AR087086A1 - Mezclas fungicidas - Google Patents
Mezclas fungicidasInfo
- Publication number
- AR087086A1 AR087086A1 ARP120102459A ARP120102459A AR087086A1 AR 087086 A1 AR087086 A1 AR 087086A1 AR P120102459 A ARP120102459 A AR P120102459A AR P120102459 A ARP120102459 A AR P120102459A AR 087086 A1 AR087086 A1 AR 087086A1
- Authority
- AR
- Argentina
- Prior art keywords
- thiaxamide
- chlorophenyl
- hydroxymethyl
- isoxazole
- pyrimidyl
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title abstract 5
- 230000000855 fungicidal effect Effects 0.000 title abstract 2
- 239000000417 fungicide Substances 0.000 title 1
- -1 alkoxyalkynyl Chemical group 0.000 abstract 8
- 125000003342 alkenyl group Chemical group 0.000 abstract 5
- 125000003545 alkoxy group Chemical group 0.000 abstract 5
- 125000000217 alkyl group Chemical group 0.000 abstract 5
- 125000004414 alkyl thio group Chemical group 0.000 abstract 5
- 125000000304 alkynyl group Chemical group 0.000 abstract 5
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 5
- 125000004438 haloalkoxy group Chemical group 0.000 abstract 5
- 125000001188 haloalkyl group Chemical group 0.000 abstract 5
- 229910052736 halogen Inorganic materials 0.000 abstract 5
- 150000002367 halogens Chemical class 0.000 abstract 5
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 5
- 150000001875 compounds Chemical class 0.000 abstract 3
- RFHAOTPXVQNOHP-UHFFFAOYSA-N fluconazole Chemical compound C1=NC=NN1CC(C=1C(=CC(F)=CC=1)F)(O)CN1C=NC=N1 RFHAOTPXVQNOHP-UHFFFAOYSA-N 0.000 abstract 3
- 229960004884 fluconazole Drugs 0.000 abstract 3
- 125000001072 heteroaryl group Chemical group 0.000 abstract 3
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 abstract 3
- DGOAXBPOVUPPEB-UHFFFAOYSA-N 3-(difluoromethyl)-N-methoxy-1-methyl-N-[1-(2,4,6-trichlorophenyl)propan-2-yl]pyrazole-4-carboxamide Chemical compound C=1N(C)N=C(C(F)F)C=1C(=O)N(OC)C(C)CC1=C(Cl)C=C(Cl)C=C1Cl DGOAXBPOVUPPEB-UHFFFAOYSA-N 0.000 abstract 2
- 201000010099 disease Diseases 0.000 abstract 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 2
- CCCGEKHKTPTUHJ-ZJUUUORDSA-N solatenol Chemical compound C1([C@]2([H])CC[C@]3(C2=C(Cl)Cl)[H])=C3C=CC=C1NC(=O)C1=CN(C)N=C1C(F)F CCCGEKHKTPTUHJ-ZJUUUORDSA-N 0.000 abstract 2
- ZMYFCFLJBGAQRS-IRXDYDNUSA-N (2R,3S)-epoxiconazole Chemical compound C1=CC(F)=CC=C1[C@@]1(CN2N=CN=C2)[C@H](C=2C(=CC=CC=2)Cl)O1 ZMYFCFLJBGAQRS-IRXDYDNUSA-N 0.000 abstract 1
- RYAUSSKQMZRMAI-ALOPSCKCSA-N (2S,6R)-4-[3-(4-tert-butylphenyl)-2-methylpropyl]-2,6-dimethylmorpholine Chemical compound C=1C=C(C(C)(C)C)C=CC=1CC(C)CN1C[C@H](C)O[C@H](C)C1 RYAUSSKQMZRMAI-ALOPSCKCSA-N 0.000 abstract 1
- PXMNMQRDXWABCY-UHFFFAOYSA-N 1-(4-chlorophenyl)-4,4-dimethyl-3-(1H-1,2,4-triazol-1-ylmethyl)pentan-3-ol Chemical compound C1=NC=NN1CC(O)(C(C)(C)C)CCC1=CC=C(Cl)C=C1 PXMNMQRDXWABCY-UHFFFAOYSA-N 0.000 abstract 1
- MGNFYQILYYYUBS-UHFFFAOYSA-N 1-[3-(4-tert-butylphenyl)-2-methylpropyl]piperidine Chemical compound C=1C=C(C(C)(C)C)C=CC=1CC(C)CN1CCCCC1 MGNFYQILYYYUBS-UHFFFAOYSA-N 0.000 abstract 1
- 125000001255 4-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1F 0.000 abstract 1
- PCCSBWNGDMYFCW-UHFFFAOYSA-N 5-methyl-5-(4-phenoxyphenyl)-3-(phenylamino)-1,3-oxazolidine-2,4-dione Chemical compound O=C1C(C)(C=2C=CC(OC=3C=CC=CC=3)=CC=2)OC(=O)N1NC1=CC=CC=C1 PCCSBWNGDMYFCW-UHFFFAOYSA-N 0.000 abstract 1
- 239000005738 Bixafen Substances 0.000 abstract 1
- 239000005740 Boscalid Substances 0.000 abstract 1
- 239000005747 Chlorothalonil Substances 0.000 abstract 1
- 239000005767 Epoxiconazole Substances 0.000 abstract 1
- 239000005772 Famoxadone Substances 0.000 abstract 1
- 239000005777 Fenpropidin Substances 0.000 abstract 1
- 239000005778 Fenpropimorph Substances 0.000 abstract 1
- 239000005781 Fludioxonil Substances 0.000 abstract 1
- 239000005784 Fluoxastrobin Substances 0.000 abstract 1
- 239000005796 Ipconazole Substances 0.000 abstract 1
- 239000005800 Kresoxim-methyl Substances 0.000 abstract 1
- 239000005868 Metconazole Substances 0.000 abstract 1
- 239000005810 Metrafenone Substances 0.000 abstract 1
- 239000005822 Propiconazole Substances 0.000 abstract 1
- 239000005824 Proquinazid Substances 0.000 abstract 1
- 239000005869 Pyraclostrobin Substances 0.000 abstract 1
- 239000005839 Tebuconazole Substances 0.000 abstract 1
- GNOOFMLHHSDFAO-UHFFFAOYSA-N [3-(4-chloro-2-fluorophenyl)-5-(2,4-difluorophenyl)-1,2-oxazol-4-yl]-(2h-pyrimidin-1-yl)methanol Chemical compound C=1C=C(Cl)C=C(F)C=1C1=NOC(C=2C(=CC(F)=CC=2)F)=C1C(O)N1CN=CC=C1 GNOOFMLHHSDFAO-UHFFFAOYSA-N 0.000 abstract 1
- YDHZUCLRCLIJRL-UHFFFAOYSA-N [3-(4-chloro-2-fluorophenyl)-5-(2,4-difluorophenyl)-1,2-oxazol-4-yl]-pyridin-3-ylmethanol Chemical compound C=1C=CN=CC=1C(O)C=1C(C=2C(=CC(Cl)=CC=2)F)=NOC=1C1=CC=C(F)C=C1F YDHZUCLRCLIJRL-UHFFFAOYSA-N 0.000 abstract 1
- RCJDGDWLBUUSLS-UHFFFAOYSA-N [3-(4-chloro-2-fluorophenyl)-5-(2-chlorophenyl)-1,2-oxazol-4-yl]-(2h-pyrimidin-1-yl)methanol Chemical compound C=1C=C(Cl)C=C(F)C=1C1=NOC(C=2C(=CC=CC=2)Cl)=C1C(O)N1CN=CC=C1 RCJDGDWLBUUSLS-UHFFFAOYSA-N 0.000 abstract 1
- HNACKEBCZPTUOQ-UHFFFAOYSA-N [3-(4-chlorophenyl)-5-(2,4-difluorophenyl)-1,2-oxazol-4-yl]-(2h-pyrimidin-1-yl)methanol Chemical compound C=1C=C(Cl)C=CC=1C1=NOC(C=2C(=CC(F)=CC=2)F)=C1C(O)N1CN=CC=C1 HNACKEBCZPTUOQ-UHFFFAOYSA-N 0.000 abstract 1
- BNBVHUBZMYFNLO-UHFFFAOYSA-N [3-(4-chlorophenyl)-5-(4-fluorophenyl)-1,2-oxazol-4-yl]-(2h-pyrimidin-1-yl)methanol Chemical compound C=1C=C(Cl)C=CC=1C1=NOC(C=2C=CC(F)=CC=2)=C1C(O)N1CN=CC=C1 BNBVHUBZMYFNLO-UHFFFAOYSA-N 0.000 abstract 1
- BUBJDEVOMATXCE-UHFFFAOYSA-N [5-(2-chloro-4-fluorophenyl)-3-(2,4-difluorophenyl)-1,2-oxazol-4-yl]-pyridin-3-ylmethanol Chemical compound C=1C=CN=CC=1C(O)C=1C(C=2C(=CC(F)=CC=2)F)=NOC=1C1=CC=C(F)C=C1Cl BUBJDEVOMATXCE-UHFFFAOYSA-N 0.000 abstract 1
- 125000002252 acyl group Chemical group 0.000 abstract 1
- 125000005103 alkyl silyl group Chemical group 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 abstract 1
- LDLMOOXUCMHBMZ-UHFFFAOYSA-N bixafen Chemical compound FC(F)C1=NN(C)C=C1C(=O)NC1=CC=C(F)C=C1C1=CC=C(Cl)C(Cl)=C1 LDLMOOXUCMHBMZ-UHFFFAOYSA-N 0.000 abstract 1
- WYEMLYFITZORAB-UHFFFAOYSA-N boscalid Chemical compound C1=CC(Cl)=CC=C1C1=CC=CC=C1NC(=O)C1=CC=CN=C1Cl WYEMLYFITZORAB-UHFFFAOYSA-N 0.000 abstract 1
- 229940118790 boscalid Drugs 0.000 abstract 1
- CRQQGFGUEAVUIL-UHFFFAOYSA-N chlorothalonil Chemical compound ClC1=C(Cl)C(C#N)=C(Cl)C(C#N)=C1Cl CRQQGFGUEAVUIL-UHFFFAOYSA-N 0.000 abstract 1
- 244000038559 crop plants Species 0.000 abstract 1
- MUJOIMFVNIBMKC-UHFFFAOYSA-N fludioxonil Chemical compound C=12OC(F)(F)OC2=CC=CC=1C1=CNC=C1C#N MUJOIMFVNIBMKC-UHFFFAOYSA-N 0.000 abstract 1
- UFEODZBUAFNAEU-NLRVBDNBSA-N fluoxastrobin Chemical compound C=1C=CC=C(OC=2C(=C(OC=3C(=CC=CC=3)Cl)N=CN=2)F)C=1C(=N/OC)\C1=NOCCO1 UFEODZBUAFNAEU-NLRVBDNBSA-N 0.000 abstract 1
- QTYCMDBMOLSEAM-UHFFFAOYSA-N ipconazole Chemical compound C1=NC=NN1CC1(O)C(C(C)C)CCC1CC1=CC=C(Cl)C=C1 QTYCMDBMOLSEAM-UHFFFAOYSA-N 0.000 abstract 1
- ZOTBXTZVPHCKPN-HTXNQAPBSA-N kresoxim-methyl Chemical compound CO\N=C(\C(=O)OC)C1=CC=CC=C1COC1=CC=CC=C1C ZOTBXTZVPHCKPN-HTXNQAPBSA-N 0.000 abstract 1
- 239000000463 material Substances 0.000 abstract 1
- XWPZUHJBOLQNMN-UHFFFAOYSA-N metconazole Chemical compound C1=NC=NN1CC1(O)C(C)(C)CCC1CC1=CC=C(Cl)C=C1 XWPZUHJBOLQNMN-UHFFFAOYSA-N 0.000 abstract 1
- AMSPWOYQQAWRRM-UHFFFAOYSA-N metrafenone Chemical compound COC1=CC=C(Br)C(C)=C1C(=O)C1=C(C)C=C(OC)C(OC)=C1OC AMSPWOYQQAWRRM-UHFFFAOYSA-N 0.000 abstract 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 abstract 1
- STJLVHWMYQXCPB-UHFFFAOYSA-N propiconazole Chemical compound O1C(CCC)COC1(C=1C(=CC(Cl)=CC=1)Cl)CN1N=CN=C1 STJLVHWMYQXCPB-UHFFFAOYSA-N 0.000 abstract 1
- FLVBXVXXXMLMOX-UHFFFAOYSA-N proquinazid Chemical compound C1=C(I)C=C2C(=O)N(CCC)C(OCCC)=NC2=C1 FLVBXVXXXMLMOX-UHFFFAOYSA-N 0.000 abstract 1
- HZRSNVGNWUDEFX-UHFFFAOYSA-N pyraclostrobin Chemical compound COC(=O)N(OC)C1=CC=CC=C1COC1=NN(C=2C=CC(Cl)=CC=2)C=C1 HZRSNVGNWUDEFX-UHFFFAOYSA-N 0.000 abstract 1
- 230000001105 regulatory effect Effects 0.000 abstract 1
- 125000003107 substituted aryl group Chemical group 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
- A01N43/80—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 one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,2
Landscapes
- 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)
Abstract
Reivindicación 1: Una composición fungicida sinergísticamente activa que comprende un componente (A) y un componente (B), en donde el componente (A) se selecciona de al menos un compuesto de fórmula (1), en donde: R¹ es arilo opcionalmente sustituido por halógeno, alquilo, alquenilo, alquinilo, haloalquilo, alcoxi, alquiltio, haloalcoxi, fenoxi, alcoxialquinilo, ciano o nitro; o heteroarilo opcionalmente sustituido por halógeno, alquilo, alquenilo, alquinilo, haloalquilo, alcoxi, alquiltio, haloalcoxi, ciano o nitro; R² es heteroarilo opcionalmente sustituido por halógeno, alquilo, alquenilo, alquinilo, haloalquilo, alcoxi, alquiltio, haloalcoxi, ciano o nitro; R³ es arilo opcionalmente sustituido por halógeno, alquilo, alquenilo, alquinilo, haloalquilo, alcoxi, alquiltio, haloalcoxi, alcoxialquinilo, ciano, nitro; heteroarilo opcionalmente sustituido por halógeno, alquilo, alquenilo, alquinilo, haloalquilo, alcoxi, alquiltio, haloalcoxi, ciano o nitro; o alquilsililo; y R⁴ es H o acilo, benzoilo y fenilacetilo; y el componente (B) se selecciona de al menos uno que se selecciona del grupo que consiste en Isopirazam, N-[9-(diclorometileno)-1,2,3,4-tetrahidro-1,4-metanonaftalen-5-il]-3-(difluorometil)-1-metil-1H-pirazol-4-carboxamida, 3-(difluorometil)-N-metoxi-1-metil-N-[1-metil-2-(2,4,6-triclorofenil)etil]-1H-pirazol-4-carboxamida, Bixafen, Boscalid, Fluxapiroxad, Pentiopirad, Fluopiram, Protioconazol, Propiconazol, Difenconazol, Ipconazol, Ciproconazol, Epoxiconazol, Metconazol, Tebuconazol, Procloraz, Flusilazol, Flutriafol, Fluquinconazol, Azoxistrobín, Trifloxistrobín, Piraclostrobín, Fluoxastrobín, Picoxistrobín, Kresoxim-metilo, Dimoxistrobín, Famoxadona, Ciprodinil, Clorotalonil, Fludioxonil, Metrafenona, Proquinazid, Ciflufenamid, Fenpropidín, Fenpropimorf, Espiroxamina, Trinexapac-etilo, Tiametoxam, Clotianidina, Imidaclodprid o Teflutrina. Reivindicación 2: Una composición adecuada para el control de enfermedades causadas por fitopatógenos de acuerdo con la reivindicación 1, en donde el o los compuestos adicionales del componente (B) se seleccionan del grupo de Isopirazam, N-[9-(diclorometileno)-1,2,3,4-tetrahidro-1,4-metanonaftalen-5-il]-3-(difluorometil)-1-metil-1H-pirazol-4-carboxamida y 3-(difluorometil)-N-metoxi-1-metil-N-[1-metil-2-(2,4,6-triclorofenil)etil]-1H-pirazol-4-carboxamida. Reivindicación 9: Una composición adecuada para el control de enfermedades causadas por fitopatógenos de acuerdo con la reivindicación 1, en donde el compuesto de fórmula (1) se selecciona de: 3-(2-fluoro-4-clorofenil)-5-(2,4-difluorofenil)-4-[(3-pirimidil)hidroximetil]-isoxazol; 3-(4-clorofenil)-5-(2,4-difluorofenil)-4-[(3-pirimidil)hidroximetil]-isoxazol; 3-(2-fluoro-4-clorofenil)-5-(2,4-difluorofenil)-4-[(3-piridil)hidroximetil]-isoxazol; 3-(2,4-clorofenil)-5-(2-clorofenil)-4-[(3-pirimidil)hidroximetil]-isoxazol; 3-(2-fluoro-4-clorofenil)-5-(2-clorofenil)-4-[(3-pirimidil)hidroximetil]-isoxazol; 3-(4-clorofenil)-5-(2-metoxipiridina)-4-[(3-pirimidil)hidroximetil]-isoxazol; 3-(4-clorofenil)-5-(4-fluorofenil)-4-[(3-pirimidil)hidroximetil]-isoxazol; 3-(4-clorofenil)-5-(2,4-fluorofenil)-4-[(3-pirimidil)hidroximetil]-isoxazol; 3-(2,4-difluorofenil)-5-(2-cloro-4-fluorofenil)-4-[(3-piridil)hidroximetil]-isoxazol y@@@(S)-3-(2-fluoro-4-clorofenil)-5-(2,4-difluorofenil)-4-[(3-piridil)hidroximetil]-isoxazol; y sales de los mismos. Reivindicación 11: Un método para regular el crecimiento de plantas de cultivos de plantas útiles que comprende aplicar a dichas plantas, a una o más partes de dichas plantas o al locus de las mismas o material de propagación de planta, una mezcla tal como se define en cualquiera de las reivindicaciones 1 a 10.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP11173202 | 2011-07-08 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR087086A1 true AR087086A1 (es) | 2014-02-12 |
Family
ID=46420204
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP120102459A AR087086A1 (es) | 2011-07-08 | 2012-07-06 | Mezclas fungicidas |
Country Status (3)
| Country | Link |
|---|---|
| AR (1) | AR087086A1 (es) |
| UY (1) | UY34189A (es) |
| WO (1) | WO2013007550A1 (es) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| PL3051945T3 (pl) | 2013-10-03 | 2023-02-20 | Syngenta Participations Ag | Kompozycje fungicydowe |
| GB2521255A (en) * | 2013-10-22 | 2015-06-17 | Syngenta Participations Ag | Method of combating corynespora |
| US10130095B2 (en) | 2014-02-19 | 2018-11-20 | BASF Agro B.V. | Fungicidal compositions of pyrazolecarboxylic acid alkoxyamides |
| CN106942237A (zh) * | 2017-05-18 | 2017-07-14 | 佛山市盈辉作物科学有限公司 | 含有吡噻菌胺和氟吡菌酰胺的杀菌组合物 |
Family Cites Families (28)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BR8600161A (pt) | 1985-01-18 | 1986-09-23 | Plant Genetic Systems Nv | Gene quimerico,vetores de plasmidio hibrido,intermediario,processo para controlar insetos em agricultura ou horticultura,composicao inseticida,processo para transformar celulas de plantas para expressar uma toxina de polipeptideo produzida por bacillus thuringiensis,planta,semente de planta,cultura de celulas e plasmidio |
| CA1340685C (en) | 1988-07-29 | 1999-07-27 | Frederick Meins | Dna sequences encoding polypeptides having beta-1,3-glucanase activity |
| US5169629A (en) | 1988-11-01 | 1992-12-08 | Mycogen Corporation | Process of controlling lepidopteran pests, using bacillus thuringiensis isolate denoted b.t ps81gg |
| NZ231804A (en) | 1988-12-19 | 1993-03-26 | Ciba Geigy Ag | Insecticidal toxin from leiurus quinquestriatus hebraeus |
| EP0392225B1 (en) | 1989-03-24 | 2003-05-28 | Syngenta Participations AG | Disease-resistant transgenic plants |
| GB8910624D0 (en) | 1989-05-09 | 1989-06-21 | Ici Plc | Bacterial strains |
| CA2015951A1 (en) | 1989-05-18 | 1990-11-18 | Mycogen Corporation | Novel bacillus thuringiensis isolates active against lepidopteran pests, and genes encoding novel lepidopteran-active toxins |
| DE69018772T2 (de) | 1989-11-07 | 1996-03-14 | Pioneer Hi Bred Int | Larven abtötende Lektine und darauf beruhende Pflanzenresistenz gegen Insekten. |
| US5639949A (en) | 1990-08-20 | 1997-06-17 | Ciba-Geigy Corporation | Genes for the synthesis of antipathogenic substances |
| UA48104C2 (uk) | 1991-10-04 | 2002-08-15 | Новартіс Аг | Фрагмент днк, який містить послідовність,що кодує інсектицидний протеїн, оптимізовану для кукурудзи,фрагмент днк, який забезпечує направлену бажану для серцевини стебла експресію зв'язаного з нею структурного гена в рослині, фрагмент днк, який забезпечує специфічну для пилку експресію зв`язаного з нею структурного гена в рослині, рекомбінантна молекула днк, спосіб одержання оптимізованої для кукурудзи кодуючої послідовності інсектицидного протеїну, спосіб захисту рослин кукурудзи щонайменше від однієї комахи-шкідника |
| US5530195A (en) | 1994-06-10 | 1996-06-25 | Ciba-Geigy Corporation | Bacillus thuringiensis gene encoding a toxin active against insects |
| WO2002015701A2 (en) | 2000-08-25 | 2002-02-28 | Syngenta Participations Ag | Bacillus thuringiensis crystal protein hybrids |
| US7230167B2 (en) | 2001-08-31 | 2007-06-12 | Syngenta Participations Ag | Modified Cry3A toxins and nucleic acid sequences coding therefor |
| WO2003052073A2 (en) | 2001-12-17 | 2003-06-26 | Syngenta Participations Ag | Novel corn event |
| CN1625336A (zh) | 2002-04-04 | 2005-06-08 | 瓦伦特生物科学公司 | 增强的除草剂组合物 |
| US20050239751A1 (en) | 2004-03-26 | 2005-10-27 | Rigel Pharmaceuticals, Inc. | Heterocyclic anti-viral compounds comprising metabolizable moieties and their uses |
| CA2579199C (en) | 2004-09-10 | 2013-04-30 | Syngenta Limited | Substituted isoxazoles as fungicides |
| DE102005007160A1 (de) | 2005-02-16 | 2006-08-24 | Basf Ag | Pyrazolcarbonsäureanilide, Verfahren zu ihrer Herstellung und sie enthaltende Mittel zur Bekämpfung von Schadpilzen |
| CA2626312C (en) | 2005-10-25 | 2014-10-07 | Hans Tobler | Heterocyclic amide derivatives useful as microbiocides |
| TW200803740A (en) | 2005-12-16 | 2008-01-16 | Du Pont | 5-aryl isoxazolines for controlling invertebrate pests |
| WO2008013622A2 (en) | 2006-07-27 | 2008-01-31 | E. I. Du Pont De Nemours And Company | Fungicidal azocyclic amides |
| BRPI0812269A2 (pt) * | 2007-06-06 | 2014-09-30 | Basf Se | Misturas fungicidas, composição fungicida, método para controlar fungos nocivos fitopatogênicos, e para proteger semente, e, semente. |
| CL2008001647A1 (es) | 2007-06-08 | 2008-10-10 | Syngenta Participations Ag | Compuestos derivados de feniletil-amida de acido-1h-pirazol-4-carboxilico; compuestos derivados de (feniletil)amina; metodo para controlar o prevenir la infestacion de plantas por parte de microorganismos fitopatogenos; y composicion para el control |
| GB0823002D0 (en) | 2008-12-17 | 2009-01-28 | Syngenta Participations Ag | Isoxazoles derivatives with plant growth regulating properties |
| TWI508962B (zh) | 2009-04-22 | 2015-11-21 | Du Pont | 氮雜環醯胺之固體形態 |
| WO2011051243A1 (en) | 2009-10-29 | 2011-05-05 | Bayer Cropscience Ag | Active compound combinations |
| TW201117722A (en) * | 2009-11-04 | 2011-06-01 | Du Pont | Fungicidal mixtures |
| EP2539335B1 (en) | 2010-02-25 | 2016-12-21 | Syngenta Participations AG | Process for the preparation of isoxazoline derivatives |
-
2012
- 2012-07-02 WO PCT/EP2012/062831 patent/WO2013007550A1/en not_active Ceased
- 2012-07-06 AR ARP120102459A patent/AR087086A1/es not_active Application Discontinuation
- 2012-07-06 UY UY0001034189A patent/UY34189A/es unknown
Also Published As
| Publication number | Publication date |
|---|---|
| UY34189A (es) | 2013-02-28 |
| WO2013007550A1 (en) | 2013-01-17 |
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