JP2017522374A5 - - Google Patents
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- Publication number
- JP2017522374A5 JP2017522374A5 JP2017521023A JP2017521023A JP2017522374A5 JP 2017522374 A5 JP2017522374 A5 JP 2017522374A5 JP 2017521023 A JP2017521023 A JP 2017521023A JP 2017521023 A JP2017521023 A JP 2017521023A JP 2017522374 A5 JP2017522374 A5 JP 2017522374A5
- Authority
- JP
- Japan
- Prior art keywords
- phenyl
- alkyl
- cycloalkyl
- piperidinecarboxamide
- oxo
- 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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- -1 hydroxy, amino Chemical group 0.000 claims description 24
- 125000000217 alkyl group Chemical group 0.000 claims description 11
- 125000003545 alkoxy group Chemical group 0.000 claims description 10
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 8
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims description 6
- 125000004644 alkyl sulfinyl group Chemical group 0.000 claims description 6
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 5
- 125000003302 alkenyloxy group Chemical group 0.000 claims description 4
- 125000005081 alkoxyalkoxyalkyl group Chemical group 0.000 claims description 4
- 125000004687 alkyl sulfinyl alkyl group Chemical group 0.000 claims description 4
- 125000006350 alkyl thio alkyl group Chemical group 0.000 claims description 4
- 125000004414 alkyl thio group Chemical group 0.000 claims description 4
- 125000005133 alkynyloxy group Chemical group 0.000 claims description 4
- 125000001316 cycloalkyl alkyl group Chemical group 0.000 claims description 4
- 125000004473 dialkylaminocarbonyl group Chemical group 0.000 claims description 4
- 125000005083 alkoxyalkoxy group Chemical group 0.000 claims description 3
- 125000004466 alkoxycarbonylamino group Chemical group 0.000 claims description 3
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims description 3
- 125000005112 cycloalkylalkoxy group Chemical group 0.000 claims description 3
- 125000004663 dialkyl amino group Chemical group 0.000 claims description 3
- 125000004472 dialkylaminosulfonyl group Chemical group 0.000 claims description 3
- 125000000278 alkyl amino alkyl group Chemical group 0.000 claims description 2
- 125000003282 alkyl amino group Chemical group 0.000 claims description 2
- 125000005119 alkyl cycloalkyl group Chemical group 0.000 claims description 2
- 125000000392 cycloalkenyl group Chemical group 0.000 claims description 2
- 125000000000 cycloalkoxy group Chemical group 0.000 claims description 2
- 125000006310 cycloalkyl amino group Chemical group 0.000 claims description 2
- 125000004985 dialkyl amino alkyl group Chemical group 0.000 claims description 2
- 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 claims 26
- 125000001424 substituent group Chemical group 0.000 claims 5
- 150000001875 compounds Chemical class 0.000 claims 4
- 125000004433 nitrogen atom Chemical group 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
- 125000004741 (C1-C6) haloalkylsulfonyl group Chemical group 0.000 claims 3
- 125000004457 alkyl amino carbonyl group Chemical group 0.000 claims 3
- 125000004448 alkyl carbonyl group Chemical group 0.000 claims 3
- 125000004692 haloalkylcarbonyl group Chemical group 0.000 claims 3
- 125000004665 trialkylsilyl group Chemical group 0.000 claims 3
- 125000004738 (C1-C6) alkyl sulfinyl group Chemical group 0.000 claims 2
- 125000004750 (C1-C6) alkylaminosulfonyl group Chemical group 0.000 claims 2
- 125000004845 (C1-C6) alkylsulfonylamino group Chemical group 0.000 claims 2
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 claims 2
- 125000004749 (C1-C6) haloalkylsulfinyl 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
- 125000006815 (C4-C10) cycloalkylaminocarbonyl group Chemical group 0.000 claims 2
- 125000006781 (C4-C10) cycloalkylcarbonyl group Chemical group 0.000 claims 2
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims 2
- 125000003806 alkyl carbonyl amino group Chemical group 0.000 claims 2
- 125000005196 alkyl carbonyloxy group Chemical group 0.000 claims 2
- 125000004688 alkyl sulfonyl alkyl group Chemical group 0.000 claims 2
- 125000002619 bicyclic group Chemical group 0.000 claims 2
- 150000001721 carbon Chemical group 0.000 claims 2
- 125000004432 carbon atom Chemical group C* 0.000 claims 2
- 125000004093 cyano group Chemical group *C#N 0.000 claims 2
- 125000005144 cycloalkylsulfonyl group Chemical group 0.000 claims 2
- 125000005366 cycloalkylthio group Chemical group 0.000 claims 2
- 239000003085 diluting agent Substances 0.000 claims 2
- 125000004994 halo alkoxy alkyl group Chemical group 0.000 claims 2
- 125000004993 haloalkoxycarbonyl group Chemical group 0.000 claims 2
- 229910052736 halogen Inorganic materials 0.000 claims 2
- 150000002367 halogens Chemical class 0.000 claims 2
- 125000005842 heteroatom Chemical group 0.000 claims 2
- 125000004434 sulfur atom Chemical group 0.000 claims 2
- SXUBVSXXRKXIQW-IUODEOHRSA-N (3R,4S)-4-(3-chlorophenyl)-N-(2,3-difluorophenyl)-2-oxopiperidine-3-carboxamide Chemical compound ClC=1C=C(C=CC=1)[C@@H]1[C@H](C(NCC1)=O)C(=O)NC1=C(C(=CC=C1)F)F SXUBVSXXRKXIQW-IUODEOHRSA-N 0.000 claims 1
- KSFKMZVIVWNXME-IUODEOHRSA-N (3R,4S)-N-(2,3-difluorophenyl)-2-oxo-4-[3-(trifluoromethyl)phenyl]piperidine-3-carboxamide Chemical compound FC1=C(C=CC=C1F)NC(=O)[C@H]1C(NCC[C@@H]1C1=CC(=CC=C1)C(F)(F)F)=O KSFKMZVIVWNXME-IUODEOHRSA-N 0.000 claims 1
- GHSUTCLEVLBVEL-IUODEOHRSA-N (3R,4S)-N-(2,3-difluorophenyl)-2-oxo-4-[4-(trifluoromethyl)phenyl]piperidine-3-carboxamide Chemical compound FC1=C(C=CC=C1F)NC(=O)[C@H]1C(NCC[C@@H]1C1=CC=C(C=C1)C(F)(F)F)=O GHSUTCLEVLBVEL-IUODEOHRSA-N 0.000 claims 1
- GERCBSOTQXAVBS-IUODEOHRSA-N (3R,4S)-N-(3-chloro-2-fluorophenyl)-2-oxo-4-[3-(trifluoromethyl)phenyl]piperidine-3-carboxamide Chemical compound ClC=1C(=C(C=CC=1)NC(=O)[C@H]1C(NCC[C@@H]1C1=CC(=CC=C1)C(F)(F)F)=O)F GERCBSOTQXAVBS-IUODEOHRSA-N 0.000 claims 1
- KNJJANUGPUMOGP-CJNGLKHVSA-N (3S,4S)-N-(2,3-difluorophenyl)-4-(4-fluorophenyl)-1-methyl-2-oxopiperidine-3-carboxamide Chemical compound FC1=C(C=CC=C1F)NC(=O)[C@H]1C(N(CC[C@@H]1C1=CC=C(C=C1)F)C)=O KNJJANUGPUMOGP-CJNGLKHVSA-N 0.000 claims 1
- 125000004890 (C1-C6) alkylamino group Chemical group 0.000 claims 1
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 claims 1
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 claims 1
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims 1
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims 1
- XTFIVUDBNACUBN-UHFFFAOYSA-N 1,3,5-trinitro-1,3,5-triazinane Chemical compound [O-][N+](=O)N1CN([N+]([O-])=O)CN([N+]([O-])=O)C1 XTFIVUDBNACUBN-UHFFFAOYSA-N 0.000 claims 1
- LTRLUOORVJPZDA-UHFFFAOYSA-N 2-oxo-4-[3-(trifluoromethyl)phenyl]-N-(2,3,4-trifluorophenyl)piperidine-3-carboxamide Chemical compound O=C1NCCC(C1C(=O)NC1=C(C(=C(C=C1)F)F)F)C1=CC(=CC=C1)C(F)(F)F LTRLUOORVJPZDA-UHFFFAOYSA-N 0.000 claims 1
- GSTKTRLJYUFJFV-UHFFFAOYSA-N 2-oxo-N-[2-(trifluoromethyl)phenyl]-4-[3-(trifluoromethyl)phenyl]piperidine-3-carboxamide Chemical compound O=C1NCCC(C1C(=O)NC1=C(C=CC=C1)C(F)(F)F)C1=CC(=CC=C1)C(F)(F)F GSTKTRLJYUFJFV-UHFFFAOYSA-N 0.000 claims 1
- SXUBVSXXRKXIQW-UHFFFAOYSA-N 4-(3-chlorophenyl)-N-(2,3-difluorophenyl)-2-oxopiperidine-3-carboxamide Chemical compound ClC=1C=C(C=CC=1)C1C(C(NCC1)=O)C(=O)NC1=C(C(=CC=C1)F)F SXUBVSXXRKXIQW-UHFFFAOYSA-N 0.000 claims 1
- JXKXEUHAXJIBBI-UHFFFAOYSA-N 4-[3-(difluoromethyl)phenyl]-N-(2,3-difluorophenyl)-2-oxopiperidine-3-carboxamide Chemical compound FC(C=1C=C(C=CC=1)C1C(C(NCC1)=O)C(=O)NC1=C(C(=CC=C1)F)F)F JXKXEUHAXJIBBI-UHFFFAOYSA-N 0.000 claims 1
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims 1
- 125000004648 C2-C8 alkenyl group Chemical group 0.000 claims 1
- 125000004649 C2-C8 alkynyl group Chemical group 0.000 claims 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 1
- KSFKMZVIVWNXME-UHFFFAOYSA-N N-(2,3-difluorophenyl)-2-oxo-4-[3-(trifluoromethyl)phenyl]piperidine-3-carboxamide Chemical compound FC1=C(C=CC=C1F)NC(=O)C1C(NCCC1C1=CC(=CC=C1)C(F)(F)F)=O KSFKMZVIVWNXME-UHFFFAOYSA-N 0.000 claims 1
- GHSUTCLEVLBVEL-UHFFFAOYSA-N N-(2,3-difluorophenyl)-2-oxo-4-[4-(trifluoromethyl)phenyl]piperidine-3-carboxamide Chemical compound FC1=C(C=CC=C1F)NC(=O)C1C(NCCC1C1=CC=C(C=C1)C(F)(F)F)=O GHSUTCLEVLBVEL-UHFFFAOYSA-N 0.000 claims 1
- 150000001204 N-oxides Chemical class 0.000 claims 1
- 125000005093 alkyl carbonyl alkyl group Chemical group 0.000 claims 1
- 125000005120 alkyl cycloalkyl alkyl group Chemical group 0.000 claims 1
- 125000005278 alkyl sulfonyloxy group Chemical group 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
- 125000002837 carbocyclic group Chemical group 0.000 claims 1
- 230000006315 carbonylation Effects 0.000 claims 1
- 238000005810 carbonylation reaction Methods 0.000 claims 1
- 125000005159 cyanoalkoxy group Chemical group 0.000 claims 1
- 125000004966 cyanoalkyl group Chemical group 0.000 claims 1
- 125000005357 cycloalkylalkynyl group Chemical group 0.000 claims 1
- 125000005201 cycloalkylcarbonyloxy group Chemical group 0.000 claims 1
- 125000005149 cycloalkylsulfinyl group Chemical group 0.000 claims 1
- 125000005221 halo alkyl carbonyl amino group Chemical group 0.000 claims 1
- 125000005280 halo alkyl sulfonyloxy group Chemical group 0.000 claims 1
- 125000000262 haloalkenyl group Chemical group 0.000 claims 1
- 125000005291 haloalkenyloxy group Chemical group 0.000 claims 1
- 125000004438 haloalkoxy group Chemical group 0.000 claims 1
- 125000001188 haloalkyl group Chemical group 0.000 claims 1
- 125000005203 haloalkylcarbonyloxy 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
- 125000004995 haloalkylthio group Chemical group 0.000 claims 1
- 125000000232 haloalkynyl group Chemical group 0.000 claims 1
- 125000005292 haloalkynyloxy group Chemical group 0.000 claims 1
- 125000005347 halocycloalkyl group Chemical group 0.000 claims 1
- 125000004461 halocycloalkylalkyl group Chemical group 0.000 claims 1
- 230000002363 herbicidal effect Effects 0.000 claims 1
- 125000004356 hydroxy functional group Chemical group O* 0.000 claims 1
- 239000007788 liquid Substances 0.000 claims 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 1
- 125000004971 nitroalkyl group Chemical group 0.000 claims 1
- GJVFBWCTGUSGDD-UHFFFAOYSA-L pentamethonium bromide Chemical compound [Br-].[Br-].C[N+](C)(C)CCCCC[N+](C)(C)C GJVFBWCTGUSGDD-UHFFFAOYSA-L 0.000 claims 1
- 125000003170 phenylsulfonyl group Chemical group C1(=CC=CC=C1)S(=O)(=O)* 0.000 claims 1
- 125000006513 pyridinyl methyl group Chemical group 0.000 claims 1
- 125000004076 pyridyl group Chemical group 0.000 claims 1
- 150000003839 salts Chemical class 0.000 claims 1
- 239000007787 solid Substances 0.000 claims 1
- 229910052717 sulfur Inorganic materials 0.000 claims 1
- 239000004094 surface-active agent Substances 0.000 claims 1
- 125000001544 thienyl group Chemical group 0.000 claims 1
- 238000006467 substitution reaction Methods 0.000 description 8
- GVNVAWHJIKLAGL-UHFFFAOYSA-N 2-(cyclohexen-1-yl)cyclohexan-1-one Chemical compound O=C1CCCCC1C1=CCCCC1 GVNVAWHJIKLAGL-UHFFFAOYSA-N 0.000 description 4
- 101150065749 Churc1 gene Proteins 0.000 description 4
- 102100038239 Protein Churchill Human genes 0.000 description 4
- 125000004430 oxygen atom Chemical group O* 0.000 description 2
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 description 1
- SSUFDOMYCBCHML-UHFFFAOYSA-N CCCCC[S](=O)=O Chemical class CCCCC[S](=O)=O SSUFDOMYCBCHML-UHFFFAOYSA-N 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- 125000000596 cyclohexenyl group Chemical group C1(=CCCCC1)* 0.000 description 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 125000002933 cyclohexyloxy group Chemical group C1(CCCCC1)O* 0.000 description 1
- 125000002433 cyclopentenyl group Chemical group C1(=CCCC1)* 0.000 description 1
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- 125000001887 cyclopentyloxy group Chemical group C1(CCCC1)O* 0.000 description 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 1
- 125000004186 cyclopropylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C1([H])[H] 0.000 description 1
- 125000003707 hexyloxy group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])O* 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201462020140P | 2014-07-02 | 2014-07-02 | |
| US62/020,140 | 2014-07-02 | ||
| PCT/US2015/038473 WO2016003997A1 (en) | 2014-07-02 | 2015-06-30 | Piperidinone herbicides |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2020093072A Division JP7088984B2 (ja) | 2014-07-02 | 2020-05-28 | ピペリジノン除草剤 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2017522374A JP2017522374A (ja) | 2017-08-10 |
| JP2017522374A5 true JP2017522374A5 (enExample) | 2019-10-03 |
Family
ID=53511066
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2017521023A Pending JP2017522374A (ja) | 2014-07-02 | 2015-06-30 | ピペリジノン除草剤 |
| JP2020093072A Expired - Fee Related JP7088984B2 (ja) | 2014-07-02 | 2020-05-28 | ピペリジノン除草剤 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2020093072A Expired - Fee Related JP7088984B2 (ja) | 2014-07-02 | 2020-05-28 | ピペリジノン除草剤 |
Country Status (21)
| Country | Link |
|---|---|
| US (1) | US9944602B2 (enExample) |
| EP (1) | EP3164386B1 (enExample) |
| JP (2) | JP2017522374A (enExample) |
| KR (1) | KR102479858B1 (enExample) |
| CN (1) | CN106715412B (enExample) |
| AR (1) | AR101102A1 (enExample) |
| AU (1) | AU2015284280C1 (enExample) |
| BR (1) | BR112016030930B1 (enExample) |
| CA (1) | CA2953548C (enExample) |
| CL (1) | CL2016003416A1 (enExample) |
| EA (1) | EA032798B1 (enExample) |
| IL (1) | IL249699B (enExample) |
| MX (1) | MX389921B (enExample) |
| MY (1) | MY178627A (enExample) |
| PE (1) | PE20170444A1 (enExample) |
| PH (1) | PH12016502594A1 (enExample) |
| SG (1) | SG11201610720VA (enExample) |
| TW (1) | TWI691487B (enExample) |
| UA (1) | UA125012C2 (enExample) |
| UY (1) | UY36201A (enExample) |
| WO (1) | WO2016003997A1 (enExample) |
Families Citing this family (24)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US11589583B2 (en) | 2013-12-03 | 2023-02-28 | Fmc Corporation | Pyrrolidinones herbicides |
| HUE049827T2 (hu) | 2013-12-03 | 2020-10-28 | Fmc Corp | Pirrolidinonok mint herbicidek |
| AU2015361018B2 (en) | 2014-12-08 | 2020-01-16 | Fmc Corporation | 3-oxo-3-(arylamino)propanoates, a process for their preparation, and their use in preparing pyrrolidinones |
| AU2016246410B2 (en) * | 2015-04-10 | 2020-11-05 | Fmc Corporation | Substituted cyclic amides as herbicides |
| BR112017020094B1 (pt) | 2015-04-27 | 2022-01-11 | Fmc Corporation | Composto, composições herbicidas, mistura de herbicida e método para controlar o crescimento de vegetação indesejada |
| WO2016182780A1 (en) | 2015-05-12 | 2016-11-17 | E I Du Pont De Nemours And Company | Aryl substituted bicyclic compounds as herbicides |
| JP6869192B2 (ja) | 2015-05-29 | 2021-05-12 | エフ エム シー コーポレーションＦｍｃ Ｃｏｒｐｏｒａｔｉｏｎ | 除草剤としての置換環状アミド |
| RU2017142979A (ru) | 2015-06-02 | 2019-07-15 | ЭфЭмСи Корпорейшн | Замещенные циклические амиды и их применение в качестве гербицидов |
| CA2993000C (en) | 2015-07-31 | 2024-01-23 | E.I. Du Pont De Nemours & Company | Cyclic n-carboxamide compounds useful as herbicides |
| GB201617062D0 (en) | 2016-10-07 | 2016-11-23 | Syngenta Participations Ag | Herbicidal mixtures |
| US11447455B2 (en) | 2016-12-20 | 2022-09-20 | Fmc Corporation | Polymorphs of herbicidal sulfonamides |
| AU2017378640B2 (en) * | 2016-12-21 | 2022-03-03 | Fmc Corporation | Nitrone herbicides |
| US20210051963A1 (en) * | 2017-03-14 | 2021-02-25 | PlantResponse Biotech, S.L. | Methods and compositions to improve plant health and/or plant performance |
| WO2018175231A1 (en) | 2017-03-21 | 2018-09-27 | Fmc Corporation | Herbicidal mixture, composition and method |
| JP7201609B2 (ja) | 2017-03-21 | 2023-01-10 | エフ エム シー コーポレーション | ピロリジノン及びこれらを調製するためのプロセス |
| WO2018178012A1 (de) * | 2017-03-30 | 2018-10-04 | Bayer Aktiengesellschaft | N-benzyl-2-oxo-4-phenyl-piperidin-3-carboxamid-derivate und verwandte verbindungen als herbizide pflanzenschutzmittel |
| WO2018178010A1 (de) * | 2017-03-30 | 2018-10-04 | Bayer Aktiengesellschaft | N-cyclopropyl-2-oxo-4-phenyl-piperidin-3-carboxamid-derivate und verwandte verbindungen als herbizide pflanzenschutzmittel |
| WO2018177836A1 (de) | 2017-03-30 | 2018-10-04 | Bayer Aktiengesellschaft | N-cyclopropyl-2-oxopyrrolidin-3-carboxamid-derivate und verwandte verbindungen als herbizide pflanzenschutzmittel |
| WO2018177837A1 (de) | 2017-03-30 | 2018-10-04 | Bayer Aktiengesellschaft | 4-cyclopentyl- und 4-cyclopropyl-2-oxopyrrolidin-3-carboxami d-derivate und verwandte verbindungen als herbizide pflanzenschutzmittel |
| WO2018184891A1 (de) * | 2017-04-05 | 2018-10-11 | Bayer Aktiengesellschaft | 4-substituierte n-amino und n-hydroxy 2-oxo-piperidin-3-carboxamid-derivate, deren salze und ihre verwendung als herbizide wirkstoffe |
| AR111967A1 (es) | 2017-05-30 | 2019-09-04 | Fmc Corp | Amidas herbicidas |
| AR111839A1 (es) * | 2017-05-30 | 2019-08-21 | Fmc Corp | Lactamas 3-sustituidas herbicidas |
| CN110934149B (zh) * | 2018-09-21 | 2021-03-02 | 华中师范大学 | 含氯酰草膦除草剂的微乳剂制剂及其制备方法和应用 |
| CN118401112A (zh) | 2021-12-15 | 2024-07-26 | 安道麦阿甘有限公司 | 用于制备各种农用化学品的化合物及其标记 |
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