WO2007115644A1 - Substituierte enaminocarbonylverbindungen - Google Patents
Substituierte enaminocarbonylverbindungen Download PDFInfo
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- WO2007115644A1 WO2007115644A1 PCT/EP2007/002386 EP2007002386W WO2007115644A1 WO 2007115644 A1 WO2007115644 A1 WO 2007115644A1 EP 2007002386 W EP2007002386 W EP 2007002386W WO 2007115644 A1 WO2007115644 A1 WO 2007115644A1
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- formula
- compounds
- hydrogen
- methyl
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- 150000001875 compounds Chemical class 0.000 title claims abstract description 241
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- 238000000034 method Methods 0.000 claims description 60
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- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 31
- 239000001301 oxygen Substances 0.000 claims description 31
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- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 28
- 239000003795 chemical substances by application Substances 0.000 claims description 27
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- DQJCHOQLCLEDLL-UHFFFAOYSA-N tricyclazole Chemical compound CC1=CC=CC2=C1N1C=NN=C1S2 DQJCHOQLCLEDLL-UHFFFAOYSA-N 0.000 description 1
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- HSMVPDGQOIQYSR-KGENOOAVSA-N triflumizole Chemical compound C1=CN=CN1C(/COCCC)=N/C1=CC=C(Cl)C=C1C(F)(F)F HSMVPDGQOIQYSR-KGENOOAVSA-N 0.000 description 1
- XAIPTRIXGHTTNT-UHFFFAOYSA-N triflumuron Chemical compound C1=CC(OC(F)(F)F)=CC=C1NC(=O)NC(=O)C1=CC=CC=C1Cl XAIPTRIXGHTTNT-UHFFFAOYSA-N 0.000 description 1
- RROQIUMZODEXOR-UHFFFAOYSA-N triforine Chemical compound O=CNC(C(Cl)(Cl)Cl)N1CCN(C(NC=O)C(Cl)(Cl)Cl)CC1 RROQIUMZODEXOR-UHFFFAOYSA-N 0.000 description 1
- RKBCYCFRFCNLTO-UHFFFAOYSA-N triisopropylamine Chemical compound CC(C)N(C(C)C)C(C)C RKBCYCFRFCNLTO-UHFFFAOYSA-N 0.000 description 1
- JARYYMUOCXVXNK-CSLFJTBJSA-N validamycin A Chemical compound N([C@H]1C[C@@H]([C@H]([C@H](O)[C@H]1O)O[C@H]1[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O1)O)CO)[C@H]1C=C(CO)[C@@H](O)[C@H](O)[C@H]1O JARYYMUOCXVXNK-CSLFJTBJSA-N 0.000 description 1
- LESVOLZBIFDZGS-UHFFFAOYSA-N vamidothion Chemical compound CNC(=O)C(C)SCCSP(=O)(OC)OC LESVOLZBIFDZGS-UHFFFAOYSA-N 0.000 description 1
- 230000008016 vaporization Effects 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 239000003981 vehicle Substances 0.000 description 1
- 125000002348 vinylic group Chemical group 0.000 description 1
- 229960004740 voriconazole Drugs 0.000 description 1
- BCEHBSKCWLPMDN-MGPLVRAMSA-N voriconazole Chemical compound C1([C@H](C)[C@](O)(CN2N=CN=C2)C=2C(=CC(F)=CC=2)F)=NC=NC=C1F BCEHBSKCWLPMDN-MGPLVRAMSA-N 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- AMHNZOICSMBGDH-UHFFFAOYSA-L zineb Chemical compound [Zn+2].[S-]C(=S)NCCNC([S-])=S AMHNZOICSMBGDH-UHFFFAOYSA-L 0.000 description 1
- DUBNHZYBDBBJHD-UHFFFAOYSA-L ziram Chemical compound [Zn+2].CN(C)C([S-])=S.CN(C)C([S-])=S DUBNHZYBDBBJHD-UHFFFAOYSA-L 0.000 description 1
- FJBGIXKIXPUXBY-UHFFFAOYSA-N {2-[3-(4-chlorophenyl)propyl]-2,4,4-trimethyl-1,3-oxazolidin-3-yl}(imidazol-1-yl)methanone Chemical compound C1=CN=CN1C(=O)N1C(C)(C)COC1(C)CCCC1=CC=C(Cl)C=C1 FJBGIXKIXPUXBY-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom 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
- C07D213/61—Halogen atoms or nitro radicals
-
- 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
- A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-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
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/74—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,3
- A01N43/78—1,3-Thiazoles; Hydrogenated 1,3-thiazoles
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D213/26—Radicals substituted by halogen atoms or nitro radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D277/22—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D277/32—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
Definitions
- the present application relates to novel substituted enaminocarbonyl compounds, processes for their preparation and their use for controlling animal pests, especially arthropods, in particular insects.
- A is pyrid-2-yl or pyrid-4-yl or pyrid-3-yl, which may be present in 6-
- Position is substituted by fluorine, chlorine, bromine, methyl, trifluoromethyl or trifluoromethoxy or for pyridazin-3-yl which is optionally substituted in the 6-position by chlorine or methyl or for pyrazine-3-yl or for 2-chloro pyrazine-5-yl or 1,3-thiazol-5-yl, which is optionally substituted in the 2-position by chlorine or methyl,
- B is oxygen, sulfur or methylene
- R 1 is haloalkyl, haloalkenyl, halocycloalkyl or halocycloalkylalkyl,
- R 2 is hydrogen or halogen
- R 3 is hydrogen or alkyl.
- a and R 1 have the meanings mentioned above,
- A, B, R 2 and R 3 have the meanings mentioned above
- R 1 has the meanings mentioned above and E is a suitable leaving group such as, for example, halogen (in particular bromine, chlorine, iodine) or O-sulfonylalkyl and O-sulfonylaryl (in particular O-mesyl, O-tosyl),
- R 1 has the meaning mentioned above
- R 1 , R 2 and R 3 have the meanings mentioned above,
- novel compounds of the formula (I) have pronounced biological properties and, above all, for controlling animal pests, in particular insects, arachnids and nematodes, which are used in agriculture, in forestry, in the protection of stored products and materials, and on the hygiene sector are suitable.
- the compounds of the formula (I) may optionally be present as geometrical and / or as optically active isomers or corresponding isomer mixtures in different compositions.
- the invention relates to both the pure isomers and the isomer mixtures.
- the compounds of the invention are generally defined by the formula (I).
- A is preferably 6-fluoropyrid-3-yl, 6-chloropyrid-3-yl, 6-bromo-pyrid-3-yl, 6-methyl-pyrid-3-yl, 6-trifluoromethyl-pyridine 3-yl, 6-trifluoromethoxypyrid-3-yl, 6-chloro-1, 4-pyridazin-3-yl, 6-methyl-1,4-pyridazin-3-yl, 2-chloro-1,3-thiazole 5-yl or 2-methyl-1,3-thiazol-5-yl.
- B is preferably oxygen or methylene.
- R 1 preferably represents fluorine-substituted C r C 5 alkyl, C 2 -C 5 alkenyl, C 3 -C 5 cycloalkyl or Cs-Cs-cycloalkylalkyl.
- R 2 is preferably hydrogen or halogen (where halogen is in particular fluorine or chlorine),
- R 3 is preferably in each case hydrogen or methyl.
- Bromopyrid-3-yl, 6-chloro-1, 4-pyridazin-3-yl, 2-chloro-1, 3-thiazol-5-yl, B is particularly preferably oxygen or methylene.
- R 1 particularly preferably represents 2-fluoroethyl, 2,2-difluoroethyl, 2-fluoro-cyclopropyl.
- R 2 is particularly preferably hydrogen.
- R 3 is particularly preferably hydrogen.
- A is very particularly preferably the radical 6-chloropyrid-3-yl, 6-bromo-pyrid-3-yl, or 6-chloro-1, 4-pyridazin-3-yl,
- B is most preferably oxygen.
- R 1 very particularly preferably represents 2,2-difluoroethyl.
- R 2 very particularly preferably represents hydrogen.
- R 3 is very particularly preferably hydrogen.
- A is 6-chloro-pyrid-3-yl
- A represents pyrid-3-yl which is substituted in the 6-position by fluorine, chlorine, bromine, methyl or trifluoromethyl or represents 2-chloro-pyrazine-5-yl or 2-chloro-1,3-thiazole 5-yl stands,
- B is oxygen, sulfur or methylene
- R 2 is hydrogen or halogen
- R 3 is hydrogen or methyl.
- A preferably represents 6-fluoropyrid-3-yl, 6-chloropyrid-3-yl, 6-bromo-pyrid-3-yl, 6-trifluoromethyl-pyrid-3-yl, 2-chloro-pyrazine 5-yl or 2-chloro-l, 3-thiazol-5-yl.
- B is preferably oxygen or methylene.
- R 1 is preferably difluoromethyl, 2-fluoroethyl, 2,2-difluoroethyl, 2-chloro-2-fluoroethyl, 3-fluoro-w-propyl, 2-fluoro-vinyl, 3,3-difluoro-prop-2-enyl or 3,3-dichloro-prop-2-enyl.
- R 2 is preferably hydrogen or halogen (where halogen is in particular fluorine or chlorine).
- R 3 is preferably in each case hydrogen.
- B is particularly preferably oxygen.
- R 1 particularly preferably represents 2-fluoroethyl or 2,2-difluoroethyl.
- R 2 is particularly preferably hydrogen.
- R 3 is particularly preferably hydrogen.
- a very particularly preferably represents the radical 6-chloropyrid-3-yl or 6-bromo-pyrid-3-yl.
- B is most preferably oxygen.
- R 1 very particularly preferably represents 2,2-difluoroethyl.
- R 2 very particularly preferably represents hydrogen.
- R is most preferably hydrogen.
- R 3 is hydrogen, B is oxygen and A is 6-chloro-pyrid-3-yl
- R 3 is hydrogen, B is oxygen and A is 6-bromo-pyrid-3-yl
- R 3 is hydrogen, B is oxygen and A is 6-fluoropyrid-3-yl
- R 3 is hydrogen, B is oxygen and A is 6-trifluoromethylpyrid-3-yl
- R 3 is hydrogen, B is oxygen and A is 2-chloro-1,3-thiazol-5-yl
- R 2 and R 3 are hydrogen, B is oxygen and A is 6-chloro-pyrid-3-yl
- R 2 and R 3 are hydrogen, B is oxygen and A is 6-bromo-pyrid-3-yl
- R 2 and R 3 are hydrogen, B is oxygen and A is 6-fluoro-pyrid-3-yl
- R 2 and R 3 are hydrogen, B is oxygen and A is 6-trifluoromethylpyrid-3-yl
- R 2 and R 3 are hydrogen, B is oxygen and A is 2-chloro-1,3-thiazol-5-yl
- R 2 and R 3 are hydrogen, B is methylene and A is 6-chloro-pyrid-3-yl
- R 2 and R 3 are hydrogen, B is methylene and A is 6-bromo-pyrid-3-yl
- R 2 and R 3 are hydrogen, B is methylene and A is 6-fluoro-pyrid-3-yl
- R 2 and R 3 are hydrogen, B is methylene and A is 6-trifluoromethylpyrid-3-yl
- R 2 and R 3 are hydrogen, B is methylene and A is 2-chloro-1,3-thiazol-5-yl
- R 1 is difluoromethyl, R 2 and R 3 are hydrogen and B is oxygen.
- R 1 is 2-fluoroethyl, R 2 and R 3 are hydrogen and B is oxygen.
- R 1 is 2,2-difluoroethyl
- R 2 and R 3 are hydrogen and B is oxygen
- R 1 is difluoromethyl
- R 2 and R 3 are hydrogen
- B is methylene
- R 1 is 2-fluoroethyl
- R 2 and R 3 are hydrogen
- B is methylene
- R 1 is 2,2-difluoroethyl
- R 2 and R 3 are hydrogen
- B is methylene
- B, R 2 and R 3 preferably represent those radicals which are already mentioned in connection with the description of the substances of the formula (I) according to the invention as preferred substituents.
- the compounds of formula (II) may, for.
- B oxygen: tetronic acids
- Rao YS Chem Rev. (1976), 76, 625-694; Tejedor, D. Garcia-Tellado, F. Org., Preparations and Procedures International (2004), 36, 35-59; Reviews
- B for sulfur: thiotetronic acids Thiomas, EJ Special Publication - Royal Society of Chemistry (1988), 65 (Top Med. Chem.), 284-307, Review
- B is methylene: cyclopentane-1,3-dione ( Schick, Hans; Eichhorn, Inge. Synthesis (1989), (7), 477-492, Review).
- a and R 1 have the meanings which have already been mentioned in connection with the description of the substances of the formula (I) according to the invention.
- the compounds of formula (III) may, for. T. commercially available or by literature methods (see, for example, BS Patai "The Chemistry of Amino Group", Interscience Publishers, New York, 1968.
- the compounds of the formula (III) can also be prepared from compounds of the formula (VII) (cf., Scheme III below).
- the compounds of formula (VII) are z. T. commercially available, some known and can be obtained by known methods (eg., 2-chloro-5-chloromethyl-l, 3-thiazole: DE 3 631 538 (1988), EP 446 913 (1991), EP 780) 384 (1997), EP 775 700 (1997), EP 794 180 (1997), WO 9 710 226 (1997); ⁇ -chloro-chloromethylpyridine: DE 3 630 046 A1 (1988), EP 373 464 A2 ( 1990), EP 373 464 A2 (1990), EP 393 453 A2 (1990), EP 569 947 A1 (1993); 6-chloro-3-bromomethylpyridine: I.
- E Hal, for example chlorine, bromine, iodine; O-tosyl, O-mesyl,
- the latter can also be obtained from corresponding methyl group-containing heterocycles (A-CH 3 ) using suitable literature-known halogenating agents.
- the compounds of formula (V) may, for. T. commercially available (see, for example, 2-fluoroethylamine or 2,2-difluoroethylamine) or by literature methods are obtained (see, for example, 3-fluoro -? - propylamine: US 6252087 Bl; 3,3-difluoro -prop-2-enylamine hydrochloride: WO 2001/007414 A1; 3,3-dichloro-prop-2-enylamine: DE 2747814).
- aldehydes (A-CHO) are z. T. commercially available
- 6-chloro-nicotinaldehyde 6-fluoro-nicotinaldehyde, 6-bromo-nicotinaldehyde, 2-chloro-1, 3-thiazole-5-carbaldehyde
- 6-methyl-nicotinaldehyde EP 104876 A2
- 2-chloro-pyrazine-5-caboxaldehyde DE 3314196 A1
- diluents are advantageously used in such an amount that the reaction mixture remains easy to stir throughout the process.
- Suitable diluents for carrying out process 1 according to the invention are all organic solvents which are inert under the reaction conditions.
- halogenated hydrocarbons in particular chlorohydrocarbons, such as tetrachlorethylene, tetrachloroethane, dichloropropane, methylene chloride, dichlorobutane, chloroform, carbon tetrachloride, trichloroethane, trichlorethylene, pentachloroethane, difluorobenzene, 1,2-dichloroethane, chlorobenzene, bromobenzene, dichlorobenzene, chlorotoluene, trichlorobenzene; Alcohols such as methanol, ethanol, isopropanol, butanol; Ethers such as ethyl propyl ether, methyl tert-butyl ether, Butyl ether, anisole, phenol, cyclohexylmethyl ether, dimethyl ether, diethyl ether, dipropl ether, diisopropyl
- Preferred diluents for carrying out the process according to the invention are aromatic hydrocarbons, such as benzene, toluene, chlorobenzene, bromobenzene, nitrobenzene or xylene, in particular benzene and toluene.
- the preparation of compounds of the formula (I) according to preparation process 1 is carried out by reacting compounds of the formula (II) in the presence of compounds of the formula (III), if appropriate in the presence of an acidic auxiliary and, if appropriate, in one of the diluents given ,
- the reaction time is generally 10 minutes to 48 hours.
- the reaction is carried out at temperatures between -10 0 C and +200 0 C, preferably between +10 0 C and 180 0 C, more preferably between 60 0 C and 14O 0 C. It is preferably carried out under reaction conditions, the Allow separation or removal of water, for example with the aid of a water separator.
- Suitable acidic agents are, for example, 7-toluenesulfonic acid or acetic acid.
- the compounds required as starting materials for carrying out the process 2 according to the invention are generally defined by the formula (Ia).
- A, B, R 2 and R 3 are preferably those radicals which have already been mentioned as preferred substituents in connection with the description of the substances of the formula (I) according to the invention.
- the compounds of the formula (Ia) can be obtained by the preparation process 1 described above, for example by reaction of compounds of the formula (II) with compounds of the formula (III) in which R 1 is hydrogen.
- the compounds of formula (IV) may, for. T. are obtained commercially (see, for example, chlorodifluoromethane, 1-bromo-2-fluoroethane, 2-bromo-1, 1-difluoroethane, 2-bromo-1-chloro-1-fluoroethane, 1-bromo- 3-fluoropropane, 3-bromo-l, l-difluoro-prop-l-ene, or obtained by literature methods (see, for example, 3-bromo-l, l-dichloro-prop-l-en: WO 8800183 Al (1988); compounds of general formula IV in which E represents halogen such as chlorine, bromine and iodine: Houben-Weyl, Methods of Organic Chemistry, Bd, V / 3, Georg Thieme Verlag Stuttgart, p 503 and Bd.
- E represents halogen such as chlorine, bromine and iodine
- E 1 is mesylate: Crossland, RK, Servis, KLJ Org. Chem. (1970), 35, 3195;
- E is tosylate: Roos, AT et al., Org. Synth. , Coli. Vol. I, (1941), 145; Marvel, CS, Sekera, VC Org. Synth., Coli. Vol. III, (1955), 366.
- Diluents are advantageously used in such an amount that the reaction mixture remains easy to stir throughout the process.
- Suitable diluents for carrying out process 2 according to the invention are all inert organic solvents.
- Preferred diluents for carrying out process 2 according to the invention are ethers, such as methyl tert-butyl ether, n-butyl ether, anisole, phenetole, cyclohexyl methyl ether, diisopropyl ether, diisobutyl ether, diisoamyl ether, ethylene glycol dimethyl ether, tetrahydrofuran, dioxane, dichlorodiethyl ether and polyethers of ethylene oxide and / or Propylene oxide, amides such as hexamethylenephosphoric triamide, formamide, N-methylformamide, N, N-dimethylformamide, N, N-dipropylformamide, N, N-dibutylformamide, benzene, toluene, chlorobenzene, bromobenzene, nitrobenzene, xylene; Ketones such as acetone, acetophenone, methyl
- preferred diluents for carrying out the process according to the invention are ethers such as methyl / er / butyl ether or cyclic ethers such as tetrahydrofuran and dioxane, amides such as N, N-dimethylformamide, aromatic hydrocarbons such as benzene or toluene; Ketones such as acetone, methyl ethyl ketone or methyl butyl ketone.
- acid binders such as amines, in particular tertiary amines and also alkali metal and alkaline earth metal compounds.
- hydroxides, hydrides, oxides and carbonates of lithium, sodium, potassium, magnesium, calcium and barium and further basic compounds such as amidine bases or guanidine bases such as 7-methyl-l, 5,7-triaza-bicyclo (4.4.
- dec-5-ene MTBD
- Diazabicyclo (4.3.0) nonene DBN
- diazabicyclo 2.2.2 octane
- DBU 1,8-diazabicyclo- (5.4.0) undecene
- CyTBG cyclohexyltetrabutyl-guanidine
- CyTMG cyclohexyltetramethylguanidine
- NNNN-tetramethyl-l 8-naphthalenediamine
- pentamethylpiperidine tertiary amines such as triethylamine, trimethylamine, tribenzylamine, triisopropylamine, tributylamine, tricyclohexylamine, triamylamine, trihexylamine, N, N-dimethylaniline, N, N-dimethyl-toluidine, N, N-dimethyl-p - aminopyridine, N-methyl-pyrrolidine, N
- hydrides of lithium or sodium are used.
- the reaction time is generally 10 minutes to 48 hours.
- the reaction is carried out at temperatures between -10 0 C and +200 0 C, preferably between +10 0 C and 180 0 C, more preferably between 6O 0 C and 14O 0 C. It can in principle be carried out under atmospheric pressure. Preferably, working at atmospheric pressure or at pressures up to 15 bar and optionally under a protective gas atmosphere (nitrogen, helium or argon).
- a protective gas atmosphere nitrogen, helium or argon
- 0.7 to 3.0 mol, particularly preferably 1.0 to 2 are added per mol of compound of the formula (IIII)) in the case of all alcoholic compounds, 00, 55, 55 bbiiss 44, 00 MMooll, vvoorrzzuuggsswweeiissee 0 mole of alkylating agent of the formula (IV)
- the entire reaction mixture is concentrated.
- the products obtained after working up can be purified in a customary manner by recrystallization, vacuum distillation or column chromatography (see also the Preparation Examples).
- the compounds to be used as starting materials for carrying out the process 3 according to the invention are generally defined by the formula (V).
- R 1 has the meaning which has already been mentioned in connection with the description of the substances of the formula (I) according to the invention.
- the amino compounds of the formula (V) are generally defined and can in many cases, for. T. commercial (see, for example, 2-fluoroethylamine or 2,2-Difiuorethylamin) or in a conventional manner according to the "Leuckart-Wallach reaction (eg 2-fluoro-ethylamine: US Pat 4030994 (1977); compounds of the formula (V) in which R 1 is alkyl, primary amines: see, for example, Houben-Weyl, Methods of Organic Chemistry, Vol. XI / 1, 4th Edition 1957, Georg Thieme Verlag Stuttgart Gart, p. 648; ML Moore in "The Leuckart Reaction” in: Organic Reactions, Vol.
- R ' halogen-containing radical
- the preferred reducing agent is, for example, the known borane-dimethyl sulfide complex (compare also the preparation of 2-chloro-2-fluoroethane-1-amine from commercially available 2-chloro-2-fluoroacetamide).
- the compounds to be used as starting materials for carrying out the process 3 according to the invention are generally defined by the formula (VII).
- diluents are advantageously used in such an amount that the reaction mixture remains easy to stir throughout the process.
- Suitable diluents for carrying out the process 3 according to the invention are all inert organic solvents.
- Preferred diluents for carrying out the first reaction step of process 3 according to the invention are aromatic hydrocarbons, such as benzene, toluene, chlorobenzene, bromobenzene, nitrobenzene or xylene, but especially benzene and toluene.
- the compounds of the formula (VI) are N-alkylated with compounds of the formula (VII).
- Suitable diluents for this reaction step are, for example, ethers, such as tetrahydrofuran or dioxane.
- Diluents are advantageously used in such an amount that the reaction mixture remains easy to stir throughout the process.
- the reaction time is generally 10 minutes to 48 hours.
- the reaction takes place at temperatures between -1O 0 C and +200 0 C, preferably between +10 0 C and 18O 0 C, more preferably between 60 0 C and 140 0 C. It is preferably carried out under reaction conditions, the deposition or removal of Allow water, for example with the aid of a water separator.
- reaction products may be in the form of geometric isomers, for example (E) and (Z) isomers (or trans and c / s isomers, respectively).
- diluents are advantageously used in such an amount that the reaction mixture remains easy to stir throughout the process.
- Suitable diluents for carrying out the C-alkylation are all organic solvents which are inert under the reaction conditions.
- Preferred diluents for carrying out the dehydrohalogenation are alcohols, such as methanol, ethanol, isopropanol, butanol; It is also possible to use mixtures of the solvents and diluents mentioned in the process according to the invention.
- Preferred diluents for carrying out the process according to the invention are alcohols, such as ethanol or butanol.
- the dehydrohalogenation of compounds of the formula (I) is carried out by reacting these with compounds of the general formula (I) in the presence of basic reaction auxiliaries.
- alkali metal hydroxides such as sodium hydroxide or potassium hydroxide as basic reaction auxiliaries.
- the reaction time is generally 10 minutes to 48 hours.
- the reaction takes place at temperatures between -100 0 C and + 8O 0 C, preferably between -20 0 C and 5O 0 C, particularly preferably at room temperature.
- diluents are advantageously used in such an amount that the reaction mixture remains easy to stir throughout the process.
- Suitable diluents for carrying out the C-alkylation are all inert organic solvents.
- Preferred diluents for carrying out the C-alkylation are ethers, such as methyl tert-butyl ether, butyl ether, anisole, phenetole, cyclohexylmethyl ether, diisopropyl ether, diisobutyl ether, diisoamyl ether, ethylene glycol dimethyl ether, tetrahydrofuran, dioxane, dichlorodiethyl ether and polyethers of ethylene oxide and / or propylene oxide.
- ethers such as methyl tert-butyl ether, butyl ether, anisole, phenetole, cyclohexylmethyl ether, diisopropyl ether, diisobutyl ether, diisoamyl ether, ethylene glycol dimethyl ether, tetrahydrofuran, dioxane, dichlorodiethyl ether and polyethers of ethylene oxide and
- Preferred diluents for carrying out the process according to the invention are ethers, such as methyl tert-butyl ether or cyclic ethers, such as tetrahydrofuran and dioxane.
- the C-alkylation is carried out by reacting suitable starting compounds of the formula I with compounds of the formula (IV) in the presence of basic reaction auxiliaries.
- the reaction time is generally 10 minutes to 48 hours.
- the reaction takes place at temperatures between -100 0 C and + 20 0 C, preferably between -9O 0 C and 10 0 C, more preferably between -80 0 C and 0 0 C.
- diluents are advantageously used in such an amount that the reaction mixture remains easy to stir throughout the process.
- Suitable diluents for carrying out the halogenation are all organic solvents which are inert under the reaction conditions.
- Suitable halogenating agents for carrying out the process according to the invention are any suitable halogenating agents, for example N-halogen compounds.
- N-halo amines such as l-chloromethyl-4-fluordiazoniabicyclo [2.2.2] - octane bis (tetrafluoroborate) (Selectfluor ®), NN-Dihalogenamine, N-halo-carboxylic acid amides, N-halo-carbamic acid ester, N- Halogen-urea, N-halogeno-sulfonylamides, N-halo-disulfonylamides, N-halo-sulfonylimides such as N-fluoro-bis [(trifluoromethyl) sulfonyl] imide and N-halo-carbodiamides such as N-chloro-phthalimide, N-bromine phthalimide, N-iodophthalimide, N-chloro-succinimide ( ⁇ CS), N-bromo-succinimide ( ⁇ BS), N-bromo-sacchar
- Preferred halogenating agents for carrying out the halogenation are N-halogenated carboxylic acid diamides or 1 -chloromethyl-4-fluordiazoniabicyclo [2.2.2] octane bis (tetrafluoroborate) (Selectfluor ®).
- Preferred diluents for carrying out the halogenation are nitriles such as acetonitrile, propionitrile, butyronitrile, isobutyronitrile, benzonitrile, m-chlorobenzonitrile.
- Particularly preferred diluents for carrying out the process according to the invention are nitriles, such as acetonitrile, propionitrile or butyronitrile.
- the reaction time in this process is generally 10 minutes to 48 hours.
- the reaction takes place at temperatures between -10 0 C and + 100 0 C, preferably between 0 0 C and 60 ° C, more preferably between 10 0 C and room temperature.
- the compounds of formula (I) may optionally be present in different polymorphic forms or as a mixture of different polymorphic forms. Both the pure polymorphs and the polymorph mixtures are the subject of the invention and can be used according to the invention.
- the active compounds according to the invention are suitable for plant tolerance, favorable warm-blood toxicity and good environmental compatibility for the protection of plants and plant organs, for increasing crop yields, improving the quality of the crop and for controlling animal pests, in particular insects, arachnids, helminths, nematodes and molluscs which are found in agriculture, horticulture, livestock, forests, gardens and recreational facilities, in the protection of materials and materials and in the hygiene sector. They can preferably be used as crop protection agents. They are effective against normally sensitive and resistant species as well as against all or individual stages of development.
- the above mentioned pests include:
- Anoplura e.g. Damalinia spp., Haematopinus spp., Ligognathus spp., Pediculus spp., Trichodectes spp.
- Ceuthorhynchus spp. Ceuthorhynchus spp., Cleonus mendicus, Conoderus spp., Cosmopolites spp., Costelytra zealandica, Curculio spp., Cryptorhynchus lapathi, Dermestes spp., Diabrotica spp., Epilachna spp., Faustinus cubae, Gibbium psylloides, Heteronychus arator, Hylamorpha elegans, Hylotrupes bajulus, Hypera postica, Hypothenemus spp., Lachnosterna consanguinea, Leptinotarsa decemlineata, Lissorhoptrus oryzophilus, Lixus spp., Lyctus spp., Meligethes aeneus, Melolontha melolontha, Migdolus spp., Mono
- Gastropoda From the class of Gastropoda, for example Arion spp., Biomphalaria spp., Bulinus spp., Deroceras spp., Galba spp., Lymnaea spp., Oncomelania spp., Succinea spp.
- helminths from the class of helminths, for example, Ancylostoma duodenale, Ancylostoma ceylanicum, Acyostoma braziliensis, Ancylostoma spp., Ascaris lubricoides, Ascaris spp., Brugia malayi, Brugia timori, Bunostomum spp., Chabertia spp., Clonorchis spp., Cooperia spp.
- Dicrocoelium spp Dictyocaulus filaria, Diphyllobothrium latum, Dracunculus medinensis, Echinococcus granulosus, Echinococcus multilocularis, Enterobius vermicularis, Faciola spp., Haemonchus spp., Heterakis spp., Hymenolepis nana, Hyostrongulus spp., Loa Loa, Nematodirus spp., Oesophagostomum spp., Opisthorchis spp., Onchocerca volvulus, Ostertagia spp., Paragonimus spp., Schistosome spp, Strongyloides fuelleborni, Strongyloides stercoralis, Stronyloides spp., Taenia saginata, Tae- nia solium, Trichinella spiralis, Trichinella spiral
- protozoa such as Eimeria
- Eimeria protozoa
- Heliopeltis spp. Horcias nobilellus, Leptocorisa spp., Leptoglossus phyllopus, Lygus spp., Macropes excavatus, Miridae, Nezara spp., Oebalus spp., Pentomidae, Piesma quadrata, Piezodorus spp., Psallus seriatetus, Pseudacysta persea, Rhodnius spp , Sahlbergella singularis, Scotinophora spp., Stephanitis nashi, Tibraca spp., Triatoma spp.
- Hymenoptera e.g. Diprion spp., Hoplocampa spp., Lasius spp., Monomorium pharaonis, Vespa spp.
- xylostella Prodenia spp., Pseudaletia spp., Pseudoplusia includens, Pyrausta nubilalis, Spodoptera spp., Thermesia gemmatalis, Tinea pellionella, Tineola bisselliella, Tortri x viridana, Trichoplusia spp.
- Orthoptera e.g. Acheta domesticus, Blatta orientalis, Blattella germanica, Gryllotalpa spp., Leucophaea maderae, Locusta spp., Melanoplus spp., Periplaneta americana, Schistocerca gregaria.
- siphonaptera e.g. Ceratophyllus spp., Xenopsylla cheopis.
- Symphyla e.g. Scutigerella immaculata.
- Thysanoptera eg Basothrips biformis, Enneothrips flavens, Frankliniella spp., Heliothrips spp., Hercinothrips femoralis, Kakothrips spp., Rhipiphorothrips cruentatus, Scirtothrips spp., Taeniothrips cardamoni, Thrips spp. From the order of Thysanura eg Lepisma saccharina.
- the plant parasitic nematodes include e.g. Anguina spp., Aphelenchoides spp., Belonoclampus spp., Bursaphelenchus spp., Ditylenchus dipsaci, Globodera spp., Heliocotylenchus spp., Heterodera spp., Longidorus spp., Meloidogyne spp., Pratylenchus spp., Radopholus similis, Ro- Tylenchus spp., Trichodorus spp., Tylenchorhynchus spp., Tylenchulus spp., Tylenchulus semipetnetrans, Xiphinema spp.
- Anguina spp. Aphelenchoides spp., Belonoclampus spp., Bursaphelenchus spp., Ditylenchus dipsaci, Globod
- the compounds according to the invention may optionally also be used in certain concentrations or application rates as herbicides, safeners, growth regulators or agents for improving plant properties, or as microbicides, for example as fungicides, antimycotics, bactericides, viricides (including agents against viroids) or as agents MLO (mycoplasma-like-organism) and RLO (Rickettsia-like-organism) are used. If appropriate, they can also be used as intermediates or precursors for the synthesis of further active ingredients.
- the active compounds can be converted into the customary formulations, such as solutions, emulsions, wettable powders, water- and oil-based suspensions, powders, dusts, pastes, soluble powders, soluble granules, scattering granules, suspension-emulsion concentrates, active substance-impregnated natural substances, Active substance-impregnated synthetic substances, fertilizers and ultrafine encapsulations in polymeric substances.
- customary formulations such as solutions, emulsions, wettable powders, water- and oil-based suspensions, powders, dusts, pastes, soluble powders, soluble granules, scattering granules, suspension-emulsion concentrates, active substance-impregnated natural substances, Active substance-impregnated synthetic substances, fertilizers and ultrafine encapsulations in polymeric substances.
- formulations are prepared in a known manner, e.g. by mixing the active substances with extenders, ie liquid solvents and / or solid carriers, optionally with the use of surface-active agents, ie emulsifiers and / or dispersants and / or foam-forming agents.
- extenders ie liquid solvents and / or solid carriers
- surface-active agents ie emulsifiers and / or dispersants and / or foam-forming agents.
- Excipients which can be used are those which are suitable for imparting special properties to the composition itself and / or preparations derived therefrom (for example spray liquor, seed dressing), such as certain technical properties and / or specific biological properties.
- Typical auxiliaries are: extenders, solvents and carriers.
- Suitable extenders include, for example, water, polar and non-polar organic chemical liquids, for example from the classes of aromatic and non-aromatic hydrocarbons (such as paraffins, alkylbenzenes, alkylnaphthalenes, chlorobenzenes), alcohols and polyols (which may also be substituted, etherified and / or esterified), ketones (such as acetone, cyclohexanone), esters (also fats and oils) and (poly) ethers, the simple and substituted amines, amides, lactams (such as N-alkylpyrrolidones) and lactones, the sulfones and sulfoxides (such as dimethyl sulfoxide).
- aromatic and non-aromatic hydrocarbons such as paraffins, alkylbenzenes, alkylnaphthalenes, chlorobenzenes
- alcohols and polyols which may also be substituted, etherified and
- Suitable liquid solvents are essentially: aromatics, such as xylene, toluene, or alkylnaphthalenes, chlorinated aromatics and chlorinated aliphatic hydrocarbons, such as chlorobenzenes, chloroethylenes or methylene chloride, aliphatic hydrocarbons, such as cyclohexane or paraffins, e.g.
- Petroleum fractions mineral and vegetable oils, alcohols such as butanol or glycol and their ethers and esters, ketones such as acetone, methyl ethyl ketone, methyl isobutyl ketone or cyclohexanone, strongly polar solvents such as dimethyl sulfoxide, and water.
- Suitable solid carriers are:
- Ammonium salts and ground natural minerals such as kaolins, clays, talc, chalk, quartz, attapulgite, montmorillonite or diatomaceous earth, and ground synthetic minerals, such as finely divided silica, alumina and silicates, as solid carriers for granules are suitable: e.g. crushed and fractionated natural rocks such as calcite, marble, pumice, sepiolite, dolomite and synthetic granules of inorganic and organic flours and granules of organic material such as paper, sawdust, coconut shells, corn cobs and tobacco stems; suitable emulsifiers and / or foam formers are: e.g.
- nonionic and anionic emulsifiers such as polyoxyethylene fatty acid esters, polyoxyethylene fatty alcohol ethers, e.g. Alkylaryl polyglycol ethers, alkylsulfonates, alkyl sulfates, arylsulfonates and protein hydrolysates;
- suitable dispersants are non-ionic and / or ionic substances, e.g.
- Adhesives such as carboxymethylcellulose, natural and synthetic powdery, granular or latex-type polymers can be used in the formulations, such as gum arabic, polyvinyl alcohol, polyvinyl acetate, as well as natural phospholipids such as cephalins and lecithins and synthetic phospholipids.
- Dyes such as inorganic pigments such as iron oxide, titanium oxide, ferrocyan blue and organic dyes such as alizarin, azo and metal phthalocyanine dyes and trace nutrients such as salts of iron, manganese, boron, copper, cobalt, molybdenum and zinc can be used.
- additives may be fragrances, mineral or vegetable optionally modified oils, waxes and nutrients (also trace nutrients), such as salts of iron, manganese, boron, copper, cobalt, molybdenum and zinc.
- Stabilizers such as low-temperature stabilizers, preservatives, antioxidants, light stabilizers or other agents which improve the chemical and / or physical stability, may furthermore be present.
- the formulations generally contain between 0.01 and 98% by weight of active ingredient, preferably between 0.5 and 90%.
- the active ingredient according to the invention can be present in its commercial formulations and in the formulations prepared from these formulations in admixture with other active ingredients such as insecticides, attractants, sterilants, bactericides, acaricides, nematicides, fungicides, growth-regulating substances, herbicides, safeners, fertilizers or semiochemicals.
- active ingredients such as insecticides, attractants, sterilants, bactericides, acaricides, nematicides, fungicides, growth-regulating substances, herbicides, safeners, fertilizers or semiochemicals.
- Particularly favorable mixing partners are e.g. the following:
- Azoxystrobin Cyazofamide, Dimoxystrobin, Enestrobin, Famoxadon, Fenamidon, FIuoxastrobin, Kresoximmethyl, Metominostrobin, Orysastrobin, Pyraclostrobin, Picoxystrobin, Trifloxystrobin
- Isofenphos isopropyl-o-salicylates, isoxathione, malathion, mecarbam, methacrifos, methamidophos, methidathion, mevinphos, monocrotophos, saled, omethoates, oxymethyl-methyl, parathion (-methyl / -ethyl), phenthoates, phorates, phosalones, Phosmet, phosphamidone, phosphocarb, phoxim, pirimiphos (-methylethyl), profenofos, pro- paphos, propetamphos, prothiofos, prothoates, pyraclofos, pyridaphenthione, pyridathion, Quinalphos, Sebufos, Sulfotep, Sulprofos, Tebupirimfos, Temephos, Terbufos, Tetrachlorino
- acrinathrin for example, acrinathrin, allethrin (d-cis-trans, d-trans), beta-cyfluthrin, bifenthrin, biotethrin, bioallethrin-S-cyclopentyl isomer, bioethanomethrin, biopermethrin, bioresmethrin, chlovaporthrin, cis-cypermethrin, cis -Resmethrin, cis-permethrin, clocthrin, cycloprothrin, cyfluthrin, cyhalothrin, cypermethrin (alpha-, beta-, theta-, zeta-), cyphenothrin, deltamethrin, empenthrin (IR isomer), esfenvalerate, etofenprox, fenfluthrin,
- Flufenprox Flumethrin, Fluvalinate, Fubfenprox, Gamma-Cyhalothrin, Imiprothrin, Kadhrin, Lambda-Cyhalothrin, Metofluthrin, Permethrin (cis, trans), Phenothrin (IR trans isomer), Prallethrin, Profuthrin, Protrifenbute, Pyresmethrin, Resmethrin , RU 15525, silafluofen, tau-fluvalinate, tefluthrin, terallethrin, tetramethrin (-1R- isomer), tralomethrin, transfluthrin, ZXI 8901, pyrethrin (pyrethrum)
- Metaflumizone (BAS3201)
- Acetylcholine receptor modulators are Acetylcholine receptor modulators
- spinosyns for example spinosad, spinetoram (XDE-175)
- camphechlor for example, camphechlor, chlordane, endosulfan, gamma-HCH, HCH, heptachlor, lindane, methoxychlor
- acetoprole for example, acetoprole, ethiprole, fipronil, pyrafluprole, pyriprole, vaniliprole
- abamectin for example, abamectin, emamectin, emamectin benzoate, ivermectin, lepimectin, mi-bemycin
- diofenolane for example, diofenolane, epofenonans, fenoxycarb, hydroprene, kinoprenes, methoprenes, pyriproxifen, triprene
- chromium afenozide for example chromium afenozide, halofenozide, methoxyfenozide, tebufenozide
- azocyclotin for example, azocyclotin, cyhexatin, fenbutatin oxides
- fenazaquin for example, fenazaquin, fenpyroximate, pyrimidifen, pyridaben, tebufenpyrad, tolfenpyrad
- tetronic acids for example spirodiclofen, spiromesifen
- rynaxypyr (3-bromo-N- ⁇ 4-chloro-2-methyl-6 - [(methylamino) carbonyl] -phenyl ⁇ -1- (3-chloropyridin-2-yl) -1H-pyrazole-5-carboxamide )
- a mixture with other known active ingredients, such as herbicides, fertilizers, growth regulators, safeners, semiochemicals, or with agents for improving the plant properties is possible.
- the active compounds according to the invention can furthermore be present in the form of insecticides in their commercial formulations and in the formulations prepared from these formulations in admixture with synergists.
- Synergists are compounds that increase the effect of the active ingredients without the added synergist itself having to be active.
- the active compounds according to the invention may furthermore, when used as insecticides in their commercial formulations and in the forms of use prepared from these formulations, be present in mixtures with inhibitors which reduce degradation of the active ingredient after application in the environment of the plant, on the surface of plant parts or in plant tissues ,
- the active substance content of the application forms prepared from the commercial formulations can vary within wide ranges.
- the active ingredient concentration of the use forms may be from 0.00000001 up to 95% by weight of active compound, preferably between 0.00001 and 1% by weight.
- the application is done in a custom forms adapted to the application forms.
- plants and parts of plants can be treated.
- plants are understood as meaning all plants and plant populations, such as desired and undesired wild plants or crop plants (including naturally occurring crop plants).
- Crop plants can be plants that are produced by conventional breeding and optimization methods or by biotechnological and genetic engineering methods or combinations thereof Methods can be obtained, including transgenic plants and including those protected by plant breeders' rights or non-protectable plant varieties.
- Plant parts are to be understood as meaning all aboveground and underground parts and organs of the plants, such as shoot, leaf, flower and root, examples of which include leaves, needles, stems, stems, flowers, fruiting bodies, fruits and seeds, as well as roots, tubers and rhizomes become.
- the plant parts also include crops and vegetative and generative propagation material, such as cuttings, tubers, rhizomes, offshoots and seeds.
- the treatment according to the invention of the plants and plant parts with the active substances takes place directly or by acting on their environment, habitat or storage space according to the usual treatment methods, e.g. by dipping, spraying, evaporating, atomizing, spreading, brushing, injecting and in propagating material, in particular in seeds, further by single or multilayer coating.
- the treatment according to the invention of the plants and plant parts with the active compound combinations takes place directly or by acting on their environment, habitat or storage space according to the usual treatment methods, e.g. by dipping, spraying, vaporizing, atomizing, spreading, spreading and in propagation material, in particular in seeds, further by single or multi-layer wrapping.
- the mixtures according to the invention are suitable for the treatment of seed.
- This phase is particularly critical, as the roots and shoots of the growing plant are particularly sensitive and even minor damage can lead to the death of the entire plant. There is therefore a particular interest in protecting the seed and the germinating plant by the use of suitable agents.
- the present invention therefore more particularly relates to a method of protecting seed and germinating plants from infestation by pests by treating the seed with an agent according to the invention.
- the invention also relates to the use of the agents according to the invention for the treatment of seeds for the protection of the seed and the resulting plant from pests.
- the invention relates to seed, which has been treated for protection against pests with a erf ⁇ ndungsdorfen agent.
- One of the advantages of the present invention is that because of the particular systemic properties of the compositions of the invention, treatment of the seed with these agents not only protects the seed itself, but also the resulting plants after emergence from pests. In this way, the immediate treatment of the culture at the time of sowing or shortly afterwards can be omitted.
- a further advantage consists in the synergistic increase of the insecticidal activity of the agents according to the invention over the insecticidal single active substance, which goes beyond the expected effectiveness of the two individually applied active substances. Also advantageous is the synergistic increase in the fungicidal activity of the compositions of the invention over the fungicidal single active ingredient, which goes beyond the expected efficacy of the single active ingredient. This allows optimization of the amount of active ingredients used.
- the mixtures according to the invention can also be used in particular in the case of transgenic seed, wherein the plants resulting from this seed are capable of expressing a protein directed against pests.
- certain pests may be affected by the expression of e.g. insecticidal protein and, in addition, be protected from damage by the means of the invention.
- compositions of the invention are suitable for the protection of seed of any plant variety as mentioned above, which is used in agriculture, in the greenhouse, in forests or in horticulture.
- these are corn, peanut, canola, rapeseed, poppy seeds, soya, cotton, beet (eg sugar beet and fodder beet), rice, millet, wheat, cereal oats, rye, sunflower, tobacco, potatoes or vegetables (eg tomatoes, cabbages).
- the compositions according to the invention are likewise suitable for the treatment of the seed of fruit plants and vegetables as already mentioned above. Of particular importance is the treatment of the seeds of maize, soya, cotton, wheat and canola or rapeseed.
- transgenic seed contains at least one heterologous gene which controls the expression of a polypeptide with in particular insecticidal properties.
- the heterologous genes in transgenic seed can come from microorganisms such as Bacillus, Rhizobium, Pseudomonas, Serratia, Trichoderma, Clavibacter, Glomus or Gliocladium.
- the present invention is particularly useful for the treatment of transgenic seed containing at least one heterologous gene derived from Bacillus sp. and whose gene product shows activity against corn borer and / or corn rootworm. Most preferably, this is a heterologous gene derived from Bacillus thuringiensis.
- the agent according to the invention is applied to the seed alone or in a suitable formulation.
- the seed is treated in a condition that is so stable that no damage occurs during the treatment.
- the treatment of the seed can be done at any time between harvesting and sowing.
- seed is used which has been separated from the plant and freed from corms, shells, stems, hull, wool or pulp.
- plants and their parts can be treated.
- wild-type or plant species obtained by conventional biological breeding methods such as crossing or protoplast fusion
- plant cultivars and their parts are treated.
- transgenic plants and plant cultivars obtained by genetic engineering if appropriate in combination with conventional methods (Genetically Modified Organisms), and parts thereof are treated.
- the terms "parts” or “parts of plants” or “plant parts” have been explained above. It is particularly preferred according to the invention to treat plants of the respective commercially available or in use plant cultivars. Plant varieties are understood as meaning plants having new traits which have been bred by conventional breeding, by mutagenesis or by recombinant DNA techniques. These can be varieties, biotypes and genotypes.
- the treatment according to the invention may also give rise to superadditive ("synergistic") effects.
- superadditive for example, reduced application rates and / or extensions of the spectrum of action and / or an increase in the effect of the substances and agents usable in the invention, better plant growth, increased tolerance to high or low temperatures, increased tolerance to drought or to water or soil salt content, increased flowering power facilitated harvest, acceleration of ripeness, higher crop yields, higher quality and / or higher nutritional value of the harvested products, higher shelf life and / or machinability of the harvested products, which exceed the actual expected effects.
- the preferred plants or plant varieties to be treated according to the invention to be treated include all plants which, as a result of the genetic engineering modification, obtained genetic material which gives these plants particularly advantageous valuable properties ("traits").
- traits are better plant growth, increased tolerance to high or low temperatures, increased tolerance to dryness or to bottoms salt, increased flowering, easier harvesting, acceleration of ripeness, higher crop yields, higher quality and / or higher nutritional value of the harvested products , higher shelf life and / or workability of the harvested products.
- Further and particularly emphasized examples of such properties are an increased defense of the plants against animal and microbial pests, such as against insects, mites, phytopathogenic fungi, bacteria and / or viruses as well as an increased tolerance of the plants to certain herbicidal active compounds.
- transgenic plants are the important crops, such as cereals (wheat, rice), corn, soybeans, potatoes, sugar beets, tomatoes, peas and other vegetables, cotton, tobacco, rapeseed, and fruit plants (with the fruits apples, pears, citrus fruits). fruit and grapes), with special emphasis on maize, soya, potato, cotton, tobacco and oilseed rape.
- Traits that are particularly emphasized are the increased defense of the plants against insects, arachnids, nematodes and snails by toxins produced in the plants, in particular those which are produced by the genetic material from Bacillus thuringiensis (eg by the genes Cry ⁇ A (a) , Cry ⁇ A (b), Cry ⁇ A (c), CryllA, CrylllA, Cryl IIB2, Cry9c Cry2Ab, Cry3Bb and CrylF and combinations thereof) in the plants (hereinafter "Bt plants”). Traits also highlight the increased resistance of plants to fungi, bacteria and viruses by systemic acquired resistance (SAR), systemin, phytoalexins, elicitors and resistance genes and correspondingly expressed proteins and toxins.
- SAR systemic acquired resistance
- “traits” which continue to be particularly emphasized are the increased tolerance of the plants to certain herbicidal active compounds, for example imidazolinones, sulfonylureas, glyphosate or phosphinotricin (eg "PAT” gene).
- the genes which confer the desired properties (“traits”) can also occur in combinations with one another in the transgenic plants.
- “Bt plants” are maize varieties, cotton varieties, soybean varieties and potato varieties which are sold under the trade names YIELD GARD® (eg corn, cotton, soya), KnockOut® (eg maize), StarLink® (eg maize), Bollgard® ( Cotton), Nucotn® (cotton) and NewLeaf® (potato).
- herbicide-tolerant plants are maize varieties, cotton varieties and soybean varieties, which are sold under the trade names Roundup Ready® (tolerance to glyphosate eg corn, cotton, soy), Liberty Link® (tolerance to phosphinotricin, eg rapeseed), IMI® (tolerance against imidazolinone) and STS® (tolerance to sulfonylureas eg corn).
- Roundup Ready® tolerance to glyphosate eg corn, cotton, soy
- Liberty Link® tolerance to phosphinotricin, eg rapeseed
- IMI® tolerance against imidazolinone
- STS® tolerance to sulfonylureas eg corn
- Clearfield® varieties eg corn
- the listed plants can be treated particularly advantageously according to the invention with the compounds of the general formula I or the active substance mixtures according to the invention.
- the preferred ranges given above for the active compounds or mixtures also apply to the treatment of these plants.
- Particularly emphasized is the plant treatment with the compounds or mixtures specifically mentioned in the present text.
- the active compounds of the invention not only against plant, hygiene and storage pests, but also in the veterinary sector against animal parasites (ecto- and endoparasites) such as ticks, leather ticks, mange mites, running mites, flies (stinging and licking), parasitic fly larvae, lice , Hair pieces, featherlings and fleas.
- animal parasites ecto- and endoparasites
- ticks ecto- and endoparasites
- leather ticks such as ticks, leather ticks, mange mites, running mites, flies (stinging and licking), parasitic fly larvae, lice , Hair pieces, featherlings and fleas.
- flies stinging and licking
- parasitic fly larvae such as ticks, leather ticks, mange mites, running mites, flies (stinging and licking), parasitic fly larvae, lice , Hair pieces, featherlings and fleas.
- Anoplurida eg Haematopinus spp., Linognathus spp., Pediculus spp., Phytus spp., Solenopotes spp. From the order of Mallophagida and the suborders Amblycerina and Ischnocerina eg Trimenopon spp., Menopon spp., Trinoton spp., Bovicola spp., Werneckiella spp., Lepikentron spp., Damalina spp., Trichodectes spp., Felicola spp.
- Nematocerina and Brachycerina e.g. Aedes spp., Anopheles spp., Culex spp., Simulium spp., Eusimulium spp., Phlebotomus spp., Lutzomyia spp., Culicoides spp., Chrysops spp., Hybomitra spp., Atylotus spp., Tabanus spp., Haematopota spp , Philipomyia spp., Braula spp., Musca spp., Hydrotaea spp., Stomoxys spp., Haematobia spp.,
- siphonaptrida e.g. Pulex spp., Ctenocephalides spp., Xenopsylla spp., Ceratophyllus spp.
- heteropterid e.g. Cimex spp., Triatoma spp., Rhodnius spp., Panstrongylus spp.
- Actinedida Prostigmata
- Acaridida e.g. Acarapis spp., Cheyletiella spp., Ornitrocheyletia spp., Myobia spp., Psorergates spp., Demodex spp., Trombicula spp., Listrophorus spp., Acarus spp., Tyrophagus spp., Caloglyphus spp., Hypodectes spp.
- Pterolichus spp. Psoroptes spp., Chorioptes spp., Otodectes spp., Sarcoptes spp., Notoedres spp., Knemidocoptes spp., Cytodites spp., Laminosioptes spp.
- the active compounds of the formula (I) according to the invention are also suitable for controlling arthropods, the livestock, such as cattle, sheep, goats, horses, pigs, donkeys, camels, buffalos, rabbits, chickens, turkeys, ducks, geese, bees, other pets such as dogs, cats, caged birds, aquarium fish and so-called experimental animals, such as hamsters, guinea pigs, rats and mice infested.
- livestock such as cattle, sheep, goats, horses, pigs, donkeys, camels, buffalos, rabbits, chickens, turkeys, ducks, geese, bees, other pets such as dogs, cats, caged birds, aquarium fish and so-called experimental animals, such as hamsters, guinea pigs, rats and mice infested.
- the use of the active compounds according to the invention takes place in the veterinary sector and in animal husbandry in a known manner by enteral administration in the form of, for example, tablets, capsules, infusions, drenches, granules, pastes, boilies, the feed-through process, suppositories, by parenteral administration, as by injections (intramuscular, subcutaneous, intravenous, intraperitoneal, etc.), implants, by nasal application, by dermal application in the form of, for example, diving or bathing (dipping), spraying, pouring (pour-on and spot-on ), washing, powdering and with the aid of active substance-containing moldings, such as collars, ear tags, tail marks, limb bands, holsters, marking devices, etc.
- enteral administration in the form of, for example, tablets, capsules, infusions, drenches, granules, pastes, boilies, the feed-through process, suppositories
- parenteral administration as by injections (intr
- the active compounds of the formula (I) can be used as formulations (for example powders, emulsions, flowable agents) which contain the active ingredients in an amount of from 1 to 80% by weight, directly or apply after 100 to 10,000 times dilution or use as a chemical bath.
- formulations for example powders, emulsions, flowable agents
- the compounds according to the invention have a high insecticidal activity against insects which destroy industrial materials.
- insects By way of example and preferably without limiting however, the following insects are mentioned:
- Hymenoptera such as Sirex juvencus, Urocerus gigas, Urocerus gigas taignus, Urocerus augur;
- Termites such as Kalotermes flavicollis, Cryptotermes brevis, Heterotermes indicola, Reticulitermes flavipes, Reticulitermes santonensis, Reticulitermes lucifugus, Mastotermes darwiniensis, Zooter- mopsis nevadensis, Coptotermes formosanus;
- Bristle tails like Lepisma saccharina.
- Technical materials in the present context are non-living materials, such as preferably plastics, adhesives, glues, papers and cardboard, leather, wood, wood processing products and paints.
- the ready-to-use agents may optionally contain further insecticides and, if appropriate, one or more fungicides.
- the compounds according to the invention can be used for protection against the growth of objects, in particular hulls, sieves, nets, structures, quays and signal systems, which come into contact with seawater or brackish water.
- the compounds according to the invention can be used alone or in combinations with other active substances as antifouling agents.
- the active substances are also suitable for controlling animal pests in household, hygiene and storage protection, in particular insects, arachnids and mites, which are used in closed rooms, such as apartments, factory halls, offices, vehicle cabins and the like. occurrence. They can be used to control these pests, alone or in combination with other active ingredients and adjuvants in household insecticide products. They are effective against sensitive and resistant species and against all stages of development. These pests include:
- Acarina e.g. Argas persicus, Argas reflexus, Bryobia ssp., Dermanyssus gallinae, Glyciphagus domesticus, Ornithodorus moubat, Rhipicephalus sanguineus, Trombicula alfreddugesi, Neutrombicula autumnalis, Dermatophagoides pteronissimus, Dermatophagoides forinae.
- Opiliones e.g. Pseudoscorpiones chelifer, Pseudoscorpiones cheiridium, Opiliones phalangium.
- Zygentoma e.g. Ctenolepisma spp., Lepisma saccharina, Lepismodes inqui- linus.
- Diptera e.g. Aedes aegypti, Aedes albopictus, Aedes taeniorhynchus, Anopheles spp., Calliphora erythrocephala, Chrysozona pluvialis, Culex quinquefasciatus, Culex pipiens, Culex tarsalis, Drosophila spp., Fannia canicularis, Musca domestica, Phlebotomus spp., Sarcophaga carnaria, Simulium spp. , Stomoxys calcitrans, Tipula paludosa.
- Lepidoptera e.g. Achroia grisella, Galleria mellonella, Plodia interpunctella, Tinea cloacella, Tinea pellionella, Tineola bisselliella.
- Ctenocephalides canis Ctenocephalides felis, Pulex irri- tans, Tunga penetrans, Xenopsylla cheopis.
- Hymenoptera e.g. Camponotus herculeanus, Lasius fuliginosus, Lasius niger, Lasius umbratus, Monomorium pharaonis, Paravespula spp., Tetramorium caespitum.
- the application is carried out in aerosols, non-pressurized sprays, eg pump and atomizer sprays, fog machines, foggers, foams, gels, evaporator products with evaporator plates of cellulose or plastic, liquid evaporators, gel and membrane evaporators, propeller driven evaporators, energy-less or passive evaporation systems, moth papers, Mot - bags and moth gels, as granules or dusts, in straw baits or bait stations.
- Example (2) 0.52 g (5.18 mmol) of tetronic acid is initially introduced in 1.13 ml of acetic acid and slowly at room temperature with 1.00 g (4.93 mmol) of N - [(6-chloro-pyridin-3-yl) -methyl] -3-fluoro-propan-1-amine (III-2). Subsequently, the entire reaction mixture is stirred for about 18 hours at room temperature. After concentration of the reaction mixture in vacuo, take up with dichloromethane and washed with water. After phase separation, the aqueous phase is extracted twice with dichloromethane. The combined organic phases are then made alkaline with 1 N sodium hydroxide solution (pH> 9) and the phases are separated.
- the aqueous phase is extracted twice with dichloromethane and, after phase separation, the combined organic phases are dried over sodium sulfate. After concentration of the organic phase in vacuo and purification of the residue by column chromatography on silica gel (silica gel 60 - Merck, particle size: 0.04 to 0.063 mm) with the mobile phase mixture ethyl acetate: cyclohexane (9: 1) to obtain 191 mg (14% of theory). 4 - [[(6-chloro-pyridin-3-yl) methyl] (3-fluoro -propyl) amino] furan-2 (5H) -one.
- the mixture is taken up in ethyl acetate, washed successively twice with 1 N aqueous hydrochloric acid, twice with 1 N aqueous sodium hydroxide solution and once with saturated sodium chloride solution. The organic phase is then dried over sodium sulfate and concentrated in vacuo.
- Emulsifier 0.5 part by weight of alkylaryl polyglycol ether
- active compound 1 part by weight of active compound is mixed with the indicated amounts of solvent and emulsifier, and the concentrate is diluted with emulsifier-containing water to the desired concentration.
- Chinese cabbage leaf discs (Brassica pekinensis) infested with all stages of the green peach aphid (Myzus persicae) are sprayed with an active compound preparation of the desired concentration.
- Vessels are populated with all stages of the green peach aphid (Myzus persicae), by sucking on the preparation of active compound of the desired concentration is treated. After the desired time, the effect is determined in%. 100% means that all aphids have been killed; 0% means that no aphids have been killed. In this test, z. B. the following compounds of the preparation examples good activity: see table
- Nilaparvata lugens test (NILALU hydroponic treatment)
- Emulsifier 0.5 part by weight of alkylaryl polyglycol ether
- a suitable preparation of active compound 1 part by weight of the compound is mixed with the stated amounts of solvent and emulsifier, and the concentrate is diluted with emulsifier-containing water to the desired concentration.
- the preparation of active compound is pipetted in water.
- Emulsifier 0.5 part by weight of alkylaryl polyglycol ether
- active compound 1 part by weight of active compound is mixed with the indicated amounts of solvent and emulsifier, and the concentrate is diluted with emulsifier-containing water to the desired concentration.
- Chinese cabbage leaf discs (Brassica pekinensis) are sprayed with a preparation of active compound of the desired concentration and, after drying, are populated with larvae of the horseradish leaf beetle (Phaedon cochleariae).
- the effect is determined in%. 100% means that all beetle larvae have been killed; 0% means that no beetle larvae have been killed.
- Vessels are filled with sand, drug solution, Meloidogyne incognita egg larvae suspension and lettuce seeds.
- the lettuce seeds germinate and the plantlets develop.
- the galls develop at the roots.
- the nematicidal activity is determined by means of bile formation in%. 100% means that no bile was found; 0% means that the number of bile on the treated plants corresponds to that of the untreated control.
- Emulsifier parts by weight of alkylaryl polyglycol ether
- active compound 1 part by weight of active compound is mixed with the indicated amounts of solvent and emulsifier, and the concentrate is diluted with water to the desired concentration.
- the preparation of active compound is mixed with water.
- the treated water is filled into peas (Pisum sativum), then infected with the green peach aphid ⁇ Myzus persicae)
- the kill is determined in%. 100% means that all aphids have been killed; 0% means that no aphids have been killed.
- Emulsifier parts by weight of alkylaryl polyglycol ether
- active compound 1 part by weight of active compound is mixed with the indicated amounts of solvent and emulsifier, and the concentrate is diluted with emulsifier-containing water to the desired concentration.
- Cotton leaves which are heavily infested with the cotton aphid ⁇ Aphis gossypii) are treated by being dipped into the preparation of active compound of the desired concentration.
- the kill is determined in%. 100% means that all aphids have been killed; 0% means that no aphids have been killed.
- Emulsifier parts by weight of alkylaryl polyglycol ether To prepare a suitable preparation of active compound, 1 part by weight of active compound is mixed with the indicated amounts of solvent and emulsifier, and the concentrate is diluted with water to the desired concentration.
- Cotton plants which are heavily attacked by the cotton aphid (Aphis gossypi ⁇ ), are cast with a preparation of active compound of the desired concentration.
- the kill is determined in%. 100% means that all aphids have been killed; 0% means that no aphids have been killed.
- Emulsifier 2 parts by weight of alkylaryl polyglycol ether
- active compound 1 part by weight of active compound is mixed with the indicated amounts of solvent and emulsifier, and the concentrate is diluted with water to the desired concentration.
- Cabbages (Brassica oleraceä) which are heavily infested with the green peach aphid (Myzus persicae) are infused with an active compound preparation of the desired concentration.
- the kill is determined in%. 100% means that all aphids have been killed; 0% means that no aphids have been killed.
- Emulsifier 0.5 part by weight of alkylaryl polyglycol ether
- Cotton leaf discs (Gossypium hirsutum) infested with larvae of the white fly (Bemisia tabaci) are sprayed with an active compound preparation of the desired concentration.
- the effect is determined in%. 100% means that all white flies have been killed; 0% means that no white fly has been killed.
- active compound For the preparation of a suitable preparation of active compound, 1 part by weight of active compound is mixed with the stated amount of water. A portion of the concentrate is diluted with citrated bovine blood and the desired concentration produced.
- fasting adult fleas (Ctenocephalides felis) are placed in a chamber sealed with gauze on top and bottom.
- a metal cylinder is placed on the chamber, the underside of which is sealed with parafilm.
- the cylinder contains the blood-drug preparation that can be absorbed by the fleas through the parafilm membrane. While the blood is heated to 37 ° C, room temperature is in the area of the flea chambers.
- the kill is determined in%. 100% means that all fleas have been killed; 0% means that no flea has been killed.
- the kill is determined in%. 100% means that all larvae have been killed; 0% means that no larvae have been killed.
- Boophilus microplus test (BOOPMI injection)
- the drug solution is injected into the abdomen (Boophilus microplus), the animals are transferred to trays and stored in an air-conditioned room.
- the effect is determined in%. 100% means that no ticks have laid fertile eggs.
- Emulsifier parts by weight of alkylaryl polyglycol ether
- active compound 1 part by weight of active compound is mixed with the indicated amounts of solvent and emulsifier, and the concentrate is diluted with emulsifier-containing water to the desired concentration.
- Cabbage leaves (Brassica olerace ⁇ ) which are heavily infested with the green peach aphid ⁇ Myzus persicae) are treated by being dipped into the preparation of active compound of the desired concentration.
- the kill is determined in%. 100% means that all aphids have been killed; 0% means that no aphids have been killed.
- active compound 1 part by weight of active compound is mixed with the indicated amounts of solvent and emulsifier, and the concentrate is diluted with emulsifier-containing water to the desired concentration.
- Chinese cabbage leaf discs (Brassica pekinensis) infested with all stages of the green peach aphid (Myzus persicae) are sprayed with an active compound preparation of the desired concentration.
- the effect is determined in%. 100% means that all aphids have been killed; 0% means that no aphids have been killed.
- Emulsifier parts by weight of alkylaryl polyglycol ether
- active compound 1 part by weight of active compound is mixed with the indicated amounts of solvent and emulsifier, and the concentrate is diluted with water to the desired concentration.
- the preparation of active compound is mixed with water.
- the treated water is filled into peas (Pisum sativum), then infected with the green peach aphid ⁇ Myzus persicae)
- the kill is determined in%. 100% means that all aphids have been killed; 0% means that no aphids have been killed.
- Emulsifier part by weight of alkylaryl polyglycol ether
- active compound 1 part by weight of active compound is mixed with the indicated amounts of solvent and emulsifier, and the concentrate is diluted with emulsifier-containing water to the desired concentration.
- the corresponding amount is pipetted after dilution of each of the finished preparation solution.
- Paprika plants (Capsicum cmnuum) which are heavily infested with the green peach aphid ⁇ Myzus persicae ⁇ ) are treated by spraying with the preparation of active compound in the desired concentration.
- Vessels are filled with all stages of the Green Peach aphid (Myzus persicae), by sucking on the preparation of active compound of the desired concentration is treated.
- Green Peach aphid Myzus persicae
- the effect is determined in%. 100% means that all aphids have been killed; 0% means that no aphids have been killed.
- Emulsifier 2 parts by weight of alkylaryl polyglycol ether
- a suitable preparation of active compound 1 part by weight of active compound is mixed with the indicated amounts of solvent and emulsifier, and the concentrate is diluted with emulsifier-containing water to the desired concentration.
- Cotton leaves ⁇ Gossypium hirsutum) which are heavily infested with cotton aphid (Aphis gossypn) are treated by being dipped into the preparation of active compound of the desired concentration.
- the kill is determined in%. 100% means that all aphids have been killed; 0% means that no aphids have been killed.
- Vessels are filled with sand, drug solution, Meloidogyne incognita egg larvae suspension and lettuce seeds.
- the lettuce seeds germinate and the plantlets develop.
- the galls develop at the roots.
- the nematicidal activity is determined by means of bile formation in%. 100% means that no bile was found; O% means that the number of bile on the treated plants corresponds to that of the untreated control.
- Vessels containing horsemeat treated with the preparation of active compound of the desired concentration are infested with Lucilia cuprina larvae.
- the kill is determined in%. 100% means that all larvae have been killed; 0% means that no larvae have been killed.
- active compound For the preparation of a suitable preparation of active compound, 1 part by weight of active compound is mixed with the stated amount of water. A portion of the concentrate is diluted with citrated bovine blood and the desired concentration produced.
- fasting adult fleas (Ctenocephalides felis) are placed in a chamber sealed with gauze on top and bottom.
- a metal cylinder is placed on the chamber, the underside of which is sealed with parafilm.
- the cylinder contains the blood-drug preparation that can be absorbed by the fleas through the parafilm membrane. While the blood is heated to 37 ° C, room temperature is in the area of the flea chambers.
- the kill is determined in%. 100% means that all fleas have been killed; 0% means that no flea has been killed.
- Boophilus microplus test (BOOPMI injection)
- the drug solution is injected into the abdomen (Boophilus microplus), the animals are transferred to trays and stored in an air-conditioned room.
- the effect is determined in%. 100% means that no ticks have laid fertile eggs.
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Abstract
Description
Claims
Priority Applications (19)
Application Number | Priority Date | Filing Date | Title |
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DK07723355.9T DK2004635T3 (en) | 2006-03-31 | 2007-03-19 | SUBSTITUTED ENAMINOCARBONYL COMPOUNDS |
KR1020137032091A KR101423077B1 (ko) | 2006-03-31 | 2007-03-19 | 치환된 엔아미노카보닐 화합물 |
BRPI0710103A BRPI0710103B1 (pt) | 2006-03-31 | 2007-03-19 | compostos enaminocarbonila substituídos, composição, seus usos, e processo para combate de pragas |
MX2013013408A MX363983B (es) | 2006-03-31 | 2007-03-19 | Compuestos de enaminocarbonilo sustituidos. |
PL07723355T PL2004635T3 (pl) | 2006-03-31 | 2007-03-19 | Podstawione związki enaminokarbonylowe |
EP07723355.9A EP2004635B1 (de) | 2006-03-31 | 2007-03-19 | Substituierte enaminocarbonylverbindungen |
KR1020087026049A KR101407042B1 (ko) | 2006-03-31 | 2007-03-19 | 치환된 엔아미노카보닐 화합물 |
MX2008012350A MX2008012350A (es) | 2006-03-31 | 2007-03-19 | Compuestos de enaminocarbonilo sustituidos. |
JP2009501903A JP5213847B2 (ja) | 2006-03-31 | 2007-03-19 | 置換されたエナミノカルボニル化合物 |
CN2007800191007A CN101466705B (zh) | 2006-03-31 | 2007-03-19 | 被取代的烯氨羰基化合物 |
US12/295,355 US8106211B2 (en) | 2006-03-31 | 2007-03-19 | Substituted enaminocarbonyl compounds |
SI200731718T SI2004635T1 (sl) | 2006-03-31 | 2007-03-19 | Substituirane spojine enaminokarbonila |
ES07723355.9T ES2553720T3 (es) | 2006-03-31 | 2007-03-19 | Compuestos de enaminocarbonilo sustituidos |
AU2007236295A AU2007236295B2 (en) | 2006-03-31 | 2007-03-19 | Substituted enaminocarbonyl compounds |
US13/334,949 US8404855B2 (en) | 2006-03-31 | 2011-12-22 | Substituted enaminocarbonyl compounds |
US13/717,624 US8546577B2 (en) | 2006-03-31 | 2012-12-17 | Substituted enaminocarbonyl compounds |
NL350090C NL350090I2 (nl) | 2006-03-31 | 2018-09-11 | flupyradifurone |
CY2019001C CY2019001I2 (el) | 2006-03-31 | 2019-01-25 | Υποκατεστημενες εναμινοκαρβονυλ ενωσεις |
LTPA2020501C LTC2004635I2 (lt) | 2006-03-31 | 2020-01-24 | Pakeistieji enaminokarbonilo junginiai |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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DE102006015467A DE102006015467A1 (de) | 2006-03-31 | 2006-03-31 | Substituierte Enaminocarbonylverbindungen |
DE102006015467.3 | 2006-03-31 |
Related Child Applications (2)
Application Number | Title | Priority Date | Filing Date |
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US12/295,355 A-371-Of-International US8106211B2 (en) | 2006-03-31 | 2007-03-19 | Substituted enaminocarbonyl compounds |
US13/334,949 Continuation US8404855B2 (en) | 2006-03-31 | 2011-12-22 | Substituted enaminocarbonyl compounds |
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WO2007115644A1 true WO2007115644A1 (de) | 2007-10-18 |
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PCT/EP2007/002386 WO2007115644A1 (de) | 2006-03-31 | 2007-03-19 | Substituierte enaminocarbonylverbindungen |
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US (3) | US8106211B2 (de) |
EP (2) | EP2327304B1 (de) |
JP (1) | JP5213847B2 (de) |
KR (2) | KR101407042B1 (de) |
CN (2) | CN101466705B (de) |
AR (1) | AR060185A1 (de) |
AU (1) | AU2007236295B2 (de) |
BR (1) | BRPI0710103B1 (de) |
CY (2) | CY1117038T1 (de) |
DE (1) | DE102006015467A1 (de) |
DK (1) | DK2004635T3 (de) |
ES (2) | ES2515221T3 (de) |
FI (1) | FIC20190019I1 (de) |
HU (2) | HUE028208T2 (de) |
LT (1) | LTC2004635I2 (de) |
MX (2) | MX363983B (de) |
NL (1) | NL350090I2 (de) |
PL (2) | PL2004635T3 (de) |
PT (1) | PT2004635E (de) |
SI (1) | SI2004635T1 (de) |
TW (1) | TWI386404B (de) |
WO (1) | WO2007115644A1 (de) |
ZA (1) | ZA200808376B (de) |
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WO2010063465A1 (de) * | 2008-12-05 | 2010-06-10 | Bayer Cropscience Aktiengesellschaft | Enaminocarbonylverbindung-nützlings-kombinationen |
EP2198709A1 (de) | 2008-12-19 | 2010-06-23 | Bayer CropScience AG | Verfahren zur Bekämpfung resistenter tierischer Schädlinge |
EP2201841A1 (de) | 2008-12-29 | 2010-06-30 | Bayer CropScience AG | Synergistische insektizide Mischungen |
EP2204094A1 (de) | 2008-12-29 | 2010-07-07 | Bayer CropScience AG | Verfahren zur verbesserten Verwendung des Herstellungspotentials von transgenen Pflanzen |
WO2010083955A2 (de) | 2009-01-23 | 2010-07-29 | Bayer Cropscience Aktiengesellschaft | Verwendung von enaminocarbonylverbindungen zur bekämpfung von durch insekten übertragenen virosen |
WO2010086095A1 (en) | 2009-01-29 | 2010-08-05 | Bayer Cropscience Ag | Method for improved utilization of the production potential of transgenic plants introduction |
WO2010086303A2 (en) | 2009-01-27 | 2010-08-05 | Basf Se | Method for dressing seeds |
WO2010089244A1 (en) | 2009-02-03 | 2010-08-12 | Basf Se | Method for dressing seeds |
DE102008063561A1 (de) | 2008-12-18 | 2010-08-19 | Bayer Cropscience Ag | Hydrazide, Verfahren zu deren Herstellung und deren Verwendung als Herbizide und Insektizide |
WO2010094728A1 (en) | 2009-02-19 | 2010-08-26 | Bayer Cropscience Ag | Pesticide composition comprising a tetrazolyloxime derivative and a fungicide or an insecticide active substance |
EP2223602A1 (de) | 2009-02-23 | 2010-09-01 | Bayer CropScience AG | Verfahren zur verbesserten Nutzung des Produktionspotentials genetisch modifizierter Pflanzen |
WO2010100189A1 (en) | 2009-03-04 | 2010-09-10 | Basf Se | 3-arylquinazolin-4-one compounds for combating invertebrate pests |
EP2230237A1 (de) | 2009-03-16 | 2010-09-22 | Bayer CropScience AG | Neues Verfahren zur Herstellung von Enaminocarbonyl-Verbindungen |
EP2230231A1 (de) | 2009-03-16 | 2010-09-22 | Bayer CropScience AG | Verfahren zur Herstellung von 2,2-Difluorethylamin-Derivaten durch Imin-Hydrierung |
EP2230236A1 (de) | 2009-03-16 | 2010-09-22 | Bayer CropScience AG | Neues Verfahren zur Herstellung von Enaminocarbonyl-Verbindungen |
EP2232995A1 (de) | 2009-03-25 | 2010-09-29 | Bayer CropScience AG | Verfahren zur verbesserten Nutzung des Produktionspotentials transgener Pflanzen |
WO2010108616A1 (de) | 2009-03-25 | 2010-09-30 | Bayer Cropscience Ag | Nematizide, insektizide und akarizide wirkstoffkombinationen umfassend pyridylethylbenzamide und insektizide |
WO2010108507A2 (de) * | 2009-03-25 | 2010-09-30 | Bayer Cropscience Ag | Synergistische wirkstoffkombinationen |
WO2010108506A1 (de) * | 2009-03-25 | 2010-09-30 | Bayer Cropscience Ag | Wirkstoffkombinationen mit insektiziden und akariziden eigenschaften |
WO2010108504A1 (de) * | 2009-03-25 | 2010-09-30 | Bayer Cropscience Ag | Wirkstoffkombinationen mit insektiziden und akariziden eigenschaften |
WO2010108505A1 (de) * | 2009-03-25 | 2010-09-30 | Bayer Cropscience Ag | Wirkstoffkombinationen mit insektiziden und akariziden eigenschaften |
WO2010112545A1 (en) | 2009-04-01 | 2010-10-07 | Basf Se | Isoxazoline compounds for combating invertebrate pests |
EP2239331A1 (de) | 2009-04-07 | 2010-10-13 | Bayer CropScience AG | Verfahren zur verbesserten Verwendung des Herstellungspotentials von transgenen Pflanzen |
WO2010121735A1 (en) | 2009-04-22 | 2010-10-28 | Bayer Cropscience Ag | Use of propineb as bird repellent |
EP2253610A1 (de) | 2007-09-18 | 2010-11-24 | Bayer CropScience AG | Verfahren zum Herstellen von 4-Aminobut-2-enoliden |
JP2010538026A (ja) * | 2007-09-05 | 2010-12-09 | バイエル・クロツプサイエンス・アクチエンゲゼルシヤフト | 殺虫及び殺ダニ特性を有する活性成分組合せ |
JP2010539202A (ja) * | 2007-09-18 | 2010-12-16 | バイエル・クロツプサイエンス・アクチエンゲゼルシヤフト | イミン水素化により2,2−ジフルオロエチルアミン誘導体を製造する方法 |
EP2264008A1 (de) | 2009-06-18 | 2010-12-22 | Bayer CropScience AG | Substituierte Enaminocarbonylverbindungen |
WO2010149370A1 (en) | 2009-06-24 | 2010-12-29 | Bayer Cropscience Ag | Combinations of biological control agents and insecticides |
WO2011003796A1 (en) | 2009-07-06 | 2011-01-13 | Basf Se | Pyridazine compounds for controlling invertebrate pests |
WO2011009804A2 (en) | 2009-07-24 | 2011-01-27 | Basf Se | Pyridine derivatives compounds for controlling invertebrate pests |
WO2011009540A2 (en) | 2009-07-24 | 2011-01-27 | Bayer Cropscience Ag | Pesticidal carboxamides |
WO2011014660A1 (en) | 2009-07-30 | 2011-02-03 | Merial Limited | Insecticidal 4-amino-thieno[2,3-d]-pyrimidine compounds and methods of their use |
WO2011020567A1 (de) | 2009-08-20 | 2011-02-24 | Bayer Cropscience Ag | 3-triazolylphenyl-substituierte sulfid-derivate als akarizide und insektizide |
WO2011020564A1 (de) | 2009-08-18 | 2011-02-24 | Bayer Cropscience Ag | Neues verfahren zur herstellung von 4-aminobut-2-enoliden |
WO2010108508A3 (de) * | 2009-03-25 | 2011-03-03 | Bayer Cropscience Ag | Wirkstoffkombinationen mit insektiziden und akariziden eigenschaften |
WO2011025789A2 (en) | 2009-08-28 | 2011-03-03 | Basf Corporation | Foamable pesticide compositions and methods of application |
WO2011029506A1 (de) | 2009-08-20 | 2011-03-17 | Bayer Cropscience Ag | 3-[1-(3-haloalkyl)-triazolyl]-phenyl-sulfid-derivate als akarizide und insektizide |
WO2011036074A1 (en) | 2009-09-24 | 2011-03-31 | Basf Se | Aminoquinazoline compounds for combating invertebrate pests |
US20110086848A1 (en) * | 2009-09-14 | 2011-04-14 | Bayer Cropscience Ag | Agrochemical Compositions Comprising Alkyl Polypropylene Glycol Polyethylene Glycol |
WO2011045240A1 (de) | 2009-10-12 | 2011-04-21 | Bayer Cropscience Ag | Amide und thioamide als schädlingsbekämpfungsmittel |
WO2011045224A1 (de) | 2009-10-12 | 2011-04-21 | Bayer Cropscience Ag | 1- (pyrid-3-yl) -pyrazole und 1- (pyrimid-5-yl) -pyrazole als schädlingsbekämpfungsmittel |
WO2011051151A1 (de) | 2009-10-26 | 2011-05-05 | Bayer Cropscience Ag | Neue feste form von 4-[[(6-chlorpyridin-3-yl)methyl](2,2-difluorethyl)amino]furan-2(5h)-on |
WO2011051455A1 (en) | 2009-10-30 | 2011-05-05 | Bayer Cropscience Ag | Pesticidal heterocyclic compounds |
WO2011051240A1 (de) | 2009-10-27 | 2011-05-05 | Bayer Technology Services Gmbh | Co-kristall von 4-{[(6-chlorpyrid-3-yl)methyl](2,2-difluorethyl)amino}furan-2(5h)-on mit benzoesäure und dessen verwendung als pestizid |
WO2011051241A1 (de) | 2009-10-27 | 2011-05-05 | Bayer Technology Services Gmbh | Co-kristall von 4-{[(6-chlorpyrid-3yl)methyl](2,2-difluorethyl)amino}furan-2(5h)-on mit oxalsäure und dessen verwendung als pestizid |
WO2011051242A1 (de) | 2009-10-27 | 2011-05-05 | Bayer Technology Services Gmbh | Co-kristall von 4- { [ (6-chlorpyrid-3-yl) methyl] (2,2-difluorethyl) amino} furan-2 (5h) -on mit salizylsäure und dessen verwendung als pestizid |
WO2011054436A2 (de) | 2009-10-27 | 2011-05-12 | Bayer Cropscience Ag | Halogenalkyl-substituierte amide als insektizide und akarizide |
WO2011057942A1 (en) | 2009-11-12 | 2011-05-19 | Basf Se | Insecticidal methods using pyridine compounds |
WO2011061110A1 (en) | 2009-11-17 | 2011-05-26 | Basf Se | Fluorinated oxa or thia heteroarylalkylsulfide derivatives for combating invertebrate pests |
WO2011061156A1 (en) | 2009-11-17 | 2011-05-26 | Bayer Cropscience Ag | Active compound combinations |
WO2011064188A1 (en) | 2009-11-27 | 2011-06-03 | Basf Se | Insecticidal methods using nitrogen-containing heteroaromatic compounds |
WO2011069143A1 (en) | 2009-12-04 | 2011-06-09 | Merial Limited | Pesticidal bis-organosulfur compounds |
WO2011069955A1 (en) | 2009-12-07 | 2011-06-16 | Basf Se | Sulfonimidamide compounds for combating animal pests |
WO2011073444A2 (en) | 2009-12-18 | 2011-06-23 | Basf Se | Azoline compounds for combating invertebrate pests |
WO2011076726A2 (en) | 2009-12-23 | 2011-06-30 | Bayer Cropscience Ag | Pesticidal compound mixtures |
WO2011076727A2 (en) | 2009-12-23 | 2011-06-30 | Bayer Cropscience Ag | Pesticidal compound mixtures |
WO2011076715A1 (de) | 2009-12-23 | 2011-06-30 | Bayer Cropscience Ag | Neues verfahren zur herstellung von 4-aminobut-2-enoliden ausgehend von 4-alkoxyfuran-2(5h)-on oder 4-arylalkoxyfuran-2-(5h)-on |
WO2011076724A2 (en) | 2009-12-23 | 2011-06-30 | Bayer Cropscience Ag | Pesticidal compound mixtures |
WO2011080211A1 (en) | 2009-12-28 | 2011-07-07 | Bayer Cropscience Ag | Pesticidal arylpyrrolidines |
WO2011080044A2 (en) | 2009-12-16 | 2011-07-07 | Bayer Cropscience Ag | Active compound combinations |
WO2011092147A1 (en) | 2010-01-29 | 2011-08-04 | Bayer Cropscience Ag | Method to reduce the frequency and/or intensity of blossom-end rot disorder in horticultural crops |
WO2011092287A1 (en) | 2010-02-01 | 2011-08-04 | Basf Se | Substituted ketonic isoxazoline compounds and derivatives for combating animal pests |
EP2353386A1 (de) | 2010-02-05 | 2011-08-10 | Bayer CropScience AG | Wirkstoffkombination enthaltend Azadirachtin und eine substituierte Enaminocarbonylverbindung |
WO2011098443A1 (de) | 2010-02-10 | 2011-08-18 | Bayer Cropscience Ag | Spiroheterocyclisch-substituierte tetramsäure-derivate |
WO2011098440A2 (de) | 2010-02-10 | 2011-08-18 | Bayer Cropscience Ag | Biphenylsubstituierte cyclische ketoenole |
WO2011107504A1 (de) | 2010-03-04 | 2011-09-09 | Bayer Cropscience Ag | Fluoralkyl- substituierte 2 -amidobenzimidazole und deren verwendung zur steigerung der stresstoleranz in pflanzen |
WO2011107443A1 (en) | 2010-03-02 | 2011-09-09 | Bayer Cropscience Ag | Use of propineb for physiological curative treatment under zinc deficiency |
WO2011117213A1 (en) | 2010-03-23 | 2011-09-29 | Basf Se | Pyridazine compounds for controlling invertebrate pests |
WO2011117286A1 (en) | 2010-03-23 | 2011-09-29 | Basf Se | Pyridazine compounds for controlling invertebrate pests |
WO2011117198A2 (en) | 2010-03-23 | 2011-09-29 | Basf Se | Pyridazine compounds for controlling invertebrate pests |
WO2011131616A2 (de) | 2010-04-23 | 2011-10-27 | Bayer Cropscience Ag | Triglyzerid-enthaltende winterspritzmittel |
EP2382865A1 (de) | 2010-04-28 | 2011-11-02 | Bayer CropScience AG | Synergistische Wirkstoffkombinationen |
WO2011138285A1 (de) | 2010-05-05 | 2011-11-10 | Bayer Cropscience Ag | Thiazolderivate als schädlingsbekämpfungsmittel |
WO2011147952A1 (en) | 2010-05-28 | 2011-12-01 | Basf Se | Pesticidal mixtures |
WO2011148886A1 (ja) | 2010-05-24 | 2011-12-01 | Meiji Seikaファルマ株式会社 | 有害生物防除剤 |
WO2011157778A1 (de) | 2010-06-18 | 2011-12-22 | Bayer Cropscience Ag | Wirkstoffkombinationen mit insektiziden und akariziden eigenschaften |
WO2011157650A1 (de) | 2010-06-15 | 2011-12-22 | Bayer Cropscience Ag | Verfahren zur herstellung von 2, 2-difluorethylamin- derivaten durch alkylierung mit 2,2- difluor-1-halogenethanen |
WO2011157663A1 (de) | 2010-06-15 | 2011-12-22 | Bayer Cropscience Ag | Neue ortho-substituierte arylamid-derivate |
WO2012001068A2 (de) | 2010-07-02 | 2012-01-05 | Bayer Cropscience Ag | Insektizide oder akarizide formulierungen mit verbesserter verfügbarkeit auf pflanzenoberflächen |
WO2012000896A2 (de) | 2010-06-28 | 2012-01-05 | Bayer Cropscience Ag | Heterocyclische verbindungen als schädlingsbekämpfungsmittel |
WO2012000902A1 (de) | 2010-06-29 | 2012-01-05 | Bayer Cropscience Ag | Verbesserte insektizide zusammensetzungen enthaltend cyclische carbonylamidine |
WO2012004326A1 (en) | 2010-07-08 | 2012-01-12 | Bayer Cropscience Ag | Pesticidal pyrroline derivatives |
WO2012004208A1 (de) | 2010-07-09 | 2012-01-12 | Bayer Cropscience Ag | Anthranilsäurediamid-derivate als pestizide |
WO2012004293A2 (de) | 2010-07-08 | 2012-01-12 | Bayer Cropscience Ag | Insektizide und fungizide wirkstoffkombinationen |
WO2012007426A1 (en) | 2010-07-13 | 2012-01-19 | Basf Se | Azoline substituted isoxazoline benzamide compounds for combating animal pests |
WO2012007505A2 (en) | 2010-07-16 | 2012-01-19 | Bayer Innovation Gmbh | Polymer composite material with biocide functionality |
WO2012007500A2 (de) | 2010-07-15 | 2012-01-19 | Bayer Cropscience Ag | Neue heterocyclische verbindungen als schädlingsbekämpfungsmittel |
WO2012010509A2 (de) | 2010-07-20 | 2012-01-26 | Bayer Cropscience Ag | Gelköder zur bekämpfung von kriechenden schadinsekten |
WO2012010534A1 (en) | 2010-07-22 | 2012-01-26 | Basf Se | Novel hetaryl (thio)carboxamide compounds for controlling invertebrate pests |
EP2422620A1 (de) | 2010-08-26 | 2012-02-29 | Bayer CropScience AG | Insektizide Wirkstoffkombinationen enthaltend Ethiprole und Pymetrozin |
WO2012028583A1 (de) | 2010-09-03 | 2012-03-08 | Bayer Cropscience Ag | Deltamethrin enthaltende formulierungen |
WO2012034959A2 (en) | 2010-09-13 | 2012-03-22 | Basf Se | Pyridine compounds for controlling invertebrate pests iii |
WO2012034960A1 (en) | 2010-09-13 | 2012-03-22 | Basf Se | Pyridine compounds for controlling invertebrate pests ii |
WO2012034961A1 (en) | 2010-09-13 | 2012-03-22 | Basf Se | Pyridine compounds for controlling invertebrate pests i |
WO2012034957A1 (en) | 2010-09-15 | 2012-03-22 | Bayer Cropscience Ag | Pesticidal pyrroline n-oxide derivatives |
WO2012035011A1 (en) | 2010-09-15 | 2012-03-22 | Bayer Cropscience Ag | Pesticidal arylpyrrolidines |
WO2012038476A1 (en) | 2010-09-22 | 2012-03-29 | Bayer Cropscience Ag | Use of active ingredients for controlling nematodes in nematode-resistant crops |
WO2012042006A1 (en) | 2010-10-01 | 2012-04-05 | Basf Se | Imine compounds |
WO2012042007A1 (en) | 2010-10-01 | 2012-04-05 | Basf Se | Imine substituted 2, 4 - diaryl - pyrroline derivatives as pesticides |
WO2012041874A1 (en) | 2010-10-01 | 2012-04-05 | Syngenta Participations Ag | Fungicidal compositions |
WO2012045798A1 (en) | 2010-10-07 | 2012-04-12 | Bayer Cropscience Ag | Fungicide composition comprising a tetrazolyloxime derivative and a thiazolylpiperidine derivative |
WO2012045680A2 (de) | 2010-10-04 | 2012-04-12 | Bayer Cropscience Ag | Insektizide und fungizide wirkstoffkombinationen |
WO2012052412A1 (de) | 2010-10-22 | 2012-04-26 | Bayer Cropscience Ag | Neue heterocylische verbindungen als schädlingsbekämpfungsmittel |
WO2012052490A1 (en) | 2010-10-21 | 2012-04-26 | Bayer Cropscience Ag | N-benzyl heterocyclic carboxamides |
EP2446742A1 (de) | 2010-10-28 | 2012-05-02 | Bayer CropScience AG | Insektizide oder akarizide Zusammensetzungen enthaltend Mono- oder Disacchariden als Wirkungsverstärker |
WO2012059497A1 (en) | 2010-11-02 | 2012-05-10 | Bayer Cropscience Ag | N-hetarylmethyl pyrazolylcarboxamides |
WO2012062740A1 (de) | 2010-11-12 | 2012-05-18 | Bayer Cropscience Ag | Verfahren zur herstellung von 2,2-difluorethylamin-derivaten ausgehend von n-(2,2-difluorethyl)prop-2-en-1-amin |
WO2012065944A1 (en) | 2010-11-15 | 2012-05-24 | Bayer Cropscience Ag | N-aryl pyrazole(thio)carboxamides |
EP2460406A1 (de) | 2010-12-01 | 2012-06-06 | Bayer CropScience AG | Verwendung von Fluopyram zum Steuern von Nematoden in nematodresistentem Pflanzen |
WO2012072489A1 (de) | 2010-11-29 | 2012-06-07 | Bayer Cropscience Ag | Alpha-beta-ungesättigte imine |
WO2012072660A1 (en) | 2010-12-01 | 2012-06-07 | Bayer Cropscience Ag | Use of fluopyram for controlling nematodes in crops and for increasing yield |
WO2012076704A2 (en) | 2010-12-10 | 2012-06-14 | Basf Se | Pyrazole compounds for controlling invertebrate pests |
WO2012076470A1 (en) | 2010-12-09 | 2012-06-14 | Bayer Cropscience Ag | Pesticidal mixtures with improved properties |
WO2012076471A1 (en) | 2010-12-09 | 2012-06-14 | Bayer Cropscience Ag | Insecticidal mixtures with improved properties |
WO2012080188A1 (de) | 2010-12-17 | 2012-06-21 | Bayer Cropscience Ag | Insektizid-wachs-partikel enthaltende zusammensetzung |
DE102010063691A1 (de) | 2010-12-21 | 2012-06-21 | Bayer Animal Health Gmbh | Ektoparasitizide Wirkstoffkombinationen |
WO2012082548A2 (en) | 2010-12-15 | 2012-06-21 | Syngenta Participations Ag | Soybean event syht0h2 and compositions and methods for detection thereof |
EP2468097A1 (de) | 2010-12-21 | 2012-06-27 | Bayer CropScience AG | Verwendung von Isothiazolcarboxamiden für latente Wirtsabwehr bei einer Pflanze |
WO2012084670A1 (en) | 2010-12-20 | 2012-06-28 | Basf Se | Pesticidal active mixtures comprising pyrazole compounds |
WO2012085081A1 (en) | 2010-12-22 | 2012-06-28 | Basf Se | Sulfoximinamide compounds for combating invertebrate pests ii |
WO2012084900A1 (fr) | 2010-12-20 | 2012-06-28 | Universite De Poitiers | Composition phytosanitaire à base de zéolithe |
WO2012089722A2 (de) | 2010-12-30 | 2012-07-05 | Bayer Cropscience Ag | Verwendung von offenkettigen aryl-, heteroaryl- und benzylsulfonamidocarbonsäuren, -carbonsäureestern, -carbonsäureamiden und -carbonitrilen oder deren salze zur steigerung der stresstoleranz in pflanzen |
US20120190867A1 (en) * | 2011-01-24 | 2012-07-26 | Bayer Cropscience Ag | Process for the preparation of 2,2-difluoroethylamine |
WO2012110519A1 (de) | 2011-02-17 | 2012-08-23 | Bayer Cropscience Ag | Substituierte 3-(biphenyl-3-yl)-8,8-difluor-4-hydroxy-1-azaspiro[4.5]dec-3-en-2-one zur therapie und halogensubstituierte spirocyclische ketoenole |
WO2012110464A1 (en) | 2011-02-17 | 2012-08-23 | Bayer Cropscience Ag | Use of sdhi fungicides on conventionally bred asr-tolerant, stem canker resistant and/or frog-eye leaf spot resistant soybean varieties |
WO2012116960A1 (de) | 2011-03-01 | 2012-09-07 | Bayer Cropscience Ag | 2-acyloxy-pyrrolin-4-one |
WO2012120105A1 (en) | 2011-03-10 | 2012-09-13 | Bayer Cropscience Ag | Use of lipochito-oligosaccharide compounds for safeguarding seed safety of treated seeds |
WO2012119984A1 (de) | 2011-03-09 | 2012-09-13 | Bayer Cropscience Ag | Indol- und benzimidazolcarbonsäureamide als insektizide und akarizide |
US8273904B2 (en) | 2007-09-18 | 2012-09-25 | Bayer Cropscience Ag | Method for preparing 4-aminobut-2-enolides |
US8273897B2 (en) | 2007-09-18 | 2012-09-25 | Bayer Cropscience Ag | Method for producing 2,2-difluoroethylamine derivative by amide hydrogenation |
WO2012126766A1 (de) | 2011-03-18 | 2012-09-27 | Bayer Cropscience Ag | N- (3 -carbamoylphenyl) - 1h - pyrazol - 5 - carboxamid - derivate und ihre verwendung zur bekämpfung von tierischen schädlingen |
WO2012136724A1 (en) | 2011-04-06 | 2012-10-11 | Basf Se | Substituted pyrimidinium compounds for combating animal pests |
WO2012136751A1 (en) | 2011-04-08 | 2012-10-11 | Basf Se | N-substituted hetero-bicyclic compounds and derivatives for combating animal pests |
WO2012139890A1 (de) | 2011-04-15 | 2012-10-18 | Bayer Cropscience Ag | Substituierte 5-(cyclohex-2-en-1-yl)-penta-2,4-diene und 5-(cyclohex-2-en-1-yl)-pent-2-en-4-ine als wirkstoffe gegen abiotischen pflanzenstress |
WO2012139891A1 (de) | 2011-04-15 | 2012-10-18 | Bayer Cropscience Ag | Substituierte vinyl- und alkinyl-cyclohexenole als wirkstoffe gegen abiotischen pflanzenstress |
WO2012139892A1 (de) | 2011-04-15 | 2012-10-18 | Bayer Cropscience Ag | Substituierte 5-(bicyclo[4.1.0]hept-3-en-2-yl)-penta-2,4-diene und 5-(bicyclo[4.1.0]hept-3-en-2-yl)-pent-2-en-4-ine als wirkstoffe gegen abiotischen pflanzenstress |
WO2012143317A1 (en) | 2011-04-21 | 2012-10-26 | Basf Se | Novel pesticidal pyrazole compounds |
EP2529927A2 (de) | 2007-07-20 | 2012-12-05 | Bayer Innovation Gmbh | Polymerverbundwerkstoff mit biozider Funktion |
EP2535334A1 (de) | 2011-06-17 | 2012-12-19 | Bayer CropScience AG | Kristalline Modifikationen von Penflufen |
EP2534951A1 (de) | 2007-04-17 | 2012-12-19 | Bayer CropScience AG | Bekämpfung von Schädlingen durch Kombination von Insektiziden und transgenen Pflanzen mittels Blatt- und Drenchanwendung |
WO2012171914A1 (en) | 2011-06-14 | 2012-12-20 | Bayer Intellectual Property Gmbh | Use of an enaminocarbonyl compound in combination with a biological control agent |
EP2540163A1 (de) | 2011-06-30 | 2013-01-02 | Bayer CropScience AG | Nematozide N-Cyclopropylsulfonylamidderivate |
WO2013004652A1 (de) | 2011-07-04 | 2013-01-10 | Bayer Intellectual Property Gmbh | Verwendung substituierter isochinolinone, isochinolindione, isochinolintrione und dihydroisochinolinone oder jeweils deren salze als wirkstoffe gegen abiotischen pflanzenstress |
WO2013010947A2 (en) | 2011-07-15 | 2013-01-24 | Basf Se | Pesticidal methods using substituted 3-pyridyl thiazole compounds and derivatives for combating animal pests ii |
WO2013014227A1 (en) | 2011-07-27 | 2013-01-31 | Bayer Intellectual Property Gmbh | Seed dressing for controlling phytopathogenic fungi |
WO2013014126A1 (de) | 2011-07-26 | 2013-01-31 | Bayer Intellectual Property Gmbh | Veretherte laktatester, verfahren zu ihrer herstellung und ihre verwendung zur verbesserung der wirkung von pflanzenschutzmitteln |
US8372417B2 (en) | 2007-07-20 | 2013-02-12 | Bayer Innovation Gmbh | Polymer composite film with barrier functionality |
WO2013024003A1 (en) | 2011-08-12 | 2013-02-21 | Basf Se | N-thio-anthranilamide compounds and their use as pesticides |
WO2013024008A1 (en) | 2011-08-12 | 2013-02-21 | Basf Se | Aniline type compounds |
WO2013024010A1 (en) | 2011-08-12 | 2013-02-21 | Basf Se | N-thio-anthranilamide compounds and their use as pesticides |
WO2013024006A1 (en) | 2011-08-12 | 2013-02-21 | Basf Se | Anthranilamide compounds and their use as pesticides |
WO2013024169A1 (en) | 2011-08-18 | 2013-02-21 | Basf Se | Carbamoylmethoxy- and carbamoylmethylthio- and carbamoylmethylamino benzamides for combating invertebrate pests |
WO2013024170A1 (en) | 2011-08-18 | 2013-02-21 | Basf Se | Carbamoylmethoxy- and carbamoylmethylthio- and carbamoylmethylamino benzamides for combating invertebrate pests |
WO2013024171A1 (en) | 2011-08-18 | 2013-02-21 | Basf Se | Carbamoylmethoxy- and carbamoylmethylthio- and carbamoylmethylamino benzamides for combating invertebrate pests |
WO2013024005A1 (en) | 2011-08-12 | 2013-02-21 | Basf Se | Anthranilamide compounds and their use as pesticides |
WO2013024004A1 (en) | 2011-08-12 | 2013-02-21 | Basf Se | N-thio-anthranilamide compounds and their use as pesticides |
WO2013024009A1 (en) | 2011-08-12 | 2013-02-21 | Basf Se | N-thio-anthranilamide compounds and their use as pesticides |
US8383549B2 (en) | 2007-07-20 | 2013-02-26 | Bayer Cropscience Lp | Methods of increasing crop yield and controlling the growth of weeds using a polymer composite film |
EP2561759A1 (de) | 2011-08-26 | 2013-02-27 | Bayer Cropscience AG | Fluoralkyl-substituierte 2-amidobenzimidazole und ihre Wirkung auf das Pflanzenwachstum |
WO2013030262A1 (en) | 2011-09-02 | 2013-03-07 | Basf Se | Insecticidal active mixtures comprising arylquinazolinone compounds |
WO2013030319A2 (en) | 2011-09-02 | 2013-03-07 | Basf Se | Use of pesticidal active 3-arylquinazolin-4-one derivatives in soil application methods |
WO2013037956A1 (en) | 2011-09-16 | 2013-03-21 | Bayer Intellectual Property Gmbh | Use of 5-phenyl- or 5-benzyl-2 isoxazoline-3 carboxylates for improving plant yield |
WO2013037955A1 (en) | 2011-09-16 | 2013-03-21 | Bayer Intellectual Property Gmbh | Use of acylsulfonamides for improving plant yield |
WO2013037958A1 (en) | 2011-09-16 | 2013-03-21 | Bayer Intellectual Property Gmbh | Use of phenylpyrazolin-3-carboxylates for improving plant yield |
WO2013050433A1 (en) | 2011-10-05 | 2013-04-11 | Bayer Intellectual Property Gmbh | Pesticide preparation and process for producing the same |
WO2013079601A1 (en) | 2011-12-02 | 2013-06-06 | Basf Se | Method and system for monitoring crops and/or infestation of crops with harmful organismus during storage |
WO2013079600A1 (en) | 2011-12-02 | 2013-06-06 | Basf Se | Method and system for monitoring crops during storage |
EP2604118A1 (de) | 2011-12-15 | 2013-06-19 | Bayer CropScience AG | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
EP2606726A1 (de) | 2011-12-21 | 2013-06-26 | Bayer CropScience AG | N-Arylamidine-substituierte trifluoroethylsulfid-Derivate als Akarizide und Insektizide |
WO2013092522A1 (de) | 2011-12-20 | 2013-06-27 | Bayer Intellectual Property Gmbh | Neue insektizide aromatische amide |
WO2013092519A1 (en) | 2011-12-19 | 2013-06-27 | Bayer Cropscience Ag | Use of anthranilic acid diamide derivatives for pest control in transgenic crops |
WO2013092868A1 (en) | 2011-12-21 | 2013-06-27 | Basf Se | N-thio-anthranilamide compounds and their use as pesticides |
WO2013092943A1 (en) | 2011-12-23 | 2013-06-27 | Basf Se | Isothiazoline compounds for combating invertebrate pests |
WO2013107785A1 (en) | 2012-01-21 | 2013-07-25 | Bayer Intellectual Property Gmbh | Use of host defense inducers for controlling bacterial harmful organisms in useful plants |
WO2013113789A1 (en) | 2012-02-02 | 2013-08-08 | Basf Se | N-thio-anthranilamide compounds and their use as pesticides |
WO2013135724A1 (en) | 2012-03-14 | 2013-09-19 | Bayer Intellectual Property Gmbh | Pesticidal arylpyrrolidines |
WO2013144223A1 (en) | 2012-03-30 | 2013-10-03 | Basf Se | N-substituted pyrimidinylidene compounds and derivatives for combating animal pests |
WO2013144228A1 (en) | 2012-03-29 | 2013-10-03 | Basf Se | Pesticidal methods using heterocyclic compounds and derivatives for combating animal pests |
WO2013144213A1 (en) | 2012-03-30 | 2013-10-03 | Basf Se | N-substituted pyridinylidene compounds and derivatives for combating animal pests |
WO2013150115A1 (en) | 2012-04-05 | 2013-10-10 | Basf Se | N- substituted hetero - bicyclic compounds and derivatives for combating animal pests |
WO2013149903A1 (en) | 2012-04-03 | 2013-10-10 | Basf Se | N- substituted hetero - bicyclic furanone derivatives for combating animal |
WO2013149940A1 (en) | 2012-04-02 | 2013-10-10 | Basf Se | Acrylamide compounds for combating invertebrate pests |
WO2013164295A1 (en) | 2012-05-04 | 2013-11-07 | Basf Se | Substituted pyrazole-containing compounds and their use as pesticides |
WO2013167633A1 (en) | 2012-05-09 | 2013-11-14 | Basf Se | Acrylamide compounds for combating invertebrate pests |
WO2013171201A1 (de) | 2012-05-16 | 2013-11-21 | Bayer Cropscience Ag | Insektizide öl-in-wasser (o/w) formulierung |
WO2013171199A1 (de) | 2012-05-16 | 2013-11-21 | Bayer Cropscience Ag | Insektizide wasser-in-öl (w/o) formulierung |
WO2013174645A1 (en) | 2012-05-24 | 2013-11-28 | Basf Se | N-thio-anthranilamide compounds and their use as pesticides |
WO2013174836A1 (en) | 2012-05-22 | 2013-11-28 | Bayer Cropscience Ag | Active compounds combinations comprising a lipo-chitooligosaccharide derivative and a nematicide, insecticidal or fungicidal compound |
WO2013182613A1 (en) | 2012-06-08 | 2013-12-12 | Bayer Cropscience Ag | Detection system for the identification of insecticide resistance |
WO2013186089A2 (en) | 2012-06-14 | 2013-12-19 | Basf Se | Pesticidal methods using substituted 3-pyridyl thiazole compounds and derivatives for combating animal pests |
WO2013189801A1 (en) | 2012-06-20 | 2013-12-27 | Basf Se | Pyrazole compound and pesticidal mixtures comprising a pyrazole compound |
WO2014001245A1 (de) | 2012-06-29 | 2014-01-03 | Bayer Cropscience Ag | Verfahren zur herstellung von 2,2-difluorethylamin-derivaten durch alkylierung von 2,2-difluorethylamin |
EP2684879A1 (de) | 2012-07-09 | 2014-01-15 | Basf Se | Substituierte mesoionische Verbindungen zur Bekämpfung von Tierschädlingen |
WO2014019983A1 (en) | 2012-07-31 | 2014-02-06 | Bayer Cropscience Ag | Compositions comprising a pesticidal terpene mixture and an insecticide |
EP2698063A1 (de) | 2008-04-07 | 2014-02-19 | Bayer CropScience AG | Kombination aus biologischen Steuerungsmitteln und Insektiziden oder Fungiziden |
WO2014026984A1 (de) | 2012-08-17 | 2014-02-20 | Bayer Cropscience Ag | Azaindolcarbonsäure- und -thiocarbonsäureamide als insektizide und akarizide |
WO2014037340A1 (de) | 2012-09-05 | 2014-03-13 | Bayer Cropscience Ag | Verwendung substituierter 2-amidobenzimidazole, 2-amidobenzoxazole und 2-amidobenzothiazole oder deren salze als wirkstoffe gegen abiotischen pflanzenstress |
WO2014045228A1 (en) | 2012-09-21 | 2014-03-27 | Basf Se | Pyrethroid insecticide for protecting plants and seed |
WO2014047334A1 (en) | 2012-09-21 | 2014-03-27 | Basf Se | Methods for preventing pest infestations |
WO2014053401A2 (en) | 2012-10-01 | 2014-04-10 | Basf Se | Method of improving plant health |
WO2014053406A1 (en) | 2012-10-01 | 2014-04-10 | Basf Se | Method of controlling ryanodine-modulator insecticide resistant insects |
WO2014053403A1 (en) | 2012-10-01 | 2014-04-10 | Basf Se | Method of controlling insecticide resistant insects |
WO2014053407A1 (en) | 2012-10-01 | 2014-04-10 | Basf Se | N-thio-anthranilamide compounds and their use as pesticides |
WO2014053404A1 (en) | 2012-10-01 | 2014-04-10 | Basf Se | Pesticidally active mixtures comprising anthranilamide compounds |
WO2014053405A1 (en) | 2012-10-01 | 2014-04-10 | Basf Se | Pesticidally active mixtures comprising anthranilamide compounds |
WO2014053450A1 (de) | 2012-10-02 | 2014-04-10 | Bayer Cropscience Ag | Heterocyclische verbindungen als schädlingsbekämpfungsmittel |
WO2014053395A1 (en) | 2012-10-01 | 2014-04-10 | Basf Se | Use of n-thio-anthranilamide compounds on cultivated plants |
WO2014060381A1 (de) | 2012-10-18 | 2014-04-24 | Bayer Cropscience Ag | Heterocyclische verbindungen als schädlingsbekämpfungsmittel |
WO2014067962A1 (de) | 2012-10-31 | 2014-05-08 | Bayer Cropscience Ag | Neue heterocylische verbindungen als schädlingsbekämpfungsmittel |
WO2014072250A1 (en) | 2012-11-06 | 2014-05-15 | Bayer Cropscience Ag | Herbicidal combinations for tolerant soybean cultures |
WO2014079820A1 (en) | 2012-11-22 | 2014-05-30 | Basf Se | Use of anthranilamide compounds for reducing insect-vectored viral infections |
WO2014083088A2 (en) | 2012-11-30 | 2014-06-05 | Bayer Cropscience Ag | Binary fungicidal mixtures |
WO2014083033A1 (en) | 2012-11-30 | 2014-06-05 | Bayer Cropsience Ag | Binary fungicidal or pesticidal mixture |
EP2740357A1 (de) | 2013-10-10 | 2014-06-11 | Bayer CropScience AG | Aktive Verbindungen zur Behandlung von Saatgut |
WO2014086751A1 (de) | 2012-12-05 | 2014-06-12 | Bayer Cropscience Ag | Verwendung substituierter 1-(arylethinyl)-, 1-(heteroarylethinyl)-, 1-(heterocyclylethinyl)- und 1-(cyloalkenylethinyl)-cyclohexanole als wirkstoffe gegen abiotischen pflanzenstress |
WO2014086750A2 (en) | 2012-12-03 | 2014-06-12 | Bayer Cropscience Ag | Composition comprising a biological control agent and an insecticide |
WO2014086759A2 (en) | 2012-12-03 | 2014-06-12 | Bayer Cropscience Ag | Composition comprising biological control agents |
WO2014086749A2 (en) | 2012-12-03 | 2014-06-12 | Bayer Cropscience Ag | Composition comprising a biological control agent and an insecticide |
WO2014086758A2 (en) | 2012-12-03 | 2014-06-12 | Bayer Cropscience Ag | Composition comprising a biological control agent and an insecticide |
WO2014086753A2 (en) | 2012-12-03 | 2014-06-12 | Bayer Cropscience Ag | Composition comprising biological control agents |
WO2014090765A1 (en) | 2012-12-12 | 2014-06-19 | Bayer Cropscience Ag | Use of 1-[2-fluoro-4-methyl-5-(2,2,2-trifluoroethylsulfinyl)phenyl]-5-amino-3-trifluoromethyl)-1 h-1,2,4 tfia zole for controlling nematodes in nematode-resistant crops |
WO2014090700A1 (en) | 2012-12-14 | 2014-06-19 | Basf Se | Malononitrile compounds for controlling animal pests |
WO2014096238A1 (en) | 2012-12-21 | 2014-06-26 | Basf Se | Cycloclavine and derivatives thereof for controlling invertebrate pests |
WO2014095826A1 (en) | 2012-12-18 | 2014-06-26 | Bayer Cropscience Ag | Binary fungicidal and bactericidal combinations |
WO2014102244A1 (en) | 2012-12-27 | 2014-07-03 | Basf Se | 2-(pyridin-3-yl)-5-hetaryl-thiazole compounds carrying an imine or imine-derived substituent for combating invertebrate pests |
KR20140084163A (ko) | 2011-10-18 | 2014-07-04 | 스미또모 가가꾸 가부시끼가이샤 | 유해 생물 방제 조성물 및 유해 생물의 방제 방법 |
WO2014119670A1 (ja) | 2013-01-31 | 2014-08-07 | 住友化学株式会社 | 有害生物防除組成物及び有害生物の防除方法 |
WO2014124375A1 (en) | 2013-02-11 | 2014-08-14 | Bayer Cropscience Lp | Compositions comprising gougerotin and a biological control agent |
WO2014124373A1 (en) | 2013-02-11 | 2014-08-14 | Bayer Cropscience Lp | Compositions comprising gougerotin and an insecticide |
WO2014122083A1 (de) | 2013-02-06 | 2014-08-14 | Bayer Cropscience Ag | Halogensubstituierte pyrazolderivate als schädlingsbekämpfungsmittel |
WO2014128069A1 (en) | 2013-02-19 | 2014-08-28 | Bayer Cropscience Ag | Use of prothioconazole to induce host defence responses |
WO2014128136A1 (en) | 2013-02-20 | 2014-08-28 | Basf Se | Anthranilamide compounds and their use as pesticides |
WO2014140111A1 (en) | 2013-03-13 | 2014-09-18 | Bayer Cropscience Ag | Lawn growth-promoting agent and method of using same |
WO2014139897A1 (en) | 2013-03-12 | 2014-09-18 | Bayer Cropscience Ag | Use of dithiine-tetracarboximides for controlling bacterial harmful organisms in useful plants |
WO2014170313A1 (en) | 2013-04-19 | 2014-10-23 | Bayer Cropscience Ag | Active compound combinations having insecticidal properties |
WO2014170364A1 (en) | 2013-04-19 | 2014-10-23 | Bayer Cropscience Ag | Binary insecticidal or pesticidal mixture |
WO2014170300A1 (en) | 2013-04-19 | 2014-10-23 | Basf Se | N-substituted acyl-imino-pyridine compounds and derivatives for combating animal pests |
DE202014008418U1 (de) | 2014-02-19 | 2014-11-14 | Clariant International Ltd. | Schaumarme agrochemische Zusammensetzungen |
DE202014008415U1 (de) | 2014-02-19 | 2014-11-25 | Clariant International Ltd. | Wässrige Adjuvant-Zusammensetzung zur Wirkungssteigerung von Elektrolyt-Wirkstoffen |
WO2014202510A1 (de) | 2013-06-20 | 2014-12-24 | Bayer Cropscience Ag | Arylsulfid- und arylsulfoxid-derivate als akarizide und insektizide |
WO2014202751A1 (en) | 2013-06-21 | 2014-12-24 | Basf Se | Methods for controlling pests in soybean |
WO2014202505A1 (de) | 2013-06-20 | 2014-12-24 | Bayer Cropscience Ag | Arylsulfid- und arylsulfoxid-derivate als akarizide und insektizide |
CN104255733A (zh) * | 2009-03-25 | 2015-01-07 | 拜尔农作物科学股份公司 | 具有协同作用的活性成分结合物 |
WO2015004028A1 (de) | 2013-07-08 | 2015-01-15 | Bayer Cropscience Ag | Sechsgliedrige c-n-verknüpfte arylsulfid- und arylsulfoxid- derivate als schädlingsbekämpfungsmittel |
WO2015007682A1 (en) | 2013-07-15 | 2015-01-22 | Basf Se | Pesticide compounds |
US8940662B2 (en) | 2009-04-28 | 2015-01-27 | Basf Corporation | Methods for controlling pests |
EP2848124A1 (de) | 2014-08-19 | 2015-03-18 | Bayer CropScience AG | Wirkstoff zur Bekämpfung von Rhynchophorus ferrugineus |
WO2015040116A1 (en) | 2013-09-19 | 2015-03-26 | Basf Se | N-acylimino heterocyclic compounds |
WO2015055757A1 (en) | 2013-10-18 | 2015-04-23 | Basf Se | Use of pesticidal active carboxamide derivative in soil and seed application and treatment methods |
WO2015055497A1 (en) | 2013-10-16 | 2015-04-23 | Basf Se | Substituted pesticidal pyrazole compounds |
CN104604929A (zh) * | 2009-03-25 | 2015-05-13 | 拜尔农作物科学股份公司 | 具有杀昆虫和杀螨特性的活性成分结合物 |
WO2015091649A1 (en) | 2013-12-18 | 2015-06-25 | Basf Se | N-substituted imino heterocyclic compounds |
WO2015091645A1 (en) | 2013-12-18 | 2015-06-25 | Basf Se | Azole compounds carrying an imine-derived substituent |
WO2015101622A1 (de) | 2014-01-03 | 2015-07-09 | Bayer Cropscience Ag | Neue pyrazolyl-heteroarylamide als schädlingsbekämpfungsmittel |
WO2015104422A1 (en) | 2014-01-13 | 2015-07-16 | Basf Se | Dihydrothiophene compounds for controlling invertebrate pests |
DE102014018274A1 (de) | 2014-12-12 | 2015-07-30 | Clariant International Ltd. | Zuckertenside und deren Verwendung in agrochemischen Zusammensetzungen |
WO2015118479A1 (en) | 2014-02-05 | 2015-08-13 | Basf Corporation | Seed coating formulations and their use for yield increase |
CN104886059A (zh) * | 2009-03-25 | 2015-09-09 | 拜尔农作物科学股份公司 | 具有杀昆虫和杀螨虫特性的活性成分结合物 |
WO2015140198A1 (de) * | 2014-03-21 | 2015-09-24 | Bayer Cropscience Ag | Verfahren zur herstellung von n-[(6-chlorpyridin-3-yl)methyl]-2,2-difluorethan-1-amin durch alkylierung von 2,2-difluorethylamin |
WO2015160618A1 (en) | 2014-04-16 | 2015-10-22 | Bayer Cropscience Lp | Compositions comprising ningnanmycin and a biological control agent |
WO2015160620A1 (en) | 2014-04-16 | 2015-10-22 | Bayer Cropscience Lp | Compositions comprising ningnanmycin and an insecticide |
WO2016001129A1 (de) | 2014-07-01 | 2016-01-07 | Bayer Cropscience Aktiengesellschaft | Verbesserte insektizide zusammensetzungen |
WO2016008830A1 (de) | 2014-07-15 | 2016-01-21 | Bayer Cropscience Aktiengesellschaft | Aryl-triazolyl-pyridine als schädlingsbekämpfungsmittel |
DE102014012022A1 (de) | 2014-08-13 | 2016-02-18 | Clariant International Ltd. | Organische Ammoniumsalze von anionischen Pestiziden |
WO2016106063A1 (en) | 2014-12-22 | 2016-06-30 | Bayer Corpscience Lp | Method for using a bacillus subtilis or bacillus pumilus strain to treat or prevent pineapple disease |
WO2016166252A1 (en) | 2015-04-17 | 2016-10-20 | Basf Agrochemical Products B.V. | Method for controlling non-crop pests |
US9504250B2 (en) | 2011-07-13 | 2016-11-29 | Sumitomo Chemical Company, Limited | Arthropod pest control composition and method for controlling arthropod pests |
US9510594B2 (en) | 2011-02-17 | 2016-12-06 | Bayer Intellectual Property Gmbh | Use of SDHI fungicides on conventionally bred ASR-tolerant, stem canker resistant and/or frog-eye leaf spot resistant soybean varieties |
WO2017147352A1 (en) | 2016-02-24 | 2017-08-31 | Merial, Inc. | Antiparasitic isoxazoline compounds, long-acting injectable formulations comprising them, methods and uses thereof |
EP3238540A1 (de) | 2016-04-28 | 2017-11-01 | Bayer CropScience Aktiengesellschaft | Agrochemische zusammensetzungen mit kontrollierter granulatfreisetzung und verfahren zu ihrer herstellung |
WO2017186543A2 (en) | 2016-04-24 | 2017-11-02 | Bayer Cropscience Aktiengesellschaft | Use of fluopyram and/or bacillus subtilis for controlling fusarium wilt in plants of the musaceae family |
EP3243387A2 (de) | 2012-05-30 | 2017-11-15 | Bayer CropScience Aktiengesellschaft | Zusammensetzungen mit einem biologischen schädlingsbekämpfungsmittel und einem insektizid |
EP3272217A1 (de) * | 2014-06-25 | 2018-01-24 | BASF Agro B.V. | Pestizidische zusammensetzungen |
WO2018019676A1 (en) | 2016-07-29 | 2018-02-01 | Bayer Cropscience Aktiengesellschaft | Active compound combinations and methods to protect the propagation material of plants |
EP3363289A2 (de) | 2012-05-30 | 2018-08-22 | Bayer CropScience Aktiengesellschaft | Zusammensetzungen mit einem biologischen schädlingsbekämpfungsmittel und einem insektizid |
WO2019197635A1 (de) | 2018-04-13 | 2019-10-17 | Bayer Aktiengesellschaft | Formulierung insektizider mischungen mit propylencarbonat |
US10512267B2 (en) | 2013-07-08 | 2019-12-24 | BASF Agro, B.V. | Compositions comprising a triazole compound and a biopesticide |
US10519122B2 (en) | 2013-01-09 | 2019-12-31 | BASF Agro B.V. | Process for the preparation of substituted oxiranes and triazoles |
US10759767B2 (en) | 2012-12-20 | 2020-09-01 | BASF Agro B.V. | Compositions comprising a triazole compound |
US10772324B2 (en) | 2012-11-03 | 2020-09-15 | Clariant International Ltd. | Aqueous adjuvant-compositions |
US10813862B2 (en) | 2012-05-30 | 2020-10-27 | Clariant International Ltd. | Use of N-methyl-N-acylglucamines as solubilizers |
US10864275B2 (en) | 2012-05-30 | 2020-12-15 | Clariant International Ltd. | N-methyl-N-acylglucamine-containing composition |
US10920080B2 (en) | 2015-10-09 | 2021-02-16 | Clariant International Ltd. | N-Alkyl glucamine-based universal pigment dispersions |
US10961484B2 (en) | 2015-10-09 | 2021-03-30 | Clariant International Ltd. | Compositions comprising sugar amine and fatty acid |
WO2021069628A1 (en) | 2019-10-10 | 2021-04-15 | Bayer Aktiengesellschaft | Formulation of insecticidal mixtures comprising glycol ether solvents |
US11220603B2 (en) | 2016-05-09 | 2022-01-11 | Clariant International Ltd. | Stabilizers for silicate paints |
US11425904B2 (en) | 2014-04-23 | 2022-08-30 | Clariant International Ltd. | Use of aqueous drift-reducing compositions |
US11700852B2 (en) | 2014-12-19 | 2023-07-18 | Clariant International Ltd | Aqueous electrolyte-containing adjuvant compositions, active ingredient-containing compositions and the use thereof |
WO2023237444A1 (en) | 2022-06-06 | 2023-12-14 | Bayer Aktiengesellschaft | Agrochemical formulations comprising crystalline form a of 4-[(6-chloro-3-pyridylmethyl)(2,2-difluoroethyl)amino]furan-2(5h)-one |
EP4295683A1 (de) | 2022-06-21 | 2023-12-27 | Bayer Aktiengesellschaft | Agrochemische formulierungen, die die kristalline form a von 4-[(6-chlor-3-pyridylmethyl)(2,2-difluorethyl)amino]furan-2(5h)-on umfassen |
Families Citing this family (64)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP2000027A1 (de) * | 2007-06-06 | 2008-12-10 | Bayer CropScience AG | Insektizide Zusammensetzungen mit verbesserter Wirkung |
EP2039248A1 (de) * | 2007-09-21 | 2009-03-25 | Bayer CropScience AG | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
BRPI0912431B1 (pt) * | 2008-05-07 | 2017-04-04 | Bayer Cropscience Ag | combinações de substâncias ativas, sua utilização, composição e seu processo de preparação, e processo para combater parasitas animais |
DE102008041695A1 (de) * | 2008-08-29 | 2010-03-04 | Bayer Cropscience Ag | Methoden zur Verbesserung des Pflanzenwachstums |
WO2010069495A1 (de) * | 2008-12-18 | 2010-06-24 | Bayer Cropscience Aktiengesellschaft | Atpenine |
TWI487486B (zh) | 2009-12-01 | 2015-06-11 | Syngenta Participations Ag | 以異唑啉衍生物為主之殺蟲化合物 |
WO2011101402A1 (en) | 2010-02-17 | 2011-08-25 | Syngenta Participations Ag | Isoxazoline derivatives as insecticides |
JP2013520403A (ja) | 2010-02-22 | 2013-06-06 | 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 | 殺虫化合物としてのジヒドロフラン誘導体 |
JP2013520456A (ja) | 2010-02-25 | 2013-06-06 | 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 | イソオキサゾリン誘導体の製造方法 |
TW201211057A (en) | 2010-06-11 | 2012-03-16 | Syngenta Participations Ag | Process for the preparation of dihydropyrrole derivatives |
EP2625165B1 (de) | 2010-10-05 | 2018-07-04 | Syngenta Participations AG | Insektizide pyrrolidin-yl-aryl-carboxamide |
MX345768B (es) * | 2010-11-12 | 2017-02-14 | Bayer Ip Gmbh | Procedimiento para la preparación de 2,2-dufluoroetilamina partiendo de un compuesto de bencilamina. |
UY33887A (es) | 2011-02-03 | 2012-09-28 | Syngenta Ltd | Métodos de control de plagas en la soja |
AR086587A1 (es) | 2011-05-31 | 2014-01-08 | Syngenta Participations Ag | Compuestos insecticidas |
CN103732567A (zh) | 2011-08-22 | 2014-04-16 | 先正达参股股份有限公司 | 作为杀虫化合物的二氢呋喃衍生物 |
US20140343049A1 (en) | 2011-08-22 | 2014-11-20 | Syngenta Participations Ag | Dihydrofuran derivatives as insecticidal compounds |
BR112014003730A2 (pt) | 2011-08-25 | 2017-03-14 | Syngenta Participations Ag | processo para a preparação de derivados de tietano |
WO2013026695A1 (en) | 2011-08-25 | 2013-02-28 | Syngenta Participations Ag | Isoxazoline derivatives as insecticidal compounds |
WO2013026929A1 (en) | 2011-08-25 | 2013-02-28 | Syngenta Participations Ag | Dihydropyrrole derivatives as insecticidal compounds |
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Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0539588A1 (de) * | 1990-07-05 | 1993-05-05 | Nippon Soda Co., Ltd. | Aminderivat |
WO2006037475A1 (de) * | 2004-10-01 | 2006-04-13 | Bayer Cropscience Ag | Wirkstoffe für die saatgutbehandlung |
Family Cites Families (28)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4030994A (en) | 1971-06-18 | 1977-06-21 | Merck & Co., Inc. | Substitutive fluorination of organic compounds |
IT1079199B (it) | 1976-10-29 | 1985-05-08 | Montedison Spa | Antidoti,della classe delle dicloroacetamidi particolarmente attivi a proteggere il mais dalla azione tossica esercitata da esteri delle glicine n,n sostituite ebricide e associazione erbicida per culture di mais |
DE3314196A1 (de) | 1982-07-16 | 1983-09-29 | CIBA-GEIGY AG, 4002 Basel | Heterocyclylaether |
NZ205525A (en) | 1982-09-29 | 1985-12-13 | Ici Australia Ltd | 5-(pyridyl)-cyclohexene-1,3-dione derivatives and herbicidal compositions |
US4748186A (en) | 1986-06-30 | 1988-05-31 | Fmc Corporation | S-trifluorobutenyl derivatives and pesticidal uses thereof |
DE3630046A1 (de) | 1986-09-04 | 1988-03-17 | Bayer Ag | Verfahren zur herstellung von 5-chlormethylpyridinen |
DE3631538A1 (de) | 1986-09-17 | 1988-03-24 | Bayer Ag | Verfahren zur herstellung von 2-chlor-5-chlormethylthiazol |
DE3886467T2 (de) * | 1987-08-01 | 1994-06-01 | Takeda Chemical Industries Ltd | Alpha-ungesättigte Amine, ihre Herstellung und Verwendung. |
DE58908969D1 (de) | 1988-12-16 | 1995-03-16 | Bayer Ag | Verfahren zur Herstellung von 2-Chlor-5-chlormethylpyridin. |
DE3912964A1 (de) | 1989-04-20 | 1990-10-25 | Bayer Ag | Verfahren zur herstellung von 2-chlor-5-chlormethyl-pyridin und neue zwischenprodukte |
DE4014420A1 (de) * | 1989-09-23 | 1991-04-04 | Bayer Ag | 5h-furan-2-on-derivate |
US5180833A (en) | 1990-03-16 | 1993-01-19 | Takeda Chemical Industries, Ltd. | Process for the preparation of chlorothiazole derivatives |
JPH054966A (ja) * | 1990-07-05 | 1993-01-14 | Nippon Soda Co Ltd | アミン誘導体、その製法及び殺虫剤 |
JPH0713063B2 (ja) | 1992-04-30 | 1995-02-15 | 日本バイエルアグロケム株式会社 | 新規ジアミン類 |
KR930023342A (ko) | 1992-05-12 | 1993-12-18 | 비트 라우버, 토마스 케플러 | 2-클로로-5-클로로메틸- 피리딘의 제조방법 |
US6252087B1 (en) | 1992-11-19 | 2001-06-26 | The Trustees Of The University Of Pennsylvania | Nitroaromatic compounds for the detection of hypoxia |
US5420270A (en) | 1993-10-07 | 1995-05-30 | G. D. Searle & Co. | Aryl substituted dibenzoxazepine compounds, pharmaceutical compositions and methods of use |
DK0850231T3 (da) | 1995-09-11 | 2003-07-21 | Syngenta Participations Ag | Fremgangsmåde til fremstilling af en 2-chlor-5-chlormethyl-thiazolforbindelse |
US5811555A (en) | 1995-11-22 | 1998-09-22 | Kureha Chemical Industry Co., Ltd. | Method for substitution of an amino group of a primary amine by a chlorine atom and a synthetic method by application thereof |
DE19548417A1 (de) | 1995-12-22 | 1997-06-26 | Bayer Ag | Verfahren zur Herstellung von 2-Chlor-5-chlormethylthiazol |
IN182219B (de) | 1996-02-21 | 1999-02-06 | Kuraray Co | |
DE19838138A1 (de) * | 1997-08-25 | 1999-03-04 | Novartis Ag | Isoxazol-Derivate |
WO2001007414A1 (en) | 1999-07-21 | 2001-02-01 | The Trustees Of The University Of Pennsylvania | Preparation of compounds useful for the detection of hypoxia |
US6303638B1 (en) * | 1999-08-06 | 2001-10-16 | The Regents Of The University Of California | Substituted pyridines as modulators of the mammalian neuronal nicotinic acetylcholine receptor |
DE10119423A1 (de) * | 2001-04-20 | 2002-10-24 | Bayer Ag | Neue insektizid wirkende Azole |
JP2007524590A (ja) | 2003-03-18 | 2007-08-30 | メルク エンド カムパニー インコーポレーテッド | ケモカイン受容体活性の調節剤であるテトラヒドロピラニルシクロペンチル複素環アミド |
DE102006015468A1 (de) * | 2006-03-31 | 2007-10-04 | Bayer Cropscience Ag | Substituierte Enaminocarbonylverbindungen |
DE102006033572A1 (de) * | 2006-07-20 | 2008-01-24 | Bayer Cropscience Ag | N'-Cyano-N-halogenalkyl-imidamid Derivate |
-
2006
- 2006-03-31 DE DE102006015467A patent/DE102006015467A1/de not_active Withdrawn
-
2007
- 2007-03-19 JP JP2009501903A patent/JP5213847B2/ja active Active
- 2007-03-19 ES ES10197164.6T patent/ES2515221T3/es active Active
- 2007-03-19 BR BRPI0710103A patent/BRPI0710103B1/pt active IP Right Grant
- 2007-03-19 WO PCT/EP2007/002386 patent/WO2007115644A1/de active Application Filing
- 2007-03-19 MX MX2013013408A patent/MX363983B/es unknown
- 2007-03-19 CN CN2007800191007A patent/CN101466705B/zh active Active
- 2007-03-19 EP EP10197164.6A patent/EP2327304B1/de active Active
- 2007-03-19 ES ES07723355.9T patent/ES2553720T3/es active Active
- 2007-03-19 HU HUE07723355A patent/HUE028208T2/en unknown
- 2007-03-19 EP EP07723355.9A patent/EP2004635B1/de active Active
- 2007-03-19 PL PL07723355T patent/PL2004635T3/pl unknown
- 2007-03-19 KR KR1020087026049A patent/KR101407042B1/ko active Protection Beyond IP Right Term
- 2007-03-19 PL PL10197164T patent/PL2327304T3/pl unknown
- 2007-03-19 US US12/295,355 patent/US8106211B2/en active Active
- 2007-03-19 CN CN201110271830.4A patent/CN102336747B/zh active Active
- 2007-03-19 SI SI200731718T patent/SI2004635T1/sl unknown
- 2007-03-19 MX MX2008012350A patent/MX2008012350A/es active IP Right Grant
- 2007-03-19 AU AU2007236295A patent/AU2007236295B2/en active Active
- 2007-03-19 DK DK07723355.9T patent/DK2004635T3/en active
- 2007-03-19 PT PT77233559T patent/PT2004635E/pt unknown
- 2007-03-19 KR KR1020137032091A patent/KR101423077B1/ko active IP Right Grant
- 2007-03-28 AR ARP070101304A patent/AR060185A1/es active IP Right Grant
- 2007-03-30 TW TW096111131A patent/TWI386404B/zh active
-
2008
- 2008-09-29 ZA ZA200808376A patent/ZA200808376B/xx unknown
-
2011
- 2011-12-22 US US13/334,949 patent/US8404855B2/en active Active
-
2012
- 2012-12-17 US US13/717,624 patent/US8546577B2/en active Active
-
2015
- 2015-12-10 CY CY20151101133T patent/CY1117038T1/el unknown
-
2018
- 2018-09-11 NL NL350090C patent/NL350090I2/nl unknown
-
2019
- 2019-01-25 CY CY2019001C patent/CY2019001I2/el unknown
- 2019-04-16 FI FIC20190019C patent/FIC20190019I1/fi unknown
- 2019-06-25 HU HUS1900033C patent/HUS1900033I1/hu unknown
-
2020
- 2020-01-24 LT LTPA2020501C patent/LTC2004635I2/lt unknown
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0539588A1 (de) * | 1990-07-05 | 1993-05-05 | Nippon Soda Co., Ltd. | Aminderivat |
WO2006037475A1 (de) * | 2004-10-01 | 2006-04-13 | Bayer Cropscience Ag | Wirkstoffe für die saatgutbehandlung |
Cited By (445)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
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US8372418B2 (en) | 2007-07-20 | 2013-02-12 | Bayer Innovation Gmbh | Polymer composite film with biocide functionality |
EP2529927A2 (de) | 2007-07-20 | 2012-12-05 | Bayer Innovation Gmbh | Polymerverbundwerkstoff mit biozider Funktion |
US8372417B2 (en) | 2007-07-20 | 2013-02-12 | Bayer Innovation Gmbh | Polymer composite film with barrier functionality |
US8383549B2 (en) | 2007-07-20 | 2013-02-26 | Bayer Cropscience Lp | Methods of increasing crop yield and controlling the growth of weeds using a polymer composite film |
JP2010538026A (ja) * | 2007-09-05 | 2010-12-09 | バイエル・クロツプサイエンス・アクチエンゲゼルシヤフト | 殺虫及び殺ダニ特性を有する活性成分組合せ |
US8497228B2 (en) | 2007-09-05 | 2013-07-30 | Bayer Cropscience Ag | Active substance combinations with insecticidal and acaricidal properties |
US8324393B2 (en) | 2007-09-18 | 2012-12-04 | Bayer Cropscience Ag | Method for producing 2,2-difluoroethylamine derivatives by imine hydrogenation |
US9550745B2 (en) | 2007-09-18 | 2017-01-24 | Bayer Cropscience Ag | Method for preparing 4-aminobut-2-enolides |
US8273897B2 (en) | 2007-09-18 | 2012-09-25 | Bayer Cropscience Ag | Method for producing 2,2-difluoroethylamine derivative by amide hydrogenation |
EP2253610A1 (de) | 2007-09-18 | 2010-11-24 | Bayer CropScience AG | Verfahren zum Herstellen von 4-Aminobut-2-enoliden |
JP2010539202A (ja) * | 2007-09-18 | 2010-12-16 | バイエル・クロツプサイエンス・アクチエンゲゼルシヤフト | イミン水素化により2,2−ジフルオロエチルアミン誘導体を製造する方法 |
US8487112B2 (en) | 2007-09-18 | 2013-07-16 | Bayer Cropscience Ag | Method for producing 4-aminobut-2-enolides |
US8273904B2 (en) | 2007-09-18 | 2012-09-25 | Bayer Cropscience Ag | Method for preparing 4-aminobut-2-enolides |
AU2008306243B2 (en) * | 2007-09-26 | 2014-08-07 | Bayer Cropscience Aktiengesellschaft | Method for the improved use of the production potential of transgenic plants |
US20100197494A1 (en) * | 2007-09-26 | 2010-08-05 | Heike Hungenberg | Active agent combinations having insecticidal and acaricidal properties |
US9173394B2 (en) * | 2007-09-26 | 2015-11-03 | Bayer Intellectual Property Gmbh | Active agent combinations having insecticidal and acaricidal properties |
DE102007045921A1 (de) | 2007-09-26 | 2009-04-02 | Bayer Cropscience Ag | Verfahren zur verbesserten Nutzung des Produktionspotentials transgener Pflanzen |
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WO2009043438A1 (de) * | 2007-09-26 | 2009-04-09 | Bayer Cropscience Ag | Verfahren zur verbesserten nutzung des produktionspotentials transgener pflanzen |
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DE102008063561A1 (de) | 2008-12-18 | 2010-08-19 | Bayer Cropscience Ag | Hydrazide, Verfahren zu deren Herstellung und deren Verwendung als Herbizide und Insektizide |
EP2198709A1 (de) | 2008-12-19 | 2010-06-23 | Bayer CropScience AG | Verfahren zur Bekämpfung resistenter tierischer Schädlinge |
WO2010078899A3 (de) * | 2008-12-19 | 2011-05-12 | Bayer Cropscience Aktiengesellschaft | Verfahren zur bekämpfung resistenter tierischer schädlinge |
WO2010078899A2 (de) * | 2008-12-19 | 2010-07-15 | Bayer Cropscience Aktiengesellschaft | Verfahren zur bekämpfung resistenter tierischer schädlinge |
EP2204094A1 (de) | 2008-12-29 | 2010-07-07 | Bayer CropScience AG | Verfahren zur verbesserten Verwendung des Herstellungspotentials von transgenen Pflanzen |
EP2201841A1 (de) | 2008-12-29 | 2010-06-30 | Bayer CropScience AG | Synergistische insektizide Mischungen |
WO2010075994A1 (en) | 2008-12-29 | 2010-07-08 | Bayer Cropscience Aktiengesellschaft | Treatment of transgenic crops with mixtures of fiproles and chloronicotinyls |
EP2039770A2 (de) | 2009-01-06 | 2009-03-25 | Bayer CropScience AG | Verfahren zur verbesserten Nutzung des Produktionspotentials transgener Pflanzen |
EP2039772A2 (de) | 2009-01-06 | 2009-03-25 | Bayer CropScience AG | Verfahren zur verbesserten Nutzung des Produktionspotentials transgener Pflanzen |
EP2039771A2 (de) | 2009-01-06 | 2009-03-25 | Bayer CropScience AG | Verfahren zur verbesserten Nutzung des Produktionspotentials transgener Pflanzen |
WO2010083955A3 (de) * | 2009-01-23 | 2011-08-25 | Bayer Cropscience Aktiengesellschaft | Verwendung von enaminocarbonylverbindungen zur bekämpfung von durch insekten übertragenen virosen |
WO2010083955A2 (de) | 2009-01-23 | 2010-07-29 | Bayer Cropscience Aktiengesellschaft | Verwendung von enaminocarbonylverbindungen zur bekämpfung von durch insekten übertragenen virosen |
EP2227951A1 (de) | 2009-01-23 | 2010-09-15 | Bayer CropScience AG | Verwendung von Enaminocarbonylverbindungen zur Bekämpfung von durch Insekten übertragenen Viren |
WO2010086303A2 (en) | 2009-01-27 | 2010-08-05 | Basf Se | Method for dressing seeds |
EP2837286A1 (de) | 2009-01-27 | 2015-02-18 | Basf Se | Verfahren zur Behandlung von Saatgut |
WO2010086095A1 (en) | 2009-01-29 | 2010-08-05 | Bayer Cropscience Ag | Method for improved utilization of the production potential of transgenic plants introduction |
WO2010089244A1 (en) | 2009-02-03 | 2010-08-12 | Basf Se | Method for dressing seeds |
WO2010094728A1 (en) | 2009-02-19 | 2010-08-26 | Bayer Cropscience Ag | Pesticide composition comprising a tetrazolyloxime derivative and a fungicide or an insecticide active substance |
EP2223602A1 (de) | 2009-02-23 | 2010-09-01 | Bayer CropScience AG | Verfahren zur verbesserten Nutzung des Produktionspotentials genetisch modifizierter Pflanzen |
WO2010100189A1 (en) | 2009-03-04 | 2010-09-10 | Basf Se | 3-arylquinazolin-4-one compounds for combating invertebrate pests |
CN102356078A (zh) * | 2009-03-16 | 2012-02-15 | 拜耳作物科学公司 | 制备烯胺羰基化合物的新方法 |
TWI491597B (zh) * | 2009-03-16 | 2015-07-11 | Bayer Cropscience Ag | 製備烯胺羰基化合物之新穎方法 |
CN102356077B (zh) * | 2009-03-16 | 2014-07-23 | 拜耳作物科学公司 | 制备烯胺羰基化合物的新方法 |
US8637673B2 (en) | 2009-03-16 | 2014-01-28 | Bayer Cropscience Ag | Method for producing 2,2-difluoroethylamine derivatives by imine hydrogenation |
US8680286B2 (en) | 2009-03-16 | 2014-03-25 | Bayer Cropscience Ag | Method for producing enaminocarbonyl compounds |
CN102356077A (zh) * | 2009-03-16 | 2012-02-15 | 拜耳作物科学公司 | 制备烯胺羰基化合物的新方法 |
US8680285B2 (en) | 2009-03-16 | 2014-03-25 | Bayer Cropscience Ag | Method for producing enaminocarbonyl compounds |
CN102356078B (zh) * | 2009-03-16 | 2014-10-15 | 拜耳作物科学公司 | 制备烯胺羰基化合物的新方法 |
EP2230237A1 (de) | 2009-03-16 | 2010-09-22 | Bayer CropScience AG | Neues Verfahren zur Herstellung von Enaminocarbonyl-Verbindungen |
WO2010105772A1 (de) | 2009-03-16 | 2010-09-23 | Bayer Cropscience Ag | Neues verfahren zur herstellung von enaminocarbonyl-verbindungen |
KR20110127750A (ko) * | 2009-03-16 | 2011-11-25 | 바이엘 크롭사이언스 아게 | 이민 수소화에 의한 2,2-다이플루오로에틸아민 유도체의 제조방법 |
JP2012520331A (ja) * | 2009-03-16 | 2012-09-06 | バイエル・クロップサイエンス・アーゲー | イミン水素化により2,2−ジフルオロエチルアミン誘導体を調製する方法 |
EP2230231A1 (de) | 2009-03-16 | 2010-09-22 | Bayer CropScience AG | Verfahren zur Herstellung von 2,2-Difluorethylamin-Derivaten durch Imin-Hydrierung |
KR101672721B1 (ko) | 2009-03-16 | 2016-11-04 | 바이엘 인텔렉쳐 프로퍼티 게엠베하 | 이민 수소화에 의한 2,2-다이플루오로에틸아민 유도체의 제조방법 |
EP2230236A1 (de) | 2009-03-16 | 2010-09-22 | Bayer CropScience AG | Neues Verfahren zur Herstellung von Enaminocarbonyl-Verbindungen |
WO2010105779A1 (de) | 2009-03-16 | 2010-09-23 | Bayer Cropscience Ag | Neues verfahren zur herstellung von enaminocarbonyl-verbindungen |
WO2010105747A1 (de) | 2009-03-16 | 2010-09-23 | Bayer Cropscience Ag | Verfahren zur herstellung von 2,2-difluorethylamin-derivaten durch imin-hydrierung |
US8828907B2 (en) | 2009-03-25 | 2014-09-09 | Bayer Cropscience Ag | Active ingredient combinations having insecticidal and acaricidal properties |
EP2564700A1 (de) | 2009-03-25 | 2013-03-06 | Bayer CropScience AG | Nematizide Wirkstoffkombinationen umfassend Fluopyram und Hirsutella |
EP2232995A1 (de) | 2009-03-25 | 2010-09-29 | Bayer CropScience AG | Verfahren zur verbesserten Nutzung des Produktionspotentials transgener Pflanzen |
JP2012521370A (ja) * | 2009-03-25 | 2012-09-13 | バイエル・クロップサイエンス・アーゲー | 殺虫特性及び殺ダニ特性を有する活性成分組合せ |
WO2010108616A1 (de) | 2009-03-25 | 2010-09-30 | Bayer Cropscience Ag | Nematizide, insektizide und akarizide wirkstoffkombinationen umfassend pyridylethylbenzamide und insektizide |
WO2010108507A2 (de) * | 2009-03-25 | 2010-09-30 | Bayer Cropscience Ag | Synergistische wirkstoffkombinationen |
WO2010108506A1 (de) * | 2009-03-25 | 2010-09-30 | Bayer Cropscience Ag | Wirkstoffkombinationen mit insektiziden und akariziden eigenschaften |
WO2010108504A1 (de) * | 2009-03-25 | 2010-09-30 | Bayer Cropscience Ag | Wirkstoffkombinationen mit insektiziden und akariziden eigenschaften |
WO2010108505A1 (de) * | 2009-03-25 | 2010-09-30 | Bayer Cropscience Ag | Wirkstoffkombinationen mit insektiziden und akariziden eigenschaften |
EP2561756A1 (de) | 2009-03-25 | 2013-02-27 | Bayer CropScience AG | Nematizide Wirkstoffkombinationen umfassend Fluopyram und Spirotetramat |
EP2561757A1 (de) | 2009-03-25 | 2013-02-27 | Bayer CropScience AG | Nematizide Wirkstoffkombinationen umfassend Fluopyram und Ethiprole |
EP2561755A1 (de) | 2009-03-25 | 2013-02-27 | Bayer CropScience AG | Nematizide Wirkstoffkombinationen umfassend Fluopyram und Mycorrhiza |
EP2561758A1 (de) | 2009-03-25 | 2013-02-27 | Bayer CropScience AG | Nematizide Wirkstoffkombinationen umfassend Fluopyram und Thiodicarb |
EP2564698A1 (de) | 2009-03-25 | 2013-03-06 | Bayer CropScience AG | Nematizide Wirkstoffkombinationen umfassend Fluopyram und Bacillus firmus |
EP2564703A1 (de) | 2009-03-25 | 2013-03-06 | Bayer CropScience AG | Nematizide Wirkstoffkombinationen umfassend Fluopyram und Rynaxypyr oder Cyazypyr |
EP2564699A1 (de) | 2009-03-25 | 2013-03-06 | Bayer CropScience AG | Nematizide Wirkstoffkombinationen umfassend Fluopyram und Metarhizium |
EP2564702A1 (de) | 2009-03-25 | 2013-03-06 | Bayer CropScience AG | Nematizide Wirkstoffkombinationen umfassend Fluopyram und ein weiterer Wirkstoff |
EP2564701A1 (de) | 2009-03-25 | 2013-03-06 | Bayer CropScience AG | Nematizide Wirkstoffkombinationen umfassend Fluopyram und fluensulfone |
EP2564704A1 (de) | 2009-03-25 | 2013-03-06 | Bayer CropScience AG | Nematizide Wirkstoffkombinationen umfassend Fluopyram und Methiocarb |
EP2564705A1 (de) | 2009-03-25 | 2013-03-06 | Bayer CropScience AG | Nematizide Wirkstoffkombinationen umfassend Fluopyram und Pasteuria penetrans |
CN102448305A (zh) * | 2009-03-25 | 2012-05-09 | 拜尔农作物科学股份公司 | 具有杀昆虫和杀螨虫特性的活性成分结合物 |
KR20140014347A (ko) * | 2009-03-25 | 2014-02-06 | 바이엘 크롭사이언스 아게 | 살충 및 살비성을 지니는 활성 성분 배합물 |
WO2010108508A3 (de) * | 2009-03-25 | 2011-03-03 | Bayer Cropscience Ag | Wirkstoffkombinationen mit insektiziden und akariziden eigenschaften |
US8828906B2 (en) | 2009-03-25 | 2014-09-09 | Bayer Cropscience Ag | Active compound combinations having insecticidal and acaricidal properties |
CN102361555A (zh) * | 2009-03-25 | 2012-02-22 | 拜尔农作物科学股份公司 | 具有杀昆虫和杀螨特性的活性化合物结合物 |
WO2010108507A3 (de) * | 2009-03-25 | 2011-05-05 | Bayer Cropscience Ag | Synergistische wirkstoffkombinationen |
KR101647702B1 (ko) | 2009-03-25 | 2016-08-11 | 바이엘 인텔렉쳐 프로퍼티 게엠베하 | 살충 및 살비성을 지니는 활성 성분 배합물 |
US8846567B2 (en) | 2009-03-25 | 2014-09-30 | Bayer Cropscience Ag | Active compound combinations having insecticidal and acaricidal properties |
US8846568B2 (en) | 2009-03-25 | 2014-09-30 | Bayer Cropscience Ag | Active compound combinations having insecticidal and acaricidal properties |
CN102365018B (zh) * | 2009-03-25 | 2014-10-29 | 拜尔农作物科学股份公司 | 具有协同作用的活性成分结合物 |
EA020314B1 (ru) * | 2009-03-25 | 2014-10-30 | Байер Кропсайенс Аг | Пестицидная комбинация биологически активных веществ |
CN104255733B (zh) * | 2009-03-25 | 2016-05-04 | 拜尔农作物科学股份公司 | 具有协同作用的活性成分结合物 |
CN104255733A (zh) * | 2009-03-25 | 2015-01-07 | 拜尔农作物科学股份公司 | 具有协同作用的活性成分结合物 |
CN102448304B (zh) * | 2009-03-25 | 2015-03-11 | 拜尔农作物科学股份公司 | 具有杀昆虫和杀螨特性的活性成分结合物 |
CN104886059A (zh) * | 2009-03-25 | 2015-09-09 | 拜尔农作物科学股份公司 | 具有杀昆虫和杀螨虫特性的活性成分结合物 |
US9089135B2 (en) * | 2009-03-25 | 2015-07-28 | Bayer Intellectual Property Gmbh | Nematicidal, insecticidal and acaricidal active ingredient combinations comprising pyridyl-ethylbenzamides and insecticides |
EA020314B9 (ru) * | 2009-03-25 | 2015-03-31 | Байер Кропсайенс Аг | Пестицидная комбинация биологически активных веществ |
CN104604929A (zh) * | 2009-03-25 | 2015-05-13 | 拜尔农作物科学股份公司 | 具有杀昆虫和杀螨特性的活性成分结合物 |
US9012360B2 (en) | 2009-03-25 | 2015-04-21 | Bayer Intellectual Property Gmbh | Synergistic combinations of active ingredients |
AU2009342807B2 (en) * | 2009-03-25 | 2015-04-02 | Bayer Cropscience Aktiengesellschaft | Synergistic combinations of active ingredients |
WO2010112545A1 (en) | 2009-04-01 | 2010-10-07 | Basf Se | Isoxazoline compounds for combating invertebrate pests |
EP2239331A1 (de) | 2009-04-07 | 2010-10-13 | Bayer CropScience AG | Verfahren zur verbesserten Verwendung des Herstellungspotentials von transgenen Pflanzen |
WO2010121735A1 (en) | 2009-04-22 | 2010-10-28 | Bayer Cropscience Ag | Use of propineb as bird repellent |
US8940662B2 (en) | 2009-04-28 | 2015-01-27 | Basf Corporation | Methods for controlling pests |
US8343893B2 (en) | 2009-06-18 | 2013-01-01 | Bayer Cropscience Ag | Substituted enaminocarbonyl compounds |
WO2010145764A1 (de) | 2009-06-18 | 2010-12-23 | Bayer Cropscience Ag | Substituierte enaminocarbonylverbindungen |
EP2264008A1 (de) | 2009-06-18 | 2010-12-22 | Bayer CropScience AG | Substituierte Enaminocarbonylverbindungen |
WO2010149370A1 (en) | 2009-06-24 | 2010-12-29 | Bayer Cropscience Ag | Combinations of biological control agents and insecticides |
EP2269455A1 (de) | 2009-06-24 | 2011-01-05 | Bayer CropScience AG | Kombinationen von biologischen Schädlingsbekämpfungsmittel und Insektiziden |
WO2011003796A1 (en) | 2009-07-06 | 2011-01-13 | Basf Se | Pyridazine compounds for controlling invertebrate pests |
WO2011009804A2 (en) | 2009-07-24 | 2011-01-27 | Basf Se | Pyridine derivatives compounds for controlling invertebrate pests |
WO2011009540A2 (en) | 2009-07-24 | 2011-01-27 | Bayer Cropscience Ag | Pesticidal carboxamides |
WO2011014660A1 (en) | 2009-07-30 | 2011-02-03 | Merial Limited | Insecticidal 4-amino-thieno[2,3-d]-pyrimidine compounds and methods of their use |
CN102471315A (zh) * | 2009-08-18 | 2012-05-23 | 拜耳作物科学公司 | 制备4-氨基丁-2-烯羟酸内酯的新方法 |
WO2011020564A1 (de) | 2009-08-18 | 2011-02-24 | Bayer Cropscience Ag | Neues verfahren zur herstellung von 4-aminobut-2-enoliden |
JP2013502385A (ja) * | 2009-08-18 | 2013-01-24 | バイエル・クロップサイエンス・アーゲー | 4−アミノブタ−2−エノリド類の新規調製方法 |
US8314242B2 (en) | 2009-08-18 | 2012-11-20 | BayerCrop Science AG | Process for the preparation of 4-aminobut-2-enolides |
WO2011029506A1 (de) | 2009-08-20 | 2011-03-17 | Bayer Cropscience Ag | 3-[1-(3-haloalkyl)-triazolyl]-phenyl-sulfid-derivate als akarizide und insektizide |
WO2011020567A1 (de) | 2009-08-20 | 2011-02-24 | Bayer Cropscience Ag | 3-triazolylphenyl-substituierte sulfid-derivate als akarizide und insektizide |
WO2011025789A2 (en) | 2009-08-28 | 2011-03-03 | Basf Corporation | Foamable pesticide compositions and methods of application |
US9339030B2 (en) | 2009-08-28 | 2016-05-17 | Basf Corporation | Foamable pesticide compositions and methods of application |
US20180035666A1 (en) * | 2009-09-14 | 2018-02-08 | Bayer Intellectual Property Gmbh | Agrochemical Compositions Comprising Alkyl Polypropylene Glycol Polyethylene Glycol |
US20110086848A1 (en) * | 2009-09-14 | 2011-04-14 | Bayer Cropscience Ag | Agrochemical Compositions Comprising Alkyl Polypropylene Glycol Polyethylene Glycol |
WO2011036074A1 (en) | 2009-09-24 | 2011-03-31 | Basf Se | Aminoquinazoline compounds for combating invertebrate pests |
WO2011045240A1 (de) | 2009-10-12 | 2011-04-21 | Bayer Cropscience Ag | Amide und thioamide als schädlingsbekämpfungsmittel |
WO2011045224A1 (de) | 2009-10-12 | 2011-04-21 | Bayer Cropscience Ag | 1- (pyrid-3-yl) -pyrazole und 1- (pyrimid-5-yl) -pyrazole als schädlingsbekämpfungsmittel |
US8476448B2 (en) | 2009-10-26 | 2013-07-02 | Bayer Cropscience Ag | Solid form of 4-[[(6-chloropyridin-3-yl)methyl](2,2-difluoroethyl)amino]furan-2(5H)-one |
US8324392B2 (en) | 2009-10-26 | 2012-12-04 | Bayer Cropscience Ag | Solid form of 4-[[(6-chloropyridin-3-yl)methyl](2,2-difluoroethyl)amino]furan-2(5H)-one |
WO2011051151A1 (de) | 2009-10-26 | 2011-05-05 | Bayer Cropscience Ag | Neue feste form von 4-[[(6-chlorpyridin-3-yl)methyl](2,2-difluorethyl)amino]furan-2(5h)-on |
WO2011054436A2 (de) | 2009-10-27 | 2011-05-12 | Bayer Cropscience Ag | Halogenalkyl-substituierte amide als insektizide und akarizide |
CN102712630A (zh) * | 2009-10-27 | 2012-10-03 | 拜尔技术服务有限责任公司 | 4-{[(6-氯吡啶-3-基)甲基](2,2-二氟乙基)-氨基}呋喃-2(5h)-酮与苯甲酸的共结晶及其作为杀虫剂的用途 |
WO2011051242A1 (de) | 2009-10-27 | 2011-05-05 | Bayer Technology Services Gmbh | Co-kristall von 4- { [ (6-chlorpyrid-3-yl) methyl] (2,2-difluorethyl) amino} furan-2 (5h) -on mit salizylsäure und dessen verwendung als pestizid |
WO2011051241A1 (de) | 2009-10-27 | 2011-05-05 | Bayer Technology Services Gmbh | Co-kristall von 4-{[(6-chlorpyrid-3yl)methyl](2,2-difluorethyl)amino}furan-2(5h)-on mit oxalsäure und dessen verwendung als pestizid |
WO2011051240A1 (de) | 2009-10-27 | 2011-05-05 | Bayer Technology Services Gmbh | Co-kristall von 4-{[(6-chlorpyrid-3-yl)methyl](2,2-difluorethyl)amino}furan-2(5h)-on mit benzoesäure und dessen verwendung als pestizid |
WO2011051455A1 (en) | 2009-10-30 | 2011-05-05 | Bayer Cropscience Ag | Pesticidal heterocyclic compounds |
WO2011057942A1 (en) | 2009-11-12 | 2011-05-19 | Basf Se | Insecticidal methods using pyridine compounds |
WO2011061110A1 (en) | 2009-11-17 | 2011-05-26 | Basf Se | Fluorinated oxa or thia heteroarylalkylsulfide derivatives for combating invertebrate pests |
WO2011061156A1 (en) | 2009-11-17 | 2011-05-26 | Bayer Cropscience Ag | Active compound combinations |
WO2011064188A1 (en) | 2009-11-27 | 2011-06-03 | Basf Se | Insecticidal methods using nitrogen-containing heteroaromatic compounds |
WO2011069143A1 (en) | 2009-12-04 | 2011-06-09 | Merial Limited | Pesticidal bis-organosulfur compounds |
WO2011069955A1 (en) | 2009-12-07 | 2011-06-16 | Basf Se | Sulfonimidamide compounds for combating animal pests |
WO2011080044A2 (en) | 2009-12-16 | 2011-07-07 | Bayer Cropscience Ag | Active compound combinations |
WO2011073444A2 (en) | 2009-12-18 | 2011-06-23 | Basf Se | Azoline compounds for combating invertebrate pests |
WO2011076724A2 (en) | 2009-12-23 | 2011-06-30 | Bayer Cropscience Ag | Pesticidal compound mixtures |
US8344151B2 (en) | 2009-12-23 | 2013-01-01 | Bayer Cropscience Ag | Process for the preparation of 4-aminobut-2-enolides starting from 4-alkoxyfuran-2(5H)-one or 4-arylalkoxyfuran-2(5H)-one |
WO2011076727A2 (en) | 2009-12-23 | 2011-06-30 | Bayer Cropscience Ag | Pesticidal compound mixtures |
WO2011076715A1 (de) | 2009-12-23 | 2011-06-30 | Bayer Cropscience Ag | Neues verfahren zur herstellung von 4-aminobut-2-enoliden ausgehend von 4-alkoxyfuran-2(5h)-on oder 4-arylalkoxyfuran-2-(5h)-on |
EP2516421B1 (de) * | 2009-12-23 | 2016-08-10 | Bayer Intellectual Property GmbH | Neues Verfahren zur Herstellung von 4-Aminobut-2-enoliden ausgehend von 4-Alkoxyfuran-2(5H)-on oder 4-Arylalkoxyfuran-2-(5H)-on |
WO2011076726A2 (en) | 2009-12-23 | 2011-06-30 | Bayer Cropscience Ag | Pesticidal compound mixtures |
WO2011080211A1 (en) | 2009-12-28 | 2011-07-07 | Bayer Cropscience Ag | Pesticidal arylpyrrolidines |
WO2011092147A1 (en) | 2010-01-29 | 2011-08-04 | Bayer Cropscience Ag | Method to reduce the frequency and/or intensity of blossom-end rot disorder in horticultural crops |
WO2011092287A1 (en) | 2010-02-01 | 2011-08-04 | Basf Se | Substituted ketonic isoxazoline compounds and derivatives for combating animal pests |
WO2011095554A3 (de) * | 2010-02-05 | 2011-11-03 | Bayer Cropscience Ag | Wirkstoffkombination enthaltend azadirachtin und eine substituierte enaminocarbonylverbindung |
EP2353386A1 (de) | 2010-02-05 | 2011-08-10 | Bayer CropScience AG | Wirkstoffkombination enthaltend Azadirachtin und eine substituierte Enaminocarbonylverbindung |
WO2011095554A2 (de) | 2010-02-05 | 2011-08-11 | Bayer Cropscience Ag | Wirkstoffkombination enthaltend azadirachtin und eine substituierte enaminocarbonylverbindung |
AU2011212451B2 (en) * | 2010-02-05 | 2014-04-10 | Bayer Cropscience Aktiengesellschaft | Active substance combination containing azadirachtin and a substituted enamino carbonyl compound |
US8653110B2 (en) | 2010-02-05 | 2014-02-18 | Bayer Cropscience Ag | Active compound combination comprising azadirachtin and a substituted enaminocarbonyl compound |
WO2011098443A1 (de) | 2010-02-10 | 2011-08-18 | Bayer Cropscience Ag | Spiroheterocyclisch-substituierte tetramsäure-derivate |
WO2011098440A2 (de) | 2010-02-10 | 2011-08-18 | Bayer Cropscience Ag | Biphenylsubstituierte cyclische ketoenole |
WO2011107443A1 (en) | 2010-03-02 | 2011-09-09 | Bayer Cropscience Ag | Use of propineb for physiological curative treatment under zinc deficiency |
WO2011107504A1 (de) | 2010-03-04 | 2011-09-09 | Bayer Cropscience Ag | Fluoralkyl- substituierte 2 -amidobenzimidazole und deren verwendung zur steigerung der stresstoleranz in pflanzen |
WO2011117804A1 (en) | 2010-03-23 | 2011-09-29 | Basf Se | Pyridazine compounds for controlling invertebrate pests |
WO2011117806A2 (en) | 2010-03-23 | 2011-09-29 | Basf Se | Pyridazine compounds for controlling invertebrate pests |
WO2011117198A2 (en) | 2010-03-23 | 2011-09-29 | Basf Se | Pyridazine compounds for controlling invertebrate pests |
WO2011117213A1 (en) | 2010-03-23 | 2011-09-29 | Basf Se | Pyridazine compounds for controlling invertebrate pests |
WO2011117286A1 (en) | 2010-03-23 | 2011-09-29 | Basf Se | Pyridazine compounds for controlling invertebrate pests |
WO2011131616A2 (de) | 2010-04-23 | 2011-10-27 | Bayer Cropscience Ag | Triglyzerid-enthaltende winterspritzmittel |
EP2382865A1 (de) | 2010-04-28 | 2011-11-02 | Bayer CropScience AG | Synergistische Wirkstoffkombinationen |
WO2011134964A1 (de) | 2010-04-28 | 2011-11-03 | Bayer Cropscience Ag | Synergistische wirkstoffkombinationen |
WO2011138285A1 (de) | 2010-05-05 | 2011-11-10 | Bayer Cropscience Ag | Thiazolderivate als schädlingsbekämpfungsmittel |
WO2011148886A1 (ja) | 2010-05-24 | 2011-12-01 | Meiji Seikaファルマ株式会社 | 有害生物防除剤 |
WO2011147952A1 (en) | 2010-05-28 | 2011-12-01 | Basf Se | Pesticidal mixtures |
KR101790159B1 (ko) | 2010-06-15 | 2017-10-25 | 바이엘 인텔렉쳐 프로퍼티 게엠베하 | 2,2-디플루오로-1-할로에탄의 알킬화에 의한 2,2-디플루오로에틸아민 유도체의 제조 방법 |
TWI510470B (zh) * | 2010-06-15 | 2015-12-01 | Bayer Ip Gmbh | 藉由以2,2-二氟-1-鹵乙烷烷化作用製備2,2-二氟乙胺衍生物之方法 |
WO2011157663A1 (de) | 2010-06-15 | 2011-12-22 | Bayer Cropscience Ag | Neue ortho-substituierte arylamid-derivate |
WO2011157650A1 (de) | 2010-06-15 | 2011-12-22 | Bayer Cropscience Ag | Verfahren zur herstellung von 2, 2-difluorethylamin- derivaten durch alkylierung mit 2,2- difluor-1-halogenethanen |
US8658800B2 (en) | 2010-06-15 | 2014-02-25 | Bayer Cropscience Ag | Ortho-substituted arylamide derivatives |
US9198424B2 (en) | 2010-06-18 | 2015-12-01 | Bayer Intellectual Property Gmbh | Active ingredient combinations having insecticidal and acaricidal properties |
WO2011157778A1 (de) | 2010-06-18 | 2011-12-22 | Bayer Cropscience Ag | Wirkstoffkombinationen mit insektiziden und akariziden eigenschaften |
US9968086B2 (en) | 2010-06-18 | 2018-05-15 | Bayer Intellectual Property Gmbh | Active ingredient combinations having insecticidal and acaricidal properties |
WO2012000896A2 (de) | 2010-06-28 | 2012-01-05 | Bayer Cropscience Ag | Heterocyclische verbindungen als schädlingsbekämpfungsmittel |
WO2012000902A1 (de) | 2010-06-29 | 2012-01-05 | Bayer Cropscience Ag | Verbesserte insektizide zusammensetzungen enthaltend cyclische carbonylamidine |
WO2012001068A2 (de) | 2010-07-02 | 2012-01-05 | Bayer Cropscience Ag | Insektizide oder akarizide formulierungen mit verbesserter verfügbarkeit auf pflanzenoberflächen |
WO2012004326A1 (en) | 2010-07-08 | 2012-01-12 | Bayer Cropscience Ag | Pesticidal pyrroline derivatives |
WO2012004293A2 (de) | 2010-07-08 | 2012-01-12 | Bayer Cropscience Ag | Insektizide und fungizide wirkstoffkombinationen |
US9790202B2 (en) | 2010-07-09 | 2017-10-17 | Bayer Intellectual Property Gmbh | Anthranilamide derivatives as pesticides |
WO2012004208A1 (de) | 2010-07-09 | 2012-01-12 | Bayer Cropscience Ag | Anthranilsäurediamid-derivate als pestizide |
WO2012007426A1 (en) | 2010-07-13 | 2012-01-19 | Basf Se | Azoline substituted isoxazoline benzamide compounds for combating animal pests |
WO2012007500A2 (de) | 2010-07-15 | 2012-01-19 | Bayer Cropscience Ag | Neue heterocyclische verbindungen als schädlingsbekämpfungsmittel |
WO2012007505A2 (en) | 2010-07-16 | 2012-01-19 | Bayer Innovation Gmbh | Polymer composite material with biocide functionality |
WO2012010509A2 (de) | 2010-07-20 | 2012-01-26 | Bayer Cropscience Ag | Gelköder zur bekämpfung von kriechenden schadinsekten |
WO2012010534A1 (en) | 2010-07-22 | 2012-01-26 | Basf Se | Novel hetaryl (thio)carboxamide compounds for controlling invertebrate pests |
EP2422620A1 (de) | 2010-08-26 | 2012-02-29 | Bayer CropScience AG | Insektizide Wirkstoffkombinationen enthaltend Ethiprole und Pymetrozin |
WO2012028583A1 (de) | 2010-09-03 | 2012-03-08 | Bayer Cropscience Ag | Deltamethrin enthaltende formulierungen |
WO2012034961A1 (en) | 2010-09-13 | 2012-03-22 | Basf Se | Pyridine compounds for controlling invertebrate pests i |
WO2012034959A2 (en) | 2010-09-13 | 2012-03-22 | Basf Se | Pyridine compounds for controlling invertebrate pests iii |
WO2012034960A1 (en) | 2010-09-13 | 2012-03-22 | Basf Se | Pyridine compounds for controlling invertebrate pests ii |
WO2012035011A1 (en) | 2010-09-15 | 2012-03-22 | Bayer Cropscience Ag | Pesticidal arylpyrrolidines |
WO2012034957A1 (en) | 2010-09-15 | 2012-03-22 | Bayer Cropscience Ag | Pesticidal pyrroline n-oxide derivatives |
US9375000B2 (en) | 2010-09-15 | 2016-06-28 | Bayer Intellectual Property Gmbh | Pesticidal arylpyrrolidines |
WO2012038476A1 (en) | 2010-09-22 | 2012-03-29 | Bayer Cropscience Ag | Use of active ingredients for controlling nematodes in nematode-resistant crops |
WO2012038480A2 (en) | 2010-09-22 | 2012-03-29 | Bayer Cropscience Ag | Use of biological or chemical control agents for controlling insects and nematodes in resistant crops |
WO2012042006A1 (en) | 2010-10-01 | 2012-04-05 | Basf Se | Imine compounds |
WO2012042007A1 (en) | 2010-10-01 | 2012-04-05 | Basf Se | Imine substituted 2, 4 - diaryl - pyrroline derivatives as pesticides |
WO2012041874A1 (en) | 2010-10-01 | 2012-04-05 | Syngenta Participations Ag | Fungicidal compositions |
EP3175712A1 (de) | 2010-10-01 | 2017-06-07 | Syngenta Participations Ag | Fungizidzusammensetzungen |
WO2012045680A2 (de) | 2010-10-04 | 2012-04-12 | Bayer Cropscience Ag | Insektizide und fungizide wirkstoffkombinationen |
WO2012045798A1 (en) | 2010-10-07 | 2012-04-12 | Bayer Cropscience Ag | Fungicide composition comprising a tetrazolyloxime derivative and a thiazolylpiperidine derivative |
WO2012052490A1 (en) | 2010-10-21 | 2012-04-26 | Bayer Cropscience Ag | N-benzyl heterocyclic carboxamides |
US9173396B2 (en) | 2010-10-22 | 2015-11-03 | Bayer Intellectual Property Gmbh | Heterocyclic compounds as pesticides |
WO2012052412A1 (de) | 2010-10-22 | 2012-04-26 | Bayer Cropscience Ag | Neue heterocylische verbindungen als schädlingsbekämpfungsmittel |
EP2446742A1 (de) | 2010-10-28 | 2012-05-02 | Bayer CropScience AG | Insektizide oder akarizide Zusammensetzungen enthaltend Mono- oder Disacchariden als Wirkungsverstärker |
WO2012059497A1 (en) | 2010-11-02 | 2012-05-10 | Bayer Cropscience Ag | N-hetarylmethyl pyrazolylcarboxamides |
WO2012062740A1 (de) | 2010-11-12 | 2012-05-18 | Bayer Cropscience Ag | Verfahren zur herstellung von 2,2-difluorethylamin-derivaten ausgehend von n-(2,2-difluorethyl)prop-2-en-1-amin |
US8586756B2 (en) | 2010-11-12 | 2013-11-19 | Bayer Cropscience Ag | Process for the preparation of 2,2-difluoroethylamine derivatives starting from N-(2,2-difluoroethyl)prop-2-en-1-amine |
WO2012065944A1 (en) | 2010-11-15 | 2012-05-24 | Bayer Cropscience Ag | N-aryl pyrazole(thio)carboxamides |
US9206137B2 (en) | 2010-11-15 | 2015-12-08 | Bayer Intellectual Property Gmbh | N-Aryl pyrazole(thio)carboxamides |
US9055743B2 (en) | 2010-11-29 | 2015-06-16 | Bayer Intellectual Property Gmbh | Alpha, beta-unsaturated imines |
WO2012072489A1 (de) | 2010-11-29 | 2012-06-07 | Bayer Cropscience Ag | Alpha-beta-ungesättigte imine |
EP2460406A1 (de) | 2010-12-01 | 2012-06-06 | Bayer CropScience AG | Verwendung von Fluopyram zum Steuern von Nematoden in nematodresistentem Pflanzen |
WO2012072660A1 (en) | 2010-12-01 | 2012-06-07 | Bayer Cropscience Ag | Use of fluopyram for controlling nematodes in crops and for increasing yield |
WO2012076470A1 (en) | 2010-12-09 | 2012-06-14 | Bayer Cropscience Ag | Pesticidal mixtures with improved properties |
WO2012076471A1 (en) | 2010-12-09 | 2012-06-14 | Bayer Cropscience Ag | Insecticidal mixtures with improved properties |
WO2012076704A2 (en) | 2010-12-10 | 2012-06-14 | Basf Se | Pyrazole compounds for controlling invertebrate pests |
WO2012082548A2 (en) | 2010-12-15 | 2012-06-21 | Syngenta Participations Ag | Soybean event syht0h2 and compositions and methods for detection thereof |
WO2012080188A1 (de) | 2010-12-17 | 2012-06-21 | Bayer Cropscience Ag | Insektizid-wachs-partikel enthaltende zusammensetzung |
WO2012084670A1 (en) | 2010-12-20 | 2012-06-28 | Basf Se | Pesticidal active mixtures comprising pyrazole compounds |
WO2012084900A1 (fr) | 2010-12-20 | 2012-06-28 | Universite De Poitiers | Composition phytosanitaire à base de zéolithe |
WO2012084852A2 (de) | 2010-12-21 | 2012-06-28 | Bayer Animal Health Gmbh | Ektoparasitizide wirkstoffkombinationen |
EP2468097A1 (de) | 2010-12-21 | 2012-06-27 | Bayer CropScience AG | Verwendung von Isothiazolcarboxamiden für latente Wirtsabwehr bei einer Pflanze |
DE102010063691A1 (de) | 2010-12-21 | 2012-06-21 | Bayer Animal Health Gmbh | Ektoparasitizide Wirkstoffkombinationen |
WO2012085081A1 (en) | 2010-12-22 | 2012-06-28 | Basf Se | Sulfoximinamide compounds for combating invertebrate pests ii |
WO2012089721A1 (de) | 2010-12-30 | 2012-07-05 | Bayer Cropscience Ag | Verwendung von substituierten spirocyclischen sulfonamidocarbonsäuren, deren carbonsäureestern, deren carbonsäureamiden und deren carbonitrilen oder deren salze zur steigerung der stresstoleranz in pflanzen |
WO2012089722A2 (de) | 2010-12-30 | 2012-07-05 | Bayer Cropscience Ag | Verwendung von offenkettigen aryl-, heteroaryl- und benzylsulfonamidocarbonsäuren, -carbonsäureestern, -carbonsäureamiden und -carbonitrilen oder deren salze zur steigerung der stresstoleranz in pflanzen |
US20120190867A1 (en) * | 2011-01-24 | 2012-07-26 | Bayer Cropscience Ag | Process for the preparation of 2,2-difluoroethylamine |
US8580973B2 (en) * | 2011-01-24 | 2013-11-12 | Bayer Cropscience Ag | Process for the preparation of 2,2-difluoroethylamine |
US9510594B2 (en) | 2011-02-17 | 2016-12-06 | Bayer Intellectual Property Gmbh | Use of SDHI fungicides on conventionally bred ASR-tolerant, stem canker resistant and/or frog-eye leaf spot resistant soybean varieties |
US8946124B2 (en) | 2011-02-17 | 2015-02-03 | Bayer Intellectual Property Gmbh | Substituted 3-(biphenyl-3-yl)-8,8-difluoro-4-hydroxy-1-azaspiro[4.5]dec-3-en-2-ones for therapy and halogen-substituted spirocyclic ketoenols |
WO2012110518A1 (de) | 2011-02-17 | 2012-08-23 | Bayer Pharma Aktiengesellschaft | Substituierte 3-(biphenyl-3-yl)-8,8-difluor-4-hydroxy-1-azaspiro[4.5]dec-3-en-2-one zur therapie |
WO2012110464A1 (en) | 2011-02-17 | 2012-08-23 | Bayer Cropscience Ag | Use of sdhi fungicides on conventionally bred asr-tolerant, stem canker resistant and/or frog-eye leaf spot resistant soybean varieties |
WO2012110519A1 (de) | 2011-02-17 | 2012-08-23 | Bayer Cropscience Ag | Substituierte 3-(biphenyl-3-yl)-8,8-difluor-4-hydroxy-1-azaspiro[4.5]dec-3-en-2-one zur therapie und halogensubstituierte spirocyclische ketoenole |
WO2012116960A1 (de) | 2011-03-01 | 2012-09-07 | Bayer Cropscience Ag | 2-acyloxy-pyrrolin-4-one |
US9204640B2 (en) | 2011-03-01 | 2015-12-08 | Bayer Intellectual Property Gmbh | 2-acyloxy-pyrrolin-4-ones |
WO2012119984A1 (de) | 2011-03-09 | 2012-09-13 | Bayer Cropscience Ag | Indol- und benzimidazolcarbonsäureamide als insektizide und akarizide |
US9107411B2 (en) | 2011-03-09 | 2015-08-18 | Bayer Intellectual Property Gmbh | Indolecarboxamides and benzimidazolecarboxamides as insecticides and acaricides |
WO2012120105A1 (en) | 2011-03-10 | 2012-09-13 | Bayer Cropscience Ag | Use of lipochito-oligosaccharide compounds for safeguarding seed safety of treated seeds |
WO2012126766A1 (de) | 2011-03-18 | 2012-09-27 | Bayer Cropscience Ag | N- (3 -carbamoylphenyl) - 1h - pyrazol - 5 - carboxamid - derivate und ihre verwendung zur bekämpfung von tierischen schädlingen |
WO2012136724A1 (en) | 2011-04-06 | 2012-10-11 | Basf Se | Substituted pyrimidinium compounds for combating animal pests |
WO2012136751A1 (en) | 2011-04-08 | 2012-10-11 | Basf Se | N-substituted hetero-bicyclic compounds and derivatives for combating animal pests |
WO2012139890A1 (de) | 2011-04-15 | 2012-10-18 | Bayer Cropscience Ag | Substituierte 5-(cyclohex-2-en-1-yl)-penta-2,4-diene und 5-(cyclohex-2-en-1-yl)-pent-2-en-4-ine als wirkstoffe gegen abiotischen pflanzenstress |
WO2012139892A1 (de) | 2011-04-15 | 2012-10-18 | Bayer Cropscience Ag | Substituierte 5-(bicyclo[4.1.0]hept-3-en-2-yl)-penta-2,4-diene und 5-(bicyclo[4.1.0]hept-3-en-2-yl)-pent-2-en-4-ine als wirkstoffe gegen abiotischen pflanzenstress |
WO2012139891A1 (de) | 2011-04-15 | 2012-10-18 | Bayer Cropscience Ag | Substituierte vinyl- und alkinyl-cyclohexenole als wirkstoffe gegen abiotischen pflanzenstress |
WO2012143317A1 (en) | 2011-04-21 | 2012-10-26 | Basf Se | Novel pesticidal pyrazole compounds |
WO2012171914A1 (en) | 2011-06-14 | 2012-12-20 | Bayer Intellectual Property Gmbh | Use of an enaminocarbonyl compound in combination with a biological control agent |
US9241493B2 (en) | 2011-06-14 | 2016-01-26 | Bayer Intellectual Property Gmbh | Use of an enaminocarbonyl compound in combination with a biological control agent |
EP2535334A1 (de) | 2011-06-17 | 2012-12-19 | Bayer CropScience AG | Kristalline Modifikationen von Penflufen |
WO2013010758A1 (en) | 2011-06-30 | 2013-01-24 | Bayer Intellectual Property Gmbh | Nematocide n- cyclopropyl - sulfonylamide derivatives |
EP2540163A1 (de) | 2011-06-30 | 2013-01-02 | Bayer CropScience AG | Nematozide N-Cyclopropylsulfonylamidderivate |
WO2013004652A1 (de) | 2011-07-04 | 2013-01-10 | Bayer Intellectual Property Gmbh | Verwendung substituierter isochinolinone, isochinolindione, isochinolintrione und dihydroisochinolinone oder jeweils deren salze als wirkstoffe gegen abiotischen pflanzenstress |
US9504250B2 (en) | 2011-07-13 | 2016-11-29 | Sumitomo Chemical Company, Limited | Arthropod pest control composition and method for controlling arthropod pests |
WO2013010947A2 (en) | 2011-07-15 | 2013-01-24 | Basf Se | Pesticidal methods using substituted 3-pyridyl thiazole compounds and derivatives for combating animal pests ii |
WO2013010946A2 (en) | 2011-07-15 | 2013-01-24 | Basf Se | Pesticidal methods using substituted 3-pyridyl thiazole compounds and derivatives for combating animal pests i |
WO2013014126A1 (de) | 2011-07-26 | 2013-01-31 | Bayer Intellectual Property Gmbh | Veretherte laktatester, verfahren zu ihrer herstellung und ihre verwendung zur verbesserung der wirkung von pflanzenschutzmitteln |
US9826734B2 (en) | 2011-07-26 | 2017-11-28 | Clariant International Ltd. | Etherified lactate esters, method for the production thereof and use thereof for enhancing the effect of plant protecting agents |
WO2013014227A1 (en) | 2011-07-27 | 2013-01-31 | Bayer Intellectual Property Gmbh | Seed dressing for controlling phytopathogenic fungi |
WO2013024006A1 (en) | 2011-08-12 | 2013-02-21 | Basf Se | Anthranilamide compounds and their use as pesticides |
WO2013024009A1 (en) | 2011-08-12 | 2013-02-21 | Basf Se | N-thio-anthranilamide compounds and their use as pesticides |
WO2013024004A1 (en) | 2011-08-12 | 2013-02-21 | Basf Se | N-thio-anthranilamide compounds and their use as pesticides |
WO2013024005A1 (en) | 2011-08-12 | 2013-02-21 | Basf Se | Anthranilamide compounds and their use as pesticides |
WO2013024003A1 (en) | 2011-08-12 | 2013-02-21 | Basf Se | N-thio-anthranilamide compounds and their use as pesticides |
WO2013024008A1 (en) | 2011-08-12 | 2013-02-21 | Basf Se | Aniline type compounds |
WO2013024010A1 (en) | 2011-08-12 | 2013-02-21 | Basf Se | N-thio-anthranilamide compounds and their use as pesticides |
WO2013024171A1 (en) | 2011-08-18 | 2013-02-21 | Basf Se | Carbamoylmethoxy- and carbamoylmethylthio- and carbamoylmethylamino benzamides for combating invertebrate pests |
WO2013024169A1 (en) | 2011-08-18 | 2013-02-21 | Basf Se | Carbamoylmethoxy- and carbamoylmethylthio- and carbamoylmethylamino benzamides for combating invertebrate pests |
WO2013024170A1 (en) | 2011-08-18 | 2013-02-21 | Basf Se | Carbamoylmethoxy- and carbamoylmethylthio- and carbamoylmethylamino benzamides for combating invertebrate pests |
EP2561759A1 (de) | 2011-08-26 | 2013-02-27 | Bayer Cropscience AG | Fluoralkyl-substituierte 2-amidobenzimidazole und ihre Wirkung auf das Pflanzenwachstum |
WO2013030319A2 (en) | 2011-09-02 | 2013-03-07 | Basf Se | Use of pesticidal active 3-arylquinazolin-4-one derivatives in soil application methods |
WO2013030262A1 (en) | 2011-09-02 | 2013-03-07 | Basf Se | Insecticidal active mixtures comprising arylquinazolinone compounds |
WO2013037956A1 (en) | 2011-09-16 | 2013-03-21 | Bayer Intellectual Property Gmbh | Use of 5-phenyl- or 5-benzyl-2 isoxazoline-3 carboxylates for improving plant yield |
WO2013037958A1 (en) | 2011-09-16 | 2013-03-21 | Bayer Intellectual Property Gmbh | Use of phenylpyrazolin-3-carboxylates for improving plant yield |
WO2013037955A1 (en) | 2011-09-16 | 2013-03-21 | Bayer Intellectual Property Gmbh | Use of acylsulfonamides for improving plant yield |
WO2013050433A1 (en) | 2011-10-05 | 2013-04-11 | Bayer Intellectual Property Gmbh | Pesticide preparation and process for producing the same |
KR20140084163A (ko) | 2011-10-18 | 2014-07-04 | 스미또모 가가꾸 가부시끼가이샤 | 유해 생물 방제 조성물 및 유해 생물의 방제 방법 |
WO2013079601A1 (en) | 2011-12-02 | 2013-06-06 | Basf Se | Method and system for monitoring crops and/or infestation of crops with harmful organismus during storage |
WO2013079600A1 (en) | 2011-12-02 | 2013-06-06 | Basf Se | Method and system for monitoring crops during storage |
EP2604118A1 (de) | 2011-12-15 | 2013-06-19 | Bayer CropScience AG | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
WO2013087709A1 (en) | 2011-12-15 | 2013-06-20 | Bayer Intellectual Property Gmbh | Active ingredient combinations having insecticidal and acaricidal properties |
WO2013092519A1 (en) | 2011-12-19 | 2013-06-27 | Bayer Cropscience Ag | Use of anthranilic acid diamide derivatives for pest control in transgenic crops |
WO2013092522A1 (de) | 2011-12-20 | 2013-06-27 | Bayer Intellectual Property Gmbh | Neue insektizide aromatische amide |
WO2013092868A1 (en) | 2011-12-21 | 2013-06-27 | Basf Se | N-thio-anthranilamide compounds and their use as pesticides |
EP3395171A1 (de) | 2011-12-21 | 2018-10-31 | Bayer CropScience Aktiengesellschaft | N-arylamidine-substituierte trifluoroethylsulfid-derivate als akarizide und insektizide |
EP2606726A1 (de) | 2011-12-21 | 2013-06-26 | Bayer CropScience AG | N-Arylamidine-substituierte trifluoroethylsulfid-Derivate als Akarizide und Insektizide |
WO2013092350A1 (de) | 2011-12-21 | 2013-06-27 | Bayer Cropscience Ag | N-arylamidine-substituierte trifluoroethylsulfid-derivate als akarizide und insektizide |
WO2013092943A1 (en) | 2011-12-23 | 2013-06-27 | Basf Se | Isothiazoline compounds for combating invertebrate pests |
WO2013107785A1 (en) | 2012-01-21 | 2013-07-25 | Bayer Intellectual Property Gmbh | Use of host defense inducers for controlling bacterial harmful organisms in useful plants |
WO2013113789A1 (en) | 2012-02-02 | 2013-08-08 | Basf Se | N-thio-anthranilamide compounds and their use as pesticides |
WO2013135724A1 (en) | 2012-03-14 | 2013-09-19 | Bayer Intellectual Property Gmbh | Pesticidal arylpyrrolidines |
WO2013144228A1 (en) | 2012-03-29 | 2013-10-03 | Basf Se | Pesticidal methods using heterocyclic compounds and derivatives for combating animal pests |
WO2013144213A1 (en) | 2012-03-30 | 2013-10-03 | Basf Se | N-substituted pyridinylidene compounds and derivatives for combating animal pests |
WO2013144223A1 (en) | 2012-03-30 | 2013-10-03 | Basf Se | N-substituted pyrimidinylidene compounds and derivatives for combating animal pests |
WO2013149940A1 (en) | 2012-04-02 | 2013-10-10 | Basf Se | Acrylamide compounds for combating invertebrate pests |
WO2013149903A1 (en) | 2012-04-03 | 2013-10-10 | Basf Se | N- substituted hetero - bicyclic furanone derivatives for combating animal |
WO2013150115A1 (en) | 2012-04-05 | 2013-10-10 | Basf Se | N- substituted hetero - bicyclic compounds and derivatives for combating animal pests |
WO2013164295A1 (en) | 2012-05-04 | 2013-11-07 | Basf Se | Substituted pyrazole-containing compounds and their use as pesticides |
WO2013167633A1 (en) | 2012-05-09 | 2013-11-14 | Basf Se | Acrylamide compounds for combating invertebrate pests |
WO2013171199A1 (de) | 2012-05-16 | 2013-11-21 | Bayer Cropscience Ag | Insektizide wasser-in-öl (w/o) formulierung |
WO2013171201A1 (de) | 2012-05-16 | 2013-11-21 | Bayer Cropscience Ag | Insektizide öl-in-wasser (o/w) formulierung |
WO2013174836A1 (en) | 2012-05-22 | 2013-11-28 | Bayer Cropscience Ag | Active compounds combinations comprising a lipo-chitooligosaccharide derivative and a nematicide, insecticidal or fungicidal compound |
WO2013174645A1 (en) | 2012-05-24 | 2013-11-28 | Basf Se | N-thio-anthranilamide compounds and their use as pesticides |
US10813862B2 (en) | 2012-05-30 | 2020-10-27 | Clariant International Ltd. | Use of N-methyl-N-acylglucamines as solubilizers |
EP3363289A2 (de) | 2012-05-30 | 2018-08-22 | Bayer CropScience Aktiengesellschaft | Zusammensetzungen mit einem biologischen schädlingsbekämpfungsmittel und einem insektizid |
EP3243387A2 (de) | 2012-05-30 | 2017-11-15 | Bayer CropScience Aktiengesellschaft | Zusammensetzungen mit einem biologischen schädlingsbekämpfungsmittel und einem insektizid |
US10864275B2 (en) | 2012-05-30 | 2020-12-15 | Clariant International Ltd. | N-methyl-N-acylglucamine-containing composition |
WO2013182613A1 (en) | 2012-06-08 | 2013-12-12 | Bayer Cropscience Ag | Detection system for the identification of insecticide resistance |
WO2013186089A2 (en) | 2012-06-14 | 2013-12-19 | Basf Se | Pesticidal methods using substituted 3-pyridyl thiazole compounds and derivatives for combating animal pests |
EP3646731A1 (de) | 2012-06-20 | 2020-05-06 | Basf Se | Pestizidmischungen, eine pyrazolverbindung umfassend |
EP3300602A1 (de) | 2012-06-20 | 2018-04-04 | Basf Se | Pestizidmischungen mit einer pyrazolverbindung |
WO2013189801A1 (en) | 2012-06-20 | 2013-12-27 | Basf Se | Pyrazole compound and pesticidal mixtures comprising a pyrazole compound |
WO2014001245A1 (de) | 2012-06-29 | 2014-01-03 | Bayer Cropscience Ag | Verfahren zur herstellung von 2,2-difluorethylamin-derivaten durch alkylierung von 2,2-difluorethylamin |
TWI593677B (zh) * | 2012-06-29 | 2017-08-01 | 拜耳作物科學股份有限公司 | 經烷化2,2-二氟乙胺製備2,2-二氟乙胺衍生物之方法 |
US9376389B2 (en) | 2012-06-29 | 2016-06-28 | Bayer Cropscience Ag | Process for preparing 2,2-difluoroethylamine derivatives by alkylating 2,2-difluoroethylamine |
EP2684879A1 (de) | 2012-07-09 | 2014-01-15 | Basf Se | Substituierte mesoionische Verbindungen zur Bekämpfung von Tierschädlingen |
WO2014019983A1 (en) | 2012-07-31 | 2014-02-06 | Bayer Cropscience Ag | Compositions comprising a pesticidal terpene mixture and an insecticide |
EP3424322A1 (de) | 2012-07-31 | 2019-01-09 | Bayer CropScience Aktiengesellschaft | Zusammensetzungen mit einer pestizid-terpen-mischung und einem insektizid |
WO2014026984A1 (de) | 2012-08-17 | 2014-02-20 | Bayer Cropscience Ag | Azaindolcarbonsäure- und -thiocarbonsäureamide als insektizide und akarizide |
WO2014037340A1 (de) | 2012-09-05 | 2014-03-13 | Bayer Cropscience Ag | Verwendung substituierter 2-amidobenzimidazole, 2-amidobenzoxazole und 2-amidobenzothiazole oder deren salze als wirkstoffe gegen abiotischen pflanzenstress |
WO2014045228A1 (en) | 2012-09-21 | 2014-03-27 | Basf Se | Pyrethroid insecticide for protecting plants and seed |
WO2014047334A1 (en) | 2012-09-21 | 2014-03-27 | Basf Se | Methods for preventing pest infestations |
WO2014053405A1 (en) | 2012-10-01 | 2014-04-10 | Basf Se | Pesticidally active mixtures comprising anthranilamide compounds |
WO2014053395A1 (en) | 2012-10-01 | 2014-04-10 | Basf Se | Use of n-thio-anthranilamide compounds on cultivated plants |
WO2014053403A1 (en) | 2012-10-01 | 2014-04-10 | Basf Se | Method of controlling insecticide resistant insects |
WO2014053407A1 (en) | 2012-10-01 | 2014-04-10 | Basf Se | N-thio-anthranilamide compounds and their use as pesticides |
WO2014053404A1 (en) | 2012-10-01 | 2014-04-10 | Basf Se | Pesticidally active mixtures comprising anthranilamide compounds |
WO2014053406A1 (en) | 2012-10-01 | 2014-04-10 | Basf Se | Method of controlling ryanodine-modulator insecticide resistant insects |
WO2014053401A2 (en) | 2012-10-01 | 2014-04-10 | Basf Se | Method of improving plant health |
WO2014053450A1 (de) | 2012-10-02 | 2014-04-10 | Bayer Cropscience Ag | Heterocyclische verbindungen als schädlingsbekämpfungsmittel |
WO2014060381A1 (de) | 2012-10-18 | 2014-04-24 | Bayer Cropscience Ag | Heterocyclische verbindungen als schädlingsbekämpfungsmittel |
WO2014067962A1 (de) | 2012-10-31 | 2014-05-08 | Bayer Cropscience Ag | Neue heterocylische verbindungen als schädlingsbekämpfungsmittel |
US10772324B2 (en) | 2012-11-03 | 2020-09-15 | Clariant International Ltd. | Aqueous adjuvant-compositions |
WO2014072250A1 (en) | 2012-11-06 | 2014-05-15 | Bayer Cropscience Ag | Herbicidal combinations for tolerant soybean cultures |
EP3369318A1 (de) | 2012-11-06 | 2018-09-05 | Bayer CropScience Aktiengesellschaft | Herbizidkombinationen für tolerante sojabohnenkulturen |
EP3387906A1 (de) | 2012-11-06 | 2018-10-17 | Bayer CropScience Aktiengesellschaft | Herbizidkombinationen für tolerante sojabohnenkulturen |
WO2014079820A1 (en) | 2012-11-22 | 2014-05-30 | Basf Se | Use of anthranilamide compounds for reducing insect-vectored viral infections |
WO2014083088A2 (en) | 2012-11-30 | 2014-06-05 | Bayer Cropscience Ag | Binary fungicidal mixtures |
WO2014083033A1 (en) | 2012-11-30 | 2014-06-05 | Bayer Cropsience Ag | Binary fungicidal or pesticidal mixture |
WO2014086758A2 (en) | 2012-12-03 | 2014-06-12 | Bayer Cropscience Ag | Composition comprising a biological control agent and an insecticide |
WO2014086750A2 (en) | 2012-12-03 | 2014-06-12 | Bayer Cropscience Ag | Composition comprising a biological control agent and an insecticide |
WO2014086749A2 (en) | 2012-12-03 | 2014-06-12 | Bayer Cropscience Ag | Composition comprising a biological control agent and an insecticide |
WO2014086753A2 (en) | 2012-12-03 | 2014-06-12 | Bayer Cropscience Ag | Composition comprising biological control agents |
WO2014086759A2 (en) | 2012-12-03 | 2014-06-12 | Bayer Cropscience Ag | Composition comprising biological control agents |
WO2014086751A1 (de) | 2012-12-05 | 2014-06-12 | Bayer Cropscience Ag | Verwendung substituierter 1-(arylethinyl)-, 1-(heteroarylethinyl)-, 1-(heterocyclylethinyl)- und 1-(cyloalkenylethinyl)-cyclohexanole als wirkstoffe gegen abiotischen pflanzenstress |
WO2014090765A1 (en) | 2012-12-12 | 2014-06-19 | Bayer Cropscience Ag | Use of 1-[2-fluoro-4-methyl-5-(2,2,2-trifluoroethylsulfinyl)phenyl]-5-amino-3-trifluoromethyl)-1 h-1,2,4 tfia zole for controlling nematodes in nematode-resistant crops |
WO2014090700A1 (en) | 2012-12-14 | 2014-06-19 | Basf Se | Malononitrile compounds for controlling animal pests |
WO2014095826A1 (en) | 2012-12-18 | 2014-06-26 | Bayer Cropscience Ag | Binary fungicidal and bactericidal combinations |
US10759767B2 (en) | 2012-12-20 | 2020-09-01 | BASF Agro B.V. | Compositions comprising a triazole compound |
WO2014096238A1 (en) | 2012-12-21 | 2014-06-26 | Basf Se | Cycloclavine and derivatives thereof for controlling invertebrate pests |
WO2014102244A1 (en) | 2012-12-27 | 2014-07-03 | Basf Se | 2-(pyridin-3-yl)-5-hetaryl-thiazole compounds carrying an imine or imine-derived substituent for combating invertebrate pests |
US10519122B2 (en) | 2013-01-09 | 2019-12-31 | BASF Agro B.V. | Process for the preparation of substituted oxiranes and triazoles |
US10981883B2 (en) | 2013-01-09 | 2021-04-20 | BASF Agro B.V. | Process for the preparation of substituted oxiranes and triazoles |
WO2014119670A1 (ja) | 2013-01-31 | 2014-08-07 | 住友化学株式会社 | 有害生物防除組成物及び有害生物の防除方法 |
WO2014122083A1 (de) | 2013-02-06 | 2014-08-14 | Bayer Cropscience Ag | Halogensubstituierte pyrazolderivate als schädlingsbekämpfungsmittel |
WO2014124373A1 (en) | 2013-02-11 | 2014-08-14 | Bayer Cropscience Lp | Compositions comprising gougerotin and an insecticide |
WO2014124361A1 (en) | 2013-02-11 | 2014-08-14 | Bayer Cropscience Lp | Compositions comprising a streptomyces-based biological control agent and another biological control agent |
WO2014124379A1 (en) | 2013-02-11 | 2014-08-14 | Bayer Cropscience Lp | Compositions comprising a streptomyces-based biological control agent and an insecticide |
WO2014124375A1 (en) | 2013-02-11 | 2014-08-14 | Bayer Cropscience Lp | Compositions comprising gougerotin and a biological control agent |
WO2014128069A1 (en) | 2013-02-19 | 2014-08-28 | Bayer Cropscience Ag | Use of prothioconazole to induce host defence responses |
WO2014128136A1 (en) | 2013-02-20 | 2014-08-28 | Basf Se | Anthranilamide compounds and their use as pesticides |
WO2014139897A1 (en) | 2013-03-12 | 2014-09-18 | Bayer Cropscience Ag | Use of dithiine-tetracarboximides for controlling bacterial harmful organisms in useful plants |
WO2014140111A1 (en) | 2013-03-13 | 2014-09-18 | Bayer Cropscience Ag | Lawn growth-promoting agent and method of using same |
WO2014170364A1 (en) | 2013-04-19 | 2014-10-23 | Bayer Cropscience Ag | Binary insecticidal or pesticidal mixture |
WO2014170313A1 (en) | 2013-04-19 | 2014-10-23 | Bayer Cropscience Ag | Active compound combinations having insecticidal properties |
WO2014170300A1 (en) | 2013-04-19 | 2014-10-23 | Basf Se | N-substituted acyl-imino-pyridine compounds and derivatives for combating animal pests |
WO2014202510A1 (de) | 2013-06-20 | 2014-12-24 | Bayer Cropscience Ag | Arylsulfid- und arylsulfoxid-derivate als akarizide und insektizide |
WO2014202505A1 (de) | 2013-06-20 | 2014-12-24 | Bayer Cropscience Ag | Arylsulfid- und arylsulfoxid-derivate als akarizide und insektizide |
WO2014202751A1 (en) | 2013-06-21 | 2014-12-24 | Basf Se | Methods for controlling pests in soybean |
WO2015004028A1 (de) | 2013-07-08 | 2015-01-15 | Bayer Cropscience Ag | Sechsgliedrige c-n-verknüpfte arylsulfid- und arylsulfoxid- derivate als schädlingsbekämpfungsmittel |
US10512267B2 (en) | 2013-07-08 | 2019-12-24 | BASF Agro, B.V. | Compositions comprising a triazole compound and a biopesticide |
WO2015007682A1 (en) | 2013-07-15 | 2015-01-22 | Basf Se | Pesticide compounds |
WO2015040116A1 (en) | 2013-09-19 | 2015-03-26 | Basf Se | N-acylimino heterocyclic compounds |
EP2740357A1 (de) | 2013-10-10 | 2014-06-11 | Bayer CropScience AG | Aktive Verbindungen zur Behandlung von Saatgut |
WO2015055497A1 (en) | 2013-10-16 | 2015-04-23 | Basf Se | Substituted pesticidal pyrazole compounds |
EP3456201A1 (de) | 2013-10-18 | 2019-03-20 | BASF Agrochemical Products B.V. | Verwendung von pestizidwirksamen carboxamidderivaten in der boden- und samenanwendung und behandlungsverfahren |
WO2015055757A1 (en) | 2013-10-18 | 2015-04-23 | Basf Se | Use of pesticidal active carboxamide derivative in soil and seed application and treatment methods |
WO2015091645A1 (en) | 2013-12-18 | 2015-06-25 | Basf Se | Azole compounds carrying an imine-derived substituent |
WO2015091649A1 (en) | 2013-12-18 | 2015-06-25 | Basf Se | N-substituted imino heterocyclic compounds |
WO2015101622A1 (de) | 2014-01-03 | 2015-07-09 | Bayer Cropscience Ag | Neue pyrazolyl-heteroarylamide als schädlingsbekämpfungsmittel |
WO2015104422A1 (en) | 2014-01-13 | 2015-07-16 | Basf Se | Dihydrothiophene compounds for controlling invertebrate pests |
WO2015118479A1 (en) | 2014-02-05 | 2015-08-13 | Basf Corporation | Seed coating formulations and their use for yield increase |
DE202014008418U1 (de) | 2014-02-19 | 2014-11-14 | Clariant International Ltd. | Schaumarme agrochemische Zusammensetzungen |
DE202014008415U1 (de) | 2014-02-19 | 2014-11-25 | Clariant International Ltd. | Wässrige Adjuvant-Zusammensetzung zur Wirkungssteigerung von Elektrolyt-Wirkstoffen |
US9890120B2 (en) | 2014-03-21 | 2018-02-13 | Bayer Cropscience Aktiengesellschaft | Preparation of N-[(6-chloropyridin-3-yl)methyl]-2,2-difluoroethan-1-amine by alkylation of 2,2-difluoroethylamine |
WO2015140198A1 (de) * | 2014-03-21 | 2015-09-24 | Bayer Cropscience Ag | Verfahren zur herstellung von n-[(6-chlorpyridin-3-yl)methyl]-2,2-difluorethan-1-amin durch alkylierung von 2,2-difluorethylamin |
WO2015160620A1 (en) | 2014-04-16 | 2015-10-22 | Bayer Cropscience Lp | Compositions comprising ningnanmycin and an insecticide |
WO2015160618A1 (en) | 2014-04-16 | 2015-10-22 | Bayer Cropscience Lp | Compositions comprising ningnanmycin and a biological control agent |
US11425904B2 (en) | 2014-04-23 | 2022-08-30 | Clariant International Ltd. | Use of aqueous drift-reducing compositions |
EP3272217A1 (de) * | 2014-06-25 | 2018-01-24 | BASF Agro B.V. | Pestizidische zusammensetzungen |
US10212934B2 (en) | 2014-06-25 | 2019-02-26 | BASF Agro B.V. | Pesticidal compositions |
WO2016001129A1 (de) | 2014-07-01 | 2016-01-07 | Bayer Cropscience Aktiengesellschaft | Verbesserte insektizide zusammensetzungen |
WO2016008830A1 (de) | 2014-07-15 | 2016-01-21 | Bayer Cropscience Aktiengesellschaft | Aryl-triazolyl-pyridine als schädlingsbekämpfungsmittel |
EP3556211A1 (de) | 2014-08-13 | 2019-10-23 | Clariant International Ltd | Organische ammoniumsalze von anionischen pestiziden |
DE102014012022A1 (de) | 2014-08-13 | 2016-02-18 | Clariant International Ltd. | Organische Ammoniumsalze von anionischen Pestiziden |
EP2848124A1 (de) | 2014-08-19 | 2015-03-18 | Bayer CropScience AG | Wirkstoff zur Bekämpfung von Rhynchophorus ferrugineus |
DE102014018274A1 (de) | 2014-12-12 | 2015-07-30 | Clariant International Ltd. | Zuckertenside und deren Verwendung in agrochemischen Zusammensetzungen |
US11700852B2 (en) | 2014-12-19 | 2023-07-18 | Clariant International Ltd | Aqueous electrolyte-containing adjuvant compositions, active ingredient-containing compositions and the use thereof |
WO2016106063A1 (en) | 2014-12-22 | 2016-06-30 | Bayer Corpscience Lp | Method for using a bacillus subtilis or bacillus pumilus strain to treat or prevent pineapple disease |
US11234436B2 (en) | 2015-04-17 | 2022-02-01 | Basf Agrochemical Products B.V. | Method for controlling non-crop pests |
WO2016166252A1 (en) | 2015-04-17 | 2016-10-20 | Basf Agrochemical Products B.V. | Method for controlling non-crop pests |
US10920080B2 (en) | 2015-10-09 | 2021-02-16 | Clariant International Ltd. | N-Alkyl glucamine-based universal pigment dispersions |
US10961484B2 (en) | 2015-10-09 | 2021-03-30 | Clariant International Ltd. | Compositions comprising sugar amine and fatty acid |
WO2017147352A1 (en) | 2016-02-24 | 2017-08-31 | Merial, Inc. | Antiparasitic isoxazoline compounds, long-acting injectable formulations comprising them, methods and uses thereof |
EP3763211A1 (de) | 2016-02-24 | 2021-01-13 | Boehringer Ingelheim Animal Health USA Inc. | Antiparasitäre isoxazolinverbindungen, langwirkende injizierbare formulierungen damit, verfahren und verwendungen davon |
WO2017186543A2 (en) | 2016-04-24 | 2017-11-02 | Bayer Cropscience Aktiengesellschaft | Use of fluopyram and/or bacillus subtilis for controlling fusarium wilt in plants of the musaceae family |
WO2017186577A1 (en) | 2016-04-28 | 2017-11-02 | Bayer Cropscience Aktiengesselschaft | Timed-release-type granular agrochemical composition and method for manufacturing same |
EP3238540A1 (de) | 2016-04-28 | 2017-11-01 | Bayer CropScience Aktiengesellschaft | Agrochemische zusammensetzungen mit kontrollierter granulatfreisetzung und verfahren zu ihrer herstellung |
US11220603B2 (en) | 2016-05-09 | 2022-01-11 | Clariant International Ltd. | Stabilizers for silicate paints |
WO2018019676A1 (en) | 2016-07-29 | 2018-02-01 | Bayer Cropscience Aktiengesellschaft | Active compound combinations and methods to protect the propagation material of plants |
WO2019197635A1 (de) | 2018-04-13 | 2019-10-17 | Bayer Aktiengesellschaft | Formulierung insektizider mischungen mit propylencarbonat |
WO2021069628A1 (en) | 2019-10-10 | 2021-04-15 | Bayer Aktiengesellschaft | Formulation of insecticidal mixtures comprising glycol ether solvents |
EP4275493A1 (de) | 2019-10-10 | 2023-11-15 | Bayer Aktiengesellschaft | Formulierung insektizider mischungen mit glykoletherlösungsmitteln |
WO2023237444A1 (en) | 2022-06-06 | 2023-12-14 | Bayer Aktiengesellschaft | Agrochemical formulations comprising crystalline form a of 4-[(6-chloro-3-pyridylmethyl)(2,2-difluoroethyl)amino]furan-2(5h)-one |
EP4295683A1 (de) | 2022-06-21 | 2023-12-27 | Bayer Aktiengesellschaft | Agrochemische formulierungen, die die kristalline form a von 4-[(6-chlor-3-pyridylmethyl)(2,2-difluorethyl)amino]furan-2(5h)-on umfassen |
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