JP2018532733A5 - - Google Patents
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- JP2018532733A5 JP2018532733A5 JP2018517430A JP2018517430A JP2018532733A5 JP 2018532733 A5 JP2018532733 A5 JP 2018532733A5 JP 2018517430 A JP2018517430 A JP 2018517430A JP 2018517430 A JP2018517430 A JP 2018517430A JP 2018532733 A5 JP2018532733 A5 JP 2018532733A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- methyl
- hydrogen
- ethyl
- alkoxy
- 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.)
- Pending
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- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 14
- 150000001875 compounds Chemical class 0.000 claims 12
- 229910052739 hydrogen Inorganic materials 0.000 claims 11
- 239000001257 hydrogen Substances 0.000 claims 11
- 241000196324 Embryophyta Species 0.000 claims 7
- -1 aluminum ion Chemical class 0.000 claims 7
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 7
- 150000002431 hydrogen Chemical class 0.000 claims 7
- 230000002363 herbicidal effect Effects 0.000 claims 6
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims 4
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 4
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 claims 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 4
- 230000008635 plant growth Effects 0.000 claims 4
- XSCHRSMBECNVNS-UHFFFAOYSA-N quinoxaline Chemical compound N1=CC=NC2=CC=CC=C21 XSCHRSMBECNVNS-UHFFFAOYSA-N 0.000 claims 4
- 150000003839 salts Chemical class 0.000 claims 4
- OISVCGZHLKNMSJ-UHFFFAOYSA-N 2,6-dimethylpyridine Chemical compound CC1=CC=CC(C)=N1 OISVCGZHLKNMSJ-UHFFFAOYSA-N 0.000 claims 3
- 150000001768 cations Chemical class 0.000 claims 3
- 244000038559 crop plants Species 0.000 claims 3
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims 3
- 229910052736 halogen Inorganic materials 0.000 claims 3
- 239000004009 herbicide Substances 0.000 claims 3
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 claims 3
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 3
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims 2
- GIWQSPITLQVMSG-UHFFFAOYSA-N 1,2-dimethylimidazole Chemical compound CC1=NC=CN1C GIWQSPITLQVMSG-UHFFFAOYSA-N 0.000 claims 2
- WOKQGMYCUGJNIJ-UHFFFAOYSA-M 1,3-dimethylimidazol-1-ium;methyl sulfate Chemical compound COS([O-])(=O)=O.CN1C=C[N+](C)=C1 WOKQGMYCUGJNIJ-UHFFFAOYSA-M 0.000 claims 2
- JYYNAJVZFGKDEQ-UHFFFAOYSA-N 2,4-Dimethylpyridine Chemical compound CC1=CC=NC(C)=C1 JYYNAJVZFGKDEQ-UHFFFAOYSA-N 0.000 claims 2
- BSKHPKMHTQYZBB-UHFFFAOYSA-N 2-methylpyridine Chemical compound CC1=CC=CC=N1 BSKHPKMHTQYZBB-UHFFFAOYSA-N 0.000 claims 2
- ITQTTZVARXURQS-UHFFFAOYSA-N 3-methylpyridine Chemical compound CC1=CC=CN=C1 ITQTTZVARXURQS-UHFFFAOYSA-N 0.000 claims 2
- FKNQCJSGGFJEIZ-UHFFFAOYSA-N 4-methylpyridine Chemical compound CC1=CC=NC=C1 FKNQCJSGGFJEIZ-UHFFFAOYSA-N 0.000 claims 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims 2
- KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 claims 2
- 125000001931 aliphatic group Chemical group 0.000 claims 2
- 229910001413 alkali metal ion Inorganic materials 0.000 claims 2
- 229910001420 alkaline earth metal ion Inorganic materials 0.000 claims 2
- 125000000217 alkyl group Chemical group 0.000 claims 2
- 229910052782 aluminium Inorganic materials 0.000 claims 2
- 239000003814 drug Substances 0.000 claims 2
- 229940079593 drug Drugs 0.000 claims 2
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims 2
- 150000002367 halogens Chemical class 0.000 claims 2
- 125000000623 heterocyclic group Chemical group 0.000 claims 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 2
- 239000011777 magnesium Substances 0.000 claims 2
- 229910052749 magnesium Inorganic materials 0.000 claims 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 2
- 229910052760 oxygen Inorganic materials 0.000 claims 2
- 239000001301 oxygen Substances 0.000 claims 2
- 229920006395 saturated elastomer Polymers 0.000 claims 2
- RWSOTUBLDIXVET-UHFFFAOYSA-O sulfonium Chemical compound [SH3+] RWSOTUBLDIXVET-UHFFFAOYSA-O 0.000 claims 2
- 125000004434 sulfur atom Chemical group 0.000 claims 2
- 229910001428 transition metal ion Inorganic materials 0.000 claims 2
- 244000045561 useful plants Species 0.000 claims 2
- FTTATHOUSOIFOQ-UHFFFAOYSA-N 1,2,3,4,6,7,8,8a-octahydropyrrolo[1,2-a]pyrazine Chemical compound C1NCCN2CCCC21 FTTATHOUSOIFOQ-UHFFFAOYSA-N 0.000 claims 1
- XWKFPIODWVPXLX-UHFFFAOYSA-N 2,5-dimethylpyridine Chemical compound CC1=CC=C(C)N=C1 XWKFPIODWVPXLX-UHFFFAOYSA-N 0.000 claims 1
- DLDSFSKURFXLIB-UHFFFAOYSA-N 3-phenylpyrrolidine-2,4-dione Chemical class O=C1CNC(=O)C1C1=CC=CC=C1 DLDSFSKURFXLIB-UHFFFAOYSA-N 0.000 claims 1
- NTSLROIKFLNUIJ-UHFFFAOYSA-N 5-Ethyl-2-methylpyridine Chemical compound CCC1=CC=C(C)N=C1 NTSLROIKFLNUIJ-UHFFFAOYSA-N 0.000 claims 1
- KNCHDRLWPAKSII-UHFFFAOYSA-N 5-ethyl-2-methylpyridine Natural products CCC1=CC=NC(C)=C1 KNCHDRLWPAKSII-UHFFFAOYSA-N 0.000 claims 1
- 235000007319 Avena orientalis Nutrition 0.000 claims 1
- 244000075850 Avena orientalis Species 0.000 claims 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 1
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 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
- 244000020551 Helianthus annuus Species 0.000 claims 1
- 235000003222 Helianthus annuus Nutrition 0.000 claims 1
- 240000005979 Hordeum vulgare Species 0.000 claims 1
- 235000007340 Hordeum vulgare Nutrition 0.000 claims 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical group C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims 1
- 240000007594 Oryza sativa Species 0.000 claims 1
- 235000007164 Oryza sativa Nutrition 0.000 claims 1
- NQRYJNQNLNOLGT-UHFFFAOYSA-O Piperidinium(1+) Chemical compound C1CC[NH2+]CC1 NQRYJNQNLNOLGT-UHFFFAOYSA-O 0.000 claims 1
- 241000209504 Poaceae Species 0.000 claims 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical group [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims 1
- RWRDLPDLKQPQOW-UHFFFAOYSA-O Pyrrolidinium ion Chemical compound C1CC[NH2+]C1 RWRDLPDLKQPQOW-UHFFFAOYSA-O 0.000 claims 1
- 240000000111 Saccharum officinarum Species 0.000 claims 1
- 235000007201 Saccharum officinarum Nutrition 0.000 claims 1
- 244000082988 Secale cereale Species 0.000 claims 1
- 235000007238 Secale cereale Nutrition 0.000 claims 1
- 235000021307 Triticum Nutrition 0.000 claims 1
- 244000098338 Triticum aestivum Species 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
- 230000000895 acaricidal effect Effects 0.000 claims 1
- 239000000642 acaricide Substances 0.000 claims 1
- 239000013543 active substance Substances 0.000 claims 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 1
- 229910052794 bromium Inorganic materials 0.000 claims 1
- 239000011575 calcium Substances 0.000 claims 1
- 229910052791 calcium Inorganic materials 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 claims 1
- 239000000460 chlorine Substances 0.000 claims 1
- 229910052801 chlorine Inorganic materials 0.000 claims 1
- 235000005822 corn Nutrition 0.000 claims 1
- 125000004093 cyano group Chemical group *C#N 0.000 claims 1
- 125000004122 cyclic group Chemical group 0.000 claims 1
- 239000012973 diazabicyclooctane Substances 0.000 claims 1
- 239000003085 diluting agent Substances 0.000 claims 1
- 229910052731 fluorine Inorganic materials 0.000 claims 1
- 239000011737 fluorine Substances 0.000 claims 1
- 239000000417 fungicide Substances 0.000 claims 1
- 239000003630 growth substance Substances 0.000 claims 1
- 125000004438 haloalkoxy group Chemical group 0.000 claims 1
- SMWDFEZZVXVKRB-UHFFFAOYSA-O hydron;quinoline Chemical group [NH+]1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-O 0.000 claims 1
- 239000002917 insecticide Substances 0.000 claims 1
- YNAVUWVOSKDBBP-UHFFFAOYSA-O morpholinium Chemical compound [H+].C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-O 0.000 claims 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 1
- 230000000361 pesticidal effect Effects 0.000 claims 1
- 239000011591 potassium Chemical group 0.000 claims 1
- 229910052700 potassium Inorganic materials 0.000 claims 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims 1
- 150000003222 pyridines Chemical class 0.000 claims 1
- JUJWROOIHBZHMG-UHFFFAOYSA-O pyridinium Chemical group C1=CC=[NH+]C=C1 JUJWROOIHBZHMG-UHFFFAOYSA-O 0.000 claims 1
- 235000009566 rice Nutrition 0.000 claims 1
- 239000011734 sodium Substances 0.000 claims 1
- 229910052708 sodium Inorganic materials 0.000 claims 1
- 239000002904 solvent Substances 0.000 claims 1
- 230000009261 transgenic effect Effects 0.000 claims 1
- IMNIMPAHZVJRPE-UHFFFAOYSA-N triethylenediamine Chemical compound C1CN2CCN1CC2 IMNIMPAHZVJRPE-UHFFFAOYSA-N 0.000 claims 1
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical group CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 claims 1
- NRZWQKGABZFFKE-UHFFFAOYSA-N trimethylsulfonium Chemical group C[S+](C)C NRZWQKGABZFFKE-UHFFFAOYSA-N 0.000 claims 1
- JABYJIQOLGWMQW-UHFFFAOYSA-N undec-4-ene Chemical compound CCCCCCC=CCCC JABYJIQOLGWMQW-UHFFFAOYSA-N 0.000 claims 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP15188613 | 2015-10-06 | ||
| EP15188613.2 | 2015-10-06 | ||
| PCT/EP2016/073591 WO2017060204A1 (de) | 2015-10-06 | 2016-10-04 | Neue alkinyl-substituierte 3-phenylpyrrolidin-2,4-dione und deren verwendung als herbizide |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2018532733A JP2018532733A (ja) | 2018-11-08 |
| JP2018532733A5 true JP2018532733A5 (enExample) | 2019-11-14 |
Family
ID=54266444
Family Applications (3)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2018517430A Pending JP2018532733A (ja) | 2015-10-06 | 2016-10-04 | 新規なアルキニル置換された３−フェニルピロリジン−２，４−ジオン類および除草剤としてのそれらの使用 |
| JP2018517431A Expired - Fee Related JP6886458B2 (ja) | 2015-10-06 | 2016-10-04 | 新規なアルキニル置換された３−フェニルピロリジン−２，４−ジオン類および除草剤としてのそれらの使用 |
| JP2020202924A Pending JP2021054835A (ja) | 2015-10-06 | 2020-12-07 | 新規なアルキニル置換された３−フェニルピロリジン−２，４−ジオン類および除草剤としてのそれらの使用 |
Family Applications After (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2018517431A Expired - Fee Related JP6886458B2 (ja) | 2015-10-06 | 2016-10-04 | 新規なアルキニル置換された３−フェニルピロリジン−２，４−ジオン類および除草剤としてのそれらの使用 |
| JP2020202924A Pending JP2021054835A (ja) | 2015-10-06 | 2020-12-07 | 新規なアルキニル置換された３−フェニルピロリジン−２，４−ジオン類および除草剤としてのそれらの使用 |
Country Status (14)
| Country | Link |
|---|---|
| US (3) | US11178868B2 (enExample) |
| EP (3) | EP3795557A3 (enExample) |
| JP (3) | JP2018532733A (enExample) |
| KR (2) | KR20180063253A (enExample) |
| CN (2) | CN108349889A (enExample) |
| AR (2) | AR106256A1 (enExample) |
| AU (3) | AU2016336174B2 (enExample) |
| BR (2) | BR112018006999A2 (enExample) |
| CA (2) | CA3000769A1 (enExample) |
| EA (2) | EA035255B1 (enExample) |
| PL (1) | PL3359525T3 (enExample) |
| UA (1) | UA123214C2 (enExample) |
| UY (2) | UY36930A (enExample) |
| WO (2) | WO2017060204A1 (enExample) |
Families Citing this family (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2018532733A (ja) * | 2015-10-06 | 2018-11-08 | バイエル・クロップサイエンス・アクチェンゲゼルシャフト | 新規なアルキニル置換された３−フェニルピロリジン−２，４−ジオン類および除草剤としてのそれらの使用 |
| AR115088A1 (es) * | 2018-05-15 | 2020-11-25 | Bayer Ag | Espirociclohexilpirrolin-2-onas y su uso como herbicidas |
| US20220106271A1 (en) * | 2018-05-15 | 2022-04-07 | Bayer Aktiengesellschaft | 2-bromo-6-alkoxyphenyl-substituted pyrrolin-2-ones and their use as herbicides |
| AR115089A1 (es) | 2018-05-15 | 2020-11-25 | Bayer Ag | 2-alquil-6-alcoxifenil-3-pirrolin-2-onas especialmente sustituidas y su uso como herbicidas |
| WO2019219585A1 (de) | 2018-05-15 | 2019-11-21 | Bayer Aktiengesellschaft | Neue 3-(4-alkinyl-6-alkoxy-2-chlorphenyl)-3-pyrrolin-2-one und deren verwendung als herbizide |
| WO2019228787A1 (de) * | 2018-05-29 | 2019-12-05 | Bayer Aktiengesellschaft | Speziell substituierte 2-alkyl-6-alkoxyphenyl-3-pyrrolin-2-one und deren verwendung als herbizide |
| WO2019228788A1 (de) * | 2018-05-29 | 2019-12-05 | Bayer Aktiengesellschaft | 2-brom-6-alkoxyphenyl-substituierte pyrrolin-2-one und deren verwendung als herbizide |
| EP3938346A1 (de) * | 2019-03-15 | 2022-01-19 | Bayer Aktiengesellschaft | Speziell substituierte 3-(2-halogen-6-alkyl-4-propinylphenyl)-3-pyrrolin-2-one und deren verwendung als herbizide |
| EA202192469A1 (ru) * | 2019-03-15 | 2022-02-16 | Байер Акциенгезельшафт | 3-(2-бром-4-алкинил-6-алкоксифенил)-замещенные 5-спироциклогексил-3-пирролин-2-оны и их применение в качестве гербицидов |
| EP3938349A1 (de) * | 2019-03-15 | 2022-01-19 | Bayer Aktiengesellschaft | Speziell substituierte 3-(2-alkoxy-6-alkyl-4-propinylphenyl)-3-pyrrolin-2-one und deren verwendung als herbizide |
| WO2021204884A1 (de) | 2020-04-09 | 2021-10-14 | Bayer Aktiengesellschaft | 3-(4-alkenyl-phenyl)-3-pyrrolin-2-one und deren verwendung als herbizide |
| WO2021209486A1 (de) * | 2020-04-15 | 2021-10-21 | Bayer Aktiengesellschaft | Speziell substituierte pyrrolin-2-one und deren verwendung als herbizide |
| TW202210489A (zh) | 2020-05-27 | 2022-03-16 | 德商拜耳廠股份有限公司 | 特定取代之吡咯啉－２－酮及其作為除草劑之用途 |
| WO2023274869A1 (de) | 2021-06-29 | 2023-01-05 | Bayer Aktiengesellschaft | 3-(4-alkenyl-phenyl)-3-pyrrolin-2-one und deren verwendung als herbizide |
Family Cites Families (25)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4985063A (en) | 1988-08-20 | 1991-01-15 | Bayer Aktiengesellschaft | 3-aryl-pyrrolidine-2,4-diones |
| DE3900669C1 (enExample) | 1989-01-12 | 1990-08-09 | Bemofensterbau Gmbh, 5452 Weissenthurm, De | |
| DE3929087A1 (de) | 1989-09-01 | 1991-03-07 | Bayer Ag | 3-aryl-pyrrolidin-2,4-dion-derivate |
| DE4004496A1 (de) | 1990-02-14 | 1991-08-22 | Bayer Ag | 3-aryl-pyrrolidin-2,4-dion-derivate |
| ATE177093T1 (de) * | 1993-07-05 | 1999-03-15 | Bayer Ag | Substituierte aryl-ketoenolheterocyclen |
| EP0809629B1 (de) * | 1995-02-13 | 2004-06-30 | Bayer CropScience AG | 2-phenylsubstituierte heterocyclische 1,3-ketoenole als herbizide und pestizide |
| KR100518374B1 (ko) | 1996-08-05 | 2005-10-04 | 바이엘 악티엔게젤샤프트 | 2- 및 2,5-치환된 페닐케토에놀 |
| JP2000053670A (ja) | 1998-08-10 | 2000-02-22 | Ube Ind Ltd | アルコキシメチルフラノン誘導体及び有害生物防除剤 |
| DE10016544A1 (de) * | 2000-04-03 | 2001-10-11 | Bayer Ag | C2-phenylsubstituierte Ketoenole |
| DE10354629A1 (de) * | 2003-11-22 | 2005-06-30 | Bayer Cropscience Ag | 2-Ethyl-4,6-dimethyl-phenyl substituierte spirocyclische Tetramsäure-Derivate |
| DE102004030753A1 (de) | 2004-06-25 | 2006-01-19 | Bayer Cropscience Ag | 3'-Alkoxy spirocyclische Tetram- und Tretronsäuren |
| DE102004053191A1 (de) * | 2004-11-04 | 2006-05-11 | Bayer Cropscience Ag | 2,6-Diethyl-4-methyl-phenyl substituierte Tetramsäure-Derivate |
| DE102005059471A1 (de) * | 2005-12-13 | 2007-07-12 | Bayer Cropscience Ag | Herbizide Zusammensetzungen mit verbesserter Wirkung |
| DE102006007882A1 (de) | 2006-02-21 | 2007-08-30 | Bayer Cropscience Ag | Cycloalkyl-phenylsubstituierte cyclische Ketoenole |
| DE102006057036A1 (de) * | 2006-12-04 | 2008-06-05 | Bayer Cropscience Ag | Biphenylsubstituierte spirocyclische Ketoenole |
| CL2007003587A1 (es) * | 2006-12-12 | 2008-07-04 | Anadys Pharmaceuticals Inc | Compuestos derivados de pirimidinas sustituidas; composicion farmaceutica que comprende a dichos compuestos y otro agente activo; y su uso para tratar o prevenir la infeccion de la hepatitis c. |
| CL2008002703A1 (es) * | 2007-09-14 | 2009-11-20 | Sumitomo Chemical Co | Compuestos derivados de 1,4-dihidro-2h-piridazin-3-ona; composicion herbicida que comprende a dichos compuestos; metodo de control de malezas; uso de dichos compuestos para el control de malezas; y compuestos intermediarios. |
| GB0820344D0 (en) * | 2008-11-06 | 2008-12-17 | Syngenta Ltd | Herbicidal compositions |
| CN103459370A (zh) * | 2011-01-25 | 2013-12-18 | 拜耳知识产权有限责任公司 | 制备1-h-吡咯烷-2,4-二酮衍生物的方法 |
| CN103974618B (zh) * | 2011-11-30 | 2016-02-24 | 先正达有限公司 | 2-(被取代的苯基)-环戊烷-1,3-二酮化合物及其衍生物 |
| GB201120644D0 (en) * | 2011-11-30 | 2012-01-11 | Syngenta Participations Ag | Herbicidal uses of compounds |
| WO2015032702A1 (en) | 2013-09-06 | 2015-03-12 | Syngenta Limited | Herbicidally active 2-halogen-4-alkynyl- phenyl-pyrazolidine-dione or pyrrolidine-dione derivatives |
| US20160219881A1 (en) * | 2013-09-20 | 2016-08-04 | Syngenta Limited | Herbicidally active 2-halogen-4-alkynyl-phenyl-pyrazolidine-dione or pyrrolidine-dione derivatives |
| KR20180019209A (ko) * | 2015-06-22 | 2018-02-23 | 바이엘 크롭사이언스 악티엔게젤샤프트 | 신규 알키닐-치환된 3-페닐피롤리딘-2,4-디온 및 제초제로서의 그의 용도 |
| JP2018532733A (ja) * | 2015-10-06 | 2018-11-08 | バイエル・クロップサイエンス・アクチェンゲゼルシャフト | 新規なアルキニル置換された３−フェニルピロリジン−２，４−ジオン類および除草剤としてのそれらの使用 |
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2016
- 2016-10-04 JP JP2018517430A patent/JP2018532733A/ja active Pending
- 2016-10-04 PL PL16787350T patent/PL3359525T3/pl unknown
- 2016-10-04 UY UY0001036930A patent/UY36930A/es not_active Application Discontinuation
- 2016-10-04 EP EP20200423.0A patent/EP3795557A3/de not_active Withdrawn
- 2016-10-04 EP EP16787350.4A patent/EP3359525B1/de not_active Not-in-force
- 2016-10-04 UA UAA201804990A patent/UA123214C2/uk unknown
- 2016-10-04 KR KR1020187012621A patent/KR20180063253A/ko not_active Withdrawn
- 2016-10-04 CA CA3000769A patent/CA3000769A1/en not_active Abandoned
- 2016-10-04 WO PCT/EP2016/073591 patent/WO2017060204A1/de not_active Ceased
- 2016-10-04 EA EA201890872A patent/EA035255B1/ru not_active IP Right Cessation
- 2016-10-04 WO PCT/EP2016/073590 patent/WO2017060203A1/de not_active Ceased
- 2016-10-04 BR BR112018006999-0A patent/BR112018006999A2/pt not_active IP Right Cessation
- 2016-10-04 AR ARP160103038A patent/AR106256A1/es active IP Right Grant
- 2016-10-04 CN CN201680067325.9A patent/CN108349889A/zh active Pending
- 2016-10-04 KR KR1020187012622A patent/KR20180061347A/ko not_active Withdrawn
- 2016-10-04 UY UY0001036929A patent/UY36929A/es not_active Application Discontinuation
- 2016-10-04 AU AU2016336174A patent/AU2016336174B2/en not_active Ceased
- 2016-10-04 BR BR112018007013-0A patent/BR112018007013B1/pt not_active IP Right Cessation
- 2016-10-04 US US15/765,769 patent/US11178868B2/en not_active Expired - Fee Related
- 2016-10-04 US US15/765,788 patent/US20180282275A1/en not_active Abandoned
- 2016-10-04 JP JP2018517431A patent/JP6886458B2/ja not_active Expired - Fee Related
- 2016-10-04 CN CN201680066096.9A patent/CN108349888B/zh not_active Expired - Fee Related
- 2016-10-04 EA EA201890882A patent/EA201890882A1/ru unknown
- 2016-10-04 AR ARP160103039A patent/AR106257A1/es unknown
- 2016-10-04 AU AU2016336175A patent/AU2016336175A1/en not_active Abandoned
- 2016-10-04 CA CA3000768A patent/CA3000768A1/en not_active Abandoned
- 2016-10-04 EP EP16775710.3A patent/EP3359524A1/de not_active Withdrawn
-
2020
- 2020-11-25 AU AU2020277157A patent/AU2020277157A1/en not_active Abandoned
- 2020-12-07 JP JP2020202924A patent/JP2021054835A/ja active Pending
-
2021
- 2021-09-10 US US17/471,524 patent/US20210400966A1/en not_active Abandoned
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