AR069488A1 - Derivados quirales de 2-(bencilsulfinil)-tiazol y derivados de 2-[ (1 h-pirazol-4-ilmetil)sulfinil ] -tiazol, procedimientos para su preparacion, asi como su uso como herbicidas y reguladores del crecimiento de plantas y composiciones en base al compuesto - Google Patents
Derivados quirales de 2-(bencilsulfinil)-tiazol y derivados de 2-[ (1 h-pirazol-4-ilmetil)sulfinil ] -tiazol, procedimientos para su preparacion, asi como su uso como herbicidas y reguladores del crecimiento de plantas y composiciones en base al compuestoInfo
- Publication number
- AR069488A1 AR069488A1 ARP080105199A ARP080105199A AR069488A1 AR 069488 A1 AR069488 A1 AR 069488A1 AR P080105199 A ARP080105199 A AR P080105199A AR P080105199 A ARP080105199 A AR P080105199A AR 069488 A1 AR069488 A1 AR 069488A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- alkoxy
- cycloalkenyl
- cycloalkyl
- aryl
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title abstract 4
- 239000004009 herbicide Substances 0.000 title abstract 2
- 238000000034 method Methods 0.000 title 1
- 239000000203 mixture Substances 0.000 title 1
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 29
- 125000000217 alkyl group Chemical group 0.000 abstract 17
- 125000003545 alkoxy group Chemical group 0.000 abstract 9
- -1 cyano, nitro, amino Chemical group 0.000 abstract 6
- 229910052736 halogen Inorganic materials 0.000 abstract 6
- 125000000392 cycloalkenyl group Chemical group 0.000 abstract 5
- 125000005843 halogen group Chemical group 0.000 abstract 5
- 125000003161 (C1-C6) alkylene group Chemical group 0.000 abstract 4
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 abstract 4
- 125000005196 alkyl carbonyloxy group Chemical group 0.000 abstract 4
- 150000002367 halogens Chemical class 0.000 abstract 4
- 229910052739 hydrogen Inorganic materials 0.000 abstract 4
- 239000001257 hydrogen Substances 0.000 abstract 4
- 150000002431 hydrogen Chemical class 0.000 abstract 4
- 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 abstract 3
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 3
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 abstract 3
- 125000005194 alkoxycarbonyloxy group Chemical group 0.000 abstract 3
- 229910052760 oxygen Inorganic materials 0.000 abstract 3
- 239000001301 oxygen Substances 0.000 abstract 3
- 125000001424 substituent group Chemical group 0.000 abstract 3
- 125000004434 sulfur atom Chemical group 0.000 abstract 3
- 125000006526 (C1-C2) alkyl group Chemical group 0.000 abstract 2
- 125000004916 (C1-C6) alkylcarbonyl group Chemical group 0.000 abstract 2
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 abstract 2
- 125000006619 (C1-C6) dialkylamino group Chemical group 0.000 abstract 2
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 abstract 2
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 2
- 125000005915 C6-C14 aryl group Chemical group 0.000 abstract 2
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 abstract 2
- 125000004448 alkyl carbonyl group Chemical group 0.000 abstract 2
- 125000001589 carboacyl group Chemical group 0.000 abstract 2
- 125000000000 cycloalkoxy group Chemical group 0.000 abstract 2
- 125000004438 haloalkoxy group Chemical group 0.000 abstract 2
- 125000004993 haloalkoxycarbonyl group Chemical group 0.000 abstract 2
- 125000006797 haloalkoxycarbonyloxy group Chemical group 0.000 abstract 2
- 125000000232 haloalkynyl group Chemical group 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
- 229910052717 sulfur Inorganic materials 0.000 abstract 2
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 1
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 abstract 1
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 abstract 1
- 125000006621 (C3-C8) cycloalkyl-(C1-C6) alkyl group Chemical group 0.000 abstract 1
- 125000006636 (C3-C8) cycloalkylcarbonyl group Chemical group 0.000 abstract 1
- 125000005947 C1-C6 alkylsulfonyloxy group Chemical group 0.000 abstract 1
- 101100079984 Caenorhabditis elegans nhr-9 gene Proteins 0.000 abstract 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 1
- 125000002877 alkyl aryl group Chemical group 0.000 abstract 1
- 125000004644 alkyl sulfinyl group Chemical group 0.000 abstract 1
- 125000004390 alkyl sulfonyl group Chemical group 0.000 abstract 1
- 125000004691 alkyl thio carbonyl group Chemical group 0.000 abstract 1
- 125000004414 alkyl thio group Chemical group 0.000 abstract 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 abstract 1
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 abstract 1
- 125000004356 hydroxy functional group Chemical group O* 0.000 abstract 1
- 150000002829 nitrogen Chemical class 0.000 abstract 1
- 125000005740 oxycarbonyl group Chemical group [*:1]OC([*:2])=O 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 244000045561 useful plants Species 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D277/32—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members 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
- C07D277/36—Sulfur atoms
-
- 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
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D277/32—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members 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
- C07D277/58—Nitro radicals
-
- 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
- C07D417/02—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 two hetero rings
- C07D417/12—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 two hetero rings linked by a chain containing hetero atoms as chain links
-
- 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
- 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)
- Plural Heterocyclic Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
Los compuestos de la presente son utiles en especial como herbicidas para el combate selectivo de plantas daninas en cultivos de plantas utiles. Reivindicacion 1: Compuestos opticamente activos de la formula general (1), sus sales agroquímicamente tolerables y sus derivados nitrogenados cuaternizados agroquímicamente tolerables, en donde Y es un compuesto de formula (2) o (3); y los sustituyentes R1 a R8, en cada caso de modo independiente entre sí, están seleccionados del grupo compuesto por: hidrogeno, halogeno, hidroxi, ciano, nitro, amino, C(O)OH, formilo; alquilo C1-6, halogenoalquilo C1-6, alquil C1-6-carbonilo, haloalquil C1-6-carbonilo, alquil C1-6-carboniloxi, halogenoalquil C1-6-carboniloxi, alquil C1-6-carbonil-alquilo C1-4, haloalquil C1-6-carbonil-alquilo C1-4, alquil C1-6-carbonil-haloalquilo C1-4, haloalquil C1-6-carbonil-haloalquilo C1-4; alcoxi C1-6, halogenoalcoxi C1-6, alcoxi C1-6-carbonilo, haloalcoxi C1-6-carbonilo, alcoxi C1-6-carbonil-alquilo C1-6, haloalcoxi C1-6-carbonil-alquilo C1-6, alcoxi C1-6-carbonil-halogenoalquilo C1-6, halogenoalcoxi C1-6-carbonil-halogenoalquilo C1-6; alquenilo C2-6, halogenoalquenilo C2-6, alquenil C2-6-carbonilo, haloalquenil C2-6-carbonilo, alquenil C2-6-oxi, haloalquenil C2-6-oxi, alquenil C2-6-oxicarbonilo, haloalquenil C2-6-oxicarbonilo; alquinilo C2-6, halogenoalquinilo C2-6, alquinil C2-6-carbonilo, haloalquinil C2-6-carbonilo, alquinil C2-6-oxi, haloalquinil C2-6-oxi, alquiniloxi C2-6-carbonilo, halogenoalquinil C2-6-oxicarbonilo; alquil C1-6-tiocarbonilo, haloalquil C1-6-tiocarbonilo, alquil C1-6-tiocarboniloxi, haloalquil C1-6-tiocarboniloxi; alquil C1-6-tio-alcoxi C1-6, alquil C1-6-tio-alquil C1-6-carbonilo, alquil C1-6-tio-alquil C1-6-carboniloxi; arilo C6-14, aril C6-14-oxi, aril C6-14-carbonilo, aril C6-14-oxicarbonilo; aril C6-14-alquilo C1-6, aril C6-14-alcoxi C1-6, aril C6-14-oxi-alquilo C1-6, aril C6-14-alquil C1-6-carbonilo, aril C6-14-alquil C1-6-carboniloxi, aril C6-14-alcoxi C1-6-carbonilo, aril C6-14-alcoxi C1-6-carboniloxi; alquil C1-6-sulfonilo, alquil C1-6-tio, alquil C1-6-sulfinilo, haloalquil C1-6-sulfonilo, halogenoalquil C1-6-tio, halogenoalquil C1-6-sulfinilo, alquil C1-6-sulfonil-alquilo C1-6, alquil C1-6-tio-alquilo C1-6, alquil C1-6-sulfinil-alquilo C1-6, haloalquil C1-6-sulfonil-alquilo C1-6, haloalquil C1-6-tio-alquilo C1-6, haloalquil C1-6-sulfinil-alquilo C1-6, alquil C1-6-sulfonil-haloalquilo C1-6, alquil C1-6-tio-haloalquilo C1-6, alquil C1-6-sulfinil-haloalquilo C1-6, haloalquil C1-6-sulfonil-haloalquilo C1-6, haloalquil C1-6-tio-haloalquilo C1-6, haloalquil C1-6-sulfinil-haloalquilo C1-6, alquil C1-6-sulfoniloxi, halogenoalquil C1-6-sulfoniloxi; aril C4-14-sulfonilo, aril C6-14-tio, aril C6-14-sulfinilo; mono-(alquil C1-6)-amino, mono-(haloalquil C1-6)-amino, di-(alquil C1-6)-amino, di-(haloalquil C1-6)-amino, (alquil C1-6)-haloalquil C1-6-amino, N-(alcanoil C1-6)-amino, N-(haloalcanoil C1-6)-amino, aminocarbonil-C1-6)-alquilo, mono-alquil C1-6-aminocarbonil-alquilo C1-6, di-alquil C1-6-aminocarbonil-alquilo C1-6, mono-(alquil C1-6)-aminocarbonilo; alcoxi C1-6-alquilo C1-6, alcoxi C1-6-alcoxi C1-6, alcoxi C1-6-carbonil-alcoxi C1-6; cicloalquilo C3-8, cicloalcoxi C3-8, cicloalquil C3-8-alquilo C1-6, cicloalquil C3-8-haloalquilo C1-6, cicloalquil C3-8-alcoxi C1-6, cicloalquil C3-8-haloalcoxi C1-6, cicloalquil C3-8-carbonilo, cicloalcoxi C3-8-carbonilo, cicloalquil C3-8-alquil C1-6-carbonilo, cicloalquil C3-8-haloalquil C1-6-carbonilo, cicloalquil C3-8-alcoxi C1-6-carbonilo, cicloalquil C3-8-haloalcoxi C1-6-carbonilo, cicloalquil C3-8-carboniloxi, cicloalcoxi C3-8-carboniloxi, cicloalquil C3-8-alquil C1-6-carboniloxi, cicloalquil C3-8-halogenoalquil C1-6-carboniloxi, cicloalquil C3-8-alcoxi C1-6-carboniloxi, cicloalquil C3-8-haloalcoxi C1-6-carboniloxi; cicloalquenilo C3-8, cicloalquenil C3-8-oxi, cicloalquenil C3-8-alquilo C1-6, cicloalquenil C3-8-halogenoalquilo C1-6, cicloalquenil C3-8-alcoxi C1-6, cicloalquenil C3-8-halogenoalcoxi C1-6, cicloalquenil C3-8-carbonilo, cicloalquenil C3-8-oxicarbonilo, cicloalquenil C3-8-alquil C1-6-carbonilo, cicloalquenil C3-8-halogenoalquil C1-6-carbonilo, cicloalquenil C3-8-alcoxi C1-6-carbonilo, cicloalquenil C3-8-haloalcoxi C1-6-carbonilo, cicloalquenil C3-8-carboniloxi, cicloalquenil C3-8-oxicarboniloxi, cicloalquenil C3-8-alquil C1-6-carboniloxi, cicloalquenil C3-8-halogenoalquil C1-6-carboniloxi, cicloalquenil C3-8-alcoxi C1-6-carboniloxi, cicloalquenil C3-8-haloalcoxi C1-6-carboniloxi; cicloalquil C3-8-tio, alquenil C3-8-tio, cicloalquenil C3-8-tio, alquinil C3-6-tio; hidroxi-alquilo C1-6, hidroxi-alcoxi C1-6, ciano-alcoxi C1-6, ciano-alquilo C1-6; 3-oxetaniloxi-; C(O)NR9R10, en donde R9 y R10 son, de modo independiente entre si, hidrogeno, alquilo C1-6, cicloalquilo C3-6, haloalquilo C1-6, o donde R9 y R10 forman juntos un grupo alquileno C1-6, que puede contener un átomo de oxigeno o de azufre o uno o dos grupos amino o alquil C1-6-amino, en donde los radicales mencionados pueden estar eventualmente unidos cíclicamente entre si, con la condicion de que estén en posicion orto y/o dos sustituyentes en posicion orto forman juntos un grupo alquileno C1-6, que pueden contener uno o varios átomos de oxígeno y/o de azufre, en donde el grupo alquileno C1-6 puede estar mono- o polisustituido con halogeno y los correspondientes sustituyentes de halogeno pueden ser iguales o diferentes; en donde los radicales previamente mencionados R1 a R8 pueden estar mono- o polisustituidos y, de modo independiente entre sí, con radicales que están seleccionados del grupo compuesto por alquilo C1-6, alcoxi C1-6, nitro, ciano, cicloalquilo C1-3, haloalcoxi C1-6, alquil C1-6-tio o halogeno, en donde los radicales mencionados pueden estar eventualmente unidos cíclicamente entre sí, con la condicion de que estén en posicion orto; y los sustituyentes R11 y R12, en cada caso de modo independiente entre sí, están seleccionados del grupo compuesto por hidrogeno, halogeno, nitro, ciano, formilo, C(O)OH, hidroxi, amino; alquilo C1-6, alquil C1-6-carbonilo, alquil C1-6-carbonil-alquilo C1-4, alquil C1-6-carboniloxi; alcoxi C1-6, alcoxi C1-6-carbonilo, alcoxi C1-6-carbonil-alquilo C1-6, alcoxi C1-6-alquilo C1-6, alcoxi C1-6-alcoxi C1-6, alcoxi C1-6-carbonil-alcoxi C1-6; alquenilo C2-6, alquenil C2-6-oxi, alquinilo C2-6, alquinil C2-6-oxi; alquil C1-6-tio, alquil C1-6-sulfinilo, alquil C1-6-sulfonilo, alquil C1-6-sulfoniloxi, alquil C1-6-sulfonil-alquilo C1-6, alquil C1-6-sulfinil-alquilo C1-6, alquil C1-6-tio-alquilo C1-6, alquil C1-6-tio-alcoxi C1-6; mono-(alquil C1-6)-amino, di-(alquil C1-6)-amino, N-(alcanoil C1-6)-amino, aminocarbonil-alquilo C1-6, mono-(alquil C1-6)-aminocarbonilo, di-(alquil C1-6)-aminocarbonilo, mono-(alquil C1-6)-aminosulfonilo, di-(alquil C1-6)-aminosulfonilo; cicloalquilo C3-8, cicloalcoxi C3-8, cicloalquil C3-8-alquilo C1-6, cicloalquil C3-8-alcoxi C1-6, cicloalquil C3-8-carbonilo, cicloalcoxi C3-8-carbonilo; cicloalquenilo C3-8, cicloalquenil C3-8-oxi, cicloalquil C3-8-tio, cicloalquil C3-8-sulfinilo, cicloalquil C3-8-sulfonilo, cicloalquil C3-8-sulfoniloxi; ciano-alcoxi C1-6, ciano-alquilo C1-6; arilo C6-14, aril C6-14-oxi, aril C6-14-alquilo C1-6, aril C6-14-alcoxi C1-6, aril C6-14-oxi-alquilo C1-6; -CONH-SO2-alquilo C1-6 -NHCHO, -NHCO-alquilo C1-6, -NHCO2-alquilo C1-6, -NHCONH-alquilo C1-6,-NHSO2-alquilo C1-6, -OCONH-alquilo C1-6, alquil C1-6-aminosulfonil-alquilo C1-2, di-alquil C1-6-aminosulfonil-alquilo C1-2, -C(O)NHR9; -C(O)NR9R10, en donde R9 y R10 son, de modo independiente entre sí, hidrogeno, alquilo C1-6, cicloalquilo C3-6, haloalquilo C1-6, o donde R9 y R10 forman juntos un grupo alquileno C1-6, que puede contener un átomo de oxígeno o de azufre o uno o dos grupos amino o alquil C1-6-amino, en donde los radicales previamente mencionados R11 y R12 pueden estar mono- o polisustituidos y, de modo independiente entre sí, con radicales que están seleccionados del grupo compuesto por halogeno y alquilo C1-6.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP07023198A EP2065374A1 (de) | 2007-11-30 | 2007-11-30 | 2-(Benzyl- und 1H-pyrazol-4-ylmethyl)sulfinyl-Thiazol-Derivate als Herbizide und Pflanzenwachstumsregulatoren |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR069488A1 true AR069488A1 (es) | 2010-01-27 |
Family
ID=39345214
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP080105199A AR069488A1 (es) | 2007-11-30 | 2008-11-28 | Derivados quirales de 2-(bencilsulfinil)-tiazol y derivados de 2-[ (1 h-pirazol-4-ilmetil)sulfinil ] -tiazol, procedimientos para su preparacion, asi como su uso como herbicidas y reguladores del crecimiento de plantas y composiciones en base al compuesto |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US8754234B2 (es) |
| EP (2) | EP2065374A1 (es) |
| AR (1) | AR069488A1 (es) |
| AU (1) | AU2008329194B2 (es) |
| BR (1) | BRPI0819595A8 (es) |
| CA (1) | CA2707115C (es) |
| WO (1) | WO2009068170A2 (es) |
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|---|---|---|---|---|
| US8097712B2 (en) | 2007-11-07 | 2012-01-17 | Beelogics Inc. | Compositions for conferring tolerance to viral disease in social insects, and the use thereof |
| US8962584B2 (en) | 2009-10-14 | 2015-02-24 | Yissum Research Development Company Of The Hebrew University Of Jerusalem, Ltd. | Compositions for controlling Varroa mites in bees |
| US9121022B2 (en) | 2010-03-08 | 2015-09-01 | Monsanto Technology Llc | Method for controlling herbicide-resistant plants |
| CA2848576A1 (en) | 2011-09-13 | 2013-03-21 | Monsanto Technology Llc | Methods and compositions for weed control comprising topical application of 4-hydroxyphenyl-pyruvate-dioxygenase (hppd)-inhibiting polynucleotides |
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| MX350775B (es) | 2011-09-13 | 2017-09-15 | Monsanto Technology Llc | Métodos y composiciones para el control de malezas. |
| EP3434779A1 (en) | 2011-09-13 | 2019-01-30 | Monsanto Technology LLC | Methods and compositions for weed control |
| WO2013040116A1 (en) | 2011-09-13 | 2013-03-21 | Monsanto Technology Llc | Methods and compositions for weed control |
| CN103957697B (zh) | 2011-09-13 | 2017-10-24 | 孟山都技术公司 | 用于杂草控制的方法和组合物 |
| UA116090C2 (uk) | 2011-09-13 | 2018-02-12 | Монсанто Текнолоджи Ллс | Спосіб та композиція для боротьби з бур'янами (варіанти) |
| US10829828B2 (en) | 2011-09-13 | 2020-11-10 | Monsanto Technology Llc | Methods and compositions for weed control |
| US10806146B2 (en) | 2011-09-13 | 2020-10-20 | Monsanto Technology Llc | Methods and compositions for weed control |
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| US10240162B2 (en) | 2012-05-24 | 2019-03-26 | A.B. Seeds Ltd. | Compositions and methods for silencing gene expression |
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-
2007
- 2007-11-30 EP EP07023198A patent/EP2065374A1/de not_active Withdrawn
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2008
- 2008-11-08 CA CA2707115A patent/CA2707115C/en not_active Expired - Fee Related
- 2008-11-08 EP EP08854201.4A patent/EP2227458B1/de not_active Not-in-force
- 2008-11-08 WO PCT/EP2008/009437 patent/WO2009068170A2/de not_active Ceased
- 2008-11-08 AU AU2008329194A patent/AU2008329194B2/en not_active Ceased
- 2008-11-08 US US12/743,862 patent/US8754234B2/en not_active Expired - Fee Related
- 2008-11-08 BR BRPI0819595A patent/BRPI0819595A8/pt not_active Application Discontinuation
- 2008-11-28 AR ARP080105199A patent/AR069488A1/es unknown
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|---|---|
| CA2707115C (en) | 2017-01-03 |
| AU2008329194A1 (en) | 2009-06-04 |
| BRPI0819595A8 (pt) | 2015-12-22 |
| BRPI0819595A2 (pt) | 2015-05-05 |
| US8754234B2 (en) | 2014-06-17 |
| WO2009068170A2 (de) | 2009-06-04 |
| WO2009068170A3 (de) | 2009-09-03 |
| AU2008329194B2 (en) | 2015-04-09 |
| EP2065374A1 (de) | 2009-06-03 |
| EP2227458B1 (de) | 2016-06-22 |
| CA2707115A1 (en) | 2009-06-04 |
| US20100285958A1 (en) | 2010-11-11 |
| EP2227458A2 (de) | 2010-09-15 |
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