JP2014510089A5 - - Google Patents
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- JP2014510089A5 JP2014510089A5 JP2014500369A JP2014500369A JP2014510089A5 JP 2014510089 A5 JP2014510089 A5 JP 2014510089A5 JP 2014500369 A JP2014500369 A JP 2014500369A JP 2014500369 A JP2014500369 A JP 2014500369A JP 2014510089 A5 JP2014510089 A5 JP 2014510089A5
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- JP
- Japan
- Prior art keywords
- alkyl
- halo
- cycloalkyl
- heterocycle
- cor
- 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.)
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- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 123
- -1 tetrazol-4-yl Chemical group 0.000 claims 30
- 125000001475 halogen functional group Chemical group 0.000 claims 27
- 229910052736 halogen Inorganic materials 0.000 claims 25
- 150000002367 halogens Chemical group 0.000 claims 25
- 125000000623 heterocyclic group Chemical group 0.000 claims 23
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims 20
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims 16
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims 16
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 14
- 125000004093 cyano group Chemical group *C#N 0.000 claims 13
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 13
- 229910052739 hydrogen Inorganic materials 0.000 claims 12
- 239000001257 hydrogen Substances 0.000 claims 12
- 125000004043 oxo group Chemical group O=* 0.000 claims 12
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims 11
- 125000001072 heteroaryl group Chemical group 0.000 claims 10
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 8
- 101100440696 Caenorhabditis elegans cor-1 gene Proteins 0.000 claims 5
- 241000196324 Embryophyta Species 0.000 claims 5
- 239000004009 herbicide Substances 0.000 claims 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 5
- 108091028043 Nucleic acid sequence Proteins 0.000 claims 4
- 150000002431 hydrogen Chemical group 0.000 claims 4
- 238000000034 method Methods 0.000 claims 4
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 4
- 108090000623 proteins and genes Proteins 0.000 claims 4
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims 3
- 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 claims 3
- 244000075850 Avena orientalis Species 0.000 claims 3
- 102000016680 Dioxygenases Human genes 0.000 claims 3
- 108010028143 Dioxygenases Proteins 0.000 claims 3
- 125000003545 alkoxy group Chemical group 0.000 claims 3
- 125000000217 alkyl group Chemical group 0.000 claims 3
- 239000003112 inhibitor Substances 0.000 claims 3
- 230000009261 transgenic effect Effects 0.000 claims 3
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 3
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 2
- 125000006643 (C2-C6) haloalkenyl group Chemical group 0.000 claims 2
- 125000003626 1,2,4-triazol-1-yl group Chemical group [*]N1N=C([H])N=C1[H] 0.000 claims 2
- 241001639653 Blepharismidae Species 0.000 claims 2
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 claims 2
- 241000242362 Kordia Species 0.000 claims 2
- 241000227653 Lycopersicon Species 0.000 claims 2
- 241000219833 Phaseolus Species 0.000 claims 2
- 241000589516 Pseudomonas Species 0.000 claims 2
- 241000316848 Rhodococcus <scale insect> Species 0.000 claims 2
- 241000207763 Solanum Species 0.000 claims 2
- 235000002634 Solanum Nutrition 0.000 claims 2
- 240000006394 Sorghum bicolor Species 0.000 claims 2
- 235000011684 Sorghum saccharatum Nutrition 0.000 claims 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 2
- 125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 claims 2
- 150000003254 radicals Chemical class 0.000 claims 2
- AIAYSXFWIUNXRC-PHIMTYICSA-N (1r,5s)-3-[hydroxy-[2-(2-methoxyethoxymethyl)-6-(trifluoromethyl)pyridin-3-yl]methylidene]bicyclo[3.2.1]octane-2,4-dione Chemical compound COCCOCC1=NC(C(F)(F)F)=CC=C1C(O)=C1C(=O)[C@@H](C2)CC[C@@H]2C1=O AIAYSXFWIUNXRC-PHIMTYICSA-N 0.000 claims 1
- DMLYTGPBYWHKHU-UHFFFAOYSA-N (2-amino-2-oxoethyl) acetate Chemical compound CC(=O)OCC(N)=O DMLYTGPBYWHKHU-UHFFFAOYSA-N 0.000 claims 1
- IFKKDNHJPJJLLH-UHFFFAOYSA-N (2-carbamoylphenyl) benzoate Chemical compound NC(=O)C1=CC=CC=C1OC(=O)C1=CC=CC=C1 IFKKDNHJPJJLLH-UHFFFAOYSA-N 0.000 claims 1
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims 1
- 125000006644 (C2-C6) haloalkynyl group Chemical group 0.000 claims 1
- HCUOEKSZWPGJIM-IYNMRSRQSA-N (e,2z)-2-hydroxyimino-6-methoxy-4-methyl-5-nitrohex-3-enamide Chemical compound COCC([N+]([O-])=O)\C(C)=C\C(=N\O)\C(N)=O HCUOEKSZWPGJIM-IYNMRSRQSA-N 0.000 claims 1
- XUHGTGGPZFJRMF-UHFFFAOYSA-N 1,3-dihydropyrazole-2-carboxylic acid Chemical compound OC(=O)N1CC=CN1 XUHGTGGPZFJRMF-UHFFFAOYSA-N 0.000 claims 1
- ZTTKDUXKVPEXCG-UHFFFAOYSA-N 2-cyano-3-cyclopropyl-1-(2-mesyl-4-trifluoromethylphenyl)propan-1,3-dione Chemical compound CS(=O)(=O)C1=CC(C(F)(F)F)=CC=C1C(=O)C(C#N)C(=O)C1CC1 ZTTKDUXKVPEXCG-UHFFFAOYSA-N 0.000 claims 1
- 108010000700 Acetolactate synthase Proteins 0.000 claims 1
- 102000000452 Acetyl-CoA carboxylase Human genes 0.000 claims 1
- 108010016219 Acetyl-CoA carboxylase Proteins 0.000 claims 1
- 241000234282 Allium Species 0.000 claims 1
- 244000099147 Ananas comosus Species 0.000 claims 1
- 235000003911 Arachis Nutrition 0.000 claims 1
- 244000105624 Arachis hypogaea Species 0.000 claims 1
- 235000005340 Asparagus officinalis Nutrition 0.000 claims 1
- 235000005781 Avena Nutrition 0.000 claims 1
- 108010018763 Biotin carboxylase Proteins 0.000 claims 1
- 241000219198 Brassica Species 0.000 claims 1
- 235000011331 Brassica Nutrition 0.000 claims 1
- 235000021538 Chard Nutrition 0.000 claims 1
- 229920000742 Cotton Polymers 0.000 claims 1
- 240000008067 Cucumis sativus Species 0.000 claims 1
- 235000010799 Cucumis sativus var sativus Nutrition 0.000 claims 1
- 241000219122 Cucurbita Species 0.000 claims 1
- 241000208175 Daucus Species 0.000 claims 1
- 244000000626 Daucus carota Species 0.000 claims 1
- 235000002767 Daucus carota Nutrition 0.000 claims 1
- 239000004471 Glycine Substances 0.000 claims 1
- 244000068988 Glycine max Species 0.000 claims 1
- 235000010469 Glycine max Nutrition 0.000 claims 1
- 241000208818 Helianthus Species 0.000 claims 1
- 241000209219 Hordeum Species 0.000 claims 1
- 240000005979 Hordeum vulgare Species 0.000 claims 1
- 235000007340 Hordeum vulgare Nutrition 0.000 claims 1
- 235000021506 Ipomoea Nutrition 0.000 claims 1
- 241000207783 Ipomoea Species 0.000 claims 1
- 244000017020 Ipomoea batatas Species 0.000 claims 1
- 235000002678 Ipomoea batatas Nutrition 0.000 claims 1
- 241000208822 Lactuca Species 0.000 claims 1
- 241000208204 Linum Species 0.000 claims 1
- 235000002262 Lycopersicon Nutrition 0.000 claims 1
- 235000007688 Lycopersicon esculentum Nutrition 0.000 claims 1
- 239000005578 Mesotrione Substances 0.000 claims 1
- OHLUUHNLEMFGTQ-UHFFFAOYSA-N N-methylacetamide Chemical compound CNC(C)=O OHLUUHNLEMFGTQ-UHFFFAOYSA-N 0.000 claims 1
- 241000208125 Nicotiana Species 0.000 claims 1
- 241000209094 Oryza Species 0.000 claims 1
- 229910019142 PO4 Inorganic materials 0.000 claims 1
- 241000209117 Panicum Species 0.000 claims 1
- 235000006443 Panicum miliaceum subsp. miliaceum Nutrition 0.000 claims 1
- 235000009037 Panicum miliaceum subsp. ruderale Nutrition 0.000 claims 1
- 108010081996 Photosystem I Protein Complex Proteins 0.000 claims 1
- 108010060806 Photosystem II Protein Complex Proteins 0.000 claims 1
- 108020001991 Protoporphyrinogen Oxidase Proteins 0.000 claims 1
- 102000005135 Protoporphyrinogen oxidase Human genes 0.000 claims 1
- 241000209051 Saccharum Species 0.000 claims 1
- 241000209056 Secale Species 0.000 claims 1
- 241000228160 Secale cereale x Triticum aestivum Species 0.000 claims 1
- 239000005618 Sulcotrione Substances 0.000 claims 1
- 239000005620 Tembotrione Substances 0.000 claims 1
- ZMZDMBWJUHKJPS-UHFFFAOYSA-M Thiocyanate anion Chemical group [S-]C#N ZMZDMBWJUHKJPS-UHFFFAOYSA-M 0.000 claims 1
- 235000019714 Triticale Nutrition 0.000 claims 1
- 235000021307 Triticum Nutrition 0.000 claims 1
- 241000209140 Triticum Species 0.000 claims 1
- 241000219873 Vicia Species 0.000 claims 1
- 241000209149 Zea Species 0.000 claims 1
- 239000013543 active substance Substances 0.000 claims 1
- 244000193174 agave Species 0.000 claims 1
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 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
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 1
- 108010040093 cellulose synthase Proteins 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 claims 1
- 125000000753 cycloalkyl group Chemical group 0.000 claims 1
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims 1
- 125000003754 ethoxycarbonyl group Chemical group C(=O)(OCC)* 0.000 claims 1
- 238000009472 formulation Methods 0.000 claims 1
- 102000005396 glutamine synthetase Human genes 0.000 claims 1
- 108020002326 glutamine synthetase Proteins 0.000 claims 1
- 239000003630 growth substance Substances 0.000 claims 1
- 125000004438 haloalkoxy group Chemical group 0.000 claims 1
- 230000002363 herbicidal effect Effects 0.000 claims 1
- ZMZDMBWJUHKJPS-UHFFFAOYSA-N hydrogen thiocyanate Chemical group SC#N ZMZDMBWJUHKJPS-UHFFFAOYSA-N 0.000 claims 1
- 230000005764 inhibitory process Effects 0.000 claims 1
- KPUREKXXPHOJQT-UHFFFAOYSA-N mesotrione Chemical compound [O-][N+](=O)C1=CC(S(=O)(=O)C)=CC=C1C(=O)C1C(=O)CCCC1=O KPUREKXXPHOJQT-UHFFFAOYSA-N 0.000 claims 1
- 125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 claims 1
- 125000004458 methylaminocarbonyl group Chemical group [H]N(C(*)=O)C([H])([H])[H] 0.000 claims 1
- 125000004674 methylcarbonyl group Chemical group CC(=O)* 0.000 claims 1
- 239000000203 mixture Substances 0.000 claims 1
- NCCHARWOCKOHIH-UHFFFAOYSA-N n-methylbenzamide Chemical compound CNC(=O)C1=CC=CC=C1 NCCHARWOCKOHIH-UHFFFAOYSA-N 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
- 239000010452 phosphate Substances 0.000 claims 1
- 108010001545 phytoene dehydrogenase Proteins 0.000 claims 1
- ASRAWSBMDXVNLX-UHFFFAOYSA-N pyrazolynate Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(=O)C=1C(C)=NN(C)C=1OS(=O)(=O)C1=CC=C(C)C=C1 ASRAWSBMDXVNLX-UHFFFAOYSA-N 0.000 claims 1
- 150000003839 salts Chemical class 0.000 claims 1
- PQTBTIFWAXVEPB-UHFFFAOYSA-N sulcotrione Chemical compound ClC1=CC(S(=O)(=O)C)=CC=C1C(=O)C1C(=O)CCCC1=O PQTBTIFWAXVEPB-UHFFFAOYSA-N 0.000 claims 1
- IUQAXCIUEPFPSF-UHFFFAOYSA-N tembotrione Chemical compound ClC1=C(COCC(F)(F)F)C(S(=O)(=O)C)=CC=C1C(=O)C1C(=O)CCCC1=O IUQAXCIUEPFPSF-UHFFFAOYSA-N 0.000 claims 1
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201161467619P | 2011-03-25 | 2011-03-25 | |
| EP11159755.5 | 2011-03-25 | ||
| US61/467,619 | 2011-03-25 | ||
| EP11159755 | 2011-03-25 | ||
| PCT/EP2012/054981 WO2012130685A1 (en) | 2011-03-25 | 2012-03-21 | Use of n-(tetrazol-4-yl)- or n-(triazol-3-yl)arylcarboxamides or their salts for controlling unwanted plants in areas of transgenic crop plants being tolerant to hppd inhibitor herbicides |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2014510089A JP2014510089A (ja) | 2014-04-24 |
| JP2014510089A5 true JP2014510089A5 (https=) | 2015-05-07 |
| JP5847921B2 JP5847921B2 (ja) | 2016-01-27 |
Family
ID=44352067
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2014500369A Expired - Fee Related JP5847921B2 (ja) | 2011-03-25 | 2012-03-21 | Ｈｐｐｄ阻害薬型除草剤に対して耐性であるトランスジェニック作物の区域で望ましくない植物を防除するためのｎ−（テトラゾール−４−イル）−もしくはｎ−（トリアゾール−３−イル）アリールカルボキサミド類またはそれらの塩の使用 |
Country Status (14)
| Country | Link |
|---|---|
| US (1) | US9078446B2 (https=) |
| EP (1) | EP2688406B1 (https=) |
| JP (1) | JP5847921B2 (https=) |
| KR (1) | KR20140033354A (https=) |
| AR (1) | AR085821A1 (https=) |
| AU (1) | AU2012234449B2 (https=) |
| CA (1) | CA2830782C (https=) |
| EA (1) | EA201391301A1 (https=) |
| HU (1) | HUE025756T2 (https=) |
| MX (1) | MX2013010908A (https=) |
| PL (1) | PL2688406T3 (https=) |
| UA (1) | UA111193C2 (https=) |
| WO (1) | WO2012130685A1 (https=) |
| ZA (1) | ZA201306715B (https=) |
Families Citing this family (36)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103459386B (zh) * | 2011-03-15 | 2016-06-22 | 拜耳知识产权有限责任公司 | N-(1,2,5-噁二唑-3-基)吡啶甲酰胺及其作为除草剂的用途 |
| US9303270B2 (en) | 2011-07-22 | 2016-04-05 | Ricetec Aktiengesellschaft | Rice resistant to HPPD and accase inhibiting herbicides |
| CN105745320A (zh) | 2011-07-22 | 2016-07-06 | 赖斯泰克股份公司 | 产生 acc 酶抑制剂抗性水稻的方法和组合物 |
| CN103717581B (zh) * | 2011-08-03 | 2016-04-06 | 拜耳知识产权有限责任公司 | N-(四唑-5-基)芳基甲酰胺和n-(三唑-5-基)芳基甲酰胺及其作为除草剂的用途 |
| EP2817298A1 (de) * | 2012-02-21 | 2014-12-31 | Bayer Intellectual Property GmbH | Herbizid wirksame 4-nitro substituierte n-(tetrazol-5-yl)-, n-(triazol-5-yl)- und n-(1,3,4-oxadiazol-2-yl)arylcarbonsäureamide |
| JP2015519314A (ja) * | 2012-04-27 | 2015-07-09 | ビーエーエスエフ ソシエタス・ヨーロピアＢａｓｆ Ｓｅ | 置換型ｎ−（テトラゾール−５−イル）−およびｎ−（トリアゾール−５−イル）ピリジン−３−イル−カルボキサミド化合物ならびに除草剤としてのそれらの使用 |
| UA119532C2 (uk) | 2012-09-14 | 2019-07-10 | Байєр Кропсайєнс Лп | Варіант hppd та спосіб його застосування |
| UA117816C2 (uk) * | 2012-11-06 | 2018-10-10 | Байєр Кропсайєнс Акцієнгезелльшафт | Гербіцидна комбінація для толерантних соєвих культур |
| US20170226529A1 (en) * | 2013-04-30 | 2017-08-10 | Basf Se | Plants having increased tolerance to herbicides |
| WO2014184017A1 (en) * | 2013-05-15 | 2014-11-20 | Basf Se | Substituted n-(tetrazol-5-yl)- and n-(triazol-5-yl)pyridin-3-yl-carboxamide compounds and their use as herbicides |
| MY172600A (en) | 2013-05-31 | 2019-12-05 | Nissan Chemical Ind Ltd | Heterocyclic amide compound |
| AU2014356608B2 (en) * | 2013-11-28 | 2018-09-06 | Bayer Cropscience Aktiengesellschaft | Use of 2-chloro-3-(methylsulfanyl)-N-(1-methyl-1H-tetrazol-5-yl)-4-(trifluoromethyl)benzamide or its salts for controlling unwanted plants in areas of transgenic crop plants being tolerant to HPPD inhibitor herbicides |
| BR112016020889B1 (pt) | 2014-03-11 | 2022-10-04 | BASF Agricultural Solutions Seed US LLC | Molécula de ácido nucleico recombinante, célula hospedeira bacteriana, proteína hppd recombinante, uso do ácido nucleico recombinante e produto de base |
| EP3116871A1 (en) * | 2014-03-11 | 2017-01-18 | Bayer CropScience Aktiengesellschaft | Use of n-(1,3,4-oxadiazol-2-yl)arylcarboxamides or their salts for controlling unwanted plants in areas of transgenic crop plants being tolerant to hppd inhibitor herbicides |
| CN108884471A (zh) | 2016-08-05 | 2018-11-23 | 赖斯泰克有限公司 | 组合水稻中与除草剂抗性/耐受性相关的突变的方法和组合物 |
| WO2018094008A1 (en) * | 2016-11-21 | 2018-05-24 | Fmc Corporation | Cellulose synthase inhibitors effective as herbicides |
| CN111362908B (zh) * | 2018-12-25 | 2021-03-12 | 青岛清原化合物有限公司 | 一种无定形态环吡氟草酮二甲胺盐及其制备方法和用途 |
| CN111362911B (zh) * | 2018-12-25 | 2021-03-12 | 青岛清原化合物有限公司 | 环吡氟草酮二甲胺盐及其制备方法和用途 |
| CN111362917B (zh) * | 2018-12-25 | 2021-03-12 | 青岛清原化合物有限公司 | 一种无定形态环吡氟草酮一异丙胺盐及其制备方法和用途 |
| CN111362915B (zh) * | 2018-12-25 | 2021-03-12 | 青岛清原化合物有限公司 | 环吡氟草酮一异丙胺盐及其制备方法和用途 |
| CN111362916B (zh) * | 2018-12-25 | 2021-03-05 | 青岛清原化合物有限公司 | 环吡氟草酮一异丙胺盐f晶型及其制备方法和用途 |
| CN111362905B (zh) * | 2018-12-25 | 2021-03-05 | 青岛清原化合物有限公司 | 环吡氟草酮一异丙胺盐e晶型及其制备方法和用途 |
| CN111362909B (zh) * | 2018-12-25 | 2021-03-12 | 青岛清原化合物有限公司 | 环吡氟草酮二甲胺盐c晶型及其制备方法和用途 |
| CN111362912B (zh) * | 2018-12-25 | 2021-03-12 | 青岛清原化合物有限公司 | 环吡氟草酮三乙醇胺盐及其制备方法和用途 |
| CN111362910B (zh) * | 2018-12-25 | 2021-03-12 | 青岛清原化合物有限公司 | 环吡氟草酮二甲胺盐b晶型及其制备方法和用途 |
| CN111362919B (zh) * | 2018-12-25 | 2021-03-12 | 青岛清原化合物有限公司 | 环吡氟草酮二甲胺盐d晶型及其制备方法和用途 |
| CN111362906B (zh) * | 2018-12-25 | 2021-03-05 | 青岛清原化合物有限公司 | 环吡氟草酮一异丙胺盐c晶型及其制备方法和用途 |
| CN111362914B (zh) * | 2018-12-25 | 2021-03-12 | 青岛清原化合物有限公司 | 环吡氟草酮三乙醇胺盐b晶型及其制备方法和用途 |
| CN111362913B (zh) * | 2018-12-25 | 2021-03-12 | 青岛清原化合物有限公司 | 一种无定形态环吡氟草酮三乙醇胺盐及其制备方法和用途 |
| CN111362907B (zh) * | 2018-12-25 | 2021-03-02 | 青岛清原化合物有限公司 | 环吡氟草酮一异丙胺盐d晶型及其制备方法和用途 |
| CN111362918B (zh) * | 2018-12-25 | 2021-03-05 | 青岛清原化合物有限公司 | 环吡氟草酮一异丙胺盐b晶型及其制备方法和用途 |
| CN116803993A (zh) * | 2019-10-23 | 2023-09-26 | 青岛清原化合物有限公司 | 一种含手性硫氧化物的芳基甲酰胺类化合物或其盐、制备方法、除草组合物和应用 |
| WO2021209383A1 (en) * | 2020-04-17 | 2021-10-21 | Syngenta Crop Protection Ag | Herbicidal compounds |
| EP4658770A1 (en) | 2023-02-03 | 2025-12-10 | Syngenta Crop Protection AG | Herbicide resistant plants |
| EP4698556A1 (en) | 2023-04-19 | 2026-02-25 | Syngenta Crop Protection AG | Herbicide resistant plants |
| WO2026027723A1 (en) | 2024-08-01 | 2026-02-05 | Syngenta Crop Protection Ag | Herbicide resistant plants |
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-
2012
- 2012-03-21 EA EA201391301A patent/EA201391301A1/ru unknown
- 2012-03-21 JP JP2014500369A patent/JP5847921B2/ja not_active Expired - Fee Related
- 2012-03-21 MX MX2013010908A patent/MX2013010908A/es unknown
- 2012-03-21 US US14/006,049 patent/US9078446B2/en not_active Expired - Fee Related
- 2012-03-21 PL PL12709887T patent/PL2688406T3/pl unknown
- 2012-03-21 AU AU2012234449A patent/AU2012234449B2/en not_active Ceased
- 2012-03-21 HU HUE12709887A patent/HUE025756T2/en unknown
- 2012-03-21 WO PCT/EP2012/054981 patent/WO2012130685A1/en not_active Ceased
- 2012-03-21 UA UAA201312476A patent/UA111193C2/uk unknown
- 2012-03-21 CA CA2830782A patent/CA2830782C/en not_active Expired - Fee Related
- 2012-03-21 EP EP20120709887 patent/EP2688406B1/en not_active Not-in-force
- 2012-03-21 KR KR1020137027333A patent/KR20140033354A/ko not_active Withdrawn
- 2012-03-23 AR ARP120100992A patent/AR085821A1/es unknown
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2013
- 2013-09-06 ZA ZA2013/06715A patent/ZA201306715B/en unknown
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