JP2010528074A5 - - Google Patents
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- Publication number
- JP2010528074A5 JP2010528074A5 JP2010509721A JP2010509721A JP2010528074A5 JP 2010528074 A5 JP2010528074 A5 JP 2010528074A5 JP 2010509721 A JP2010509721 A JP 2010509721A JP 2010509721 A JP2010509721 A JP 2010509721A JP 2010528074 A5 JP2010528074 A5 JP 2010528074A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- alkoxy
- haloalkyl
- haloalkoxy
- phenyl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 125000000217 alkyl group Chemical group 0.000 claims 180
- 125000003545 alkoxy group Chemical group 0.000 claims 57
- 125000001188 haloalkyl group Chemical group 0.000 claims 53
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 50
- 125000004438 haloalkoxy group Chemical group 0.000 claims 48
- 229910052736 halogen Inorganic materials 0.000 claims 48
- 150000002367 halogens Chemical class 0.000 claims 48
- 125000004093 cyano group Chemical group *C#N 0.000 claims 44
- 125000001072 heteroaryl group Chemical group 0.000 claims 43
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 43
- 150000001875 compounds Chemical class 0.000 claims 38
- 125000004644 alkyl sulfinyl group Chemical group 0.000 claims 23
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims 23
- 125000004414 alkyl thio group Chemical group 0.000 claims 23
- 229910052739 hydrogen Inorganic materials 0.000 claims 22
- 239000001257 hydrogen Substances 0.000 claims 21
- 150000002431 hydrogen Chemical class 0.000 claims 16
- -1 methoxy, ethoxy Chemical group 0.000 claims 15
- 125000003282 alkyl amino group Chemical group 0.000 claims 13
- 125000000753 cycloalkyl group Chemical group 0.000 claims 13
- 125000000304 alkynyl group Chemical group 0.000 claims 9
- 125000004663 dialkyl amino group Chemical group 0.000 claims 9
- 125000005240 diheteroarylamino group Chemical group 0.000 claims 9
- 125000005241 heteroarylamino group Chemical group 0.000 claims 9
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 9
- 125000003342 alkenyl group Chemical group 0.000 claims 8
- 125000004457 alkyl amino carbonyl group Chemical group 0.000 claims 8
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 8
- 238000000034 method Methods 0.000 claims 8
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims 7
- 125000003806 alkyl carbonyl amino group Chemical group 0.000 claims 7
- 125000004448 alkyl carbonyl group Chemical group 0.000 claims 7
- 125000000262 haloalkenyl group Chemical group 0.000 claims 7
- 239000000203 mixture Substances 0.000 claims 7
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims 6
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 6
- 125000003302 alkenyloxy group Chemical group 0.000 claims 6
- 125000002947 alkylene group Chemical group 0.000 claims 6
- 125000005133 alkynyloxy group Chemical group 0.000 claims 6
- 125000004103 aminoalkyl group Chemical group 0.000 claims 6
- 125000002490 anilino group Chemical group [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims 6
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 6
- 229910052794 bromium Inorganic materials 0.000 claims 6
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims 6
- 229910052801 chlorine Inorganic materials 0.000 claims 6
- 239000000460 chlorine Substances 0.000 claims 6
- 125000004966 cyanoalkyl group Chemical group 0.000 claims 6
- 125000006310 cycloalkyl amino group Chemical group 0.000 claims 6
- 125000004473 dialkylaminocarbonyl group Chemical group 0.000 claims 6
- 125000004971 nitroalkyl group Chemical group 0.000 claims 6
- 125000004665 trialkylsilyl group Chemical group 0.000 claims 6
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims 5
- 239000005977 Ethylene Substances 0.000 claims 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 5
- 125000004450 alkenylene group Chemical group 0.000 claims 5
- 239000002585 base Substances 0.000 claims 5
- 239000003054 catalyst Substances 0.000 claims 5
- 239000003446 ligand Substances 0.000 claims 5
- 238000004519 manufacturing process Methods 0.000 claims 5
- 238000002360 preparation method Methods 0.000 claims 5
- 150000003839 salts Chemical class 0.000 claims 5
- 239000002904 solvent Substances 0.000 claims 5
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 claims 4
- 125000001246 bromo group Chemical group Br* 0.000 claims 4
- 125000001309 chloro group Chemical group Cl* 0.000 claims 4
- 150000002148 esters Chemical class 0.000 claims 4
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 claims 4
- 125000001153 fluoro group Chemical group F* 0.000 claims 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 4
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims 4
- 229920002554 vinyl polymer Polymers 0.000 claims 4
- 241000196324 Embryophyta Species 0.000 claims 3
- 125000000000 cycloalkoxy group Chemical group 0.000 claims 3
- 125000004970 halomethyl group Chemical group 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
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims 2
- 125000006643 (C2-C6) haloalkenyl group Chemical group 0.000 claims 2
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims 2
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims 2
- 125000000278 alkyl amino alkyl group Chemical group 0.000 claims 2
- 125000004949 alkyl amino carbonyl amino group Chemical group 0.000 claims 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 2
- 125000004969 haloethyl group Chemical group 0.000 claims 2
- 239000004009 herbicide Substances 0.000 claims 2
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 claims 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 2
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 claims 2
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 2
- 229910052760 oxygen Inorganic materials 0.000 claims 2
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims 2
- 229910052717 sulfur Inorganic materials 0.000 claims 2
- 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 claims 1
- 125000004738 (C1-C6) alkyl sulfinyl group Chemical group 0.000 claims 1
- 125000004916 (C1-C6) alkylcarbonyl group Chemical group 0.000 claims 1
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 claims 1
- 125000006772 (C1-C6) haloalkylsulfonyloxy group Chemical group 0.000 claims 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims 1
- 241000219310 Beta vulgaris subsp. vulgaris Species 0.000 claims 1
- 240000002791 Brassica napus Species 0.000 claims 1
- 235000004977 Brassica sinapistrum Nutrition 0.000 claims 1
- 125000005947 C1-C6 alkylsulfonyloxy group Chemical group 0.000 claims 1
- 229920000742 Cotton Polymers 0.000 claims 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims 1
- 244000068988 Glycine max Species 0.000 claims 1
- 235000010469 Glycine max Nutrition 0.000 claims 1
- 241000219146 Gossypium Species 0.000 claims 1
- 240000007594 Oryza sativa Species 0.000 claims 1
- 235000007164 Oryza sativa Nutrition 0.000 claims 1
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 claims 1
- 229930006000 Sucrose Natural products 0.000 claims 1
- 235000021536 Sugar beet Nutrition 0.000 claims 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 1
- 240000008042 Zea mays Species 0.000 claims 1
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 claims 1
- 235000002017 Zea mays subsp mays Nutrition 0.000 claims 1
- 239000002671 adjuvant Substances 0.000 claims 1
- 229910052783 alkali metal Inorganic materials 0.000 claims 1
- 150000001340 alkali metals Chemical class 0.000 claims 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims 1
- 150000001342 alkaline earth metals Chemical class 0.000 claims 1
- 125000004466 alkoxycarbonylamino group Chemical group 0.000 claims 1
- 125000004656 alkyl sulfonylamino group Chemical group 0.000 claims 1
- 125000005278 alkyl sulfonyloxy group Chemical group 0.000 claims 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 1
- 125000000051 benzyloxy group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])O* 0.000 claims 1
- 229910052799 carbon Inorganic materials 0.000 claims 1
- 235000013339 cereals Nutrition 0.000 claims 1
- 235000005822 corn Nutrition 0.000 claims 1
- 244000038559 crop plants Species 0.000 claims 1
- 125000000392 cycloalkenyl group Chemical group 0.000 claims 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims 1
- 125000005678 ethenylene group Chemical group [H]C([*:1])=C([H])[*:2] 0.000 claims 1
- 229910052731 fluorine Inorganic materials 0.000 claims 1
- 239000011737 fluorine Substances 0.000 claims 1
- 238000009472 formulation Methods 0.000 claims 1
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 claims 1
- 125000002541 furyl group Chemical group 0.000 claims 1
- 125000005280 halo alkyl sulfonyloxy group Chemical group 0.000 claims 1
- 125000004440 haloalkylsulfinyl group Chemical group 0.000 claims 1
- 125000004441 haloalkylsulfonyl group Chemical group 0.000 claims 1
- 125000004664 haloalkylsulfonylamino group Chemical group 0.000 claims 1
- 125000004995 haloalkylthio group Chemical group 0.000 claims 1
- 230000002363 herbicidal effect Effects 0.000 claims 1
- 125000005842 heteroatom Chemical group 0.000 claims 1
- 125000002883 imidazolyl group Chemical group 0.000 claims 1
- 229910052740 iodine Inorganic materials 0.000 claims 1
- 239000011630 iodine Substances 0.000 claims 1
- 125000001786 isothiazolyl group Chemical group 0.000 claims 1
- 125000000842 isoxazolyl group Chemical group 0.000 claims 1
- 125000001181 organosilyl group Chemical group [SiH3]* 0.000 claims 1
- 125000001715 oxadiazolyl group Chemical group 0.000 claims 1
- 125000002971 oxazolyl group Chemical group 0.000 claims 1
- 239000001301 oxygen Substances 0.000 claims 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 1
- 125000003373 pyrazinyl group Chemical group 0.000 claims 1
- 125000003226 pyrazolyl group Chemical group 0.000 claims 1
- 125000002098 pyridazinyl group Chemical group 0.000 claims 1
- 125000004076 pyridyl group Chemical group 0.000 claims 1
- 125000000714 pyrimidinyl group Chemical group 0.000 claims 1
- 125000000168 pyrrolyl group Chemical group 0.000 claims 1
- 235000009566 rice Nutrition 0.000 claims 1
- 125000004469 siloxy group Chemical group [SiH3]O* 0.000 claims 1
- 125000001424 substituent group Chemical group 0.000 claims 1
- 239000005720 sucrose Substances 0.000 claims 1
- RWSOTUBLDIXVET-UHFFFAOYSA-O sulfonium Chemical compound [SH3+] RWSOTUBLDIXVET-UHFFFAOYSA-O 0.000 claims 1
- 239000011593 sulfur Substances 0.000 claims 1
- 125000003831 tetrazolyl group Chemical group 0.000 claims 1
- 125000001113 thiadiazolyl group Chemical group 0.000 claims 1
- 125000000335 thiazolyl group Chemical group 0.000 claims 1
- 125000001544 thienyl group Chemical group 0.000 claims 1
- 125000004306 triazinyl group Chemical group 0.000 claims 1
- 125000001425 triazolyl group Chemical group 0.000 claims 1
- 244000045561 useful plants Species 0.000 claims 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB0710223.9 | 2007-05-29 | ||
| GBGB0710223.9A GB0710223D0 (en) | 2007-05-29 | 2007-05-29 | Novel Herbicides |
| PCT/EP2008/004195 WO2008145336A1 (en) | 2007-05-29 | 2008-05-27 | Herbicidally active bicyclic 1,3-dione compounds |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2010528074A JP2010528074A (ja) | 2010-08-19 |
| JP2010528074A5 true JP2010528074A5 (OSRAM) | 2011-07-14 |
| JP5373775B2 JP5373775B2 (ja) | 2013-12-18 |
Family
ID=38289466
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2010509721A Expired - Fee Related JP5373775B2 (ja) | 2007-05-29 | 2008-05-27 | 除草活性のある二環１，３−ジオン化合物 |
Country Status (28)
| Country | Link |
|---|---|
| US (1) | US8828908B2 (OSRAM) |
| EP (1) | EP2155645B1 (OSRAM) |
| JP (1) | JP5373775B2 (OSRAM) |
| KR (1) | KR20100017455A (OSRAM) |
| CN (1) | CN101679177B (OSRAM) |
| AP (1) | AP2521A (OSRAM) |
| AR (1) | AR069264A1 (OSRAM) |
| AU (1) | AU2008256487B2 (OSRAM) |
| BR (1) | BRPI0812027B1 (OSRAM) |
| CA (1) | CA2687202C (OSRAM) |
| CL (1) | CL2008001545A1 (OSRAM) |
| CO (1) | CO6251202A2 (OSRAM) |
| CU (1) | CU23836B1 (OSRAM) |
| EA (1) | EA020771B1 (OSRAM) |
| EC (1) | ECSP099760A (OSRAM) |
| ES (1) | ES2638441T3 (OSRAM) |
| GB (1) | GB0710223D0 (OSRAM) |
| HN (1) | HN2009003299A (OSRAM) |
| MA (1) | MA31467B1 (OSRAM) |
| MX (1) | MX2009012687A (OSRAM) |
| NZ (1) | NZ581078A (OSRAM) |
| SA (1) | SA08290322B1 (OSRAM) |
| SV (1) | SV2009003432A (OSRAM) |
| TN (1) | TN2009000499A1 (OSRAM) |
| TW (1) | TW200906300A (OSRAM) |
| UA (1) | UA99728C2 (OSRAM) |
| WO (1) | WO2008145336A1 (OSRAM) |
| ZA (1) | ZA200907894B (OSRAM) |
Families Citing this family (27)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB0712653D0 (en) | 2007-06-28 | 2007-08-08 | Syngenta Ltd | Novel herbicides |
| GB0714981D0 (en) | 2007-08-01 | 2007-09-12 | Syngenta Ltd | Novel herbicides |
| GB0715454D0 (en) | 2007-08-08 | 2007-09-19 | Syngenta Ltd | Novel herbicides |
| GB0715576D0 (en) | 2007-08-09 | 2007-09-19 | Syngenta Ltd | Novel herbicides |
| WO2009150095A1 (en) * | 2008-06-12 | 2009-12-17 | Syngenta Participations Ag | Pesticidal compositions containing a pyrandione or a thiopyrandione or a cyclohexanetrione derivative |
| GB0812310D0 (en) | 2008-07-03 | 2008-08-13 | Syngenta Ltd | Novel herbicides |
| GB0819205D0 (en) | 2008-10-20 | 2008-11-26 | Syngenta Ltd | Novel herbicides |
| GB0822834D0 (en) | 2008-12-15 | 2009-01-21 | Syngenta Ltd | Novel herbicides |
| GB0900641D0 (en) * | 2009-01-15 | 2009-02-25 | Syngenta Ltd | Novel herbicides |
| KR20110106447A (ko) * | 2009-01-19 | 2011-09-28 | 바이엘 크롭사이언스 아게 | 비사이클릭 1,3-디온 및 살충제, 살비제 및/또는 살진균제로서의 그의 용도 |
| GB0901086D0 (en) | 2009-01-22 | 2009-03-11 | Syngenta Ltd | Novel herbicides |
| GB0901834D0 (en) | 2009-02-04 | 2009-03-11 | Syngenta Ltd | Novel herbicides |
| GB0901835D0 (en) | 2009-02-04 | 2009-03-11 | Syngenta Ltd | Novel herbicides |
| AU2010223535B2 (en) | 2009-03-11 | 2015-09-10 | Bayer Intellectual Property Gmbh | Halogenalkylmethylenoxy-phenyl-substituted ketoenols |
| GB0912385D0 (en) | 2009-07-16 | 2009-08-26 | Syngenta Ltd | Novel herbicides |
| US9051300B2 (en) | 2009-07-31 | 2015-06-09 | Syngenta Limited | Herbicides |
| DE102010008644A1 (de) | 2010-02-15 | 2011-08-18 | Bayer Schering Pharma Aktiengesellschaft, 13353 | Zyklische Ketoenole zur Therapie |
| UA113753C2 (xx) | 2012-01-26 | 2017-03-10 | Фенілзаміщені кетоеноли для боротьби з паразитами риб | |
| JP6047166B2 (ja) * | 2012-10-04 | 2016-12-21 | バイエル・インテレクチュアル・プロパティ・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツングＢａｙｅｒ Ｉｎｔｅｌｌｅｃｔｕａｌ Ｐｒｏｐｅｒｔｙ ＧｍｂＨ | 農薬製剤及びその製造方法 |
| AU2013366561B2 (en) * | 2012-12-21 | 2017-12-21 | Syngenta Limited | Herbicidally active cyclic dione compounds, or derivatives thereof, substituted by a phenyl which has an alkynyl-containing substituent |
| BR112015029940B1 (pt) * | 2013-05-30 | 2021-08-17 | Syngenta Limited | Compostos de dionas cíclicas substituídas com alquinilfenil e seus derivados, composição herbicida compreendendo os referidos compostos e método de controle de ervas daninhas de gramíneas monocotiledôneas |
| GB201310047D0 (en) | 2013-06-05 | 2013-07-17 | Syngenta Ltd | Compounds |
| GB201411418D0 (en) * | 2014-06-26 | 2014-08-13 | Syngenta Participations Ag | Compounds |
| GB201802558D0 (en) * | 2018-02-16 | 2018-04-04 | Syngenta Participations Ag | Improvements in or relating to organic compounds |
| CA3221821A1 (en) * | 2021-07-09 | 2023-01-12 | Philip Matthew JOYCE | Herbicidal compositions |
| PE20240771A1 (es) * | 2021-07-09 | 2024-04-17 | Syngenta Crop Protection Ag | Composiciones herbicidas |
| EP4366527A1 (en) * | 2021-07-09 | 2024-05-15 | Syngenta Crop Protection AG | Herbicidal compositions |
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| US4209532A (en) | 1977-03-28 | 1980-06-24 | Union Carbide Corporation | Biocidal 2-aryl-1,3-cyclohexane dione compounds and alkali metal and ammonium salts thereof |
| US4659372A (en) | 1977-03-28 | 1987-04-21 | Union Carbide Corporation | Biocidal 2-aryl-1,3-cyclohexanedione enol ester compounds |
| US4422870A (en) | 1977-03-28 | 1983-12-27 | Union Carbide Corporation | Biocidal 2-aryl-1, 3-cyclohexanedione enol ester compounds |
| PT67818A (en) | 1977-03-28 | 1978-04-01 | Union Carbide Corp | Process for the synthesis of biocidal 2-aryl-1,3-cycloalkanedionas and their enol esters |
| US4175135A (en) | 1978-07-18 | 1979-11-20 | Union Carbide Corporation | Method of controlling acarina ectoparasites on warmblooded animals by orally administering to the animal an ectoparasitically effective amount of a 2-aryl-1,3-cyclohexanedione compound, and alkali metal salts, ammonium salts and enol esters thereof |
| US4436666A (en) | 1978-09-22 | 1984-03-13 | Union Carbide Corporation | Biocidal enol derivatives of 2-aryl-1,3-cycloalkanedione compounds |
| US4526723A (en) * | 1978-09-27 | 1985-07-02 | Union Carbide Corporation | Biocidal enol esters of non-ortho substituted 2-aryl-1-3-cycloalkanedione compounds |
| US4409153A (en) * | 1980-03-28 | 1983-10-11 | Union Carbide Corporation | O-(2-Aryl-3-oxo-1-cyclohexenyl) phosphates |
| US4489012A (en) * | 1982-02-23 | 1984-12-18 | Union Carbide Corporation | Enol-phosphorous esters of 2-aryl-1,3-cycloalkanediones compounds |
| BR8600161A (pt) | 1985-01-18 | 1986-09-23 | Plant Genetic Systems Nv | Gene quimerico,vetores de plasmidio hibrido,intermediario,processo para controlar insetos em agricultura ou horticultura,composicao inseticida,processo para transformar celulas de plantas para expressar uma toxina de polipeptideo produzida por bacillus thuringiensis,planta,semente de planta,cultura de celulas e plasmidio |
| US4834908A (en) | 1987-10-05 | 1989-05-30 | Basf Corporation | Antagonism defeating crop oil concentrates |
| CN1038093A (zh) * | 1988-04-18 | 1989-12-20 | 山道士有限公司 | 对有机化合物和关于有机化合物的改进 |
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| EP0374753A3 (de) | 1988-12-19 | 1991-05-29 | American Cyanamid Company | Insektizide Toxine, Gene, die diese Toxine kodieren, Antikörper, die sie binden, sowie transgene Pflanzenzellen und transgene Pflanzen, die diese Toxine exprimieren |
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| BR9107199A (pt) | 1990-12-31 | 1994-04-05 | Monsanto Co | Preservacao contra interacao de pesticidas em plantacoes |
| UA48104C2 (uk) | 1991-10-04 | 2002-08-15 | Новартіс Аг | Фрагмент днк, який містить послідовність,що кодує інсектицидний протеїн, оптимізовану для кукурудзи,фрагмент днк, який забезпечує направлену бажану для серцевини стебла експресію зв'язаного з нею структурного гена в рослині, фрагмент днк, який забезпечує специфічну для пилку експресію зв`язаного з нею структурного гена в рослині, рекомбінантна молекула днк, спосіб одержання оптимізованої для кукурудзи кодуючої послідовності інсектицидного протеїну, спосіб захисту рослин кукурудзи щонайменше від однієї комахи-шкідника |
| US5530195A (en) | 1994-06-10 | 1996-06-25 | Ciba-Geigy Corporation | Bacillus thuringiensis gene encoding a toxin active against insects |
| EP0773920B1 (de) * | 1994-07-21 | 2000-01-26 | Bayer Ag | 2-(2,4,6-trimethylphenyl)-cyclopentan-1,3-dion-derivate |
| PL186631B1 (pl) | 1996-03-15 | 2004-02-27 | Syngenta Participations Ag | Synergistyczna kompozycja herbicydowa oraz sposóbzwalczania niepożądanych roślin |
| DE19808261A1 (de) * | 1998-02-27 | 1999-10-28 | Bayer Ag | Arylphenylsubstituierte cyclische Ketoenole |
| CZ301369B6 (cs) | 1998-03-13 | 2010-02-03 | Syngenta Participations Ag | Herbicidne aktivní deriváty 3-hydroxy-4-aryl-5-oxopyrazolinu |
| DE19813354A1 (de) | 1998-03-26 | 1999-09-30 | Bayer Ag | Arylphenylsubstituierte cyclische Ketoenole |
| CA2341291C (en) * | 1998-09-15 | 2009-11-03 | Syngenta Participations Ag | Pyridine ketones useful as herbicides |
| EP1140811B1 (en) | 1998-12-21 | 2006-08-02 | Syngenta Participations AG | Novel herbicides |
| DE19935963A1 (de) * | 1999-07-30 | 2001-02-01 | Bayer Ag | Biphenylsubstituierte cyclische Ketoenole |
| EP1210333B1 (de) * | 1999-09-07 | 2004-11-17 | Syngenta Participations AG | p-Tolyl-Heterocyclen als Herbizide |
| WO2001017973A2 (de) | 1999-09-07 | 2001-03-15 | Syngenta Participations Ag | Neue herbizide |
| DE10016544A1 (de) | 2000-04-03 | 2001-10-11 | Bayer Ag | C2-phenylsubstituierte Ketoenole |
| GT200100103A (es) * | 2000-06-09 | 2002-02-21 | Nuevos herbicidas | |
| DE10139465A1 (de) | 2001-08-10 | 2003-02-20 | Bayer Cropscience Ag | Selektive Herbizide auf Basis von substituierten, cayclischen Ketoenolen und Safenern |
| WO2003052073A2 (en) | 2001-12-17 | 2003-06-26 | Syngenta Participations Ag | Novel corn event |
| AU2003203482B2 (en) * | 2002-04-09 | 2005-06-02 | Syngenta Participations Ag | Process for the preparation of cyclic diketones |
| AU2003203479B2 (en) | 2002-04-09 | 2005-10-06 | Syngenta Participations Ag | Process for the preparation of bicyclic diketone salts |
| GT200300290A (es) * | 2002-12-30 | 2004-10-13 | Herbicidas novedosos | |
| DE10326386A1 (de) * | 2003-06-12 | 2004-12-30 | Bayer Cropscience Ag | N-Heterocyclyl-phenylsubstituierte cyclische Ketoenole |
| EP1636160A4 (en) | 2003-06-23 | 2006-09-27 | Auspex Pharmaceuticals | NEW THERAPEUTIC AGENTS FOR THE TREATMENT OF CANCER, METABOLISM AND SKIN DISEASES |
| WO2005105717A1 (en) * | 2004-04-30 | 2005-11-10 | Syngenta Participations Ag | Process for the production of cyclic diketones |
| BRPI0510502B1 (pt) * | 2004-04-30 | 2015-07-21 | Syngenta Participations Ag | Processo para a produção de dicetonas cíclicas, bem como seus intermediários |
| US7179943B2 (en) | 2004-06-14 | 2007-02-20 | Wyeth | Bicyclic derivatives that modulate voltage-gated potassium channels and methods of use thereof |
| AR049448A1 (es) | 2004-06-22 | 2006-08-02 | Syngenta Participations Ag | Biciclooctenos sustituidos y usos como herbicidas |
| US7919496B2 (en) | 2004-09-20 | 2011-04-05 | Xenon Pharmaceuticals Inc. | Heterocyclic derivatives for the treatment of diseases mediated by stearoyl-CoA desaturase enzymes |
| MX2007003330A (es) | 2004-09-20 | 2007-06-05 | Xenon Pharmaceuticals Inc | Derivados heterociclicos y su uso como agentes terapeuticos. |
| SA07280691B1 (ar) * | 2006-12-14 | 2010-11-02 | سينجنتا بارتسبيشنز ايه جي | مركبات جديدة من 4- باي فينيل- بيران -3،5-دايون وإستخدامها كمبيدات أعشاب |
| GB0704652D0 (en) * | 2007-03-09 | 2007-04-18 | Syngenta Participations Ag | Novel herbicides |
| GB0704653D0 (en) | 2007-03-09 | 2007-04-18 | Syngenta Participations Ag | Novel herbicides |
| GB0714981D0 (en) * | 2007-08-01 | 2007-09-12 | Syngenta Ltd | Novel herbicides |
-
2007
- 2007-05-29 GB GBGB0710223.9A patent/GB0710223D0/en not_active Ceased
-
2008
- 2008-05-27 BR BRPI0812027-7A patent/BRPI0812027B1/pt active IP Right Grant
- 2008-05-27 WO PCT/EP2008/004195 patent/WO2008145336A1/en not_active Ceased
- 2008-05-27 EP EP08758780.4A patent/EP2155645B1/en active Active
- 2008-05-27 SA SA8290322A patent/SA08290322B1/ar unknown
- 2008-05-27 TW TW097119523A patent/TW200906300A/zh unknown
- 2008-05-27 AP AP2009005043A patent/AP2521A/xx active
- 2008-05-27 CN CN2008800177150A patent/CN101679177B/zh active Active
- 2008-05-27 EA EA200901597A patent/EA020771B1/ru not_active IP Right Cessation
- 2008-05-27 CA CA2687202A patent/CA2687202C/en active Active
- 2008-05-27 JP JP2010509721A patent/JP5373775B2/ja not_active Expired - Fee Related
- 2008-05-27 AR ARP080102222A patent/AR069264A1/es active IP Right Grant
- 2008-05-27 NZ NZ581078A patent/NZ581078A/en not_active IP Right Cessation
- 2008-05-27 ES ES08758780.4T patent/ES2638441T3/es active Active
- 2008-05-27 AU AU2008256487A patent/AU2008256487B2/en active Active
- 2008-05-27 KR KR1020097024835A patent/KR20100017455A/ko not_active Ceased
- 2008-05-27 MX MX2009012687A patent/MX2009012687A/es active IP Right Grant
- 2008-05-27 US US12/601,619 patent/US8828908B2/en active Active
- 2008-05-27 UA UAA200913024A patent/UA99728C2/ru unknown
- 2008-05-28 CL CL200801545A patent/CL2008001545A1/es unknown
-
2009
- 2009-11-10 ZA ZA200907894A patent/ZA200907894B/xx unknown
- 2009-11-23 CO CO09132859A patent/CO6251202A2/es active IP Right Grant
- 2009-11-24 HN HN2009003299A patent/HN2009003299A/es unknown
- 2009-11-25 EC EC2009009760A patent/ECSP099760A/es unknown
- 2009-11-26 CU CU2009000202A patent/CU23836B1/es not_active IP Right Cessation
- 2009-11-30 TN TNP2009000499A patent/TN2009000499A1/fr unknown
- 2009-12-04 SV SV2009003432A patent/SV2009003432A/es not_active Application Discontinuation
- 2009-12-29 MA MA32455A patent/MA31467B1/fr unknown
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