AR082405A1 - Derivados microbicidas de eteres de dioximas - Google Patents
Derivados microbicidas de eteres de dioximasInfo
- Publication number
- AR082405A1 AR082405A1 ARP110102730A ARP110102730A AR082405A1 AR 082405 A1 AR082405 A1 AR 082405A1 AR P110102730 A ARP110102730 A AR P110102730A AR P110102730 A ARP110102730 A AR P110102730A AR 082405 A1 AR082405 A1 AR 082405A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- alkoxy
- halogen
- haloalkyl
- radicals
- Prior art date
Links
- 230000003641 microbiacidal effect Effects 0.000 title 1
- 229940124561 microbicide Drugs 0.000 title 1
- 239000002855 microbicide agent Substances 0.000 title 1
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 13
- 229910052736 halogen Inorganic materials 0.000 abstract 13
- 150000002367 halogens Chemical class 0.000 abstract 13
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 abstract 11
- 125000000229 (C1-C4)alkoxy 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
- 229910052739 hydrogen Inorganic materials 0.000 abstract 9
- 239000001257 hydrogen Substances 0.000 abstract 9
- 125000004435 hydrogen atom Chemical class [H]* 0.000 abstract 9
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 abstract 8
- 125000000217 alkyl group Chemical group 0.000 abstract 7
- 229910052757 nitrogen Inorganic materials 0.000 abstract 7
- 125000004076 pyridyl group Chemical group 0.000 abstract 7
- 125000003342 alkenyl group Chemical group 0.000 abstract 6
- 125000000304 alkynyl group Chemical group 0.000 abstract 6
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 5
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 4
- 125000005347 halocycloalkyl group Chemical group 0.000 abstract 4
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 4
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 abstract 3
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 abstract 3
- 125000003545 alkoxy group Chemical group 0.000 abstract 3
- 125000004414 alkyl thio group Chemical group 0.000 abstract 3
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 3
- 229910052760 oxygen Inorganic materials 0.000 abstract 3
- 125000004769 (C1-C4) alkylsulfonyl group Chemical group 0.000 abstract 2
- 125000004648 C2-C8 alkenyl group Chemical group 0.000 abstract 2
- 125000004649 C2-C8 alkynyl group Chemical group 0.000 abstract 2
- 101100134929 Gallus gallus COR9 gene Proteins 0.000 abstract 2
- 229910052799 carbon Inorganic materials 0.000 abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 125000000714 pyrimidinyl group Chemical group 0.000 abstract 2
- 125000004434 sulfur atom Chemical group 0.000 abstract 2
- 125000004768 (C1-C4) alkylsulfinyl group Chemical group 0.000 abstract 1
- 125000001960 7 membered carbocyclic group Chemical group 0.000 abstract 1
- -1 C1-4-sulfinyl alkyl Chemical group 0.000 abstract 1
- 241000233866 Fungi Species 0.000 abstract 1
- 206010061217 Infestation Diseases 0.000 abstract 1
- 150000001204 N-oxides Chemical class 0.000 abstract 1
- 125000004448 alkyl carbonyl group Chemical group 0.000 abstract 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 239000012634 fragment Substances 0.000 abstract 1
- 125000004438 haloalkoxy group Chemical group 0.000 abstract 1
- 125000004692 haloalkylcarbonyl group Chemical group 0.000 abstract 1
- 125000005842 heteroatom Chemical group 0.000 abstract 1
- 125000000623 heterocyclic group Chemical group 0.000 abstract 1
- 238000003898 horticulture Methods 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 244000005700 microbiome Species 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 239000001301 oxygen Chemical group 0.000 abstract 1
- 125000004430 oxygen atom Chemical group O* 0.000 abstract 1
- 230000003032 phytopathogenic effect Effects 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 229910052717 sulfur Inorganic materials 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
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
- A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
- A01N43/42—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings condensed with carbocyclic rings
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D215/38—Nitrogen atoms
- C07D215/40—Nitrogen atoms attached in position 8
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom 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)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Pyridine Compounds (AREA)
Abstract
La solicitud se refiere además a composiciones que comprenden estos compuestos y a su uso en agricultura u horticultura para controlar o prevenir la infestación de plantas provocada por microorganismos fitopatógenos, especialmente hongos, y a métodos para controlar o prevenir estas enfermedades.Reivindicación 1: Un compuesto de fórmula (1) donde X representa #-Z1-Z2-#, #-Z3-Z4-Z5-#, #-Z6-Z7-Z8-Z9-#, #-Z10-Z11-Z12-Z13-Z14-#; Z1, Z2, Z3, Z5, Z6, Z7, Z8, Z9, Z10, Z11, Z13 y Z14 representan independientemente entre sí CR1R2, C=CR3R4 o C=O; Z4 y Z12 representan independientemente entre sí C=CR3R4, CR5R6, SiR7R8 o C=O; cada R1 y R2 representan independientemente entre si hidrógeno, halógeno, OH, alquilo C1-4, haloalquilo C1-4, cicloalquilo C3-6, halocicloalquilo C3-6, alquiltio C1-4, alquilo C1-4-sulfinilo, alquilo C1-4-sulfonilo, fenilo o CN, donde el fenilo está sustituido opcionalmente con uno o varios grupos seleccionados en forma independiente entre halógeno, CN, alquilo C1-4, haloalquilo C1-4, alcoxi C1-4 y haloalcoxi C1-4; o R1 y R2 junto con el átomo de carbono al cual están unidos pueden formar un grupo cicloalquilo C3-6 o un grupo halocicloalquilo C3-6; cada R3 y R4 representan independientemente entre sí hidrógeno, halógeno, alquilo C1-4 o haloalquilo C1-4; cada R5, R6, R7 y R8 representan independientemente entre si hidrógeno, halógeno, OH, alquilo C1-4, haloalquilo C1-4, cicloalquilo C3-6, halocicloalquilo C3-6, fenilo o CN, donde el fenilo está sustituido opcionalmente con uno o varios grupos seleccionados en forma independiente entre halógeno, CN, alquilo C1-4, haloalquilo C1-4, alcoxi C1-4 y haloalcoxi C1-4; o R5 y R6 junto con el átomo de carbono al cual están unidos pueden formar un grupo cicloalquilo C3-6 o un grupo halocicloalquilo C3-6 donde los agrupamientos #-Z1-Z2-#, #-Z3-Z4-Z5-#, #-Z6-Z7-Z8-Z9-#, #-Z10-Z11-Z12-Z13-Z14-# pueden contener como máximo un anillo que contiene solamente uno de los radicales Z1 a Z14 o dos radicales Z1 a Z14 o tres radicales Z1 a Z14 o cuatro radicales Z1 a Z14 como miembros del anillo; y donde los radicales Z1, Z2, Z3, Z5, Z6, Z9, Z10 y Z14 no están sustituidos con OH; Y1, Y2, Y3, Y4, Y5 e Y6 representan independientemente entre sí hidrógeno, halógeno, CN, NO2, alquilo C1-8, alcoxi C1-4-alquilo C1-4, alcoxi C1-4-alcoxi C1-4-alquilo C1-4, cicloalquilo C3-8, alquenilo C2-8, alquinilo C2-8, fenilo, piridilo, pirimidinilo, COR9, OR10, SH, alquiltio C1-8, alquilo C1-8-sulfinilo, alquilo C1-8-sulfonilo, N(R11)2, CO2R10, O(CO)R9, CON(R11)2, NR11COR9 o CR9N-OR10, donde el alquilo, cicloalquilo, alquenilo, alquinilo, fenilo, pirimidinilo y piridilo están sustituidos opcionalmente con uno o varios grupos seleccionados en forma independiente entre halógeno, CN, NH2, NO2, OH, alquilo C1-4, haloalquilo C1-4, alcoxi C1-4, haloalcoxi C1-4, alquiltio C1-4, alquilo C1-4-sulfinilo y alquilo C1-4-sulfonilo; o independientemente Y1 e Y2, Y2 e Y3, Y4 e Y5, Y5 e Y6, junto con el fragmento del anillo piridilo al cual están unidos, pueden formar un anillo carbocíclico de 5 a 7 miembros parcial o totalmente insaturado o un anillo heterocíclico de 5 a 7 miembros que contiene uno a tres heteroátomos seleccionados en forma independiente entre O, S, N y N(R11), con la condición de que el heterociclo no contenga átomos de oxígeno adyacentes, átomos de azufre adyacentes, o átomos de oxígeno y azufre adyacentes, y donde el anillo formado por Y1 e Y2, Y2 e Y3, Y4 e Y5, Y5 e Y6 está sustituido opcionalmente con uno o varios grupos seleccionados en forma independiente entre halógeno, CN, NH2, NO2, OH, alquilo C1-4, haloalquilo C1-4, alcoxi C1-4 y haloalcoxi C1-4; cada R9 representa independientemente entre sí un hidrógeno, alquilo C1-8, cicloalquilo C3-8, alquenilo C2-8, alquinilo C2-8, bencilo, fenilo o piridilo, donde el alquilo, cicloalquilo, alquenilo, alquinilo, fenilo, bencilo y piridilo están sustituidos opcionalmente con uno o varios grupos seleccionados en forma independiente entre halógeno, CN, NH2, NO2, OH, alquilo C1-4, haloalquilo C1-4, alcoxi C1-4 y haloalcoxi C1-4; cada R10 representa independientemente entre sí un hidrógeno, alquilo C1-8, cicloalquilo C3-8, alquenilo C3-8, alquinilo C3-8, bencilo, fenilo o piridilo, donde el alquilo, cicloalquilo, alquenilo, alquinilo, fenilo, bencilo y piridilo están sustituidos opcionalmente con uno o varios grupos seleccionados en forma independiente entre halógeno, CN, NH2, NO2, OH, alquilo C1-4, haloalquilo C1-4-, alcoxi C1-4, haloalcoxi C1-4 y alcoxi C1-4-alquilo C1-4; cada R11 representa independientemente entre sí un hidrógeno, OH, alquilo C1-8, alcoxi C1-8, alcoxi C1-8-alquilo C1-4, alquenilo C3-8, alquinilo C3-8, o COR9, donde el alquilo, alcoxi, alquenilo y alquinilo están sustituidos opcionalmente con uno o varios halógeno; donde, cuando dos radicales R11 están unidos al mismo átomo de nitrógeno, estos radicales pueden ser iguales o diferentes, donde, cuando dos radicales R11 están unidos al mismo átomo de nitrógeno, estos dos radicales no pueden ser OH, alcoxi C1-4 o haloalcoxi C1-4; y donde, cuando dos radicales R11 están unidos al mismo átomo de nitrógeno, estos dos radicales junto con el átomo de nitrógeno al cual están unidos pueden formar un ciclo seleccionado del grupo de fórmulas (2), donde el ciclo formado está sustituido opcionalmente con uno o varios grupos seleccionados en forma independiente entre halógeno, CN, NH2, NO2, OH, alquilo C1-4, haloalquilo C1-4, alcoxi C1-4 y haloalcoxi C1-4; G1, G2, G4 y G5 representan independientemente entre sí -C(R12R13)-; G3 y G6 representan independientemente entre sí -C(R12R13)-, O, N(R14) o S; o G1 y G2, o G2 y G3, o G1 y G1, o G4 y G5, o G5 y G6, o G4 y G4, juntos representan -CR12=R13-; cada R12 y R13 representan independientemente entre si hidrógeno, halógeno, alquilo C1-4, haloalquilo C1-4, alcoxi C1-4 o haloalcoxi C1-4; R14 representa hidrógeno, OH, alquilo C1-4, alcoxi C1-4, cicloalquilo C3-6, alquilo C1-8-carbonilo o haloalquilo C1-8-carbonilo; y p y q son cada uno independientemente 0, 1 ó 2; o una sal o un N-óxido de estos.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP10171257 | 2010-07-29 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR082405A1 true AR082405A1 (es) | 2012-12-05 |
Family
ID=44454756
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP110102730A AR082405A1 (es) | 2010-07-29 | 2011-07-28 | Derivados microbicidas de eteres de dioximas |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US20140162980A1 (es) |
| EP (1) | EP2598487A1 (es) |
| CN (1) | CN103038217A (es) |
| AR (1) | AR082405A1 (es) |
| AU (1) | AU2011284714A1 (es) |
| BR (1) | BR112013002073A2 (es) |
| CA (1) | CA2804355A1 (es) |
| TW (1) | TW201211005A (es) |
| UY (1) | UY33538A (es) |
| WO (1) | WO2012013754A1 (es) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2641901A1 (en) * | 2012-03-22 | 2013-09-25 | Syngenta Participations AG. | Novel microbiocides |
| MX359619B (es) | 2014-07-14 | 2018-10-04 | Adjuvants Plus Usa Inc | Materiales vegetales inoculados con clonostachys rosea con fungicidas y adyuvantes. |
| CN106478494B (zh) * | 2016-09-22 | 2019-03-15 | 南通海迪新材料有限公司 | 2,3,5,6-四氯-4-甲磺酰基吡啶的生产方法 |
Family Cites Families (42)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA1340685C (en) | 1988-07-29 | 1999-07-27 | Frederick Meins | Dna sequences encoding polypeptides having beta-1,3-glucanase activity |
| EP0392225B1 (en) | 1989-03-24 | 2003-05-28 | Syngenta Participations AG | Disease-resistant transgenic plants |
| US5006153A (en) * | 1989-11-29 | 1991-04-09 | Uniroyal Chemical Company, Inc. | Azole derivatives of naphthalenone oxime ethers |
| US5639949A (en) | 1990-08-20 | 1997-06-17 | Ciba-Geigy Corporation | Genes for the synthesis of antipathogenic substances |
| UA51635C2 (uk) | 1994-12-19 | 2002-12-16 | Ніппон Сода Ко., Лтд | Похідні бензамідоксиму, спосіб їх одержання та фунгіцид на їх основі |
| CN1155977A (zh) | 1995-08-28 | 1997-08-06 | 化学工业部沈阳化工研究院 | 含氟二苯基丙烯酰胺类杀菌剂 |
| CN1043720C (zh) | 1995-08-28 | 1999-06-23 | 化学工业部沈阳化工研究院 | 含氟二苯基丙烯酰胺类杀菌剂 |
| EA001148B1 (ru) | 1996-03-11 | 2000-10-30 | Новартис Аг | Производные пиримидин-4-она |
| US6020332A (en) | 1997-02-20 | 2000-02-01 | Shenyang Research Institute Of Chemical Industry | Fluorine-containing diphenyl acrylamide antimicrobial agents |
| EP0860438B1 (en) | 1997-02-21 | 2003-01-08 | Shenyang Research Institute of Chemical Industry | Fluorine-containing diphenyl acrylamide antimicrobial agents |
| TWI252231B (en) | 1997-04-14 | 2006-04-01 | American Cyanamid Co | Fungicidal trifluorophenyl-triazolopyrimidines |
| NZ503594A (en) | 1997-09-18 | 2001-08-31 | Basf Ag | (Phenyl, thienyl or pyrazolyl)-substituted and alkyl-substituted benzamidoxime derivatives, and benzonitrile intermediates, useful as fungicides |
| DE69906170T2 (de) | 1998-02-10 | 2003-10-23 | Dow Agrosciences Llc, Indianapolis | Ungesättigte Oxim-Ether und ihre Verwendung als Fungizide oder Insectizide |
| TW575562B (en) | 1998-02-19 | 2004-02-11 | Agrevo Uk Ltd | Fungicides |
| US6344330B1 (en) | 1998-03-27 | 2002-02-05 | The Regents Of The University Of California | Pharmacophore recombination for the identification of small molecule drug lead compounds |
| GB9919558D0 (en) * | 1999-08-18 | 1999-10-20 | Hoechst Schering Agrevo Gmbh | Fungicidal compounds |
| GB0011944D0 (en) | 2000-05-17 | 2000-07-05 | Novartis Ag | Organic compounds |
| GT200100103A (es) | 2000-06-09 | 2002-02-21 | Nuevos herbicidas | |
| DE10136065A1 (de) | 2001-07-25 | 2003-02-13 | Bayer Cropscience Ag | Pyrazolylcarboxanilide |
| AR036872A1 (es) | 2001-08-13 | 2004-10-13 | Du Pont | Compuesto de antranilamida, composicion que lo comprende y metodo para controlar una plaga de invertebrados |
| DE10215292A1 (de) | 2002-02-19 | 2003-08-28 | Bayer Cropscience Ag | Disubstitutierte Pyrazolylcarbocanilide |
| BR0308230B1 (pt) | 2002-03-05 | 2014-05-20 | Syngenta Participations Ag | O-ciclopropil-carboxanilida, composição e método de controle ou prevenção de infestação de plantas cultivadas por microorganismos fitopatogênicos |
| WO2004016088A2 (en) | 2002-08-12 | 2004-02-26 | Bayer Cropscience S.A. | Novel 2-pyridylethylbenzamide derivative |
| GB0224316D0 (en) | 2002-10-18 | 2002-11-27 | Syngenta Participations Ag | Chemical compounds |
| IN243219B (es) | 2003-01-28 | 2010-10-01 | Du Pont | |
| AR048669A1 (es) | 2004-03-03 | 2006-05-17 | Syngenta Ltd | Derivados biciclicos de bisamida |
| GB0422401D0 (en) | 2004-10-08 | 2004-11-10 | Syngenta Participations Ag | Fungicidal compositions |
| GB0422556D0 (en) | 2004-10-11 | 2004-11-10 | Syngenta Participations Ag | Novel insecticides |
| EP1871760B1 (en) | 2005-04-20 | 2010-08-11 | Syngenta Participations AG | Cyano anthranilamide insecticides |
| EP1881964A1 (de) | 2005-05-11 | 2008-01-30 | Basf Aktiengesellschaft | Pyrazolcarbonsäureamide als fungizide |
| EP1888063B1 (en) | 2005-05-18 | 2009-01-14 | F2G Ltd. | Antifungal agents |
| US7476764B2 (en) | 2005-08-04 | 2009-01-13 | Bristol-Myers Squibb Company | Phenylcarboxyamides as beta-secretase inhibitors |
| US20100222217A1 (en) | 2005-08-05 | 2010-09-02 | Markus Gewehr | Fungicidal N-[2-(Haloalkoxy)Phenyl]Heteroarylcarboxamides |
| GB0516703D0 (en) | 2005-08-15 | 2005-09-21 | Syngenta Participations Ag | Novel insecticides |
| CA2626312C (en) | 2005-10-25 | 2014-10-07 | Hans Tobler | Heterocyclic amide derivatives useful as microbiocides |
| WO2007058504A1 (en) | 2005-11-21 | 2007-05-24 | Lg Life Sciences, Ltd. | Novel compounds as agonist for ppar gamma and ppar alpha, method for preparation of the same, and pharmaceutical composition containing the same |
| AU2007214661B2 (en) | 2006-02-16 | 2012-05-17 | Syngenta Limited | Pesticides containing a bicyclic bisamide structure |
| DE102006035991A1 (de) | 2006-08-02 | 2008-02-14 | A. Raymond Et Cie | Vorrichtung zum Halten einer Kamera an einem Träger |
| DE102007023102A1 (de) | 2006-12-19 | 2008-06-26 | Bayer Cropscience Ag | Bisoxime als Fungizide |
| GB0720232D0 (en) | 2007-10-16 | 2007-11-28 | Syngenta Participations Ag | Insecticidal compounds |
| TWI508962B (zh) | 2009-04-22 | 2015-11-21 | Du Pont | 氮雜環醯胺之固體形態 |
| CN103153958A (zh) * | 2010-07-02 | 2013-06-12 | 先正达参股股份有限公司 | 新颖的杀微生物的二肟醚衍生物 |
-
2011
- 2011-07-28 AR ARP110102730A patent/AR082405A1/es unknown
- 2011-07-28 WO PCT/EP2011/063018 patent/WO2012013754A1/en not_active Ceased
- 2011-07-28 CN CN201180037088.9A patent/CN103038217A/zh active Pending
- 2011-07-28 EP EP11736114.7A patent/EP2598487A1/en not_active Withdrawn
- 2011-07-28 TW TW100126768A patent/TW201211005A/zh unknown
- 2011-07-28 CA CA2804355A patent/CA2804355A1/en not_active Abandoned
- 2011-07-28 US US13/813,131 patent/US20140162980A1/en not_active Abandoned
- 2011-07-28 AU AU2011284714A patent/AU2011284714A1/en not_active Abandoned
- 2011-07-28 BR BR112013002073A patent/BR112013002073A2/pt not_active Application Discontinuation
- 2011-07-29 UY UY0001033538A patent/UY33538A/es not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| US20140162980A1 (en) | 2014-06-12 |
| BR112013002073A2 (pt) | 2016-05-24 |
| UY33538A (es) | 2012-02-29 |
| TW201211005A (en) | 2012-03-16 |
| EP2598487A1 (en) | 2013-06-05 |
| CN103038217A (zh) | 2013-04-10 |
| CA2804355A1 (en) | 2012-02-02 |
| AU2011284714A1 (en) | 2013-01-31 |
| WO2012013754A1 (en) | 2012-02-02 |
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