 2
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 abstract 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 abstract 1
- 125000005108 alkenylthio group Chemical group 0.000 abstract 1
- 125000003282 alkyl amino group Chemical group 0.000 abstract 1
- 125000000304 alkynyl group Chemical group 0.000 abstract 1
- 125000000051 benzyloxy group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])O* 0.000 abstract 1
- 244000038559 crop plants Species 0.000 abstract 1
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 1
- 125000004122 cyclic group Chemical group 0.000 abstract 1
- 125000005366 cycloalkylthio group Chemical group 0.000 abstract 1
- 125000004663 dialkyl amino group Chemical group 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- 239000013067 intermediate product Substances 0.000 abstract 1
- 229910052740 iodine Inorganic materials 0.000 abstract 1
- 239000011630 iodine Substances 0.000 abstract 1
- 229910021645 metal ion Inorganic materials 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 abstract 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 1
- 230000000361 pesticidal effect Effects 0.000 abstract 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 abstract 1
- 125000005359 phenoxyalkyl group Chemical group 0.000 abstract 1
- 125000003884 phenylalkyl group Chemical group 0.000 abstract 1
- 125000003356 phenylsulfanyl group Chemical group [*]SC1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/34—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D307/56—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D307/60—Two oxygen atoms, e.g. succinic anhydride
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C233/00—Carboxylic acid amides
- C07C233/01—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C233/45—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by carboxyl groups
- C07C233/52—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by carboxyl groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by a carbon atom of a ring other than a six-membered aromatic ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C235/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms
- C07C235/02—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to acyclic carbon atoms and singly-bound oxygen atoms bound to the same carbon skeleton
- C07C235/32—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to acyclic carbon atoms and singly-bound oxygen atoms bound to the same carbon skeleton the carbon skeleton containing six-membered aromatic rings
- C07C235/36—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to acyclic carbon atoms and singly-bound oxygen atoms bound to the same carbon skeleton the carbon skeleton containing six-membered aromatic rings having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a ring other than a six-membered aromatic ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C57/00—Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms
- C07C57/52—Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms containing halogen
- C07C57/58—Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms containing halogen containing six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/30—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members
- C07D207/34—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D207/36—Oxygen or sulfur atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/54—Spiro-condensed
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D237/00—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings
- C07D237/02—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings
- C07D237/04—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having less than three double bonds between ring members or between ring members and non-ring members
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/94—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom spiro-condensed with carbocyclic rings or ring systems, e.g. griseofulvins
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D311/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/10—Spiro-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D493/00—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system
- C07D493/02—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system in which the condensed system contains two hetero rings
- C07D493/10—Spiro-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/10—Spiro-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/12—Systems containing only non-condensed rings with a six-membered ring
- C07C2601/14—The ring being saturated
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Furan Compounds (AREA)
- Pyrrole Compounds (AREA)
- Indole Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
La presente se refiere a varios procedimientos y a productos intermedios para su obtencion y a su empleo como agentes pesticidas y/o herbicidas, así como a agentes herbicidas selectivos, que contienen, por un lado, cetoenoles cíclicos, substituidos con yodo-fenilo de la formula (1) y, por otro lado, al menos un compuesto mejorador de la compatibilidad con las plantas de cultivo. Reivindicacion 1: Compuestos de la formula (1), en la que: J significa yodo; X significa hidrogeno, alquilo, halogeno, halogenoalquilo, alcoxi o halogenoalcoxi; I significa hidrogeno, alquilo, halogeno o alcoxi, con la condicion de que se encuentre, al menos, uno de los restos J, X o Y en la posicion 2 del resto de fenilo y que, en este caso, sea diferente de hidrogeno; CKE significa uno de los grupos de formulas (2) a (9): donde A significa hidrogeno, alquilo, alquenilo, alcoxialquilo, alquiltioalquilo, substituidos respectivamente, en caso dado, con halogeno, cicloalquilo saturado o insaturado, substituido en caso dado, en el que está reemplazado, en caso dado, al menos, un átomo del anillo por un heteroátomo, o arilo, arilalquilo o hetarilo substituidos respectivamente, en caso dado, con halogeno, con alquilo, con halogenoalquilo, con alcoxi, con halogenoalcoxi, con ciano o con nitro; B significa hidrogeno, alquilo o alcoxialquilo; o A y B significan, junto con el átomo de carbono, con el que están enlazados, un ciclo saturado o insaturado, insubstituido o substituido, que contiene, en caso dado, al menos un heteroátomo; D significa hidrogeno o un resto, substituido en caso dado, elegido de la serie formada por alquilo, alquenilo, alquinilo, alcoxialquilo, cicloalquilo saturado o insaturado, en el que están reemplazados, en caso dado, uno o varios miembros del anillo por heteroátomos, arilalquilo, arilo, hetarilalquilo o hetarilo o; A y D significan junto con los átomos, con los que están enlazados, un ciclo saturado o insaturado y que contiene en caso dado, al menos, un heteroátomo (en el caso en que CKE=8 otro heteroátomo), insubstituido o substituido en la A, D, o bien; A y Q1 significan, conjuntamente, alcanodiilo o alquenodiilo substituidos, en caso dado, con hidroxi, con alquilo, con alcoxi, con alquiltio, con cicloalquilo, con benciloxi o con arilo substituidos respectivamente, en caso dado o; Q1 significa hidrogeno o alquilo; Q2, Q4, Q5 y Q6 significan, independientemente entre sí, hidrogeno o alquilo; Q3 significa hidrogeno, significa alquilo, alcoxialquilo, alquiltioalquilo substituidos en caso dado, significa cicloalquilo substituido en caso dado (estando reemplazado, en caso dado, un grupo metileno por oxígeno o por azufre) o significa fenilo substituido en caso dado; o Q3 y Q4 significan junto con el átomo de carbono, con el que están enlazados, un ciclo saturado o insaturado, insubstituido o substituido, que contiene, en caso dado, un heteroátomo; G significa hidrogeno a) o significa uno de los grupos de formulas (10) a (15), donde E significa un equivalente de ion metálico o un ion amonio; L significa oxígeno o azufre; M significa oxígeno o azufre; R1 significa alquilo, alquenilo, alcoxialquilo, alquiltioalquilo, polialcoxialquilo substituidos respectivamente, en caso dado, con halogeno o significa, cicloalquilo substituidos, en caso dado, con halogeno, con alquilo o con alcoxi, que puede estar interrumpido, al menos, por un heteroátomo, significa fenilo, fenilalquilo, hetarilo, fenoxialquilo o hetariloxialquilo substituidos respectivamente, en caso dado; R2 significa alquilo, alquenilo, alcoxialquilo, polialcoxialquilo substituidos respectivamente, en caso dado, con halogeno o significa cicloalquilo, fenilo o bencilo substituidos respectivamente, en caso dado; R3, R4 y R5 significan, independientemente entre sí, alquilo, alcoxi, alquilamino, dialquilamino, alquiltio, alqueniltio, cicloalquiltio substituidos respectivamente, en caso dado, con halogeno o significan fenilo, bencilo, fenoxi o feniltio substituidos respectivamente, en caso dado; R6 y R7 significan, independientemente entre sí, hidrogeno, alquilo, cicloalquilo, alquenilo, alcoxi, alcoxialquilo substituidos respectivamente, en caso dado, con halogeno, significan fenilo substituido, en caso dado, significan bencilo substituido, en caso dado, o junto con el átomo de N, con el que están enlazados, significa un ciclo interrumpido, en caso dado, por oxígeno o por azufre.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102004044827A DE102004044827A1 (de) | 2004-09-16 | 2004-09-16 | Jod-phenylsubstituierte cyclische Ketoenole |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR051096A1 true AR051096A1 (es) | 2006-12-20 |
Family
ID=35351612
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP050103913A AR051096A1 (es) | 2004-09-16 | 2005-09-20 | Cetoenoles ciclicos substituidos por yodo-fenilo |
Country Status (15)
| Country | Link |
|---|---|
| US (1) | US8629084B2 (es) |
| EP (1) | EP1791816B1 (es) |
| JP (1) | JP5136981B2 (es) |
| KR (1) | KR20070054240A (es) |
| CN (3) | CN101696197A (es) |
| AR (1) | AR051096A1 (es) |
| AU (1) | AU2005284318A1 (es) |
| BR (1) | BRPI0515398B1 (es) |
| CA (1) | CA2580328A1 (es) |
| DE (1) | DE102004044827A1 (es) |
| MX (1) | MX2007003100A (es) |
| RU (1) | RU2007113905A (es) |
| UA (1) | UA87161C2 (es) |
| WO (1) | WO2006029799A1 (es) |
| ZA (1) | ZA200702178B (es) |
Families Citing this family (63)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102005051325A1 (de) | 2005-10-27 | 2007-05-03 | Bayer Cropscience Ag | Alkoxyalkyl spirocyclische Tetram- und Tetronsäuren |
| DE102005059469A1 (de) | 2005-12-13 | 2007-06-14 | Bayer Cropscience Ag | Insektizide Zusammensetzungen mit verbesserter Wirkung |
| DE102005059891A1 (de) | 2005-12-15 | 2007-06-28 | Bayer Cropscience Ag | 3'-Alkoxy-spirocyclopentyl substituierte Tetram- und Tetronsäuren |
| DE102006007882A1 (de) | 2006-02-21 | 2007-08-30 | Bayer Cropscience Ag | Cycloalkyl-phenylsubstituierte cyclische Ketoenole |
| DE102006018828A1 (de) | 2006-04-22 | 2007-10-25 | Bayer Cropscience Ag | Alkoxyalkyl-substituierte cyclische Ketoenole |
| DE102006022821A1 (de) | 2006-05-12 | 2007-11-15 | Bayer Cropscience Ag | Verwendung von Tetramsäurederivaten zur Bekämpfung von Insekten aus der Ordnung der Käfer (Coleoptera), Thrips (Tysanoptera), Wanzen (Hemiptera), Fliegen (Diptera) und Zikaden (Auchenorrhynchae) |
| 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 |
| DE102006033154A1 (de) | 2006-07-18 | 2008-01-24 | Bayer Cropscience Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| DE102006050148A1 (de) | 2006-10-25 | 2008-04-30 | Bayer Cropscience Ag | Trifluormethoxy-phenylsubstituierte Tetramsäure-Derivate |
| DE102006057036A1 (de) | 2006-12-04 | 2008-06-05 | Bayer Cropscience Ag | Biphenylsubstituierte spirocyclische Ketoenole |
| DE102006057037A1 (de) | 2006-12-04 | 2008-06-05 | Bayer Cropscience Ag | cis-Alkoxyspirocyclische biphenylsubstituierte Tetramsäure-Derivate |
| DE102007009957A1 (de) | 2006-12-27 | 2008-07-03 | Bayer Cropscience Ag | Verfahren zur verbesserten Nutzung des Produktionsptentials transgener Pflanzen |
| DE102007001866A1 (de) * | 2007-01-12 | 2008-07-17 | Bayer Cropscience Ag | Spirocyclische Tetronsäure-Derivate |
| EP2011394A1 (de) * | 2007-07-03 | 2009-01-07 | Bayer CropScience AG | Verwendung von Tetramsäure - Derivaten zur Bekämpfung von virusübertragenden Vektoren |
| EP2014169A1 (de) | 2007-07-09 | 2009-01-14 | Bayer CropScience AG | Wasserlösliche Konzentrate von 3-(2-Alkoxy-4-chlor-6-alkyl-phenyl)-substituierten Tetramaten und ihren korrespondierenden Enolen |
| EP2014164A1 (de) * | 2007-07-11 | 2009-01-14 | Bayer CropScience AG | Wirkstoffkombinationen mit insektiziden, akariziden und nematiziden Eigenschaften |
| US9044261B2 (en) * | 2007-07-31 | 2015-06-02 | Ethicon Endo-Surgery, Inc. | Temperature controlled ultrasonic surgical instruments |
| EP2020413A1 (de) | 2007-08-02 | 2009-02-04 | Bayer CropScience AG | Oxaspirocyclische-spiro-substituierte Tetram- und Tetronsäure-Derivate |
| GB0715454D0 (en) | 2007-08-08 | 2007-09-19 | Syngenta Ltd | Novel herbicides |
| GB0715576D0 (en) | 2007-08-09 | 2007-09-19 | Syngenta Ltd | Novel herbicides |
| EP2039248A1 (de) * | 2007-09-21 | 2009-03-25 | Bayer CropScience AG | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| EP2045240A1 (de) | 2007-09-25 | 2009-04-08 | Bayer CropScience AG | Halogenalkoxyspirocyclische Tetram- und Tetronsäure-Derivate |
| EP2103615A1 (de) | 2008-03-19 | 2009-09-23 | Bayer CropScience AG | 4'4'-Dioxaspiro-spirocyclisch substituierte Tetramate |
| MX2010010114A (es) * | 2008-03-27 | 2010-09-30 | Bayer Cropscience Ag | Uso de derivados de acido tetronico para el combate de insectos y acaros tetraniquidos por riego, aplicacion de gotitas o aplicacion por inmersion. |
| EP2113172A1 (de) | 2008-04-28 | 2009-11-04 | Bayer CropScience AG | Verfahren zur verbesserten Nutzung des Produktionspotentials transgener Pflanzen |
| EP2127522A1 (de) | 2008-05-29 | 2009-12-02 | Bayer CropScience AG | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
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| DE10139465A1 (de) | 2001-08-10 | 2003-02-20 | Bayer Cropscience Ag | Selektive Herbizide auf Basis von substituierten, cayclischen Ketoenolen und Safenern |
| PL207276B1 (pl) | 2001-09-27 | 2010-11-30 | Syngenta Participations Ag | Kompozycja chwastobójcza oraz sposób selektywnego zwalczania chwastów i traw w uprawach roślin użytkowych |
| JP2005516973A (ja) | 2002-01-22 | 2005-06-09 | シンジェンタ パーティシペーションズ アクチェンゲゼルシャフト | 除草剤として有用なフェニル置換ヘテロ環化合物 |
| WO2004000152A2 (en) | 2002-06-21 | 2003-12-31 | Hauck Douglas J D D S | Oral disease prevention and treatment |
| DE10231333A1 (de) | 2002-07-11 | 2004-01-22 | Bayer Cropscience Ag | Cis-Alkoxysubstituierte spirocyclische 1-H-Pyrrolidin-2,4-dion-Derivate |
| DE10239479A1 (de) | 2002-08-28 | 2004-03-04 | Bayer Cropscience Ag | Substituierte spirocyclische Ketoenole |
| AR042206A1 (es) | 2002-11-26 | 2005-06-15 | Novartis Ag | Acidos fenilaceticos y derivados |
| DE10301806A1 (de) | 2003-01-20 | 2004-07-29 | Bayer Cropscience Ag | Selektive Herbizide auf Basis von substituierten, cyclischen Dicarbonylverbindungen und Safenern |
| DE10301804A1 (de) | 2003-01-20 | 2004-07-29 | Bayer Cropscience Ag | 2,4-Dihalogen-6-(C2-C3-alkyl)-phenyl substituierte Tetramsäure-Derivate |
| DE10302960A1 (de) * | 2003-01-24 | 2004-08-05 | Kalle Gmbh & Co. Kg | Rauchdurchlässige Nahrungsmittelhülle auf Basis von Polyamid und wasserlöslichen Polymeren |
| 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 |
| DE10330724A1 (de) | 2003-07-08 | 2005-01-27 | Bayer Cropscience Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| DE10331674A1 (de) | 2003-07-14 | 2005-02-10 | Bayer Cropscience Ag | Verwendung von 2,2-Dimethyl-3(2,4-dichlorophenyl)-2-oxo-1-oxaspiro[4.5]dec-3-en-4-yl butanoat zur Bekämpfung von Akariden |
| DE10331675A1 (de) | 2003-07-14 | 2005-02-10 | Bayer Cropscience Ag | Hetarylsubstituierte Pyrazolidindion-Derivate |
| DE10337496A1 (de) | 2003-08-14 | 2005-04-14 | Bayer Cropscience Ag | 4-Biphenylsubstituierte-4-substituierte-pyrazolidin-3,5-dione |
| DE10337497A1 (de) | 2003-08-14 | 2005-03-10 | Bayer Cropscience Ag | 4-Biphenylsubstituierte-Pyrazolidin-3,5-dion-Derivate |
| DE10351647A1 (de) | 2003-11-05 | 2005-06-09 | Bayer Cropscience Ag | 2-Halogen-6-alkyl-phenyl substituierte Tetramsäure-Derivate |
| DE10351646A1 (de) | 2003-11-05 | 2005-06-09 | Bayer Cropscience Ag | 2-Halogen-6-alkyl-phenyl substituierte spirocyclische Tetramsäure-Derivate |
| DE10354629A1 (de) | 2003-11-22 | 2005-06-30 | Bayer Cropscience Ag | 2-Ethyl-4,6-dimethyl-phenyl substituierte spirocyclische Tetramsäure-Derivate |
| DE10354628A1 (de) | 2003-11-22 | 2005-06-16 | Bayer Cropscience Ag | 2-Ethyl-4,6-dimethyl-phenyl-substituierte Tetramsäure-Derivate |
| WO2005053405A1 (de) | 2003-12-04 | 2005-06-16 | Bayer Cropscience Aktiengesellschaft | Wirkstoffkombinationen mit insektiziden und akariziden eigenschaften |
| 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 |
| DE102004032420A1 (de) | 2004-07-05 | 2006-01-26 | Bayer Cropscience Ag | Verwendung von 3-(2,4,6-Trimethylphenyl)-4-neopentylcarbonyloxy-5,5-tetramethylen-Δ3-dihydrofuran-2-on zur Bekämpfung von Psylliden |
-
2004
- 2004-09-16 DE DE102004044827A patent/DE102004044827A1/de not_active Withdrawn
-
2005
- 2005-09-13 BR BRPI0515398A patent/BRPI0515398B1/pt not_active IP Right Cessation
- 2005-09-13 WO PCT/EP2005/009807 patent/WO2006029799A1/de not_active Ceased
- 2005-09-13 CN CN200910161343A patent/CN101696197A/zh active Pending
- 2005-09-13 AU AU2005284318A patent/AU2005284318A1/en not_active Abandoned
- 2005-09-13 CN CN2005800382908A patent/CN101056852B/zh not_active Expired - Fee Related
- 2005-09-13 EP EP05783004A patent/EP1791816B1/de not_active Expired - Lifetime
- 2005-09-13 KR KR1020077008281A patent/KR20070054240A/ko not_active Ceased
- 2005-09-13 CA CA002580328A patent/CA2580328A1/en not_active Abandoned
- 2005-09-13 CN CN200910161342A patent/CN101696184A/zh active Pending
- 2005-09-13 UA UAA200704234A patent/UA87161C2/ru unknown
- 2005-09-13 JP JP2007531656A patent/JP5136981B2/ja not_active Expired - Fee Related
- 2005-09-13 RU RU2007113905/04A patent/RU2007113905A/ru not_active Application Discontinuation
- 2005-09-13 US US11/663,029 patent/US8629084B2/en active Active
- 2005-09-13 MX MX2007003100A patent/MX2007003100A/es active IP Right Grant
- 2005-09-20 AR ARP050103913A patent/AR051096A1/es not_active Application Discontinuation
-
2007
- 2007-03-15 ZA ZA200702178A patent/ZA200702178B/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| CA2580328A1 (en) | 2006-03-23 |
| WO2006029799A1 (de) | 2006-03-23 |
| BRPI0515398B1 (pt) | 2016-03-01 |
| ZA200702178B (en) | 2009-10-28 |
| CN101056852B (zh) | 2013-05-01 |
| AU2005284318A1 (en) | 2006-03-23 |
| US8629084B2 (en) | 2014-01-14 |
| CN101696184A (zh) | 2010-04-21 |
| JP5136981B2 (ja) | 2013-02-06 |
| CN101696197A (zh) | 2010-04-21 |
| EP1791816B1 (de) | 2012-08-22 |
| RU2007113905A (ru) | 2008-10-27 |
| KR20070054240A (ko) | 2007-05-28 |
| EP1791816A1 (de) | 2007-06-06 |
| DE102004044827A1 (de) | 2006-03-23 |
| CN101056852A (zh) | 2007-10-17 |
| UA87161C2 (ru) | 2009-06-25 |
| US20100009850A1 (en) | 2010-01-14 |
| BRPI0515398A (pt) | 2008-07-22 |
| MX2007003100A (es) | 2009-02-16 |
| JP2008513391A (ja) | 2008-05-01 |
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