WO1997040678A1 - Fungizide mischungen - Google Patents
Fungizide mischungen Download PDFInfo
- Publication number
- WO1997040678A1 WO1997040678A1 PCT/EP1997/002048 EP9702048W WO9740678A1 WO 1997040678 A1 WO1997040678 A1 WO 1997040678A1 EP 9702048 W EP9702048 W EP 9702048W WO 9740678 A1 WO9740678 A1 WO 9740678A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- formula
- alkyl
- compound
- iii
- compounds
- Prior art date
Links
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
- A01N37/52—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 containing groups, e.g. carboxylic acid amidines
-
- 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
- A01N47/08—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
Definitions
- the present invention relates to a fungicidal mixture, which
- T is CH and N
- n is 0, 1 or 2
- R is halogen, C 1 -C 4 -alkyl or C] .
- -C 4 -haloalkyl means, where the radicals R can be different if n is 2, and / or
- X is oxygen or amino (NH);
- Y is CH or N
- Z is oxygen, sulfur, amino (NH) or C 1 -C 4 alkylamino (N-C ⁇ -C 4 alkyl);
- the invention relates to methods for controlling harmful fungi with mixtures of the compounds I and / or II and III and the use of the compounds I and / or II and the compound III for the preparation of such mixtures.
- the present invention was based on the problem of mixtures which, with a reduced total amount of active compounds applied, have an improved activity against harmful fungi (synergistic mixtures).
- Formula I in particular represents carbamates in which the combination of the substituents corresponds to one row of the following table:
- the general formula II is particularly representative of methoxy-acrylic esters and oxime ethers in which X is oxygen and Y is CH or X is amino and Y is N.
- the E / Z isomer mixture or the E isomer is preferably used in each case, the E isomer being particularly preferred in the case of the compound II.
- the compounds II can be used both as isomer mixtures and as pure isomers in the mixtures according to the invention. With regard to their use, particular preference is given to compounds II in which the terminal oxime ether grouping of the side chain is in the ice configuration (OCH 3 group to ZR ').
- the compounds I and II are able to form salts or adducts with inorganic or organic acids or with metal ions.
- inorganic acids are hydrohalic acids such as hydrogen fluoride, hydrogen chloride, hydrogen bromide and hydrogen iodide, sulfuric acid, phosphoric acid and nitric acid.
- suitable organic acids are formic acid, carbonic acid and alkanoic acids such as acetic acid, trifluoroacetic acid, trichloroacetic acid and propionic acid as well as glycolic acid, thiocyanic acid, lactic acid, succinic acid, citric acid, benzoic acid, cinnamic acid, oxalic acid, alkylsulfonic acids (sulfonic acids with branched chain radicals or with straight-chain fatty acids) 1 to 20 carbon atoms), arylsulfonic acids or disulfonic acids (aromatic radicals such as phenyl and naphthyl which carry one or two sulfonic acid groups), alkylphosphonic acids (phosphonic acids with straight-chain or branched alkyl radicals with 1 to 20 carbon atoms), Arylphosphonsauren or aryldiphosphonic acids (aromatic radicals such as phenyl and naphthyl, which one or two phosphoric acid radicals wear),
- the ions of the elements of the second main group, in particular calcium and magnesium, the third and fourth main group, in particular aluminum, tin and lead, and the first to eighth subgroups, in particular chromium, manganese, iron, cobalt, nickel, copper, come as metal ions. Zinc and others into consideration.
- the metal ions of the elements of the subgroups of the fourth period are particularly preferred. The metals can be present in the various valences that they have.
- the mixtures of the compounds I and / or II and III or the simultaneous joint or separate use of the compounds I and / or II and III are distinguished by an excellent action against a broad spectrum of phytopathogenic fungi, in particular from the class the Ascomycetes, Deuteromycetes, Phycomycetes and Basidiomycetes. Some of them are systemically active and can therefore also be used as foliar and soil fungicides. They are of particular importance for combating a large number of fungi on various crop plants such as cotton, vegetable plants (for example cucumbers, beans and pumpkin plants), barley, grass, oats, coffee, corn, fruit plants, rice, rye, soybeans, wine, wheat , Ornamental plants, sugar cane and a variety of seeds.
- Ascomycetes, Deuteromycetes, Phycomycetes and Basidiomycetes Some of them are systemically active and can therefore also be used as foliar and soil fungicides. They are of particular importance for combating a large number
- the compounds I and / or II and III can be applied simultaneously together or separately or in succession, the sequence in the case of separate application generally not having any effect on the success of the control measures.
- the compounds I and / or II and III are usually in a weight ratio of 200: 1 to 0.1: 1, preferably 100: 1 to 1: 1, in particular 50: 1 to 5: 1 (III: I and / or II ) applied.
- the application rates of the mixtures according to the invention are in general from 0.005 to 0.5 kg / ha, preferably 0.01 to 0.5 kg / ha, in particular 0.01 to 0 , 3 kg / ha.
- the application rates for the compounds III are accordingly 0.1 to 10 kg / ha, preferably 0.5 to 5 kg / ha, in particular 1 to 4 kg / ha.
- the compounds I and / or II and II or the mixtures of the compounds I and / or II and II are applied separately or together by spraying or dusting the seeds, the plants or the Soils before or after sowing the plants or before or after emergence of the plants.
- the fungicidal synergistic mixtures according to the invention or the compounds I and / or II and III can be used, for example, in the form of directly sprayable solutions, powders and suspensions or in the form of high-strength aqueous, oily or other suspensions, dispersions, emulsions, old-dispersions, pastes, dusts, Spreading agents or granules are prepared and applied by spraying, atomizing, dusting, scattering or pouring.
- the form of application depends on the purpose; in any case, it should ensure as fine and uniform a distribution of the mixture according to the invention as possible.
- the formulations are prepared in a manner known per se, e.g. by adding solvents and / or carriers. Inert additives such as emulsifiers or dispersants are usually added to the formulations.
- alkali, alkaline earth, ammonium salts of aromatic sulfonic acids e.g. Lignin-,
- Granules e.g. coating, impregnation or homogeneous granules
- a solid carrier e.g., a wax, a wax, or a wax.
- Mineral earths such as silica gel, silicas, silica gels, silicates, talc, kaolin, limestone, lime, chalk, boluses, loess, clay, dolomite, diatomaceous earth, calcium and magnesium sulfate, magnesium oxide, ground plastics serve as fillers or solid carriers, for example. and fertilizers such as ammonium sulfate, ammonium phosphate, ammonium nitrate, ureas and vegetable products such as cereal flour, tree bark, wood and nutshell flour, cellulose powder or other solid carriers.
- fertilizers such as ammonium sulfate, ammonium phosphate, ammonium nitrate, ureas and vegetable products such as cereal flour, tree bark, wood and nutshell flour, cellulose powder or other solid carriers.
- the formulations generally contain 0.1 to 95% by weight, preferably 0.5 to 90% by weight, of one of the compounds I and / or II or III or the mixture of the compounds I and / or II and III.
- the active ingredients are used in a purity of 90% to 100%, preferably 95% to 100% (according to the NMR or HPLC spectrum).
- the compounds I and / or II and III or the mixtures or the corresponding formulations are used by mixing the harmful fungi, the plants, seeds, soils, surfaces, materials or spaces to be kept free of them with a fungicidally effective amount of the mixture, or the compounds I and / or II and III treated separately.
- the application can take place before or after the infestation by the harmful fungi.
- the fungicidal activity of the compound and the mixtures can be demonstrated by the following tests:
- the active ingredients are separated or together as a 10% emulsion in a mixture of 70% by weight cyclohexanone, 20% by weight Nekanil® LN (Lutensol® AP6, wetting agent with emulsifying and dispersing action based on ethoxylated alkylphenols) and 10% by weight -% Emulphor® EL (Emulan® EL, emulsifier based on ethoxylated fatty alcohols) prepared and diluted with water according to the desired concentration.
- Nekanil® LN Litensol® AP6, wetting agent with emulsifying and dispersing action based on ethoxylated alkylphenols
- Emulphor® EL Emulphor® EL
- the evaluation is carried out by determining the affected leaf areas in percent. These percentages are converted into efficiencies.
- the expected efficacies of the active ingredient Mixtures are determined using Colby's formula [RS Colby, Weeds 15, 20-22 (1967)] and compared with the observed efficiencies.
- ⁇ corresponds to the fungal attack of the treated plants in%
- ß corresponds to the fungal infection of the untreated (control) plants in%
- the infection of the treated plants corresponds to that of the untreated control plants; with an efficiency of 100, the treated plants are not infected.
- Leaves of potted plants of the "large meat tomato" variety were sprayed to runoff point with an aqueous suspension which was prepared from a stock solution of 10% active ingredient, 63% cyclohexanone and 27% emulsifier. The following day, the leaves were infected with an aqueous suspension of zoospores from Phytophthora infestans. The plants were then placed in a water vapor-saturated chamber at temperatures between 16 and 18 ° C. After 6 days, the late blight on the untreated but infected control plants developed so strongly that the infestation could be determined visually in%.
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)
Abstract
Description
Claims
Priority Applications (16)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US09/171,563 US6028093A (en) | 1996-04-26 | 1997-04-23 | Fungicide compositions |
DE59706871T DE59706871D1 (de) | 1996-04-26 | 1997-04-23 | Fungizide mischungen |
EA199800895A EA001105B1 (ru) | 1996-04-26 | 1997-04-23 | Фунгицидные смеси |
NZ332077A NZ332077A (en) | 1996-04-26 | 1997-04-23 | Fungicide mixture containing a carbamate derivative and propamcarb and/or an oxime ether derivative |
SK1443-98A SK144398A3 (en) | 1996-04-26 | 1997-04-23 | Fungicidal mixtures |
PL97329522A PL329522A1 (en) | 1996-04-26 | 1997-04-23 | Fungicidal mixture |
DK97920739T DK0900011T3 (da) | 1996-04-26 | 1997-04-23 | Fungicide blandinger |
SI9730301T SI0900011T1 (en) | 1996-04-26 | 1997-04-23 | Fungicide mixtures |
CA002252641A CA2252641A1 (en) | 1996-04-26 | 1997-04-23 | Fungicide mixtures |
EP97920739A EP0900011B1 (de) | 1996-04-26 | 1997-04-23 | Fungizide mischungen |
AT97920739T ATE215309T1 (de) | 1996-04-26 | 1997-04-23 | Fungizide mischungen |
AU27009/97A AU722194B2 (en) | 1996-04-26 | 1997-04-23 | Fungicidal mixtures |
JP9538551A JP2000509062A (ja) | 1996-04-26 | 1997-04-23 | 殺菌剤混合物 |
IL12623097A IL126230A0 (en) | 1996-04-26 | 1997-04-23 | Fungicidal mixtures |
BR9708805A BR9708805A (pt) | 1996-04-26 | 1997-04-23 | Mistura fungicida e processo para controlar fungos daninhos |
KR1019980708551A KR20000065014A (ko) | 1996-04-26 | 1997-04-23 | 살진균제혼합물 |
Applications Claiming Priority (6)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19616689 | 1996-04-26 | ||
DE19616689.6 | 1996-04-26 | ||
DE19617069 | 1996-04-29 | ||
DE19617069.9 | 1996-04-29 | ||
DE19635505 | 1996-09-02 | ||
DE19635505.2 | 1996-09-02 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO1997040678A1 true WO1997040678A1 (de) | 1997-11-06 |
Family
ID=27216187
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/EP1997/002048 WO1997040678A1 (de) | 1996-04-26 | 1997-04-23 | Fungizide mischungen |
Country Status (21)
Country | Link |
---|---|
US (1) | US6028093A (de) |
EP (1) | EP0900011B1 (de) |
JP (1) | JP2000509062A (de) |
KR (1) | KR20000065014A (de) |
CN (1) | CN1216440A (de) |
AR (1) | AR006857A1 (de) |
AT (1) | ATE215309T1 (de) |
AU (1) | AU722194B2 (de) |
BR (1) | BR9708805A (de) |
CA (1) | CA2252641A1 (de) |
CO (1) | CO4761030A1 (de) |
CZ (1) | CZ289349B6 (de) |
DE (1) | DE59706871D1 (de) |
DK (1) | DK0900011T3 (de) |
EA (1) | EA001105B1 (de) |
IL (1) | IL126230A0 (de) |
NZ (1) | NZ332077A (de) |
PL (1) | PL329522A1 (de) |
SK (1) | SK144398A3 (de) |
TW (1) | TW337981B (de) |
WO (1) | WO1997040678A1 (de) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2006040123A3 (de) * | 2004-10-12 | 2006-06-29 | Bayer Cropscience Ag | Fluoxastrobin enthaltende fungizide wirkstoffkombinationen |
US8592412B1 (en) | 2008-03-24 | 2013-11-26 | Nippon Soda Co., Ltd. | Plant disease control agent |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU4400497A (en) * | 1996-10-15 | 1998-05-11 | Shionogi & Co., Ltd. | Oxime derivatives, hydrazone derivatives, and use thereof |
US8188003B2 (en) * | 2000-05-03 | 2012-05-29 | Basf Aktiengesellschaft | Method of inducing virus tolerance of plants |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0610764A1 (de) * | 1993-02-12 | 1994-08-17 | Bayer Ag | Fungizide Wirkstoffkombinationen |
WO1995021153A1 (de) * | 1994-02-04 | 1995-08-10 | Basf Aktiengesellschaft | Phenylessigsäurederivate, verfahren und zwischenprodukte zu ihrer herstellung und sie enthaltende mittel |
WO1996001256A1 (de) * | 1994-07-06 | 1996-01-18 | Basf Aktiengesellschaft | 2-[(dihydro)pyrazolyl-3'-oxymethylen]-anilide als schädlingsbekämpfungsmittel und fungizide |
WO1996001258A1 (de) * | 1994-07-06 | 1996-01-18 | Basf Aktiengesellschaft | 2-(1',2',4'-triazol-3'yloxymethylen)-anilide und ihre verwendung als schädlingsbekämpfungsmittel |
DE19528651A1 (de) * | 1995-08-04 | 1997-02-06 | Basf Ag | Hydroximsäurederivate, Verfahren zu ihrer Herstellung und sie enthaltende Mittel |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NL157191C (nl) * | 1966-12-17 | Schering Ag | Werkwijze voor het bereiden van een preparaat met fungicide en fungistatische werking. | |
JPS6425763A (en) * | 1987-04-24 | 1989-01-27 | Mitsubishi Chem Ind | Pyrazoles and insecticide and acaricide containing said pyrazoles as active ingredient |
AU681932B2 (en) * | 1994-02-04 | 1997-09-11 | Basf Aktiengesellschaft | Phenyl acetic acid derivatives, process and intermediate products for their production and agents containing them |
TW401275B (en) * | 1995-09-25 | 2000-08-11 | Basf Ag | Compositions and methods of controlling harmful fungi |
-
1997
- 1997-04-23 EA EA199800895A patent/EA001105B1/ru not_active IP Right Cessation
- 1997-04-23 IL IL12623097A patent/IL126230A0/xx not_active IP Right Cessation
- 1997-04-23 CZ CZ19983378A patent/CZ289349B6/cs not_active IP Right Cessation
- 1997-04-23 BR BR9708805A patent/BR9708805A/pt unknown
- 1997-04-23 NZ NZ332077A patent/NZ332077A/en unknown
- 1997-04-23 US US09/171,563 patent/US6028093A/en not_active Expired - Fee Related
- 1997-04-23 DE DE59706871T patent/DE59706871D1/de not_active Expired - Lifetime
- 1997-04-23 SK SK1443-98A patent/SK144398A3/sk unknown
- 1997-04-23 CA CA002252641A patent/CA2252641A1/en not_active Abandoned
- 1997-04-23 DK DK97920739T patent/DK0900011T3/da active
- 1997-04-23 AT AT97920739T patent/ATE215309T1/de not_active IP Right Cessation
- 1997-04-23 JP JP9538551A patent/JP2000509062A/ja active Pending
- 1997-04-23 WO PCT/EP1997/002048 patent/WO1997040678A1/de not_active Application Discontinuation
- 1997-04-23 PL PL97329522A patent/PL329522A1/xx unknown
- 1997-04-23 CN CN97194053A patent/CN1216440A/zh active Pending
- 1997-04-23 AU AU27009/97A patent/AU722194B2/en not_active Ceased
- 1997-04-23 EP EP97920739A patent/EP0900011B1/de not_active Expired - Lifetime
- 1997-04-23 KR KR1019980708551A patent/KR20000065014A/ko not_active Application Discontinuation
- 1997-04-25 AR ARP970101708A patent/AR006857A1/es unknown
- 1997-04-25 CO CO97022200A patent/CO4761030A1/es unknown
- 1997-04-25 TW TW086105452A patent/TW337981B/zh active
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0610764A1 (de) * | 1993-02-12 | 1994-08-17 | Bayer Ag | Fungizide Wirkstoffkombinationen |
WO1995021153A1 (de) * | 1994-02-04 | 1995-08-10 | Basf Aktiengesellschaft | Phenylessigsäurederivate, verfahren und zwischenprodukte zu ihrer herstellung und sie enthaltende mittel |
WO1996001256A1 (de) * | 1994-07-06 | 1996-01-18 | Basf Aktiengesellschaft | 2-[(dihydro)pyrazolyl-3'-oxymethylen]-anilide als schädlingsbekämpfungsmittel und fungizide |
WO1996001258A1 (de) * | 1994-07-06 | 1996-01-18 | Basf Aktiengesellschaft | 2-(1',2',4'-triazol-3'yloxymethylen)-anilide und ihre verwendung als schädlingsbekämpfungsmittel |
DE19528651A1 (de) * | 1995-08-04 | 1997-02-06 | Basf Ag | Hydroximsäurederivate, Verfahren zu ihrer Herstellung und sie enthaltende Mittel |
Non-Patent Citations (2)
Title |
---|
"MIXTURES OF FUNGICIDES AND HERBICIDES", RESEARCH DISCLOSURE, no. 348, 1 April 1993 (1993-04-01), pages 267, COMPL, XP000304224 * |
FRAINE DE P J ET AL: "A NEW SERIES OF BROAD-SPECTRUM BETA-METHOXYACRYLATE FUNGICIDES WITH AN OXIME ETHER SIDE-CHAIN", PESTICIDE SCIENCE, vol. 44, no. 1, May 1995 (1995-05-01), pages 77 - 79, XP002020496 * |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2006040123A3 (de) * | 2004-10-12 | 2006-06-29 | Bayer Cropscience Ag | Fluoxastrobin enthaltende fungizide wirkstoffkombinationen |
US8592412B1 (en) | 2008-03-24 | 2013-11-26 | Nippon Soda Co., Ltd. | Plant disease control agent |
US8592461B2 (en) | 2008-03-24 | 2013-11-26 | Nippon Soda Co., Ltd. | Plant disease control agent |
Also Published As
Publication number | Publication date |
---|---|
AU2700997A (en) | 1997-11-19 |
EP0900011B1 (de) | 2002-04-03 |
AR006857A1 (es) | 1999-09-29 |
DK0900011T3 (da) | 2002-07-01 |
ATE215309T1 (de) | 2002-04-15 |
EA199800895A1 (ru) | 1999-06-24 |
EP0900011A1 (de) | 1999-03-10 |
DE59706871D1 (de) | 2002-05-08 |
AU722194B2 (en) | 2000-07-27 |
NZ332077A (en) | 2000-02-28 |
CZ289349B6 (cs) | 2002-01-16 |
CN1216440A (zh) | 1999-05-12 |
US6028093A (en) | 2000-02-22 |
TW337981B (en) | 1998-08-11 |
IL126230A0 (en) | 1999-05-09 |
CZ337898A3 (cs) | 1999-04-14 |
SK144398A3 (en) | 1999-04-13 |
PL329522A1 (en) | 1999-03-29 |
CA2252641A1 (en) | 1997-11-06 |
JP2000509062A (ja) | 2000-07-18 |
EA001105B1 (ru) | 2000-10-30 |
CO4761030A1 (es) | 1999-04-27 |
KR20000065014A (ko) | 2000-11-06 |
BR9708805A (pt) | 1999-08-03 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
WO1998058544A1 (de) | Fungizide mischungen | |
WO1998052417A1 (de) | Fungizide mischungen | |
EP0901322B1 (de) | Fungizide mischungen | |
EP0906017B1 (de) | Fungizide mischungen | |
EP0900020B1 (de) | Fungizide mischungen | |
EP0900008A1 (de) | Fungizide mischungen | |
EP0984696B1 (de) | Fungizide mischungen | |
EP0844819B1 (de) | Fungizide mischungen eines oximethercarbonsäureamids mit fenarimol | |
EP0763976B1 (de) | Fungizide mischungen | |
EP0900011B1 (de) | Fungizide mischungen | |
EP0984689B1 (de) | Fungizide mischung | |
EP0900013B1 (de) | Fungizide mischungen | |
EP1083792A1 (de) | Fungizide mischungen | |
EP0912088B1 (de) | Fungizide mischungen | |
EP0984687A1 (de) | Fungizide mischungen | |
EP0984695A1 (de) | Fungizide mischungen | |
WO2003022053A1 (de) | Fungizide mischungen | |
EP0763975B1 (de) | Fungizide mischungen | |
WO1998008384A1 (de) | Fungizide mischungen | |
WO1997040675A1 (de) | Fungizide mischungen | |
EP0900018B1 (de) | Fungizide mischungen | |
EP0900014A1 (de) | Fungizide mischungen | |
WO1998053693A1 (de) | Fungizide mischungen |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
WWE | Wipo information: entry into national phase |
Ref document number: 97194053.3 Country of ref document: CN |
|
AK | Designated states |
Kind code of ref document: A1 Designated state(s): AU BG BR CA CN CZ GE HU IL JP KR LV MX NO NZ PL RO SG SI SK TR UA US AM AZ BY KG KZ MD RU TJ TM |
|
AL | Designated countries for regional patents |
Kind code of ref document: A1 Designated state(s): AT BE CH DE DK ES FI FR GB GR IE IT LU MC NL PT SE |
|
DFPE | Request for preliminary examination filed prior to expiration of 19th month from priority date (pct application filed before 20040101) | ||
121 | Ep: the epo has been informed by wipo that ep was designated in this application | ||
WWE | Wipo information: entry into national phase |
Ref document number: 1997920739 Country of ref document: EP |
|
WWE | Wipo information: entry into national phase |
Ref document number: 332077 Country of ref document: NZ |
|
WWE | Wipo information: entry into national phase |
Ref document number: 144398 Country of ref document: SK |
|
WWE | Wipo information: entry into national phase |
Ref document number: PV1998-3378 Country of ref document: CZ |
|
WWE | Wipo information: entry into national phase |
Ref document number: 09171563 Country of ref document: US |
|
ENP | Entry into the national phase |
Ref document number: 2252641 Country of ref document: CA Ref document number: 2252641 Country of ref document: CA Kind code of ref document: A |
|
WWE | Wipo information: entry into national phase |
Ref document number: PA/a/1998/008776 Country of ref document: MX |
|
WWE | Wipo information: entry into national phase |
Ref document number: 1019980708551 Country of ref document: KR |
|
WWE | Wipo information: entry into national phase |
Ref document number: 199800895 Country of ref document: EA |
|
WWP | Wipo information: published in national office |
Ref document number: 1997920739 Country of ref document: EP |
|
WWP | Wipo information: published in national office |
Ref document number: PV1998-3378 Country of ref document: CZ |
|
WWP | Wipo information: published in national office |
Ref document number: 1019980708551 Country of ref document: KR |
|
WWG | Wipo information: grant in national office |
Ref document number: PV1998-3378 Country of ref document: CZ |
|
WWG | Wipo information: grant in national office |
Ref document number: 1997920739 Country of ref document: EP |
|
WWW | Wipo information: withdrawn in national office |
Ref document number: 1019980708551 Country of ref document: KR |