JP2004501071A5 - - Google Patents
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- JP2004501071A5 JP2004501071A5 JP2001572465A JP2001572465A JP2004501071A5 JP 2004501071 A5 JP2004501071 A5 JP 2004501071A5 JP 2001572465 A JP2001572465 A JP 2001572465A JP 2001572465 A JP2001572465 A JP 2001572465A JP 2004501071 A5 JP2004501071 A5 JP 2004501071A5
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- 150000001875 compounds Chemical class 0.000 description 36
- 0 *c1cc(*)c(*)c(*)c1* Chemical compound *c1cc(*)c(*)c(*)c1* 0.000 description 28
- 125000000217 alkyl group Chemical group 0.000 description 23
- 229910052739 hydrogen Inorganic materials 0.000 description 16
- 239000001257 hydrogen Substances 0.000 description 16
- 239000003085 diluting agent Substances 0.000 description 14
- 239000002253 acid Substances 0.000 description 11
- 125000003342 alkenyl group Chemical group 0.000 description 10
- 150000002431 hydrogen Chemical class 0.000 description 10
- 125000004183 alkoxy alkyl group Chemical group 0.000 description 7
- 229910052736 halogen Inorganic materials 0.000 description 7
- 150000002367 halogens Chemical group 0.000 description 7
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 6
- 125000003545 alkoxy group Chemical group 0.000 description 6
- 125000000304 alkynyl group Chemical group 0.000 description 6
- 125000005842 heteroatom Chemical group 0.000 description 6
- -1 Q 4 Chemical compound 0.000 description 5
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 5
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 5
- 239000011230 binding agent Substances 0.000 description 5
- 125000000753 cycloalkyl group Chemical group 0.000 description 5
- 229910052760 oxygen Inorganic materials 0.000 description 5
- 239000001301 oxygen Substances 0.000 description 5
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 5
- 229920006395 saturated elastomer Polymers 0.000 description 5
- 229910052717 sulfur Inorganic materials 0.000 description 5
- 239000011593 sulfur Substances 0.000 description 5
- 125000006350 alkyl thio alkyl group Chemical group 0.000 description 3
- 125000003118 aryl group Chemical group 0.000 description 3
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 3
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- 230000005494 condensation Effects 0.000 description 3
- 238000009833 condensation Methods 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 150000004820 halides Chemical class 0.000 description 3
- 125000001072 heteroaryl group Chemical group 0.000 description 3
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
- 241000607479 Yersinia pestis Species 0.000 description 2
- 125000004414 alkyl thio group Chemical group 0.000 description 2
- 125000003710 aryl alkyl group Chemical group 0.000 description 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 2
- 229910052794 bromium Inorganic materials 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000000460 chlorine Substances 0.000 description 2
- 229910052801 chlorine Inorganic materials 0.000 description 2
- 229910021419 crystalline silicon Inorganic materials 0.000 description 2
- 125000005843 halogen group Chemical group 0.000 description 2
- 238000003402 intramolecular cyclocondensation reaction Methods 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- ZNLONTGEVCATRW-UHFFFAOYSA-N 2-phenyl-2h-1,3-thiazine Chemical class S1C=CC=NC1C1=CC=CC=C1 ZNLONTGEVCATRW-UHFFFAOYSA-N 0.000 description 1
- YYCQUUTYXPMBLY-UHFFFAOYSA-N 3-phenylpyran-2-one Chemical class O=C1OC=CC=C1C1=CC=CC=C1 YYCQUUTYXPMBLY-UHFFFAOYSA-N 0.000 description 1
- DLDSFSKURFXLIB-UHFFFAOYSA-N 3-phenylpyrrolidine-2,4-dione Chemical compound O=C1CNC(=O)C1C1=CC=CC=C1 DLDSFSKURFXLIB-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- CKDWPUIZGOQOOM-UHFFFAOYSA-N Carbamyl chloride Chemical compound NC(Cl)=O CKDWPUIZGOQOOM-UHFFFAOYSA-N 0.000 description 1
- 125000005108 alkenylthio group Chemical group 0.000 description 1
- 125000003282 alkyl amino group Chemical group 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 125000000051 benzyloxy group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])O* 0.000 description 1
- 150000001728 carbonyl compounds Chemical class 0.000 description 1
- 150000001733 carboxylic acid esters Chemical class 0.000 description 1
- LRYSUGTXBIPBGB-UHFFFAOYSA-N chloromethanedithioic acid Chemical class SC(Cl)=S LRYSUGTXBIPBGB-UHFFFAOYSA-N 0.000 description 1
- KTRFZWJCHOQHMN-UHFFFAOYSA-N chloromethanethioic s-acid Chemical class SC(Cl)=O KTRFZWJCHOQHMN-UHFFFAOYSA-N 0.000 description 1
- 125000005366 cycloalkylthio group Chemical group 0.000 description 1
- 125000004663 dialkyl amino group Chemical group 0.000 description 1
- 150000002085 enols Chemical class 0.000 description 1
- BADWIIDKTXQYLW-UHFFFAOYSA-N ethenylstannane Chemical compound [SnH3]C=C BADWIIDKTXQYLW-UHFFFAOYSA-N 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- KUFWTXSQQKDMAI-UHFFFAOYSA-N ethynylsilicon Chemical group [Si]C#C KUFWTXSQQKDMAI-UHFFFAOYSA-N 0.000 description 1
- 125000004438 haloalkoxy group Chemical group 0.000 description 1
- 125000001188 haloalkyl group Chemical group 0.000 description 1
- 230000002363 herbicidal effect Effects 0.000 description 1
- 239000004009 herbicide Substances 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 150000002540 isothiocyanates Chemical class 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 150000002736 metal compounds Chemical class 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- JLPJFSCQKHRSQR-UHFFFAOYSA-N oxolan-3-one Chemical class O=C1CCOC1 JLPJFSCQKHRSQR-UHFFFAOYSA-N 0.000 description 1
- 230000000361 pesticidal effect Effects 0.000 description 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 1
- 125000005359 phenoxyalkyl group Chemical group 0.000 description 1
- 125000003884 phenylalkyl group Chemical group 0.000 description 1
- 125000003356 phenylsulfanyl group Chemical group [*]SC1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 125000006413 ring segment Chemical group 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 125000005346 substituted cycloalkyl group Chemical group 0.000 description 1
- DSXFPRKPFJRPIB-UHFFFAOYSA-N thiolan-3-one Chemical class O=C1CCSC1 DSXFPRKPFJRPIB-UHFFFAOYSA-N 0.000 description 1
- SQQWBSBBCSFQGC-JLHYYAGUSA-N ubiquinone-2 Chemical compound COC1=C(OC)C(=O)C(C\C=C(/C)CCC=C(C)C)=C(C)C1=O SQQWBSBBCSFQGC-JLHYYAGUSA-N 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10016544A DE10016544A1 (de) | 2000-04-03 | 2000-04-03 | C2-phenylsubstituierte Ketoenole |
| DE10016544.3 | 2000-04-03 | ||
| PCT/EP2001/003215 WO2001074770A1 (de) | 2000-04-03 | 2001-03-21 | C2-phenylsubstituierte cyclische ketoenole als schädlingsbekämpfungsmittel und herbizide |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2011136575A Division JP5685153B2 (ja) | 2000-04-03 | 2011-06-20 | Ｃ２フェニル−置換環状ケト−エノール |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2004501071A JP2004501071A (ja) | 2004-01-15 |
| JP2004501071A5 true JP2004501071A5 (https=) | 2008-05-15 |
| JP4947868B2 JP4947868B2 (ja) | 2012-06-06 |
Family
ID=7637441
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2001572465A Expired - Fee Related JP4947868B2 (ja) | 2000-04-03 | 2001-03-21 | 有害生物防除剤及び除草剤として用いられるｃ２フェニル−置換環状ケト−エノール |
| JP2011136575A Expired - Fee Related JP5685153B2 (ja) | 2000-04-03 | 2011-06-20 | Ｃ２フェニル−置換環状ケト−エノール |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2011136575A Expired - Fee Related JP5685153B2 (ja) | 2000-04-03 | 2011-06-20 | Ｃ２フェニル−置換環状ケト−エノール |
Country Status (17)
| Country | Link |
|---|---|
| US (4) | US7915282B2 (https=) |
| EP (1) | EP1280770B1 (https=) |
| JP (2) | JP4947868B2 (https=) |
| KR (1) | KR100704719B1 (https=) |
| CN (7) | CN1880293A (https=) |
| AT (1) | ATE471929T1 (https=) |
| AU (1) | AU782557C (https=) |
| BR (3) | BR0117375B1 (https=) |
| CA (2) | CA2404868C (https=) |
| DE (2) | DE10016544A1 (https=) |
| ES (1) | ES2346039T3 (https=) |
| MX (1) | MXPA02009730A (https=) |
| PL (1) | PL362703A1 (https=) |
| RU (1) | RU2280643C2 (https=) |
| UA (1) | UA73984C2 (https=) |
| WO (1) | WO2001074770A1 (https=) |
| ZA (1) | ZA200206836B (https=) |
Families Citing this family (139)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE10016544A1 (de) | 2000-04-03 | 2001-10-11 | Bayer Ag | C2-phenylsubstituierte Ketoenole |
| DE10146910A1 (de) | 2001-09-24 | 2003-04-10 | Bayer Cropscience Ag | Spirocyclische 3-Phenyl-3-substituierte-4-ketolaktame und -laktone |
| DE10213051B4 (de) * | 2002-03-23 | 2013-03-07 | Grünenthal GmbH | Substituierte 4-Aminocyclohexanole |
| DE10231333A1 (de) * | 2002-07-11 | 2004-01-22 | Bayer Cropscience Ag | Cis-Alkoxysubstituierte spirocyclische 1-H-Pyrrolidin-2,4-dion-Derivate |
| DE10239479A1 (de) * | 2002-08-28 | 2004-03-04 | Bayer Cropscience Ag | Substituierte spirocyclische Ketoenole |
| DE10249055A1 (de) * | 2002-10-22 | 2004-05-06 | Bayer Cropscience Ag | 2-Phenyl-2-substituierte-1,3-diketone |
| DE10311300A1 (de) | 2003-03-14 | 2004-09-23 | Bayer Cropscience Ag | 2,4,6-Phenylsubstituierte cyclische Ketoenole |
| DE10326386A1 (de) | 2003-06-12 | 2004-12-30 | Bayer Cropscience Ag | N-Heterocyclyl-phenylsubstituierte cyclische Ketoenole |
| DE10330723A1 (de) * | 2003-07-08 | 2005-02-03 | Bayer Cropscience Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| DE10330724A1 (de) | 2003-07-08 | 2005-01-27 | Bayer Cropscience Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| DE10353281A1 (de) | 2003-11-14 | 2005-06-16 | Bayer Cropscience Ag | Wirkstoffkombination mit insektiziden und akariziden Eigenschaften |
| DE10354629A1 (de) * | 2003-11-22 | 2005-06-30 | Bayer Cropscience Ag | 2-Ethyl-4,6-dimethyl-phenyl substituierte spirocyclische Tetramsäure-Derivate |
| DE10354628A1 (de) | 2003-11-22 | 2005-06-16 | Bayer Cropscience Ag | 2-Ethyl-4,6-dimethyl-phenyl-substituierte Tetramsäure-Derivate |
| WO2005053405A1 (de) | 2003-12-04 | 2005-06-16 | Bayer Cropscience Aktiengesellschaft | Wirkstoffkombinationen mit insektiziden und akariziden eigenschaften |
| DE102004014620A1 (de) * | 2004-03-25 | 2005-10-06 | Bayer Cropscience Ag | 2,4,6-phenylsubstituierte cyclische Ketoenole |
| DE102004030753A1 (de) * | 2004-06-25 | 2006-01-19 | Bayer Cropscience Ag | 3'-Alkoxy spirocyclische Tetram- und Tretronsäuren |
| DE102004035133A1 (de) * | 2004-07-20 | 2006-02-16 | Bayer Cropscience Ag | Selektive Insektizide auf Basis von substituierten, cyclischen Ketoenolen und Safenern |
| DE102004044827A1 (de) | 2004-09-16 | 2006-03-23 | Bayer Cropscience Ag | Jod-phenylsubstituierte cyclische Ketoenole |
| DE102004053192A1 (de) * | 2004-11-04 | 2006-05-11 | Bayer Cropscience Ag | 2-Alkoxy-6-alkyl-phenyl substituierte spirocyclische Tetramsäure-Derivate |
| DE102004053191A1 (de) * | 2004-11-04 | 2006-05-11 | Bayer Cropscience Ag | 2,6-Diethyl-4-methyl-phenyl substituierte Tetramsäure-Derivate |
| DE102005003076A1 (de) * | 2005-01-22 | 2006-07-27 | Bayer Cropscience Ag | Verwendung von Tetramsäurederivaten zur Bekämpfung von Insekten aus der Gattung der Pflanzenläuse (Sternorrhyncha) |
| DE102005008021A1 (de) | 2005-02-22 | 2006-08-24 | Bayer Cropscience Ag | Spiroketal-substituierte cyclische Ketoenole |
| DE102005051325A1 (de) | 2005-10-27 | 2007-05-03 | Bayer Cropscience Ag | Alkoxyalkyl spirocyclische Tetram- und Tetronsäuren |
| DE102005059469A1 (de) * | 2005-12-13 | 2007-06-14 | Bayer Cropscience Ag | Insektizide Zusammensetzungen mit verbesserter Wirkung |
| DE102005059891A1 (de) | 2005-12-15 | 2007-06-28 | Bayer Cropscience Ag | 3'-Alkoxy-spirocyclopentyl substituierte Tetram- und Tetronsäuren |
| DE102006000971A1 (de) * | 2006-01-07 | 2007-07-12 | Bayer Cropscience Ag | 2,4,6-Trialkylphenylsubstituierte Cyclopentan-1,3-dione |
| DE102006007882A1 (de) | 2006-02-21 | 2007-08-30 | Bayer Cropscience Ag | Cycloalkyl-phenylsubstituierte cyclische Ketoenole |
| DE102006014653A1 (de) * | 2006-03-28 | 2007-10-04 | Bayer Cropscience Ag | Verwendung von Tetramsäurederivaten zur Bekämpfung von Insekten durch Angiessen, Tröpfchenapplikation oder Bodeninjektion |
| AU2013200343B2 (en) * | 2006-03-28 | 2014-12-04 | Bayer Intellectual Property Gmbh | Use of tetramic acid derivatives for controlling pests by drenching, drip application, dip application or soil injection |
| DE102006018828A1 (de) | 2006-04-22 | 2007-10-25 | Bayer Cropscience Ag | Alkoxyalkyl-substituierte cyclische Ketoenole |
| DE102006022821A1 (de) | 2006-05-12 | 2007-11-15 | Bayer Cropscience Ag | Verwendung von Tetramsäurederivaten zur Bekämpfung von Insekten aus der Ordnung der Käfer (Coleoptera), Thrips (Tysanoptera), Wanzen (Hemiptera), Fliegen (Diptera) und Zikaden (Auchenorrhynchae) |
| DE102006025874A1 (de) | 2006-06-02 | 2007-12-06 | Bayer Cropscience Ag | Alkoxyalkyl-substituierte cyclische Ketoenole |
| DE102006027731A1 (de) | 2006-06-16 | 2007-12-20 | Bayer Cropscience Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| DE102006027730A1 (de) * | 2006-06-16 | 2007-12-20 | Bayer Cropscience Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| DE102006027732A1 (de) | 2006-06-16 | 2008-01-10 | Bayer Cropscience Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| DE102006033154A1 (de) | 2006-07-18 | 2008-01-24 | Bayer Cropscience Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| DE102006050148A1 (de) | 2006-10-25 | 2008-04-30 | Bayer Cropscience Ag | Trifluormethoxy-phenylsubstituierte Tetramsäure-Derivate |
| DE102006057037A1 (de) | 2006-12-04 | 2008-06-05 | Bayer Cropscience Ag | cis-Alkoxyspirocyclische biphenylsubstituierte Tetramsäure-Derivate |
| DE102006057036A1 (de) | 2006-12-04 | 2008-06-05 | Bayer Cropscience Ag | Biphenylsubstituierte spirocyclische Ketoenole |
| AU2007331723B2 (en) | 2006-12-14 | 2013-05-30 | Syngenta Limited | 4-phenyl-pyrane-3,5-diones, 4-phenyl-thiopyrane-3,5-diones and cyclohexanetriones as novel herbicides |
| DE102007009957A1 (de) | 2006-12-27 | 2008-07-03 | Bayer Cropscience Ag | Verfahren zur verbesserten Nutzung des Produktionsptentials transgener Pflanzen |
| DE102007001866A1 (de) | 2007-01-12 | 2008-07-17 | Bayer Cropscience Ag | Spirocyclische Tetronsäure-Derivate |
| GB0704653D0 (en) | 2007-03-09 | 2007-04-18 | Syngenta Participations Ag | Novel herbicides |
| GB0704652D0 (en) * | 2007-03-09 | 2007-04-18 | Syngenta Participations Ag | Novel herbicides |
| JP2008266230A (ja) | 2007-04-23 | 2008-11-06 | Bayer Cropscience Ag | 殺虫性アリールピロリジン類 |
| US9266830B2 (en) | 2007-04-23 | 2016-02-23 | Bayer Intellectual Property Gmbh | Pesticidal arylpyrrolidines |
| GB0710223D0 (en) | 2007-05-29 | 2007-07-11 | Syngenta Ltd | Novel Herbicides |
| GB0712653D0 (en) * | 2007-06-28 | 2007-08-08 | Syngenta Ltd | Novel herbicides |
| EP2014169A1 (de) | 2007-07-09 | 2009-01-14 | Bayer CropScience AG | Wasserlösliche Konzentrate von 3-(2-Alkoxy-4-chlor-6-alkyl-phenyl)-substituierten Tetramaten und ihren korrespondierenden Enolen |
| GB0714981D0 (en) | 2007-08-01 | 2007-09-12 | Syngenta Ltd | Novel herbicides |
| EP2020413A1 (de) | 2007-08-02 | 2009-02-04 | Bayer CropScience AG | Oxaspirocyclische-spiro-substituierte Tetram- und Tetronsäure-Derivate |
| GB0715454D0 (en) | 2007-08-08 | 2007-09-19 | Syngenta Ltd | Novel herbicides |
| GB0715576D0 (en) | 2007-08-09 | 2007-09-19 | Syngenta Ltd | Novel herbicides |
| GB0717082D0 (en) * | 2007-09-03 | 2007-10-10 | Syngenta Ltd | Novel herbicides |
| EP2045240A1 (de) | 2007-09-25 | 2009-04-08 | Bayer CropScience AG | Halogenalkoxyspirocyclische Tetram- und Tetronsäure-Derivate |
| PL2222657T3 (pl) | 2007-12-13 | 2013-03-29 | Syngenta Ltd | Piranodiony, tiopiranodiony i cykloheksanotriony o właściwościach chwastobójczych |
| EP2103615A1 (de) * | 2008-03-19 | 2009-09-23 | Bayer CropScience AG | 4'4'-Dioxaspiro-spirocyclisch substituierte Tetramate |
| MX2010010114A (es) * | 2008-03-27 | 2010-09-30 | Bayer Cropscience Ag | Uso de derivados de acido tetronico para el combate de insectos y acaros tetraniquidos por riego, aplicacion de gotitas o aplicacion por inmersion. |
| EP2113172A1 (de) | 2008-04-28 | 2009-11-04 | Bayer CropScience AG | Verfahren zur verbesserten Nutzung des Produktionspotentials transgener Pflanzen |
| EP2127522A1 (de) | 2008-05-29 | 2009-12-02 | Bayer CropScience AG | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| GB0810728D0 (en) | 2008-06-11 | 2008-07-16 | Syngenta Ltd | Novel herbicides |
| GB0810815D0 (en) * | 2008-06-12 | 2008-07-23 | Syngenta Ltd | Novel herbicides |
| GB0812310D0 (en) * | 2008-07-03 | 2008-08-13 | Syngenta Ltd | Novel herbicides |
| US8367873B2 (en) * | 2008-10-10 | 2013-02-05 | Bayer Cropscience Ag | Phenyl-substituted bicyclooctane-1,3-dione derivatives |
| GB0819205D0 (en) | 2008-10-20 | 2008-11-26 | Syngenta Ltd | Novel herbicides |
| GB0820344D0 (en) * | 2008-11-06 | 2008-12-17 | Syngenta Ltd | Herbicidal compositions |
| TW201031327A (en) | 2008-11-14 | 2010-09-01 | Bayer Cropscience Ag | Active compound combinations having insecticidal and acaricidal properties |
| US8389443B2 (en) | 2008-12-02 | 2013-03-05 | Bayer Cropscience Ag | Geminal alkoxy/alkylspirocyclic substituted tetramate derivatives |
| US8846946B2 (en) | 2008-12-02 | 2014-09-30 | Bayer Cropscience Ag | Germinal alkoxy/alkylspirocyclic substituted tetramate derivatives |
| GB0822834D0 (en) | 2008-12-15 | 2009-01-21 | Syngenta Ltd | Novel herbicides |
| GB0900641D0 (en) | 2009-01-15 | 2009-02-25 | Syngenta Ltd | Novel herbicides |
| JP2012515179A (ja) * | 2009-01-19 | 2012-07-05 | バイエル・クロップサイエンス・アーゲー | 殺虫剤、殺ダニ剤および／または殺真菌剤としての２−アリール−５−ヘテロシクリル−シクロヘキサン−１，３−ジオン化合物の使用 |
| JP5558490B2 (ja) * | 2009-01-19 | 2014-07-23 | バイエル・クロップサイエンス・アーゲー | 環状ジオンならびに殺虫剤、殺ダニ剤および／または殺真菌剤としてのその使用 |
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| ES2251022T3 (es) | 1996-05-10 | 2006-04-16 | Bayer Cropscience Ag | Nuevos piridilcetoenoles sustituidos. |
| ES2275796T3 (es) * | 1996-08-05 | 2007-06-16 | Bayer Cropscience Ag | Fenilcetoenoles 2- y 2,5-substituidos. |
| DE19632126A1 (de) | 1996-08-09 | 1998-02-12 | Bayer Ag | Phenylsubstituierte cyclische Ketoenole |
| US6391912B1 (en) | 1996-12-12 | 2002-05-21 | Bayer Aktiengesellschaft | Substituted phenylketoenols |
| DE19651686A1 (de) | 1996-12-12 | 1998-06-18 | Bayer Ag | Neue substituierte Phenylketoenole |
| DE19708607A1 (de) | 1997-03-03 | 1998-09-10 | Bayer Ag | 2-Arylcyclopentan-1,3-dione |
| DE19742492A1 (de) | 1997-09-26 | 1999-04-01 | Bayer Ag | Spirocyclische Phenylketoenole |
| DE19749720A1 (de) | 1997-11-11 | 1999-05-12 | Bayer Ag | Neue substituierte Phenylketoenole |
| DE19808261A1 (de) | 1998-02-27 | 1999-10-28 | Bayer Ag | Arylphenylsubstituierte cyclische Ketoenole |
| UA66837C2 (uk) * | 1998-03-13 | 2004-06-15 | Сінгента Партісіпейшнс Аг | Похідні 3-гідроксі-4-арил-5-оксопіразоліну, які проявляють гербіцидну активність |
| DE19813354A1 (de) | 1998-03-26 | 1999-09-30 | Bayer Ag | Arylphenylsubstituierte cyclische Ketoenole |
| DE19818732A1 (de) | 1998-04-27 | 1999-10-28 | Bayer Ag | Arylphenylsubstituierte cyclische Ketoenole |
| RU2269537C2 (ru) * | 1999-09-07 | 2006-02-10 | Зингента Партисипейшнс Аг | Фенилзамещенные гетероциклические 1,3-кетоенолы, способ их получения, гербицидное средство на их основе и способ борьбы с ростом нежелательной растительности |
| DE10016554A1 (de) | 2000-04-03 | 2001-10-18 | Rootec Ges Fuer Bioaktive Wirk | Vorrichtung zum Kultivieren von pflanzlichen oder tierischen Gewebekulturen |
| DE10016544A1 (de) * | 2000-04-03 | 2001-10-11 | Bayer Ag | C2-phenylsubstituierte Ketoenole |
| DE102006000971A1 (de) | 2006-01-07 | 2007-07-12 | Bayer Cropscience Ag | 2,4,6-Trialkylphenylsubstituierte Cyclopentan-1,3-dione |
-
2000
- 2000-04-03 DE DE10016544A patent/DE10016544A1/de not_active Withdrawn
-
2001
- 2001-03-21 CA CA2404868A patent/CA2404868C/en not_active Expired - Lifetime
- 2001-03-21 JP JP2001572465A patent/JP4947868B2/ja not_active Expired - Fee Related
- 2001-03-21 KR KR1020027012218A patent/KR100704719B1/ko not_active Expired - Lifetime
- 2001-03-21 AU AU44215/01A patent/AU782557C/en not_active Expired
- 2001-03-21 CN CNA2006101014026A patent/CN1880293A/zh active Pending
- 2001-03-21 BR BRPI0117375-8A patent/BR0117375B1/pt active IP Right Grant
- 2001-03-21 PL PL01362703A patent/PL362703A1/xx not_active Application Discontinuation
- 2001-03-21 BR BRPI0109750-4A patent/BR0109750B1/pt not_active IP Right Cessation
- 2001-03-21 CN CNB01810651XA patent/CN1309709C/zh not_active Expired - Lifetime
- 2001-03-21 BR BRPI0117376-6A patent/BRPI0117376B1/pt not_active IP Right Cessation
- 2001-03-21 CA CA2829534A patent/CA2829534C/en not_active Expired - Lifetime
- 2001-03-21 ES ES01917102T patent/ES2346039T3/es not_active Expired - Lifetime
- 2001-03-21 WO PCT/EP2001/003215 patent/WO2001074770A1/de not_active Ceased
- 2001-03-21 CN CN2011102105146A patent/CN102408369A/zh active Pending
- 2001-03-21 UA UA2002118712A patent/UA73984C2/uk unknown
- 2001-03-21 RU RU2002129566/04A patent/RU2280643C2/ru not_active IP Right Cessation
- 2001-03-21 DE DE50115530T patent/DE50115530D1/de not_active Expired - Lifetime
- 2001-03-21 CN CNB2005100712543A patent/CN100526287C/zh not_active Expired - Lifetime
- 2001-03-21 CN CN200910175740A patent/CN101676258A/zh active Pending
- 2001-03-21 MX MXPA02009730A patent/MXPA02009730A/es active IP Right Grant
- 2001-03-21 CN CN2004100974842A patent/CN1631878B/zh not_active Expired - Lifetime
- 2001-03-21 CN CNA2006101728204A patent/CN1982296A/zh active Pending
- 2001-03-21 AT AT01917102T patent/ATE471929T1/de active
- 2001-03-21 EP EP01917102A patent/EP1280770B1/de not_active Revoked
- 2001-03-21 US US10/239,331 patent/US7915282B2/en not_active Expired - Fee Related
-
2002
- 2002-08-27 ZA ZA200206836A patent/ZA200206836B/en unknown
-
2011
- 2011-02-17 US US13/029,497 patent/US8193120B2/en not_active Expired - Fee Related
- 2011-03-24 US US13/071,171 patent/US8334300B2/en not_active Expired - Fee Related
- 2011-06-20 JP JP2011136575A patent/JP5685153B2/ja not_active Expired - Fee Related
-
2012
- 2012-04-25 US US13/455,416 patent/US8673818B2/en not_active Expired - Fee Related
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