AR078830A1 - Fungicidas de azolil benceno sustituido por heterobiciclos - Google Patents
Fungicidas de azolil benceno sustituido por heterobiciclosInfo
- Publication number
- AR078830A1 AR078830A1 ARP100103996A ARP100103996A AR078830A1 AR 078830 A1 AR078830 A1 AR 078830A1 AR P100103996 A ARP100103996 A AR P100103996A AR P100103996 A ARP100103996 A AR P100103996A AR 078830 A1 AR078830 A1 AR 078830A1
- Authority
- AR
- Argentina
- Prior art keywords
- haloalkyl
- alkyl
- ring
- cycloalkyl
- atoms
- Prior art date
Links
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 title 3
- 239000000417 fungicide Substances 0.000 title 1
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 abstract 9
- 125000006583 (C1-C3) haloalkyl group Chemical group 0.000 abstract 8
- 125000004432 carbon atom Chemical group C* 0.000 abstract 6
- -1 hydroxy, amino Chemical group 0.000 abstract 6
- 125000004448 alkyl carbonyl group Chemical group 0.000 abstract 5
- 125000004438 haloalkoxy group Chemical group 0.000 abstract 5
- 125000004692 haloalkylcarbonyl group Chemical group 0.000 abstract 5
- 125000005347 halocycloalkyl group Chemical group 0.000 abstract 5
- 229910052736 halogen Inorganic materials 0.000 abstract 5
- 125000006274 (C1-C3)alkoxy group Chemical group 0.000 abstract 4
- 125000004429 atom Chemical group 0.000 abstract 4
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 abstract 3
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 abstract 3
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 3
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 abstract 3
- 125000006645 (C3-C4) cycloalkyl group Chemical group 0.000 abstract 3
- 125000006555 (C3-C5) cycloalkyl group Chemical group 0.000 abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 3
- 125000000000 cycloalkoxy group Chemical group 0.000 abstract 3
- 125000005843 halogen group Chemical group 0.000 abstract 3
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 3
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 2
- 125000004769 (C1-C4) alkylsulfonyl group Chemical group 0.000 abstract 2
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 2
- 125000006656 (C2-C4) alkenyl group Chemical group 0.000 abstract 2
- 125000006650 (C2-C4) alkynyl group Chemical group 0.000 abstract 2
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 2
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 2
- 125000004183 alkoxy alkyl group Chemical group 0.000 abstract 2
- 125000003545 alkoxy group Chemical group 0.000 abstract 2
- 125000005083 alkoxyalkoxy group Chemical group 0.000 abstract 2
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 2
- 125000004457 alkyl amino carbonyl group Chemical group 0.000 abstract 2
- 125000003282 alkyl amino group Chemical group 0.000 abstract 2
- 125000005196 alkyl carbonyloxy group Chemical group 0.000 abstract 2
- 125000006254 cycloalkyl carbonyl group Chemical group 0.000 abstract 2
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 2
- 125000005167 cycloalkylaminocarbonyl group Chemical group 0.000 abstract 2
- 125000005201 cycloalkylcarbonyloxy group Chemical group 0.000 abstract 2
- 125000005144 cycloalkylsulfonyl group Chemical group 0.000 abstract 2
- 125000004663 dialkyl amino group Chemical group 0.000 abstract 2
- 125000004473 dialkylaminocarbonyl group Chemical group 0.000 abstract 2
- 125000005291 haloalkenyloxy group Chemical group 0.000 abstract 2
- 125000005203 haloalkylcarbonyloxy group Chemical group 0.000 abstract 2
- 125000004441 haloalkylsulfonyl group Chemical group 0.000 abstract 2
- 125000006769 halocycloalkoxy group Chemical group 0.000 abstract 2
- 150000002367 halogens Chemical class 0.000 abstract 2
- 239000000203 mixture Substances 0.000 abstract 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 2
- 125000001424 substituent group Chemical group 0.000 abstract 2
- 125000004434 sulfur atom Chemical group 0.000 abstract 2
- 125000004665 trialkylsilyl group Chemical group 0.000 abstract 2
- 125000006594 (C1-C3) alkylsulfony group Chemical group 0.000 abstract 1
- 125000006677 (C1-C3) haloalkoxy group Chemical group 0.000 abstract 1
- 125000004768 (C1-C4) alkylsulfinyl group Chemical group 0.000 abstract 1
- 125000004771 (C1-C4) haloalkylsulfinyl group Chemical group 0.000 abstract 1
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 abstract 1
- 125000002373 5 membered heterocyclic group Chemical group 0.000 abstract 1
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 abstract 1
- 150000001204 N-oxides Chemical class 0.000 abstract 1
- 125000003806 alkyl carbonyl amino group Chemical group 0.000 abstract 1
- 125000000304 alkynyl group Chemical group 0.000 abstract 1
- 125000005133 alkynyloxy group Chemical group 0.000 abstract 1
- 229910052799 carbon Inorganic materials 0.000 abstract 1
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 1
- 125000004122 cyclic group Chemical group 0.000 abstract 1
- 125000006310 cycloalkyl amino group Chemical group 0.000 abstract 1
- 125000005112 cycloalkylalkoxy group Chemical group 0.000 abstract 1
- 125000005366 cycloalkylthio group Chemical group 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 244000053095 fungal pathogen Species 0.000 abstract 1
- 125000005221 halo alkyl carbonyl amino group Chemical group 0.000 abstract 1
- 125000004993 haloalkoxycarbonyl group Chemical group 0.000 abstract 1
- 125000004992 haloalkylamino group Chemical group 0.000 abstract 1
- 125000005842 heteroatom Chemical group 0.000 abstract 1
- 125000000623 heterocyclic group Chemical group 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 125000004430 oxygen atom Chemical group O* 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 229910052717 sulfur Inorganic materials 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/04—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- 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
- A01N43/56—1,2-Diazoles; Hydrogenated 1,2-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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
- A01N47/18—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing a —O—CO—N< group, or a thio analogue thereof, directly attached to a heterocyclic or cycloaliphatic ring
-
- 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D411/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen and sulfur atoms as the only ring hetero atoms
- C07D411/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen and sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D411/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen and sulfur atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Abstract
También se describen composiciones que contienen los compuestos de la formula (1) y métodos para controlar enfermedades de las plantas causadas por un patogeno fungico; el método comprende aplicar una cantidad eficaz de un compuesto o una composicion de la solicitud. Reivindicacion 1: Un compuesto seleccionado de la formula (1), N-oxidos y sus sales, caracterizado porque Y es un anillo heterocíclico de 5 miembros, parcial o totalmente insaturado, que contiene 2-4 átomos de carbono y 2-3 átomos de nitrogeno como miembros anulares, el anillo se encuentra sustituido con Z en un átomo miembro del anillo conectado, a través de un unico átomo miembro del anillo adyacente, con el átomo miembro del anillo que une el anillo heterocíclico al anillo de fenilo de la formula (1) y, opcionalmente, también sustituido con hasta 2 sustituyentes seleccionados independientemente de R5 en miembros anulares de átomos de carbono y de R6 en miembros anulares de átomos de nitrogeno; Z es un sistema anular heterobicíclico fundido de 8, 9, 10 u 11 miembros que contiene miembros anulares seleccionados de átomos de carbono y 1 a 4 heteroátomos seleccionados independientemente de hasta 2 átomos de O, hasta 2 átomos de S y hasta 4 átomos de N, en donde hasta 3 miembros anulares de átomos de carbono se seleccionan independientemente de C(=O) y C(=S), y los miembros anulares de átomos de azufre se seleccionan independiente de S(=O)u(=NR7)z, el sistema anular sustituido opcionalmente con sustituyentes seleccionados independientemente de R8 en miembros anulares de átomos de carbono y de R9 en miembros anulares de átomos de nitrogeno; W es O o S; Q es CR10aR10b, O o NR11; R1 es halogeno, CN, alquilo C1-3, alcoxi C1-3, haloalquilo C1-3, haloalcoxi C1-3 o cicloalquilo C3-6; R2 es H, halogeno, CN, alquilo C1-3, alcoxi C1-3, haloalquilo C1-3, haloalcoxi C1-3 o cicloalquilo C3-6; R3 es H, alquilo C1-3, haloalquilo C1-3, cicloalquilo C3-4, halocicloalquilo C3-4, alquilcarbonilo C2-6, haloalquilcarbonilo C2-6, alcoxicarbonilo C2-6 o haloalcoxicarbonilo C2-6; R4 es H, hidroxilo, amino, alquilo C1-3, haloalquilo C1-4, cicloalquilo C3-4, halocicloalquilo C3-4, alcoxi C1-4, haloalcoxi C1-4, cicloalcoxi C3-4, alquilamino C1-4, haloalquilamino C1-4, dialquilamino C2-6, halodialquilamino C2-6 o cicloalquilamino C3-4; cada R5 es independientemente halogeno, ciano, hidroxilo, amino, nitro, alquilo C1-6, cicloalquilo C3-5, halocicloalquilo C3-5, alquenilo C2-6, alquinilo C2-6 o haloalquilo C1-6; cada R6 es independientemente ciano, hidroxilo, alquilo C1-6, haloalquilo C1-6, cicloalquilo C3-5, halocicloalquilo C3-5, alquenilo C2-6 o alquinilo C3-6; cada R8 es independientemente halogeno, ciano, hidroxilo, amino, nitro, -CH(=O), -C(=O)OH, -C(=O)NH2, -C(R12)=N-O-R13, -C(R12)=N-R13, alquilo C1-4, haloalquilo C1-4, cicloalquilo C3-4, alquenilo C2-4, alquinilo C2-4, alquilcarbonilo C2-5, haloalquilcarbonilo C2-5, cicloalquilcarbonilo C4-5, alcoxicarbonilo C2-5, cicloalcoxicarbonilo C4-10, alquilaminocarbonilo C2-8, dialquilaminocarbonilo C3-10, cicloalquilaminocarbonilo C4-5, alcoxi C1-4, haloalcoxi C1-4, cicloalcoxi C3-4, halocicloalcoxi C3-4, cicloalquilalcoxi C4-5, alqueniloxi C2-4, haloalqueniloxi C2-4, alquiniloxi C2-4, haloalquiniloxi C3-4, alcoxialcoxi C2-4, alquilcarboniloxi C2-8, haloalquilcarboniloxi C2-8, cicloalquilcarboniloxi C4-10, alquiltio C1-4, haloalquiltio C1-4, cicloalquiltio C3-6, alquilsulfinilo C1-4, haloalquilsulfinilo C1-4, alquilsulfonilo C1-4, haloalquilsulfonilo C1-4, cicloalquilsulfonilo C3-5, trialquilsililo C3-7, alquilamino C1-4, dialquilamino C2-8, haloalquilamino C1-4, halodialquilamino C2-8, cicloalquilamino C3-6, alquilcarbonilamino C2-5 o haloalquilcarbonilamino C2-5; cada R9 es independientemente ciano, hidroxilo, -CH(=O), -C(=O)NH2, -C(R12)=N-O-R13, -C(R12)=N-R13, alquilo C1-4, cicloalquilo C3-4, alquenilo C2-4, alquinilo C2-4, haloalquilo C1-4, alquilcarbonilo C2-5, haloalquilcarbonilo C2-5, cicloalquilcarbonilo C4-5, alcoxicarbonilo C2-5, cicloalcoxicarbonilo C4-10, alquilaminocarbonilo C2-8, dialquilaminocarbonilo C3-10, cicloalquilaminocarbonilo C4-5, alcoxi C1-4, haloalcoxi C1-4, cicloalcoxi C3-4, halocicloalcoxi C3-4, cicloalquilalcoxi C4-5, alqueniloxi C2-4, haloalqueniloxi C2-4, alquiniloxi C2-4, haloalquiniloxi C3-4, alcoxialcoxi C2-4, alquilcarboniloxi C2-8, haloalquilcarboniloxi C2-8, cicloalquilcarboniloxi C4-10, benciltio, alquiltio C1-6, haloalquiltio C1-6, cicloalquiltio C3-8, alquilsulfonilo C1-4, haloalquilsulfonilo C1-4, cicloalquilsulfonilo C3-6 o trialquilsililo C3-10; cada R7 y R13 es independientemente H, alquilo C1-3, haloalquilo C1-3, alquilcarbonilo C2-3 o haloalquilcarbonilo C2-3; R10a es H, OH, halogeno, ciano, alquilo C1-3, haloalquilo C1-3, alcoxialquilo C2-3, alcoxi C1-3, haloalcoxi C1-C3 o alquilsulfonilo C1-3; R10b es H, alquilo C1-3, haloalquilo C1-3, alcoxialquilo C2-3, alcoxi C1-3 o haloalcoxi C1-3 o R10a y R10b se toman junto con el átomo de carbono al que están unidos para formar un anillo de cicloalquilo C3-4 o halocicloalquilo C3-4; R11 es H, alquilo C1-3, haloalquilo C1-3, alquilcarbonilo C2-3 o haloalquilcarbonilo C2-3; cada R12 es independientemente H, alquilo C1-3, cicloalquilo C3-5 o haloalquilo C1-3; y u y z en cada instancia de S(=O)u(=NR7)z son independientemente 0, 1 o 2, siempre que la suma de u y z en cada instancia de S(=O)u(=NR7)z sea 0, 1 o 2.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US25599609P | 2009-10-29 | 2009-10-29 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR078830A1 true AR078830A1 (es) | 2011-12-07 |
Family
ID=43548802
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP100103996A AR078830A1 (es) | 2009-10-29 | 2010-10-29 | Fungicidas de azolil benceno sustituido por heterobiciclos |
Country Status (25)
| Country | Link |
|---|---|
| US (1) | US8921360B2 (es) |
| EP (1) | EP2493880B1 (es) |
| JP (1) | JP2013509408A (es) |
| KR (1) | KR20120112423A (es) |
| CN (1) | CN102596940B (es) |
| AR (1) | AR078830A1 (es) |
| AU (1) | AU2010318557A1 (es) |
| BR (1) | BR112012009998A2 (es) |
| CA (1) | CA2790361A1 (es) |
| CL (1) | CL2012001071A1 (es) |
| CO (1) | CO6551700A2 (es) |
| ES (1) | ES2435298T3 (es) |
| GE (1) | GEP20135951B (es) |
| IL (1) | IL218942A0 (es) |
| IN (1) | IN2012DN02871A (es) |
| MX (1) | MX2012004808A (es) |
| NZ (1) | NZ599070A (es) |
| PE (1) | PE20121357A1 (es) |
| PH (1) | PH12012500749A1 (es) |
| PL (1) | PL2493880T3 (es) |
| RU (1) | RU2012122017A (es) |
| TW (1) | TW201116212A (es) |
| UY (1) | UY32983A (es) |
| WO (1) | WO2011059619A1 (es) |
| ZA (1) | ZA201202421B (es) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA3066423A1 (en) * | 2017-06-14 | 2018-12-20 | Trevena, Inc. | Compounds for modulating s1p1 activity and methods of using the same |
| TWI832917B (zh) | 2018-11-06 | 2024-02-21 | 美商富曼西公司 | 經取代之甲苯基殺真菌劑 |
| MX2022005766A (es) | 2019-11-19 | 2022-08-08 | Trevena Inc | Compuestos y métodos para la preparación de compuestos moduladores de esfingosina 1-fosfato tipo 1 (s1p1). |
| UY39189A (es) | 2020-05-06 | 2021-12-31 | Fmc Corp | Fungicidas de tolilo sustituido y sus mezclas |
| CN116768875B (zh) * | 2022-03-10 | 2025-08-15 | 河北大学 | 一种含二氢苯并呋喃基的异噁唑啉类化合物及其制备方法与应用 |
| CN116768876B (zh) * | 2022-03-10 | 2025-08-15 | 河北大学 | 一种含二氢苯并呋喃基的异噁唑类化合物及其制备方法与应用 |
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| GB2095558B (en) | 1981-03-30 | 1984-10-24 | Avon Packers Ltd | Formulation of agricultural chemicals |
| DE3246493A1 (de) | 1982-12-16 | 1984-06-20 | Bayer Ag, 5090 Leverkusen | Verfahren zur herstellung von wasserdispergierbaren granulaten |
| US5180587A (en) | 1988-06-28 | 1993-01-19 | E. I. Du Pont De Nemours And Company | Tablet formulations of pesticides |
| DK0777964T3 (da) | 1989-08-30 | 2002-03-11 | Kynoch Agrochemicals Proprieta | Fremgangsmåde til fremstilling af et doseringssystem |
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| TW200301698A (en) | 2001-12-21 | 2003-07-16 | Bristol Myers Squibb Co | Acridone inhibitors of IMPDH enzyme |
| WO2004037770A1 (ja) | 2002-10-23 | 2004-05-06 | Nippon Soda Co.,Ltd. | ヒドラジン誘導体、製造中間体および農園芸用殺菌剤および殺虫剤 |
| CN100503551C (zh) | 2002-12-26 | 2009-06-24 | 庵原化学工业株式会社 | 制备苄胺衍生物的方法 |
| WO2005051932A1 (ja) * | 2003-11-28 | 2005-06-09 | Nippon Soda Co., Ltd. | アリール複素環誘導体および農園芸用殺菌剤および殺虫剤 |
| US7241773B2 (en) | 2003-12-22 | 2007-07-10 | Abbott Laboratories | 3-quinuclidinyl heteroatom bridged biaryl derivatives |
| EP1746099A1 (en) | 2004-12-23 | 2007-01-24 | DeveloGen Aktiengesellschaft | Mnk1 or Mnk2 inhibitors |
| JP2006327973A (ja) * | 2005-05-25 | 2006-12-07 | Nippon Soda Co Ltd | アリール複素環誘導体および農園芸用殺菌剤 |
| AU2006322067A1 (en) | 2005-12-06 | 2007-06-14 | Merck Sharp & Dohme Corp. | Morpholine carboxamide prokineticin receptor antagonists |
| ES2643082T3 (es) | 2007-04-03 | 2017-11-21 | E. I. Du Pont De Nemours And Company | Fungicidas de benceno sustituido |
| EP2005995A1 (en) | 2007-06-22 | 2008-12-24 | Glaxo Group Limited | Heterocyclic compounds for the treatment of tuberculosis |
| ATE541841T1 (de) | 2007-11-15 | 2012-02-15 | Boehringer Ingelheim Int | Inhibitoren der replikation des human immunodeficiency virus |
-
2010
- 2010-10-05 TW TW099133915A patent/TW201116212A/zh unknown
- 2010-10-12 CA CA2790361A patent/CA2790361A1/en not_active Abandoned
- 2010-10-12 RU RU2012122017/04A patent/RU2012122017A/ru unknown
- 2010-10-12 ES ES10768149T patent/ES2435298T3/es active Active
- 2010-10-12 JP JP2012536841A patent/JP2013509408A/ja active Pending
- 2010-10-12 GE GEAP201012723A patent/GEP20135951B/en unknown
- 2010-10-12 US US13/500,928 patent/US8921360B2/en not_active Expired - Fee Related
- 2010-10-12 BR BR112012009998A patent/BR112012009998A2/pt not_active IP Right Cessation
- 2010-10-12 KR KR1020127013672A patent/KR20120112423A/ko not_active Withdrawn
- 2010-10-12 PL PL10768149T patent/PL2493880T3/pl unknown
- 2010-10-12 PE PE2012000569A patent/PE20121357A1/es not_active Application Discontinuation
- 2010-10-12 EP EP10768149.6A patent/EP2493880B1/en active Active
- 2010-10-12 MX MX2012004808A patent/MX2012004808A/es active IP Right Grant
- 2010-10-12 WO PCT/US2010/052228 patent/WO2011059619A1/en not_active Ceased
- 2010-10-12 CN CN201080049706.7A patent/CN102596940B/zh not_active Expired - Fee Related
- 2010-10-12 NZ NZ599070A patent/NZ599070A/xx not_active IP Right Cessation
- 2010-10-12 IN IN2871DEN2012 patent/IN2012DN02871A/en unknown
- 2010-10-12 AU AU2010318557A patent/AU2010318557A1/en not_active Abandoned
- 2010-10-12 PH PH1/2012/500749A patent/PH12012500749A1/en unknown
- 2010-10-28 UY UY0001032983A patent/UY32983A/es not_active Application Discontinuation
- 2010-10-29 AR ARP100103996A patent/AR078830A1/es unknown
-
2012
- 2012-03-29 IL IL218942A patent/IL218942A0/en unknown
- 2012-04-03 ZA ZA2012/02421A patent/ZA201202421B/en unknown
- 2012-04-26 CL CL2012001071A patent/CL2012001071A1/es unknown
- 2012-05-22 CO CO12084046A patent/CO6551700A2/es not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| JP2013509408A (ja) | 2013-03-14 |
| BR112012009998A2 (pt) | 2019-09-24 |
| PH12012500749A1 (en) | 2012-10-29 |
| GEP20135951B (en) | 2013-10-25 |
| PE20121357A1 (es) | 2012-10-15 |
| NZ599070A (en) | 2013-09-27 |
| CN102596940A (zh) | 2012-07-18 |
| IL218942A0 (en) | 2012-07-31 |
| IN2012DN02871A (es) | 2015-07-24 |
| RU2012122017A (ru) | 2013-12-10 |
| TW201116212A (en) | 2011-05-16 |
| PL2493880T3 (pl) | 2014-02-28 |
| ES2435298T3 (es) | 2013-12-18 |
| EP2493880A1 (en) | 2012-09-05 |
| CL2012001071A1 (es) | 2012-09-14 |
| ZA201202421B (en) | 2013-06-26 |
| US20120202815A1 (en) | 2012-08-09 |
| CO6551700A2 (es) | 2012-10-31 |
| KR20120112423A (ko) | 2012-10-11 |
| AU2010318557A1 (en) | 2012-04-19 |
| MX2012004808A (es) | 2012-06-14 |
| WO2011059619A1 (en) | 2011-05-19 |
| CN102596940B (zh) | 2015-01-28 |
| CA2790361A1 (en) | 2011-05-19 |
| UY32983A (es) | 2011-05-31 |
| EP2493880B1 (en) | 2013-09-18 |
| US8921360B2 (en) | 2014-12-30 |
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