DK2904901T3 - Synergistisk fungicid blanding til svampebekæmpelse i kornplanter - Google Patents
Synergistisk fungicid blanding til svampebekæmpelse i kornplanter Download PDFInfo
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- DK2904901T3 DK2904901T3 DK15156066.1T DK15156066T DK2904901T3 DK 2904901 T3 DK2904901 T3 DK 2904901T3 DK 15156066 T DK15156066 T DK 15156066T DK 2904901 T3 DK2904901 T3 DK 2904901T3
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- synergistic
- compound
- anamorph
- fungicidal
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- 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/34—Nitriles
-
- 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
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
- A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
-
- 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
-
- 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
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/56—1,2-Diazoles; Hydrogenated 1,2-diazoles
-
- 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
- A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three 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
- A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
- A01N43/647—Triazoles; Hydrogenated triazoles
- A01N43/653—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
-
- 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/02—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having no bond to a nitrogen atom
- A01N47/06—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having no bond to a nitrogen atom containing —O—CO—O— groups; Thio analogues 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
- A01N47/24—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing the groups, or; Thio analogues 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/40—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having a double or triple bond to nitrogen, e.g. cyanates, cyanamides
-
- 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
-
- 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
- C07D405/14—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 three or more hetero rings
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Claims (9)
1. Synergistisk fungicid blanding, hvilken blanding omfatter en fungicid effektiv mængde af en forbindelse med formel l-V og mindst et fungicid, der er valgt fra gruppen bestående af azoxystrobin og pyraclostrobin
2. Blandingen ifølge krav 1, hvor vægtforholdet af forbindelsen l-V til azoxystrobin er på mellem 1 : 10 og 10 : 1.
3. Blandingen ifølge krav 1, hvor vægtforholdet af forbindelsen l-V til pyraclostrobin er på mellem 1 :10 og 10 :1.
4. Fungicid sammensætning, hvilken sammensætning omfatter en fungicid effektiv mængde af den fungicide blanding ifølge krav 1 og en landbrugsmæssig acceptabel adjuvans eller bærer.
5. Anvendelse af blandingen eller sammensætningen ifølge et hvilket som helst af de foregående krav til at bekæmpe svampe, som inficerer planteafgrøder.
6. Anvendelsen ifølge krav 5, hvori svampene er af klasserne Ascomycetes og Basidiomycetes.
7. Anvendelsen ifølge krav 5, hvori svampene er valgt fra gruppen, der består af hvedebrun rust (Puccinia recondita; PUCCRT); striberust af hvede (Puccinia striiformis', PUCCST); bladplet af hvede (Mycosphaerella graminicola; anamorph: Septoria triticr, SEPTTR); glumeplet af hvede (Leptosphaeria nodorurrr, LEPTNO; anamorph: Stagonospora nodorum); spotplet af byg (Cochliobolus sativum, COCHSA; anamorph: Helminthosporium sativum); bladplet af sukkerroer (Cercospora beticola; CERCBE); bladplet af jordnød (Mycosphaerella arachidis; MYCOAR; anamorph: Cercospora arachidicola); agurk-anthracnose (Glomerella lagenarium; anamorph: Colletotrichum lagenarium; COLLLA) og sort-sigatoka-sygdom af banan (Mycosphaerella fijiensis; MYCOFI).
8. Anvendelsen ifølge krav 5, hvor sammensætningen anvendes ved en dosering på mellem 65 gram pr. hektar (g/ha) til 2.300 g/ha baseret på den totale mængde aktive ingredienser i sammensætningen.
9. Anvendelsen ifølge krav 5, hvor azoxystrobin anvendes ved en dosering på mellem 50 g/ha og 250 g/ha eller pyraclostrobin anvendes ved en dosering på mellem 50 g/ha og 250 g/ha, og forbindelsen med formel l-V anvendes ved en dosering på mellem 35 g/ha og 300 g/ha.
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US24947909P | 2009-10-07 | 2009-10-07 | |
EP10822587.1A EP2485592B1 (en) | 2009-10-07 | 2010-10-06 | Synergistic fungicidal mixtures for fungal control in cereals |
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DK16202262.8T DK3153021T3 (da) | 2009-10-07 | 2010-10-06 | Synergistiske fungicide blandinger til svampebekæmpelse i kornplanter |
DK15156066.1T DK2904901T3 (da) | 2009-10-07 | 2010-10-06 | Synergistisk fungicid blanding til svampebekæmpelse i kornplanter |
DK10822587.1T DK2485592T3 (da) | 2009-10-07 | 2010-10-06 | Synergistiske fungicide blandinger til svampebekæmpelse i kornsorter |
DK16202257.8T DK3153020T3 (da) | 2009-10-07 | 2010-10-06 | Synergistiske fungicide blandinger til svampebekæmpelse i kornplanter |
DK17152922.5T DK3178321T3 (da) | 2009-10-07 | 2010-10-06 | Synergistiske fungicide blandninger af epoxiconazol til bekæmpelse af svamp i korn |
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DK16202262.8T DK3153021T3 (da) | 2009-10-07 | 2010-10-06 | Synergistiske fungicide blandinger til svampebekæmpelse i kornplanter |
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DK10822587.1T DK2485592T3 (da) | 2009-10-07 | 2010-10-06 | Synergistiske fungicide blandinger til svampebekæmpelse i kornsorter |
DK16202257.8T DK3153020T3 (da) | 2009-10-07 | 2010-10-06 | Synergistiske fungicide blandinger til svampebekæmpelse i kornplanter |
DK17152922.5T DK3178321T3 (da) | 2009-10-07 | 2010-10-06 | Synergistiske fungicide blandninger af epoxiconazol til bekæmpelse af svamp i korn |
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US (3) | US8883811B2 (da) |
EP (5) | EP3153021B1 (da) |
JP (3) | JP5905826B2 (da) |
KR (3) | KR20120093925A (da) |
CN (2) | CN102711477B (da) |
AU (2) | AU2010303529B2 (da) |
BR (1) | BR112012008010A2 (da) |
CA (1) | CA2776746C (da) |
CL (2) | CL2012000888A1 (da) |
CO (1) | CO6541551A2 (da) |
CR (3) | CR20180237A (da) |
DK (5) | DK3153021T3 (da) |
EC (1) | ECSP12011870A (da) |
ES (5) | ES2712081T3 (da) |
FR (1) | FR21C1047I2 (da) |
HK (2) | HK1222298A1 (da) |
HU (6) | HUE042624T2 (da) |
IL (1) | IL219032A (da) |
IN (1) | IN2012DN03101A (da) |
LT (5) | LT3153021T (da) |
MX (3) | MX2012004048A (da) |
MY (1) | MY175147A (da) |
NL (1) | NL350111I2 (da) |
NZ (3) | NZ625074A (da) |
PH (1) | PH12015501443A1 (da) |
PL (5) | PL3178321T3 (da) |
PT (5) | PT3153021T (da) |
RU (2) | RU2547554C2 (da) |
TR (3) | TR201900242T4 (da) |
UA (2) | UA115314C2 (da) |
WO (1) | WO2011044213A1 (da) |
ZA (1) | ZA201202424B (da) |
Families Citing this family (77)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP5683592B2 (ja) * | 2009-09-01 | 2015-03-11 | ダウ アグロサイエンシィズ エルエルシー | 穀類における菌類防除のための5−フルオロピリミジン誘導体を含有する相乗性殺菌剤組成物 |
CA2776562A1 (en) * | 2009-10-07 | 2011-04-14 | Dow Agrosciences Llc | Synergistic fungicidal composition containing 5-fluorocytosine for fungal control in cereals |
PL3178321T3 (pl) | 2009-10-07 | 2019-10-31 | Dow Agrosciences Llc | Synergistyczne grzybobójcze mieszaniny epoksykonazolu do zwalczania grzybów w zbożach |
TWI568721B (zh) | 2012-02-01 | 2017-02-01 | 杜邦股份有限公司 | 殺真菌之吡唑混合物 |
WO2013169662A2 (en) | 2012-05-07 | 2013-11-14 | Dow Agrosciences Llc | Macrocyclic picolinamides as fungicides |
WO2013169661A1 (en) * | 2012-05-07 | 2013-11-14 | Dow Agrosciences Llp | Use of pro-fungicides of uk-2a for control of black sigatoka |
PL2847188T3 (pl) | 2012-05-07 | 2017-07-31 | Dow Agrosciences Llc | Makrocykliczne pikolinamidy jako fungicydy |
CN104703984A (zh) | 2012-05-07 | 2015-06-10 | 陶氏益农公司 | 作为杀真菌剂的大环吡啶-2-甲酰胺 |
BR112014027591A2 (pt) * | 2012-05-07 | 2017-06-27 | Dow Agrosciences Llc | uso de pró-fungicidas de uk-2a para controle de ferrugem de soja |
EP2864293B1 (en) | 2012-06-22 | 2016-04-27 | E. I. du Pont de Nemours and Company | Fungicidal 4-methylanilino pyrazoles |
BR112015015351B8 (pt) * | 2012-12-28 | 2022-08-23 | Dow Agrosciences Llc | Mistura fungicida sinérgica, composição fungicida, e método para tratamento de uma planta |
US9247742B2 (en) * | 2012-12-31 | 2016-02-02 | Dow Agrosciences Llc | Synergistic fungicidal compositions |
US9750248B2 (en) * | 2012-12-31 | 2017-09-05 | Dow Agrosciences Llc | Synergistic fungicidal compositions |
US9482661B2 (en) | 2012-12-31 | 2016-11-01 | Dow Agrosciences Llc | Synthesis and use of isotopically labeled macrocyclic compounds |
JP2016507511A (ja) | 2012-12-31 | 2016-03-10 | ダウ アグロサイエンシィズ エルエルシー | 殺真菌剤としての大環状ピコリンアミド |
US10455835B2 (en) | 2012-12-31 | 2019-10-29 | Dow Agrosciences Llc | Fungicidal compositions for controlling leaf spots in sugar beets |
WO2014130409A2 (en) | 2013-02-21 | 2014-08-28 | E. I. Du Pont De Nemours And Company | Fungicidal pyrazole mixtures |
CN103988840A (zh) * | 2013-03-20 | 2014-08-20 | 海南正业中农高科股份有限公司 | 含有吡噻菌胺与咪鲜胺的杀菌组合物 |
JP6419783B2 (ja) | 2013-04-15 | 2018-11-07 | エフ エム シー コーポレーションFmc Corporation | 殺菌・殺カビ性アミド |
MX2015014406A (es) | 2013-04-15 | 2016-02-16 | Du Pont | Carboxamidas fungicidas. |
AR097314A1 (es) * | 2013-07-10 | 2016-03-09 | Meiji Seika Pharma Co Ltd | Composiciones sinérgicas para el control de enfermedades en plantas, que comprenden derivados del ácido picolínico |
CN105705502A (zh) | 2013-10-01 | 2016-06-22 | 美国陶氏益农公司 | 具有杀真菌活性的大环吡啶酰胺化合物 |
BR112016006366A2 (pt) | 2013-10-01 | 2017-08-01 | Dow Agrosciences Llc | uso de picolinamidas macrocíclicas como fungicidas |
WO2015100182A1 (en) | 2013-12-26 | 2015-07-02 | Dow Agrosciences Llc | Use of macrocyclic picolinamides as fungicides |
CN106028815A (zh) * | 2013-12-26 | 2016-10-12 | 美国陶氏益农公司 | 作为杀真菌剂的大环吡啶酰胺 |
NZ720916A (en) * | 2013-12-31 | 2017-06-30 | Dow Agrosciences Llc | Synergistic fungicidal mixtures for fungal control in cereals |
MX2016008737A (es) | 2013-12-31 | 2017-02-28 | Adama Makhteshim Ltd | Mezclas fungicidas sinergicas para el control fungico en cereales. |
GB201401117D0 (en) * | 2014-01-23 | 2014-03-12 | Univ Sussex The | Antifungal composition |
WO2015123193A1 (en) | 2014-02-12 | 2015-08-20 | E. I. Du Pont De Nemours And Company | Fungicidal benzodipyrazoles |
WO2015157005A1 (en) | 2014-04-10 | 2015-10-15 | E I Du Pont De Nemours And Company | Substituted tolyl fungicide mixtures |
BR112016025397A2 (pt) | 2014-05-06 | 2017-08-15 | Dow Agrosciences Llc | picolinamidas macrocíclicas como fungicidas |
US20170037014A1 (en) | 2014-05-06 | 2017-02-09 | E. I. Du Pont De Nemours And Company | Fungicidal pyrazoles |
WO2016007532A1 (en) | 2014-07-08 | 2016-01-14 | Dow Agrosciences Llc | Process for the preparation of 3-hydroxypicolinic acids |
US9686984B2 (en) | 2014-07-08 | 2017-06-27 | Dow Agrosciences Llc | Macrocyclic picolinamides as fungicides |
WO2016007529A1 (en) | 2014-07-08 | 2016-01-14 | Dow Agrosciences Llc | Macrocyclic picolinamides as fungicides |
WO2016007638A1 (en) | 2014-07-08 | 2016-01-14 | Dow Agrosciences Llc | Process for the preparation of 4-alkoxy-3-hydroxypicolinic acids |
US20160037774A1 (en) * | 2014-08-08 | 2016-02-11 | Dow Agrosciences Llc | Synergistic fungicidal mixtures for fungal control in cereals |
AU2015380298B2 (en) | 2014-12-30 | 2019-02-21 | Corteva Agriscience Llc | Picolinamide compounds with fungicidal activity |
PL3240415T3 (pl) | 2014-12-30 | 2022-11-21 | Corteva Agriscience Llc | Kompozycje fungicydowe |
CN107205398B (zh) | 2014-12-30 | 2020-08-21 | 美国陶氏益农公司 | 具有杀真菌活性的吡啶酰胺化合物 |
BR112017013653A2 (pt) | 2014-12-30 | 2018-03-13 | Dow Agrosciences Llc | uso de compostos de picolinamida com atividade fungicida |
CA2972034A1 (en) | 2014-12-30 | 2016-07-07 | Dow Agrosciences Llc | Picolinamides with fungicidal activity |
ES2841906T3 (es) | 2014-12-30 | 2021-07-12 | Dow Agrosciences Llc | Picolinamidas como fungicidas |
US20180042234A1 (en) | 2015-03-19 | 2018-02-15 | E I Du Pont De Nemours And Company | Fungicidal pyrazoles |
EP3141118A1 (en) | 2015-09-14 | 2017-03-15 | Bayer CropScience AG | Compound combination for controlling control phytopathogenic harmful fungi |
AU2016381095B2 (en) * | 2015-12-30 | 2020-11-12 | Corteva Agriscience Llc | Fungal control of white mold |
WO2017194363A1 (en) * | 2016-05-10 | 2017-11-16 | Bayer Cropscience Aktiengesellschaft | Compound combination for controlling phytopathogenic harmful fungi |
EP3245872A1 (en) * | 2016-05-20 | 2017-11-22 | BASF Agro B.V. | Pesticidal compositions |
EP3504202A4 (en) * | 2016-08-26 | 2020-03-11 | Dow Agrosciences LLC | USE OF UK-2A PRO-FUNGICIDES TO CONTROL RICE TANKS |
WO2018039546A1 (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 |
WO2018045003A1 (en) | 2016-08-30 | 2018-03-08 | Dow Agrosciences Llc | Picolinamide n-oxide compounds with fungicidal activity |
US10173982B2 (en) | 2016-08-30 | 2019-01-08 | Dow Agrosciences Llc | Picolinamides as fungicides |
WO2018045010A1 (en) | 2016-08-30 | 2018-03-08 | Dow Agrosciences Llc | Pyrido-1,3-oxazine-2,4-dione compounds with fungicidal activity |
US10172358B2 (en) | 2016-08-30 | 2019-01-08 | Dow Agrosciences Llc | Thiopicolinamide compounds with fungicidal activity |
EP3558984B1 (en) | 2016-12-20 | 2023-08-02 | FMC Corporation | Fungicidal oxadiazoles |
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 |
CN114424771A (zh) * | 2017-03-07 | 2022-05-03 | Upl有限公司 | 杀真菌组合 |
TW202334101A (zh) | 2017-04-06 | 2023-09-01 | 美商富曼西公司 | 殺真菌之噁二唑 |
CN110996665B (zh) | 2017-05-02 | 2021-10-26 | 陶氏益农公司 | 无环吡啶酰胺化合物作为针对草坪草上的真菌病害的杀真菌剂的用途 |
TWI774760B (zh) * | 2017-05-02 | 2022-08-21 | 美商科迪華農業科技有限責任公司 | 用於蔬菜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 |
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 |
AR112221A1 (es) | 2017-07-05 | 2019-10-02 | Fmc Corp | Oxadiazoles fungicidas, composición que los comprende y un método para controlar fitoenfermedades que los emplea |
EA202091234A1 (ru) | 2017-11-21 | 2020-10-05 | Зингента Партисипейшнс Аг | Фунгицидные композиции |
US11319553B2 (en) | 2017-11-29 | 2022-05-03 | Rahan Meristem (1998) Ltd. | Compositions and methods conferring resistance to fungal diseases |
RU2672493C1 (ru) * | 2018-02-14 | 2018-11-15 | ООО "Агро Эксперт Груп" | Фунгицидная композиция (варианты) |
RU2661392C1 (ru) * | 2018-02-14 | 2018-07-16 | Общество с ограниченной ответственностью "Агро Эксперт Груп" | Фунгицидная композиция (Варианты) |
BR102019004480B1 (pt) | 2018-03-08 | 2023-03-28 | Dow Agrosciences Llc | Picolinamidas como fungicidas |
TW202400547A (zh) | 2018-09-06 | 2024-01-01 | 美商富曼西公司 | 殺真菌之經硝苯胺基取代之吡唑 |
WO2020056090A1 (en) | 2018-09-14 | 2020-03-19 | Fmc Corporation | Fungicidal halomethyl ketones and hydrates |
CA3114046C (en) | 2018-09-27 | 2022-07-19 | 0903608 B.C. Ltd. | Synergistic pesticidal compositions and methods for delivery of insecticidal active ingredients |
WO2020081382A1 (en) | 2018-10-15 | 2020-04-23 | Dow Agrosciences Llc | Methods for sythesis of oxypicolinamides |
TWI846654B (zh) | 2018-11-06 | 2024-06-21 | 美商富曼西公司 | 經取代之甲苯基殺真菌劑 |
MX2022008688A (es) | 2020-01-15 | 2022-08-04 | Fmc Corp | Amidas fungicidas. |
UY39082A (es) | 2020-02-14 | 2021-09-30 | Fmc Corp | Piridazinonas fungicidas |
RU2763596C1 (ru) * | 2021-07-19 | 2021-12-30 | Акционерное общество "Щелково Агрохим" | Фунгицидная синергетическая комбинация биологически активных веществ |
CN115299449B (zh) * | 2022-09-20 | 2023-10-27 | 允发化工(上海)有限公司 | 一种农药组合物及其应用 |
Family Cites Families (63)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4051173A (en) | 1974-04-02 | 1977-09-27 | Merck Patent Gesellschaft Mit Beschrankter Haftung | Phenoxyalkanol derivatives |
ES2120523T3 (es) | 1993-02-25 | 1998-11-01 | Goldschmidt Ag Th | Organopolisiloxano-polieteres y su empleo como agentes de reticulacion estables a la hidrolisis en sistemas acuosos. |
ATE242962T1 (de) | 1997-03-03 | 2003-07-15 | Rohm & Haas | Pestizide zusammensetzungen |
WO1999011127A1 (fr) * | 1997-08-29 | 1999-03-11 | Meiji Seika Kaisha, Ltd. | Agent de lutte contre la piriculariose du riz et agent de lutte contre la tavelure du ble |
TW491686B (en) | 1997-12-18 | 2002-06-21 | Basf Ag | Fungicidal mixtures based on amide compounds and tetrachloroisophthalonitrile |
US7250389B1 (en) * | 1998-02-06 | 2007-07-31 | Meiji Seika Kaisha, Ltd. | Antifungal compound and process for producing the same |
WO2000026191A1 (fr) | 1998-11-04 | 2000-05-11 | Meiji Seika Kaisha, Ltd. | Derives de picolinamide et pesticides contenant ces derives comme ingredient actif |
EP1516874B1 (en) * | 1999-07-20 | 2015-08-19 | Dow AgroSciences LLC | Fungicidal heterocyclic aromatic amides and their compositions, methods of use and preparation |
US20030018052A1 (en) | 1999-07-20 | 2003-01-23 | Ricks Michael J. | Fungicidal heterocyclic aromatic amides and their compositions, methods of use and preparation |
UA73519C2 (en) | 1999-07-20 | 2005-08-15 | Dow Agrosciences Llc | Heterocyclic aromatic amide, fungicide mixture based thereon and a method for control or prevention of fungous affection |
US6355660B1 (en) | 1999-07-20 | 2002-03-12 | Dow Agrosciences Llc | Fungicidal heterocyclic aromatic amides and their compositions, methods of use and preparation |
US20050239873A1 (en) | 1999-08-20 | 2005-10-27 | Fred Hutchinson Cancer Research Center | 2 Methoxy antimycin a derivatives and methods of use |
EP1204643B1 (en) * | 1999-08-20 | 2008-06-04 | Dow AgroSciences LLC | Fungicidal heterocyclic aromatic amides and their compositions, methods of use and preparation |
EP1218368B1 (en) | 1999-08-20 | 2007-05-23 | Fred Hutchinson Cancer Research Center | COMPOSITIONS AND METHODS FOR MODULATING APOPTOSIS IN CELLS OVER-EXPRESSING bcl-2 FAMILY MEMBER PROTEINS |
FR2803592A1 (fr) | 2000-01-06 | 2001-07-13 | Aventis Cropscience Sa | Nouveaux derives de l'acide 3-hydroxypicolinique, leur procede de preparation et compositions fongicides les contenant. |
US20020119979A1 (en) | 2000-10-17 | 2002-08-29 | Degenhardt Charles Raymond | Acyclic compounds and methods for treating multidrug resistance |
EP1275653A1 (en) | 2001-07-10 | 2003-01-15 | Bayer CropScience S.A. | Oxazolopyridines and their use as fungicides |
WO2003011857A1 (en) * | 2001-07-31 | 2003-02-13 | Dow Agrosciences Llc | Reductive cleavage of the exocyclic ester of uk-2a or its derivatives and products formed therefrom |
US6903219B2 (en) | 2001-10-05 | 2005-06-07 | Dow Agrosciences Llc | Process to produce derivatives from UK-2A derivatives |
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 |
AP2063A (en) * | 2003-05-28 | 2009-10-29 | Basf Ag | Fungicidal mixtures for controlling rice pathogens |
CN1794914A (zh) * | 2003-05-28 | 2006-06-28 | 巴斯福股份公司 | 用于防治稻病原体的杀真菌混合物 |
DE10347090A1 (de) * | 2003-10-10 | 2005-05-04 | Bayer Cropscience Ag | Synergistische fungizide Wirkstoffkombinationen |
EP1713331B1 (en) * | 2004-02-04 | 2007-08-29 | Janssen Pharmaceutica N.V. | Synergistic antifungal ddac compositions |
GB0419694D0 (en) | 2004-09-06 | 2004-10-06 | Givaudan Sa | Anti-bacterial compounds |
US9185911B2 (en) * | 2005-02-04 | 2015-11-17 | Mitsui Chemicals, Inc. | Composition for preventing plant diseases and method for preventing the diseases |
PL1931197T3 (pl) * | 2005-04-18 | 2015-09-30 | Basf Se | Preparat zawierający co najmniej jeden fungicyd konazolowy, inny fungicyd i jeden kopolimer stabilizujący |
WO2007054835A2 (en) * | 2005-06-21 | 2007-05-18 | Cheminova Agro A/S | Synergistic combination of a glyphosate herbicide and a triazole fungicide |
PL1912503T3 (pl) | 2005-08-05 | 2014-12-31 | Basf Se | Mieszaniny grzybobójcze zawierające podstawione anilidy kwasu 1-metylopirazol-4-ilokarboksylowego |
US8008231B2 (en) | 2005-10-13 | 2011-08-30 | Momentive Performance Materials Inc. | Extreme environment surfactant compositions comprising hydrolysis resistant organomodified disiloxane surfactants |
WO2008105964A1 (en) | 2007-02-26 | 2008-09-04 | Stepan Company | Adjuvants for agricultural applications |
CN101808521A (zh) * | 2007-09-26 | 2010-08-18 | 巴斯夫欧洲公司 | 包含啶酰菌胺和百菌清的三元杀真菌组合物 |
DK2296467T3 (da) * | 2008-05-30 | 2016-02-15 | Dow Agrosciences Llc | FREMGANGSMÅDER TIL BEKÆMPELSE AF QoI-RESISTENTE SVAMPEPATOGENER |
TWI504598B (zh) | 2009-03-20 | 2015-10-21 | Onyx Therapeutics Inc | 結晶性三肽環氧酮蛋白酶抑制劑 |
MX2012001622A (es) | 2009-08-07 | 2012-04-11 | Dow Agrosciences Llc | Derivados de n1-sulfonil-5-fluoropirimidinona. |
UA112284C2 (uk) | 2009-08-07 | 2016-08-25 | ДАУ АГРОСАЙЄНСІЗ ЕлЕлСі | Похідні 5-фторпіримідинону |
JP5683592B2 (ja) | 2009-09-01 | 2015-03-11 | ダウ アグロサイエンシィズ エルエルシー | 穀類における菌類防除のための5−フルオロピリミジン誘導体を含有する相乗性殺菌剤組成物 |
US20110070278A1 (en) | 2009-09-22 | 2011-03-24 | Humberto Benito Lopez | Metconazole compositions and methods of use |
UA109416C2 (xx) | 2009-10-06 | 2015-08-25 | Стабільні емульсії типу "масло в воді" | |
PL3178321T3 (pl) | 2009-10-07 | 2019-10-31 | Dow Agrosciences Llc | Synergistyczne grzybobójcze mieszaniny epoksykonazolu do zwalczania grzybów w zbożach |
CA2776562A1 (en) | 2009-10-07 | 2011-04-14 | Dow Agrosciences Llc | Synergistic fungicidal composition containing 5-fluorocytosine for fungal control in cereals |
AU2010330080B2 (en) | 2009-12-08 | 2014-07-31 | Basf Se | Pesticidal mixtures |
PT2563771E (pt) | 2010-04-24 | 2016-03-31 | Viamet Pharmaceuticals Inc | Compostos inibidores de metaloenzimas |
KR101466838B1 (ko) | 2010-06-18 | 2014-11-28 | 주식회사 녹십자 | Sglt2 억제제로서의 티아졸 유도체 및 이를 포함하는 약학 조성물 |
WO2012016989A2 (en) | 2010-08-03 | 2012-02-09 | Basf Se | Fungicidal compositions |
CN104365610A (zh) | 2010-08-05 | 2015-02-25 | 拜耳知识产权有限责任公司 | 包含丙硫菌唑和氟唑菌酰胺的活性化合物组合产品 |
UA111167C2 (uk) | 2010-08-05 | 2016-04-11 | ДАУ АГРОСАЙЄНСІЗ ЕлЕлСі | Пестицидні композиції мезорозмірних частинок з підсиленою дією |
JP2012036143A (ja) | 2010-08-10 | 2012-02-23 | Sumitomo Chemical Co Ltd | 植物病害防除組成物およびその用途 |
EP2643300A1 (en) | 2010-11-24 | 2013-10-02 | Stemergie Biotechnology SA | Inhibitors of the activity of complex iii of the mitochondrial electron transport chain and use thereof for treating diseases |
JP6013032B2 (ja) | 2011-07-08 | 2016-10-25 | 石原産業株式会社 | 殺菌剤組成物及び植物病害の防除方法 |
BR112014017799A8 (pt) | 2012-01-20 | 2017-07-11 | Viamet Pharmaceuticals Inc | Compostos inibidores de metaloenzima |
TWI568721B (zh) | 2012-02-01 | 2017-02-01 | 杜邦股份有限公司 | 殺真菌之吡唑混合物 |
BR112014027591A2 (pt) | 2012-05-07 | 2017-06-27 | Dow Agrosciences Llc | uso de pró-fungicidas de uk-2a para controle de ferrugem de soja |
WO2013169661A1 (en) | 2012-05-07 | 2013-11-14 | Dow Agrosciences Llp | Use of pro-fungicides of uk-2a for control of black sigatoka |
WO2013169662A2 (en) | 2012-05-07 | 2013-11-14 | Dow Agrosciences Llc | Macrocyclic picolinamides as fungicides |
CN104703984A (zh) | 2012-05-07 | 2015-06-10 | 陶氏益农公司 | 作为杀真菌剂的大环吡啶-2-甲酰胺 |
PL2847188T3 (pl) | 2012-05-07 | 2017-07-31 | Dow Agrosciences Llc | Makrocykliczne pikolinamidy jako fungicydy |
BR112015015351B8 (pt) | 2012-12-28 | 2022-08-23 | Dow Agrosciences Llc | Mistura fungicida sinérgica, composição fungicida, e método para tratamento de uma planta |
US9750248B2 (en) | 2012-12-31 | 2017-09-05 | Dow Agrosciences Llc | Synergistic fungicidal compositions |
JP2016507511A (ja) | 2012-12-31 | 2016-03-10 | ダウ アグロサイエンシィズ エルエルシー | 殺真菌剤としての大環状ピコリンアミド |
CN105705502A (zh) | 2013-10-01 | 2016-06-22 | 美国陶氏益农公司 | 具有杀真菌活性的大环吡啶酰胺化合物 |
WO2015100182A1 (en) | 2013-12-26 | 2015-07-02 | Dow Agrosciences Llc | Use of macrocyclic picolinamides as fungicides |
NZ720916A (en) | 2013-12-31 | 2017-06-30 | Dow Agrosciences Llc | Synergistic fungicidal mixtures for fungal control in cereals |
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