HRP20100294T1 - Derivati izoksazolina i njihova uporaba kao herbicida - Google Patents
Derivati izoksazolina i njihova uporaba kao herbicida Download PDFInfo
- Publication number
- HRP20100294T1 HRP20100294T1 HR20100294T HRP20100294T HRP20100294T1 HR P20100294 T1 HRP20100294 T1 HR P20100294T1 HR 20100294 T HR20100294 T HR 20100294T HR P20100294 T HRP20100294 T HR P20100294T HR P20100294 T1 HRP20100294 T1 HR P20100294T1
- Authority
- HR
- Croatia
- Prior art keywords
- formula
- compound
- attached form
- carbon atom
- c6alkyl
- Prior art date
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- 239000004009 herbicide Substances 0.000 title claims 2
- 150000002547 isoxazolines Chemical class 0.000 title 1
- -1 methylsulfinylmethyl Chemical group 0.000 claims abstract 84
- 150000001875 compounds Chemical class 0.000 claims abstract 34
- 229910052799 carbon Inorganic materials 0.000 claims abstract 16
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract 16
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract 16
- 239000001257 hydrogen Substances 0.000 claims abstract 16
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract 14
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims abstract 12
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims abstract 8
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract 7
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims abstract 5
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims abstract 5
- 229910052794 bromium Inorganic materials 0.000 claims abstract 5
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims abstract 5
- 125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 claims abstract 5
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims abstract 4
- 125000001028 difluoromethyl group Chemical group [H]C(F)(F)* 0.000 claims abstract 4
- 125000001889 triflyl group Chemical group FC(F)(F)S(*)(=O)=O 0.000 claims abstract 4
- 125000001494 2-propynyl group Chemical group [H]C#CC([H])([H])* 0.000 claims abstract 3
- 150000001204 N-oxides Chemical class 0.000 claims abstract 3
- 125000000217 alkyl group Chemical group 0.000 claims abstract 3
- 125000003754 ethoxycarbonyl group Chemical group C(=O)(OCC)* 0.000 claims abstract 3
- 125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 claims abstract 3
- 125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 claims abstract 3
- 230000003287 optical effect Effects 0.000 claims abstract 3
- 150000003839 salts Chemical class 0.000 claims abstract 3
- 125000004502 1,2,3-oxadiazolyl group Chemical group 0.000 claims abstract 2
- 125000004511 1,2,3-thiadiazolyl group Chemical group 0.000 claims abstract 2
- 125000004529 1,2,3-triazinyl group Chemical group N1=NN=C(C=C1)* 0.000 claims abstract 2
- 125000001399 1,2,3-triazolyl group Chemical group N1N=NC(=C1)* 0.000 claims abstract 2
- 125000004504 1,2,4-oxadiazolyl group Chemical group 0.000 claims abstract 2
- 125000004514 1,2,4-thiadiazolyl group Chemical group 0.000 claims abstract 2
- 125000004530 1,2,4-triazinyl group Chemical group N1=NC(=NC=C1)* 0.000 claims abstract 2
- 125000001376 1,2,4-triazolyl group Chemical group N1N=C(N=C1)* 0.000 claims abstract 2
- 125000004506 1,2,5-oxadiazolyl group Chemical group 0.000 claims abstract 2
- 125000004517 1,2,5-thiadiazolyl group Chemical group 0.000 claims abstract 2
- 125000001781 1,3,4-oxadiazolyl group Chemical group 0.000 claims abstract 2
- 125000004520 1,3,4-thiadiazolyl group Chemical group 0.000 claims abstract 2
- 125000003363 1,3,5-triazinyl group Chemical group N1=C(N=CN=C1)* 0.000 claims abstract 2
- 125000000166 1,3-dioxalanyl group Chemical group 0.000 claims abstract 2
- 125000001731 2-cyanoethyl group Chemical group [H]C([H])(*)C([H])([H])C#N 0.000 claims abstract 2
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 claims abstract 2
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 claims abstract 2
- 125000003785 benzimidazolyl group Chemical group N1=C(NC2=C1C=CC=C2)* 0.000 claims abstract 2
- 125000004618 benzofuryl group Chemical group O1C(=CC2=C1C=CC=C2)* 0.000 claims abstract 2
- 125000004196 benzothienyl group Chemical group S1C(=CC2=C1C=CC=C2)* 0.000 claims abstract 2
- 125000001584 benzyloxycarbonyl group Chemical group C(=O)(OCC1=CC=CC=C1)* 0.000 claims abstract 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims abstract 2
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 claims abstract 2
- 125000002541 furyl group Chemical group 0.000 claims abstract 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract 2
- 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 claims abstract 2
- 125000002883 imidazolyl group Chemical group 0.000 claims abstract 2
- 125000001041 indolyl group Chemical group 0.000 claims abstract 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims abstract 2
- 125000005956 isoquinolyl group Chemical group 0.000 claims abstract 2
- 125000001786 isothiazolyl group Chemical group 0.000 claims abstract 2
- 125000000842 isoxazolyl group Chemical group 0.000 claims abstract 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims abstract 2
- 125000004092 methylthiomethyl group Chemical group [H]C([H])([H])SC([H])([H])* 0.000 claims abstract 2
- 125000002757 morpholinyl group Chemical group 0.000 claims abstract 2
- 125000001624 naphthyl group Chemical group 0.000 claims abstract 2
- 125000002971 oxazolyl group Chemical group 0.000 claims abstract 2
- UYWQUFXKFGHYNT-UHFFFAOYSA-N phenylmethyl ester of formic acid Natural products O=COCC1=CC=CC=C1 UYWQUFXKFGHYNT-UHFFFAOYSA-N 0.000 claims abstract 2
- 125000003170 phenylsulfonyl group Chemical group C1(=CC=CC=C1)S(=O)(=O)* 0.000 claims abstract 2
- 125000004592 phthalazinyl group Chemical group C1(=NN=CC2=CC=CC=C12)* 0.000 claims abstract 2
- 125000000561 purinyl group Chemical group N1=C(N=C2N=CNC2=C1)* 0.000 claims abstract 2
- 125000003373 pyrazinyl group Chemical group 0.000 claims abstract 2
- 125000003226 pyrazolyl group Chemical group 0.000 claims abstract 2
- 125000002098 pyridazinyl group Chemical group 0.000 claims abstract 2
- 125000004076 pyridyl group Chemical group 0.000 claims abstract 2
- 125000000714 pyrimidinyl group Chemical group 0.000 claims abstract 2
- 125000000168 pyrrolyl group Chemical group 0.000 claims abstract 2
- 125000002294 quinazolinyl group Chemical group N1=C(N=CC2=CC=CC=C12)* 0.000 claims abstract 2
- 125000005493 quinolyl group Chemical group 0.000 claims abstract 2
- 125000001567 quinoxalinyl group Chemical group N1=C(C=NC2=CC=CC=C12)* 0.000 claims abstract 2
- 125000003718 tetrahydrofuranyl group Chemical group 0.000 claims abstract 2
- 125000001712 tetrahydronaphthyl group Chemical group C1(CCCC2=CC=CC=C12)* 0.000 claims abstract 2
- 125000005247 tetrazinyl group Chemical group N1=NN=NC(=C1)* 0.000 claims abstract 2
- 125000003831 tetrazolyl group Chemical group 0.000 claims abstract 2
- 125000001544 thienyl group Chemical group 0.000 claims abstract 2
- 125000004205 trifluoroethyl group Chemical group [H]C([H])(*)C(F)(F)F 0.000 claims abstract 2
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 claims abstract 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims abstract 2
- 229920002554 vinyl polymer Polymers 0.000 claims abstract 2
- 229910052736 halogen Inorganic materials 0.000 claims 15
- 150000002367 halogens Chemical group 0.000 claims 15
- 150000002431 hydrogen Chemical group 0.000 claims 10
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 6
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims 6
- 238000000034 method Methods 0.000 claims 6
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 6
- 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 claims 5
- 125000004093 cyano group Chemical group *C#N 0.000 claims 5
- 229910052731 fluorine Inorganic materials 0.000 claims 5
- 239000011737 fluorine Chemical group 0.000 claims 5
- 239000000203 mixture Substances 0.000 claims 5
- 125000004916 (C1-C6) alkylcarbonyl group Chemical group 0.000 claims 4
- 229910052801 chlorine Inorganic materials 0.000 claims 4
- 239000000460 chlorine Chemical group 0.000 claims 4
- 239000012442 inert solvent Substances 0.000 claims 4
- 125000001424 substituent group Chemical group 0.000 claims 4
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 claims 3
- 125000004741 (C1-C6) haloalkylsulfonyl group Chemical group 0.000 claims 3
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical group [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 3
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims 3
- 125000001153 fluoro group Chemical group F* 0.000 claims 3
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 claims 2
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 claims 2
- 125000006771 (C1-C6) haloalkylthio group Chemical group 0.000 claims 2
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims 2
- 101100273567 Arabidopsis thaliana CYCL1-1 gene Proteins 0.000 claims 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 2
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims 2
- 241000196324 Embryophyta Species 0.000 claims 2
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical group FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims 2
- 101100412046 Saccharomyces cerevisiae (strain ATCC 204508 / S288c) RCY1 gene Proteins 0.000 claims 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 2
- 125000004218 chloromethyl group Chemical group [H]C([H])(Cl)* 0.000 claims 2
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims 2
- 125000004216 fluoromethyl group Chemical group [H]C([H])(F)* 0.000 claims 2
- 125000000008 (C1-C10) alkyl group Chemical group 0.000 claims 1
- 125000004738 (C1-C6) alkyl sulfinyl group Chemical group 0.000 claims 1
- 125000004749 (C1-C6) haloalkylsulfinyl group Chemical group 0.000 claims 1
- 125000006772 (C1-C6) haloalkylsulfonyloxy group Chemical group 0.000 claims 1
- 125000006766 (C2-C6) alkynyloxy group Chemical group 0.000 claims 1
- 125000006643 (C2-C6) haloalkenyl group Chemical group 0.000 claims 1
- OTTXCOAOKOEENK-UHFFFAOYSA-N 2,2-difluoroethenone Chemical group FC(F)=C=O OTTXCOAOKOEENK-UHFFFAOYSA-N 0.000 claims 1
- 125000004176 4-fluorobenzyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1F)C([H])([H])* 0.000 claims 1
- 125000005947 C1-C6 alkylsulfonyloxy group Chemical group 0.000 claims 1
- 125000006577 C1-C6 hydroxyalkyl group Chemical group 0.000 claims 1
- 125000003320 C2-C6 alkenyloxy group Chemical group 0.000 claims 1
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims 1
- 241000209504 Poaceae Species 0.000 claims 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 1
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims 1
- 125000001309 chloro group Chemical group Cl* 0.000 claims 1
- 125000002668 chloroacetyl group Chemical group ClCC(=O)* 0.000 claims 1
- 125000006255 cyclopropyl carbonyl group Chemical group [H]C1([H])C([H])([H])C1([H])C(*)=O 0.000 claims 1
- 238000009472 formulation Methods 0.000 claims 1
- 230000002363 herbicidal effect Effects 0.000 claims 1
- 125000003406 indolizinyl group Chemical group C=1(C=CN2C=CC=CC12)* 0.000 claims 1
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical group II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 claims 1
- 125000002346 iodo group Chemical group I* 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 229910052757 nitrogen Inorganic materials 0.000 claims 1
- 239000007800 oxidant agent Substances 0.000 claims 1
- UUEVFMOUBSLVJW-UHFFFAOYSA-N oxo-[[1-[2-[2-[2-[4-(oxoazaniumylmethylidene)pyridin-1-yl]ethoxy]ethoxy]ethyl]pyridin-4-ylidene]methyl]azanium;dibromide Chemical compound [Br-].[Br-].C1=CC(=C[NH+]=O)C=CN1CCOCCOCCN1C=CC(=C[NH+]=O)C=C1 UUEVFMOUBSLVJW-UHFFFAOYSA-N 0.000 claims 1
- 229910052760 oxygen Inorganic materials 0.000 claims 1
- 239000001301 oxygen Substances 0.000 claims 1
- 125000004430 oxygen atom Chemical group O* 0.000 claims 1
- 239000003223 protective agent Substances 0.000 claims 1
- 125000001042 pteridinyl group Chemical group N1=C(N=CC2=NC=CN=C12)* 0.000 claims 1
- 125000004434 sulfur atom Chemical group 0.000 claims 1
- 125000005034 trifluormethylthio group Chemical group FC(S*)(F)F 0.000 claims 1
- 125000004044 trifluoroacetyl group Chemical group FC(C(=O)*)(F)F 0.000 claims 1
- 244000045561 useful plants Species 0.000 claims 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 abstract 3
- 125000000259 cinnolinyl group Chemical group N1=NC(=CC2=CC=CC=C12)* 0.000 abstract 1
- 125000001188 haloalkyl group Chemical group 0.000 abstract 1
- 125000004593 naphthyridinyl group Chemical group N1=C(C=CC2=CC=CN=C12)* 0.000 abstract 1
- SNOOUWRIMMFWNE-UHFFFAOYSA-M sodium;6-[(3,4,5-trimethoxybenzoyl)amino]hexanoate Chemical compound [Na+].COC1=CC(C(=O)NCCCCCC([O-])=O)=CC(OC)=C1OC SNOOUWRIMMFWNE-UHFFFAOYSA-M 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D261/00—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
- C07D261/02—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings
- C07D261/06—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members
- C07D261/10—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more 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
-
- 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
- A01N43/80—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 1,2
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms 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
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB0419634A GB0419634D0 (en) | 2004-09-03 | 2004-09-03 | Novel herbicides |
| GB0420645A GB0420645D0 (en) | 2004-09-16 | 2004-09-16 | Novel herbicides |
| GB0502486A GB0502486D0 (en) | 2005-02-07 | 2005-02-07 | Novel herbicides |
| PCT/GB2005/003228 WO2006024820A1 (en) | 2004-09-03 | 2005-08-17 | Isoxazoline derivatives and their use as herbicides |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| HRP20100294T1 true HRP20100294T1 (hr) | 2010-06-30 |
Family
ID=35431596
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| HR20100294T HRP20100294T1 (hr) | 2004-09-03 | 2010-05-25 | Derivati izoksazolina i njihova uporaba kao herbicida |
Country Status (27)
| Country | Link |
|---|---|
| US (1) | US8680290B2 (de) |
| EP (1) | EP1789401B1 (de) |
| JP (2) | JP2008511596A (de) |
| KR (1) | KR101278609B1 (de) |
| AR (1) | AR050793A1 (de) |
| AT (1) | ATE459605T1 (de) |
| AU (1) | AU2005279042A1 (de) |
| BR (1) | BRPI0514880A (de) |
| CA (1) | CA2577495C (de) |
| CY (1) | CY1110025T1 (de) |
| DE (1) | DE602005019752D1 (de) |
| DK (1) | DK1789401T3 (de) |
| EA (1) | EA012848B1 (de) |
| EC (1) | ECSP077290A (de) |
| ES (1) | ES2338135T3 (de) |
| GT (1) | GT200500240A (de) |
| HN (1) | HN2005000497A (de) |
| HR (1) | HRP20100294T1 (de) |
| IL (1) | IL181512A0 (de) |
| MX (1) | MX2007002645A (de) |
| NZ (1) | NZ553172A (de) |
| PL (1) | PL1789401T3 (de) |
| PT (1) | PT1789401E (de) |
| RS (1) | RS51323B (de) |
| SI (1) | SI1789401T1 (de) |
| SV (1) | SV2006002215A (de) |
| WO (1) | WO2006024820A1 (de) |
Families Citing this family (188)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| UA78071C2 (en) * | 2002-08-07 | 2007-02-15 | Kumiai Chemical Industry Co | Herbicidal composition |
| ATE450517T1 (de) | 2004-10-05 | 2009-12-15 | Syngenta Ltd | Isoxazolinderivate und ihre verwendung als herbizide |
| DE102005031412A1 (de) * | 2005-07-06 | 2007-01-11 | Bayer Cropscience Gmbh | 3-[1-Halo-1-aryl-methan-sulfonyl]-und 3-[1-Halo-1-heteroaryl-methan-sulfonyl]-isoxazolin-Derivate, Verfahren zu deren Herstellung und Verwendung als Herbizide und Pflanzenwachstumsregulatoren |
| WO2007003296A1 (de) * | 2005-07-06 | 2007-01-11 | Bayer Cropscience Ag | Herbizid-safener-kombination |
| WO2007006409A2 (de) * | 2005-07-07 | 2007-01-18 | Bayer Cropscience Ag | Herbizid-safener-kombination |
| GB0526044D0 (en) * | 2005-12-21 | 2006-02-01 | Syngenta Ltd | Novel herbicides |
| GB0603891D0 (en) * | 2006-02-27 | 2006-04-05 | Syngenta Ltd | Novel herbicides |
| DE102006050148A1 (de) * | 2006-10-25 | 2008-04-30 | Bayer Cropscience Ag | Trifluormethoxy-phenylsubstituierte Tetramsäure-Derivate |
| US8110530B2 (en) | 2006-12-21 | 2012-02-07 | Kumiai Chemical Industry Co., Ltd. | Herbicidal composition |
| GB0625598D0 (en) * | 2006-12-21 | 2007-01-31 | Syngenta Ltd | Novel herbicides |
| DE102007012168A1 (de) | 2007-03-12 | 2008-09-18 | Bayer Cropscience Ag | 2-[Heteroarylalkyl-sulfonyl]-thiazol-Derivate und 2-[Heteroarylalkyl-sulfinyl]-thiazol-Derivate, Verfahren zu deren Herstellung, sowie deren Verwendung als Herbizide und Pflanzenwachstumsregulatoren |
| EP2135508B1 (de) * | 2007-03-16 | 2016-05-11 | Kumiai Chemical Industry CO., LTD. | Herbizidzusammensetzung |
| US8097712B2 (en) | 2007-11-07 | 2012-01-17 | Beelogics Inc. | Compositions for conferring tolerance to viral disease in social insects, and the use thereof |
| EP2065374A1 (de) | 2007-11-30 | 2009-06-03 | Bayer CropScience AG | 2-(Benzyl- und 1H-pyrazol-4-ylmethyl)sulfinyl-Thiazol-Derivate als Herbizide und Pflanzenwachstumsregulatoren |
| EP2065373A1 (de) | 2007-11-30 | 2009-06-03 | Bayer CropScience AG | Chirale 3-(Benzylsulfinyl)-5,5-dimethyl-4,5-dihydroisoxazol-Derivate und 5,5-Dimethyl-3-[(1H-pyrazol-4-ylmethyl) sulfinyl]-4,5-dihydroisoxazol-Derivate, Verfahren zu deren Herstellung sowie deren Verwendung als Herbizide und Pflanzenwachstumsregulatoren |
| JP5472638B2 (ja) * | 2008-03-18 | 2014-04-16 | 日産化学工業株式会社 | １−（置換フェニル）−１−置換シリルエーテル、アルコールまたはケトンの製造方法および中間体 |
| EP2112149A1 (de) | 2008-04-22 | 2009-10-28 | Bayer CropScience Aktiengesellschaft | 2-[(1h-Pyrazol-4-ylmethyl)-sulfonyl]-Oxazol-Derivate, 2-[(1H-Pyrazol-4-ylmethyl)-sulfanyl]-Oxazol-Derivate und chirale 2-[(1H-Pyrazol-4-ylmethyl)-sulfinyl]-Oxazol-Derivate, Verfahren zu deren Herstellung sowie deren Verwendung als Herbizide und Pflanzenwachstumsregulatoren |
| EP2112143A1 (de) | 2008-04-22 | 2009-10-28 | Bayer CropScience AG | 2-(Benzylsulfonyl)-Oxazol-Derivate, chirale 2-(Benzylsulfinyl)-Oxazol-Derivate 2-(Benzylsulfanyl-Oxazol Derivate, Verfahren zu deren Herstellung sowie deren Verwendung als Herbizide und Pflanzenwachstumsregulatoren |
| WO2009158258A1 (en) * | 2008-06-25 | 2009-12-30 | E. I. Du Pont De Nemours And Company | Herbicidal dihydro oxo six-membered azinyl isoxazolines |
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| WO2023110491A1 (en) | 2021-12-16 | 2023-06-22 | BASF Agro B.V. | Method for controlling undesirable vegetation in an aquatic environment |
| WO2023194957A1 (en) * | 2022-04-08 | 2023-10-12 | Upl Limited | A process for preparation of 3-[5-(difluoromethoxy)-1- methyl-3-(trifluoromethyl)pyrazol-4- ylmethylsulfonyl]-4,5-dihydro-5,5-dimethyl-1,2-oxazole and its intermediates |
| WO2023208447A1 (en) | 2022-04-25 | 2023-11-02 | Basf Se | An emulsifiable concentrate having a (substituted) benzaldehyde-based solvent system |
| WO2023227676A1 (en) | 2022-05-25 | 2023-11-30 | Basf Se | Herbicidal malonic acid monoamides and malonamide esters |
| WO2024012905A1 (en) | 2022-07-13 | 2024-01-18 | Basf Se | Herbicidal composition comprising azine compounds |
| WO2024056517A1 (en) | 2022-09-14 | 2024-03-21 | Basf Se | Use of an alkylether sulfate for improving the efficacy of herbicides |
| EP4338592A1 (de) | 2022-09-15 | 2024-03-20 | Basf Se | Verwendung einer verbindung zur verbesserung der wirksamkeit von herbiziden |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| US4394155A (en) * | 1981-02-05 | 1983-07-19 | Uniroyal, Inc. | Substituted pyridine 1-oxide herbicides |
| DE3310337A1 (de) * | 1983-03-22 | 1984-09-27 | Europäisches Laboratorium für Molekularbiologie (EMBL), 6900 Heidelberg | Verfahren zur durchfuehrung von hybridisierungsreaktionen |
| GB2145558A (en) * | 1983-08-23 | 1985-03-27 | Standard Telephones Cables Ltd | Field effect transistor |
| JP3810838B2 (ja) | 1994-12-12 | 2006-08-16 | 三共アグロ株式会社 | 除草性イソオキサゾリン誘導体 |
| JPH09328483A (ja) * | 1996-06-11 | 1997-12-22 | Sankyo Co Ltd | 除草性イソオキサゾリン誘導体 |
| US6461997B1 (en) * | 1999-01-14 | 2002-10-08 | Monsanto Technology Llc | Triazole sulfones having herbicidal activity |
| BR0013251B1 (pt) | 1999-08-10 | 2010-11-30 | derivado de isoxazolina e herbicida que contém o mesmo como ingrediente ativo. | |
| JP4465133B2 (ja) * | 2001-02-08 | 2010-05-19 | クミアイ化学工業株式会社 | イソオキサゾリン誘導体及びこれを有効成分とする除草剤 |
| JP4317445B2 (ja) | 2001-06-21 | 2009-08-19 | クミアイ化学工業株式会社 | イソオキサゾリン誘導体及び除草剤 |
| WO2003010165A1 (fr) * | 2001-07-24 | 2003-02-06 | Kumiai Chemical Industry Co., Ltd. | Derives d'isoxazoline et herbicides destines a un usage agricole ou horticole |
| JP2003096059A (ja) * | 2001-09-21 | 2003-04-03 | Otsuka Chem Co Ltd | チアゾール化合物及び除草剤組成物 |
| US6886994B2 (en) | 2002-07-18 | 2005-05-03 | Chiaro Networks Ltd. | Optical assembly and method for manufacture thereof |
| EP1541561B1 (de) * | 2002-08-01 | 2014-07-23 | Ihara Chemical Industry Co., Ltd. | Pyrazolderivate und verfahren zu deren herstellung |
| JP4570015B2 (ja) * | 2003-07-14 | 2010-10-27 | クミアイ化学工業株式会社 | ２−イソオキサゾリン誘導体及びそれを有効成分として含有する除草剤 |
-
2005
- 2005-08-17 DK DK05771917.1T patent/DK1789401T3/da active
- 2005-08-17 CA CA2577495A patent/CA2577495C/en not_active Expired - Fee Related
- 2005-08-17 SI SI200530996T patent/SI1789401T1/sl unknown
- 2005-08-17 EP EP05771917A patent/EP1789401B1/de active Active
- 2005-08-17 NZ NZ553172A patent/NZ553172A/en not_active IP Right Cessation
- 2005-08-17 PT PT05771917T patent/PT1789401E/pt unknown
- 2005-08-17 PL PL05771917T patent/PL1789401T3/pl unknown
- 2005-08-17 ES ES05771917T patent/ES2338135T3/es active Active
- 2005-08-17 AT AT05771917T patent/ATE459605T1/de active
- 2005-08-17 MX MX2007002645A patent/MX2007002645A/es active IP Right Grant
- 2005-08-17 DE DE602005019752T patent/DE602005019752D1/de active Active
- 2005-08-17 AU AU2005279042A patent/AU2005279042A1/en not_active Abandoned
- 2005-08-17 WO PCT/GB2005/003228 patent/WO2006024820A1/en active Application Filing
- 2005-08-17 JP JP2007528958A patent/JP2008511596A/ja not_active Withdrawn
- 2005-08-17 US US11/574,648 patent/US8680290B2/en not_active Expired - Fee Related
- 2005-08-17 EA EA200700545A patent/EA012848B1/ru not_active IP Right Cessation
- 2005-08-17 RS RSP-2010/0243A patent/RS51323B/sr unknown
- 2005-08-17 BR BRPI0514880-4A patent/BRPI0514880A/pt not_active Application Discontinuation
- 2005-08-17 KR KR1020077006965A patent/KR101278609B1/ko not_active IP Right Cessation
- 2005-08-31 HN HN2005000497A patent/HN2005000497A/es unknown
- 2005-09-01 GT GT200500240A patent/GT200500240A/es unknown
- 2005-09-02 AR ARP050103680A patent/AR050793A1/es unknown
- 2005-09-02 SV SV2005002215A patent/SV2006002215A/es unknown
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2007
- 2007-02-22 IL IL181512A patent/IL181512A0/en unknown
- 2007-03-01 EC EC2007007290A patent/ECSP077290A/es unknown
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2010
- 2010-05-13 CY CY20101100412T patent/CY1110025T1/el unknown
- 2010-05-25 HR HR20100294T patent/HRP20100294T1/hr unknown
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- 2012-04-19 JP JP2012095363A patent/JP5559237B2/ja not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| AR050793A1 (es) | 2006-11-22 |
| MX2007002645A (es) | 2007-04-27 |
| JP2008511596A (ja) | 2008-04-17 |
| JP2012149091A (ja) | 2012-08-09 |
| RS51323B (sr) | 2010-12-31 |
| KR20070047838A (ko) | 2007-05-07 |
| ES2338135T3 (es) | 2010-05-04 |
| NZ553172A (en) | 2009-07-31 |
| HN2005000497A (es) | 2010-06-08 |
| CY1110025T1 (el) | 2015-01-14 |
| DK1789401T3 (da) | 2010-05-25 |
| WO2006024820A1 (en) | 2006-03-09 |
| AU2005279042A1 (en) | 2006-03-09 |
| EA200700545A1 (ru) | 2007-08-31 |
| PT1789401E (pt) | 2010-03-18 |
| SI1789401T1 (sl) | 2010-07-30 |
| BRPI0514880A (pt) | 2008-06-24 |
| CA2577495A1 (en) | 2006-03-09 |
| SV2006002215A (es) | 2006-05-25 |
| GT200500240A (es) | 2006-04-10 |
| CA2577495C (en) | 2013-08-06 |
| US8680290B2 (en) | 2014-03-25 |
| ATE459605T1 (de) | 2010-03-15 |
| EP1789401A1 (de) | 2007-05-30 |
| ECSP077290A (es) | 2007-04-26 |
| EA012848B1 (ru) | 2009-12-30 |
| IL181512A0 (en) | 2007-07-04 |
| EP1789401B1 (de) | 2010-03-03 |
| PL1789401T3 (pl) | 2010-07-30 |
| KR101278609B1 (ko) | 2013-06-25 |
| US20080139390A1 (en) | 2008-06-12 |
| JP5559237B2 (ja) | 2014-07-23 |
| DE602005019752D1 (de) | 2010-04-15 |
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