AU2010303832B2 - Synergistic fungicidal composition containing 5-fluorocytosine for fungal control in cereals - Google Patents
Synergistic fungicidal composition containing 5-fluorocytosine for fungal control in cereals Download PDFInfo
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- AU2010303832B2 AU2010303832B2 AU2010303832A AU2010303832A AU2010303832B2 AU 2010303832 B2 AU2010303832 B2 AU 2010303832B2 AU 2010303832 A AU2010303832 A AU 2010303832A AU 2010303832 A AU2010303832 A AU 2010303832A AU 2010303832 B2 AU2010303832 B2 AU 2010303832B2
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- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- ONCZDRURRATYFI-TVJDWZFNSA-N trifloxystrobin Chemical compound CO\N=C(\C(=O)OC)C1=CC=CC=C1CO\N=C(/C)C1=CC=CC(C(F)(F)F)=C1 ONCZDRURRATYFI-TVJDWZFNSA-N 0.000 description 1
- HSMVPDGQOIQYSR-KGENOOAVSA-N triflumizole Chemical compound C1=CN=CN1C(/COCCC)=N/C1=CC=C(Cl)C=C1C(F)(F)F HSMVPDGQOIQYSR-KGENOOAVSA-N 0.000 description 1
- RROQIUMZODEXOR-UHFFFAOYSA-N triforine Chemical compound O=CNC(C(Cl)(Cl)Cl)N1CCN(C(NC=O)C(Cl)(Cl)Cl)CC1 RROQIUMZODEXOR-UHFFFAOYSA-N 0.000 description 1
- JARYYMUOCXVXNK-IMTORBKUSA-N validamycin Chemical compound N([C@H]1C[C@@H]([C@H]([C@H](O)[C@H]1O)O[C@H]1[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O1)O)CO)[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O JARYYMUOCXVXNK-IMTORBKUSA-N 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 239000004562 water dispersible granule Substances 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- DUBNHZYBDBBJHD-UHFFFAOYSA-L ziram Chemical compound [Zn+2].CN(C)C([S-])=S.CN(C)C([S-])=S DUBNHZYBDBBJHD-UHFFFAOYSA-L 0.000 description 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
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
-
- 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
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)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US24947509P | 2009-10-07 | 2009-10-07 | |
| US61/249,475 | 2009-10-07 | ||
| PCT/US2010/047142 WO2011043876A1 (en) | 2009-10-07 | 2010-08-30 | Synergistic fungicidal composition containing 5-fluorocytosine for fungal control in cereals |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| AU2010303832A1 AU2010303832A1 (en) | 2012-05-03 |
| AU2010303832B2 true AU2010303832B2 (en) | 2015-02-12 |
Family
ID=43823670
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU2010303832A Ceased AU2010303832B2 (en) | 2009-10-07 | 2010-08-30 | Synergistic fungicidal composition containing 5-fluorocytosine for fungal control in cereals |
Country Status (21)
| Country | Link |
|---|---|
| US (1) | US20110082162A1 (enExample) |
| EP (1) | EP2485732A4 (enExample) |
| JP (1) | JP5655080B2 (enExample) |
| KR (1) | KR20120093264A (enExample) |
| CN (1) | CN102858341B (enExample) |
| AR (1) | AR078250A1 (enExample) |
| AU (1) | AU2010303832B2 (enExample) |
| BR (1) | BR112012007975A2 (enExample) |
| CA (1) | CA2776562A1 (enExample) |
| CL (1) | CL2012000887A1 (enExample) |
| CR (1) | CR20120196A (enExample) |
| EC (1) | ECSP12011869A (enExample) |
| IL (1) | IL219031A0 (enExample) |
| IN (1) | IN2012DN03094A (enExample) |
| MX (1) | MX2012004046A (enExample) |
| NZ (1) | NZ599124A (enExample) |
| PH (1) | PH12012500678A1 (enExample) |
| RU (1) | RU2012118395A (enExample) |
| UA (1) | UA106246C2 (enExample) |
| WO (1) | WO2011043876A1 (enExample) |
| ZA (1) | ZA201202423B (enExample) |
Families Citing this family (69)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NZ598809A (en) * | 2009-09-01 | 2014-02-28 | Dow Agrosciences Llc | Synergistic fungicidal compositions containing a 5-fluoropyrimidine derivative for fungal control in cereals |
| CA2776746C (en) | 2009-10-07 | 2019-06-18 | Dow Agrosciences Llc | Synergistic fungicidal mixtures for fungal control in cereals |
| EP2651224A4 (en) * | 2010-12-16 | 2014-06-04 | Dow Agrosciences Llc | SYNERGISTIC FUNGICIDE INTERACTIONS OF 5-FLUOROCYTOSINE AND OTHER FUNGICIDES |
| JP6128658B2 (ja) * | 2011-08-17 | 2017-05-17 | アダマ・マクテシム・リミテッド | ５−フルオロ−４−イミノ−３−（置換）−３，４−ジヒドロピリミジン−２−（１ｈ）−オン誘導体 |
| AU2013259790B2 (en) | 2012-05-07 | 2016-09-08 | Corteva Agriscience Llc | Use of pro-fungicides of UK-2A for control of Black Sigatoka |
| CN104284590B (zh) * | 2012-05-07 | 2018-05-04 | 陶氏益农公司 | Uk-2a的前杀真菌剂在防治大豆锈病中的用途 |
| US8906826B2 (en) | 2012-07-24 | 2014-12-09 | Dow Agrosciences, Llc. | Herbicidal compositions comprising 4-amino-3-chloro-5-fluoro-6-(4-chloro-2-fluoro-3-methoxyphenyl) pyridine-2-carboxylic acid or a derivative thereof and imidazolinones |
| US8796177B2 (en) | 2012-07-24 | 2014-08-05 | Dow Agrosciences Llc | Herbicidal compositions comprising 4-amino-3-chloro-5-fluoro-6-(4-chloro-2-fluoro-3-methoxyphenyl)pyridine-2-carboxylic acid or a derivative thereof and acetyl-CoA carboxylase (ACCase) inhibitors |
| US8871680B2 (en) * | 2012-07-24 | 2014-10-28 | Dow Agrosciences, Llc. | Herbicidal compositions comprising 4-amino-3-chloro-5-fluoro-6-(4-chloro-2-fluoro-3-methoxyphenyl) pyridine-2-carboxylic acid or a derivative thereof and a di-methoxy-pyrimidine and derivatives thereof |
| US8809232B2 (en) * | 2012-07-24 | 2014-08-19 | Dow Agroscience Llc | Herbicidal compositions comprising 4-amino-3-chloro-5-fluoro-6-(4-chloro-2-fluoro-3-methoxyphenyl) pyridine-2-carboxylic acid or a derivative thereof and halosulfuron, pyrazosulfuron and esprocarb |
| US8916499B2 (en) | 2012-07-24 | 2014-12-23 | Dow Agrosciences, Llc. | Herbicidal compositions comprising 4-amino-3-chloro-5-fluoro-6-(4-chloro-2-fluoro-3-methoxyphenyl) pyridine-2-carboxylic acid or a derivative thereof and a protoporphyrinogen oxidase inhibitor |
| US8912121B2 (en) | 2012-07-24 | 2014-12-16 | Dow Agrosciences, Llc. | Herbicidal compositions comprising 4-amino-3-chloro-5-fluoro-6-(4-chloro-2-fluoro-3-methoxyphenyl)pyridine-2-carboxylic acid or a derivative thereof and certain PS II inhibitors |
| US8912120B2 (en) | 2012-07-24 | 2014-12-16 | Dow Agrosciences, Llc. | Herbicidal compositions comprising 4-amino-3-chloro-5-fluoro-6-(4-chloro-2-fluoro-3-methoxyphenyl) pyridine-2-carboxylic acid or a derivative thereof and synthetic auxin herbicides |
| US8871681B2 (en) * | 2012-07-24 | 2014-10-28 | Dow Agrosciences Llc | Herbicidal compositions comprising 4-amino-3-chloro-5-fluoro-6-(4-chloro-2-fluoro-3-methoxyphenyl) pyridine-2-carboxylic acid or a derivative thereof and certain sulfonylureas |
| US8841233B2 (en) * | 2012-07-24 | 2014-09-23 | Dow Agrosciences Llc | Herbicidal compositions comprising 4-amino-3-chloro-5-fluoro-6-(4-chloro-2-fluoro-3-methoxyphenyl) pyridine-2-carboxylic acid or a derivative thereof and 4-hydroxyphenyl-pyruvate dioxygenase (HPPD) inhibitors |
| US8883682B2 (en) | 2012-07-24 | 2014-11-11 | Dow Agrosciences, Llc. | Herbicidal compositions comprising 4-amino-3-chloro-5-fluoro-6-(4-chloro-2-fluoro-3-methoxyphenyl)pyridine-2-carboxylic acid or a derivative thereof and auxin transport inhibitors |
| US9644469B2 (en) | 2012-07-24 | 2017-05-09 | Dow Agrosciences Llc | Herbicidal compositions comprising 4-amino-3-chloro-5-fluoro-6-(4-chloro-2-fluoro-3-methoxyphenyl) pyridine-2-carboxylic acid or a derivative thereof and VLCFA and lipid synthesis inhibiting herbicides |
| US8846570B2 (en) * | 2012-07-24 | 2014-09-30 | Dow Agrosciences, Llc. | Herbicidal compositions comprising 4-amino-3-chloro-5-fluoro-6-(4-chloro-2-fluoro-3-methoxyphenyl)pyridine-2-carboxylic acid or a derivative thereof and microtubule inhibiting herbicides |
| US8889591B2 (en) | 2012-07-24 | 2014-11-18 | Dow Agrosciences, Llc. | Herbicidal compositions comprising 4-amino-3-chloro-5-fluoro-6-(4-chloro-2-fluoro-3-methoxyphenyl)pyridine-2-carboxylic acid or a derivative thereof and bromobutide, daimuron, oxaziclomefone or pyributicarb |
| US8906825B2 (en) | 2012-07-24 | 2014-12-09 | Dow Agrosciences, Llc. | Herbicidal compositions comprising 4-amino-3-chloro-5-fluoro-6-(4-chloro-2-fluoro-3-methoxyphenyl) pyridine-2-carboxylic acid or a derivative thereof and triazolopyrimidine sulfonamides |
| US8901035B2 (en) | 2012-07-24 | 2014-12-02 | Dow Agrosciences, Llc. | Herbicidal compositions comprising 4-amino-3-chloro-5-fluoro-6-(4-chloro-2-fluoro-3-methoxyphenyl) pyridine-2-carboxylic acid or a derivative thereof and cellulose biosynthesis inhibitor herbicides |
| US8895470B2 (en) | 2012-07-24 | 2014-11-25 | Dow Agrosciences, Llc. | Herbicidal compositions comprising 4-amino-3-chloro-5-fluoro-6-(4-chloro-2-fluoro-3-methoxyphenyl) pyridine-2-carboxylic acid or a derivative thereof and glyphosate or glufosinate |
| US8791048B2 (en) * | 2012-07-24 | 2014-07-29 | Dow Agrosciences Llc | Herbicidal compositions comprising 4-amino-3-chloro-5-fluoro-6-(4-chloro-2-fluoro-3-methoxyphenyl) pyridine-2-carboxylic acid or a derivative thereof and clomazone |
| JP6469581B2 (ja) * | 2012-11-19 | 2019-02-13 | アーチ ウッド プロテクション，インコーポレーテッド | コハク酸デヒドロゲナーゼ阻害剤含有組成物 |
| RU2638556C2 (ru) | 2012-12-28 | 2017-12-14 | Адама Мактешим Лтд. | Производные n-(замещенного)-5-фтор-4-имино-3-метил-2-оксо-3,4-дигидропиримидин-1(2н)-карбоксилата |
| UA117743C2 (uk) | 2012-12-28 | 2018-09-25 | Адама Махтешім Лтд. | N-(заміщені)-5-фтор-4-іміно-3-метил-2-оксо-3,4-дигідропіримідин-1(2h)-карбоксамідні похідні |
| DK2938191T3 (en) * | 2012-12-28 | 2018-05-07 | Dow Agrosciences Llc | SYNERGISTIC FUNGICIDE MIXTURES FOR FERTILIZER IN GRAIN PLANTS |
| KR20150103175A (ko) | 2012-12-31 | 2015-09-09 | 다우 아그로사이언시즈 엘엘씨 | 살진균제로서의 마크로시클릭 피콜린아미드 |
| RU2644014C2 (ru) | 2012-12-31 | 2018-02-07 | Адама Мактешим Лтд. | Производные 3-алкил-5-фтор-4-замещенного-имино-3,4-дигидропиримидин-2(н)-она в качестве фунгицидов |
| US9247742B2 (en) * | 2012-12-31 | 2016-02-02 | Dow Agrosciences Llc | Synergistic fungicidal compositions |
| US9730445B2 (en) | 2013-03-15 | 2017-08-15 | Dow Agrosciences Llc | Herbicidal compositions comprising 4-amino-3-chloro-5-fluoro-6-(4-chloro-2-fluoro-3-methoxyphenyl) pyridine-2-carboxylic acid or a derivative thereof and fungicides |
| US8841234B1 (en) * | 2013-03-15 | 2014-09-23 | Dow Agrosciences, Llc. | Herbicidal compositions comprising 4-amino-3-chloro-5-fluoro-6-(4-chloro-2-fluoro-3-methoxyphenyl) pyridine-2-carboxylic acid or a derivative thereof and fungicides |
| WO2015005355A1 (ja) * | 2013-07-10 | 2015-01-15 | Ｍｅｉｊｉ Ｓｅｉｋａファルマ株式会社 | ピコリン酸誘導体を含んでなる相乗性植物病害防除用組成物 |
| EP3086642A4 (en) | 2013-12-26 | 2017-09-27 | Dow Agrosciences LLC | Use of macrocyclic picolinamides as fungicides |
| CN106028814A (zh) | 2013-12-26 | 2016-10-12 | 美国陶氏益农公司 | 大环吡啶酰胺作为杀真菌剂的用途 |
| AU2014373959B2 (en) | 2013-12-31 | 2017-10-26 | Adama Makhteshim Ltd. | 5-fluoro-4-imino-3-(alkyl/substituted alkyl)-1- (arylsulfonyl)-3,4-dihydropyrimidin-2(1H)-one and processes for their preparation |
| NZ722436A (en) | 2013-12-31 | 2018-01-26 | Adama Makhteshim Ltd | Synergistic fungicidal mixtures and compositions for fungal control |
| EP3089587B1 (en) * | 2013-12-31 | 2019-07-24 | Dow AgroSciences LLC | Synergistic fungicidal mixtures for fungal control in cereals |
| WO2015171408A1 (en) | 2014-05-06 | 2015-11-12 | Dow Agrosciences Llc | Macrocyclic picolinamides as fungicides |
| JP6560335B2 (ja) | 2014-07-08 | 2019-08-14 | ダウ アグロサイエンシィズ エルエルシー | ３−ヒドロキシピコリン酸の製造方法 |
| TW201625576A (zh) | 2014-07-08 | 2016-07-16 | 陶氏農業科學公司 | 作爲殺真菌劑之巨環吡啶醯胺（一） |
| TWI720647B (zh) | 2014-07-08 | 2021-03-01 | 美商陶氏農業科學公司 | 用於製備4-烷氧基-3-羥基吡啶甲酸之方法（三） |
| TW201625577A (zh) | 2014-07-08 | 2016-07-16 | 陶氏農業科學公司 | 作爲殺真菌劑之巨環吡啶醯胺（二） |
| US20160037774A1 (en) * | 2014-08-08 | 2016-02-11 | Dow Agrosciences Llc | Synergistic fungicidal mixtures for fungal control in cereals |
| CN107205385A (zh) | 2014-12-30 | 2017-09-26 | 美国陶氏益农公司 | 吡啶酰胺作为杀真菌剂的用途 |
| CN107205386B (zh) | 2014-12-30 | 2021-07-23 | 美国陶氏益农公司 | 具有杀真菌活性的吡啶酰胺 |
| RU2708392C2 (ru) | 2014-12-30 | 2019-12-06 | ДАУ АГРОСАЙЕНСИЗ ЭлЭлСи | Соединения пиколинамида с фунгицидной активностью |
| TWI700037B (zh) | 2014-12-30 | 2020-08-01 | 美商陶氏農業科學公司 | 殺真菌組成物（二） |
| EP3240413B1 (en) | 2014-12-30 | 2020-05-13 | Dow Agrosciences LLC | Picolinamide compounds with fungicidal activity |
| CA2972408A1 (en) | 2014-12-30 | 2016-07-07 | Dow Agrosciences Llc | Use of picolinamide compounds with fungicidal activity |
| CN105994284A (zh) * | 2016-05-25 | 2016-10-12 | 南京华洲药业有限公司 | 一种含联苯吡菌胺和咪唑菌酮的杀菌组合物及其应用 |
| CN105994285A (zh) * | 2016-05-25 | 2016-10-12 | 南京华洲药业有限公司 | 一种含联苯吡菌胺和苯菌酮的杀菌组合物及其应用 |
| CN105994294A (zh) * | 2016-05-25 | 2016-10-12 | 南京华洲药业有限公司 | 一种含联苯吡菌胺和丙环唑的杀菌组合物及其应用 |
| US20180055049A1 (en) * | 2016-08-26 | 2018-03-01 | Dow Agrosciences Llc | Use of pro-fungicides of uk-2a for control of brown rot diesease on stone and pome fruits |
| WO2018039548A1 (en) * | 2016-08-26 | 2018-03-01 | Dow Agrosciences Llc | Use of pro-fungicides of uk-2a for control of rice blast |
| US10111432B2 (en) | 2016-08-30 | 2018-10-30 | Dow Agrosciences Llc | Picolinamide N-oxide compounds with fungicidal activity |
| US10334852B2 (en) | 2016-08-30 | 2019-07-02 | Dow Agrosciences Llc | Pyrido-1,3-oxazine-2,4-dione compounds with fungicidal activity |
| US10231452B2 (en) | 2016-08-30 | 2019-03-19 | Dow Agrosciences Llc | Thiopicolinamide compounds with fungicidal activity |
| US10173982B2 (en) | 2016-08-30 | 2019-01-08 | Dow Agrosciences Llc | Picolinamides as fungicides |
| CN106390130B (zh) * | 2016-09-18 | 2018-06-01 | 中国人民解放军第二军医大学 | 烟酰胺作为抗真菌药物增效剂的用途 |
| BR102018000183B1 (pt) | 2017-01-05 | 2023-04-25 | Dow Agrosciences Llc | Picolinamidas, composição para controle de um patógeno fúngico, e método para controle e prevenção de um ataque por fungos em uma planta |
| EA201991994A1 (ru) | 2017-03-07 | 2020-01-30 | Юпл Лтд | Фунгицидные комбинации |
| TWI774761B (zh) | 2017-05-02 | 2022-08-21 | 美商科迪華農業科技有限責任公司 | 用於穀物中的真菌防治之協同性混合物 |
| TW201842851A (zh) | 2017-05-02 | 2018-12-16 | 美商陶氏農業科學公司 | 用於穀類中的真菌防治之協同性混合物 |
| US11191269B2 (en) | 2017-05-02 | 2021-12-07 | Dow Agrosciences Llc | Use of an acyclic picolinamide compound as a fungicide for fungal diseases on turfgrasses |
| US11632954B2 (en) | 2017-07-17 | 2023-04-25 | Adama Makhteshim Ltd. | Polymorphs of 5-fluoro-4-imino-3-methyl-1 -tosyl-3,4-dihydropyrimidin-2-one |
| BR102019004480B1 (pt) | 2018-03-08 | 2023-03-28 | Dow Agrosciences Llc | Picolinamidas como fungicidas |
| US11639334B2 (en) | 2018-10-15 | 2023-05-02 | Corteva Agriscience Llc | Methods for synthesis of oxypicolinamides |
| EP4044811A4 (en) | 2019-10-18 | 2023-09-27 | Corteva Agriscience LLC | METHOD FOR SYNTHESIS OF PICOLINAMIDS |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20090203647A1 (en) * | 2008-01-22 | 2009-08-13 | Dow Agrosciences Llc | 5-fluoro pyrimidine derivatives |
Family Cites Families (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3368938A (en) * | 1966-01-13 | 1968-02-13 | Hoffmann La Roche | Controlling fungi with 5-fluorocytosine |
| IL48039A0 (en) * | 1974-09-20 | 1975-11-25 | Sparamedica Ag | Pharmaceutical compositions containing an active substance combination |
| DE19716257A1 (de) * | 1997-04-18 | 1998-10-22 | Bayer Ag | Fungizide Wirkstoffkombination |
| WO1999040081A1 (en) * | 1998-02-06 | 1999-08-12 | Meiji Seika Kaisha, Ltd. | Novel antifungal compounds and process for producing the same |
| CN1208321C (zh) * | 1999-07-20 | 2005-06-29 | 道农业科学公司 | 杀真菌的杂环芳族酰胺和它们的组合物、使用方法和制备 |
| AR037328A1 (es) * | 2001-10-23 | 2004-11-03 | Dow Agrosciences Llc | Compuesto de [7-bencil-2,6-dioxo-1,5-dioxonan-3-il]-4-metoxipiridin-2-carboxamida, composicion que lo comprende y metodo que lo utiliza |
| EP2187747B1 (de) * | 2007-08-09 | 2011-04-13 | Basf Se | Fungizide mischungen |
| WO2009106633A2 (en) * | 2008-02-28 | 2009-09-03 | Basf Se | Method for protecting cereals from being infected by fungi |
| MX2010010950A (es) * | 2008-04-08 | 2010-11-12 | Dow Agrosciences Llc | 2-alquinil-6-piridin-2-il-piridazinonas, 2-alquinil-6-piridin-2-il -dihidropiridazinonas, 2-alquinil-6-pirimidin-2-il-piridazinonas y 2-alquinil-6-pirimidin-2-il-dihidropiridazinonas y su uso como fungicidas. |
| UA107651C2 (en) * | 2008-08-01 | 2015-02-10 | Dow Agrosciences Llc | Use of 5-fluorocytosine as a fungicide |
| WO2010025451A2 (en) * | 2008-08-29 | 2010-03-04 | Dow Agrosciences Llc | 5,8-difluoro-4-(2-(4-(heteroaryloxy)-phenyl)ethylamino)quinazolines and their use as agrochemicals |
| NZ598809A (en) * | 2009-09-01 | 2014-02-28 | Dow Agrosciences Llc | Synergistic fungicidal compositions containing a 5-fluoropyrimidine derivative for fungal control in cereals |
| CA2776746C (en) * | 2009-10-07 | 2019-06-18 | Dow Agrosciences Llc | Synergistic fungicidal mixtures for fungal control in cereals |
| EP2651224A4 (en) * | 2010-12-16 | 2014-06-04 | Dow Agrosciences Llc | SYNERGISTIC FUNGICIDE INTERACTIONS OF 5-FLUOROCYTOSINE AND OTHER FUNGICIDES |
-
2010
- 2010-08-30 UA UAA201205522A patent/UA106246C2/ru unknown
- 2010-08-30 JP JP2012533181A patent/JP5655080B2/ja not_active Expired - Fee Related
- 2010-08-30 BR BR112012007975A patent/BR112012007975A2/pt not_active IP Right Cessation
- 2010-08-30 RU RU2012118395/15A patent/RU2012118395A/ru unknown
- 2010-08-30 WO PCT/US2010/047142 patent/WO2011043876A1/en not_active Ceased
- 2010-08-30 AU AU2010303832A patent/AU2010303832B2/en not_active Ceased
- 2010-08-30 IN IN3094DEN2012 patent/IN2012DN03094A/en unknown
- 2010-08-30 EP EP10822395.9A patent/EP2485732A4/en not_active Withdrawn
- 2010-08-30 KR KR1020127011642A patent/KR20120093264A/ko not_active Withdrawn
- 2010-08-30 US US12/871,444 patent/US20110082162A1/en not_active Abandoned
- 2010-08-30 MX MX2012004046A patent/MX2012004046A/es active IP Right Grant
- 2010-08-30 NZ NZ599124A patent/NZ599124A/en not_active IP Right Cessation
- 2010-08-30 PH PH1/2012/500678A patent/PH12012500678A1/en unknown
- 2010-08-30 CA CA2776562A patent/CA2776562A1/en not_active Abandoned
- 2010-08-30 CN CN201080055453.4A patent/CN102858341B/zh not_active Expired - Fee Related
- 2010-09-01 AR ARP100103202A patent/AR078250A1/es unknown
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2012
- 2012-04-03 ZA ZA2012/02423A patent/ZA201202423B/en unknown
- 2012-04-03 IL IL219031A patent/IL219031A0/en unknown
- 2012-04-05 CL CL2012000887A patent/CL2012000887A1/es unknown
- 2012-04-23 CR CR20120196A patent/CR20120196A/es unknown
- 2012-05-04 EC ECSP12011869 patent/ECSP12011869A/es unknown
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20090203647A1 (en) * | 2008-01-22 | 2009-08-13 | Dow Agrosciences Llc | 5-fluoro pyrimidine derivatives |
Also Published As
| Publication number | Publication date |
|---|---|
| CN102858341B (zh) | 2015-01-21 |
| IL219031A0 (en) | 2012-06-28 |
| BR112012007975A2 (pt) | 2016-03-29 |
| ECSP12011869A (es) | 2012-07-31 |
| US20110082162A1 (en) | 2011-04-07 |
| KR20120093264A (ko) | 2012-08-22 |
| RU2012118395A (ru) | 2013-11-20 |
| ZA201202423B (en) | 2013-06-26 |
| CA2776562A1 (en) | 2011-04-14 |
| PH12012500678A1 (en) | 2012-10-29 |
| MX2012004046A (es) | 2012-05-22 |
| CN102858341A (zh) | 2013-01-02 |
| AU2010303832A1 (en) | 2012-05-03 |
| IN2012DN03094A (enExample) | 2015-09-18 |
| NZ599124A (en) | 2014-03-28 |
| EP2485732A4 (en) | 2013-10-09 |
| UA106246C2 (ru) | 2014-08-11 |
| CR20120196A (es) | 2012-06-01 |
| AR078250A1 (es) | 2011-10-26 |
| EP2485732A1 (en) | 2012-08-15 |
| JP5655080B2 (ja) | 2015-01-14 |
| JP2013507362A (ja) | 2013-03-04 |
| WO2011043876A1 (en) | 2011-04-14 |
| CL2012000887A1 (es) | 2012-10-19 |
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