AR095928A1 - Métodos para controlar las plagas resistentes a neonicotinoides - Google Patents
Métodos para controlar las plagas resistentes a neonicotinoidesInfo
- Publication number
- AR095928A1 AR095928A1 ARP140101404A ARP140101404A AR095928A1 AR 095928 A1 AR095928 A1 AR 095928A1 AR P140101404 A ARP140101404 A AR P140101404A AR P140101404 A ARP140101404 A AR P140101404A AR 095928 A1 AR095928 A1 AR 095928A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- alkoxy
- haloalkyl
- optionally substituted
- cyano
- Prior art date
Links
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 20
- 125000000217 alkyl group Chemical group 0.000 abstract 16
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 abstract 14
- 125000001424 substituent group Chemical group 0.000 abstract 12
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 11
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 11
- 229910052736 halogen Inorganic materials 0.000 abstract 9
- 150000002367 halogens Chemical class 0.000 abstract 9
- 229910052739 hydrogen Inorganic materials 0.000 abstract 9
- 239000001257 hydrogen Substances 0.000 abstract 9
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 9
- 125000003545 alkoxy group Chemical group 0.000 abstract 6
- 150000002431 hydrogen Chemical group 0.000 abstract 6
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 5
- 125000005133 alkynyloxy group Chemical group 0.000 abstract 5
- 241000238631 Hexapoda Species 0.000 abstract 4
- 125000003342 alkenyl group Chemical group 0.000 abstract 4
- 125000003118 aryl group Chemical group 0.000 abstract 4
- 230000009286 beneficial effect Effects 0.000 abstract 4
- 125000000262 haloalkenyl group Chemical group 0.000 abstract 4
- 125000001188 haloalkyl group Chemical group 0.000 abstract 4
- 241000238421 Arthropoda Species 0.000 abstract 3
- 125000003302 alkenyloxy group Chemical group 0.000 abstract 3
- 125000000304 alkynyl group Chemical group 0.000 abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 3
- -1 cyano, hydroxy Chemical group 0.000 abstract 3
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 abstract 2
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 2
- 241000258937 Hemiptera Species 0.000 abstract 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 2
- 125000005097 aminocarbonylalkyl group Chemical group 0.000 abstract 2
- 125000004682 aminothiocarbonyl group Chemical group NC(=S)* 0.000 abstract 2
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 2
- 125000004104 aryloxy group Chemical group 0.000 abstract 2
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 2
- 125000004966 cyanoalkyl group Chemical group 0.000 abstract 2
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 abstract 2
- 125000001072 heteroaryl group Chemical group 0.000 abstract 2
- 125000000623 heterocyclic group Chemical group 0.000 abstract 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 2
- 239000002917 insecticide Substances 0.000 abstract 2
- 125000006526 (C1-C2) alkyl group Chemical group 0.000 abstract 1
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 1
- 125000006642 (C1-C6) cyanoalkyl group Chemical group 0.000 abstract 1
- 125000006619 (C1-C6) dialkylamino group Chemical group 0.000 abstract 1
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 abstract 1
- 241000238876 Acari Species 0.000 abstract 1
- 241000255769 Adalia bipunctata Species 0.000 abstract 1
- 241001541099 Amblydromalus limonicus Species 0.000 abstract 1
- 241000124899 Amblyseius andersoni Species 0.000 abstract 1
- 241001664794 Amblyseius swirskii Species 0.000 abstract 1
- 241000131068 Coccinella septempunctata Species 0.000 abstract 1
- 150000001204 N-oxides Chemical class 0.000 abstract 1
- 241001206567 Neoseiulus barkeri Species 0.000 abstract 1
- 241001658757 Neoseiulus californicus Species 0.000 abstract 1
- 241001455175 Neoseiulus cucumeris Species 0.000 abstract 1
- 241001647846 Orius insidiosus Species 0.000 abstract 1
- 241001635530 Orius laevigatus Species 0.000 abstract 1
- 241001635527 Orius majusculus Species 0.000 abstract 1
- 241000275633 Syrphus Species 0.000 abstract 1
- 241001621303 Typhlodromips montdorensis Species 0.000 abstract 1
- MDFFNEOEWAXZRQ-UHFFFAOYSA-N aminyl Chemical group [NH2] MDFFNEOEWAXZRQ-UHFFFAOYSA-N 0.000 abstract 1
- 125000005161 aryl oxy carbonyl group Chemical group 0.000 abstract 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 abstract 1
- 125000000392 cycloalkenyl group Chemical group 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- 125000006576 di-(C1-C3-alkyl)-aminocarbonyl group Chemical group 0.000 abstract 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 1
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 abstract 1
- 125000000232 haloalkynyl group Chemical group 0.000 abstract 1
- 125000005347 halocycloalkyl group Chemical group 0.000 abstract 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
- 125000005016 hydroxyalkynyl group Chemical group 0.000 abstract 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 abstract 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 125000004469 siloxy group Chemical group [SiH3]O* 0.000 abstract 1
- 125000002813 thiocarbonyl group Chemical group *C(*)=S 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D451/00—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof
- C07D451/02—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof containing not further condensed 8-azabicyclo [3.2.1] octane or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane; Cyclic acetals thereof
-
- 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
- A01N63/00—Biocides, pest repellants or attractants, or plant growth regulators containing microorganisms, viruses, microbial fungi, animals or substances produced by, or obtained from, microorganisms, viruses, microbial fungi or animals, e.g. enzymes or fermentates
- A01N63/10—Animals; Substances produced thereby or obtained therefrom
- A01N63/14—Insects
-
- 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
- A01N63/00—Biocides, pest repellants or attractants, or plant growth regulators containing microorganisms, viruses, microbial fungi, animals or substances produced by, or obtained from, microorganisms, viruses, microbial fungi or animals, e.g. enzymes or fermentates
- A01N63/10—Animals; Substances produced thereby or obtained therefrom
- A01N63/16—Arachnids
Landscapes
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Zoology (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Environmental Sciences (AREA)
- Wood Science & Technology (AREA)
- Dentistry (AREA)
- Plant Pathology (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Biotechnology (AREA)
- Microbiology (AREA)
- Virology (AREA)
- Insects & Arthropods (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
Reivindicación 1: Un método para controlar insectos del orden de los Hemípteros, que son resistentes a insecticidas neonicotinoides, método que comprende la aplicación a dichos insectos resistentes a neonicotinoides de un compuesto de fórmula (1), donde A es -CH₂-CH₂- o -CH=CH-; R¹ es hidrógeno, formilo, ciano, hidroxi, NH₂, alquilo C₁₋₆ (opcionalmente sustituido por arilo, ariloxi, heteroarilo o heterociclilo, donde ellos mismos pueden estar opcionalmente sustituidos por uno a tres sustituyentes que se seleccionan independientemente de halógeno, ciano, nitro, alquilo C₁₋₄, haloalquilo C₁₋₄, y alcoxi C₁₋₄), haloalquilo C₁₋₆ (opcionalmente sustituido por uno a dos sustituyentes que se seleccionan independientemente de hidroxi, alcoxi C₁₋₄, tri(alquil C₁₋₄)sililoxi, alquil C₁₋₂-carboniloxi, y alquenil C₃₋₅), cianoalquilo C₁₋₆, alcoxi C₁₋₆alquilo C₁₋₆, alcoxi C₁₋₄alcoxi C₁₋₄alquilo C₁₋₄, alquil C₁₋₆carbonilalquilo C₁₋₆, alcoxi C₁₋₆iminoalquilo C₁₋₄, haloalcoxi C₁₋₄alquilo C₁₋₄, alcoxi C₁₋₆carbonilalquilo C₁₋₆, alcoxi C₁₋₄alcoxi C₁₋₄carbonilalquilo C₁₋₆, hidroxicarbonilalquilo C₁₋₆, ariloxicarbonilalquilo C₁₋₆ (donde el grupo arilo puede estar opcionalmente sustituido por uno o dos sustituyentes que se seleccionan independientemente de halógeno, ciano, nitro, alquilo C₁₋₄, haloalquilo C₁₋₄, y alcoxi C₁₋₄), alquil C₁₋₄aminocarbonilalquilo C₁₋₆, di(alquil C₁₋₄)aminocarbonilalquilo C₁₋₆, haloalquil C₁₋₄aminocarbonilalquilo C₁₋₆, di(haloalquil C₁₋₄)aminocarbonilalquilo C₁₋₆, alcoxi C₁₋₂alquil C₂₋₄aminocarbonilalquilo C₁₋₄, alqueniloxi C₂₋₆carbonilalquilo C₁₋₆, alquiniloxi C₃₋₆carbonilalquilo C₁₋₆, (R³O)₂(O=)P-alquilo C₁₋₆ donde R³ es hidrógeno, alquilo C₁₋₄ o bencilo, cicloalquilo C₃₋₇ (opcionalmente sustituido por uno a tres sustituyentes que se seleccionan independientemente de alquilo C₁₋₄, haloalquilo C₁₋₄, y alcoxi C₁₋₄ y, adicionalmente, una de las unidades de miembro del anillo puede representar opcionalmente C=O o C=NR² donde R² es hidrógeno, alquilo C₁₋₄, haloalquilo C₁₋₄, cianoalquilo C₁₋₄, alcoxi C₁₋₄, o cicloalquilo C₃₋₆), halocicloalquilo C₃₋₇, cicloalquenilo C₃₋₇ (opcionalmente sustituido por uno o dos sustituyentes que se seleccionan independientemente de alquilo C₁₋₄, y haloalquilo C₁₋₄, y, adicionalmente, una de las unidades de miembro del anillo puede representar opcionalmente C=O), halocicloalquenilo C₃₋₇, alquil C₁₋₆-S(=O)ₙ₅-alquilo C₁₋₆ donde n⁵ es 0, 1 ó 2, alquenilo C₃₋₆, haloalquenilo C₃₋₆, arilalquenilo C₃₋₆, alquinilo C₃₋₆, haloalquinilo C₃₋₆, arilalquinilo C₃₋₆, hidroxialquinilo C₃₋₆, alcoxi C₁₋₆carbonilo (opcionalmente sustituido por uno a tres sustituyentes que se seleccionan independientemente de halógeno, hidroxi, ciano, alcoxi C₁₋₄, haloalquilo C₁₋₄ y arilo), ariloxicarbonilo (opcionalmente sustituido por uno a tres sustituyentes que se seleccionan independientemente de halógeno, ciano, nitro, alquilo C₁₋₄, haloalquilo C₁₋₄, alcoxi C₁₋₄), alqueniloxi C₃₋₆carbonilo, alquiniloxi C₃₋₆carbonilo, alquil C₁₋₆carbonilo, haloalquil C₁₋₆carbonilo, aminocarbonilo, alquil C₁₋₆aminocarbonilo, di(alquil C₁₋₆)aminocarbonilo, aminotiocarbonilo, alquil C₁₋₆aminotiocarbonilo, di(alquil C₁₋₆)aminotiocarbonilo, alcoxi C₁₋₆, alqueniloxi C₃₋₆, alquiniloxi C₃₋₆, ariloxi (opcionalmente sustituido por uno a tres sustituyentes que se seleccionan independientemente de halógeno, ciano, nitro, alquilo C₁₋₄, haloalquilo C₁₋₄, y alcoxi C₁₋₄), alquil C₁₋₆amino, di(alquil C₁₋₆)amino, cicloalquil C₃₋₆amino, alquil C₁₋₄tio, alquil C₁₋₄sulfinilo, alquil C₁₋₄sulfonilo, haloalquil C₁₋₄sulfonilo, aril-S(=O)ₙ₆ (opcionalmente sustituido por uno o dos sustituyentes que se seleccionan independientemente de halógeno, nitro, y alquilo C₁₋₄) donde n₆ es 0, 1 ó 2, arilo (opcionalmente sustituido por uno a tres sustituyentes que se seleccionan independientemente de halógeno, ciano, nitro, alquilo C₁₋₄, haloalquilo C₁₋₄, alcoxi C₁₋₄, y haloalcoxi C₁₋₄), heteroarilo (opcionalmente sustituido por uno a tres sustituyentes que se seleccionan independientemente de halógeno, ciano, nitro, alquilo C₁₋₄, haloalquilo C₁₋₄, alcoxi C₁₋₄, y haloalcoxi C₁₋₄), heterociclilo (opcionalmente sustituido por uno a tres sustituyentes que se seleccionan independientemente de halógeno, ciano, nitro, alquilo C₁₋₄, haloalquilo C₁₋₄, alcoxi C₁₋₄, y haloalcoxi C₁₋₄, y, adicionalmente, una de las unidades de miembro del anillo puede representar opcionalmente C=O o C=NR² donde R² es hidrógeno, alquilo C₁₋₄, haloalquilo C₁₋₄, cianoalquilo C₁₋₄, alcoxi C₁₋₄, o cicloalquilo C₃₋₆), (alquil C₁₋₆tio)carbonilo, (alquil C₁₋₆tio)tiocarbonilo, alquil C₁₋₆-S(=O)ₙ₇(=NR⁴)-alquilo C₁₋₄ donde R⁴ es hidrógeno, ciano, nitro, alquilo C₁₋₄ y n⁷ es 0 ó 1; o R¹ representa el grupo -C(R⁵)(R⁶)(R⁷) donde R⁵ es alquilo C₁₋₄, haloalquilo C₁₋₄, o ciclopropilo; R⁶ es hidrógeno, alquilo C₁₋₄ haloalquilo C₁₋₄, o ciclopropilo, preferentemente hidrógeno; y R⁷ es ciano, alquilo C₁₋₄, alquenilo C₁₋₆, haloalquenilo C₂₋₆, alcoxi C₁₋₄, alquinilo C₂₋₅, alcoxi C₂₋₄carbonilo, alquil C₁₋₄aminocarbonilo, di(alquil C₁₋₃)aminocarbonilo, haloalquil C₁₋₂aminocarbonilo, alqueniloxi C₃₋₆carbonilo, alquiniloxi C₃₋₆carbonilo, o alquil C₃₋₆carbonilo; o una sal agroquímicamente aceptable, N-óxido o isómero del mismo. Reivindicación 4: Un método de conformidad con cualquier reivindicación anterior donde se controlan insectos indeseables del orden de los Hemípteros que son resistentes a uno o más de los insecticidas neonicotinoides pero los artrópodos beneficiosos no son afectados. Reivindicación 5: Un método de conformidad con cualquier reivindicación anterior donde el método comprende la aplicación de un compuesto de fórmula (1) y uno o más artrópodos beneficiosos. Reivindicación 6: Un método de conformidad con la reivindicación 4 o la reivindicación 5 donde los artrópodos beneficiosos son uno o más insectos beneficiosos o ácaros depredadores que se seleccionan de Orius insidiosus, Orius laevigatus, Orius majusculus, Coccinella septempunctata, Adalia bipunctata, Amblydromalus limonicus, Amblyseius andersoni, Amblyseius barkeri, Amblyseius californicus, Amblyseius cucumeris, Amblyseius montdorensis, Amblyseius swirskii, Phitoseiulus persimilis, Syrphus spp., y Phitoseiulus persimilis. Reivindicación 8: Un compuesto de fórmula (1H), donde A es -CH₂-CH₂- o -CH=CH-; R¹ es etilo, propilo, isopropilo, 2-metilprop-2-enilo, alcoxi C₁₋₂alquilo C₁₋₂, alquil C₁₋₂-S(=O)ₙ₅-alquilo C₁₋₂ donde n⁵ es 0, 1 ó 2 (preferentemente n⁵ es 0), haloalquenilo C₃, alcoxi C₂₋₄carbonilalquilo C₁₋₂, o R¹ representa el grupo -C(R⁵)(R⁶)(R⁷) donde R⁵ es alquilo C₁₋₂; R⁶ es hidrógeno o alquilo C₁₋₂, preferentemente hidrógeno; y R⁷ es ciano, alquenilo C₂, haloalquenilo C₂, alquinilo C₂, alcoxi
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IN962DE2013 | 2013-03-28 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR095928A1 true AR095928A1 (es) | 2015-11-25 |
Family
ID=50382418
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP140101404A AR095928A1 (es) | 2013-03-28 | 2014-03-27 | Métodos para controlar las plagas resistentes a neonicotinoides |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US20160046620A1 (es) |
| EP (1) | EP2978318A1 (es) |
| JP (1) | JP2016515551A (es) |
| CN (1) | CN105072910A (es) |
| AR (1) | AR095928A1 (es) |
| BR (1) | BR112015024305A2 (es) |
| CA (1) | CA2907749A1 (es) |
| EA (1) | EA201500982A1 (es) |
| MX (1) | MX2015013617A (es) |
| WO (1) | WO2014154487A1 (es) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2978316A1 (en) * | 2013-03-28 | 2016-02-03 | Syngenta Participations AG | Methods of controlling neonicotinoid resistant pests |
| WO2016050567A1 (en) * | 2014-10-01 | 2016-04-07 | Syngenta Participations Ag | Insecticidal cyanotropane derivatives |
| CN118620907B (zh) * | 2024-04-01 | 2025-05-23 | 安徽农业大学 | 一种增强植物抵抗蚜虫的rta1基因及其应用 |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB9510459D0 (en) * | 1995-05-24 | 1995-07-19 | Zeneca Ltd | Bicyclic amines |
| CZ287821B6 (en) * | 1996-05-13 | 2001-02-14 | Zeneca Ltd | Bicyclic amines, process of their preparation and insecticidal, acaricidal and nematocidal agent containing thereof |
| CN1186154A (zh) * | 1996-10-26 | 1998-07-01 | 李国富 | 凸头转子发动机 |
| GB9623944D0 (en) * | 1996-11-15 | 1997-01-08 | Zeneca Ltd | Bicyclic amine derivatives |
| GB9624501D0 (en) * | 1996-11-26 | 1997-01-15 | Zeneca Ltd | Insecticial compositions and method |
| EA199900502A1 (ru) * | 1996-11-26 | 2000-02-28 | Зенека Лимитед | 8-азабицикло[3.2.1]октан-, 8-азабицикло[3.2.1]окт-6-ен-, 9-азабицикло[3.3.1]нонан-, 9-аза-3-оксабицикло[3.3.1]нонан- и 9-аза-3-тиабицикло[3.3.1]нонанпроизводные, их получение и их применение в качестве инсектицидов |
| GB9724693D0 (en) * | 1997-11-21 | 1998-01-21 | Zeneca Ltd | Chemical compounds |
| WO2002057262A2 (en) * | 2001-01-17 | 2002-07-25 | Syngenta Limited | Bicyclic amines as insecticides |
-
2014
- 2014-03-12 US US14/780,571 patent/US20160046620A1/en not_active Abandoned
- 2014-03-12 CA CA2907749A patent/CA2907749A1/en not_active Abandoned
- 2014-03-12 BR BR112015024305A patent/BR112015024305A2/pt not_active Application Discontinuation
- 2014-03-12 EA EA201500982A patent/EA201500982A1/ru unknown
- 2014-03-12 CN CN201480018635.2A patent/CN105072910A/zh active Pending
- 2014-03-12 MX MX2015013617A patent/MX2015013617A/es unknown
- 2014-03-12 JP JP2016504553A patent/JP2016515551A/ja active Pending
- 2014-03-12 WO PCT/EP2014/054847 patent/WO2014154487A1/en not_active Ceased
- 2014-03-12 EP EP14712617.1A patent/EP2978318A1/en not_active Withdrawn
- 2014-03-27 AR ARP140101404A patent/AR095928A1/es unknown
Also Published As
| Publication number | Publication date |
|---|---|
| BR112015024305A2 (pt) | 2017-07-18 |
| MX2015013617A (es) | 2016-02-25 |
| WO2014154487A1 (en) | 2014-10-02 |
| CN105072910A (zh) | 2015-11-18 |
| EA201500982A1 (ru) | 2016-03-31 |
| US20160046620A1 (en) | 2016-02-18 |
| EP2978318A1 (en) | 2016-02-03 |
| JP2016515551A (ja) | 2016-05-30 |
| CA2907749A1 (en) | 2014-10-02 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| AR095929A1 (es) | Métodos para controlar las plagas resistentes a neonicotinoides | |
| AR118275A2 (es) | 4-amino-6-(heterocíclico)picolinatos y 6-amino-2-(heterocíclico)pirimidin-4-carboxilatos y su uso como herbicidas | |
| AR104714A1 (es) | Compuestos depsipeptídicos como antihelmínticos | |
| EA201400138A1 (ru) | Пестицидные способы применения замещенных 3-пиридилтиазольных соединений и производных для борьбы с животными-вредителями ii | |
| AR106314A1 (es) | COMPUESTOS DE ESPIRO[3H-INDOL-3,2-PIRROLIDIN]-2(1H)-ONA Y DERIVADOS COMO INHIBIDORES DE MDM2 - p53 | |
| AR095728A1 (es) | Métodos para controlar las plagas resistentes a neonicotinoides | |
| AR107249A1 (es) | Compuestos depsipeptídicos como anthelmínticos | |
| AR101558A1 (es) | Difluoropirrolidinas como moduladores del receptor de orexina | |
| EA201792212A1 (ru) | Гербицидные смеси | |
| AR099677A1 (es) | Compuesto heterocíclico fusionado y su uso para el control de plagas | |
| EA201300894A1 (ru) | Инсектицидные соединения | |
| EA201400212A1 (ru) | N-тиоантраниламидные соединения и их применение в качестве пестицидов | |
| AR084308A1 (es) | Compuestos insecticidas derivados de triazol | |
| RU2015116670A (ru) | Гетероциклические соединения в качестве пестицидов | |
| AR093818A1 (es) | Compuesto de 1-(bencil sustituido)piperazina sustituida | |
| PH12018500009A1 (en) | Heterocyclic compounds as pesticides | |
| AR086819A1 (es) | 3-alcoxi, tioalquil y amino-4-amino-6-picolinatos (sustituidos) y su uso como herbicidas | |
| RU2017107553A (ru) | Новые галоген-замещенные соединения | |
| PH12019500267A1 (en) | Substituted 2-heterocyclyl imidazolyl-carboxamides as pest control agents | |
| PH12018501705A1 (en) | Substituted imidazolyl-carboxamides as pest control agents | |
| PH12018501706A1 (en) | Substituted 2-oxyimidazolyl-carboxamides as pest control agents | |
| EA201400819A1 (ru) | Пестицидные смеси, содержащие спирогетероциклические пирролидиндионы | |
| UY36368A (es) | Compuestos herbicidas | |
| MX387107B (es) | Compuestos insecticidas. | |
| AR095928A1 (es) | Métodos para controlar las plagas resistentes a neonicotinoides |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FB | Suspension of granting procedure |