AR085811A1 - N-(1,2,5-oxadiazol-3-il)piridincarboxamidas y su uso como herbicidas - Google Patents
N-(1,2,5-oxadiazol-3-il)piridincarboxamidas y su uso como herbicidasInfo
- Publication number
- AR085811A1 AR085811A1 ARP120100835A AR085811A1 AR 085811 A1 AR085811 A1 AR 085811A1 AR P120100835 A ARP120100835 A AR P120100835A AR 085811 A1 AR085811 A1 AR 085811A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- cycloalkyl
- heterocyclyl
- cyano
- nitro
- Prior art date
Links
- 239000004009 herbicide Substances 0.000 title abstract 3
- 125000000217 alkyl group Chemical group 0.000 abstract 30
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 20
- -1 cyano, nitro, methylsulfenyl Chemical group 0.000 abstract 15
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 8
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 8
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 8
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 abstract 7
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 abstract 7
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 7
- 229910052736 halogen Inorganic materials 0.000 abstract 7
- 150000002367 halogens Chemical class 0.000 abstract 7
- 125000000623 heterocyclic group Chemical group 0.000 abstract 7
- 229910052739 hydrogen Inorganic materials 0.000 abstract 7
- 239000001257 hydrogen Substances 0.000 abstract 7
- 150000002431 hydrogen Chemical class 0.000 abstract 6
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 6
- NJYFRQQXXXRJHK-UHFFFAOYSA-N (4-aminophenyl) thiocyanate Chemical compound NC1=CC=C(SC#N)C=C1 NJYFRQQXXXRJHK-UHFFFAOYSA-N 0.000 abstract 5
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 abstract 5
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 5
- 125000000262 haloalkenyl group Chemical group 0.000 abstract 5
- 125000000232 haloalkynyl group Chemical group 0.000 abstract 5
- 125000005347 halocycloalkyl group Chemical group 0.000 abstract 4
- 125000001072 heteroaryl group Chemical group 0.000 abstract 4
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 3
- 101100496169 Arabidopsis thaliana CLH1 gene Proteins 0.000 abstract 3
- 101100044057 Mesocricetus auratus SYCP3 gene Proteins 0.000 abstract 3
- 102000003728 Peroxisome Proliferator-Activated Receptors Human genes 0.000 abstract 3
- 108090000029 Peroxisome Proliferator-Activated Receptors Proteins 0.000 abstract 3
- 101100080600 Schizosaccharomyces pombe (strain 972 / ATCC 24843) nse6 gene Proteins 0.000 abstract 3
- 125000003545 alkoxy group Chemical group 0.000 abstract 3
- 101150111293 cor-1 gene Proteins 0.000 abstract 3
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 3
- 125000004043 oxo group Chemical group O=* 0.000 abstract 3
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 2
- 101100295738 Gallus gallus COR3 gene Proteins 0.000 abstract 2
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 2
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 abstract 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 2
- 125000005843 halogen group Chemical group 0.000 abstract 2
- 125000004458 methylaminocarbonyl group Chemical group [H]N(C(*)=O)C([H])([H])[H] 0.000 abstract 2
- 125000004674 methylcarbonyl group Chemical group CC(=O)* 0.000 abstract 2
- QDDAWCPKZGZBPN-UHFFFAOYSA-N n-(1,2,5-oxadiazol-3-yl)pyridine-2-carboxamide Chemical class C=1C=CC=NC=1C(=O)NC=1C=NON=1 QDDAWCPKZGZBPN-UHFFFAOYSA-N 0.000 abstract 2
- 125000001424 substituent group Chemical group 0.000 abstract 2
- 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 abstract 1
- HCUOEKSZWPGJIM-YBRHCDHNSA-N (e,2e)-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-YBRHCDHNSA-N 0.000 abstract 1
- 125000003320 C2-C6 alkenyloxy group Chemical group 0.000 abstract 1
- 101001109689 Homo sapiens Nuclear receptor subfamily 4 group A member 3 Proteins 0.000 abstract 1
- 101000598778 Homo sapiens Protein OSCP1 Proteins 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- 101001067395 Mus musculus Phospholipid scramblase 1 Proteins 0.000 abstract 1
- 102100022673 Nuclear receptor subfamily 4 group A member 3 Human genes 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 125000000392 cycloalkenyl group Chemical group 0.000 abstract 1
- 125000003754 ethoxycarbonyl group Chemical group C(=O)(OCC)* 0.000 abstract 1
- 125000004995 haloalkylthio group Chemical group 0.000 abstract 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 abstract 1
- 125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 abstract 1
- 125000006216 methylsulfinyl group Chemical group [H]C([H])([H])S(*)=O 0.000 abstract 1
- 125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 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
- 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
-
- 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
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Plural Heterocyclic Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
Se describen N-(1,2,5-oxadiazol-3-il)piridin-carboxamidas de la fórmula general (1). Su uso como herbicidas, agentes herbicidas conteniendo el compuesto activo y procedimiento para combatir plantas indeseadas.Reivindicación 1: N-(1,2,5-oxadiazol-3-il)piridincarboxamidas de la fórmula (1) o sus sales, en la que W significa un grupo de fórmula (W1), (W2) ó (W3); R significa hidrógeno, alquilo C1-6, cicloalquilo C3-7, haloalquilo C1-6, alcoxi C1-6, haloalcoxi C1-6, alquenilo C2-6, alqueniloxi C2-6, haloalquenilo C2-6, alquinilo C2-6, alquiniloxi C2-6, haloalquinilo C2-6, ciano, nitro, metilsulfenilo, metilsulfinilo, metilsulfonilo, alquilcarbonil C1-6-amino, benzoilamino, fenoxi, metoxicarbonilo, etoxicarbonilo, metoxicarbonilmetilo, etoxicarbonilmetilo, benzoílo, metilcarbonilo, piperidinilcarbonilo, trifluorometilcarbonilo, halógeno, amino, aminocarbonilo, metilaminocarbonilo, dimetilaminocarbonilo, metoximetilo o heteroarilo, heterociclilo o fenilo sustituidos respectivamente con s restos del grupo de metilo, etilo, metoxi, trifluorometilo y halógeno; X y V significan independientemente entre sí respectivamente hidrógeno, nitro, halógeno, ciano, formilo, rodano, alquilo C1-6, haloalquilo C1-6, alquenilo C2-6, haloalquenilo C2-6, alquinilo C2-6, haloalquinilo C3-6, cicloalquilo C3-6, halocicloalquilo C3-6, cicloalquilo C3-6-alquilo C1-6, halocicloalquilo C3-6-alquilo C1-6, COR1, COOR1, OCOOR1, NR1COOR1, C(O)N(R1)2, NR1C(O)N(R1)2, OC(O)N(R1)2, C(O)NR1OR1, OR1, OCOR1, OSO2R2, S(O)nR2, SO2OR1, SO2N(R1)2, NR1SO2R2, NR1COR1, alquil C1-6-S(O)nR2, alquil C1-6-OR1, alquil C1-6-OCOR1, alquil C1-6-OSO2R2, alquil C1-6-CO2R1, alquil C1-6-SO2OR1, alquil C1-6-CON(R1)2, alquil C1-6-SO2N(R1)2, alquil C1-6-NR1COR1, alquil C1-6-NR1SO2R2, NR1R2, P(O)(OR5)2, CH2P(O)(OR5)2, alquil C1-6-heteroarilo, alquil C1-5-heterociclilo, fenilo, heteroarilo o heterociclilo, estando los últimos 5 restos sustituidos respectivamente con s restos del grupo de halógeno, nitro, ciano, alquilo C1-6, haloalquilo C1-6, cicloalquilo C3-6, S(O)n-alquilo C1-6, alcoxi C1-6, haloalcoxi C1-6, alcoxi C1-6-alquilo C1-4 y cianometilo y portando el heterociclilo n grupos oxo; Y y U significan independientemente entre sí respectivamente hidrógeno, nitro, halógeno, ciano, rodano, alquilo C1-6, haloalquilo C1-6, alquenilo C2-6, haloalquenilo C2-6, alquinilo C2-6, haloalquinilo C2-6, cicloalquilo C3-6, cicloalquenilo C3-6, halocicloalquilo C3-6, cicloalquilo C3-6-alquilo C1-6, halocicloalquilo C3-6-alquilo C1-6, COR1, COOR1, OCOOR1, NR1COOR1, C(O)N(R1)2, NR1C(O)N(R1)2, OC(O)N(R1)2, CO(NOR1)R1, NR1SO2R2, NR1COR1, OR1, OSO2R2, S(O)nR2, SO2OR1, SO2N(R1)2, alquil C1-6-S(O)nR2, alquil C1-6-OR1, alquil C1-6-OCOR1, alquil C1-6-OSO2R2, alquil C1-6-CO2R1, alquil C1-6-CN, alquil C1-6-SO2OR1, alquil C1-6-CON(R1)2, alquil C1-6-SO2N(R1)2, alquil C1-6-NR1COR1, alquil C1-6-NR1SO2R2, N(R1)2, P(O)(OR5)2, CH2P(O)(OR5)2, alquil C1-6-fenilo, alquil C1-6-heteroarilo, alquil C1-6-heterociclilo, fenilo, heteroarilo o heterociclilo, estando los últimos 6 restos sustituidos respectivamente con s restos del grupo de halógeno, nitro, ciano, alquilo C1-6, haloalquilo C1-6, cicloalquilo C3-6, S(O)n-alquilo C1-6, alcoxi C1-6, haloalcoxi C1-6, alcoxi C1-6-alquilo C1-4 y cianometilo, y portando el heterociclilo n grupos oxo; Z significa hidrógeno, halógeno, ciano, rodano, nitro, alquilo C1-6, alcoxi C1-6, haloalquilo C1-6, haloalcoxi C1-6, haloalquiltio C1-6, alquenilo C2-6, haloalquenilo C2-6, alquinilo C2-6, haloalquinilo C2-6, cicloalquilo C3-6, halocicloalquilo C3-6, cicloalquilo C3-6-alquilo C1-6, halocicloalquilo C3-6-alquilo C1-6, COR1, COOR1, OCOOR1, NR1COOR1, C(O)N(R1)2, NR1C(O)N(R1)2, OC(O)N(R1)2, C(O)NR1OR1, OSO2R2, S(O)nR2, SO2OR1, SO2N(R1)2, NR1SO2R2, NR1COR1, alquil C1-6-S(O)nR2, alquil C1-6-OR1, alquil C1-6-OCOR1, alquil C1-6-OSO2R2, alquil C1-6-CO2R1, alquil C1-6-SO2OR1, alquil C1-6-CON(R1)2, alquil C1-6-SO2N(R1)2, alquil C1-5-NR1COR1, alquil C1-6-NR1SO2R2, N(R1)2, P(O)(OR5)2, heteroarilo, heterociclilo o fenilo, estando los últimos tres restos sustituidos respectivamente con s restos del grupo de halógeno, nitro, ciano, alquilo C1-6, haloalquilo C1-6, cicloalquilo C3-6, S(O)n-alquilo C1-6, alcoxi C1-6 o haloalcoxi C1-6 y portando el heterociclilo n grupos oxo; R1 significa hidrógeno, alquilo C1-6, haloalquilo C1-6, alquenilo C2-6, haloalquenilo C2-6, alquinilo C2-6, haloalquinilo C2-6, cicloalquilo C3-6, halocicloalquilo C3-6, alquil C1-6-O-alquilo C1-6, cicloalquilo C3-6-alquilo C1-6, fenilo o fenil-alquilo C1-6, estando los 12 últimos restos mencionados sustituidos con s restos del grupo que se compone de ciano, halógeno, nitro, rodano, OR3, S(O)nR4, N(R3)2, NR3OR3, COR3, OCOR3, SCOR3, NR3COR3, CO2R3, COSR3, CON(R3)2 y alcoxi C1-4-alcoxicarbonilo C2-6; R2 significa alquilo C1-6, alquenilo C2-6, alquinilo C2-6, cicloalquilo C3-6, cicloalquilo C3-6-alquilo C1-6, fenilo o fenil-alquilo C1-6, estando los siete últimos restos mencionados sustituidos con s restos del grupo que se compone de ciano, halógeno, nitro, rodano, OR3, S(O)nR4, N(R3)2, NR3OR3, COR3, OCOR3, SCOR3, NR3COR3, CO2R3, COSR3, CON(R3)2 y alcoxi C1-4-alcoxicarbonilo C2-6; R3 significa hidrógeno, alquilo C1-6, alquenilo C2-6 o alquinilo C2-6; R4 significa alquilo C1-6, alquenilo C2-6 o alquinilo C2-6; R5 significa metilo o etilo; n significa 0, 1 ó 2, s significa 0, 1, 2 ó 3; con la condición que en el resto de fórmula (W1) los sustituyentes U, y, X y Z o bien en el resto de fórmula (W2) los sustituyentes U, y, X e Y no signifiquen todos simultáneamente hidrógeno.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP11158253 | 2011-03-15 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR085811A1 true AR085811A1 (es) | 2013-10-30 |
Family
ID=44226888
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP120100835 AR085811A1 (es) | 2011-03-15 | 2012-03-14 | N-(1,2,5-oxadiazol-3-il)piridincarboxamidas y su uso como herbicidas |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US9035064B2 (es) |
| EP (1) | EP2686316B1 (es) |
| JP (1) | JP6008881B2 (es) |
| CN (1) | CN103459386B (es) |
| AR (1) | AR085811A1 (es) |
| BR (1) | BR112013023603A2 (es) |
| WO (1) | WO2012123416A1 (es) |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ES2532486T3 (es) * | 2011-03-15 | 2015-03-27 | Bayer Intellectual Property Gmbh | Amidas de ácidos N-(1,2,5-oxadiazol-3-il)-, N-(tetrazol-5-il)- y N-(triazol-5-il) bicicloarilcarboxílico y su uso como herbicidas |
| US9332759B2 (en) * | 2011-03-15 | 2016-05-10 | Bayer Intellectual Property Gmbh | Herbicide safener compositions |
| KR20140107280A (ko) * | 2011-11-18 | 2014-09-04 | 바스프 에스이 | 치환된 1,2,5-옥사디아졸 화합물 및 이의 제초제 iii 로서의 용도 |
| WO2013164333A1 (de) * | 2012-05-03 | 2013-11-07 | Bayer Cropscience Ag | 6-pyridon-2-carbamoyl-azole und ihre verwendung als herbizide |
| US9512113B2 (en) | 2012-05-24 | 2016-12-06 | Bayer Cropscience Ag | N-(tetrazol-5-yl)- and N-(triazol-5-yl)arylcarboxylic thioamides and use thereof as herbicides |
| WO2014086737A1 (de) | 2012-12-06 | 2014-06-12 | Bayer Cropscience Ag | Kondensierte 2-pyridon-3-carboxamide und ihre verwendung als herbizide |
| WO2014184014A1 (en) * | 2013-05-15 | 2014-11-20 | Basf Se | N-(1,2,5-oxadiazol-3-yl)carboxamide compounds and their use as herbicides |
| CN103242308B (zh) * | 2013-05-24 | 2015-07-01 | 青岛农业大学 | 2-氟烟酰衍生物及其制备方法和其应用 |
| 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 |
| WO2015007633A1 (de) * | 2013-07-16 | 2015-01-22 | Bayer Cropscience Ag | 6-azinon-2-carbonyl-derivate und ihre verwendung als herbizide |
| EP3055305A1 (en) * | 2013-10-10 | 2016-08-17 | Basf Se | Substituted 1,2,5-oxadiazole compounds and their use as herbicides |
| CN103524407B (zh) * | 2013-11-01 | 2015-12-02 | 青岛农业大学 | 一组2-氟-3-吡啶甲酰化合物 |
| KR20180043838A (ko) | 2015-09-11 | 2018-04-30 | 바이엘 크롭사이언스 악티엔게젤샤프트 | Hppd 변이체 및 사용 방법 |
| JP6932125B2 (ja) | 2015-09-28 | 2021-09-08 | 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 | アシル化n−(1,2,5−オキサジアゾール−3−イル)−、n−(1,3,4−オキサジアゾール−2−イル)−、n−(テトラゾール−5−イル)−およびn−(トリアゾール−5−イル)−アリールカルボキサミド、および除草剤としてのそれらの使用 |
| BR112019018175A2 (pt) | 2017-03-07 | 2020-04-07 | BASF Agricultural Solutions Seed US LLC | molécula, célula, planta, sementes, polipeptídeos recombinantes, método para produzir um polipeptídeo, planta, método para controlar ervas, uso do ácido nucleico e produto de utilidade |
| US12156523B2 (en) * | 2017-03-17 | 2024-12-03 | Mmag Co., Ltd. | Plant disease control agent |
| WO2020050297A1 (ja) * | 2018-09-06 | 2020-03-12 | Meiji Seikaファルマ株式会社 | 植物病害防除剤 |
| CN109232566B (zh) * | 2018-11-05 | 2021-03-12 | 中新科农(山东)生态农业有限公司 | 酰胺类化合物及其制备方法和在除草剂中的应用 |
| CN109111432B (zh) * | 2018-11-05 | 2020-10-30 | 潍坊科技学院 | 一种化合物及其制备方法和其作物除草作用 |
| US12497365B2 (en) | 2019-01-14 | 2025-12-16 | Qingdao Kingagroot Chemical Compound Co., Ltd. | 4-pyridinyl formamide compound or derivative thereof, preparation method therefor, herbicidal composition and use thereof |
| TW202134214A (zh) * | 2020-03-04 | 2021-09-16 | 瑞士商先正達農作物保護公司 | 用於製備具有3-含硫取代基的5-氯-吡啶-2-甲酸醯胺以及甲酸鹽之方法 |
| UA129277C2 (uk) * | 2020-04-07 | 2025-03-05 | Байєр Акцієнгезелльшафт | Заміщені діаміди ізофталевої кислоти та їх застосування як гербіцидів |
| US20230150953A1 (en) * | 2020-04-07 | 2023-05-18 | Bayer Aktiengesellschaft | Substituted isophthalic acid diamides |
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| DE69133261D1 (de) | 1990-03-16 | 2003-06-26 | Calgene Llc Davis | Dnas, die für pflanzliche desaturasen kodieren und deren anwendungen |
| DE69132916T2 (de) | 1990-06-18 | 2002-10-31 | Monsanto Technology Llc, St. Louis | Erhöhter stärkegehalt in pflanzen |
| JP3173784B2 (ja) | 1990-06-25 | 2001-06-04 | モンサント カンパニー | グリホセート耐性植物 |
| SE467358B (sv) | 1990-12-21 | 1992-07-06 | Amylogene Hb | Genteknisk foeraendring av potatis foer bildning av staerkelse av amylopektintyp |
| DE4104782B4 (de) | 1991-02-13 | 2006-05-11 | Bayer Cropscience Gmbh | Neue Plasmide, enthaltend DNA-Sequenzen, die Veränderungen der Karbohydratkonzentration und Karbohydratzusammensetzung in Pflanzen hervorrufen, sowie Pflanzen und Pflanzenzellen enthaltend dieses Plasmide |
| JP4689042B2 (ja) * | 1998-11-04 | 2011-05-25 | 明治製菓株式会社 | ピコリン酸アミド誘導体、それを有効成分として含有する有害生物防除剤 |
| DE19854081A1 (de) * | 1998-11-24 | 2000-05-25 | Bayer Ag | Substituierte N-Pyrazolyl-phenoxynicotinsäure-(thio)amide |
| EP1351571A2 (de) * | 1999-11-17 | 2003-10-15 | Bayer CropScience AG | Selektive herbizide auf basis von 2,6-disubstituierten pyridin-derivaten |
| RU2260949C2 (ru) | 2000-01-25 | 2005-09-27 | Зингента Партисипейшнс Аг | Композиции селективного гербицидного действия, способы борьбы с нежелательными растениями в культурах полезных растений |
| GT200100103A (es) | 2000-06-09 | 2002-02-21 | Nuevos herbicidas | |
| US20050256003A1 (en) | 2002-06-14 | 2005-11-17 | Christoph Luthy | Novel herbicides |
| JP5728480B2 (ja) | 2009-09-25 | 2015-06-03 | バイエル・インテレクチュアル・プロパティ・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツングBayer Intellectual Property GmbH | N−(1,2,5−オキサジアゾール−3−イル)ベンズアミド類および除草剤としてのそれの使用 |
| JP5805767B2 (ja) * | 2010-09-01 | 2015-11-10 | バイエル・インテレクチュアル・プロパティ・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツングBayer Intellectual Property GmbH | N−(テトラゾール−5−イル)アリールカルボキサミド類及びn−(トリアゾール−5−イル)アリールカルボキサミド類並びに除草剤としてのそれらの使用 |
| ES2532486T3 (es) * | 2011-03-15 | 2015-03-27 | Bayer Intellectual Property Gmbh | Amidas de ácidos N-(1,2,5-oxadiazol-3-il)-, N-(tetrazol-5-il)- y N-(triazol-5-il) bicicloarilcarboxílico y su uso como herbicidas |
| US9332759B2 (en) * | 2011-03-15 | 2016-05-10 | Bayer Intellectual Property Gmbh | Herbicide safener compositions |
| UA115424C2 (uk) * | 2011-03-22 | 2017-11-10 | Баєр Інтеллекчуел Проперті Гмбх | Аміди n-(1,3,4-оксадіазол-2-іл)арилкарбонової кислоти та їх застосування як гербіцидів |
| KR20140033354A (ko) * | 2011-03-25 | 2014-03-18 | 바이엘 인텔렉쳐 프로퍼티 게엠베하 | Hppd 억제 제초제에 대해서 내성인 유전자이식 농작물의 영역에서 원치 않는 식물을 방제하기 위한 n-(테트라졸-4-일)- 또는 n-(트리아졸-3-일)아릴카복사미드 또는 그의 염의 용도 |
| JP5847920B2 (ja) * | 2011-03-25 | 2016-01-27 | バイエル・インテレクチュアル・プロパティ・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツングBayer Intellectual Property GmbH | Hppdインヒビター除草剤に対して耐性であるトランスジェニック作物植物の領域において望まぬ植物を制御するためのn−(1,2,5−オキサジアゾール−3−イル)ベンズアミドの使用 |
| AR087385A1 (es) * | 2011-08-03 | 2014-03-19 | Bayer Ip Gmbh | Amidas de acidos n-(tetrazol-5-il)-arilcarboxilico y n-(triazol-5-il)-arilcarboxilico y su uso como herbicidas |
| KR20140107280A (ko) * | 2011-11-18 | 2014-09-04 | 바스프 에스이 | 치환된 1,2,5-옥사디아졸 화합물 및 이의 제초제 iii 로서의 용도 |
| UA116532C2 (uk) * | 2011-12-13 | 2018-04-10 | Байєр Інтеллектуал Проперті Гмбх | Аміди n-(1,2,5-оксадіазол-3-іл)-, n-(1,3,4-оксадіазол-2-іл)- або n-(тетразол-5-іл)арилкарбоксильної кислоти й застосування їх як гербіцидів |
| US9169219B2 (en) * | 2012-02-21 | 2015-10-27 | Bayer Intellectual Property Gmbh | Herbicidally active 4-nitro-substituted N-(tetrazol-5-yl)-, N-(triazol-5-yl)-, and N-(1,3,4-0XADIAZOL-2-yl)aryl carboxylic acid amides |
-
2012
- 2012-03-12 CN CN201280013525.8A patent/CN103459386B/zh active Active
- 2012-03-12 JP JP2013558395A patent/JP6008881B2/ja active Active
- 2012-03-12 BR BR112013023603A patent/BR112013023603A2/pt not_active Application Discontinuation
- 2012-03-12 US US14/004,833 patent/US9035064B2/en active Active
- 2012-03-12 EP EP20120708329 patent/EP2686316B1/de not_active Not-in-force
- 2012-03-12 WO PCT/EP2012/054281 patent/WO2012123416A1/de not_active Ceased
- 2012-03-14 AR ARP120100835 patent/AR085811A1/es not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| CN103459386A (zh) | 2013-12-18 |
| CN103459386B (zh) | 2016-06-22 |
| EP2686316A1 (de) | 2014-01-22 |
| EP2686316B1 (de) | 2015-04-22 |
| BR112013023603A2 (pt) | 2016-08-02 |
| US20140066301A1 (en) | 2014-03-06 |
| JP6008881B2 (ja) | 2016-10-19 |
| WO2012123416A1 (de) | 2012-09-20 |
| US9035064B2 (en) | 2015-05-19 |
| JP2014509597A (ja) | 2014-04-21 |
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