AR074921A1 - Derivados de pirimidina y su utilizacion para la represion de un crecimiento indeseado de plantas - Google Patents
Derivados de pirimidina y su utilizacion para la represion de un crecimiento indeseado de plantasInfo
- Publication number
- AR074921A1 AR074921A1 ARP090105132A ARP090105132A AR074921A1 AR 074921 A1 AR074921 A1 AR 074921A1 AR P090105132 A ARP090105132 A AR P090105132A AR P090105132 A ARP090105132 A AR P090105132A AR 074921 A1 AR074921 A1 AR 074921A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- halo
- halogen
- carbonyl
- alkoxy
- Prior art date
Links
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical class C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 title 1
- 125000000217 alkyl group Chemical group 0.000 abstract 21
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 18
- 229910052736 halogen Inorganic materials 0.000 abstract 12
- 125000003545 alkoxy group Chemical group 0.000 abstract 9
- 150000002367 halogens Chemical class 0.000 abstract 9
- 229910052739 hydrogen Inorganic materials 0.000 abstract 7
- 239000001257 hydrogen Substances 0.000 abstract 7
- 125000004435 hydrogen atom Chemical class [H]* 0.000 abstract 7
- 125000005196 alkyl carbonyloxy group Chemical group 0.000 abstract 6
- 125000005194 alkoxycarbonyloxy group Chemical group 0.000 abstract 5
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 abstract 4
- 125000002947 alkylene group Chemical group 0.000 abstract 4
- 125000005843 halogen group Chemical group 0.000 abstract 4
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 3
- 125000006621 (C3-C8) cycloalkyl-(C1-C6) alkyl group Chemical group 0.000 abstract 3
- 125000000392 cycloalkenyl group Chemical group 0.000 abstract 3
- 229910052760 oxygen Inorganic materials 0.000 abstract 3
- 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 abstract 2
- 125000004916 (C1-C6) alkylcarbonyl group Chemical group 0.000 abstract 2
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 abstract 2
- 125000005236 alkanoylamino group Chemical group 0.000 abstract 2
- 125000004691 alkyl thio carbonyl group Chemical group 0.000 abstract 2
- 125000005087 alkynylcarbonyl group Chemical group 0.000 abstract 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 2
- -1 cyano, nitro, amino Chemical group 0.000 abstract 2
- 125000004356 hydroxy functional group Chemical group O* 0.000 abstract 2
- 239000001301 oxygen Substances 0.000 abstract 2
- 125000004434 sulfur atom Chemical group 0.000 abstract 2
- 125000004738 (C1-C6) alkyl sulfinyl group Chemical group 0.000 abstract 1
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 abstract 1
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 abstract 1
- 125000005947 C1-C6 alkylsulfonyloxy group Chemical group 0.000 abstract 1
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 1
- 125000005915 C6-C14 aryl group Chemical group 0.000 abstract 1
- 125000005974 C6-C14 arylcarbonyl group Chemical group 0.000 abstract 1
- 125000005090 alkenylcarbonyl group Chemical group 0.000 abstract 1
- 125000000304 alkynyl group Chemical group 0.000 abstract 1
- 125000005225 alkynyloxycarbonyl group Chemical group 0.000 abstract 1
- MDFFNEOEWAXZRQ-UHFFFAOYSA-N aminyl Chemical compound [NH2] MDFFNEOEWAXZRQ-UHFFFAOYSA-N 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 229910052799 carbon Inorganic materials 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 1
- 125000000000 cycloalkoxy group Chemical group 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- 125000000262 haloalkenyl group Chemical group 0.000 abstract 1
- 125000006788 haloalkenyloxycarbonyl group Chemical group 0.000 abstract 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 229910052717 sulfur Inorganic materials 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more 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, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/48—Two nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more 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, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/50—Three nitrogen atoms
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
Reivindicación 1: Compuestos de la fórmula general (1) y sus sales agroquímicamente compatibles en los/las que R1 y R2, independientemente uno de otro, están seleccionados entre el conjunto, que se compone de hidrógeno, halógeno, hidroxi, ciano, nitro, amino, C(O)OH, C(O)NH2, alquilo C1-6, halógeno-alquilo C1-6, alquil C1-6-carbonilo, halo-alquil C1-6-carbonilo, alquil C1-6-carboniloxi, halógeno-alquil C1-6-carboniloxi, alquil C1-6-carbonil-alquilo C1-4, alcoxi C1-6, halógeno-alcoxi C1-6, alcoxi C1-6-carbonilo, halo-alcoxi C1-6-carbonilo, alcoxi C1-6-carbonil-alquilo C1-6, halo-alcoxi C1-6-carbonil-alquilo C1-6, alcoxi C1-6-carbonil-halógeno-alquilo C1-6, halógeno-alcoxi C1-6-carbonil-halógeno-alquilo C1-6; alquenilo C2-6, halógeno-alquenilo C2-6, alquenil C2-6-carbonilo, halo-alquenil C2-6-carbonilo, alquenil C2-6-oxi, halo-alquenil C2-6-oxi, alquenil C2-6-oxicarbonilo, halo-alquenil C2-6-oxicarbonilo; alquinilo C2-6, halógeno-alquinilo C2-6, alquinil C2-6-carbonilo, halo-alquinil C2-6-carbonilo, alquinil C2-6-oxi, halo-alquinil C2-6-oxi, alquinil C2-6-oxicarbonilo, halógeno-alquinil C2-6-oxicarbonilo; tri-alquil C1-6-silil-alquinilo C2-6, di-alquil C1-6-silil-alquinilo C2-6, mono-alquil C1-6-silil-alquinilo C2-6, fenil-silil-alquinilo C2-6; arilo C6-14, aril C6-14-oxi, aril C6-14-carbonilo y aril C6-14-oxicarbonilo, que pueden estar sustituidos en cada caso en la parte de arilo con halógeno, alquilo C1-6 y/o halo-alquilo C1-6; aril C6-14-alquilo C1-6, aril C6-14-alcoxi 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; mono-alquil C1-6-amino, mono-halo-alquil C1-6-amino, di-alquil C1-6-amino, di-halo-alquil C1-6-amino, alquil C1-6-halo-alquil C1-6-amino, N-alcanoil C1-6-amino, N-halo-alcanoil C1-6-amino, aminocarbonil-alquilo C1-6, di-alquil C1-6-aminocarbonil-alquilo C1-6; mono-alquil C1-6-amino-carbonilo, mono-halo-alquil C1-6-amino-carbonilo, di-alquil C1-6-amino-carbonilo, di-halo-alquil C1-6-amino-carbonilo, alquil C1-6-halo-alquil C1-6-amino-carbonillo, N-alcanoil C1-6-amino-carbonilo, N-halo-alcanoil C1-6-amino-carbonilo, mono-aril C6-14-amino-carbonilo, di-aril C6-14-amino-carbonilo, alcoxi C1-6-alquilo C1-6, alcoxi C1-6-alcoxi C1-6, alcoxi C1-6-carbonil-alcoxi C1-6; cicloalquilo C3-8, que eventualmente puede estar sustituido en el radical cicloalquilo con alquilo C1-6 y/o halógeno; cicloalcoxi C3-8, cicloalquil C3-8-alquilo C1-6, cicloalquil C3-8-halo-alquilo C1-6, cicloalquil C3-8-alcoxi C1-6, cicloalquil C3-8-halo-alcoxi C1-6, cicloalquil C3-8-carbonilo, cicloalcoxi C3-8-carbonilo, cicloalquil C3-8-alquil C1-6-carbonilo, cicloalquil C3-8-halo-alquil C1-6-carbonilo, cicloalquil C3-8-alcoxi C1-6-carbonilo, cicloalquil C3-8-halo-alcoxi C1-6-carbonilo, cicloalquil C3-8-carboniloxi, cicloalcoxi C3-8-carboniloxi, cicloalquil C3-8-alquil C1-6-carboniloxi, cicloalquil C3-8-halógeno-alquil C1-6-carboniloxi, cicloalquil C3-8-alcoxi C1-6-carboniloxi, cicloalquil C3-8-halo-alcoxi C1-6-carboniloxi; cicloalquenilo C3-8, cicloalquenil C3-8-oxi, cicloalquenil C3-8-alquilo C1-6, cicloalquenil C3-8-halógeno-aIquilo C1-6, cicloalquenil C3-8-alcoxi C1-6, cicloalquenil C3-8-halógeno-alcoxi C1-6, cicloalquenil C3-8-carbonilo, cicloalquenil C3-8-oxicarbonilo, cicloalquenil C3-8-alquil C1-6-carbonilo, cicloalquenil C3-8-halógeno-alquil C1-6-carbonilo, cicloalquenil C3-8-alcoxi C1-6-carbonilo, cicloalquenil C3-8-halo-alcoxi C1-6-carbonilo, cicloalquenil C3-8-carboniloxi, cicloalquenil C3-8-oxicarboniloxi, cicloalquenil C3-8-alquil C1-6-carboniloxi, cicloalquenil C3-8-halógeno-alquil C1-6-carboniloxi, cicloalquenil C3-8-alcoxi C1-6-carboniloxi, cicloalquenil C3-8-halo-alcoxi C1-6-carboniloxi; hidroxi-alquilo de C1-6, hidroxi-alcoxi C1-6, ciano-alcoxi C1-6, ciano-alquilo C1-6; alquil C1-6-sulfonilo, alquil C1-6-tio, alquil C1-6-sulfinilo, halo-alquil C1-6-sulfonilo, halógeno-alquil C1-6-tio, halógeno-alquil C1-6-sulfinilo, alquil C1-6-sulfonil-alquilo C1-6, alquil C1-6-tio-alquilo C1-6, alquil C1-6-sulfinil-alquilo C1-6, halo-alquil C1-6-sulfonil-alquilo C1-6, halo-alquil C1-6-tio-alquilo C1-6, halo-alquil C1-6-sulfinil-alquilo C1-6, alquil C1-6-sulfonil-halo-alquilo C1-6, alquil C1-6-tio-halo-alquilo C1-6, alquil C1-6-sulfinil-halo-alquilo C1-6, halo-alquil C1-6-sulfonil-halo-alquilo C1-6, halo-alquil C1-6-tio- halo-alquilo C1-6, halo-alquil C1-6-sulfinil-halo-alquilo C1-6, alquil C1-6-sulfoniloxi, halógeno C1-6-alquil C1-6-sulfoniloxi, alquil C1-6-tiocarbonilo, halo-alquil C1-6-tiocarbonilo, alquil C1-6-tiocarboniloxi, halo-alquil C1-6-tiocarboniloxi, alquil C1-6-tio-alquilo C1-6, alquil C1-6-tio-alcoxi C1-6, alquil C1-6-tio-alquil C1-6-carbonilo, alquil C1-6-tio-alquil C1-6-carboniloxi, aril C4-14-sulfonilo, aril C6-14-tio, aril C6-14-sulfinilo, cicloalquil C3-8-tio, alquenil C3-8-tio, cicloalquenil C3-8-tio, alquinil C3-6-tio; los radicales R1 y R2 en común forman un grupo alquileno C2-6, que puede contener uno o varios átomos de oxigeno y/o azufre, realizándose que el grupo alquileno C2-6 puede estar sustituido una vez o múltiples veces con halógeno y los respectivos sustituyentes halógenos pueden ser iguales o diferentes; R3 se selecciona entre el conjunto, que se compone de hidrógeno, alquilo C1-6 y halo-alquilo C1-6; R4 y R5 en cada caso independientemente uno de otro, están seleccionados entre el conjunto, que se compone de hidrógeno, alquilo C1-6, halo-alquilo C1-6, hidroxi, alcoxi C1-6 y halógeno-alcoxi C1-6; o en común con el átomo de carbono, al que ellos están unidos, forman un anillo de tres a siete miembros; R6 y R7 en cada caso independientemente uno de otro, están seleccionados entre el conjunto, que se compone de hidrógeno, alquilo C1-6, halo-alquilo C1-6, alcoxi C1-6, halógeno-alcoxi C1-6, arilo C6-14, aril C6-14-oxi, aril C6-14-carbonilo y aril C6-14-oxicarbonilo; o los radicales R6 y R7 en común forman un grupo alquileno C2-7, que puede contener uno o varios átomos de oxígeno y/o azufre, realizándose que el grupo alquileno C2-7 puede estar sustituido una vez o múltiples veces con halógeno y los respectivos sustituyentes halógenos pueden ser iguales o diferentes; R8, R9, R10 y R11, independientemente unos de otros, en cada caso están seleccionados entre el conjunto, que se compone de hidrógeno, halógeno, ciano, alquilo C1-6, alquil C1-6-carbonilo, alquil C1-6-oxicarbonilo, alquil C1-6-aminocarbonilo, di-alquil C1-6-aminocarbonilo, halo-alquilo C1-6, alcoxi C1-6, halógeno-alcoxi C1-6, alquinilo C2-6, halógeno-alquinilo C2-6, alquinil C2-6-carbonilo, halo-alquinil C2-6-carbonilo, alquinil C2-6-oxi, halo-alquinil C2-6-oxi, alquinil C2-6-oxicarbonilo y halógeno-alquinil C2-6-oxicarbonilo; y X representa un enlace, CH2, O, S, carbonilo, NH, CR12R13 y NR14; R12 y R13, en cada caso independientemente uno de otro, están seleccionados entre el conjunto, que se compone de hidrógeno, alquilo C1-6 y halo-alquilo C1-6; y R14 se selecciona entre el conjunto, que se compone de hidrógeno, alquilo C1-6, halo-alquilo C1-6, a) con la condición de que por lo menos un radical de R1, R4, R5, R6, R7, R8, R9, R10 o R11 ha de ser distinto de H, cuando R2 es igual a CF3, y b) de que R2 no ha de significar Cl, cuando R1 representa NH2.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP08022522A EP2206703A1 (de) | 2008-12-30 | 2008-12-30 | Pyrimidinderivate und ihre Verwendung zur Bekämpfung unerwünschten Pflanzenwachstums |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR074921A1 true AR074921A1 (es) | 2011-02-23 |
Family
ID=40395202
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP090105132A AR074921A1 (es) | 2008-12-30 | 2009-12-28 | Derivados de pirimidina y su utilizacion para la represion de un crecimiento indeseado de plantas |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US8445408B2 (es) |
| EP (2) | EP2206703A1 (es) |
| JP (1) | JP5826633B2 (es) |
| KR (1) | KR20110102482A (es) |
| CN (1) | CN102272107B (es) |
| AR (1) | AR074921A1 (es) |
| AU (1) | AU2009335286A1 (es) |
| BR (1) | BRPI0923893B1 (es) |
| CA (1) | CA2748577A1 (es) |
| MX (1) | MX2011006278A (es) |
| TW (1) | TW201034572A (es) |
| WO (1) | WO2010076009A1 (es) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2210879A1 (de) * | 2008-12-30 | 2010-07-28 | Bayer CropScience AG | Pyrimidinderivate und ihre Verwendung zur Bekämpfung unerwünschten Pflanzenwachstums |
| CN104203925A (zh) * | 2012-03-29 | 2014-12-10 | 拜耳知识产权有限责任公司 | 5-氨基嘧啶衍生物及其用于防治不希望的植物生长的用途 |
| JP6629311B2 (ja) | 2014-07-01 | 2020-01-15 | バイエル・クロップサイエンス・アクチェンゲゼルシャフト | 2−アミノ−5−ケト−ピリミジン誘導体および望ましくない植物成長を制御するためのその使用 |
| CN108026086B (zh) | 2015-07-24 | 2021-02-19 | 拜耳作物科学股份公司 | 取代的呋喃并/噻吩并环烷基氨基-2-嘧啶衍生物及其用于防治不想要的植物生长的用途 |
| WO2017108656A1 (de) * | 2015-12-21 | 2017-06-29 | Bayer Cropscience Aktiengesellschaft | 2-amino-5-ketoxim-pyrimidinderivate und deren verwendung zur bekämpfung unerwünschten pflanzenwachstums |
| CN109415352B (zh) * | 2016-06-24 | 2022-04-26 | 拜耳作物科学股份公司 | 3-氨基-1,2,4-三嗪衍生物及其用于防治不想要的植物生长的用途 |
| WO2018184978A1 (de) | 2017-04-05 | 2018-10-11 | Bayer Cropscience Aktiengesellschaft | 2-amino-5-oxyalkyl-pyrimidinderivate und deren verwendung zur bekämpfung unerwünschten pflanzenwachstums |
| US12304890B2 (en) | 2018-12-27 | 2025-05-20 | Qingdao Kingagroot Chemical Compound Co., Ltd. | R-type pyridyloxycarboxylic acid, salt and ester derivative thereof, and preparation method therefor, and herbicidal composition and application thereof |
| US12435076B2 (en) | 2019-11-01 | 2025-10-07 | Unimatec Co., Ltd. | Fluorine-containing pyrimidine compound and method for producing same |
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-
2008
- 2008-12-30 EP EP08022522A patent/EP2206703A1/de not_active Withdrawn
-
2009
- 2009-12-28 CN CN200980153524.1A patent/CN102272107B/zh not_active Expired - Fee Related
- 2009-12-28 JP JP2011543990A patent/JP5826633B2/ja active Active
- 2009-12-28 WO PCT/EP2009/009287 patent/WO2010076009A1/de not_active Ceased
- 2009-12-28 BR BRPI0923893-0A patent/BRPI0923893B1/pt not_active IP Right Cessation
- 2009-12-28 TW TW098145310A patent/TW201034572A/zh unknown
- 2009-12-28 AR ARP090105132A patent/AR074921A1/es not_active Application Discontinuation
- 2009-12-28 MX MX2011006278A patent/MX2011006278A/es not_active Application Discontinuation
- 2009-12-28 AU AU2009335286A patent/AU2009335286A1/en not_active Abandoned
- 2009-12-28 EP EP09799289.5A patent/EP2384322B1/de not_active Not-in-force
- 2009-12-28 KR KR1020117017807A patent/KR20110102482A/ko not_active Withdrawn
- 2009-12-28 US US12/647,608 patent/US8445408B2/en not_active Expired - Fee Related
- 2009-12-28 CA CA2748577A patent/CA2748577A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| CN102272107A (zh) | 2011-12-07 |
| WO2010076009A8 (de) | 2011-06-23 |
| CN102272107B (zh) | 2015-10-14 |
| TW201034572A (en) | 2010-10-01 |
| JP2012514016A (ja) | 2012-06-21 |
| KR20110102482A (ko) | 2011-09-16 |
| BRPI0923893A2 (pt) | 2020-08-11 |
| AU2009335286A1 (en) | 2011-07-21 |
| US8445408B2 (en) | 2013-05-21 |
| JP5826633B2 (ja) | 2015-12-02 |
| MX2011006278A (es) | 2011-06-24 |
| CA2748577A1 (en) | 2010-07-08 |
| BRPI0923893B1 (pt) | 2021-03-09 |
| EP2384322B1 (de) | 2014-08-27 |
| WO2010076009A1 (de) | 2010-07-08 |
| EP2206703A1 (de) | 2010-07-14 |
| EP2384322A1 (de) | 2011-11-09 |
| US20100167935A1 (en) | 2010-07-01 |
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| FA | Abandonment or withdrawal |