JP2018522832A5 - - Google Patents
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- Publication number
- JP2018522832A5 JP2018522832A5 JP2017562771A JP2017562771A JP2018522832A5 JP 2018522832 A5 JP2018522832 A5 JP 2018522832A5 JP 2017562771 A JP2017562771 A JP 2017562771A JP 2017562771 A JP2017562771 A JP 2017562771A JP 2018522832 A5 JP2018522832 A5 JP 2018522832A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- cycloalkyl
- independently
- alkoxy
- haloalkyl
- 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
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- -1 hydroxy, amino Chemical group 0.000 claims description 108
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 94
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims description 93
- 125000001316 cycloalkyl alkyl group Chemical group 0.000 claims description 87
- 125000004665 trialkylsilyl group Chemical group 0.000 claims description 85
- 125000001424 substituent group Chemical group 0.000 claims description 84
- 125000004994 halo alkoxy alkyl group Chemical group 0.000 claims description 79
- 125000004687 alkyl sulfinyl alkyl group Chemical group 0.000 claims description 78
- 125000006350 alkyl thio alkyl group Chemical group 0.000 claims description 77
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 76
- 125000004448 alkyl carbonyl group Chemical group 0.000 claims description 75
- 125000004122 cyclic group Chemical group 0.000 claims description 73
- 125000004688 alkyl sulfonyl alkyl group Chemical group 0.000 claims description 70
- 125000004692 haloalkylcarbonyl group Chemical group 0.000 claims description 63
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 63
- 125000004473 dialkylaminocarbonyl group Chemical group 0.000 claims description 62
- 125000004457 alkyl amino carbonyl group Chemical group 0.000 claims description 61
- 229910052799 carbon Inorganic materials 0.000 claims description 61
- 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 description 58
- 125000005144 cycloalkylsulfonyl group Chemical group 0.000 claims description 54
- 125000004993 haloalkoxycarbonyl group Chemical group 0.000 claims description 53
- 125000004434 sulfur atom Chemical group 0.000 claims description 51
- 125000004472 dialkylaminosulfonyl group Chemical group 0.000 claims description 50
- 229910052739 hydrogen Inorganic materials 0.000 claims description 48
- 150000001721 carbon Chemical group 0.000 claims description 46
- 125000005149 cycloalkylsulfinyl group Chemical group 0.000 claims description 46
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 44
- 125000006254 cycloalkyl carbonyl group Chemical group 0.000 claims description 39
- 229910052736 halogen Inorganic materials 0.000 claims description 39
- 150000002367 halogens Chemical class 0.000 claims description 39
- 150000001875 compounds Chemical class 0.000 claims description 36
- 125000005167 cycloalkylaminocarbonyl group Chemical group 0.000 claims description 35
- 125000005366 cycloalkylthio group Chemical group 0.000 claims description 34
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 33
- 125000005842 heteroatom Chemical group 0.000 claims description 33
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims description 32
- 125000002619 bicyclic group Chemical group 0.000 claims description 27
- 125000004432 carbon atom Chemical group C* 0.000 claims description 27
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 26
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 25
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 24
- 125000000392 cycloalkenyl group Chemical group 0.000 claims description 24
- 125000000623 heterocyclic group Chemical group 0.000 claims description 24
- 125000005081 alkoxyalkoxyalkyl group Chemical group 0.000 claims description 23
- 125000000262 haloalkenyl group Chemical group 0.000 claims description 23
- 125000000232 haloalkynyl group Chemical group 0.000 claims description 23
- 229910052717 sulfur Inorganic materials 0.000 claims description 22
- 125000006546 (C4-C10) cycloalkyl group Chemical group 0.000 claims description 19
- 150000001204 N-oxides Chemical class 0.000 claims description 19
- 125000005083 alkoxyalkoxy group Chemical group 0.000 claims description 16
- 125000005196 alkyl carbonyloxy group Chemical group 0.000 claims description 16
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims description 16
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 16
- 125000000000 cycloalkoxy group Chemical group 0.000 claims description 16
- 125000004663 dialkyl amino group Chemical group 0.000 claims description 16
- 125000006781 (C4-C10) cycloalkylcarbonyl group Chemical group 0.000 claims description 15
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 15
- 125000003806 alkyl carbonyl amino group Chemical group 0.000 claims description 15
- 239000011593 sulfur Substances 0.000 claims description 15
- 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 description 14
- 150000003839 salts Chemical class 0.000 claims description 14
- 125000004845 (C1-C6) alkylsulfonylamino group Chemical group 0.000 claims description 12
- 125000004076 pyridyl group Chemical group 0.000 claims description 10
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 claims description 9
- 125000004466 alkoxycarbonylamino group Chemical group 0.000 claims description 9
- 125000004440 haloalkylsulfinyl group Chemical group 0.000 claims description 9
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 claims description 8
- 125000006771 (C1-C6) haloalkylthio group Chemical group 0.000 claims description 8
- 125000006432 1-methyl cyclopropyl group Chemical group [H]C([H])([H])C1(*)C([H])([H])C1([H])[H] 0.000 claims description 8
- 125000004648 C2-C8 alkenyl group Chemical group 0.000 claims description 8
- 125000004649 C2-C8 alkynyl group Chemical group 0.000 claims description 8
- 125000003545 alkoxy group Chemical group 0.000 claims description 8
- 125000003282 alkyl amino group Chemical group 0.000 claims description 8
- 125000005093 alkyl carbonyl alkyl group Chemical group 0.000 claims description 8
- 125000005120 alkyl cycloalkyl alkyl group Chemical group 0.000 claims description 8
- 125000000217 alkyl group Chemical group 0.000 claims description 8
- 125000004644 alkyl sulfinyl group Chemical group 0.000 claims description 8
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims description 8
- 125000005278 alkyl sulfonyloxy group Chemical group 0.000 claims description 8
- 125000004414 alkyl thio group Chemical group 0.000 claims description 8
- 125000002947 alkylene group Chemical group 0.000 claims description 8
- 125000005133 alkynyloxy group Chemical group 0.000 claims description 8
- 125000004429 atom Chemical group 0.000 claims description 8
- 125000005159 cyanoalkoxy group Chemical group 0.000 claims description 8
- 125000004966 cyanoalkyl group Chemical group 0.000 claims description 8
- 125000004858 cycloalkoxyalkyl group Chemical group 0.000 claims description 8
- 125000006310 cycloalkyl amino group Chemical group 0.000 claims description 8
- 125000006448 cycloalkyl cycloalkyl group Chemical group 0.000 claims description 8
- 125000005112 cycloalkylalkoxy group Chemical group 0.000 claims description 8
- 125000004985 dialkyl amino alkyl group Chemical group 0.000 claims description 8
- 125000005221 halo alkyl carbonyl amino group Chemical group 0.000 claims description 8
- 125000005280 halo alkyl sulfonyloxy group Chemical group 0.000 claims description 8
- 125000004438 haloalkoxy group Chemical group 0.000 claims description 8
- 125000001188 haloalkyl group Chemical group 0.000 claims description 8
- 125000005203 haloalkylcarbonyloxy group Chemical group 0.000 claims description 8
- 125000004441 haloalkylsulfonyl group Chemical group 0.000 claims description 8
- 125000005347 halocycloalkyl group Chemical group 0.000 claims description 8
- 125000004461 halocycloalkylalkyl group Chemical group 0.000 claims description 8
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 8
- 125000004971 nitroalkyl group Chemical group 0.000 claims description 8
- 125000003170 phenylsulfonyl group Chemical group C1(=CC=CC=C1)S(=O)(=O)* 0.000 claims description 8
- 125000006513 pyridinyl methyl group Chemical group 0.000 claims description 8
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims description 7
- 125000004749 (C1-C6) haloalkylsulfinyl group Chemical group 0.000 claims description 7
- 125000005292 haloalkynyloxy group Chemical group 0.000 claims description 7
- 229910052760 oxygen Inorganic materials 0.000 claims description 7
- 125000006815 (C4-C10) cycloalkylaminocarbonyl group Chemical group 0.000 claims description 6
- 230000008878 coupling Effects 0.000 claims description 6
- 238000010168 coupling process Methods 0.000 claims description 6
- 238000005859 coupling reaction Methods 0.000 claims description 6
- 125000001544 thienyl group Chemical group 0.000 claims description 6
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 claims description 5
- 125000006374 C2-C10 alkenyl group Chemical group 0.000 claims description 4
- 125000005865 C2-C10alkynyl group Chemical group 0.000 claims description 4
- CRZSWQNUVZTVTQ-UHFFFAOYSA-N N-(benzotriazol-1-yl)-2-oxo-4-phenylpyrrolidine-3-carboxamide Chemical compound N1(N=NC2=C1C=CC=C2)NC(=O)C1C(NCC1C1=CC=CC=C1)=O CRZSWQNUVZTVTQ-UHFFFAOYSA-N 0.000 claims description 4
- 125000000278 alkyl amino alkyl group Chemical group 0.000 claims description 4
- 125000004984 dialkylaminoalkoxy group Chemical group 0.000 claims description 4
- 125000005843 halogen group Chemical group 0.000 claims description 2
- 125000004356 hydroxy functional group Chemical group O* 0.000 claims 29
- 239000003112 inhibitor Substances 0.000 claims 15
- 125000004741 (C1-C6) haloalkylsulfonyl group Chemical group 0.000 claims 12
- 125000003342 alkenyl group Chemical group 0.000 claims 11
- 125000000304 alkynyl group Chemical group 0.000 claims 11
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 11
- 125000004750 (C1-C6) alkylaminosulfonyl group Chemical group 0.000 claims 8
- 239000004009 herbicide Substances 0.000 claims 8
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 claims 7
- 125000006665 (C2 to C4) alkoxycarbonyl group Chemical group 0.000 claims 7
- 125000004186 cyclopropylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C1([H])[H] 0.000 claims 7
- 125000004995 haloalkylthio group Chemical group 0.000 claims 7
- 229910052757 nitrogen Inorganic materials 0.000 claims 7
- 125000003302 alkenyloxy group Chemical group 0.000 claims 6
- 230000002363 herbicidal effect Effects 0.000 claims 6
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 6
- 239000000203 mixture Substances 0.000 claims 5
- 125000004938 5-pyridyl group Chemical group N1=CC=CC(=C1)* 0.000 claims 4
- 125000003418 alkyl amino alkoxy group Chemical group 0.000 claims 4
- 108010068327 4-hydroxyphenylpyruvate dioxygenase Proteins 0.000 claims 3
- 102100028626 4-hydroxyphenylpyruvate dioxygenase Human genes 0.000 claims 3
- 239000004480 active ingredient Substances 0.000 claims 3
- 125000005291 haloalkenyloxy group Chemical group 0.000 claims 3
- 150000004669 very long chain fatty acids Chemical class 0.000 claims 3
- 102000000452 Acetyl-CoA carboxylase Human genes 0.000 claims 2
- 108010016219 Acetyl-CoA carboxylase Proteins 0.000 claims 2
- 108010018763 Biotin carboxylase Proteins 0.000 claims 2
- 108020001991 Protoporphyrinogen Oxidase Proteins 0.000 claims 2
- 102000005135 Protoporphyrinogen oxidase Human genes 0.000 claims 2
- 125000005201 cycloalkylcarbonyloxy group Chemical group 0.000 claims 2
- 102000005396 glutamine synthetase Human genes 0.000 claims 2
- 108020002326 glutamine synthetase Proteins 0.000 claims 2
- 125000006769 halocycloalkoxy group Chemical group 0.000 claims 2
- 238000000034 method Methods 0.000 claims 2
- FBUKVWPVBMHYJY-UHFFFAOYSA-N nonanoic acid Chemical compound CCCCCCCCC(O)=O FBUKVWPVBMHYJY-UHFFFAOYSA-N 0.000 claims 2
- LCDCPQHFCOBUEF-UHFFFAOYSA-N pyrrolidine-1-carboxamide Chemical compound NC(=O)N1CCCC1 LCDCPQHFCOBUEF-UHFFFAOYSA-N 0.000 claims 2
- 230000001988 toxicity Effects 0.000 claims 2
- 231100000419 toxicity Toxicity 0.000 claims 2
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 claims 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 claims 1
- 125000001963 4 membered heterocyclic group Chemical group 0.000 claims 1
- 125000003341 7 membered heterocyclic group Chemical group 0.000 claims 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 claims 1
- 229930192334 Auxin Natural products 0.000 claims 1
- NNYRZQHKCHEXSD-UHFFFAOYSA-N Daimuron Chemical compound C1=CC(C)=CC=C1NC(=O)NC(C)(C)C1=CC=CC=C1 NNYRZQHKCHEXSD-UHFFFAOYSA-N 0.000 claims 1
- 108010028143 Dioxygenases Proteins 0.000 claims 1
- 102000016680 Dioxygenases Human genes 0.000 claims 1
- 229940106987 Elongase inhibitor Drugs 0.000 claims 1
- ICWUMLXQKFTJMH-UHFFFAOYSA-N Etobenzanid Chemical compound C1=CC(OCOCC)=CC=C1C(=O)NC1=CC=CC(Cl)=C1Cl ICWUMLXQKFTJMH-UHFFFAOYSA-N 0.000 claims 1
- GXAMYUGOODKVRM-UHFFFAOYSA-N Flurecol Chemical compound C1=CC=C2C(C(=O)O)(O)C3=CC=CC=C3C2=C1 GXAMYUGOODKVRM-UHFFFAOYSA-N 0.000 claims 1
- 239000002169 Metam Substances 0.000 claims 1
- FMINYZXVCTYSNY-UHFFFAOYSA-N Methyldymron Chemical compound C=1C=CC=CC=1N(C)C(=O)NC(C)(C)C1=CC=CC=C1 FMINYZXVCTYSNY-UHFFFAOYSA-N 0.000 claims 1
- 239000005642 Oleic acid Substances 0.000 claims 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 claims 1
- 229910019142 PO4 Inorganic materials 0.000 claims 1
- 239000005643 Pelargonic acid Substances 0.000 claims 1
- 239000002253 acid Substances 0.000 claims 1
- 125000004694 alkoxyaminocarbonyl group Chemical group 0.000 claims 1
- 229910052785 arsenic Inorganic materials 0.000 claims 1
- RQNWIZPPADIBDY-UHFFFAOYSA-N arsenic atom Chemical compound [As] RQNWIZPPADIBDY-UHFFFAOYSA-N 0.000 claims 1
- 125000005129 aryl carbonyl group Chemical group 0.000 claims 1
- 239000002363 auxin Substances 0.000 claims 1
- WZDDLAZXUYIVMU-UHFFFAOYSA-N bromobutide Chemical compound CC(C)(C)C(Br)C(=O)NC(C)(C)C1=CC=CC=C1 WZDDLAZXUYIVMU-UHFFFAOYSA-N 0.000 claims 1
- 230000008166 cellulose biosynthesis Effects 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 claims 1
- 239000003085 diluting agent Substances 0.000 claims 1
- 230000004992 fission Effects 0.000 claims 1
- SEOVTRFCIGRIMH-UHFFFAOYSA-N indole-3-acetic acid Chemical compound C1=CC=C2C(CC(=O)O)=CNC2=C1 SEOVTRFCIGRIMH-UHFFFAOYSA-N 0.000 claims 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 claims 1
- 239000007788 liquid Substances 0.000 claims 1
- HYVVJDQGXFXBRZ-UHFFFAOYSA-N metam Chemical compound CNC(S)=S HYVVJDQGXFXBRZ-UHFFFAOYSA-N 0.000 claims 1
- 230000003278 mimic effect Effects 0.000 claims 1
- 230000000116 mitigating effect Effects 0.000 claims 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 claims 1
- 239000010452 phosphate Substances 0.000 claims 1
- MCJGNVYPOGVAJF-UHFFFAOYSA-N quinolin-8-ol Chemical compound C1=CN=C2C(O)=CC=CC2=C1 MCJGNVYPOGVAJF-UHFFFAOYSA-N 0.000 claims 1
- 239000007787 solid Substances 0.000 claims 1
- 239000004094 surface-active agent Substances 0.000 claims 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 4
- 125000002768 hydroxyalkyl group Chemical group 0.000 description 2
- 125000004738 (C1-C6) alkyl sulfinyl group Chemical group 0.000 description 1
- 125000003682 3-furyl group Chemical group O1C([H])=C([*])C([H])=C1[H] 0.000 description 1
- 125000004471 alkyl aminosulfonyl group Chemical group 0.000 description 1
- 125000005119 alkyl cycloalkyl group Chemical group 0.000 description 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 1
- CMWTZPSULFXXJA-VIFPVBQESA-N naproxen Chemical group C1=C([C@H](C)C(O)=O)C=CC2=CC(OC)=CC=C21 CMWTZPSULFXXJA-VIFPVBQESA-N 0.000 description 1
- GJVFBWCTGUSGDD-UHFFFAOYSA-L pentamethonium bromide Chemical compound [Br-].[Br-].C[N+](C)(C)CCCCC[N+](C)(C)C GJVFBWCTGUSGDD-UHFFFAOYSA-L 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
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201562170129P | 2015-06-02 | 2015-06-02 | |
| US62/170,129 | 2015-06-02 | ||
| PCT/US2016/035214 WO2016196593A1 (en) | 2015-06-02 | 2016-06-01 | Substituted cyclic amides and their use as herbicides |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2018522832A JP2018522832A (ja) | 2018-08-16 |
| JP2018522832A5 true JP2018522832A5 (enExample) | 2020-11-12 |
| JP6949730B2 JP6949730B2 (ja) | 2021-10-13 |
Family
ID=56118067
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2017562771A Active JP6949730B2 (ja) | 2015-06-02 | 2016-06-01 | 置換環状アミドおよび除草剤としてのそれらの使用 |
Country Status (9)
| Country | Link |
|---|---|
| US (4) | US10654804B2 (enExample) |
| EP (1) | EP3303321A1 (enExample) |
| JP (1) | JP6949730B2 (enExample) |
| CN (1) | CN107709310B (enExample) |
| AR (1) | AR104866A1 (enExample) |
| AU (1) | AU2016271374B2 (enExample) |
| CA (1) | CA2983759A1 (enExample) |
| RU (1) | RU2017142979A (enExample) |
| WO (1) | WO2016196593A1 (enExample) |
Families Citing this family (40)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| MX2016007259A (es) | 2013-12-03 | 2016-08-04 | Du Pont | Pirrolidinonas como herbicidas. |
| US11589583B2 (en) | 2013-12-03 | 2023-02-28 | Fmc Corporation | Pyrrolidinones herbicides |
| US9944602B2 (en) | 2014-07-02 | 2018-04-17 | E. I. Du Pont De Nemours And Company | Piperidinone herbicides |
| EP3230264B1 (en) * | 2014-12-08 | 2019-09-11 | FMC Corporation | 3-oxo-3-(arylamino)propanoates, a process for their preparation, and their use in preparing pyrrolidinones |
| EP3280709B1 (en) | 2015-04-10 | 2021-05-26 | FMC Corporation | Substituted cyclic amides as herbicides |
| CN107531658B (zh) | 2015-04-27 | 2021-07-27 | Fmc公司 | 作为除草剂的丁内酯 |
| PL3294743T3 (pl) | 2015-05-12 | 2020-03-31 | Fmc Corporation | Podstawione arylem związki bicykliczne jako środki chwastobójcze |
| WO2016196019A1 (en) | 2015-05-29 | 2016-12-08 | E I Du Pont De Nemours And Company | Substituted cyclic amides as herbicides |
| CN107709310B (zh) | 2015-06-02 | 2021-09-24 | Fmc公司 | 取代的环酰胺及其作为除草剂的用途 |
| CN108137512B (zh) | 2015-07-31 | 2022-05-31 | Fmc公司 | 用作除草剂的环状n-酰胺化合物 |
| CA3047724A1 (en) | 2016-12-21 | 2018-06-28 | Fmc Corporation | Nitrone herbicides |
| CA3057297A1 (en) * | 2017-03-21 | 2018-09-27 | Fmc Corporation | Pyrrolidinones and a process to prepare them |
| WO2018175231A1 (en) * | 2017-03-21 | 2018-09-27 | Fmc Corporation | Herbicidal mixture, composition and method |
| WO2018178014A1 (de) * | 2017-03-30 | 2018-10-04 | Bayer Aktiengesellschaft | 4-cyclopropyl-2-oxopyrrolidin-3-carboxamid-derivate und verwandte verbindungen als herbizide pflanzenschutzmittel |
| WO2018178008A1 (de) * | 2017-03-30 | 2018-10-04 | Bayer Aktiengesellschaft | Substituierte isoazolidin-5-one sowie deren salze und ihre verwendung als herbizide wirkstoffe |
| 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 |
| 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 |
| WO2019025156A1 (de) | 2017-08-03 | 2019-02-07 | Bayer Aktiengesellschaft | Substituierte pyrrolidinone sowie deren salze und ihre verwendung als herbizide wirkstoffe |
| WO2019179928A1 (de) * | 2018-03-20 | 2019-09-26 | Bayer Aktiengesellschaft | Substituierte succinimid-3-carboxamide sowie deren salze und ihre verwendung als herbizide wirkstoffe |
| WO2020064260A1 (de) | 2018-09-24 | 2020-04-02 | Bayer Aktiengesellschaft | Substituierte 5-(sulfanyl)-3,4-dihydro-2h-pyrrol-4-carboxamide sowie deren salze und ihre verwendung als herbizide wirkstoffe |
| CA3121202A1 (en) | 2018-11-30 | 2020-06-04 | Nuvation Bio Inc. | Pyrrole and pyrazole compounds and methods of use thereof |
| GB201901559D0 (en) * | 2019-02-05 | 2019-03-27 | Syngenta Crop Protection Ag | Herbicidal compositions |
| JP2022532929A (ja) * | 2019-05-24 | 2022-07-20 | エフ エム シー コーポレーション | 除草剤としてのピラゾール－置換されたピロリジノン |
| BR112022010924A2 (pt) | 2019-12-06 | 2022-09-06 | Vertex Pharma | Tetra-hidrofuranos substituídos como moduladores de canais de sódio |
| GB202012143D0 (en) * | 2020-08-05 | 2020-09-16 | Syngenta Crop Protection Ag | Herbicidal compounds |
| GB202012651D0 (en) * | 2020-08-13 | 2020-09-30 | Syngenta Crop Protection Ag | Herbicidal compositions |
| GB202016569D0 (en) * | 2020-10-19 | 2020-12-02 | Syngenta Crop Protection Ag | Herbicidal compositions |
| GB202016568D0 (en) * | 2020-10-19 | 2020-12-02 | Syngenta Crop Protection Ag | Herbicidal compositions |
| EP4337014A1 (en) * | 2021-05-10 | 2024-03-20 | Syngenta Crop Protection AG | Herbicidal compositions |
| SMT202500481T1 (it) | 2021-06-04 | 2026-01-12 | Vertex Pharma | N-(idrossialchil(etero)aril)tetraidrofuran carbossammidi come modulatori di canali del sodio |
| CN113475508B (zh) * | 2021-08-27 | 2023-08-08 | 青岛奥迪斯生物科技有限公司 | 一种除草组合物 |
| EP4508980A3 (en) | 2021-12-15 | 2025-07-16 | Adama Agan Ltd. | Compounds useful for the preparation of various agrochemicals and markers thereof |
| WO2023222834A1 (en) | 2022-05-20 | 2023-11-23 | Syngenta Crop Protection Ag | Herbicidal compositions |
| CN118496201A (zh) * | 2023-02-16 | 2024-08-16 | 青岛清原化合物有限公司 | 一种取代的吡咯烷酮类化合物及其制备方法、除草组合物和应用 |
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2016
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- 2016-06-01 AU AU2016271374A patent/AU2016271374B2/en active Active
- 2016-06-01 RU RU2017142979A patent/RU2017142979A/ru unknown
- 2016-06-01 WO PCT/US2016/035214 patent/WO2016196593A1/en not_active Ceased
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