JP2014533254A - 置換型１，２，５−オキサジアゾール化合物及びその除草剤としての使用 - Google Patents
置換型１，２，５−オキサジアゾール化合物及びその除草剤としての使用 Download PDFInfo
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- JP2014533254A JP2014533254A JP2014540513A JP2014540513A JP2014533254A JP 2014533254 A JP2014533254 A JP 2014533254A JP 2014540513 A JP2014540513 A JP 2014540513A JP 2014540513 A JP2014540513 A JP 2014540513A JP 2014533254 A JP2014533254 A JP 2014533254A
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- JP
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- Prior art keywords
- alkyl
- isoxazolinyl
- group
- 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.)
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- 150000002244 furazanes Chemical class 0.000 title claims abstract description 6
- 239000004009 herbicide Substances 0.000 title description 20
- -1 1,2,5-oxadiazole compound Chemical class 0.000 claims abstract description 701
- 150000001875 compounds Chemical class 0.000 claims abstract description 230
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 108
- 229910052736 halogen Inorganic materials 0.000 claims abstract description 107
- 150000002367 halogens Chemical class 0.000 claims abstract description 104
- 239000001257 hydrogen Substances 0.000 claims abstract description 91
- 239000000203 mixture Substances 0.000 claims abstract description 85
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims abstract description 75
- 150000002431 hydrogen Chemical class 0.000 claims abstract description 69
- 150000003839 salts Chemical class 0.000 claims abstract description 55
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims abstract description 46
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims abstract description 45
- 125000006643 (C2-C6) haloalkenyl group Chemical group 0.000 claims abstract description 37
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims abstract description 37
- 150000001204 N-oxides Chemical class 0.000 claims abstract description 21
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims abstract description 21
- 125000004093 cyano group Chemical group *C#N 0.000 claims abstract description 14
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 claims abstract description 7
- 125000004649 C2-C8 alkynyl group Chemical group 0.000 claims abstract description 7
- 125000006766 (C2-C6) alkynyloxy group Chemical group 0.000 claims abstract description 5
- 125000003320 C2-C6 alkenyloxy group Chemical group 0.000 claims abstract description 5
- 125000004648 C2-C8 alkenyl group Chemical group 0.000 claims abstract description 5
- 125000001181 organosilyl group Chemical group [SiH3]* 0.000 claims abstract description 3
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 238
- 125000000623 heterocyclic group Chemical group 0.000 claims description 89
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 79
- 239000000460 chlorine Substances 0.000 claims description 71
- 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 66
- 229910052757 nitrogen Inorganic materials 0.000 claims description 58
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 41
- 229910052801 chlorine Inorganic materials 0.000 claims description 41
- 229910052760 oxygen Inorganic materials 0.000 claims description 41
- 229910052731 fluorine Inorganic materials 0.000 claims description 40
- 229920006395 saturated elastomer Polymers 0.000 claims description 40
- 229910052717 sulfur Inorganic materials 0.000 claims description 40
- 125000005842 heteroatom Chemical group 0.000 claims description 38
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 claims description 33
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 26
- 125000002950 monocyclic group Chemical group 0.000 claims description 25
- 125000000217 alkyl group Chemical group 0.000 claims description 23
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 23
- YUCFVHQCAFKDQG-UHFFFAOYSA-N fluoromethane Chemical compound F[CH] YUCFVHQCAFKDQG-UHFFFAOYSA-N 0.000 claims description 22
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 21
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 17
- 229910052799 carbon Inorganic materials 0.000 claims description 16
- 125000003545 alkoxy group Chemical group 0.000 claims description 15
- 125000002619 bicyclic group Chemical group 0.000 claims description 15
- 239000011737 fluorine Substances 0.000 claims description 15
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 14
- 125000001188 haloalkyl group Chemical group 0.000 claims description 14
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 14
- 125000006656 (C2-C4) alkenyl group Chemical group 0.000 claims description 13
- 125000004438 haloalkoxy group Chemical group 0.000 claims description 13
- 125000006615 aromatic heterocyclic group Chemical group 0.000 claims description 12
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 12
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 12
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 12
- 125000006650 (C2-C4) alkynyl group Chemical group 0.000 claims description 10
- 239000002671 adjuvant Substances 0.000 claims description 10
- 239000003905 agrochemical Substances 0.000 claims description 10
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 9
- 125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 claims description 9
- 238000006467 substitution reaction Methods 0.000 claims description 7
- 125000004122 cyclic group Chemical group 0.000 claims description 6
- 125000000842 isoxazolyl group Chemical group 0.000 claims description 6
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims description 5
- 125000004429 atom Chemical group 0.000 claims description 4
- 125000005844 heterocyclyloxy group Chemical group 0.000 claims description 4
- 125000003971 isoxazolinyl group Chemical group 0.000 claims description 4
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims description 3
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 3
- 125000004076 pyridyl group Chemical group 0.000 claims description 3
- 125000000714 pyrimidinyl group Chemical group 0.000 claims description 3
- 125000005879 dioxolanyl group Chemical group 0.000 claims description 2
- 125000002541 furyl group Chemical group 0.000 claims description 2
- 125000002757 morpholinyl group Chemical group 0.000 claims description 2
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 2
- 125000002971 oxazolyl group Chemical group 0.000 claims description 2
- 125000004193 piperazinyl group Chemical group 0.000 claims description 2
- 125000003386 piperidinyl group Chemical group 0.000 claims description 2
- 125000003373 pyrazinyl group Chemical group 0.000 claims description 2
- 125000003226 pyrazolyl group Chemical group 0.000 claims description 2
- 125000003718 tetrahydrofuranyl group Chemical group 0.000 claims description 2
- 125000000335 thiazolyl group Chemical group 0.000 claims description 2
- 125000005133 alkynyloxy group Chemical group 0.000 claims 1
- 238000000034 method Methods 0.000 abstract description 31
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract description 4
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract description 4
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- 125000004209 (C1-C8) alkyl group Chemical group 0.000 abstract 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 abstract 1
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- 238000009472 formulation Methods 0.000 description 17
- 239000003112 inhibitor Substances 0.000 description 17
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- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 15
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 15
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- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 14
- 239000000049 pigment Substances 0.000 description 14
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- 238000006243 chemical reaction Methods 0.000 description 12
- 150000003254 radicals Chemical class 0.000 description 12
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 description 11
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- LMDZBCPBFSXMTL-UHFFFAOYSA-N 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide Chemical compound CCN=C=NCCCN(C)C LMDZBCPBFSXMTL-UHFFFAOYSA-N 0.000 description 6
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- 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 6
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- YNESATAKKCNGOF-UHFFFAOYSA-N lithium bis(trimethylsilyl)amide Chemical compound [Li+].C[Si](C)(C)[N-][Si](C)(C)C YNESATAKKCNGOF-UHFFFAOYSA-N 0.000 description 6
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- 125000004853 tetrahydropyridinyl group Chemical group N1(CCCC=C1)* 0.000 description 1
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 1
- QEMXHQIAXOOASZ-UHFFFAOYSA-N tetramethylammonium Chemical compound C[N+](C)(C)C QEMXHQIAXOOASZ-UHFFFAOYSA-N 0.000 description 1
- WROMPOXWARCANT-UHFFFAOYSA-N tfa trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F.OC(=O)C(F)(F)F WROMPOXWARCANT-UHFFFAOYSA-N 0.000 description 1
- 125000004495 thiazol-4-yl group Chemical group S1C=NC(=C1)* 0.000 description 1
- 125000004496 thiazol-5-yl group Chemical group S1C=NC=C1* 0.000 description 1
- 125000004300 thiazolidin-2-yl group Chemical group [H]N1C([H])([H])C([H])([H])SC1([H])* 0.000 description 1
- GLDAZAQRGCSFNP-UHFFFAOYSA-N thiencarbazone Chemical compound O=C1N(C)C(OC)=NN1C(=O)NS(=O)(=O)C1=C(C)SC=C1C(O)=O GLDAZAQRGCSFNP-UHFFFAOYSA-N 0.000 description 1
- XSKZXGDFSCCXQX-UHFFFAOYSA-N thiencarbazone-methyl Chemical compound COC(=O)C1=CSC(C)=C1S(=O)(=O)NC(=O)N1C(=O)N(C)C(OC)=N1 XSKZXGDFSCCXQX-UHFFFAOYSA-N 0.000 description 1
- 125000004275 thietan-2-yl group Chemical group [H]C1([H])SC([H])(*)C1([H])[H] 0.000 description 1
- 125000006300 thietan-3-yl group Chemical group [H]C1([H])SC([H])([H])C1([H])* 0.000 description 1
- LOQQVLXUKHKNIA-UHFFFAOYSA-N thifensulfuron Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C2=C(SC=C2)C(O)=O)=N1 LOQQVLXUKHKNIA-UHFFFAOYSA-N 0.000 description 1
- 150000007970 thio esters Chemical class 0.000 description 1
- 125000004569 thiomorpholin-2-yl group Chemical group N1CC(SCC1)* 0.000 description 1
- 125000004570 thiomorpholin-3-yl group Chemical group N1C(CSCC1)* 0.000 description 1
- 125000004571 thiomorpholin-4-yl group Chemical group N1(CCSCC1)* 0.000 description 1
- 210000001519 tissue Anatomy 0.000 description 1
- 235000010215 titanium dioxide Nutrition 0.000 description 1
- IYMLUHWAJFXAQP-UHFFFAOYSA-N topramezone Chemical compound CC1=C(C(=O)C2=C(N(C)N=C2)O)C=CC(S(C)(=O)=O)=C1C1=NOCC1 IYMLUHWAJFXAQP-UHFFFAOYSA-N 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- 150000003624 transition metals Chemical class 0.000 description 1
- 238000013519 translation Methods 0.000 description 1
- XOPFESVZMSQIKC-UHFFFAOYSA-N triasulfuron Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)OCCCl)=N1 XOPFESVZMSQIKC-UHFFFAOYSA-N 0.000 description 1
- BQZXUHDXIARLEO-UHFFFAOYSA-N tribenuron Chemical compound COC1=NC(C)=NC(N(C)C(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(O)=O)=N1 BQZXUHDXIARLEO-UHFFFAOYSA-N 0.000 description 1
- YMXOXAPKZDWXLY-QWRGUYRKSA-N tribenuron methyl Chemical group COC(=O)[C@H]1CCCC[C@@H]1S(=O)(=O)NC(=O)N(C)C1=NC(C)=NC(OC)=N1 YMXOXAPKZDWXLY-QWRGUYRKSA-N 0.000 description 1
- REEQLXCGVXDJSQ-UHFFFAOYSA-N trichlopyr Chemical compound OC(=O)COC1=NC(Cl)=C(Cl)C=C1Cl REEQLXCGVXDJSQ-UHFFFAOYSA-N 0.000 description 1
- AZHZOGYUMMIAOF-UHFFFAOYSA-N trifludimoxazin Chemical compound O=C1N(C)C(=S)N(C)C(=O)N1C(C(=C1)F)=CC2=C1OC(F)(F)C(=O)N2CC#C AZHZOGYUMMIAOF-UHFFFAOYSA-N 0.000 description 1
- KVEQCVKVIFQSGC-UHFFFAOYSA-N tritosulfuron Chemical compound FC(F)(F)C1=NC(OC)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(F)(F)F)=N1 KVEQCVKVIFQSGC-UHFFFAOYSA-N 0.000 description 1
- 239000002753 trypsin inhibitor Substances 0.000 description 1
- JABYJIQOLGWMQW-UHFFFAOYSA-N undec-4-ene Chemical compound CCCCCCC=CCCC JABYJIQOLGWMQW-UHFFFAOYSA-N 0.000 description 1
- 229940035893 uracil Drugs 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 150000004669 very long chain fatty acids Chemical class 0.000 description 1
- 230000003612 virological effect Effects 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 239000003021 water soluble solvent Substances 0.000 description 1
- 239000004563 wettable powder Substances 0.000 description 1
- 230000002087 whitening effect Effects 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000000230 xanthan gum Substances 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
- 235000010493 xanthan gum Nutrition 0.000 description 1
- 229940082509 xanthan gum Drugs 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/82—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with three ring hetero atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D271/00—Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms
- C07D271/02—Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms not condensed with other rings
- C07D271/08—1,2,5-Oxadiazoles; Hydrogenated 1,2,5-oxadiazoles
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Dentistry (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Agronomy & Crop Science (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Plural Heterocyclic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201161559164P | 2011-11-14 | 2011-11-14 | |
| US61/559,164 | 2011-11-14 | ||
| PCT/EP2012/072469 WO2013072300A1 (en) | 2011-11-14 | 2012-11-13 | Substituted 1,2,5-oxadiazole compounds and their use as herbicides |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JP2014533254A true JP2014533254A (ja) | 2014-12-11 |
Family
ID=47146426
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2014540513A Pending JP2014533254A (ja) | 2011-11-14 | 2012-11-13 | 置換型１，２，５−オキサジアゾール化合物及びその除草剤としての使用 |
Country Status (17)
| Country | Link |
|---|---|
| US (1) | US20140323306A1 (enExample) |
| EP (1) | EP2780334A1 (enExample) |
| JP (1) | JP2014533254A (enExample) |
| KR (1) | KR20140098134A (enExample) |
| CN (1) | CN104039770A (enExample) |
| AR (1) | AR088857A1 (enExample) |
| AU (1) | AU2012338953A1 (enExample) |
| BR (1) | BR112014011534A2 (enExample) |
| CA (1) | CA2853724A1 (enExample) |
| CO (1) | CO6950497A2 (enExample) |
| CR (1) | CR20140195A (enExample) |
| EA (1) | EA201400576A1 (enExample) |
| IL (1) | IL232235A0 (enExample) |
| IN (1) | IN2014CN03268A (enExample) |
| MX (1) | MX2014005175A (enExample) |
| WO (1) | WO2013072300A1 (enExample) |
| ZA (1) | ZA201404294B (enExample) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2019500365A (ja) * | 2015-12-17 | 2019-01-10 | ビーエーエスエフ ソシエタス・ヨーロピアＢａｓｆ Ｓｅ | ベンズアミド化合物及び除草剤としてのそれらの使用 |
Families Citing this family (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU2012338879A1 (en) | 2011-11-16 | 2014-06-05 | Basf Se | Substituted 1,2,5-oxadiazole compounds and their use as herbicides II |
| WO2014184058A1 (en) * | 2013-05-15 | 2014-11-20 | Basf Se | Substituted 1,2,5-oxadiazole compounds and their use as herbicides |
| JP6327483B2 (ja) | 2013-05-31 | 2018-05-23 | 日産化学工業株式会社 | 複素環アミド化合物 |
| WO2015052152A1 (en) * | 2013-10-10 | 2015-04-16 | Basf Se | Substituted 1,2,5-oxadiazole compounds and their use as herbicides |
| WO2015052178A1 (en) * | 2013-10-10 | 2015-04-16 | Basf Se | 1,2,5-oxadiazole compounds and their use as herbicides |
| EP2907807A1 (en) | 2014-02-18 | 2015-08-19 | Basf Se | Benzamide compounds and their use as herbicides |
| CN106459986B (zh) | 2014-03-11 | 2020-06-30 | 拜耳作物科学有限合伙公司 | Hppd变体和使用方法 |
| BR112017016789A2 (pt) | 2015-02-11 | 2018-05-08 | Basf Se | métodos para produzir uma planta transgênica, para controlar a vegetação indesejada e para o cultivo da planta, molécula de ácido nucleico, construção de ácido nucleico, vetor, polipeptídeo hppd mutado, núcleo de célula vegetal, núcleo de célula vegetal transgênica, planta transgênica, uso do ácido nucleico, combinação útil, processo para a preparação de uma combinação útil e uso de uma combinação útil |
| HK1258349A1 (zh) | 2015-09-11 | 2019-11-08 | Bayer Cropscience Ag | Hppd变体及使用方法 |
| US11624076B2 (en) | 2016-04-21 | 2023-04-11 | BASF Agricultural Solutions Seed US LLC | TAL-effector mediated herbicide tolerance |
| US11180770B2 (en) | 2017-03-07 | 2021-11-23 | BASF Agricultural Solutions Seed US LLC | HPPD variants and methods of use |
| WO2019016385A1 (en) | 2017-07-21 | 2019-01-24 | Basf Se | BENZAMIDE COMPOUNDS AND THEIR USE AS HERBICIDES |
| BR112020008092A2 (pt) | 2017-10-24 | 2020-09-15 | BASF Agricultural Solutions Seed US LLC | método para conferir tolerância a um herbicida e planta de soja transgênica |
| BR112020008096A2 (pt) | 2017-10-24 | 2020-11-03 | Basf Se | método para conferir tolerância a um herbicida e planta de soja transgênica |
| EP4132917B1 (de) | 2020-04-07 | 2024-01-24 | Bayer Aktiengesellschaft | Substituierte isophtalsäurediamide |
| CN115768752B (zh) * | 2020-04-07 | 2025-04-22 | 拜耳公司 | 取代的间苯二酸二酰胺 |
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-
2012
- 2012-11-13 BR BR112014011534A patent/BR112014011534A2/pt not_active IP Right Cessation
- 2012-11-13 CA CA2853724A patent/CA2853724A1/en not_active Abandoned
- 2012-11-13 CN CN201280067032.2A patent/CN104039770A/zh active Pending
- 2012-11-13 MX MX2014005175A patent/MX2014005175A/es unknown
- 2012-11-13 JP JP2014540513A patent/JP2014533254A/ja active Pending
- 2012-11-13 IN IN3268CHN2014 patent/IN2014CN03268A/en unknown
- 2012-11-13 AR ARP120104276A patent/AR088857A1/es unknown
- 2012-11-13 EP EP12783624.5A patent/EP2780334A1/en not_active Withdrawn
- 2012-11-13 KR KR1020147016251A patent/KR20140098134A/ko not_active Withdrawn
- 2012-11-13 US US14/357,897 patent/US20140323306A1/en not_active Abandoned
- 2012-11-13 AU AU2012338953A patent/AU2012338953A1/en not_active Abandoned
- 2012-11-13 WO PCT/EP2012/072469 patent/WO2013072300A1/en not_active Ceased
- 2012-11-13 EA EA201400576A patent/EA201400576A1/ru unknown
-
2014
- 2014-04-24 IL IL232235A patent/IL232235A0/en unknown
- 2014-04-29 CR CR20140195A patent/CR20140195A/es unknown
- 2014-05-08 CO CO14099141A patent/CO6950497A2/es unknown
- 2014-06-11 ZA ZA2014/04294A patent/ZA201404294B/en unknown
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2019500365A (ja) * | 2015-12-17 | 2019-01-10 | ビーエーエスエフ ソシエタス・ヨーロピアＢａｓｆ Ｓｅ | ベンズアミド化合物及び除草剤としてのそれらの使用 |
Also Published As
| Publication number | Publication date |
|---|---|
| CN104039770A (zh) | 2014-09-10 |
| WO2013072300A1 (en) | 2013-05-23 |
| KR20140098134A (ko) | 2014-08-07 |
| AU2012338953A1 (en) | 2014-06-05 |
| CR20140195A (es) | 2014-06-03 |
| EP2780334A1 (en) | 2014-09-24 |
| US20140323306A1 (en) | 2014-10-30 |
| ZA201404294B (en) | 2017-11-29 |
| IL232235A0 (en) | 2014-06-30 |
| BR112014011534A2 (pt) | 2017-05-09 |
| AR088857A1 (es) | 2014-07-10 |
| MX2014005175A (es) | 2014-05-28 |
| CO6950497A2 (es) | 2014-05-20 |
| EA201400576A1 (ru) | 2014-11-28 |
| CA2853724A1 (en) | 2013-05-23 |
| IN2014CN03268A (enExample) | 2015-07-03 |
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