WO2007104658A2 - Method of inducing tolerance of plants against bacterioses - Google Patents

Method of inducing tolerance of plants against bacterioses Download PDF

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Publication number
WO2007104658A2
WO2007104658A2 PCT/EP2007/051986 EP2007051986W WO2007104658A2 WO 2007104658 A2 WO2007104658 A2 WO 2007104658A2 EP 2007051986 W EP2007051986 W EP 2007051986W WO 2007104658 A2 WO2007104658 A2 WO 2007104658A2
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WO
WIPO (PCT)
Prior art keywords
methyl
amide
difluoromethyl
carboxylic acid
pyrazole
Prior art date
Application number
PCT/EP2007/051986
Other languages
French (fr)
Other versions
WO2007104658A3 (en
Inventor
Harald Köhle
Ted R. Bardinelli
Marco-Antonio Tavares-Rodrigues
Original Assignee
Basf Se
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Basf Se filed Critical Basf Se
Priority to BRPI0708283-5A priority Critical patent/BRPI0708283A2/en
Priority to CN2007800092270A priority patent/CN101400259B/en
Priority to JP2008558770A priority patent/JP2009529565A/en
Priority to AU2007224576A priority patent/AU2007224576A1/en
Priority to EP07726584A priority patent/EP1996018A2/en
Priority to US12/279,309 priority patent/US20090011935A1/en
Priority to EA200801902A priority patent/EA015354B1/en
Priority to CA002640963A priority patent/CA2640963A1/en
Publication of WO2007104658A2 publication Critical patent/WO2007104658A2/en
Publication of WO2007104658A3 publication Critical patent/WO2007104658A3/en

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    • 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
    • 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
    • A01N37/36—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 at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids
    • 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
    • A01N37/36—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 at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids
    • A01N37/38—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 at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids having at least one oxygen or sulfur atom attached to an aromatic ring system
    • 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
    • A01N37/44—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 at least one carboxylic group or a thio analogue, or a derivative thereof, and a nitrogen atom attached to the same carbon skeleton by a single or double bond, this nitrogen atom not being a member of a derivative or of a thio analogue of a carboxylic group, e.g. amino-carboxylic acids
    • A01N37/50—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 at least one carboxylic group or a thio analogue, or a derivative thereof, and a nitrogen atom attached to the same carbon skeleton by a single or double bond, this nitrogen atom not being a member of a derivative or of a thio analogue of a carboxylic group, e.g. amino-carboxylic acids the nitrogen atom being doubly bound to the carbon skeleton
    • 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
    • A01N43/64—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 method of inducing tolerance of plants against bacterioses, which comprises treating the plants, the soil or the seeds with an effective amount of a compound of the formula I, 1 ) a compound of the formula I
  • X is halogen, Ci-C4-alkyl or trifluoromethyl
  • m O or i ;
  • # denotes the bond to the phenyl ring
  • B is phenyl, naphthyl, 5-or 6-membered hetaryl or 5-or 6-membered hetero- cyclyl, containing one to three N atoms and/or one O or S atom or one or two O and/or S atoms, the ring systems being unsubstituted or substituted by one to three radicals R a :
  • R a is cyano, nitro, amino, aminocarbonyl, aminothiocarbonyl, halogen, d-Ce-alkyl, Ci-C 6 -haloalkyl, Ci-C 6 -alkylcarbonyl, Ci-C 6 -alkylsulfonyl,
  • R b is cyano, nitro, halogen, amino, aminocarbonyl, aminothio- carbonyl, Ci-C ⁇ -alkyl, Ci-C ⁇ -haloalkyl, Ci-C ⁇ -alkylsulfonyl, Ci- Ce-alkylsulfinyl, C3-C6-cycloalkyl, Ci-C ⁇ -alkoxy, Ci-C ⁇ -halo- alkoxy, Ci-C ⁇ -alkoxycarbonyl, Ci-C ⁇ -alkylthio, Ci-C6-alkylamino, di-Ci-C6-alkylamino, Ci-Ce-alkylaminocarbonyl, di-Ci-C ⁇ -alkyl- amino-carbonyl, d-Ce-alkylaminothiocarbonyl, di-Ci-C ⁇ -alkyl- aminothiocarbonyl, C2-C6-alkenyl, C2-C6-alkenyloxy, C3-C6
  • R A , R B are hydrogen or Ci-C 6 -alkyl
  • R 1 is hydrogen, cyano, Ci-C4-alkyl, Ci-C4-haloalkyl, C3-C6-cycloalkyl, C1-C4- alkoxy;
  • R 2 is phenyl, phenylcarbonyl, phenylsulfonyl, 5- or 6-membered hetaryl, 5- or 6-membered hetarylcarbonyl or 5- or 6-membered hetarylsulfonyl, the ring systems being unsubstituted or substituted by one to three radicals R a ,
  • Ci-Cio-alkyl, C3-C6-cycloalkyl, C2-Cio-alkenyl, C2-Cio-alkynyl, Ci-Cio-alkyl- carbonyl, C2-Cio-alkenylcarbonyl, Cs-Cio-alkynylcarbonyl, Ci-Cio-alkyl- sulfonyl, or C( NOR A )-R B , the hydrocarbon radicals of these groups being unsubstituted or substituted by one to three radicals R c :
  • R c is cyano, nitro, amino, aminocarbonyl, aminothiocarbonyl, halogen, d-Ce-alkyl, Ci-C 6 -haloalkyl, Ci-C 6 -alkylsulfonyl, Ci-C 6 -alkylsulfinyl, Ci-C ⁇ -alkoxy, Ci-C ⁇ -haloalkoxy, Ci-C ⁇ -alkoxycarbonyl, Ci-C ⁇ -alkyl- thio, Ci-C ⁇ -alkylamino, di-Ci-C ⁇ -alkylamino, Ci-C ⁇ -alkylamino- carbonyl, di-Ci-C ⁇ -alkylaminocarbonyl, Ci-C ⁇ -alkylaminothiocarbonyl, di-Ci-C ⁇ -alkylaminothiocarbonyl, C2-C6-alkenyl, C2-C6-alkenyloxy,
  • R 3 is hydrogen, Ci-C ⁇ -alkyl, C2-C6-alkenyl, C2-C6-alkynyl, the hydrocarbon radicals of these groups being unsubstituted or substituted by one to three radicals R c ;
  • acylalanines benalaxyl, metalaxyl, ofurace, oxadixyl,
  • D) azoles bitertanol, bromoconazole, cyproconazole, difenoconazole, dinitroconazole, enilconazole, epoxiconazole, fenbuconazole, fluquinconazole, flusilazole, flutriafol, hexaconazole, imazalil, ipconazole, metconazole, myclobutanil, penconazole, propiconazole, prochloraz, prothioconazole, simeconazole, tebuconazole, tetraconazole, triadimefon, triadimenol, triflumizol, triticonazole,
  • dicarboximides iprodione, myclozolin, procymidone, vinclozolin,
  • F) dithiocarbamates ferbam, nabam, maneb, mancozeb, metam, metiram, propineb, polycarbamate, thiram, ziram, zineb, G) heterocyclic compounds: anilazine, benomyl, boscalid, carbendazim, car- boxin, oxycarboxin, cyazofamid, dazomet, dithianon, fenamidone, fenari- mol, fuberidazole, flutolanil, furametpyr, isoprothiolane, mepronil, nuarimol, penthiopyrad, picobenzamid, probenazole, proquinazid, pyrifenox, pyroqui- lon, quinoxyfen, silthiofam, thiabendazole, thifluzamide, thiophanate- methyl, tiadinil, tricyclazole, triforine, 5-chloro-7
  • K) other fungicides selected from acibenzolar-S-methyl, benthiavalicarb, carpropamid, chlorothalonil, cyflufenamid, diclomezin, diclocymet, diethofencarb, edifenphos, ethaboxam, fenhexamid, fentin acetate, fenoxanil, ferimzone, fluazinam, phosphorous acid and its salts, fosetyl, fosetyl-aluminum, iprovalicarb, hexachlorobenzene, mandipropamid, metrafenone, pencycuron, propamocarb, phthalide, toloclofos-methyl, quintozene, zoxamid, acetyl salic acids, N-(2-(4-[3-(4-Chloro-phenyl)-prop- 2-ynyloxy]-3-methoxy-phenyl)
  • the inven- tion generally relates to the use of the combinations of a compound of formula I and a compound of the group A) to M) for immunizing plants against bacterioses.
  • Bacteria are predominantly found in moderate and humid-warm climatic regions as pathogens of diseases (bacterioses) in a large number of crop plants. Occasionally, these diseases cause substantial economic damage. Examples which are generally known are the death of entire fruit plantations caused by a variety of Erwinia species ("fireblight” in pears and apples), and bacterial soft rot in potatoes and many other plants, various plant tumors triggered by agrobacteria, and the necroses on a variety of vegetables, on rice, wheat and citrus fruit, caused by Xanthomonas species. The bac- terioses caused by Pseudomonas species, in particular in vegetables, top fruit species and tobacco are especially dreaded.
  • antibiotics for example Streptomycin, Blasticidin S or Kasugamicin
  • Streptomycin for example Streptomycin, Blasticidin S or Kasugamicin
  • this procedure is rarely practiced: the extensive use of antibiotics in agriculture is debated since, in principle, these antibiotics rely on the same mechanisms of action as are used against bacterial pathogens in human and veterinary medicine. They may thus favor the build-up of resistances.
  • antibiotics are expensive, owing to their molecular structures (most of which are complicated) and can only be produced by biotechnological methods. Therefore, it is an object of the invention to reduce the necessity to use antibiotics in agriculture.
  • Strobilurine type fungicides have a stimulatory effect on the plants' intrinsic immune system against bacteria. However, this effect is not always fully satisfactory.
  • strobilurines of formula I are known as fungicides and, in some cases, also as insecticides (EP-A 178 826; EP-A 253 213; WO 93/15046; WO
  • 3-Difluoromethyl-1-methyl-1 H-pyrazole-4-carboxylic acid [2-(1 ,1 , 2,3,3, 3-hexafluoro- propoxy)-phenyl]-amide, 3-Difluoromethyl-1-methyl-1 H-pyrazole-4-carboxylic acid [2- (1 ,1 ,2,2-tetrafluoroethoxy)-phenyl]-amide (PCT/EP2006/064988); 3-Difluoromethyl-1 -methyl-1 H-pyrazole-4-carboxylic acid (4'-trifluoromethylthiobiphenyl- 2-yl)-amide (EP Appln. 06123463.9);
  • the good compatibility, with plants, of the active ingredients of the formula I at the concentrations required for controlling plant diseases permits the treatment of aerial plant parts and also the treatment of propagation material and seed, and of the soil.
  • the active ingredients are taken up by the plant either through the leaf surface or through the roots and is distributed within the entire plant in the sap.
  • the protective action after carrying out the method according to the invention is not just found in those plant parts, which have been sprayed directly, but the tolerance to bacterial diseases of the entire plant is increased.
  • the aerial plant parts are treated with a formulation or with a tank mix of the active ingredients 1 ) and 2).
  • component 1 the active ingredients of the formulae Il to VIII, in which
  • V is OCH 3 and NHCH 3 ,
  • Y is CH and N and T and Z independently of one another are CH and N.
  • Preferred active ingredients of the formula I in which Q is N(-OCH3)-COOCH3 are the compounds described in the publications WO 93/15046 and WO 96/01256.
  • Preferred active ingredients of the formula I in which A is -O-B are the compounds described in the publications EP-A 382 375 and EP-A 398 692.
  • A is CH 2 -O- and
  • B is 3-pyrazolyl or 1 ,2,4-triazolyl, where B has attached to it one or two substituents selected from the group of halogen, methyl and trifluoromethyl and • phenyl and pyridyl, in particular 2-pyridyl, substituted by 1 to 3 radicals R b .
  • T is a carbon or a nitrogen atom
  • R a' is halogen, methyl and trifluoromethyl
  • y is zero, 1 or 2
  • R b is as defined for formula I
  • x is zero, 1 , 2, 3 or 4.
  • More preferred active ingredients are those of formula M':
  • the combination of pyraclostrobin and one of the compounds selected from the groups A) to M) is used.
  • the combination of kresoxim-methyl and one of the compounds selected from the groups A) to M) is used.
  • acylalanines such as benalaxyl, metalaxyl, ofurace, oxadixyl,
  • B) amine derivatives such as aldimorph, dodine, dodemorph, fenpropimorph, fenpropidin, guazatine, iminoctadine, spiroxamine, tridemorph
  • D) azoles such as bitertanol, bromoconazole, cyproconazole, difenoconazole, dinitroconazole, enilconazole, epoxiconazole, fenbuconazole, fluquinconazole, flusilazole, flutriafol, hexaconazole, imazalil, ipconazole, metconazole, myclobutanil, penconazole, propiconazole, prochloraz, prothioconazole, simeconazole, tebuconazole, tetraconazole, triadimefon, triadimenol, triflumizol, triticonazole, E) dicarboximides, such as iprodione, myclozolin, procymidone, vinclozolin, E) dicarboximides, such as iprodione, myclozolin, procymidone, vinclo
  • dithiocarbamates such as ferbam, nabam, maneb, mancozeb, metam, metiram, propineb, polycarbamate, thiram, ziram, zineb,
  • heterocyclic compounds such as anilazine, benomyl, boscalid, carbendazim, carboxin, oxycarboxin, cyazofamid, dazomet, dithianon, fenamidone, fenarimol, fuberidazole, flutolanil, furametpyr, isoprothiolane, mepronil, nuarimol, penthiopyrad, picobenzamid, probenazole, proquinazid, pyrifenox, pyroquilon, quinoxyfen, silthiofam, thiabendazole, thifluzamide, thiophanate-methyl, tiadinil, tricyclazole, triforine, 5-Chloro-7-(4-methyl-piperidin-1 -yl)-6-(2,4,6-trifluoro- phenyl)-[1 ,2,4]triazolo[1 ,5-a]pyrimidine, H) sulfur,
  • nitrophenyl derivatives such as binapacryl, dinocap, dinobuton, nitrophthal- isopropyl,
  • phenylpyrroles such as fenpiclonil or fludioxonil
  • K) other fungicides such as acibenzolar-S-methyl, benthiavalicarb, carpropamid, chlorothalonil, cyflufenamid, diclomezin, diclocymet, diethofencarb, edifenphos, ethaboxam, fenhexamid, fentin acetate, fenoxanil, ferimzone, fluazinam, phosphorous acid and its salts, fosetyl, fosetyl-aluminum, iprovalicarb, hexachlorobenzene, mandipropamid, metrafenone, pencycuron, propamocarb, phthalide, toloclofos-methyl, quintozene, zoxamid, acetyl salic acids, L) sulfenic acid derivatives, such as captafol, captan, dichlofluanid, folpet, tolylfluani
  • A) acylalanines especially benalaxyl, metalaxyl, ofurace, oxadixyl
  • B) amine derivatives especially dodine, fenpropimorph, tridemorph
  • D) azoles especially epoxiconazole, fluquinconazole, flutriafol, imazalil, metconazole, prochloraz, tebuconazole, triticonazole,
  • dithiocarbamates especially ferbam, nabam, maneb, mancozeb, metam, metiram, propineb, polycarbamate, thiram, ziram, zineb,
  • heterocyclic compounds especially anilazine, benomyl, boscalid, carbendazim, carboxin, oxycarboxin, cyazofamid, dithianon, flutolanil, thiabendazole, thiophanate-methyl, 5-chloro-7-(4-methyl-piperidin-1-yl)-6-(2,4,6-trifluoro-phenyl)-
  • [1 ,2,4]t ⁇ azolo[1 ,5-a]pyrimidine K) other fungicides, especially acibenzolar-S-methyl, benthiavalicarb, carpropamid, chlorothalonil, cyflufenamid, cymoxanil, ethaboxam, phosphorous acid and its salts, fosetyl, fosetyl-aluminum, metrafenone,
  • Also particularly useful is the combination of a compound of formula I with acibenzolar- S-methyl, or phosphorous acid, and its alkali- and earth alkali salts.
  • the combination of active ingredients 1) and 2) increase the tolerance of plants to bac- terioses. They are especially important for controlling bacteria on a variety of crop plants such as vegetables, top fruit species and tobacco, and all the seeds of these plants.
  • Pseudomonas species on tobacco, potatoes, tomatoes and pulses and, in particular, Erwinia species on fruit, vegetables and potatoes.
  • the compounds are applied by treating the soil or the seeds or plants to be protected against bacterial attack with an effective amount of the active ingredients.
  • Application can be effected both before and after infection of the plants or seeds by the bacteria.
  • the application of the compounds 1 ) and 2) preferably is made during the first six weeks, preferably four weeks of the growth period of the plants, long before first protec- tive application against fungi usually is made.
  • the plant is treated before infection takes place, preferably several weeks to one week before the expected bacteria attack. During such timeframe one to 10 applications are carried out. A markedly reduced susceptibility of the plant to bacterioses is observed.
  • the active ingredients are preferably applied shortly after germination of the plants, especially within the first four weeks after germination.
  • the first application is made before begin or within the first four weeks of the growth period. In all cases best efficacy is observed, when the application is repeated every 10 to 20 days.
  • the method according to the invention is preferably carried out as foliar application when applied to fruit and vegetables, such as potatoes, tomatoes, cucurbits, preferably cucumbers, melons, watermelons, garlic, onions, and lettuce.
  • fruit and vegetables such as potatoes, tomatoes, cucurbits, preferably cucumbers, melons, watermelons, garlic, onions, and lettuce.
  • more than two applications, and up to 10 applications during a season are carried out.
  • the method according to the invention is preferably carried out as foliar application when applied to fruits, such as apples, stone fruits, and citrus. Preferably more than two applications, and up to 5 applications during a season are carried out.
  • the method of the invention can also be applied to field crops, such as soybeans, corn, cotton, tobacco, common beans, wheat, barley, peas, and others.
  • field crops such as soybeans, corn, cotton, tobacco, common beans, wheat, barley, peas, and others.
  • the method is preferably applied by treating the seeds or the plants.
  • the plants are preferably treated with two to three applications.
  • the component 1 ) and the component 2) can be applied simultaneously, that is jointly or separately, or in succession, the sequence, in the case of separate application, generally not having any effect on the result of the control measures.
  • a further active com- pound 3) or two active compounds 3) and 4) are added to the components 1 ) and 2).
  • Suitable compounds 3) and 4) are selected from the compounds mentioned as component 2).
  • the ratio in which component 1 ) and the component 2) are applied depends from the specific compound 1) and compound 2), usually they are applied in a weight ratio of from 1000:1 to 1 :1000, preferable 100:1 to 1 :100, more preferably from 20:1 to 1 :20, in particular from 10: 1 to 1 : 10.
  • the components 3) and, if appropriate ⁇ ) are, if desired, added in a ratio of 20:1 to 1 :20 to the component 1 ).
  • a synergistically increased preventive effect against bacte- rioses is obseved.
  • the application rates of the mixtures according to the invention are from 5 g/ha to 2000 g/ha, preferably from 50 to 1000 g/ha, in particular from 50 to 750 g/ha.
  • the application rates for the component 1) are generally from 1 to 1000 g/ha, preferably from 10 to 900 g/ha, in particular from 20 to 750 g/ha.
  • the application rates for the component 2) are generally from 1 to 2000 g/ha, preferably from 10 to 1000 g/ha, in particular from 40 to 350 g/ha.
  • application rates of mixture are generally from 1 to 1000 g/100 kg of seed, preferably from 1 to 200 g/100 kg, in particular from 5 to 100 g/100 kg.
  • the application rates are between 0.01 and 2.0 kg, prefera- bly up to 1.0 kg of active ingredient per hectare, depending on the type of pathogen and the plant species.
  • amounts of from 0.001 to 0.1 g, preferably 0.01 to 0.05 g, of active ingredient are generally required per kilogram of seed.
  • the weight ratio in such case is preferably of from 1000:1 to 30:1 , preferably from 1000:1 to 50:1 , especially 500:1 to 100:1.
  • the application rate of diflufenzopyr is 50 mg to 10 g/ha, preferably from 100 mg to 2 g/ha.
  • diflufenzopyr For protecting dicotyledonous plants amounts of 50 mg to 5 g/ha, preferably 100 mg to 2 g/ha diflufenzopyr are used.
  • the mixtures according to the invention, or the components 1 ) and 2), can be converted into the customary formulations, for example solutions, emulsions, suspensions, dusts, powders, pastes and granules.
  • the use form depends on the particular intended purpose; in each case, it should ensure a fine and even distribution of the compound according to the invention.
  • the compounds 1) and 2) can be used as such, in the form of their formulations or the use forms prepared therefrom, for example in the form of directly sprayable solutions, powders, suspensions or dispersions, emulsions, oil dispersions, pastes, dustable products, materials for spreading, or granules, by means of spraying, atomizing, dusting, spreading or pouring.
  • the use forms depend entirely on the intended purposes; they are intended to ensure in each case the finest possible distribution of the active compound(s) according to the invention.
  • Aqueous use forms can be prepared from emulsion concentrates, pastes or wettable powders (sprayable powders, oil dispersions) by adding water.
  • emulsions, pastes or oil dispersions the substances, as such or dissolved in an oil or solvent, can be homogenized in water by means of a wetter, tackifier, dispersant or emulsifier.
  • concentrates composed of active substance, wetter, tackifier, dispersant or emulsifier and, if appropriate, solvent or oil and such concentrates are suitable for dilution with water.
  • the active compound concentrations in the ready-to-use preparations can be varied within relatively wide ranges. In general, they are from 0.0001 to 10%, preferably from 0.01 to 1 % per weight.
  • the active compound may also be used successfully in the ultra-low-volume process (ULV), it being possible to apply formulations comprising over 95% by weight of active compound, or even to apply the active compound without additives.
  • UUV ultra-low-volume process
  • the formulations are prepared in a known manner (see e.g. for review US 3,060,084, EP-A 707 445 (for liquid concentrates), Browning, "Agglomeration”, Chemical Engineering, Dec. 4, 1967, 147-48, Perry's Chemical Engineer's Handbook, 4th Ed., McGraw-Hill, New York, 1963, pages 8-57 and et seq.
  • auxiliaries suitable for the formulation of agrochemicals such as solvents and/or carriers, if desired emulsifiers, surfactants and dispersants, preservatives, anti- foaming agents, anti-freezing agents.
  • solvents examples include water, aromatic solvents (for example Solvesso products, xylene), paraffins (for example mineral oil fractions), alcohols (for example methanol, butanol, pentanol, benzyl alcohol), ketones (for example cyclohexanone, gamma-butyrolactone), pyrrolidones (NMP, NOP), acetates (glycol diacetate), glycols, fatty acid dimethylamides, fatty acids and fatty acid esters.
  • aromatic solvents for example Solvesso products, xylene
  • paraffins for example mineral oil fractions
  • alcohols for example methanol, butanol, pentanol, benzyl alcohol
  • ketones for example cyclohexanone, gamma-butyrolactone
  • NMP pyrrolidones
  • acetates glycols
  • fatty acid dimethylamides examples of fatty acids and fatty acid esters.
  • Suitable emulsifiers are nonionic and anionic emulsifiers (for example polyoxyethylene fatty alcohol ethers, alkylsulfonates and arylsulfonates).
  • dispersants examples include lignin-sulfite waste liquors and methylcellulose.
  • Suitable surfactants used are alkali metal, alkaline earth metal and ammonium salts of lignosulfonic acid, naphthalenesulfonic acid, phenolsulfonic acid, dibutylnaphthalene- sulfonic acid, alkylarylsulfonates, alkyl sulfates, alkylsulfonates, fatty alcohol sulfates, fatty acids and sulfated fatty alcohol glycol ethers, furthermore condensates of sulfonated naphthalene and naphthalene derivatives with formaldehyde, condensates of naphthalene or of naphthalenesulfonic acid with phenol and formaldehyde, polyoxyethylene octylphenol ether, ethoxylated isooctylphenol, octylphenol, nonylphenol, alkyl- phenol polyglycol ethers, tributylphen
  • Substances which are suitable for the preparation of directly sprayable solutions, emulsions, pastes or oil dispersions are mineral oil fractions of medium to high boiling point, such as kerosene or diesel oil, furthermore coal tar oils and oils of vegetable or animal origin, aliphatic, cyclic and aromatic hydrocarbons, for example toluene, xylene, paraffin, tetrahydronaphthalene, alkylated naphthalenes or their derivatives, methanol, etha- nol, propanol, butanol, cyclohexanol, cyclohexanone, isophorone, highly polar solvents, for example dimethyl sulfoxide, N-methylpyrrolidone or water.
  • mineral oil fractions of medium to high boiling point such as kerosene or diesel oil, furthermore coal tar oils and oils of vegetable or animal origin, aliphatic, cyclic and aromatic hydrocarbons, for example toluene, x
  • anti-freezing agents such as glycerin, ethylene glycol, propylene glycol and bactericides such as can be added to the formulation.
  • Suitable antifoaming agents are for example antifoaming agents based on silicon or magnesium stearate.
  • Suitable preservatives are for example dichlorophen und enzylalkoholhemiformal.
  • Seed Treatment formulations may additionally comprise binders and optionally colorants.
  • Binders can be added to improve the adhesion of the active materials on the seeds after treatment.
  • Suitable binders are block copolymers EO/PO surfactants but also po- lyvinylalcoholsl, polyvinylpyrrolidones, polyacrylates, polymethacrylates, polybutenes, polyisobutylenes, polystyrene, polyethyleneamines, polyethyleneamides, polyethyle- neimines (Lupasol®, Polymin®), polyethers, polyurethans, polyvinylacetate, tylose and copolymers derived from these polymers.
  • Powders, materials for spreading and dustable products can be prepared by mixing or concomitantly grinding the active substances with a solid carrier.
  • Granules for example coated granules, impregnated granules and homogeneous granules, can be prepared by binding the active compounds to solid carriers.
  • solid carriers examples include mineral earths such as silica gels, silicates, talc, kaolin, attaclay, limestone, lime, chalk, bole, loess, clay, dolomite, diatomaceous earth, calcium sulfate, magnesium sulfate, magnesium oxide, ground synthetic materials, fertilizers, such as, for example, ammonium sulfate, ammonium phosphate, ammonium nitrate, ureas, and products of vegetable origin, such as cereal meal, tree bark meal, wood meal and nutshell meal, cellulose powders and other solid carriers.
  • mineral earths such as silica gels, silicates, talc, kaolin, attaclay, limestone, lime, chalk, bole, loess, clay, dolomite, diatomaceous earth, calcium sulfate, magnesium sulfate, magnesium oxide, ground synthetic materials, fertilizers, such as, for example, ammonium sulfate, ammonium phosphate
  • the formulations comprise from 0.01 to 95% by weight, preferably from 0.1 to 90% by weight, of the active compound(s).
  • the active compound(s) are employed in a purity of from 90% to 100% by weight, preferably 95% to 100% by weight(according to NMR spectrum).
  • respective formulations can be diluted 2-10 fold leading to concentrations in the ready to use preparations of 0,01 to 60% by weight active compound by weight, preferably 0,1 to 40% by weight.
  • formulations 1. Products for dilution with water for foliar applications. For seed treatment purposes, such products may be applied to the seed diluted or undiluted.
  • DC Dispersible concentrates 20 parts by weight of the active compound(s) are dissolved in 70 parts by weight of cyclohexanone with addition of 10 parts by weight of a dispersant, for example polyvinylpyrrolidone. Dilution with water gives a dispersion, whereby a formulation with 20% (w/w) of active compound(s) is obtained.
  • a dispersant for example polyvinylpyrrolidone
  • Emulsions EW, EO, ES
  • 25 parts by weight of the active compound(s) are dissolved in 35 parts by weight of xylene with addition of calcium dodecylbenzenesulfonate and castor oil ethoxylate (in each case 5 parts by weight).
  • This mixture is introduced into 30 parts by weight of wa- ter by means of an emulsifier machine (e.g. Ultraturrax) and made into a homogeneous emulsion. Dilution with water gives an emulsion, whereby a formulation with 25% (w/w) of active compound(s) is obtained.
  • an emulsifier machine e.g. Ultraturrax
  • 50 parts by weight of the active compound(s) are ground finely with addition of 50 parts by weight of dispersants and wetters and made as water-dispersible or water-soluble granules by means of technical appliances (for example extrusion, spray tower, fluid- ized bed). Dilution with water gives a stable dispersion or solution of the active compound ⁇ ), whereby a formulation with 50% (w/w) of active compound(s) is obtained.
  • Dustable powders (DP, DS) 5 parts by weight of the active compound(s) are ground finely and mixed intimately with 95 parts by weight of finely divided kaolin. This gives a dustable product having 5% (w/w) of active compound(s)
  • Granules (GR, FG, GG, MG) 0.5 part by weight of the active compound(s) is ground finely and associated with 95.5 parts by weight of carriers, whereby a formulation with 0.5% (w/w) of active compound ⁇ ) is obtained.
  • Current methods are extrusion, spray-drying or the fluidized bed. This gives granules to be applied undiluted for foliar use.
  • Conventional seed treatment formulations include for example flowable concentrates FS, solutions LS, powders for dry treatment DS, water dispersible powders for slurry treatment WS, water-soluble powders SS and emulsion ES and EC and gel formulation GF. These formulation can be applied to the seed diluted or undiluted. Application to the seeds is carried out before sowing, either directly on the seeds.
  • a FS formulation is used for seed treatment.
  • a FS formulation may comprise 1-800 g/l of active ingredient, 1-200 g/l Surfactant, 0 to 200 g/l antifreezing agent, 0 to 400 g/l of binder, 0 to 200 g/l of a pigment and up to 1 liter of a solvent, preferably water.
  • Oils of various types, wetters, adjuvants, herbicides, fungicides, other pesticides, or bactericides may be added to the active compounds, even, if appropriate, not until immediately prior to use (tank mix). These agents are typically admixed with the compositions according to the invention in a weight ratio of from 1 :10 to 10:1.
  • the note mentioning the effect of the active ingredients 1) and 2) in inducing tolerance to bacteria may be present as a label on the packaging or in product data sheets.
  • the note may also be present in the case of preparations, which can be used in combination with the active ingredients 1) and 2).
  • the induction of tolerance may also constitute an indication which may be the subject of official approval of combinations of active ingredients 1) and 2).
  • Biological Examples
  • the efficacy (E) is calculated as follows using Abbot's formula:
  • ⁇ corresponds to the fungal infection of the treated plants in % and ⁇ corresponds to the fungal infection of the untreated (control) plants in %
  • An efficacy of 0 means that the infection level of the treated plants corresponds to that of the untreated control plants; an efficacy of 100 means that the treated plants were not infected.
  • the active compounds were applied as Cabrio Top® of BASF Aktiengesellschaft, which is a commercial formulation of Pyraclostrobin (5%) and Metiram (55%). The effect of metiram alone on bacteria is very close to zero. In this test the treatment with 1920 g/ha Cabrio Top® yielded 75% efficacy in preventing any damage from the leaves; the leaves of the untreated plants showed 20% infection.

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  • Life Sciences & Earth Sciences (AREA)
  • Dentistry (AREA)
  • Wood Science & Technology (AREA)
  • Plant Pathology (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Agronomy & Crop Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Pest Control & Pesticides (AREA)
  • Zoology (AREA)
  • Environmental Sciences (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Pretreatment Of Seeds And Plants (AREA)
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  • Plural Heterocyclic Compounds (AREA)

Abstract

A method of inducing tolerance of plants against bacterioses which comprises treating the plants, the soil or seeds with an effective amount of a combination of a compound of the formula (I) in which the variables have the meaning as set forth in the description, and a second active compound as defined in the description; which is taken up by the plants or seeds.

Description

Method of inducing tolerance of plants against bacterioses
Description
The present invention relates to a method of inducing tolerance of plants against bacterioses, which comprises treating the plants, the soil or the seeds with an effective amount of a compound of the formula I, 1 ) a compound of the formula I
Figure imgf000002_0001
in which
X is halogen, Ci-C4-alkyl or trifluoromethyl;
m is O or i ;
Q is C(=CH-CH3)-COOCH3, C(=CH-OCH3)-COOCH3, C(=N-OCH3)-
CONHCH3, C(=N- 3, or a group Q1
Figure imgf000002_0002
wherein # denotes the bond to the phenyl ring;
A is -O-B, -CH2O-B, -OCH2-B, -CH=CH-B, -C≡C-B, -CH2O-N=C(R1)-B, -CH2O-N=C(R1)-CH=CH-B, or -CH2O-N=C(R1)-C(R2)=N-OR3, where
B is phenyl, naphthyl, 5-or 6-membered hetaryl or 5-or 6-membered hetero- cyclyl, containing one to three N atoms and/or one O or S atom or one or two O and/or S atoms, the ring systems being unsubstituted or substituted by one to three radicals Ra:
Ra is cyano, nitro, amino, aminocarbonyl, aminothiocarbonyl, halogen, d-Ce-alkyl, Ci-C6-haloalkyl, Ci-C6-alkylcarbonyl, Ci-C6-alkylsulfonyl,
C 1 -Ce-a I ky I s u If i nyl , C3-C6-cycloalkyl, Ci-Cβ-alkoxy, Ci-Cβ-haloalkoxy, Ci-Cδ-alkyloxycarbonyl, Ci-Cβ-alkylthio, Ci-Cβ-alkylamino, di-Ci-Cβ- alkylamino, Ci-Cδ-alkylaminocarbonyl, di-Ci-Cδ-alkylamino-carbonyl, Ci-Cδ-alkylaminothiocarbonyl, di-Ci-Cδ-alkylaminothiocarbonyl, C2-Cδ- alkenyl, C2-C6-alkenyloxy, phenyl, phenoxy, benzyl, benzyloxy, 5- or
6-membered heterocyclyl, 5- or 6-membered hetaryl, 5- or 6- membered hetaryloxy, C(=NORa)-Rb or OC(Ra)2-C(Rb)=NORb, the cyclic radicals, in turn, being unsubstituted or substituted by one to three radicals Rb:
Rb is cyano, nitro, halogen, amino, aminocarbonyl, aminothio- carbonyl, Ci-Cδ-alkyl, Ci-Cβ-haloalkyl, Ci-Cδ-alkylsulfonyl, Ci- Ce-alkylsulfinyl, C3-C6-cycloalkyl, Ci-Cβ-alkoxy, Ci-Cδ-halo- alkoxy, Ci-Cδ-alkoxycarbonyl, Ci-Cβ-alkylthio, Ci-C6-alkylamino, di-Ci-C6-alkylamino, Ci-Ce-alkylaminocarbonyl, di-Ci-Cδ-alkyl- amino-carbonyl, d-Ce-alkylaminothiocarbonyl, di-Ci-Cδ-alkyl- aminothiocarbonyl, C2-C6-alkenyl, C2-C6-alkenyloxy, C3-C6- cycloalkyl, C3-C6-cycloalkenyl, phenyl, phenoxy, phenylthio, benzyl, benzyloxy, 5- or 6-membered heterocyclyl, 5- or 6- membered hetaryl, 5- or 6-membered hetaryloxy or C(=NORA)-RB;
RA, RB are hydrogen or Ci-C6-alkyl;
R1 is hydrogen, cyano, Ci-C4-alkyl, Ci-C4-haloalkyl, C3-C6-cycloalkyl, C1-C4- alkoxy;
R2 is phenyl, phenylcarbonyl, phenylsulfonyl, 5- or 6-membered hetaryl, 5- or 6-membered hetarylcarbonyl or 5- or 6-membered hetarylsulfonyl, the ring systems being unsubstituted or substituted by one to three radicals Ra,
Ci-Cio-alkyl, C3-C6-cycloalkyl, C2-Cio-alkenyl, C2-Cio-alkynyl, Ci-Cio-alkyl- carbonyl, C2-Cio-alkenylcarbonyl, Cs-Cio-alkynylcarbonyl, Ci-Cio-alkyl- sulfonyl, or C(=NORA)-RB, the hydrocarbon radicals of these groups being unsubstituted or substituted by one to three radicals Rc:
Rc is cyano, nitro, amino, aminocarbonyl, aminothiocarbonyl, halogen, d-Ce-alkyl, Ci-C6-haloalkyl, Ci-C6-alkylsulfonyl, Ci-C6-alkylsulfinyl, Ci-Cβ-alkoxy, Ci-Cβ-haloalkoxy, Ci-Cδ-alkoxycarbonyl, Ci-Cδ-alkyl- thio, Ci-Cβ-alkylamino, di-Ci-Cβ-alkylamino, Ci-Cδ-alkylamino- carbonyl, di-Ci-Cδ-alkylaminocarbonyl, Ci-Cδ-alkylaminothiocarbonyl, di-Ci-Cδ-alkylaminothiocarbonyl, C2-C6-alkenyl, C2-C6-alkenyloxy,
C3-C6-cycloalkyl, Cs-Cδ-cycloalkyloxy, 5- or 6-membered heterocyclyl, 5- or 6-membered heterocyclyloxy, benzyl, benzyloxy, phenyl, phenoxy, phenylthio, 5- or 6-membered hetaryl, 5- or 6- membered hetaryloxy and hetarylthio, it being possible for the cyclic groups, in turn, to be partially or fully halogenated or to have attached to them one to three radicals Ra; and
R3 is hydrogen, Ci-Cβ-alkyl, C2-C6-alkenyl, C2-C6-alkynyl, the hydrocarbon radicals of these groups being unsubstituted or substituted by one to three radicals Rc;
and
2) a compound selected from the groups A) to M):
A) acylalanines: benalaxyl, metalaxyl, ofurace, oxadixyl,
B) amine derivatives: aldimorph, dodine, dodemorph, fenpropimorph, fenpropidin, guazatine, iminoctadine, spiroxamine, tridemorph, C) anilinopyrimidines: pyrimethanil, mepanipyrim or cyprodinil,
D) azoles: bitertanol, bromoconazole, cyproconazole, difenoconazole, dinitroconazole, enilconazole, epoxiconazole, fenbuconazole, fluquinconazole, flusilazole, flutriafol, hexaconazole, imazalil, ipconazole, metconazole, myclobutanil, penconazole, propiconazole, prochloraz, prothioconazole, simeconazole, tebuconazole, tetraconazole, triadimefon, triadimenol, triflumizol, triticonazole,
E) dicarboximides: iprodione, myclozolin, procymidone, vinclozolin,
F) dithiocarbamates: ferbam, nabam, maneb, mancozeb, metam, metiram, propineb, polycarbamate, thiram, ziram, zineb, G) heterocyclic compounds: anilazine, benomyl, boscalid, carbendazim, car- boxin, oxycarboxin, cyazofamid, dazomet, dithianon, fenamidone, fenari- mol, fuberidazole, flutolanil, furametpyr, isoprothiolane, mepronil, nuarimol, penthiopyrad, picobenzamid, probenazole, proquinazid, pyrifenox, pyroqui- lon, quinoxyfen, silthiofam, thiabendazole, thifluzamide, thiophanate- methyl, tiadinil, tricyclazole, triforine, 5-chloro-7-(4-methyl-piperidin-1-yl)-6-
(2,4,6-trifluoro-phenyl)-[1 ,2,4]triazolo[1 ,5-a]pyrimidine, 4-difluoromethyl-2- methyl-thiazole-5-carboxylic acid-(4'-bromo-biphenyl-2-yl)-amide, 4- difluoromethyl^-methyl-thiazole-δ-carboxylic acid^'-trifluoromethyl- biphenyl-2-yl)-amide, 4-difluoromethyl-2-methyl-thiazole-5-carboxylic acid- (4'-chloro-3'-fluoro-biphenyl-2-yl)-amide, 3-difluoromethyl-1 -methyl- pyrazole-4-carboxylic acid-(3',4'-dichloro-4-fluoro-biphenyl-2-yl)-amide, 3- difluoromethyl-1-methyl-pyrazole-4-carboxylic acid-(3',4'-dichloro-5-fluoro- biphenyl-2-yl)-amide, 3-Difluoromethyl-1 -methyl-1 H-pyrazole-4-carboxylic acid (2',4'-difluorobiphenyl-2-yl)-amide, 3-Difluoromethyl-1 -methyl-1 H- pyrazole-4-carboxylic acid (2',4'-dichlorobiphenyl-2-yl)-amide, 3-
Difluoromethyl-1 -methyl-1 H-pyrazole-4-carboxylic acid (2',5'-difluoro- biphenyl-2-yl)-amide, 3-Difluoromethyl-1 -methyl-1 H-pyrazole-4-carboxylic acid (2',5'-dichlorobiphenyl-2-yl)-amide, 3-Difluoromethyl-1-methyl-1 H- pyrazole-4-carboxylic acid (3',5'-difluorobiphenyl-2-yl)-amide, 3- Difluoromethyl-1-methyl-1 H-pyrazole-4-carboxylic acid (3',5'- dichlorobiphenyl-2-yl)-amide, 3-Difluoromethyl-1 -methyl-1 H-pyrazole-4- carboxylic acid (3'-fluorobiphenyl-2-yl)-amide, 3-Difluoromethyl-1-methyl-
1 H-pyrazole-4-carboxylic acid (3'-chlorobiphenyl-2-yl)-amide, 3- Difluoromethyl-1 -methyl-1 H-pyrazole-4-carboxylic acid (2'-fluorobiphenyl-2- yl)-amide, 3-Difluoromethyl-1 -methyl-1 H-pyrazole-4-carboxylic acid (2'- chlorobiphenyl-2-yl)-amide, 3-Difluoromethyl-1 -methyl-1 H-pyrazole-4- carboxylic acid (3',4',5'-trifluorobiphenyl-2-yl)-amide, 3-Difluoromethyl-1- methyl-1 H-pyrazole-4-carboxylic acid (2',4',5'-trifluorobiphenyl-2-yl)-amide, 3-Difluoromethyl-1 -methyl-1 H-pyrazole-4-carboxylic acid [2-(1 ,1 ,2,3,3,3- hexafluoropropoxy)-phenyl]-amide, 3-Difluoromethyl-1 -methyl-1 H-pyrazole- 4-carboxylic acid [2-(1 ,1 ,2,2-tetrafluoroethoxy)-phenyl]-amide, 3- Difluoromethyl-1 -methyl-1 H-pyrazole-4-carboxylic acid (4'- trifluoromethylthiobiphenyl-2-yl)-amide, N-(2-Bicycloprop-2-ylphenyl)-3- difluoromethyl-1 -methyl-1 H-pyrazole-4-carboxamide, 3,4-dichloro- isothiazole-5-carboxylic acid (2-cyano-phenyl) amide, 3-[5-(4-chloro- phenyl)-2,3-dimethyl-isoxazolidin-3-yl]-pyridine, 2-Butoxy-6-iodo-3-propyl- chromen-4-one, 3-(3-bromo-6-fluoro-2-methyl-indole-1 -sulfonyl)-
[1 ,2,4]triazole-1 -sulfonic acid dimethylamide, (2-chloro-5-[1-(3-methyl-ben- zyloxyimino)-ethyl]-benzyl)-carbamic acid methyl ester, (2-chloro-5-[1-(6- methyl-pyridin-2-ylmethoxyimino)-ethyl]-benzyl)-carbamic acid methyl ester, H) sulfur, I) nitrophenyl derivatives: binapacryl, dinocap, dinobuton, nitrophthal- isopropyl,
J) phenylpyrroles: fenpiclonil or fludioxonil,
K) other fungicides selected from acibenzolar-S-methyl, benthiavalicarb, carpropamid, chlorothalonil, cyflufenamid, diclomezin, diclocymet, diethofencarb, edifenphos, ethaboxam, fenhexamid, fentin acetate, fenoxanil, ferimzone, fluazinam, phosphorous acid and its salts, fosetyl, fosetyl-aluminum, iprovalicarb, hexachlorobenzene, mandipropamid, metrafenone, pencycuron, propamocarb, phthalide, toloclofos-methyl, quintozene, zoxamid, acetyl salic acids, N-(2-(4-[3-(4-Chloro-phenyl)-prop- 2-ynyloxy]-3-methoxy-phenyl)-ethyl)-2-methanesulfonylamino-3-methyl- butyramide, N-(2-(4-[3-(4-Chloro-phenyl)-prop-2-ynyloxy]-3-methoxy- phenyl)-ethyl)-2-ethanesulfonylamino-3-methyl-butyramide, 3-(4-Chloro- phenyl)-3-(2-isopropoxy carbonylamino-3-methyl-butyrylamino)-propionic acid methyl ester, L) sulfenic acid derivatives: captafol, captan, dichlofluanid, folpet, tolylfluanid, and M) cinnamides and analogous compounds: dimethomorph, flumetover or flumorph,
which components 1) and 2) are taken up by the plants or seeds. In addition, the inven- tion generally relates to the use of the combinations of a compound of formula I and a compound of the group A) to M) for immunizing plants against bacterioses.
Bacteria are predominantly found in moderate and humid-warm climatic regions as pathogens of diseases (bacterioses) in a large number of crop plants. Occasionally, these diseases cause substantial economic damage. Examples which are generally known are the death of entire fruit plantations caused by a variety of Erwinia species ("fireblight" in pears and apples), and bacterial soft rot in potatoes and many other plants, various plant tumors triggered by agrobacteria, and the necroses on a variety of vegetables, on rice, wheat and citrus fruit, caused by Xanthomonas species. The bac- terioses caused by Pseudomonas species, in particular in vegetables, top fruit species and tobacco are especially dreaded.
As can be expected, conventional fungicides which engage in fungus-specific metabolic processes are not active against bacterioses. Thus, the only way of controlling them which has been possible to date was the use of antibiotics (for example Streptomycin, Blasticidin S or Kasugamicin), but this procedure is rarely practiced: the extensive use of antibiotics in agriculture is debated since, in principle, these antibiotics rely on the same mechanisms of action as are used against bacterial pathogens in human and veterinary medicine. They may thus favor the build-up of resistances. Moreover, antibiotics are expensive, owing to their molecular structures (most of which are complicated) and can only be produced by biotechnological methods. Therefore, it is an object of the invention to reduce the necessity to use antibiotics in agriculture.
An alternative way to prevent bacterial diseases in plants is taught in WO 03/075663: Strobilurine type fungicides have a stimulatory effect on the plants' intrinsic immune system against bacteria. However, this effect is not always fully satisfactory.
It is an object of the present invention to provide a highly effective method, which can be used broadly, which does not damage the plants and which brings about increased tolerance of the plants against phytobacterioses at a reduced total amount of active compounds applied.
We have found that this object is achieved by the method defined at the outset. The above-mentioned strobilurines of formula I are known as fungicides and, in some cases, also as insecticides (EP-A 178 826; EP-A 253 213; WO 93/15046; WO
95/18789; WO 95/21 153; WO 95/21 154; WO 95/24396; WO 96/01256; WO 97/15552). Prior does not teach a preventive effect of the compounds mentioned as component 2) above against bacteria, or that the known active compounds 2) might influence the plants' immune system against phytobacterioses, when applied in combination with strobilurins.
The active compounds according to the groups A) to M) mentioned above, their preparation and their action against harmful fungi are generally known in the art (cf.: http://www.hclrss.demon.co.uk/index.html; The Pecticide Manual, 10th Ed., BCPC, 1995);
4-Difluoromethyl-2-methyl-thiazole-5-carboxylic acid-(4'-bromo-biphenyl-2-yl)-amide, 4-Difluoromethyl-2-methyl-thiazole-5-carboxylic acid-(4'-trifluoromethyl-biphenyl-2-yl)- amide, 4-Difluoromethyl-2-methyl-thiazole-5-carboxylic acid-(4'-chloro-3'-fluoro-biphe- nyl-2-yl)-amide, 3-Difluoromethyl-1 -methyl-pyrazole-4-carboxylic acid-(3',4'-dichloro-4- fluoro-biphenyl-2-yl)-amide (WO 03/066610),
S^-Dichloro-isothiazole-δ-carboxylic acid (2-cyano-phenyl) amide (WO 99/24413), N-(2-(4-[3-(4-Chloro-phenyl)-prop-2-ynyloxy]-3-methoxy-phenyl)-ethyl)-2-methane- sulfonylamino-3-methyl-butyramide, N-(2-(4-[3-(4-Chloro-phenyl)-prop-2-ynyloxy]-3- methoxy-phenyl)-ethyl)-2-ethanesulfonylamino-3-methyl-butyramide (WO 04/049804), 3-[5-(4-Chloro-phenyl)-2,3-dimethyl-isoxazolidin-3-yl]-pyridine (EP-A 10 35 122), 2-Butoxy-6-iodo-3-propyl-chromen-4-one (WO 03/14103),
3-(3-Bromo-6-fluoro-2-methyl-indole-1 -sulfonyl)-[1 ,2,4]triazole-1 -sulfonic acid dimethyl- amide (EP-A 10 31 571 ), (2-Chloro-5-[1-(3-methyl-benzyloxyimino)-ethyl]-benzyl)-carbamic acid methyl ester, (2-Chloro-5-[1-(6-methyl-pyridin-2-ylmethoxyimino)-ethyl]-benzyl)-carbamic acid methyl ester (EP-A 12 01 648),
3-(4-Chloro-phenyl)-3-(2-isopropoxy carbonylamino-3-methyl-butyrylamino)-propionic acid methyl ester (EP-A 10 28 125), 3-Difluoromethyl-1-methyl-1 H-pyrazole-4-carboxylic acid (2',4'-difluorobiphenyl-2-yl)- amide, 3-Difluoromethyl-1-methyl-1 H-pyrazole-4-carboxylic acid (2',4'-dichlorobiphenyl- 2-yl)-amide (WO 2007/000462);
3-Difluoromethyl-1-methyl-1 H-pyrazole-4-carboxylic acid (2',5'-difluorobiphenyl-2-yl)- amide, 3-Difluoromethyl-1-methyl-1 H-pyrazole-4-carboxylic acid (2',5'-dichlorobiphenyl- 2-yl)-amide (WO 2007/003540); 3-Difluoromethyl-1-methyl-1 H-pyrazole-4-carboxylic acid (3',5'-difluorobiphenyl-2-yl)- amide, 3-Difluoromethyl-1-methyl-1 H-pyrazole-4-carboxylic acid (3',5'-dichlorobiphenyl- 2-yl)-amide (WO 2007/003564);
3-Difluoromethyl-1-methyl-1 H-pyrazole-4-carboxylic acid (3'-fluorobiphenyl-2-yl)-amide, 3-Difluoromethyl-1-methyl-1 H-pyrazole-4-carboxylic acid (3'-chlorobiphenyl-2-yl)-amide (WO 2007/003603); 3-Difluoromethyl-1-methyl-1 H-pyτazole-4-carboxylic acid (2'-fluorobiphenyl-2-yl)-amide, 3-Difluoromethyl-1-methyl-1 H-pyrazole-4-carboxylic acid (2'-chlorobiphenyl-2-yl)-amide (WO 2007/006806);
3-Difluoromethyl-1-methyl-1 H-pyrazole-4-carboxylic acid (3',4',5'-trifluorobiphenyl-2-yl)- amide, 3-Difluoromethyl-1-methyl-1 H-pyrazole-4-carboxylic acid (2',4',5'-trifluoro- biphenyl-2-yl)-amide (PCT/EP2006/064907);
3-Difluoromethyl-1-methyl-1 H-pyrazole-4-carboxylic acid [2-(1 ,1 , 2,3,3, 3-hexafluoro- propoxy)-phenyl]-amide, 3-Difluoromethyl-1-methyl-1 H-pyrazole-4-carboxylic acid [2- (1 ,1 ,2,2-tetrafluoroethoxy)-phenyl]-amide (PCT/EP2006/064988); 3-Difluoromethyl-1 -methyl-1 H-pyrazole-4-carboxylic acid (4'-trifluoromethylthiobiphenyl- 2-yl)-amide (EP Appln. 06123463.9);
N-(2-Bicycloprop-2-ylphenyl)-3-difluoromethyl-1 -methyl-1 H-pyrazole-4-carboxamide (WO 03/074491 ).
The publications cited above describe synthesis routes for the preparation of the active ingredients used in the method according to the invention.
The compounds identified by their common names are commercially available.
The good compatibility, with plants, of the active ingredients of the formula I at the concentrations required for controlling plant diseases permits the treatment of aerial plant parts and also the treatment of propagation material and seed, and of the soil.
In the method according to the invention, the active ingredients are taken up by the plant either through the leaf surface or through the roots and is distributed within the entire plant in the sap.
Thus, the protective action after carrying out the method according to the invention is not just found in those plant parts, which have been sprayed directly, but the tolerance to bacterial diseases of the entire plant is increased.
In a preferred embodiment of the method, the aerial plant parts are treated with a formulation or with a tank mix of the active ingredients 1 ) and 2).
Especially preferred for the method according to the invention are active ingredients with the following meanings of the substituents, in each case alone or in combination, the disclosure of the publications cited being hereby incorporated:
Especially preferred for the method according to the invention are, as component 1 , the active ingredients of the formulae Il to VIII, in which
V is OCH3 and NHCH3,
Y is CH and N and T and Z independently of one another are CH and N.
Preferred active ingredients of the formula I in which Q is N(-OCH3)-COOCH3 are the compounds described in the publications WO 93/15046 and WO 96/01256.
Preferred active ingredients of the formula I in which Q is C(=CH-OCH3)-COOCH3 are the compounds described in the publications EP-A 178 826 and EP-A 278 595.
Preferred active ingredients of the formula I in which Q is C(=N-OCH3)-COOCH3 are the compounds described in the publications EP-A 253 213 and EP-A 254 426.
Preferred active ingredients of the formula I in which Q is C(=N-OCH3)-CONHCH3 are the compounds described in the publications EP-A 398 692, EP-A 477 631 and EP-A 628 540.
Preferred active ingredients of the formula I in which Q is C(=CH-CH3)-COOCH3 are the compounds described in the publications EP-A 280 185 and EP-A 350 691.
Preferred active ingredients of the formula I in which Q is -CH2θ-N=C(R1)-B are the compounds described in the publications EP-A 460 575 and EP-A 463 488.
Preferred active ingredients of the formula I in which A is -O-B are the compounds described in the publications EP-A 382 375 and EP-A 398 692.
Preferred active ingredients of the formula I in which A is -CH2O-N=C(R1)-C(R2)=N-OR3 are the compounds described in the publications WO 95/18789, WO 95/21153, WO 95/21 154, WO 97/05103 and WO 97/06133.
Especially preferred are the active ingredients of the formula I in which Q is N(-OCH3)-COOCH3,
A is CH2-O- and
B is 3-pyrazolyl or 1 ,2,4-triazolyl, where B has attached to it one or two substituents selected from the group of halogen, methyl and trifluoromethyl and • phenyl and pyridyl, in particular 2-pyridyl, substituted by 1 to 3 radicals Rb.
These active ingredients are described by formula II,
Figure imgf000009_0001
in which T is a carbon or a nitrogen atom, Ra' is halogen, methyl and trifluoromethyl, y is zero, 1 or 2, Rb is as defined for formula I, x is zero, 1 , 2, 3 or 4.
More preferred active ingredients are those of formula M':
Figure imgf000010_0001
in which Rb is as defined for formula I.
With regard to their use, the compounds compiled in the tables, which follow, are especially preferred.
Table I
Figure imgf000010_0002
Figure imgf000010_0003
Table Il
Figure imgf000011_0001
Figure imgf000011_0003
Table
Figure imgf000011_0002
Figure imgf000011_0004
Table IV
Figure imgf000012_0001
Figure imgf000012_0003
Table V
Figure imgf000012_0002
Figure imgf000012_0004
Table Vl
Figure imgf000013_0001
Figure imgf000013_0003
Table VII
Figure imgf000013_0002
Figure imgf000013_0004
Particularly preferred are combinations of one of the following components 1 : Compound I-5 (pyraclostrobin), IM (kresoxim-methyl), II-3 (dimoxystrobin), 11-11 (ZJ 0712), III-3 (picoxystrobin), IV-6 (trifloxystrobin), IV-9 (enestroburin), V-16 (orysastrobin), VM (metominostrobin), VIM (azoxystrobin), and VII-11 (fluoxastrobin) with one of the compounds selected from the groups A) to M). In one embodiment of the invention the combination of pyraclostrobin and one of the compounds selected from the groups A) to M) is used.
In another embodiment of the invention the combination of kresoxim-methyl and one of the compounds selected from the groups A) to M) is used.
In another embodiment of the invention the combination of dimoxystrobin and one of the compounds selected from the groups A) to M) is used.
In another embodiment of the invention the combination of ZJ 0712 and one of the compounds selected from the groups A) to M) is used.
In another embodiment of the invention the combination of picoxystrobin and one of the compounds selected from the groups A) to M) is used.
In another embodiment of the invention the combination of trifloxystrobin and one of the compounds selected from the groups A) to M) is used.
In another embodiment of the invention the combination of enestroburin and one of the compounds selected from the groups A) to M) is used.
In another embodiment of the invention the combination of orysastrobin and one of the compounds selected from the groups A) to M) is used.
In another embodiment of the invention the combination of metominostrobin and one of the compounds selected from the groups A) to M) is used.
In another embodiment of the invention the combination of azoxystrobin and one of the compounds selected from the groups A) to M) is used.
In another embodiment of the invention the combination of fluoxastrobin and one of the compounds selected from the groups A) to M) is used.
In another embodiment of the invention the combination of one the compounds of for- mula I with one of the following compounds:
A) acylalanines, such as benalaxyl, metalaxyl, ofurace, oxadixyl,
B) amine derivatives, such as aldimorph, dodine, dodemorph, fenpropimorph, fenpropidin, guazatine, iminoctadine, spiroxamine, tridemorph, C) anilinopyrimidines, such as pyrimethanil, mepanipyrim or cyprodinil,
D) azoles, such as bitertanol, bromoconazole, cyproconazole, difenoconazole, dinitroconazole, enilconazole, epoxiconazole, fenbuconazole, fluquinconazole, flusilazole, flutriafol, hexaconazole, imazalil, ipconazole, metconazole, myclobutanil, penconazole, propiconazole, prochloraz, prothioconazole, simeconazole, tebuconazole, tetraconazole, triadimefon, triadimenol, triflumizol, triticonazole, E) dicarboximides, such as iprodione, myclozolin, procymidone, vinclozolin,
F) dithiocarbamates, such as ferbam, nabam, maneb, mancozeb, metam, metiram, propineb, polycarbamate, thiram, ziram, zineb,
G) heterocyclic compounds, such as anilazine, benomyl, boscalid, carbendazim, carboxin, oxycarboxin, cyazofamid, dazomet, dithianon, fenamidone, fenarimol, fuberidazole, flutolanil, furametpyr, isoprothiolane, mepronil, nuarimol, penthiopyrad, picobenzamid, probenazole, proquinazid, pyrifenox, pyroquilon, quinoxyfen, silthiofam, thiabendazole, thifluzamide, thiophanate-methyl, tiadinil, tricyclazole, triforine, 5-Chloro-7-(4-methyl-piperidin-1 -yl)-6-(2,4,6-trifluoro- phenyl)-[1 ,2,4]triazolo[1 ,5-a]pyrimidine, H) sulfur,
I) nitrophenyl derivatives, such as binapacryl, dinocap, dinobuton, nitrophthal- isopropyl,
J) phenylpyrroles, such as fenpiclonil or fludioxonil,
K) other fungicides, such as acibenzolar-S-methyl, benthiavalicarb, carpropamid, chlorothalonil, cyflufenamid, diclomezin, diclocymet, diethofencarb, edifenphos, ethaboxam, fenhexamid, fentin acetate, fenoxanil, ferimzone, fluazinam, phosphorous acid and its salts, fosetyl, fosetyl-aluminum, iprovalicarb, hexachlorobenzene, mandipropamid, metrafenone, pencycuron, propamocarb, phthalide, toloclofos-methyl, quintozene, zoxamid, acetyl salic acids, L) sulfenic acid derivatives, such as captafol, captan, dichlofluanid, folpet, tolylfluanid, and
M) cinnamides and analogous compounds, such as dimethomorph, flumetover or flumorph,
is used.
More preferably the method is carried out with a compound of formula I as defined above and a compound selected from the following groups:
A) acylalanines, especially benalaxyl, metalaxyl, ofurace, oxadixyl, B) amine derivatives, especially dodine, fenpropimorph, tridemorph, D) azoles, especially epoxiconazole, fluquinconazole, flutriafol, imazalil, metconazole, prochloraz, tebuconazole, triticonazole,
F) dithiocarbamates, especially ferbam, nabam, maneb, mancozeb, metam, metiram, propineb, polycarbamate, thiram, ziram, zineb,
G) heterocyclic compounds, especially anilazine, benomyl, boscalid, carbendazim, carboxin, oxycarboxin, cyazofamid, dithianon, flutolanil, thiabendazole, thiophanate-methyl, 5-chloro-7-(4-methyl-piperidin-1-yl)-6-(2,4,6-trifluoro-phenyl)-
[1 ,2,4]tιϊazolo[1 ,5-a]pyrimidine, K) other fungicides, especially acibenzolar-S-methyl, benthiavalicarb, carpropamid, chlorothalonil, cyflufenamid, cymoxanil, ethaboxam, phosphorous acid and its salts, fosetyl, fosetyl-aluminum, metrafenone,
L) sulfenic acid derivatives, especially folpet, and M) cinnamides and analogous compounds, especially dimethomorph.
Particular preference is given to combinations containing as component 2) one of the following compounds:
F) dithiocarbamates, especially mancozeb, metiram,
G) heterocyclic compounds, especially carbendazim, dithianon, thiophanate-methyl, K) other fungicides, especially acibenzolar-S-methyl, phosphorous acid and its salts.
In one embodiment of the invention the combination of a compound of formula I with dithiocarbamates, especially mancozeb, or metiram is used.
Furthermore particularly useful is the combination of a compound of formula I with het- erocyclic compounds, especially carbendazim, dithianon, or thiophanate-methyl.
Also particularly useful is the combination of a compound of formula I with acibenzolar- S-methyl, or phosphorous acid, and its alkali- and earth alkali salts.
The combination of active ingredients 1) and 2) increase the tolerance of plants to bac- terioses. They are especially important for controlling bacteria on a variety of crop plants such as vegetables, top fruit species and tobacco, and all the seeds of these plants.
Specifically, they are suitable for controlling the following plant diseases:
Pseudomonas species on tobacco, potatoes, tomatoes and pulses, and, in particular, Erwinia species on fruit, vegetables and potatoes.
The compounds are applied by treating the soil or the seeds or plants to be protected against bacterial attack with an effective amount of the active ingredients. Application can be effected both before and after infection of the plants or seeds by the bacteria.
The application of the compounds 1 ) and 2) preferably is made during the first six weeks, preferably four weeks of the growth period of the plants, long before first protec- tive application against fungi usually is made. The plant is treated before infection takes place, preferably several weeks to one week before the expected bacteria attack. During such timeframe one to 10 applications are carried out. A markedly reduced susceptibility of the plant to bacterioses is observed.
In case of vegetables and field crops the active ingredients are preferably applied shortly after germination of the plants, especially within the first four weeks after germination. In case of fruits and other perennial plants the first application is made before begin or within the first four weeks of the growth period. In all cases best efficacy is observed, when the application is repeated every 10 to 20 days.
The method according to the invention is preferably carried out as foliar application when applied to fruit and vegetables, such as potatoes, tomatoes, cucurbits, preferably cucumbers, melons, watermelons, garlic, onions, and lettuce. Preferably more than two applications, and up to 10 applications during a season are carried out.
The method according to the invention is preferably carried out as foliar application when applied to fruits, such as apples, stone fruits, and citrus. Preferably more than two applications, and up to 5 applications during a season are carried out.
The method of the invention can also be applied to field crops, such as soybeans, corn, cotton, tobacco, common beans, wheat, barley, peas, and others. In relation to these crops the method is preferably applied by treating the seeds or the plants. The plants are preferably treated with two to three applications.
The component 1 ) and the component 2) can be applied simultaneously, that is jointly or separately, or in succession, the sequence, in the case of separate application, generally not having any effect on the result of the control measures.
In one embodiment of the mixtures according to the invention, a further active com- pound 3) or two active compounds 3) and 4) are added to the components 1 ) and 2). Suitable compounds 3) and 4) are selected from the compounds mentioned as component 2).
Preference is given to mixtures of the components 1) and 2) and a component 3). Par- ticular preference is given to mixtures of the components 1) and 2).
The ratio in which component 1 ) and the component 2) are applied depends from the specific compound 1) and compound 2), usually they are applied in a weight ratio of from 1000:1 to 1 :1000, preferable 100:1 to 1 :100, more preferably from 20:1 to 1 :20, in particular from 10: 1 to 1 : 10.
The components 3) and, if appropriate^) are, if desired, added in a ratio of 20:1 to 1 :20 to the component 1 ).
In a preferred embodiment a synergistically increased preventive effect against bacte- rioses is obseved.
Depending on the type of compound and the desired effect, the application rates of the mixtures according to the invention are from 5 g/ha to 2000 g/ha, preferably from 50 to 1000 g/ha, in particular from 50 to 750 g/ha.
Correspondingly, the application rates for the component 1) are generally from 1 to 1000 g/ha, preferably from 10 to 900 g/ha, in particular from 20 to 750 g/ha.
Correspondingly, the application rates for the component 2) are generally from 1 to 2000 g/ha, preferably from 10 to 1000 g/ha, in particular from 40 to 350 g/ha.
In the treatment of seed, application rates of mixture are generally from 1 to 1000 g/100 kg of seed, preferably from 1 to 200 g/100 kg, in particular from 5 to 100 g/100 kg.
For use in crop protection, the application rates are between 0.01 and 2.0 kg, prefera- bly up to 1.0 kg of active ingredient per hectare, depending on the type of pathogen and the plant species.
In the treatment of seed, amounts of from 0.001 to 0.1 g, preferably 0.01 to 0.05 g, of active ingredient are generally required per kilogram of seed.
If diflufenzopyr is used as component 2) it is used in very low doses, the weight ratio in such case is preferably of from 1000:1 to 30:1 , preferably from 1000:1 to 50:1 , especially 500:1 to 100:1.
Depending on the type of plant to be protected, the application rate of diflufenzopyr is 50 mg to 10 g/ha, preferably from 100 mg to 2 g/ha.
For protecting monocotyledonous plants amounts of 100 mg to 10 g/ha, preferably between 100 mg and 5 g/ha diflufenzopyr are sufficient to enhance resistibility of the plants.
For protecting dicotyledonous plants amounts of 50 mg to 5 g/ha, preferably 100 mg to 2 g/ha diflufenzopyr are used.
The mixtures according to the invention, or the components 1 ) and 2), can be converted into the customary formulations, for example solutions, emulsions, suspensions, dusts, powders, pastes and granules. The use form depends on the particular intended purpose; in each case, it should ensure a fine and even distribution of the compound according to the invention.
Best results are obtained when a formulation is used which supports the transport of the active compounds into the plants, and the distribution within the entire plant in the sap. Such especially suitable formulations are, e. g. EC, DC, and SE.
The compounds 1) and 2) can be used as such, in the form of their formulations or the use forms prepared therefrom, for example in the form of directly sprayable solutions, powders, suspensions or dispersions, emulsions, oil dispersions, pastes, dustable products, materials for spreading, or granules, by means of spraying, atomizing, dusting, spreading or pouring. The use forms depend entirely on the intended purposes; they are intended to ensure in each case the finest possible distribution of the active compound(s) according to the invention.
Aqueous use forms can be prepared from emulsion concentrates, pastes or wettable powders (sprayable powders, oil dispersions) by adding water. To prepare emulsions, pastes or oil dispersions, the substances, as such or dissolved in an oil or solvent, can be homogenized in water by means of a wetter, tackifier, dispersant or emulsifier. However, it is also possible to prepare concentrates composed of active substance, wetter, tackifier, dispersant or emulsifier and, if appropriate, solvent or oil, and such concentrates are suitable for dilution with water.
The active compound concentrations in the ready-to-use preparations can be varied within relatively wide ranges. In general, they are from 0.0001 to 10%, preferably from 0.01 to 1 % per weight.
The active compound may also be used successfully in the ultra-low-volume process (ULV), it being possible to apply formulations comprising over 95% by weight of active compound, or even to apply the active compound without additives.
The formulations are prepared in a known manner (see e.g. for review US 3,060,084, EP-A 707 445 (for liquid concentrates), Browning, "Agglomeration", Chemical Engineering, Dec. 4, 1967, 147-48, Perry's Chemical Engineer's Handbook, 4th Ed., McGraw-Hill, New York, 1963, pages 8-57 and et seq. WO 91/13546, US 4,172,714, US 4,144,050, US 3,920,442, US 5,180,587, US 5,232,701 , US 5,208,030, GB 2,095,558, US 3,299,566, Klingman, Weed Control as a Science, John Wiley and Sons, Inc., New York, 1961 , Hance et al., Weed Control Handbook, 8th Ed., Blackwell Scientific Publications, Oxford, 1989 and Mollet, H., Grubemann, A., Formulation tech- nology, Wiley VCH Verlag GmbH, Weinheim (Germany), 2001 , 2. D. A. Knowles,
Chemistry and Technology of Agrochemical Formulations, Kluwer Academic Publishers, Dordrecht, 1998 (ISBN 0-7514-0443-8), for example by extending the active com- pound with auxiliaries suitable for the formulation of agrochemicals, such as solvents and/or carriers, if desired emulsifiers, surfactants and dispersants, preservatives, anti- foaming agents, anti-freezing agents.
Examples of suitable solvents are water, aromatic solvents (for example Solvesso products, xylene), paraffins (for example mineral oil fractions), alcohols (for example methanol, butanol, pentanol, benzyl alcohol), ketones (for example cyclohexanone, gamma-butyrolactone), pyrrolidones (NMP, NOP), acetates (glycol diacetate), glycols, fatty acid dimethylamides, fatty acids and fatty acid esters. In principle, solvent mix- tures may also be used.
Suitable emulsifiers are nonionic and anionic emulsifiers (for example polyoxyethylene fatty alcohol ethers, alkylsulfonates and arylsulfonates).
Examples of dispersants are lignin-sulfite waste liquors and methylcellulose.
Suitable surfactants used are alkali metal, alkaline earth metal and ammonium salts of lignosulfonic acid, naphthalenesulfonic acid, phenolsulfonic acid, dibutylnaphthalene- sulfonic acid, alkylarylsulfonates, alkyl sulfates, alkylsulfonates, fatty alcohol sulfates, fatty acids and sulfated fatty alcohol glycol ethers, furthermore condensates of sulfonated naphthalene and naphthalene derivatives with formaldehyde, condensates of naphthalene or of naphthalenesulfonic acid with phenol and formaldehyde, polyoxyethylene octylphenol ether, ethoxylated isooctylphenol, octylphenol, nonylphenol, alkyl- phenol polyglycol ethers, tributylphenyl polyglycol ether, tristearyl phenyl polyglycol ether, alkylaryl polyether alcohols, alcohol and fatty alcohol ethylene oxide condensates, ethoxylated castor oil, polyoxyethylene alkyl ethers, ethoxylated polyoxypropyl- ene, lauryl alcohol polyglycol ether acetal, sorbitol esters, lignosulfite waste liquors and methylcellulose.
Substances which are suitable for the preparation of directly sprayable solutions, emulsions, pastes or oil dispersions are mineral oil fractions of medium to high boiling point, such as kerosene or diesel oil, furthermore coal tar oils and oils of vegetable or animal origin, aliphatic, cyclic and aromatic hydrocarbons, for example toluene, xylene, paraffin, tetrahydronaphthalene, alkylated naphthalenes or their derivatives, methanol, etha- nol, propanol, butanol, cyclohexanol, cyclohexanone, isophorone, highly polar solvents, for example dimethyl sulfoxide, N-methylpyrrolidone or water.
Also anti-freezing agents such as glycerin, ethylene glycol, propylene glycol and bactericides such as can be added to the formulation.
Suitable antifoaming agents are for example antifoaming agents based on silicon or magnesium stearate. Suitable preservatives are for example dichlorophen und enzylalkoholhemiformal.
Seed Treatment formulations may additionally comprise binders and optionally colorants.
Binders can be added to improve the adhesion of the active materials on the seeds after treatment. Suitable binders are block copolymers EO/PO surfactants but also po- lyvinylalcoholsl, polyvinylpyrrolidones, polyacrylates, polymethacrylates, polybutenes, polyisobutylenes, polystyrene, polyethyleneamines, polyethyleneamides, polyethyle- neimines (Lupasol®, Polymin®), polyethers, polyurethans, polyvinylacetate, tylose and copolymers derived from these polymers.
Powders, materials for spreading and dustable products can be prepared by mixing or concomitantly grinding the active substances with a solid carrier.
Granules, for example coated granules, impregnated granules and homogeneous granules, can be prepared by binding the active compounds to solid carriers.
Examples of solid carriers are mineral earths such as silica gels, silicates, talc, kaolin, attaclay, limestone, lime, chalk, bole, loess, clay, dolomite, diatomaceous earth, calcium sulfate, magnesium sulfate, magnesium oxide, ground synthetic materials, fertilizers, such as, for example, ammonium sulfate, ammonium phosphate, ammonium nitrate, ureas, and products of vegetable origin, such as cereal meal, tree bark meal, wood meal and nutshell meal, cellulose powders and other solid carriers.
In general, the formulations comprise from 0.01 to 95% by weight, preferably from 0.1 to 90% by weight, of the active compound(s). In this case, the active compound(s) are employed in a purity of from 90% to 100% by weight, preferably 95% to 100% by weight(according to NMR spectrum).
For seed treatment purposes, respective formulations can be diluted 2-10 fold leading to concentrations in the ready to use preparations of 0,01 to 60% by weight active compound by weight, preferably 0,1 to 40% by weight.
The following are examples of formulations: 1. Products for dilution with water for foliar applications. For seed treatment purposes, such products may be applied to the seed diluted or undiluted.
A) Water-soluble concentrates (SL, LS) 10 parts by weight of the active compound(s) are dissolved in 90 parts by weight of water or a water-soluble solvent. As an alternative, wetters or other auxiliaries are added. The active compound(s) dissolves upon dilution with water, whereby a formulation with 10 % (w/w) of active compound(s) is obtained.
B) Dispersible concentrates (DC) 20 parts by weight of the active compound(s) are dissolved in 70 parts by weight of cyclohexanone with addition of 10 parts by weight of a dispersant, for example polyvinylpyrrolidone. Dilution with water gives a dispersion, whereby a formulation with 20% (w/w) of active compound(s) is obtained.
C) Emulsifiable concentrates (EC)
15 parts by weight of the active compound(s) are dissolved in 7 parts by weight of xylene with addition of calcium dodecylbenzenesulfonate and castor oil ethoxylate (in each case 5 parts by weight). Dilution with water gives an emulsion, whereby a formulation with 15% (w/w) of active compound(s) is obtained.
D) Emulsions (EW, EO, ES)
25 parts by weight of the active compound(s) are dissolved in 35 parts by weight of xylene with addition of calcium dodecylbenzenesulfonate and castor oil ethoxylate (in each case 5 parts by weight). This mixture is introduced into 30 parts by weight of wa- ter by means of an emulsifier machine (e.g. Ultraturrax) and made into a homogeneous emulsion. Dilution with water gives an emulsion, whereby a formulation with 25% (w/w) of active compound(s) is obtained.
E) Suspensions (SC, OD, FS) In an agitated ball mill, 20 parts by weight of the active compound(s) are comminuted with addition of 10 parts by weight of dispersants, wetters and 70 parts by weight of water or of an organic solvent to give a fine active compound(s) suspension. Dilution with water gives a stable suspension of the active compound(s), whereby a formulation with 20% (w/w) of active compound(s) is obtained.
F) Water-dispersible granules and water-soluble granules (WG, SG)
50 parts by weight of the active compound(s) are ground finely with addition of 50 parts by weight of dispersants and wetters and made as water-dispersible or water-soluble granules by means of technical appliances (for example extrusion, spray tower, fluid- ized bed). Dilution with water gives a stable dispersion or solution of the active compound^), whereby a formulation with 50% (w/w) of active compound(s) is obtained.
G) Water-dispersible powders and water-soluble powders (WP, SP, SS, WS)
75 parts by weight of the active compound(s) are ground in a rotor-stator mill with addi- tion of 25 parts by weight of dispersants, wetters and silica gel. Dilution with water gives a stable dispersion or solution of the active compound(s) , whereby a formulation with 75% (w/w) of active compound(s) is obtained. 2. Products to be applied undiluted for foliar applications. For seed treatment purposes, such products may be applied to the seed diluted
I) Dustable powders (DP, DS) 5 parts by weight of the active compound(s) are ground finely and mixed intimately with 95 parts by weight of finely divided kaolin. This gives a dustable product having 5% (w/w) of active compound(s)
J) Granules (GR, FG, GG, MG) 0.5 part by weight of the active compound(s) is ground finely and associated with 95.5 parts by weight of carriers, whereby a formulation with 0.5% (w/w) of active compound^) is obtained. Current methods are extrusion, spray-drying or the fluidized bed. This gives granules to be applied undiluted for foliar use.
K) ULV solutions (UL)
10 parts by weight of the active compound(s) are dissolved in 90 parts by weight of an organic solvent, for example xylene. This gives a product having 10% (w/w) of active compound(s), which is applied undiluted for foliar use.
Conventional seed treatment formulations include for example flowable concentrates FS, solutions LS, powders for dry treatment DS, water dispersible powders for slurry treatment WS, water-soluble powders SS and emulsion ES and EC and gel formulation GF. These formulation can be applied to the seed diluted or undiluted. Application to the seeds is carried out before sowing, either directly on the seeds.
In a preferred embodiment a FS formulation is used for seed treatment. Typcially, a FS formulation may comprise 1-800 g/l of active ingredient, 1-200 g/l Surfactant, 0 to 200 g/l antifreezing agent, 0 to 400 g/l of binder, 0 to 200 g/l of a pigment and up to 1 liter of a solvent, preferably water.
Oils of various types, wetters, adjuvants, herbicides, fungicides, other pesticides, or bactericides may be added to the active compounds, even, if appropriate, not until immediately prior to use (tank mix). These agents are typically admixed with the compositions according to the invention in a weight ratio of from 1 :10 to 10:1.
The note mentioning the effect of the active ingredients 1) and 2) in inducing tolerance to bacteria may be present as a label on the packaging or in product data sheets. The note may also be present in the case of preparations, which can be used in combination with the active ingredients 1) and 2).
The induction of tolerance may also constitute an indication which may be the subject of official approval of combinations of active ingredients 1) and 2). Biological Examples
Preventive action on tomatoes against Xathomonas ssp.
The trial was conducted under field conditions. Tomato plants of variety Carmen at a height of app. 10 cm were planted and grown under standard conditions with adequate supply of water and nutrients. After 18 days a first application of active compounds was made, which was repeated five times every 5 to 8 days. No other compounds were applied for pathogen control. Infection with pathogens occurred naturally. Each treat- ment consisted of four parallels in a randomized block design. The disease incidences were evaluated 46 days after the first application (Xathomonas ssp.). The dosages used and the obtained results are shown below:
The visually determined percentages of infected leaf areas were converted into effica- cies in % of the untreated control:
The efficacy (E) is calculated as follows using Abbot's formula:
E = (1 - α/β) - 100
α corresponds to the fungal infection of the treated plants in % and β corresponds to the fungal infection of the untreated (control) plants in %
An efficacy of 0 means that the infection level of the treated plants corresponds to that of the untreated control plants; an efficacy of 100 means that the treated plants were not infected.
The expected efficacies of mixtures of active compounds were determined using Colby's formula (Colby, S. R. "Calculating synergistic and antagonistic responses of herbicide combinations", Weeds, j_5, 20-22, 1967) and compared with the observed efficacies.
Colby's formula:
E = x + y - x-y/100
E expected efficacy, expressed in % of the untreated control, when using the mixture of the active compounds A and B at the concentrations a and b x efficacy, expressed in % of the untreated control, when using the active compound A at the concentration a y efficacy, expressed in % of the untreated control, when using the active compound B at the concentration b The active compounds were applied as Cabrio Top® of BASF Aktiengesellschaft, which is a commercial formulation of Pyraclostrobin (5%) and Metiram (55%). The effect of metiram alone on bacteria is very close to zero. In this test the treatment with 1920 g/ha Cabrio Top® yielded 75% efficacy in preventing any damage from the leaves; the leaves of the untreated plants showed 20% infection.

Claims

Claims:
1. A method of inducing tolerance against bacterioses of plants which comprises treating the plants, the soil or seeds with an effective amount of a combination of
1 ) a compound of the formula I
Figure imgf000026_0001
in which
X is halogen, Ci-C4-alkyl or trifluoromethyl;
m is O or i ;
Q is C(=CH-CH3)-COOCH3, C(=CH-OCH3)-COOCH3, C(=N-OCH3)-CONHCH3, C(=N-OCH3)-COOCH3 ,
N(-OCH3)-CO
Figure imgf000026_0002
wherein # denotes the bond to the phenyl ring;
A is -O-B, -CH2O-B, -OCH2-B, -CH=CH-B, -C≡C-B, -CH2O-N=C(R1)-B,
-CH2O-N=C(R1)-CH=CH-B, or -CH2O-N=C(R1)-C(R2)=N-OR3, where
B is phenyl, naphthyl, 5-membered or 6-membered hetaryl or 5- membered or 6-membered heterocyclyl, containing one to three N atoms and/or one O or S atom or one or two O and/or S atoms, the ring systems being unsubstituted or substituted by one to three radicals Ra:
Ra is cyano, nitro, amino, aminocarbonyl, aminothiocarbonyl, halo- gen, Ci-C6-alkyl, Ci-C6-haloalkyl, Ci-C6-alkylcarbonyl, Ci-C6-al- kylsulfonyl, Ci-Ce-alkylsulfinyl, C3-C6-cycloalkyl, Ci-Cβ-alkoxy, Ci-Cβ-haloalkoxy, Ci-Cδ-alkyloxycarbonyl, Ci-Cβ-alkylthio, Ci- Cδ-alkylamino, di-Ci-Cβ-alkylamino, Ci-Cδ-alkylaminocarbonyl, di-Ci-Cδ-alkylaminocarbonyl, Ci-Cδ-alkylaminothiocarbonyl, di- Ci-Cδ-alkylaminothiocarbonyl, C2-C6-alkenyl, C2-C6-alkenyloxy, phenyl, phenoxy, benzyl, benzyloxy, 5- or 6-membered hetero- cyclyl, 5- or 6-membered hetaryl, 5- or 6-membered hetaryl- oxy, C(=NORa)-Rb or OC(Ra)2-C(Rb)=NORb, the cyclic radicals, in turn, being unsubstituted or substituted by one to three radicals Rb:
Rb is cyano, nitro, halogen, amino, aminocarbonyl, aminothio- carbonyl, Ci-Cδ-alkyl, Ci-Cβ-haloalkyl, Ci-Cδ-alkylsulfonyl, Ci- Ce-alkylsulfinyl, C3-C6-cycloalkyl, Ci-Cβ-alkoxy, Ci-Cδ-halo- alkoxy, Ci-Cδ-alkoxycarbonyl, C-i-Cδ-alkylthio, Ci-C6-alkylamino, di-Ci-C6-alkylamino, Ci-Ce-alkylaminocarbonyl, di-Ci-Cδ-alkyl- aminocarbonyl, d-Ce-alkylaminothiocarbonyl, di-Ci-Cδ-alkyl- aminothiocarbonyl, C2-C6-alkenyl, C2-C6-alkenyloxy, C3-C6- cycloalkyl, C3-C6-cycloalkenyl, phenyl, phenoxy, phenylthio, benzyl, benzyloxy, 5- or 6-membered heterocyclyl, 5- or 6- membered hetaryl, 5- or 6-membered hetaryloxy or
C(=NORA)-RB;
RA, RB are hydrogen or Ci-C6-alkyl;
R1 is hydrogen, cyano, Ci-C4-alkyl, Ci-C4-haloalkyl, C3-C6-cycloalkyl, Ci-
C4-alkoxy;
R2 is phenyl, phenylcarbonyl, phenylsulfonyl, 5- or 6-membered hetaryl,
5- or 6-membered hetarylcarbonyl or 5- or 6-membered hetaryl- sulfonyl, the ring systems being unsubstituted or substituted by one to three radicals Ra,
Ci-Cio-alkyl, C3-C6-cycloalkyl, C2-Cio-alkenyl, C2-Cio-alkynyl, C1-C10- alkylcarbonyl, C2-Cio-alkenylcarbonyl, Cs-Cio-alkynylcarbonyl, C1-C10- alkylsulfonyl, or C(=NORa)-Rb, the hydrocarbon radicals of these groups being unsubstituted or substituted by one to three radicals Rc:
Rc is cyano, nitro, amino, aminocarbonyl, aminothiocarbonyl, halogen, d-Ce-alkyl, Ci-C6-haloalkyl, Ci-C6-alkylsulfonyl, CrC6- alkylsulfinyl, Ci-Cβ-alkoxy, Ci-Cβ-haloalkoxy, Ci-Cδ-alkoxy- carbonyl, Ci-Cβ-alkylthio, Ci-Cβ-alkylamino, di-Ci-Cδ-alkyl- amino, Ci-Cδ-alkylaminocarbonyl, di-Ci-Cδ-alkylaminocarbonyl, Ci-Cδ-alkylaminothiocarbonyl, di-Ci-Cδ-alkylaminothiocarbonyl, C2-C6-alkenyl, C2-C6-alkenyloxy,
C3-C6-cycloalkyl, C3-C6-cycloalkyloxy, 5- or 6-membered heterocyclyl, 5- or 6-membered heterocyclyloxy, benzyl, benzyloxy, phenyl, phenoxy, phenylthio, 5- or 6-membered hetaryl, 5- or 6-membered hetaryloxy and hetarylthio, it being possible for the cyclic groups, in turn, to be partially or fully halogenated or to have attached to them one to three radicals Ra; and
R3 is hydrogen, Ci-Cβ-alkyl, C2-C6-alkenyl, C2-C6-alkynyl, the hydrocarbon radicals of these groups being unsubstituted or substituted by one to three radicals Rc;
and
2) a compound selected from the groups A) to M):
A) acylalanines: benalaxyl, metalaxyl, ofurace, oxadixyl,
B) amine derivatives: aldimorph, dodine, dodemorph, fenpropimorph, fenpropidin, guazatine, iminoctadine, spiroxamine, tridemorph,
C) anilinopyrimidines: pyrimethanil, mepanipyrim or cyprodinil,
D) azoles: bitertanol, bromoconazole, cyproconazole, difenoconazole, dinitroconazole, enilconazole, epoxiconazole, fenbuconazole, fluquinconazole, flusilazole, flutriafol, hexaconazole, imazalil, ipconazole, metconazole, myclobutanil, penconazole, propiconazole, prochloraz, prothioconazole, simeconazole, tebuconazole, tetraconazole, triadimefon, triadimenol, triflumizol, triticonazole, E) dicarboximides: iprodione, myclozolin, procymidone, vinclozolin,
F) dithiocarbamates: ferbam, nabam, maneb, mancozeb, metam, metiram, propineb, polycarbamate, thiram, ziram, zineb,
G) heterocyclic compounds: anilazine, benomyl, boscalid, carbendazim, carboxin, oxycarboxin, cyazofamid, dazomet, dithianon, fenamidone, fenarimol, fuberidazole, flutolanil, furametpyr, isoprothiolane, mepro- nil, nuarimol, picobenzamid, probenazole, proquinazid, pyrifenox, pyroquilon, quinoxyfen, silthiofam, thiabendazole, thifluzamide, thio- phanate-methyl, tiadinil, tricyclazole, triforine, 5-chloro-7-(4-methyl- piperidin-1 -yl)-6-(2,4,6-trifluoro-phenyl)-[1 ,2,4]triazolo[1 ,5- a]pyrimidine, 4-difluoromethyl-2-methyl-thiazole-5-carboxylic acid-(4'- bromo-biphenyl-2-yl)-amide, 4-difluoromethyl-2-methyl-thiazole-5-car- boxylic acid-(4'-trifluoromethyl-biphenyl-2-yl)-amide, 4-difluoromethyl- 2-methyl-thiazole-5-carboxylic acid-(4'-chloro-3'-fluoro-biphenyl-2-yl)- amide, 3-difluoromethyl-1 -methyl-pyrazole-4-carboxylic acid-(3',4'- dichloro-4-fluoro-biphenyl-2-yl)-amide, 3-difluoromethyl-1 -methyl- pyrazole-4-carboxylic acid-(3',4'-dichloro-5-fluoro-biphenyl-2-yl)- amide, 3-Difluoromethyl-1-methyl-1 H-pyrazole-4-carboxylic acid (2',4'-difluorobiphenyl-2-yl)-amide, 3-Difluoromethyl-1 -methyl-1 H- pyrazole-4-carboxylic acid (2',4'-dichlorobiphenyl-2-yl)-amide, 3- Difluoromethyl-1 -methyl-1 H-pyrazole-4-carboxylic acid (2',5'-difluoro- biphenyl-2-yl)-amide, 3-Difluoromethyl-1 -methyl-1 H-pyrazole-4- carboxylic acid (2',5'-dichlorobiphenyl-2-yl)-amide, 3-Difluoromethyl-1- methyl-1 H-pyrazole-4-carboxylic acid (3',5'-difluorobiphenyl-2-yl)- amide, 3-Difluoromethyl-1 -methyl-1 H-pyrazole-4-carboxylic acid (3',5'-dichlorobiphenyl-2-yl)-amide, 3-Difluoromethyl-1 -methyl-1 H- pyrazole-4-carboxylic acid (3'-fluorobiphenyl-2-yl)-amide, 3- Difluoromethyl-1 -methyl-1 H-pyrazole-4-carboxylic acid (3'- chlorobiphenyl-2-yl)-amide, 3-Difluoromethyl-1 -methyl-1 H-pyrazole-4- carboxylic acid (2'-fluorobiphenyl-2-yl)-amide, 3-Difluoromethyl-1- methyl-1 H-pyrazole-4-carboxylic acid (2'-chlorobiphenyl-2-yl)-amide, 3-Difluoromethyl-1 -methyl-1 H-pyrazole-4-carboxylic acid (3',4',5'- trifluorobiphenyl-2-yl)-amide, 3-Difluoromethyl-1 -methyl-1 H-pyrazole-
4-carboxylic acid (2',4',5'-trifluorobiphenyl-2-yl)-amide, 3- Difluoromethyl-1 -methyl-1 H-pyrazole-4-carboxylic acid [2-(1 ,1 ,2,3,3,3- hexafluoropropoxy)-phenyl]-amide, 3-Difluoromethyl-1 -methyl-1 H- pyrazole-4-carboxylic acid [2-(1 ,1 ,2,2-tetrafluoroethoxy)-phenyl]- amide, 3-Difluoromethyl-1 -methyl-1 H-pyrazole-4-carboxylic acid (4'- trifluoromethylthiobiphenyl-2-yl)-amide, N-(2-Bicycloprop-2-ylphenyl)- 3-difluoromethyl-1 -methyl-1 H-pyrazole-4-carboxamide, 3,4-dichloro- isothiazole-5-carboxylic acid (2-cyano-phenyl) amide, 3-[5-(4-chloro- phenyl)-2,3-dimethyl-isoxazolidin-3-yl]-pyridine, 2-Butoxy-6-iodo-3- propyl-chromen-4-one, 3-(3-bromo-6-fluoro-2-methyl-indole-1- sulfonyl)-[1 ,2,4]triazole-1 -sulfonic acid dimethylamide, (2-chloro-5-[1- (3-methyl-benzyloxyimino)-ethyl]-benzyl)-carbamic acid methyl ester, (2-chloro-5-[1-(6-methyl-pyridin-2-ylmethoxyimino)-ethyl]-benzyl)- carbamic acid methyl ester, H) sulfur,
I) nitrophenyl derivatives: binapacryl, dinocap, dinobuton, nitrophthal- isopropyl,
J) phenylpyrroles: fenpiclonil or fludioxonil, K) other fungicides: acibenzolar-S-methyl, benthiavalicarb, carpropamid, chlorothalonil, cyflufenamid, diclomezin, diclocymet, diethofencarb, edifenphos, ethaboxam, fenhexamid, fentin acetate, fenoxanil, ferimzone, fluazinam, phosphorous acid and its salts, fosetyl, fosetyl- aluminum, iprovalicarb, hexachlorobenzene, metrafenone, pencycuron, penthiopyrad, propamocarb, phthalide, toloclofos-methyl, quintozene, zoxamid, acetyl salic acids, N-(2-(4-[3-(4-Chloro-phenyl)- prop-2-ynyloxy]-3-methoxy-phenyl)-ethyl)-2-methanesulfonylamino-3- methyl-butyramide, N-(2-(4-[3-(4-Chloro-phenyl)-prop-2-ynyloxy]-3- methoxy-phenyl)-ethyl)-2-ethanesulfonylamino-3-methyl-butyramide,
3-(4-Chloro-phenyl)-3-(2-isopropoxy carbonylamino-3-methyl-butyr- ylamino)-propionic acid methyl ester,
L) sulfenic acid derivatives: captafol, captan, dichlofluanid, folpet, tolylfluanid, and
M) cinnamides and analogous compounds: dimethomorph, flumetover or flumorph,
which active compounds 1 ) and 2) are taken up by the plants or seeds.
2. A method as claimed in claim 1 , wherein component 1) is selected from: pyraclostrobin, kresoxim-methyl, dimoxystrobin, 2-(ortho-((2,5-Dimethylphenyl- oxymethylene)phenyl)-3-methoxy-acrylic acid methyl ester, picoxystrobin, trifloxy- strobin, enestroburin, orysastrobin, metominostrobin, azoxystrobin, and fluoxa- strobin.
3. A method as claimed in claim 1 , wherein component 1 ) is pyraclostrobin.
4. A method as claimed in any one of claims 1 , 2 or 3, wherein component 2) is se- lected from benalaxyl, metalaxyl, ofurace, and oxadixyl.
5. A method as claimed in any one of claims 1 , 2 or 3, wherein component 2) is selected from dodine, fenpropimorph, and tridemorph.
6. A method as claimed in any one of claims 1 , 2 or 3, wherein component 2) is selected from epoxiconazole, fluquinconazole, flutriafol, metconazole, prochloraz, tebuconazole, and triticonazole.
7. A method as claimed in any one of claims 1 , 2 or 3, wherein component 2) is se- lected from ferbam, nabam, maneb, mancozeb, metam, metiram, propineb, poly- carbamate, thiram, ziram, and zineb.
8. A method as claimed in any one of claims 1 , 2 or 3, wherein heterocyclic compounds of group G) in component 2) are selected from anilazine, benomyl, boscalid, carbendazim, carboxin, oxycarboxin, cyazofamid, dazomet, dithianon, fenamidone, fenarimol, fuberidazole, flutolanil, furametpyr, isoprothiolane, me- pronil, nuarimol, picobenzamid, probenazole, proquinazid, pyrifenox, pyroquilon, quinoxyfen, silthiofam, thiabendazole, thifluzamide, thiophanate-methyl, tiadinil, tricyclazole, triforine, 5-Chloro-7-(4-methyl-piperidin-1 -yl)-6-(2,4,6-trifluoro- phenyl)-[1 ,2,4]triazolo[1 ,5-a]pyrimidine, 4-Difluoromethyl-2-methyl-thiazole-5- carboxylic acid-(4'-bromo-biphenyl-2-yl)-amide, 4-Difluoromethyl-2-methyl- thiazole-5-carboxylic acid-(4'-trifluoromethyl-biphenyl-2-yl)-amide, 4-Difluoro- methyl^-methyl-thiazole-δ-carboxylic acid-(4'-chloro-3'-fluoro-biphenyl-2-yl)- amide, 3-Difluoromethyl-1 -methyl-pyrazole-4-carboxylic acid-(3',4'-dichloro-4-flu- oro-biphenyl-2-yl)-amide, S^-Dichloro-isothiazole-δ-carboxylic acid (2-cyano- phenyl) amide, 3-[5-(4-Chloro-phenyl)-2,3-dimethyl-isoxazolidin-3-yl]-pyridine, 2- Butoxy-δ-iodo-S-propyl-chromen^-one, 3-(3-Bromo-6-fluoro-2-methyl-indole-1 - sulfonyl)-[1 ,2,4]triazole-1 -sulfonic acid dimethylamide, (2-Chloro-5-[1-(3-methyl- benzyloxyiminoj-ethyll-benzylj-carbamic acid methyl ester, (2-Chloro-5-[1-(6- methyl-pyridin-2-ylmethoxyimino)-ethyl]-benzyl)-carbamic acid methyl ester.
9. A method as claimed in any one of claims 1 , 2, 3 or 8 wherein component 2) is selected from anilazine, benomyl, boscalid, carbendazim, carboxin, oxycarboxin, cyazofamid, dithianon, flutolanil, thiabendazole, thiophanate-methyl, and 5- chloro-7-(4-methyl-piperidin-1 -yl)-6-(2,4,6-trifluoro-phenyl)-[1 ,2,4]triazolo[1 ,5- a]pyrimidine.
10. A method as claimed in any one of claims 1 , 2 or 3, wherein component 2) is selected from boscalid, 3-Difluoromethyl-1 -methyl-pyrazole-4-carboxylic acid-(3',4'- dichloro-4-fluoro-biphenyl-2-yl)-amide, 3-Difluoromethyl-1-methyl-pyrazole-4- carboxylic acid-(3',4'-dichloro-5-fluoro-biphenyl-2-yl)-amide, 3-Difluoromethyl-1 - methyl-1 H-pyrazole-4-carboxylic acid (2',4'-difluorobiphenyl-2-yl)-amide, 3-Di- fluoromethyl-1-methyl-1 H-pyrazole-4-carboxylic acid (2',4'-dichlorobiphenyl-2-yl)- amide, 3-Difluoromethyl-1 -methyl-1 H-pyrazole-4-carboxylic acid (2',5'-difluoro- biphenyl-2-yl)-amide, 3-Difluoromethyl-1 -methyl-1 H-pyrazole-4-carboxylic acid (2',5'-dichlorobiphenyl-2-yl)-amide, 3-Difluoromethyl-1 -methyl-1 H-pyrazole-4- carboxylic acid (3',5'-difluorobiphenyl-2-yl)-amide, 3-Difluoromethyl-1 -methyl-1 H- pyrazole-4-carboxylic acid (3',5'-dichlorobiphenyl-2-yl)-amide, 3-Difluoromethyl-1- methyl-1 H-pyrazole-4-carboxylic acid (3'-fluorobiphenyl-2-yl)-amide, 3-Difluoro- methyl-1 -methyl-1 H-pyrazole-4-carboxylic acid (3'-chlorobiphenyl-2-yl)-amide, 3- Difluoromethyl-1 -methyl-1 H-pyrazole-4-carboxylic acid (2'-fluorobiphenyl-2-yl)- amide, 3-Difluoromethyl-1 -methyl-1 H-pyrazole-4-carboxylic acid (2'- chlorobiphenyl-2-yl)-amide, 3-Difluoromethyl-1 -methyl-1 H-pyrazole-4-carboxylic acid (3',4',5'-trifluorobiphenyl-2-yl)-amide, 3-Difluoromethyl-1 -methyl-1 H-pyrazole- 4-carboxylic acid (2',4',5'-trifluorobiphenyl-2-yl)-amide, 3-Difluoromethyl-1-methyl- 1 H-pyrazole-4-carboxylic acid [2-(1 ,1 ,2,3,3,3-hexafluoropropoxy)-phenyl]-amide, 3-Difluoromethyl-1 -methyl-1 H-pyrazole-4-carboxylic acid [2-(1 , 1 ,2,2- tetrafluoroethoxy)-phenyl]-amide, 3-Difluoromethyl-1 -methyl-1 H-pyrazole-4- carboxylic acid (4'-trifluoromethylthiobiphenyl-2-yl)-amide, N-(2-Bicycloprop-2-yl- phenyl)-3-difluoromethyl-1 -methyl-1 H-pyrazole-4-carboxamide.
1 1. A method as claimed in any one of claims 1 , 2 or 3, wherein component 2) is selected from acibenzolar-S-methyl, benthiavalicarb, chlorothalonil, cyflufenamid, phosphorous acid and its salts, and metrafenone.
12. A method as claimed in any one of claims 1 , 2 or 3, wherein component 2) is selected from captan, and folpet.
13. A method as claimed in any one of claims 1 , 2 or 3, wherein component 2) is se- lected from dimethomorph and flumorph.
14. A method as claimed in any one of claims 1 , 2, 3 or 7, wherein component 2) is selected from mancozeb, and metiram.
15. A method as claimed in any one of claims 1 , 2, 3, 8 or 9, wherein component 2) is selected from carbendazim, dithianon, and thiophanate-methyl.
16. A method as claimed in any one of claims 1 , 2, 3 or 11 , wherein component 2) is selected from acibenzolar-S-methyl, and phosphorous acid and its salts.
17. A method as claimed in any one of claims 1 to 16, wherein components 1 ) and 2) are applied in synergistically effective amounts.
18. A method as claimed in any one of claims 1 to 17, wherein components 1 ) and 2) are used in ratios of from 100:1 to 1 :100.
19. A method as claimed in any one of claims 1 to 18 wherein application of components 1 ) and 2) is carried out during the first six weeks of the growth period of the plants.
20. A method as claimed in any one of claims 1 to 18 wherein application of components 1 ) and 2) is carried out within the first four weeks after germination of the plants.
21. A method as claimed in any one of claims 1 to 20 wherein application of components 1) and 2) is carried out one to ten times before expected bacteria attack.
22. A method as claimed in any one of claims 1 to 21 wherein components 1 ) and 2) are applied to potato, or tomato plants.
23. A method as claimed in any one of claims 1 to 21 wherein components 1 ) and 2) are applied to seeds.
24. The use of the combinations as defined in any of claims 1 to 18 for inducing bac- teria tolerance in plants.
PCT/EP2007/051986 2006-03-14 2007-03-02 Method of inducing tolerance of plants against bacterioses WO2007104658A2 (en)

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CN103109831A (en) * 2013-03-09 2013-05-22 海利尔药业集团股份有限公司 Bactericidal composition containing pyraclostrobin and imidazole hericenone
CN103798237B (en) * 2013-11-19 2015-09-09 广西田园生化股份有限公司 A kind of ultra low volume liquids containing Boscalid
CN103734163A (en) * 2013-12-27 2014-04-23 江苏绿叶农化有限公司 Bactericidal composition containing trifloxystrobin and application of bactericidal composition
CN105052958B (en) * 2015-07-19 2018-08-14 广东中迅农科股份有限公司 A kind of multifunctional paddy bactericidal composition
CN105766919A (en) * 2016-04-22 2016-07-20 广东中迅农科股份有限公司 Bactericidal composition containing triflumizole and (E)2-[2-(2, 5-dimethylphenoxytoluene)-phenyl]-3-methoxyacrylate
CN106879599B (en) * 2017-03-24 2018-08-03 浙江博仕达作物科技有限公司 Application of the triazole sulfonates compounds in preventing paddy bacterial disease
US10628408B2 (en) * 2017-07-20 2020-04-21 Slack Technologies, Inc. Method, apparatus, and computer program product for digital content auditing and retention in a group based communication repository

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2003045146A1 (en) * 2001-11-27 2003-06-05 Syngenta Participations Ag Seed treatment compositions
WO2003045150A2 (en) * 2001-11-30 2003-06-05 Syngenta Participations Ag Seed treatment compositions
WO2003045147A1 (en) * 2001-11-27 2003-06-05 Syngenta Participations Ag Synergistic seed treatment compositions
WO2003066610A1 (en) * 2002-02-04 2003-08-14 Bayer Cropscience Aktiengesellschaft Difluoromethyl thiazolyl carboxanilides
WO2003075663A1 (en) * 2002-03-11 2003-09-18 Basf Aktiengesellschaft Method for immunizing plants against bacterioses
EP1606999A1 (en) * 2004-06-18 2005-12-21 Bayer CropScience AG Seed treatment agent for soy
WO2007104677A1 (en) * 2006-03-14 2007-09-20 Basf Se Method of inducing tolerance of plants against bacterioses

Family Cites Families (28)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NZ213630A (en) * 1984-10-19 1990-02-26 Ici Plc Acrylic acid derivatives and fungicidal compositions
DE3623921A1 (en) * 1986-07-16 1988-01-21 Basf Ag OXIMETHER AND FUNGICIDES CONTAINING THEM
DE3705389A1 (en) * 1987-02-20 1988-09-01 Basf Ag SUBSTITUTED CROTON ACID ESTERS AND FUNGICIDES CONTAINING THEM
DE3823991A1 (en) * 1988-07-15 1990-02-15 Basf Ag HETEROCYCLICALLY SUBSTITUTED (ALPHA) -ARYL-ACRYLIC ACID ESTERS AND FUNGICIDES THAT CONTAIN THESE COMPOUNDS
PH11991042549B1 (en) * 1990-06-05 2000-12-04
DK0463488T4 (en) * 1990-06-27 2004-05-10 Basf Ag O-benzyloxymeters and plant protection agents containing these compounds
DE4030038A1 (en) * 1990-09-22 1992-03-26 Basf Ag New 2-substd. phenyl-acetamide derivs. - useful as fungicides, insecticides, acaricides and nematocides
RU2129118C1 (en) * 1992-01-29 1999-04-20 Басф Акциенгезельшафт Carbamates, intermediate compounds, a fungicide composition, a method of struggle against fungi
DE4304172A1 (en) * 1993-02-12 1994-08-25 Bayer Ag Fungicidal active ingredient combinations
DE4318917A1 (en) * 1993-06-07 1994-12-08 Bayer Ag 2-oximino-2-phenyl-acetamide
EP0738260B2 (en) * 1994-01-05 2006-12-13 Bayer CropScience AG Pesticides
WO1995021154A2 (en) * 1994-02-04 1995-08-10 Basf Aktiengesellschaft Phenyl acetic acid derivatives, process and intermediate products for their production and agents containing them
ATE195509T1 (en) * 1994-02-04 2000-09-15 Basf Ag PHENYLESACETIC ACID DERIVATIVES, PROCESSES AND INTERMEDIATE PRODUCTS FOR THE PRODUCTION THEREOF AND MATERIALS CONTAINING THEM
GB9404375D0 (en) * 1994-03-07 1994-04-20 Zeneca Ltd Fungicides
DE4423612A1 (en) * 1994-07-06 1996-01-11 Basf Ag 2 - [(Dihydro) pyrazolyl-3'-oxymethylene] anilides, process for their preparation and their use
DE19539324A1 (en) * 1995-10-23 1997-04-24 Basf Ag Phenylacetic acid derivatives, processes and intermediates for their preparation and compositions containing them
DE19602095A1 (en) * 1996-01-22 1997-07-24 Bayer Ag Halopyrimidines
KR20000065016A (en) * 1996-04-26 2000-11-06 스타르크, 카르크 Fungicide Mixture
UA73307C2 (en) * 1999-08-05 2005-07-15 Куміаі Кемікал Індастрі Ко., Лтд. Carbamate derivative and fungicide of agricultural/horticultural destination
EP1416793A4 (en) * 2001-06-14 2010-07-14 Syngenta Participations Ag Composition and method for improving plant growth
AU2003233306A1 (en) * 2002-05-17 2003-12-02 Globachem Nv Novel vegetal reinforcing agent based on phytohormones for use in the cultivation of plants or agriculture, preferably in the cultivation of fruit or in wine growing
WO2004095926A2 (en) * 2003-04-28 2004-11-11 Monsanto Technology, Llc Treatment of plants and plant propagation materials with an antioxidant to improve plant health and/or yield
CN1311746C (en) * 2003-06-10 2007-04-25 沈阳化工研究院 Bactericidal compositions of flumorph and enostroburin and synergist
CN100352347C (en) * 2003-06-10 2007-12-05 沈阳化工研究院 Bactericidal compositions containing enostroburin and thiocarbamate
DE602006012716D1 (en) * 2005-10-28 2010-04-15 Basf Se PROCESS FOR INDUCING RESISTANCE TO HARMFUL TREATMENTS
DE102005057250A1 (en) * 2005-11-29 2007-06-06 Bayer Cropscience Gmbh Active ingredients to increase stress control in plants against abiotic stress and methods for their discovery
WO2008095926A1 (en) * 2007-02-06 2008-08-14 Basf Se Plant health composition
KR101066377B1 (en) * 2008-08-01 2011-09-20 삼성전자주식회사 Method for compressing real-time transport protocol hader extension field and header compressed by the method

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2003045146A1 (en) * 2001-11-27 2003-06-05 Syngenta Participations Ag Seed treatment compositions
WO2003045147A1 (en) * 2001-11-27 2003-06-05 Syngenta Participations Ag Synergistic seed treatment compositions
WO2003045150A2 (en) * 2001-11-30 2003-06-05 Syngenta Participations Ag Seed treatment compositions
WO2003066610A1 (en) * 2002-02-04 2003-08-14 Bayer Cropscience Aktiengesellschaft Difluoromethyl thiazolyl carboxanilides
WO2003075663A1 (en) * 2002-03-11 2003-09-18 Basf Aktiengesellschaft Method for immunizing plants against bacterioses
EP1606999A1 (en) * 2004-06-18 2005-12-21 Bayer CropScience AG Seed treatment agent for soy
WO2007104677A1 (en) * 2006-03-14 2007-09-20 Basf Se Method of inducing tolerance of plants against bacterioses

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
DATABASE CABA [Online] CABA COPYRIGHT 2003 CABI; SOBOLEWSKI J ET AL: "New fungicides used for complex control of diseases on tomato growing in the field and in the greenhouse" XP002241579 retrieved from CABA accession no. 2003:69833 Database accession no. 20333035017 *

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2007110173A2 (en) * 2006-03-24 2007-10-04 Bayer Cropscience Ag Fungicidal active substance combinations
WO2007110173A3 (en) * 2006-03-24 2009-03-19 Bayer Cropscience Ag Fungicidal active substance combinations
US8273686B2 (en) 2006-03-24 2012-09-25 Basf Se Method for combating phytopathogenic fungi
EP3586631A2 (en) 2008-02-05 2020-01-01 Basf Se Plant health composition
EP4406412A2 (en) 2008-02-05 2024-07-31 Basf Se Plant health composition
EP4410099A2 (en) 2008-02-05 2024-08-07 Basf Se Plant health composition
EP4410100A2 (en) 2008-02-05 2024-08-07 Basf Se Plant health composition

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