AR104046A1 - Derivados heterobicíclicos microbicidas - Google Patents
Derivados heterobicíclicos microbicidasInfo
- Publication number
- AR104046A1 AR104046A1 ARP160100770A ARP160100770A AR104046A1 AR 104046 A1 AR104046 A1 AR 104046A1 AR P160100770 A ARP160100770 A AR P160100770A AR P160100770 A ARP160100770 A AR P160100770A AR 104046 A1 AR104046 A1 AR 104046A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- alkoxy
- cycloalkyl
- halogen
- alkylthio
- 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
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 15
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 14
- 229910052736 halogen Inorganic materials 0.000 abstract 14
- 150000002367 halogens Chemical class 0.000 abstract 14
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 abstract 11
- 125000001424 substituent group Chemical group 0.000 abstract 10
- 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 abstract 6
- 125000003342 alkenyl group Chemical group 0.000 abstract 6
- 125000000304 alkynyl group Chemical group 0.000 abstract 6
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 5
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 abstract 5
- 125000000217 alkyl group Chemical group 0.000 abstract 5
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 5
- 229910052739 hydrogen Inorganic materials 0.000 abstract 5
- 239000001257 hydrogen Substances 0.000 abstract 5
- 125000004435 hydrogen atom Chemical class [H]* 0.000 abstract 5
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 4
- 125000003302 alkenyloxy group Chemical group 0.000 abstract 3
- 125000003545 alkoxy group Chemical group 0.000 abstract 3
- 125000005133 alkynyloxy group Chemical group 0.000 abstract 3
- 229910052799 carbon Inorganic materials 0.000 abstract 3
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 3
- 239000000203 mixture Substances 0.000 abstract 3
- 229910052760 oxygen Inorganic materials 0.000 abstract 3
- 125000006376 (C3-C10) cycloalkyl group Chemical group 0.000 abstract 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 2
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 abstract 2
- 125000003118 aryl group Chemical group 0.000 abstract 2
- 150000001721 carbon Chemical group 0.000 abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 abstract 2
- -1 cyano, formyl Chemical group 0.000 abstract 2
- 125000001072 heteroaryl group Chemical group 0.000 abstract 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 2
- 239000001301 oxygen Substances 0.000 abstract 2
- 229910052717 sulfur Inorganic materials 0.000 abstract 2
- 125000004434 sulfur atom Chemical group 0.000 abstract 2
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 abstract 1
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 abstract 1
- 125000006713 (C5-C10) cycloalkyl group Chemical group 0.000 abstract 1
- 125000006705 (C5-C7) cycloalkyl group 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
- 239000003905 agrochemical Substances 0.000 abstract 1
- 125000004414 alkyl thio group Chemical group 0.000 abstract 1
- 125000004104 aryloxy group Chemical group 0.000 abstract 1
- 125000000262 haloalkenyl group Chemical group 0.000 abstract 1
- 125000004995 haloalkylthio group Chemical group 0.000 abstract 1
- 125000000232 haloalkynyl group Chemical group 0.000 abstract 1
- 125000005553 heteroaryloxy group Chemical group 0.000 abstract 1
- 238000003898 horticulture Methods 0.000 abstract 1
- 239000000463 material Substances 0.000 abstract 1
- 244000005700 microbiome Species 0.000 abstract 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
- 230000003032 phytopathogenic effect Effects 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- PXQLVRUNWNTZOS-UHFFFAOYSA-N sulfanyl Chemical class [SH] PXQLVRUNWNTZOS-UHFFFAOYSA-N 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
- A01N43/48—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
- A01N43/52—1,3-Diazoles; Hydrogenated 1,3-diazoles condensed with carbocyclic rings, e.g. benzimidazoles
-
- 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
- A01N43/54—1,3-Diazines; Hydrogenated 1,3-diazines
-
- 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
- A01N43/74—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 1,3
- A01N43/78—1,3-Thiazoles; Hydrogenated 1,3-thiazoles
-
- 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
- C07D401/04—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 directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Environmental Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Plant Pathology (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 Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Apparatus For Disinfection Or Sterilisation (AREA)
- Mushroom Cultivation (AREA)
Abstract
Además, la presente se refiere a composiciones agroquímicas que comprenden compuestos de fórmula (1), a la preparación de estas composiciones y al uso de los compuestos o composiciones en agricultura u horticultura para combatir, prevenir o controlar la infestación de las plantas, cultivos alimentarios recolectados, semillas o materiales inertes debida a microorganismos fitopatógenos, en particular, hongos. Reivindicación 1: Un compuesto de fórmula (1), donde R¹ y R² se seleccionan cada uno independientemente entre hidrógeno, ciano, alquilo C₁₋₆, cicloalquilo C₃₋₇, alquenilo C₂₋₆ y alquinilo C₂₋₆, en los cuales los grupos alquilo, cicloalquilo, alquenilo y alquinilo pueden estar sustituidos opcionalmente con de 1 a 3 sustituyentes seleccionados independientemente entre halógeno, alcoxi C₁₋₆ y alquiltio C₁₋₆; o R¹ y R² junto con el átomo de carbono al cual se encuentran unidos representan un grupo cicloalquilo C₃₋₁₀ (el cual puede estar sustituido opcionalmente con de 1 a 3 sustituyentes seleccionados independientemente a partir del grupo constituido por halógeno, alquilo C₁₋₆, alcoxi C₁₋₆ y alquiltio C₁₋₆); R³ y R⁴ se seleccionan cada uno independientemente entre hidrógeno, halógeno, hidroxilo, alquilo C₁₋₆, alcoxi C₁₋₆, cicloalquilo C₃₋₇, alquenilo C₂₋₆ y alquinilo C₂₋₆, en los cuales los grupos alquilo, alcoxi, cicloalquilo, alquenilo y alquinilo pueden estar sustituidos opcionalmente con de 1 a 3 sustituyentes seleccionados independientemente: entre halógeno, alcoxi C₁₋₆ y alquiltio C₁₋₆; o R³ y R⁴ junto con el átomo de carbono al cual se encuentran unidos representan C=O, C=NORᵃ, C=C(Rᵇ)(Rᶜ) o cicloalquilo C₃₋₁₀ (el cual puede estar sustituido opcionalmente con de 1 a 3 sustituyentes seleccionados independientemente a partir del grupo constituido por halógeno, alquilo C₁₋₆, alcoxi C₁₋₆ y alquiltio C₁₋₆); o R² y R³ junto con los átomos de carbono a los cuales se encuentran unidos representan cicloalquilo C₅₋₁₀ (el cual puede estar sustituido opcionalmente con de 1 a 3 sustituyentes seleccionados independientemente a partir del grupo constituido por halógeno, alquilo C₁₋₆, alcoxi C₁₋₆ y alquiltio C₁₋₆ y, adicionalmente, una unidad de carbono anular puede ser reemplazada por un átomo de oxígeno o azufre); cada R⁵ representa independientemente halógeno, hidroxilo, mercapto, nitro, ciano, formilo, alquilo C₁₋₆, alquenilo C₂₋₆, alquinilo C₂₋₆, cicloalquilo C₃₋₇, alcoxi C₁₋₆, alqueniloxi C₃₋₆, alquiniloxi C₃₋₆, alquiltio C₁₋₆, -C(=NORᵃ)(alquilo C₁₋₆), (alquil C₁₋₆)carbonilo, arilo, heteroarilo, ariloxi o heteroariloxi, en los cuales los grupos alquilo, cicloalquilo, alquenilo, alquinilo, alcoxi, alqueniloxi, alquiniloxi, arilo y heteroarilo pueden estar sustituidos opcionalmente con de 1 a 5 sustituyentes seleccionados independientemente entre halógeno, alquilo C₁₋₆, alcoxi C₁₋₆, ciano y alquiltio C₁₋₆; n es 0, 1, 2, 3 ó 4; R⁶ es hidrógeno, halógeno, alquilo C₁₋₆ o alcoxi C₁₋₆; cada R⁷ representa. independientemente hidroxilo, mercapto, ciano, halógeno, alquilo C₁₋₆, haloalquilo C₁₋₆, alquenilo C₂₋₆, alquinilo C₂₋₆, haloalquenilo C₂₋₆, haloalquinilo C₃₋₆, alquiltio C₁₋₆, haloalcoxi C₁₋₆, haloalquiltio C₁₋₆, (alcoxi C₁₋₆)carbonilo, (alquil C₁₋₆)carbonilo, cicloalquilo C₃₋₇, alcoxi C₁₋₆, alqueniloxi C₃₋₆ o alquiniloxi C₃₋₆; m es 0, 1, 2, 3 ó 4; o dos sustituyentes R⁷ adyacentes junto con los átomos de carbono a los cuales se encuentran unidos representan un cicloalquilo C₅₋₇ (el cual puede estar sustituido opcionalmente con de 1 a 3 sustituyentes seleccionados independientemente a partir del grupo constituido por halógeno, alquilo C₁₋₆, alcoxi C₁₋₆ y alquiltio C₁₋₆ y, adicionalmente, una unidad de carbono anular puede ser reemplazada por un átomo de oxígeno o azufre); Rᵃ se selecciona entre hidrógeno, alquilo C₁₋₆, cicloalquilo C₃₋₇, alquenilo C₃₋₆ y alquinilo C₃₋₆, en los cuales los grupos alquilo, cicloalquilo, alquenilo y alquinilo pueden estar sustituidos opcionalmente con de 1 a 3 sustituyentes seleccionados independientemente entre halógeno, alcoxi C₁₋₆ y alquiltio C₁₋₆; Rᵇ y Rᶜ se seleccionan cada uno independientemente entre hidrógeno, halógeno, ciano, alquilo C₁₋₆, cicloalquilo C₃₋₇, alquenilo C₂₋₆, alquinilo C₂₋₆, alcoxi C₁₋₆ y alquiltio C₁₋₆, en los cuales los grupos alquilo, cicloalquilo, alquenilo y alquinilo pueden estar sustituidos opcionalmente con de 1 a 3 sustituyentes seleccionados independientemente entre halógeno, alcoxi C₁₋₆ y alquiltio C₁₋₆; o una de sus sales o N-óxidos.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP15161494 | 2015-03-27 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR104046A1 true AR104046A1 (es) | 2017-06-21 |
Family
ID=53058973
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP160100770A AR104046A1 (es) | 2015-03-27 | 2016-03-22 | Derivados heterobicíclicos microbicidas |
Country Status (24)
| Country | Link |
|---|---|
| US (1) | US10273221B2 (es) |
| EP (3) | EP3848364B1 (es) |
| JP (1) | JP6662901B2 (es) |
| KR (1) | KR102565369B1 (es) |
| CN (3) | CN111303116B (es) |
| AR (1) | AR104046A1 (es) |
| AU (1) | AU2016239625B2 (es) |
| BR (1) | BR112017020349B1 (es) |
| CA (1) | CA2978996A1 (es) |
| CL (1) | CL2017002426A1 (es) |
| CO (1) | CO2017009652A2 (es) |
| CR (1) | CR20170418A (es) |
| EA (1) | EA033690B1 (es) |
| ES (3) | ES2791193T3 (es) |
| GE (2) | GEAP201914613A (es) |
| HU (1) | HUE049090T2 (es) |
| IL (1) | IL254190B (es) |
| MA (1) | MA40816A1 (es) |
| MX (1) | MX384596B (es) |
| PL (1) | PL3274343T3 (es) |
| PT (1) | PT3274343T (es) |
| TN (1) | TN2017000407A1 (es) |
| UA (1) | UA120960C2 (es) |
| WO (1) | WO2016156085A1 (es) |
Families Citing this family (203)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AR105640A1 (es) * | 2015-08-12 | 2017-10-25 | Syngenta Participations Ag | Derivados heterobicíclicos microbicidas |
| ES2829575T3 (es) * | 2016-09-28 | 2021-06-01 | Syngenta Participations Ag | Composiciones fungicidas |
| WO2018073110A1 (en) | 2016-10-20 | 2018-04-26 | Basf Se | Quinoline compounds as fungicides |
| WO2018116072A1 (en) * | 2016-12-20 | 2018-06-28 | Pi Industries Ltd. | Heterocyclic compounds |
| EP3571190A1 (en) | 2017-01-23 | 2019-11-27 | Basf Se | Fungicidal pyridine compounds |
| TWI772367B (zh) | 2017-02-16 | 2022-08-01 | 瑞士商先正達合夥公司 | 殺真菌組成物 |
| WO2018184882A1 (en) | 2017-04-06 | 2018-10-11 | Basf Se | Pyridine compounds |
| WO2018206419A1 (en) | 2017-05-12 | 2018-11-15 | Syngenta Participations Ag | Microbiocidal heterobicyclic derivatives |
| CA3082419A1 (en) | 2017-11-21 | 2019-05-31 | Syngenta Participations Ag | Fungicidal compositions |
| WO2020165403A1 (en) | 2019-02-15 | 2020-08-20 | Syngenta Crop Protection Ag | Phenyl substituted thiazole derivatives as microbiocidal compounds |
| ES2953140T3 (es) | 2019-03-08 | 2023-11-08 | Syngenta Crop Protection Ag | Compuestos de azol-amida activos de manera plaguicida |
| US20220183294A1 (en) | 2019-03-20 | 2022-06-16 | Syngenta Crop Protection Ag | Pesticidally active azole amide compounds |
| US20220306599A1 (en) | 2019-03-20 | 2022-09-29 | Syngenta Crop Protection Ag | Pesticidally active azole amide compounds |
| GB201903942D0 (en) | 2019-03-22 | 2019-05-08 | Syngenta Crop Protection Ag | Microbiocidal compounds |
| BR112021018822A2 (pt) | 2019-03-22 | 2021-11-23 | Syngenta Crop Protection Ag | Derivados de n-[1-(5-bromo-2-pirimidin-2-il-1,2,4-triazol-3-il)etil]-2-ciclopropil-6-(trifluorometil)piridina-4-carboxamida e compostos relacionados como inseticidas |
| EP3947371B1 (en) | 2019-03-27 | 2023-11-22 | Syngenta Crop Protection AG | Microbiocidal thiazole derivatives |
| TWI853009B (zh) | 2019-03-29 | 2024-08-21 | 瑞士商先正達農作物保護公司 | 殺有害生物活性之二-醯胺化合物 |
| PE20220171A1 (es) | 2019-04-05 | 2022-01-28 | Syngenta Crop Protection Ag | Compuestos de diazina-amida activos como pesticidas |
| WO2020208095A1 (en) | 2019-04-10 | 2020-10-15 | Syngenta Crop Protection Ag | Microbiocidal picolinamide derivatives |
| MX2021012352A (es) | 2019-04-10 | 2022-01-18 | Syngenta Crop Protection Ag | Composiciones fungicidas. |
| EP3953343A1 (en) | 2019-04-11 | 2022-02-16 | Syngenta Crop Protection AG | Pesticidally active diazine-amide compounds |
| US12528778B2 (en) | 2019-05-29 | 2026-01-20 | Syngenta Crop Protection Ag | Microbiocidal derivatives |
| AR119009A1 (es) | 2019-05-29 | 2021-11-17 | Syngenta Crop Protection Ag | Derivados de alcoxipiridina y alcoxipirimidina microbicidas |
| WO2020239855A1 (en) | 2019-05-29 | 2020-12-03 | Syngenta Crop Protection Ag | Microbiocidal derivatives |
| AR119011A1 (es) | 2019-05-29 | 2021-11-17 | Syngenta Crop Protection Ag | DERIVADOS DE [1,3]DIOXOLO[4,5-c]PIRIDIN-4-CARBOXAMIDA, COMPOSICIONES AGROQUÍMICAS QUE LOS COMPRENDEN Y SU EMPLEO COMO FUNGICIDA PARA CONTROLAR O PREVENIR LA INFESTACIÓN DE PLANTAS ÚTILES |
| JP2022539244A (ja) | 2019-07-05 | 2022-09-07 | シンジェンタ クロップ プロテクション アクチェンゲゼルシャフト | 殺微生物性ピコリンアミド誘導体 |
| GB201910037D0 (en) | 2019-07-12 | 2019-08-28 | Syngenta Crop Protection Ag | Microbiocidal compounds |
| WO2021037614A1 (en) | 2019-08-23 | 2021-03-04 | Syngenta Crop Protection Ag | Pesticidally active pyrazine-amide compounds |
| GB201912595D0 (en) | 2019-09-02 | 2019-10-16 | Syngenta Crop Protection Ag | Plant growth regulator compounds |
| JP7581336B2 (ja) | 2019-09-20 | 2024-11-12 | シンジェンタ クロップ プロテクション アクチェンゲゼルシャフト | 硫黄及びスルホキシミン含有置換基を有する殺有害生物的に活性な複素環式誘導体 |
| UY38885A (es) | 2019-09-20 | 2021-04-30 | Syngenta Crop Protection Ag | Compuestos de azetidinil-, pirrolidinil-,piperdinil- o piperazinil-piridinil carbonilo pesticidamente activos |
| HRP20251479T1 (hr) | 2019-11-01 | 2026-01-02 | Syngenta Crop Protection Ag | Pesticidno aktivni kondenzirani biciklički heteroaromatski spojevi |
| JP7788377B2 (ja) | 2019-12-04 | 2025-12-18 | シンジェンタ クロップ プロテクション アクチェンゲゼルシャフト | 殺有害生物的に活性な縮合二環式芳香族複素環式アミノ化合物 |
| WO2021122645A1 (en) | 2019-12-20 | 2021-06-24 | Syngenta Crop Protection Ag | Pesticidally active azole-amide compounds |
| EP4085058A1 (en) | 2019-12-31 | 2022-11-09 | Syngenta Crop Protection AG | Pesticidally active heterocyclic derivatives with sulfur containing substituents |
| TW202132300A (zh) | 2020-01-06 | 2021-09-01 | 瑞士商先正達農作物保護公司 | 具有含硫取代基的殺有害生物活性雜環衍生物 |
| BR112022014313A2 (pt) | 2020-01-24 | 2022-09-20 | Syngenta Crop Protection Ag | Compostos heteroaromáticos bicíclicos fundidos ativos em termos pesticidas |
| JP2023513047A (ja) | 2020-01-30 | 2023-03-30 | シンジェンタ クロップ プロテクション アクチェンゲゼルシャフト | 殺有害生物的に有効な縮合二環式芳香族複素環式アミノ化合物 |
| BR112022015723A2 (pt) | 2020-02-11 | 2023-02-14 | Syngenta Crop Protection Ag | Compostos de amina cíclica pesticidamente ativos |
| WO2021170881A1 (en) | 2020-02-27 | 2021-09-02 | Syngenta Crop Protection Ag | Pesticidally active diazine-bisamide compounds |
| WO2021175822A1 (en) | 2020-03-02 | 2021-09-10 | Syngenta Crop Protection Ag | Pesticidally amidine-substituted benzoic acid amide compounds |
| UY39115A (es) | 2020-03-05 | 2021-10-29 | Syngenta Crop Protection Ag | Mezclas fungicidas de derivados de arilo metoxiacrilato |
| WO2021176007A1 (en) | 2020-03-05 | 2021-09-10 | Syngenta Crop Protection Ag | Fungicidal compositions |
| EP4117435A1 (en) | 2020-03-13 | 2023-01-18 | Syngenta Crop Protection AG | Methods of controlling or preventing infestation of plants by the phytopathogenic microorganism corynespora cassiicola |
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| US20230096145A1 (en) | 2020-03-13 | 2023-03-30 | Syngenta Crop Protection Ag | Methods of controlling or preventing infestation of plants by the phytopathogenic microorganism corynespora cassiicola |
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| WO2025248032A1 (en) | 2024-05-31 | 2025-12-04 | Syngenta Crop Protection Ag | Pesticidally active indazole compounds |
| WO2025252553A1 (en) | 2024-06-04 | 2025-12-11 | Syngenta Crop Protection Ag | Pesticidally-active 2,2-dihalocyclopropyl compounds |
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| WO2025257072A1 (en) | 2024-06-14 | 2025-12-18 | Syngenta Crop Protection Ag | Pesticidally active 2-oxobenzimidazole compounds |
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