AR076838A1 - Sulfonamidas nematocidas - Google Patents
Sulfonamidas nematocidasInfo
- Publication number
- AR076838A1 AR076838A1 ARP100101511A ARP100101511A AR076838A1 AR 076838 A1 AR076838 A1 AR 076838A1 AR P100101511 A ARP100101511 A AR P100101511A AR P100101511 A ARP100101511 A AR P100101511A AR 076838 A1 AR076838 A1 AR 076838A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- haloalkyl
- cn11r12
- 2cn11r12
- cyano
- Prior art date
Links
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 26
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 26
- 125000001424 substituent group Chemical group 0.000 abstract 25
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 21
- 229910052736 halogen Inorganic materials 0.000 abstract 20
- 125000000262 haloalkenyl group Chemical group 0.000 abstract 19
- 125000005843 halogen group Chemical group 0.000 abstract 19
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 17
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 abstract 13
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 13
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 abstract 13
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 abstract 10
- 125000000232 haloalkynyl group Chemical group 0.000 abstract 10
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 10
- 125000006656 (C2-C4) alkenyl group Chemical group 0.000 abstract 9
- 125000004183 alkoxy alkyl group Chemical group 0.000 abstract 9
- 125000001316 cycloalkyl alkyl group Chemical group 0.000 abstract 9
- 125000006650 (C2-C4) alkynyl group Chemical group 0.000 abstract 8
- 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 abstract 8
- 125000000392 cycloalkenyl group Chemical group 0.000 abstract 8
- 125000001188 haloalkyl group Chemical group 0.000 abstract 7
- 125000006448 cycloalkyl cycloalkyl group Chemical group 0.000 abstract 5
- 125000001072 heteroaryl group Chemical group 0.000 abstract 4
- HCMJWOGOISXSDL-UHFFFAOYSA-N (2-isothiocyanato-1-phenylethyl)benzene Chemical group C=1C=CC=CC=1C(CN=C=S)C1=CC=CC=C1 HCMJWOGOISXSDL-UHFFFAOYSA-N 0.000 abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 3
- 125000001651 cyanato group Chemical group [*]OC#N 0.000 abstract 3
- 125000001624 naphthyl group Chemical group 0.000 abstract 3
- ZMZDMBWJUHKJPS-UHFFFAOYSA-N thiocyanic acid Chemical group SC#N ZMZDMBWJUHKJPS-UHFFFAOYSA-N 0.000 abstract 3
- 241000244206 Nematoda Species 0.000 abstract 2
- 239000000203 mixture Substances 0.000 abstract 2
- 229910052760 oxygen Inorganic materials 0.000 abstract 2
- 230000003071 parasitic effect Effects 0.000 abstract 2
- 229910052717 sulfur Inorganic materials 0.000 abstract 2
- 150000001204 N-oxides Chemical class 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 125000000304 alkynyl group Chemical group 0.000 abstract 1
- 229910052799 carbon Inorganic materials 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
Classifications
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- 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
- A01N43/90—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system
-
- 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
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/50—1,3-Diazoles; Hydrogenated 1,3-diazoles
-
- 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
- A01N55/00—Biocides, pest repellants or attractants, or plant growth regulators, containing organic compounds containing elements other than carbon, hydrogen, halogen, oxygen, nitrogen and sulfur
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/415—1,2-Diazoles
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Wood Science & Technology (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Dentistry (AREA)
- Agronomy & Crop Science (AREA)
- Engineering & Computer Science (AREA)
- Veterinary Medicine (AREA)
- Chemical & Material Sciences (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Epidemiology (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Tropical Medicine & Parasitology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
También se describen composiciones que contienen los compuestos de la formula 1 y métodos para controlar un nemátodo parasítico; los métodos comprenden poner en contacto el nemátodo parasítico o su hábitat con una cantidad biologicamente eficaz de un compuesto o una composicion de la solicitud. Reivindicacion 1: Un compuesto seleccionado de la formula (1), un N-oxido, o una sal de éste, caracterizado porque Z es O o S; cada R1 es independientemente halogeno, ciano, nitro, SF5, OCN, SCN, Si(R15)3, OR4, CN5R6, alquilo C1-6, haloalquilo C1-6, alquenilo C2-6, haloalquenilo C2-6, alquinilo C2-6, haloalquinilo C2-6, C(X)R7, C(O)OR8, C(O)CN11R12, S(O)mR9, S(O)2CN11R12, OC(O)R7, OC(O)OR8, OC(O)CN11R12, OS(O)2R9, OS(O)2CN11R12, N(R10)C(O)R7, N(R10)C(O)CN11R12, N(R10)S(O)2R9 o (R10)S(O)2CN11R12; o cicloalquilo C3-7, cicloalquilalquilo C4-8, cicloalquilcicloalquilo C6-14 o cicloalquenilo C5-7, cada uno opcionalmente sustituido con 1 a 4 sustituyentes independientemente seleccionados del grupo que consiste de halogeno, ciano, nitro, alquilo C1-4, haloalquilo C1-4, OR4a y S(O)mR9a; o alquilo C1-6 sustituido con 1 a 4 sustituyentes independientemente seleccionados del grupo que consiste de ciano, nitro, OR4, CN5R6, C(X)R7, C(O)OR8, C(O)CN11R12, S(O)mR9 y S(O)2CN11R12 o fenilo, naftalenilo o un anillo heteroaromático de 5 o 6 miembros, cada uno opcionalmente sustituido con 1 a 5 sustituyentes seleccionados independientemente del grupo que consiste de halogeno, ciano, nitro, OR4, CN5R6, alquilo C1-4, alquenilo C2-4, alquinilo C2-4, haloalquilo C1-4, haloalquenilo C2-4, alcoxialquilo C2-6, C(X)R7, C(O)OR8, C(O)CN11R12, S(O)mR9, S(O)2CN11R12, OC(O)R7a y N(R10)C(O)R7a; R2 es H, halogeno, ciano, nitro, SF5, OCN, SCN, Si(R15)3, OR4, CN5R6, alquilo C1-6, haloalquilo C1-6, alquenilo C2-6, haloalquenilo C2-6, alquinilo C2-6, haloalquinilo C2-6, C(X)R7, C(O)OR8, C(O)CN11R12, S(O)mR9, S(O)2CN11R12, OC(O)R7, OC(O)OR8, OC(O)CN11R12, OS(O)2R9, OS(O)2CN11R12, N(R10)C(O)R7, N(R10)C(O)CN11R12, N(R10)S(O)2R9 o N(R10)S(O)2CN11R12; o cicloalquilo C3-7, cicloalquilalquilo C4-8, cicloalquilcicloalquilo C6-14 o cicloalquenilo C5-7, cada uno opcionalmente sustituido con 1 a 4 sustituyentes independientemente seleccionados del grupo que consiste de halogeno, ciano, nitro, alquilo C1-4, haloalquilo C1-4, OR4a y S(O)mR9; o alquilo C1-6 sustituido con 1 a 4 sustituyentes independientemente seleccionados del grupo que consiste de ciano, nitro, OR4, CN5R6, C(X)R7, C(O)OR8, C(O)CN11R12, S(O)mR9 y S(O)2CN11R12; o fenilo, naftalenilo o un heteroaromático de 5 o 6 miembros, cada uno opcionalmente sustituido con 1 a 5 sustituyentes independientemente seleccionados del grupo que consiste de halogeno, ciano, nitro, OR4, CN5R6, alquilo C1-4, alquenilo C2-4, alquinilo C2-4, haloalquilo C1-4, haloalquenilo C2-4, alcoxialquilo C2-6, C(X)R7, C(O)OR8, C(O)CN11R12, S(O)mR9, S(O)2CN11R12, OC(O)R7a y N(R10)C(O)R7a; R3 es H, alquilo C1-6, haloalquilo C1-6, alquenilo C2-6, haloalquenilo C2-6, alquinilo C2-6, haloalquinilo C2-6, C(X)R7, C(O)OR8, C(O)CN11R12, S(O)mR9 o S(O)2CN11R12; o cicloalquilo C3-7, cicloalquilalquilo C4-8 o cicloalquenilo C5-7, cada uno opcionalmente sustituido con 1 a 4 sustituyentes independientemente seleccionados del grupo que consiste de halogeno, ciano, nitro, alquilo C1-4, haloalquilo C1-4, OR4a y S(O)mR9a; o alquilo C1-6 sustituido con 1 a 4 sustituyentes independientemente seleccionados del grupo que consiste de ciano, nitro, OR4, CN5R6, C(X)R7, C(O)OR8, C(O)CN11R12, S(O)mR9 y S(O)2CN11R12; o alquilo C1-6 sustituido con 1 o 2 sustituyentes independientemente seleccionados del grupo que consiste de fenilo o un anillo heteroaromático de 5 o 6 miembros, cada uno opcionalmente sustituido con 1 a 5 sustituyentes independientemente seleccionados del grupo que consiste de halogeno, ciano, nitro, OR4, CN5R6, alquilo C1-4, alquenilo C2-4, alquinilo C2-4, haloalquilo C1-4, haloalquenilo C2-4, alcoxialquilo C2-6, C(X)R7, C(O)OR8, C(O)CN11R12, S(O)mR9, S(O)2CN11R12, OC(O)R7a y N(R10)C(O)R7a; o fenilo opcionalmente sustituido con 1 a 5 sustituyentes independientemente seleccionados del grupo que consiste de halogeno, ciano, nitro, OR4, CN5R6, alquilo C1-4, alquenilo C2-4, alquinilo C2-4, haloalquilo C1-4, haloalquenilo C2-4, alcoxialquilo C2-6, C(X)R7, C(O)OR8, C(O)CN11R12, S(O)mR9, S(O)2CN11R12, OC(O)R7a y N(R10)C(O)R7a; Q es fenilo, naftalenilo, un anillo heteroaromático de 5 o 6 miembros o un sistema de anillos bicíclicos heteroaromáticos de 8 a 10 miembros, cada uno opcionalmente sustituido con 1 a 5 sustituyentes independientemente seleccionados del grupo que consiste de halogeno, ciano, nitro, SF5, OCN, SCN, Si(R15)3, OR4, CN5R6, alquilo C1-6, haloalquilo C1-6, alquenilo C2-6, haloalquenilo C2-6, alquinilo C2-6, haloalquinilo C2-6, C(X)R7, C(O)OR8, C(X)CN11R12, S(O)mR9, S(O)2CN11R12, OC(O)R7, OC(O)OR8, OC(O)CN11R12, OS(O)2R9, OS(O)2CN11R12, N(R10)C(O)R7, N(R10)C(O)CN11R12, N(R10)S(O)2R9, N(R10)S(O)2CN11R12 y R14; cada X es independientemente O o S; cada R4 es independientemente H, alquilo C1-6, haloalquilo C1-6, alquenilo C2-6, haloalquenilo C2-6, alquinilo C2-6 o haloalquinilo C2-6; o alquilo C1-6, alquenilo C2-6 o alquinilo C2-6, cada uno sustituido con 1 o 4 sustituyentes independientemente seleccionados del grupo que consiste de ciano, nitro, OR4a, CN5aR6a, C(X)R7a, C(O)OR8a, C(O)CN11R12, S(O)mR9a o S(O)2CN11R12; o fenilo opcionalmente sustituido con 1 o 3 sustituyentes independientemente seleccionados del grupo que consiste de halogeno, ciano, nitro, alquilo C1-4, alquenilo C2-4, alquinilo C2-4, haloalquilo C1-4, haloalquenilo C2-4, C(X)R7a, C(O)OR8a, C(O)CN11R12, OR4a, alcoxialquilo C2-6, S(O)mR9a, S(O)2CN11R12, CN5aR6a, OC(O)R7a y N(R10)C(O)R7a; cada R4a es independientemente H, alquilo C1-6 o haloalquilo C1-6; cada R5 es independientemente H, CN5aR6a, alquilo C1-6, haloalquilo C1-6, alquenilo C2-6, haloalquenilo C2-6, alquinilo C2-6, haloalquinilo C2-6, C(X)R7, C(O)OR8, C(O)CN11R12, S(O)mR9 o S(O)2CN11R12; o cicloalquilo C3-7, cicloalquilalquilo C4-8, cicloalquilcicloalquilo C6-14 o cicloalquenilo C5-7, cada uno opcionalmente sustituido con 1 a 4 sustituyentes independientemente seleccionados del grupo que consiste de halogeno, ciano, nitro, alquilo C1-4, haloalquilo C1-4, OR4a y S(O)mR9; o fenilo opcionalmente sustituido con 1 a 3 sustituyentes independientemente seleccionados del grupo que consiste de halogeno, ciano, nitro, alquilo C1-4, alquenilo C2-4, alquinilo C2-4, haloalquilo C1-4, haloalquenilo C2-4, C(X)R7a, C(O)OR8a, C(O)CN11R12, OR4a, alcoxialquilo C2-6, S(O)mR9a, S(O)2CN11R12, CN5aR6a, OC(O)R7a y N(R10)C(O)R7a; cada R5a es independientemente H o alquilo C1-6; cada R6 es independientemente H, alquilo C1-6, haloalquilo C1-6, alquenilo C2-6, haloalquenilo C2-6, alquinilo C2-6 o haloalquinilo C2-6; o cicloalquilo C3-7, cicloalquilalquilo C4-8, cicloalquilcicloalquilo C6-14 o cicloalquenilo C5-7, cada uno opcionalmente sustituido con 1 a 4 sustituyentes independientemente seleccionados del grupo que consiste de halogeno, ciano, nitro, alquilo C1-4, haloalquilo C1-4, OR4a y S(O)mR9; cada R6a es independientemente H, alquilo C1-6, C(O)R13 o C(O)OR13; cada R7 es independientemente H, alquilo C1-6, haloalquilo C1-6, alquenilo C2-6, haloalquenilo C2-6, alquinilo C2-6 o haloalquinilo C2-6; o cicloalquilo C3-7, cicloalquilalquilo C4-8, cicloalquilcicloalquilo C6-14 o cicloalquenilo C5-7, cada uno opcionalmente sustituido con 1 a 4 sustituyentes independientemente seleccionados de grupo que consiste de halogeno, ciano, nitro, alquilo C1-4, haloalquilo C1-4, OR4a y S(O)mR9; o fenilo opcionalmente sustituido con 1 a 3 sustituyentes independientemente seleccionados del grupo que consiste de halogeno, ciano, nitro, alquilo C1-4, alquenilo C2-4, alquinilo C2-4, haloalquilo C1-4, haloalquenilo C2-4, C(X)R7a, C(O)OR8a, C(O)CN11R12, OR4, alcoxialquilo C2-6, S(O)mR9a, S(O)2CN11R12, CN5aR6a, OC(O)R7a y N(R10)C(O)R7a; cada R7 es independientemente alquilo C1-6 o haloalquilo C1-6; cada R8 es independientemente H, alquilo C1-6, haloalquilo C1-6, alquenilo C2-6, haloalquenilo C2-6, alquinilo C2-6 o haloalquinilo C2-6; o cicloalquilo C3-7, cicloalquilalquilo C4-8, cicloalquilcicloalquilo C6-14 o cicloalquenilo C5-7, cada uno opcionalmente sustituido con 1 a 4 sustituyentes independientemente seleccionados del grupo que consiste de halogeno, ciano, nitro, alquilo C1-4, haloalquilo C1-4, OR4 y S(O)mR9a; o alquilo C1-6, alquenilo C2-6 o alquinilo C2-6, cada uno sustituido con 1 a 4 sustituyentes seleccionados del grupo que consiste de ciano, nitro, OR4, CN5R6, C(X)R7, C(O)OR8, C(O)CN11R12, S(O)mR9 y S(O)2CN11R12; o fenilo opcionalmente sustituido con 1 a 3 sustituyentes independientemente seleccionados del grupo que consiste de halogeno, ciano, nitro, alquilo C1-4, alquenilo C2-4, alquinilo C2-4, haloalquilo C1-4, haloalquenilo C2-4, C(X)R7a, C(O)OR8a, C(O)CN11R12, OR4a, alcoxialquilo C2-6, S(O)mR9a, S(O)2CN11R12, CN5aR6a, OC(O)R7a y N(R10)C(O)R7a; cada R8a es independientemente alquilo C1-6 o haloalquilo C1-6; cada R9 es independientemente H, alquilo C1-6, haloalquilo C1-6, alquenilo C2-6, haloalquenilo C2-6, alquinilo C2-6 o haloalquinilo C2-6; o cicloalquilo C3-7, cicloalquilalquilo C4-8, cicloalquilcicloalquilo C6-14 o cicloalquenilo C5-7, cada uno opcionalmente sustituido con 1 a 4 sustituyentes independientemente seleccionados del grupo que consiste de halogeno, ciano, nitro, alquilo C1-4, haloalquilo C1-4, OR4, S(O)mR9a; o alquilo C1-6, alquenilo C2-6 o alquinilo C2-6, cada uno sustituido con 1 a 4 sustituyentes seleccionados del grupo que consiste de ciano, nitro, OR4, CN5R6, C(X)R7, C(O)OR8, C(O)CN11R12, S(O)mR9 y S(O)2CN11R12; o fenilo opcionalmente sustituido con 1 a 3 sustituyentes independientemente seleccionados del grupo que consiste de halogeno, ciano, nitro, alquilo C1-4, alquenilo C2-4, alquinilo C2-4, haloalquilo C1-4, haloalquenilo C2-4, C(X)R7a, C(O)OR8a, C(O)CN11R12, OR4a, alcoxialquilo C2-6, S(O)mR9a, S(O)2CN11R12, CN5aR6a, OC(O)R7a y N
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US17520609P | 2009-05-04 | 2009-05-04 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR076838A1 true AR076838A1 (es) | 2011-07-13 |
Family
ID=43050805
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP100101511A AR076838A1 (es) | 2009-05-04 | 2010-05-04 | Sulfonamidas nematocidas |
Country Status (31)
| Country | Link |
|---|---|
| US (3) | US8623890B2 (es) |
| EP (1) | EP2427058B1 (es) |
| JP (1) | JP5634504B2 (es) |
| KR (1) | KR101769162B1 (es) |
| CN (1) | CN102413693B (es) |
| AR (1) | AR076838A1 (es) |
| AU (1) | AU2010246105B2 (es) |
| BR (1) | BRPI1007622B8 (es) |
| CA (1) | CA2757075C (es) |
| CL (1) | CL2011002726A1 (es) |
| CO (1) | CO6450621A2 (es) |
| DK (1) | DK2427058T3 (es) |
| ES (1) | ES2530268T3 (es) |
| HR (1) | HRP20150065T1 (es) |
| HU (1) | HUE024909T2 (es) |
| IL (1) | IL215105A0 (es) |
| MA (1) | MA33261B1 (es) |
| ME (1) | ME02284B (es) |
| MX (1) | MX2011011485A (es) |
| MY (1) | MY152267A (es) |
| NZ (1) | NZ595152A (es) |
| PL (1) | PL2427058T3 (es) |
| PT (1) | PT2427058E (es) |
| RS (1) | RS54208B1 (es) |
| RU (1) | RU2531317C2 (es) |
| SI (1) | SI2427058T1 (es) |
| TW (1) | TWI482771B (es) |
| UA (1) | UA120828C2 (es) |
| UY (1) | UY32606A (es) |
| WO (1) | WO2010129500A2 (es) |
| ZA (1) | ZA201106729B (es) |
Families Citing this family (65)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TWI482771B (zh) * | 2009-05-04 | 2015-05-01 | Du Pont | 磺醯胺殺線蟲劑 |
| CA2803695A1 (en) * | 2010-06-28 | 2012-01-05 | Bayer Intellectual Property Gmbh | Heteroaryl-substituted pyridine compounds for use as pesticides |
| MX343596B (es) * | 2010-10-18 | 2016-11-11 | E I Du Pont De Nemours And Company * | Sulfonamidas nematocidas. |
| EP2540163A1 (en) * | 2011-06-30 | 2013-01-02 | Bayer CropScience AG | Nematocide N-cyclopropyl-sulfonylamide derivatives |
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