WO2019197615A1 - Active ingredient combinations with fungicides, insecticides and acaricidal properties - Google Patents

Active ingredient combinations with fungicides, insecticides and acaricidal properties Download PDF

Info

Publication number
WO2019197615A1
WO2019197615A1 PCT/EP2019/059434 EP2019059434W WO2019197615A1 WO 2019197615 A1 WO2019197615 A1 WO 2019197615A1 EP 2019059434 W EP2019059434 W EP 2019059434W WO 2019197615 A1 WO2019197615 A1 WO 2019197615A1
Authority
WO
WIPO (PCT)
Prior art keywords
methyl
spp
pyrazole
fluoro
difluoromethyl
Prior art date
Application number
PCT/EP2019/059434
Other languages
German (de)
French (fr)
Inventor
Reiner Fischer
Holger Weckwert
Matthias Haas
Stefan Herrmann
Marita JOHN
Original Assignee
Bayer Aktiengesellschaft
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 Bayer Aktiengesellschaft filed Critical Bayer Aktiengesellschaft
Publication of WO2019197615A1 publication Critical patent/WO2019197615A1/en

Links

Classifications

    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION 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
    • A01N43/00Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/90Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system

Definitions

  • the present invention relates to novel drug combinations which consist of known compounds of the formula (I) on the one hand and other known fungicidal active compounds on the other hand and are very suitable for controlling animal and / or microbial pests such as phytopathogenic fungi, insects and / or unwanted acarids.
  • the compounds of the formula (I) are known from WO 06/089633, which describes their use for controlling animal pests. However, the efficacy and / or range of action and / or the plant tolerance of this compound, in particular to crops, is not always sufficient.
  • W and Y are independently hydrogen, C
  • X is Ct-C ⁇ alkyl, C
  • A, B and the carbon atom to which they are attached are C ⁇ -C ⁇ -cycloalkyl in which optionally one ring member is replaced by nitrogen and which is optionally monosubstituted by C t-C alkoxy, or
  • A, B and the carbon atom to which they are bonded represent O j -C ⁇ -cycloalkyl, which by an optionally by C
  • E is a metal ion or an ammonium ion
  • M is oxygen or sulfur
  • R 1 is straight-chain or branched C 1 -C 8 -alkyl
  • inhibitors of signal transmission 14) compounds that can act as decouplers,
  • the active compound combinations according to the invention comprise, in addition to at least one of the compounds of the formula (I), at least one further compound (B) selected from the following groups (classes):
  • inhibitors of ergosterol biosynthesis for example (1,001) cyproconazole, (1,002) difenoconazole, (1,003) epoxiconazole, (1,004) fenhexamide, (1,005) fenpropidin, (1,006) fenpropimorph, (1,007) fenpyrazamine, (1,008) fluquinconazole, (1.009 ) Flutriafol, (1,010) hnazalil, (1,011) imazalil sulfate, (1,012) ipconazole, (1,013) metconazole, (1,014) myclobutanil, (1,015) paclobutrazole, (1,016) prochloraz, (1,017) propiconazole, (1,018) prothioconazole, (1,019 ) Pyrisoxazole, (1,020) spiroxamine, (1,021) tebuconazole, (1,022)
  • inhibitors of mitosis and cell division for example (4,001) carbendazim, (4,002) diethofencarb,
  • Multisite action compounds for example (5,001) Bordeaux mixture, (5,002) captafol, (5,003) captan, (5,004) chlorothalonil, (5,005) copper hydroxide, (5,006) copper naphthenate , (5.007) copper oxide, (5.008) copper oxychloride, (5.009) copper (2+) sulfate, (5.010) dithianone, (5.011) dodin, (5.012) folpet, (5.013) mancozeb, (5.014) maneb, (5.015) Metiram, (5.016) Metiram Zinc, (5.017) Oxine Copper, (5.018) Propineb, (5.019) Sulfur and Sulfur Preparations including Calcium Polysulfide, (5.020) Thiram, (5.021) Zineb, (5.022) Ziram, (5.023)
  • inhibitors of amino acid and / or protein biosynthesis for example (7,001) cyprodinil, (7,002) kasugamycin, (7,003) kasugamycin hydrochloride hydrate, (7,004) oxytetracycline, (7,005) pyrimethanil, (7,006) 3- (5-fluoro) 3,3,4,4-tetramethyl-3,4-dihydroisoquinoline-l-yl) quinoline.
  • inhibitors of ATP production for example (8,001) silthiofam.
  • inhibitors of cell wall synthesis for example, (9.001) benthi- avalicarb, (9.002) benthiavalicarbisopropyl, (9.003) dimethomorph, (9.004) flumorph, (9.005) iprovalicarb, (9.006) mandipropamide, (9.007) pyrimorph, (9.008) valproate, (9.009) (2E) -3- (4-tert-butylphenyl) -3- (2-chloropyridin-4-yl) -1- (morpholin-4-yl) prop-2-en-1-one, 9,010) (2Z) -3- (4-tert-butylphenyl) -3- (2-chloropyridin-4-yl) -1- (morpholin-4-yl) prop-2-en-1-one.
  • inhibitors of lipid and membrane synthesis for example (10,001) propamocarb, (10,002) propamocarb hydrochloride, (10,003) tolclofos-methyl.
  • Inhibitors of melanin biosynthesis for example, (11.001) tricyclazole, (11.002) [3-methyl-1 - [(4-methylbenzoyl) amino] butan-2-yl ⁇ carbamic acid 2,2,2-trifluoroethyl ester.
  • inhibitors of signal transduction for example (13.001) fludioxonil, (13.002) iprodione, (13.003) procymidone, (13.004) proquinazide, (13.005) quinoxyfen, (13.006) vinclozolin.
  • All of the above-mentioned mixture partners of classes (1) to (15), if they are capable of doing so on the basis of their functional groups, may optionally form salts with suitable bases or acids.
  • All of the mentioned fungicidal mixture partners of classes (1) to (15) may optionally include tautomeric forms.
  • W is preferably methyl
  • X is preferably chlorine or methyl, (highlighted for methyl),
  • Y is preferably chlorine, bromine or methyl
  • D is preferably hydrogen
  • A, B and the carbon atom to which they are attached are preferably saturated C 1-6 cycloalkyl which is substituted with an alkylenedioxy group having a 5-ring or 6-ring ketal with the carbon atom to which it is attached forms,
  • G is preferably hydrogen (a) or one of the groups in which
  • E is a metal ion equivalent or an ammonium ion (highlighted for sodium or potassium)
  • Rl preferably represents geradkettippos or branched C
  • active ingredient combinations comprising the compound of the formula (I-2) and at least one further compound (B) of the classes (1) to (15) described above.
  • Trifloxystrobin (3.020) Trifloxystrobin, (3.025) (3S, 6S, 7R, 8R) -2-methylpropanoic acid 8-benzyl-3 - [( ⁇ 3- [(isobutyryloxy) methoxy] -4-methoxypyridin-2-yl ⁇ carbonyl) amino] -6-methyl-4,9-dioxo-l, 5-dioxonan-7-yl-ester,
  • the active compound combinations according to the invention contain the compounds of the formula (I) and the mixing partners (B) of the classes (1) to (15) as described above, preferably in synergistically effective amounts.
  • the weight ratios of the compounds in the active substance combinations can be varied within a relatively wide range.
  • the combinations according to the invention contain compounds of the formula (I) and the mixing partners (B) of the classes (1) to (15) as described above in the following mixing ratios:
  • active ingredient combinations comprising the compound of the formula (I-2) and isotianil in the mixing ratio 3: 1 to 1: 3.
  • active ingredient combination stands for different combinations of compounds of the formula (I) and the mixing partner (B), for example in the form of a single ready-mix, in a combined spray mixture composed of separate formulations of the individual active ingredients, e.g. a tank mix or in a combined use of the individual active ingredients when applied sequentially, e.g. successively within a reasonably short period of time, e.g. a few hours or days.
  • the order of application of the active compounds of the formula (I) and the mixing partner (B) is not critical to the practice of the present invention.
  • the active compound combinations according to the invention have a potent microbicidal activity and / or a high potential for plant defense modulating. They can be used to control unwanted microorganisms such as unwanted fungi and bacteria. They are particularly suitable for plant protection (they control micro-organisms that cause plant diseases) or for the protection of materials (eg technical materials, timber, stored Goods), as described in more detail below. More specifically, the active compound combinations according to the invention can be used to protect against undesired microorganisms seeds, germinating seeds, accumulated seedlings, plants, plant parts, fruits, crops and / or the soil in which the plants grow.
  • control encompasses the protective, curative and eradicative treatment of undesirable microorganisms.
  • the undesirable microorganisms may be pathogenic bacteria, pathogenic viruses, pathogenic oomycetes or pathogenic fungi, specific phytopathogenic bacteria, phytopathogenic viruses, phytopathogenic oomycetes or phytopathogenic fungi. As described in detail below, these phytopathogenic microorganisms are the causative agents of a wide variety of plant diseases.
  • the active compound combinations according to the invention can be used as fungicides.
  • fungicide refers to a compound or composition which can be used in crop protection for controlling undesired fungi such as Plasmodiophoromycetes, Chytridiomycetes, Zygomycetes, Ascomycetes, Basidiomycetes and Deuteromycetes and / or for controlling Oomycetes.
  • the active compound combinations according to the invention can also be used as antibacterial agent. They can be used in particular in crop protection, for example for controlling undesired bacteria such as Pseudomonadaceae, Rhizobiaceae, Xanthomonadaceae, Enterobacteriaceae, Corynebacteriaceae and Streptomycetaceae.
  • the active compound combinations according to the invention can also be used as an antiviral agent in crop protection.
  • the compound of the present invention and the composition of the present invention may have effects on diseases of plant viruses such as Tobacco Mosaic Virus (TMV), Tobacco Rattle Virus, Tobacco Stunt Virus (TStuV), Tobacco Leaf Curl Virus (VLCV), Tobacco Nervilia Mosaic Virus (TVBMV), Tobacco Necrotic Dwarf Virus (TNDV), Tobacco Streak Virus (TSV), Potato Virus X (PVX), Potato Viruses Y, S, M, and A, Potato Acuba Mosaic Virus (PAMV), Potato Mop-Top Virus (PMTV), Potato Leaf Roll Virus (PLRV), Alfalfa Mosaic Virus (AMV), Cucumber Mosaic Virus (CMV), Cucumber Green Mottlemosaic Virus (CGMMV), Cucumber Yellows Virus (CuYV), Watermelon Mosaic Virus
  • the present invention also relates to a method for controlling unwanted microorganisms such as undesirable fungi, oomycetes and bacteria, which comprises the step of applying at least one active ingredient combination according to the invention to the microorganisms and / or their habitat (to the plants, plant parts, seeds, fruits or soil in which the plants grow).
  • an effective and plant compatible amount thereof is provided to the plants, plant parts, fruits, seeds or soil or substrates in which: the plants grow out.
  • Suitable substrates that can be used to cultivate plants include inorganic based substrates such as mineral wool, especially rockwool, perlite, sand or pebbles; organic substrates such as peat, pine bark or sawdust; and petroleum-based substrates such as polymeric foams or plastic beads.
  • Effective and plant-compatible amount means an amount sufficient to control or destroy the fungi present or occurring on the cultivated land, and which does not induce significant symptoms of phytotoxicity in the crops. Such an amount may vary widely depending on the fungus to be controlled, the crop type, the growth stage of the crop, the climatic conditions and the active compound combinations of the present invention used. This amount can be determined by systematic field trials familiar to the person skilled in the art.
  • Nonlimiting examples of pathogens of fungal diseases which can be treated according to the invention include:
  • Blumeria species for example Blumeria graminis
  • Podosphaera species for example Podosphaera leucotrichcr
  • Sphaerotheca species for example Sphaerotheca fuliginecr
  • Uncinula species for example Uncinula necator
  • Gymnosporangium species for example, Gymnosporangium sabinae
  • Hemileia species for example Hemileia vastatrix
  • Phakopsora species for example Phakopsora pachyrhizi or Phakopsora meibomiae
  • Puccinia species for example Puccinia recondita, Puccinia graminis or Puccinia striiformis
  • Uromyces species for example Uromyces appendiculatus, are caused
  • Diseases caused by pathogens from the group of the Oomycetes for example Albugo species, for example Albugo candida) Bremia species, for example Bremia lactucae
  • Peronospora species for example Peronospora pisi or P.
  • brassicae Phytophthora species, for example Phytophthora infestan
  • Plasmopara species for example Plasmopara viticola
  • Pseudoperonospora species for example Pseudoperonospora humuli or Pseudoperonospora cubensis
  • Pythium species for example Pythium ultimum, are caused;
  • Alternaria species for example Alternaria solani; Cercospora species, for example Cercospora beticola; Cladiosporium species, for example Cladiosporium cucumerinum; Cochliobolus species, for example Cochliobolus sativus (conidia form: Drechslera, Syn: Helminthosporium) or Cochliobolus miyabeanus; Colletotrichum species, for example Colletotrichum lindemuthanium; Corynespora species, for example Corynespora cassiicola; Cycloconium species, for example cycloconium oleaginum; Diaporthe species, for example Diaporthe citri; Citeranoe species, for example Elsinoe fawcettiv, Gloeosporium species, for example Gloeosporium laeticolor, Glomerella species, for example Glomerella cingulata; Gu
  • Corticium species for example Corticium graminearum Fusarium species, for example Fusarium oxysporum; Gaeumannomyces species, for example Gaeumannomyces graminis; Plasmodiophora species, for example Plasmodiophora brassicae, Rhizoctonia species, for example Rhizoctonia solani; Sarocladium species, for example Sarocladium oryzae; Sclerotium-Alten, for example Sclerotium oryzae; Tapesm species, for example Tapesia acuformis; Thielaviopsis species, for example Thielaviopsis basicola, are caused;
  • Ear and panicle diseases including corncob
  • Alternaria species for example Alternaria spp.
  • Aspergillus species for example Aspergillus flavus Cladosporium species, for example Cladosporium cladosporioides; C / av / cepi species, for example Claviceps purpurea; Fusarium species, for example Fusarium culmorum; Gibberella species, for example Gibberella zeae; Monographella species, for example Monographella nivalis, Stagnospora species, for example Stagnospora nodorum are caused; Diseases caused by gangrenous fungi, for example sphacelotheca species, for example Sphacelotheca reiliana; Tilletia species, for example Tilletia caries or Tilletia controverscr, Urocystis species, for example Urocystis occulta Ustilago species, for example Ustila
  • Aspergillus species for example Aspergillus flavus Botrytis species, for example Botrytis cinerea
  • Monilinia species for example Monilinia laxa Penicillium species, for example Penicillium expansum or Penicillium purpurogenum
  • Rhizopus species for example Rhizopus stolonifer, Sclerotinia species, for example Sclerotinia sclerotiorum
  • Verticilium species for example Verticilium alboatrum is caused; seed- and soil-borne rots and wilting as well as casserole diseases, the z.
  • Alternaria species for example Alternaria brassicicola; Aphanomyces species, for example Aphanomyces euteiches; Ascochyta species, for example Ascochyta lentis; Aspergillus species, for example Aspergillus flavus, Cladosporium species, for example Cladosporium herbarum; Cochliobolus species, for example Cochliobolus sativus (conidia form: Drechslera, Bipolaris Syn: Helminthosporium); Colletotrichum species, for example Colletotrichum coccodes; Fusarium species, for example Fusarium culmorum; Gibberella species, for example Gibberella zeae; Macrophomina species, for example Macrophomina phaseolina; Microdochium species, for example Microdochium nivale; Monographella species, for example Monographella nivalis, Penicillium species, for example Penicillium expansum; Phoma species, for example
  • Nectria species for example Nectria galligena
  • Verticillium species for example Verticillium longisporum
  • Fusarium species for example Fusarium oxysporum are caused
  • Exobasidium species for example Exobasidium vexans
  • Taphrina species for example, Taphrina deformans are caused
  • Degenerative diseases of woody plants the z.
  • foca species for example Phaeomoniella chlamydospora, Phaeoacremonium aleophilum or Fomitiporia mediterranea
  • Ganoderma species for example Ganoderma boninense be caused
  • Diseases of plant tubers the z.
  • Rhizoctonia species for example Rhizoctonia solani
  • Helminthosporium species for example Helminthosporium solani;
  • Xanthomonas species for example Xanthomonas campestris pv.
  • Oryzae Pseudomonas species for example Pseudomonas syringae pv.
  • Lachryman Erwinia species, for example Erwinia amylovora; Liberibacter species, for example Liberibacter asiaticu; Xyella species, for example Xylella fastidiosa Ralstonia species, for example Ralstonia solanacearum; Dickeya species, for example Dickeya solani; Clavibacter species, for example Clavibacter michiganensis; Streptomyces species, for example Streptomyces scabies are caused.
  • Black Root Red (Calonectria crotalariae), Black Rot (Macrophomina phaseolina), Fusarium Blight or Wilt, Root Red, and Pod and Collar Red (Fusarium oxysporum, Fusarium orthoceras, Fusarium semitectum, Fusarium equiseti), Mycoleptodiscus Root Red (Mycoleptodiscus terrestris ), Neocosmospora (Neocosmospora vasinfecta), Pod and Star Blight (Diaporthe phaseolorum), Stem Crab (Diaporthe phaseolorum var. Caulivora), Phytophthora rot.
  • mycotoxins include, but are not limited to, the following: desoxynivalenol (DON), nivalenol, 15-Ac-DON, 3-Ac-DON, T2 and HT2 toxin, fumonisins, zearalenone, moniliformin, fusarin, diaceotoxyscirpenol (DAS), beauvericin, enniatine, fusaroproliferin, fusarenol, ochratoxins, patulin, ergot alkaloids and aflatoxins, which can be produced, for example, by the following fungi: Fusarium spec., Such as F.
  • verticillioides etc.
  • Aspergillus spec. such as A. flavus, A. parasiticus, A. nomius, A. ochraceus, A. clavatus, A. terreus, A. versicolor, Penicillium spec. as P. verrucosum, P. viridicatum, P. citrinum, P. expansum, P. claviforme, P. roqueforti, Claviceps spec. as C. purpurea, C. fusiformis, C. paspali, C. africana, Stachybotrys spec. and other.
  • the invention also relates to methods for controlling animal pests, in which the active ingredient combinations according to the invention are allowed to act on animal pests and / or their Eebensraum.
  • the control of animal pests is preferably carried out in forestry and material protection. Excluded therefor are preferably methods for the surgical or therapeutic treatment of the human or animal body and diagnostic methods that are performed on the human or animal body.
  • the invention further relates to the use of the active compound combinations according to the invention as pesticides, in particular crop protection agents.
  • pest control always always includes the term pesticides.
  • the active compound combinations according to the invention are suitable for plant protection, favorable warm-blooded toxicity and good environmental compatibility for the protection of plants and plant organs against biotic and abiotic stress factors, for increasing crop yields, improving the quality of the crop and for controlling animal pests, in particular insects, arachnids, helminths, especially nematodes, and mollusks that occur in agriculture, horticulture, forests, gardens and recreational facilities.
  • the active compound combinations according to the invention can preferably be used as
  • Pesticides are used. They are effective against normally sensitive and resistant species as well as against all or individual stages of development.
  • the above mentioned pests include:
  • Pests from the strain of Arthropoda in particular from the class of Arachnida z. Acarus spp., E.g. Acarus siro, Aceria kuko, Aceria sheldoni, Aculops spp., Aculus spp., E.g. Aculus fockeui, Aculus badendali, Amblyomma spp., Amphitetranychus viennensis, Argas spp., Boophilus spp., Brevipalpus spp., E.g. B.
  • Oligonychus coffeae Oligonychus coniferarum, Oligonychus ilicis, Oligonychus indicus, Oligonychus mangiferus, Oligonychus pratensis, Oligonychus punicae, Oligonychus yothersi, Ornithodorus spp., Ornithonyssus spp., Panonychus spp., E.g.
  • Panonychus citri Metatetranychus citri
  • Panonychus ulmi Metatetranychus ulmi
  • Phyllocoptruta oleivora Platytetranychus multidigituli
  • Polyphagotarsonemus latus Psoroptes spp., Rhipicephalus spp., Rhizoglyphus spp., Sarcoptes spp., Scorpio maurus, Steneotarsonemus spp. Steneotarsonemus spinki, Tarsonemus spp. Tarsonemus confusus, Tarsonemus pallidus, Tetranychus spp., E.g.
  • Blatta orientalis Blattella asahinai, Blattella germanica, Leucophaea maderae, Loboptera decipiens, Neostylopyga rhombifolia, Panchlora spp., Parcoblatta spp., Periplaneta spp., E.g. Periplaneta americana, Periplaneta australasiae, Pycnoscelus surinamensis, Supella longipalpa; from the order of Coleoptera z.
  • Anoplophora glabripennis Anthonomus spp., e.g. Anthonomus grandis, Anthrenus spp., Apion spp., Apogonia spp., Atomaria spp., E.g. Eg Atomaria linearis, Attagenus spp., Baris caerulescens, Bruchidius obtectus, Bruchus spp., E.g. Bruchus pisorum, Bruchus rufimanus, Cassida spp., Cerotoma trifurcata, Ceutorrhynchus spp.
  • Diabrotica balteata Diabrotica barberi, Diabrotica undecimpunctata howardi, Diabrotica undecimpunctata undecimpunctata, Diabrotica virgifera virgifera, Diabrotica virgifera zeae, Dichocrocis spp., Dicladispa armigera, Diloboderus spp., Epicaerus spp., Epilachna spp., E.g. Epilachna borealis, Epilachna varivestis, Epitrix spp., E.g.
  • Epitrix cucumeris Epitrix fuscula, Epitrix hirtipennis, Epitrix subcrinita, Epitrix tuberis, Faustinus spp., Gibbium psylloides, Gnathocerus cornutus, Hellula and alis, Heteronychus arator, Heteronyx spp., Hylamorpha elegans, Hylotrupes b Camillus, Hypera postica, Hypomeces squamosus, Hypothenemus spp., z.
  • Hypothenemus hampei Hypothenemus obscurus, Hypothenemus pubescens, Lachnosterna consanguinea, Lasioderma serricorne, Latheticus oryzae, Lathridius spp., Lema spp., Leptinotarsa decemlineata, Leucoptera spp., E.g. Luperoptera spp., Luperodes spp., Luperomorpha xanthodera, Lyctus spp., Megacyllene spp., E.g. Megacyllene robiniae, Megascelis spp., Melanotus spp., E.g.
  • Melanotus longulus oregonensis Meligethes aeneus, Melolontha spp., E.g. Melolontha melolontha, Migdolus spp., Monochamus spp., Naupactus xanthographus, Necrobia spp., Neogalerucella spp., Niptus hololeucus, Oryctes rhinoceros, Oryzaephilus surinamensis, Oryzaphagus oryzae, Otiorhynchus spp., E.g.
  • Otiorhynchus cribricollis Otiorhynchus ligustici, Otiorhynchus ovatus, Otiorhynchus rugosostriarus, Otiorhynchus sulcatus, Oulema spp., E.g. Oulema melanopus, Oulema oryzae, Oxycetonia jucunda, Phaedon cochleariae, Phyllophaga spp., Phyllophaga helleri, Phyllotreta spp., E.g.
  • Phyllotreta armoraciae Phyllotreta pusilla, Phyllotreta ramosa, Phyllotreta striolata, Popillia japonica, Premnotrypes spp., Prostephanus truncatus, Psylliodes spp., E.g.
  • Tribolium audax Tribolium castaneum, Tribolium confusum, Trogoderma spp., Tychius spp., Xylotrechus spp., Zabrus spp., E.g. Zabrus tenebrioides; from the order of Dermaptera z.
  • Acyrthosiphon pisum Acrogonia spp., Aeneolamia spp., Agonoscena spp., Aleurocanthus spp., Aleyrodes proletella, Aleurolobus barodensis, Aleurothrixus floccosus, Allocaridara malayensis, Amrasca spp., E.g. Amrasca bigutulla, Amrasca devastans, Anuraphis cardui, Aonidiella spp.
  • Aspidiella spp. Aspidiella spp., Aspidiotus spp., E.g. Aspidiotus nerii, Atanus spp., Aulacorthum solani, Bemisia tabaci, Blastopsylla occidentalis, Boreioglycaspis melaleucae, Brachycaudus helichrysi, Brachycolus spp., Brevicoryne brassicae, Cacopsylla spp., E.g.
  • Icerya purchasi Idiocerus spp., Idioscopus spp., Laodelphax striatellus, Lecanium spp., E.g.
  • B. Lecanium corni ( Parthenolecanium corni), Lepidosaphes spp., Z. Lepidosaphes ulmi, Lipaphis erysimi, Lopholeucaspis japonica, Lycorma americanula, Macrosiphum spp., E.g.
  • Macrosiphum euphorbiae Macrosiphum lilii, Macrosiphum rosae, Macrosteies facifrons, Mahanarva spp., Melanaphis sacchari, Metcalfiella spp., Metcalfa pruinosa, Metopolophium dirhodum, Monellia costalis, Monelliopsis pecanis, Myzus spp., E.g.
  • Nephotettix spp. E.g. Nephotettix cincticeps, Nephotettix nigropictus, Nettigoniclla spectra, Nilaparvata lugens, Oncometopia spp., Orthezia praelonga, Oxya chinensis, Pachypsylla spp., Parabemisia myricae, Paratrioza spp., E.g.
  • Paratrioza cockerelli Parlatoria spp., Pemphigus spp., E.g. B. Pemphigus bursarius, Pemphigus populivenae, Peregrinus maidis, Perkinsiella spp., Phenacoccus spp., Z. Phenacoccus madeirensis, Phloeomyzus passerinii, Phorodon humuli, Phylloxera spp., E.g. Phylloxera devastatrix, Phylloxera notabilis, Pinnaspis aspidistrae, Planococcus spp., E.g. B.
  • Planococcus citri Prosopidopsylla flava, Protopulvinaria pyriformis, Pseudaulacaspis pentagona, Pseudococcus spp., Z. Pseudococcus calceolariae, Pseudococcus comstocki, Pseudococcus longispinus, Pseudococcus maritimus, Pseudococcus viburni, Psyllopsis spp., Psylla spp., E.g.
  • Rhopalosiphum maidis Rhopalosiphum oxyacanthae, Rhopalosiphum padi, Rhopalosiphum rufiabdominal, Saissetia spp., E.g.
  • Trioza spp. E.g. Trioza diospyri, Typhlocyba spp., Unaspis spp., Viteus vitifolii, Zygina spp .; from the subordination of Heteroptera z.
  • Aelia spp. Anasa tristis, Antestiopsis spp., Boisea spp., Blissus spp., Calocoris spp., Campylomma livida, Cavelerius spp., Cimex spp., E.g.
  • Cimex adjunctus Cimex hemipterus, Cimex lectularius, Cimex pilosellus, Collaria spp., Creontiades dilutus, Dasynus piperis, Dichelops furcatus, Diconocoris hewetti, Dysdercus spp., Euschistus spp., E.g.
  • Lygus elisus Lygus hesperus, Lygus lineolaris, Macropes excavatus, Megacopta cribraria, Miridae, Monalonion atratum, Nezara spp., Z. Nezara viridula, Nysius spp., Oebalus spp., Pentomidae, Piesma quadrata, Piezodorus spp., E.g.
  • Hoplocampa cookei Hoplocampa testudinea, Lasius spp., Linepithema (Iridiomyrmex) humile, Monomorium pharaonis, Paratrechina spp., Paravespula spp., Plagiolepis spp., Sirex spp., E.g. Sirex noctilio, Solenopsis invicta, Tapinoma spp., Technomyrmex albipes, Urocerus spp., Vespa spp., E.g. Vespa crabro, Wasmannia auropunctata, Xeris spp .; from the order of Isopoda z.
  • Cydia nigricana Cydia pomonella, Dalaca noctuides, Diaphania spp., Diparopsis spp., Diatraea saccharalis, Dioryctria spp., E.g. B. Dioryctria tremani, Earias spp., Ecdytolopha aurantium, Elasmopalpus lignosellus, Eldana saccharina, Ephestia spp., E.g.
  • Grapholita molesta Grapholita prunivora, Hedylepta spp., Helicoverpa spp., Z. Helicoverpa armigera, Helicoverpa zea, Heliothis spp. Homo. Spp., Hyponomeuta padella, Kakivoria flavofasciata, Lampides spp., Laphygma spp., Laspeyresia molesta, Leucinodes orbonalis, Leucoptera spp., E.g. B. Leucoptera coffeella, Lithocolletis spp., Z. B.
  • Pectinophora gossypiella, Perileucoptera spp., Phthorimaea spp., Z. Phthorimaea operculella, Phyllocnistis citrella, Phyllonorycter spp., E.g. Phyllonorycter blancardella, Phyllonorycter crataegella, Pieris spp., E.g. Pieris rapae, Platynota stultana, Plodia interpunctella, Plusia spp., Plutella xylostella ( Plutella maculipennis), Podesia spp., E.g.
  • Trichoplusia ni Tryporyza incertulas, Tuta absolutea, Virachola spp .; from the order of Orthoptera or Saltatoria z.
  • Ctenocephalides canis, Ctenocephalides felis, Pulex irritans, Tunga penetrans, Xenopsylla cheopis; from the order of Thysanoptera z.
  • Ctenolepisma spp. Lepisma saccharina, Lepismodes inquilinus, Thermobia domestica; from the class of Symphyla z. B. Scutigerella spp., Z. B. Scutigerella immaculata;
  • Bursaphelenchus cocophilus, Bursaphelenchus eremus, Bursaphelenchus xylophilus, Cacopaurus spp., E.g. Cacopaurus pestis, Criconemella spp., E.g. Criconemella curvata, Criconemella onoensis, Criconemella ornata, Criconemella rusium, Criconemella xenoplax ( Mesocriconema xenoplax), Criconemoides spp., E.g. Criconemoides ferniae, Criconemoides onoense, Criconemoides ornatum, Ditylenchus spp., E.g.
  • Meloidogyne spp. Longidorus africanus, Meloidogyne spp., E.g. Meloidogyne chitwoodi, Meloidogyne fallax, Meloidogyne hapla, Meloidogyne incognita, Meloinema spp., Nacobbus spp., Neotylenchus spp., Paralongidorus spp., Paraphelenchus spp., Paratrichodorus spp., E.g. Paratrichodorus minor, Paratylenchus spp., Pratylenchus spp., E.g.
  • Pratylenchus penetrans Pseudohalenchus spp., Psilenchus spp., Punctodera spp., Quinisulcius spp., Radopholus spp., E.g. Radopholus citrophilus, Radopholus similis, Rotylenchulus spp., Rotylenchus spp., Scutellonema spp., Subanguina spp., Trichodorus spp., E.g. Trichodorus obtusus, Trichodorus primitivus, Tylenchorhynchus spp., E.g. Tylenchorhynchus annulatus, Tylenchulus spp., E.g. B. Tylenchulus semipenetrans, Xiphinema spp., Z. B. Xiphinema index.
  • the active compound combinations according to the invention may optionally in certain con centrations or application rates as herbicides, safeners, growth regulators or agents for improving plant properties, as microbicides or gametocides, for example as Fungicides, antimycotics, bactericides, viricides (including anti-viral agents) or as agents against MLO (Mycoplasma-like-organism) and RLO (Rickettsia-like-organism). If appropriate, they can also be used as intermediates or precursors for the synthesis of further active ingredients.
  • the present invention further relates to formulations and application forms prepared therefrom as pesticides such.
  • B. drench, Drip and spray comprising at least one active ingredient combination according to the invention.
  • the uses include other pesticides and / or effect-improving adjuvants such as penetration enhancers, e.g. As vegetable oils such as rapeseed oil, sunflower oil, mineral oils such as paraffin oils, alkyl esters of fatty acids such as rapeseed oil or soybean oil or alkanol alkoxylates and / or spreading agents such as alkyl siloxanes and / or salts, eg.
  • organic or inorganic ammonium or phosphonium salts such as ammonium sulfate or diammonium hydrogen phosphate and / or retention-promoting agents such.
  • organic or inorganic ammonium or phosphonium salts such as ammonium sulfate or diammonium hydrogen phosphate and / or retention-promoting agents such.
  • dioctyl sulfosuccinate or hydroxypropyl guar polymers and / or humectants such.
  • glycerol and / or fertilizers such as ammonium, potassium or phosphorus-containing fertilizer.
  • Typical formulations are, for example, water-soluble liquids (SF), emulsion concentrates (EC), emulsions in water (EW), suspension concentrates (SC, SE, FS, OD), water-dispersible granules (WG), granules (GR) and capsule concentrates (CS). ;
  • SF water-soluble liquids
  • EC emulsion concentrates
  • EW emulsions in water
  • SC suspension concentrates
  • SC SE, SE, FS, OD
  • WG water-dispersible granules
  • GR granules
  • CS capsule concentrates
  • the formulations contain, in addition to one or more active compound combinations according to the invention, further agrochemical active substances.
  • auxiliaries such as extenders, foaming agents, spontaneity promoters, carriers, emulsifiers, dispersants, antifreeze agents, biocides, thickeners and / or further auxiliaries, for example adjuvants.
  • An adjuvant in this context is a component that enhances the biological effect of the formulation without the component itself having a biological effect.
  • adjuvants are agents that promote retention, spreading behavior, adherence to the leaf surface, or penetration.
  • These formulations are prepared in a known manner, for. Example by mixing the active compound combinations according to the invention with excipients such as extenders, solvents and / or solid carriers and / or other excipients such as surface-active substances. The preparation of the formulations is carried out either in suitable systems or before or during use.
  • Excipients which can be used are those which are suitable for the formulation of the active compound combinations according to the invention or for the use forms prepared from these formulations (such as, for example, usable pesticides such as spray mixtures or seed dressing), such as certain physical, technical and / or biological properties to rent.
  • Suitable extenders z As water, polar and nonpolar organic chemical liquids such. B. from the classes of aromatic and non-aromatic hydrocarbons (such as paraffins, alkylbenzenes, alkylnaphthalenes, chlorobenzenes), alcohols and polyols (which may also be substituted, etherified and / or esterified), the ketones (such as acetone, cyclohexanone ), esters (including fats and oils) and (poly) ethers, simple and substituted amines, amides, lactams (such as N-alkylpyrrolidones) and lactones, sulfones and sulfoxides (such as dimethylsulfoxide), carbonates and nitriles.
  • aromatic and non-aromatic hydrocarbons such as paraffins, alkylbenzenes, alkylnaphthalenes, chlorobenzenes
  • alcohols and polyols which may also be substitute
  • Suitable liquid solvents are essentially: aromatics such as xylene, toluene or alkylnaphthalenes, chlorinated aromatics or chlorinated aliphatic hydrocarbons such as chlorobenzenes, chloroethylenes or methylene chloride, aliphatic hydrocarbons such as cyclohexane or paraffins, eg.
  • Suitable solvents are, for example, aromatic hydrocarbons such. As xylene, toluene or alkylnaphthalenes, chlorinated aromatic or chlorinated aliphatic hydrocarbons such. As chlorobenzene, chloroethylene, or methylene chloride, aliphatic hydrocarbons such. As cyclohexane, paraffins, petroleum fractions, mineral and vegetable oils, alcohols such. As methanol, ethanol, iso-propanol, butanol or glycol and their ethers and esters, ketones such.
  • acetone methyl ethyl ketone, methyl isobutyl ketone or cyclohexanone
  • strong polar solvents such as dimethyl sulfoxide
  • carbonates such as propylene carbonate, butylene carbonate, diethyl carbonate or dibutyl carbonate
  • nitriles such as acetonitrile or propanenitrile
  • water water.
  • carriers are in particular question: z.
  • ammonium salts and ground natural minerals such as kaolins, clays, talc, chalk, quartz, attapulgite, montmorillonite or diatomaceous earth and synthetic minerals such as finely divided silica, alumina and natural or synthetic silicates, resins, waxes and / or solid fertilizers.
  • Suitable carriers for granules are: z. As broken and fractionated natural rocks such as calcite, marble, pumice, sepiolite, dolomite and synthetic granules of inorganic and organic flours and granules of organic material such as sawdust, paper, coconut shells, corncobs and tobacco stems.
  • liquefied gaseous diluents or solvents can be used.
  • extenders or carriers which are gaseous at normal temperature and under atmospheric pressure, for.
  • aerosol propellants such as halogenated hydrocarbons and butane, propane, nitrogen and carbon dioxide.
  • Examples of emulsifying and / or foaming agents, dispersants or wetting agents having ionic or non-ionic properties or mixtures of these surfactants are salts of polyacrylic acid, salts of lignosulfonic acid, salts of phenolsulfonic acid or naphthalenesulfonic acid, polycondensates of ethylene oxide with fatty alcohols or with fatty acids or with fatty amines, with substituted phenols (preferably alkylphenols or arylphenols), salts of sulfosuccinic acid esters, taurine derivatives (preferably alkyl taurates), isethionate derivatives, phosphoric acid esters of polyethoxylated alcohols or phenols, fatty acid esters of polyols and derivatives of the compounds containing sulfates, sulfonates and phosphates, e.g.
  • alkylaryl polyglycol ethers alkylsulfonates, alkyl sulfates, arylsulfonates, protein hydrolysates, lignin liquors and methylcellulose.
  • a surface-active substance is advantageous if one of the active compound combinations according to the invention and / or one of the inert carriers is not soluble in water and if the application is carried out in water.
  • auxiliaries can in the formulations and the applications derived therefrom dyes such as inorganic pigments, eg.
  • dyes such as inorganic pigments, eg.
  • iron oxide, titanium oxide, ferrocyan blue and organic dyes such as alizarin, azo and Metallphthalocyaninfarbstoffe and nutrient and trace nutrients such as salts of iron, manganese, boron, copper, cobalt, molybdenum and zinc may be present.
  • Stabilizers such as cold stabilizers, preservatives, antioxidants, light stabilizers or other chemical and / or physical stability-improving agents may also be present. It may also contain foam-forming agents or defoamers.
  • auxiliaries also adhesives such as carboxymethylcellulose, natural and synthetic powdery, granular or latex-like polymers such as gum arabic, polyvinyl alcohol, polyvinyl acetate and natural phospholipids such as cephalins and lecithins and synthetic phospholipids.
  • Other auxiliaries may be mineral and vegetable oils.
  • auxiliaries may be present in the formulations and in the use forms derived therefrom.
  • additives include, for example, fragrances, protective colloids, binders, adhesives, thickeners, thixotropic agents, penetrants, retention promoters, stabilizers, sequestrants, chelants, humectants, spreading agents.
  • the active compound combinations of this invention can be used with any solid or liquid additive commonly used for formulation purposes , be combined.
  • retention promoters are all those substances which reduce the dynamic surface tension such as dioctylsulfosuccinate or increase the visco-elasticity such as hydroxypropyl guar polymers.
  • Penetration promoters are in this context defined by the fact that they can penetrate from the (usually aqueous) application broth and / or from the spray coating into the cuticle of the plant and thereby increase the mobility of the active ingredients in the cuticle.
  • the method described in the literature can be used to determine this property.
  • Examples include alcohol alkoxylates such as coconut oil ethoxylate (10) or isotridecyl ethoxylate (12), fatty acid esters such as rapeseed oil or soybean oil, Fettaminalkoxylate such as tallowamine ethoxylate (15) or ammonium and / or phosphonium salts such as ammonium sulfate or diammonium hydrogen phosphate.
  • alcohol alkoxylates such as coconut oil ethoxylate (10) or isotridecyl ethoxylate (12)
  • fatty acid esters such as rapeseed oil or soybean oil
  • Fettaminalkoxylate such as tallowamine ethoxylate (15) or ammonium and / or phosphonium salts such as ammonium sulfate or diammonium hydrogen phosphate.
  • the formulations preferably contain between 0.00000001 and 98% by weight of the active ingredient combination according to the invention, more preferably between 0.01 and 95% by weight of the active ingredient combination according to the invention, very particularly preferably between 0.5 and 90% by weight of the active ingredient combination according to the invention , based on the weight of the formulation.
  • the content of the active ingredient combination according to the invention in the forms of application prepared from the formulations (in particular pesticides) can vary within wide ranges.
  • the concentration of the active ingredient combination according to the invention in the application forms can usually be between 0.00000001 and 95% by weight of the active ingredient combination according to the invention, preferably between 0.00001 and 1% by weight, based on the weight of the application form.
  • the application is done in a custom forms adapted to the application forms. mixtures
  • the active compound combinations according to the invention can also be used in admixture with one or more suitable fungicides, bactericides, acaricides, molluscicides, nematicides, insecticides, microbiologicals, beneficials, herbicides, fertilizers, avian repellents, phytotonics, sterilants, safeners, semiochemicals and / or plant growth regulators, in order to: z. B. to broaden the spectrum of action, to extend the duration of action, to increase the rate of action, to prevent repellence or to prevent development of resistance.
  • z. B. to broaden the spectrum of action, to extend the duration of action, to increase the rate of action, to prevent repellence or to prevent development of resistance.
  • such drug combinations plant growth and / or tolerance to abiotic factors such. As high or low temperatures, improve against dryness or increased water or Bodensalzgehalt. Also, flowering and fruiting behavior can be improved, germination and rooting can be improved, harvesting and crop
  • the active compound combinations according to the invention may be present in a mixture with other active substances or semiochemicals, such as attractants and / or avian repellents and / or plant activators and / or growth regulators and / or fertilizers.
  • the active compound combinations according to the invention can be used to improve the plant properties such as, for example, growth, yield and quality of the crop.
  • the active compound combinations according to the invention are present in formulations or in the use forms prepared from these formulations in admixture with further compounds, preferably those as described below.
  • Acetylcholinesterase (AChE) inhibitors preferably carbamates selected from alanycarb, aldicarb, bendiocarb, benfuracarb, butocarboxime, butoxycarboxime, carbaryl, carbofuran, carbosulfan, ethiofencarb, fenobucarb, formetanate, furathiocarb, isoprocarb, methiocarb, methomyl, metolcarb, oxamyl, Pirimicarb, propoxur, thiodicarb, thiofanox, triazamate, trimethacarb, XMC and xylylcarb, or organophosphates selected from acephate, azamethiphos, azinphos-ethyl, azinphos-methyl, cadusafos, chloroethoxyfos, chlorfenvinphos, chloroforms, chlorpyrifos-methyl, cous
  • GABA-controlled chloride channel blockers preferably cyclodiene organochlorines selected from chlordane and endosulfan, or phenylpyrazoles (fiproles) selected from ethiprole and fipronil.
  • Sodium channel modulators preferably pyrethroids selected from acrinathrin, allethrin, d-cis-trans-allethrin, d-trans-allethrin, bifenthrin, bioallethrin, bioallethrin-S-cyclopentenyl isomer, bioresmethrin, cycloprothrin, cyfluthrin, beta Cyfluthrin, cyhalothrin, lambda-cyhalothrin, gamma-cyhalothrin, cypermethrin, alpha-cypermethrin, beta-cypermethrin, theta-cypermethrin, zeta-cypermethrin, cyphenothrin [(lR) -trans isomer], deltamethrin, empenthrin [(EZ) (IR) isomer], esfenvalerate
  • nAChR nicotinic acetylcholine receptor
  • neonicotinoids selected from acetamiprid, clothianidin, dinotefuran, bnidacloprid, nitenpyram, thiacloprid and thiamethoxam, or nicotine
  • sufoximines selected from sulfoxaflor, or butenolides selected from flupyradifurone.
  • Allosteric modulators of the nicotinic acetylcholine receptor preferably spinosyns selected from spinetoram and spinosad.
  • Allosteric modulators of the glutamate-dependent chloride channel preferably avermectins / milbemycins selected from abamectin, emamectin benzoate, eepimectin and milbemectin.
  • Juvenile hormone mimetics preferably juvenile hormone analogs selected from hydroprene, kinoprene and methoprene, or fenoxycarb or pyriproxyfen.
  • Various non-specific (multi-site) inhibitors preferably alkyl halides selected from methyl bromide and other alkyl halides, or chloropicrin or sulfuryl fluoride or borax or tartaric or methyl isocyanate producers selected from Diazomet and Metam.
  • TRPV channel modulators of chordotonic organs selected from pymetrozine and pyrifluquinazone.
  • mite growth inhibitors selected from clofentezine, hexythiazox, diflovidazine and etoxazole.
  • Insect intestinal membrane microbial disruptors selected from Bacillus thuringiensis subspecies israelensis, Bacillus sphaericus, Bacillus thuringiensis subspecies aizawai, Bacillus thuringiensis subspecies kurstaki, Bacillus thuringiensis subspecies tenebrionis, and Bt plant proteins selected from CrylAb, CrylAc, CrylFa, CrylA.105, Cry2Ab, VIP3A , mCry3A, Cry3Ab, Cry3Bb and Cry34Ab 1/35 Abi.
  • inhibitors of mitochondrial ATP synthase preferably ATP disruptors selected from diafenthiuron, or organotin compounds selected from azocyclotine, cyhexatin and fenbutatin oxide, or propargite or tetradifone.
  • Blocker of the nicotinic acetylcholine receptor channel selected from Bensultap, Cartap hydrochloride, thiocyclam and thiosultap sodium.
  • Inhibitors of chitin biosynthesis type 0, selected from bistrifluron, chlorofluorazuron, diflubenzuron, flucycloxuron, flufenoxuron, hexaflumuron, lufenuron, novaluron, noviflumuron, teflubenzuron and triflumuron.
  • inhibitors of chitin biosynthesis type 1 selected from buprofezin.
  • Skinning disruptor especially in dipterans, i.e., two-winged selected from cyromazine.
  • Ecdysone receptor agonists selected from chromafenozide, halofenozide, methoxyfenozide and tebufenozide.
  • Octopamine receptor agonists selected from Amitraz.
  • Mitochondrial complex III electron transport inhibitors selected from hydramethylnone, acequinocyl and fluacrypyrim.
  • Mitochondrial Complex I Electron Transport Inhibitors preferably META acaricides selected from Fenazaquin, Fenpyroximate, Pyrimidifen, Pyridaben, Tebufenpyrad and Tolfenpyrad, or rotenone (Derris).
  • Inhibitors of acetyl-CoA carboxylase preferably tetronic and tetramic acid derivatives selected from spirodiclofen, spiromesifen and spirotetramat.
  • inhibitors of mitochondrial complex IV electron transport preferably phosphines selected from aluminum phosphide, calcium phosphide, phosphine and zinc phosphide, or cyanides selected from calcium cyanide, potassium cyanide and sodium cyanide.
  • inhibitors of mitochondrial complex II electron transport preferably beta-ketone nitrile derivatives selected from cyenopyrafen and Cyflumetofen, or carboxanilides selected from Pyflubumid.
  • ryanodine receptor modulators preferably diamides selected from chlorantraniliprole, cyantraniliprole and flubendiamide.
  • octane (known from WO 2007040280 A1, WO 2007040282 A1) (CAS 934001-66-8), N- [3-chloro-1- (3-pyridinyl) -1H-pyrazol-4-yl] -N-ethyl 3 - [(3,3,3-trifluoropropyl) thio] -propanamide (known from WO 2015/058021 A1, WO 2015/058028 A1) (CAS 1477919-27-9) and N- [4- (aminothioxomethyl) -
  • the active compound combinations according to the invention can be combined with biological pesticides.
  • Bio pesticides include, in particular, bacteria, fungi, yeasts, plant extracts and those products formed by microorganisms, including proteins and secondary metabolites.
  • Biological pesticides include bacteria such as spore-forming bacteria, root-colonizing bacteria and bacteria that act as biological insecticides, fungicides or nematicides.
  • Bacillus amyloliquefaciens strain FZB42 (DSM 231179), or Bacillus cereus, in particular B. cereus strain CNCM 1-1562 or Bacillus firmus, strain 1-1582 (Accession number CNCM 1-1582) or Bacillus pumilus, in particular strain GB34 (Accession No. ATCC 700814) and strain QST2808 (Accession No. NRRL B-30087), or Bacillus subtilis, in particular strain GB03 (Accession No. ATCC SD-1397), or Bacillus subtilis strain QST713 (Accession No. NRRL B-21661) or Bacillus subtilis strain OST 30002 (Accession No.
  • NRRL B-50421 Bacillus thuringiensis, in particular Thuringiensis subspecies israelensis (serotype H-14), strain AM65-52 (Accession No. ATCC 1276), or B. thuringiensis subsp. aizawai, in particular strain ABTS-1857 (SD-1372), or B. thuringiensis subsp. kurstaki strain HD-1, or B. thuringiensis subsp. tenebrionis strain NB 176 (SD-5428), Pasteuria penetrans, Pasteuria spp.
  • fungi and yeasts which can be used as biological pesticides are:
  • Beauveria bassiana in particular strain ATCC 74040, coniothyrium minitans, in particular strain CON / M / 91-8 (Accession No. DSM-9660), Lecanicillium spp., In particular strain HRO LEC 12, Lecanicillium lecanii (formerly known as Verticillium lecanii), in particular Strain KV01, Metarhizium anisopliae, in particular strain F52 (DSM3884 / ATCC 90448), Metschnikowia fructicola, in particular strain NRRL Y-30752, Paecilomyces fumosoroseus (new: Isaria fumosorosea), in particular strain IFPC 200613, or strain Apopka 97 (Accesion No.
  • Paecilomyces lilacinus in particular P. lilacinus strain 251 (AGAL 89/030550), Talaromyces flavus, in particular strain VI 17b, Trichoderma atroviride, in particular strain SCI (Accession Number CBS 122089), Trichoderma harzianum, in particular T. harzianum rifai T39. (Accession Number CNCM 1-952).
  • viruses that can be used or used as biological pesticides are:
  • Adoxophyes orana Apple peel winder
  • Granulosis virus GV
  • Cydia pomonella codling moth
  • Granulosis virus GV
  • Helicoverpa armigera cotton bollworm
  • Nuclear polyhedrosis virus NPV
  • Spodoptera exigua mNPV
  • Spodoptera frugiperda armyworm
  • mNPV Spodoptera littoralis
  • bacteria and fungi that are added as 'inoculant' plants or parts of plants or plant organs and promote by their special properties, plant growth and plant health. Examples are:
  • plant extracts and those products formed by microorganisms, including proteins and secondary metabolites, which can be used as biological pesticides are:
  • the active compound combinations according to the invention can be combined with safeners, for example Benoxacor, Cloquintocet (-mexyl), Cyometrinil, Cyprosulfamide, Dichlormid, Fenchlorazole (- ethyl), Fenclorim, Flurazole, Fluxofenim, Furilazole, Isoxadifen (-ethyl), Mefenpyr (-diethyl ), Naphthalene anhydrides, oxabetrinil, 2-methoxy-N - ( ⁇ 4-
  • safeners for example Benoxacor, Cloquintocet (-mexyl), Cyometrinil, Cyprosulfamide, Dichlormid, Fenchlorazole (- ethyl), Fenclorim, Flurazole, Fluxofenim, Furilazole, Isoxadifen (-ethyl), Mefenpyr (-diethyl ), Naphthalene anhydrides, o
  • plants and parts of plants can be treated.
  • Plants are understood to mean all plants and plant populations, such as desirable and unwanted wild plants or crops (including naturally occurring crops), for example cereals (wheat, rice, triticale, barley, rye, oats), corn, soybeans, potatoes, sugar beets, sugarcane, tomatoes , Paprika, cucumber, melon, carrot, watermelon, onion, lettuce, spinach, leek, beans, Brassica oleracea (eg cabbage) and other vegetables, cotton, tobacco, rapeseed, as well as fruit plants (with the fruits apples, pears, Citrus fruits and grapes).
  • Crop plants can be plants that can be obtained by conventional breeding and optimization methods or by biotechnological and genetic engineering methods or combinations of these methods, including the transgenic plants and including by Plant variety rights protectable or non-protectable plant varieties.
  • Plants are to be understood as meaning all stages of development, such as seeds, cuttings, young (unripe) plants and mature plants.
  • Plant parts are understood to mean all aboveground and subterranean parts and organs of plants such as shoot, leaf, flower and root, examples of which include leaves, needles, stems, stems, flowers, fruiting bodies, fruits and seeds, and roots, tubers and rhizomes.
  • the plant parts also include harvested plants or harvested plant parts as well as vegetative and generative propagation material, for example cuttings, tubers, rhizomes, offshoots and seeds.
  • the treatment according to the invention of the plants and plant parts with the active compound combinations according to the invention is carried out directly or by the action of the compounds on the environment, the Eebensraum or Eagerraum after the usual treatment methods, eg. B. by immersion, spraying, evaporation, nebulization, scattering, brushing, injecting and in propagating material, in particular in seeds, further by single or multi-layer wrapping.
  • plants and their parts can be treated.
  • wild-type or plant species and plant varieties obtained by conventional biological breeding methods such as crossing or protoplast fusion and parts thereof are treated.
  • transgenic plants and plant cultivars obtained by genetic engineering, if appropriate in combination with conventional methods (Genetically Modified Organisms), and parts thereof are treated.
  • the term "parts” or “parts of plants” or “plant parts” has been explained above. It is particularly preferred according to the invention to treat plants of the respective commercially available or in use plant cultivars.
  • Plant varieties are understood as meaning plants having new traits which have been obtained by conventional breeding, by mutagenesis or by recombinant DNA techniques. These may be varieties, breeds, biotypes and genotypes.
  • the preferred plants or plant varieties to be treated according to the invention to be treated include all plants which, as a result of the genetic engineering modification, obtained genetic material which gives these plants particularly advantageous valuable properties ("traits").
  • traits are better plant growth, increased tolerance to high or low temperatures, increased tolerance to dryness or to bottoms salt, increased flowering, easier harvesting, acceleration of ripeness, higher crop yields, higher quality and / or higher nutritional value of the harvested products , higher shelf life and / or workability of the harvested products.
  • Further and particularly emphasized examples of such properties are an increased resistance of the plants against animal and microbial pests, such as insects, arachnids, nematodes, mites, snails, causes z.
  • toxins produced in the plants in particular those produced by the genetic material from Bacillus thuringiensis (eg by the genes CrylA (a), CrylA (b), CrylA (c), CryflA, CrylllA, CryfIIB2, Cry9c Cry2Ab, Cry3Bb and CrylF and their combinations) are produced in the plants, further increased resistance of the plants against plant pathogenic fungi, bacteria and / or viruses, causes z.
  • systemically acquired resistance SAR
  • systemin phytoalexins
  • elicitors elicitors
  • resistance genes and correspondingly expressed proteins and toxins as well as an increased tolerance of the plants to certain herbicidal active compounds, for example imidazolinones, sulfonylureas, glyphosate or phosphinotricin (eg "PAT "-Gene).
  • herbicidal active compounds for example imidazolinones, sulfonylureas, glyphosate or phosphinotricin (eg "PAT "-Gene).
  • PAT phosphinotricin
  • the genes which confer the desired properties can also be present in combinations with one another in the transgenic plants.
  • transgenic plants are the important crops such as cereals (wheat, rice, triticale, barley, rye, oats), corn, soy, potato, sugar beets, sugarcane, tomatoes, peas and other vegetables, cotton, tobacco, oilseed rape, and fruit plants (with the fruits apples, pears, citrus fruits and grapes), with emphasis on corn, soy, wheat, rice, potato, cotton, sugar cane, tobacco and oilseed rape. Traits that are particularly emphasized are the increased resistance of the plants to insects, arachnids, nematodes and snails.
  • the treatment of the plants and plant parts with the active compound combinations according to the invention is carried out directly or by acting on their environment, habitat or storage space according to the usual treatment methods, eg. B. by dipping, spraying, spraying, sprinkling, vaporizing, atomizing, atomizing, scattering, foaming, brushing, spreading, injecting, pouring (drenchen), drip irrigation and propagating material, especially in seeds, further by dry pickling, wet pickling, slurry pickling, encrusting , single or multi-layer encasing, etc. It is also possible to apply the active compound combinations according to the invention by the ultra-low-volume method or to inject the application form or the active compound combinations according to the invention itself into the soil.
  • a preferred direct treatment of the plants is foliar application, i. H. the active compound combinations according to the invention are applied to the foliage, wherein the treatment frequency and the application rate should be matched to the infestation pressure of the respective pest.
  • Active ingredient A at a rate of m g / ha or in a concentration of
  • Y means the degree of killing, expressed in% of the untreated control, when using the active ingredient B in an application rate of n g / ha or in a concentration of n ppm
  • E means the degree of killing, expressed in% of the untreated control, when using the active compounds A and B at application rates of m and n g / ha or in a concentration of m and n ppm,
  • the combination is over-additive in its kill, ie it has a synergistic effect.
  • Emulsifier 2 parts by weight of alkylaryl polyglycol ether To prepare a suitable preparation of active compound, 1 part by weight of active compound is mixed with the stated amounts of solvent and emulsifier, and the concentrate is diluted with water to the desired concentration, whereby the volume of the earth into which it is compressed must also be taken into account. It must be ensured that a concentration of 40 ppm emulsifier is not exceeded in the soil. To prepare further test concentrations, it is diluted with water. Cotton plants (Gossypium hirsutum) in soil pots which are heavily infested with the cotton aphid (Aphis gosypii) are infused with an active compound preparation of the desired concentration.
  • the kill is determined in%. 100% means that all aphids have been killed; 0% means that no aphids have been killed.
  • the determined mortality values are calculated according to the Colby formula.

Landscapes

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

Abstract

The invention relates to the use of active ingredient combinations comprising at least one compound of formula (I) and at least one compound (B) from the classes (1) to (15) listed in the description for controlling animal and microbial pests.

Description

Wirkstoffkombinationen mit fungiziden, insektiziden und akariziden Eigenschaften  Active ingredient combinations with fungicidal, insecticidal and acaricidal properties
Die vorliegende Erfindung betrifft neue Wirkstoffkombinationen, die aus bekannten Verbindungen der Formel (I) einerseits und weiteren bekannten fungiziden Wirkstoffen andererseits bestehen und sehr gut zur Bekämpfung von tierischen und / oder mikrobiellen Schädlingen wie phytopathogenen Pilzen, Insekten und / oder unerwünschten Akariden geeignet sind. The present invention relates to novel drug combinations which consist of known compounds of the formula (I) on the one hand and other known fungicidal active compounds on the other hand and are very suitable for controlling animal and / or microbial pests such as phytopathogenic fungi, insects and / or unwanted acarids.
Die Verbindungen der Formel (I) sind bekannt aus WO 06/089633, dort wird ihre Verwendung zur Bekämpfung tierischer Schädlinge beschrieben. Die Wirksamkeit und / oder Wirkungsbreite und / oder die Pflanzenverträglichkeit dieser Verbindung, insbesondere gegenüber Kulturpflanzen, ist jedoch nicht immer ausreichend. The compounds of the formula (I) are known from WO 06/089633, which describes their use for controlling animal pests. However, the efficacy and / or range of action and / or the plant tolerance of this compound, in particular to crops, is not always sufficient.
Weiterhin bekannt sind Mischungen von Verbindungen der Formel (I) mit anderen Insektiziden und/oder Akariziden, z.Bsp. WO 2009/039951. Also known are mixtures of compounds of formula (I) with other insecticides and / or acaricides, z.Bsp. WO 2009/039951.
Es wurde nun gefunden, dass Wirkstoffkombinationen enthaltend mindestens eine Verbindung der Formel (I), It has now been found that active substance combinations comprising at least one compound of the formula (I)
Figure imgf000002_0001
in welcher
Figure imgf000002_0001
in which
W und Y unabhängig voneinander für Wasserstoff, C | -('4-Alkyl, Chlor, Brom, Jod oder Fluor stehen, W and Y are independently hydrogen, C | - ('4-alkyl, chlorine, bromine, iodine or fluorine,
X für Ct-C^Alkyl, C | -(' [-Alkoxy, Chlor, Brom oder Jod steht, X is Ct-C ^ alkyl, C | - (' [ -alkoxy, chlorine, bromine or iodine,
D für Wasserstoff oder Methyl steht, D is hydrogen or methyl,
A, B und das Kohlenstoffatom, an das sie gebunden sind, für C^-C^-Cycloalkyl stehen, in welchem gegebenenfalls ein Ringglied durch Stickstoff ersetzt ist und welches gegebenenfalls einfach durch Ci-C t-Alkoxy substituiert ist oder A, B and the carbon atom to which they are attached are C ^ -C ^ -cycloalkyl in which optionally one ring member is replaced by nitrogen and which is optionally monosubstituted by C t-C alkoxy, or
A, B und das Kohlenstoffatom, an das sie gebunden sind, für Oj-C^-Cycloalkyl stehen, welches durch eine gegebenenfalls durch C | -(' [-Alkyl oder Ci-C4-Alkoxy-Ci-C2-alkyl-substituierte Alkylendioxyl-Gruppe substituiert ist, die mit dem Kohlenstoffatom, an das sie gebunden ist, ein 5-Ring- oder 6-Ringketal bildet, G für Wasserstoff (a) oder für eine der Gruppen
Figure imgf000003_0001
A, B and the carbon atom to which they are bonded, represent O j -C ^ -cycloalkyl, which by an optionally by C | - is substituted (' [ -alkyl or C 1 -C 4 -alkoxy-C 1 -C 2 -alkyl-substituted alkylenedioxy group which forms a 5-membered or 6-membered ketal with the carbon atom to which it is attached, G is hydrogen (a) or one of the groups
Figure imgf000003_0001
stehen, stand,
in welchen in which
E für ein Metallion oder ein Ammoniumion steht, E is a metal ion or an ammonium ion,
M für Sauerstoff oder Schwefel steht,  M is oxygen or sulfur,
Rl für geradkettigtes oder verzweigtes C^ -Cg- Alkyl steht,  R 1 is straight-chain or branched C 1 -C 8 -alkyl,
für geradkettigtes oder verzweigtes Cj -Cg- Alkyl steht represents straight-chain or branched C j -Cg-alkyl
und mindestens eine weitere Verbindung (B) ausgewählt aus folgenden Gruppen (Klassen): 1) Inhibitoren der Ergosterolbiosynthese, and at least one further compound (B) selected from the following groups (classes): 1) inhibitors of ergosterol biosynthesis,
2) Inhibitoren der Atmungskette an Komplex I oder II,  2) inhibitors of the respiratory chain on complex I or II,
3) Inhibitoren der Atmungskette an Komplex PI,  3) inhibitors of the respiratory chain on complex PI,
4) Inhibitoren von Mitose und Zellteilung,  4) inhibitors of mitosis and cell division,
5) Verbindungen, die an mehreren Stellen wirken können („Multisite Action“),  5) compounds that can act in several places ("multisite action"),
6) Verbindungen, die dazu in der Lage sind, Abwehrreaktionen des Wirtes zu induzieren,6) Compounds capable of inducing host defense responses
7) Inhibitoren von Aminosäure- und/oder Proteinbiosynthese, 7) inhibitors of amino acid and / or protein biosynthesis,
8) Inhibitoren der ATP-Produktion,  8) inhibitors of ATP production,
9) Inhibitoren der Zellwandsynthese,  9) inhibitors of cell wall synthesis,
10) Inhibitoren der Lipid- und Membransynthese,  10) inhibitors of lipid and membrane synthesis,
11) Inhibitoren der Melaninbiosynthese, 11) inhibitors of melanin biosynthesis,
12) Inhibitoren der Nukleinsäuresynthese,  12) inhibitors of nucleic acid synthesis,
13) Inhibitoren der Signalübertragung, 14) Verbindungen, die als Entkoppler wirken können, 13) inhibitors of signal transmission, 14) compounds that can act as decouplers,
15) weitere Fungizide sehr gute fungizide, insektizide und / oder akarizide Eigenschaften besitzen. 15) further fungicides have very good fungicidal, insecticidal and / or acaricidal properties.
Die erfindungegemäßen Wirkstoffkombinationen enthalten in einer Ausführungsform neben mindestens einer der Verbindungen der Formel (I) mindestens eine weitere Verbindung (B) ausgewählt aus folgenden Gruppen (Klassen): In one embodiment, the active compound combinations according to the invention comprise, in addition to at least one of the compounds of the formula (I), at least one further compound (B) selected from the following groups (classes):
1) Inhibitoren der Ergosterolbiosynthese, zum Beispiel (1.001) Cyproconazol, (1.002) Difenoconazol, (1.003) Epoxiconazol, (1.004) Fenhexamid, (1.005) Fenpropidin, (1.006) Fenpropimorph, (1.007) Fenpyrazamin, (1.008) Fluquinconazol, (1.009) Flutriafol, (1.010) hnazalil, (1.011) Imazalilsulfat, (1.012) Ipconazol, (1.013) Metconazol, (1.014) Myclobutanil, (1.015) Paclobutrazol, (1.016) Prochloraz, (1.017) Propiconazol, (1.018) Prothioconazol, (1.019) Pyrisoxazol, (1.020) Spiroxamin, (1.021) Tebuconazol, (1.022) Tetraconazol, (1.023) Triadimenol, (1.024) Tridemorph, (1.025) Triticonazol, ( 1.026) ( lR,2S,5S)-5 -(4-Chlorbenzyl)-2-(chlormethyl)-2-methyl- 1 -( 1 H- 1 ,2,4-triazol- 1 - ylmethyl)cyclopentanol, (1.027) (lS,2R,5R)-5-(4-Chlorbenzyl)-2-(chlormethyl)-2-methyl-l-(lH-l,2,4- triazol-1 -ylmethyl)cyclopentanol, ( 1.028) (2R)-2-( 1 -Chlorcyclopropyl)-4-[( lR)-2,2-dichlorcyclopropyl] - 1 -( 1 H- 1 ,2,4-triazol- 1 -yl)butan-2-ol, ( 1.029) (2R)-2-( 1 -Chlorcyclopropyl)-4-[( 1 S)-2,2-dichlor- cyclopropyl] - 1 -( 1 H- 1 ,2,4-triazol- 1 -yl)butan-2-ol, ( 1.030) (2R)-2-[4-(4-Chlorphenoxy)-2-(trifluor- methyl)phenyl] - 1 -( 1 H- 1 ,2,4-triazol- 1 -yl)propan-2-ol, ( 1.031) (2S)-2-( 1 -Chlorcyclopropyl)-4-[( 1 R)-2,2- dichlorcyclopropyl] - 1 -( 1 H- 1 ,2,4-triazol- 1 -yl)butan-2-ol, ( 1.032) (2S)-2-( 1 -Chlorcyclopropyl)-4- [( 1 S)- 2,2-dichlorcyclopropyl]- 1 -( 1H- 1 ,2,4-triazol- l-yl)butan-2-ol, ( 1.033) (2S)-2-[4-(4-Chlorphenoxy)-2-1) inhibitors of ergosterol biosynthesis, for example (1,001) cyproconazole, (1,002) difenoconazole, (1,003) epoxiconazole, (1,004) fenhexamide, (1,005) fenpropidin, (1,006) fenpropimorph, (1,007) fenpyrazamine, (1,008) fluquinconazole, (1.009 ) Flutriafol, (1,010) hnazalil, (1,011) imazalil sulfate, (1,012) ipconazole, (1,013) metconazole, (1,014) myclobutanil, (1,015) paclobutrazole, (1,016) prochloraz, (1,017) propiconazole, (1,018) prothioconazole, (1,019 ) Pyrisoxazole, (1,020) spiroxamine, (1,021) tebuconazole, (1,022) tetraconazole, (1,023) triadimenol, (1,024) tridemorph, (1,025) triticonazole, (1,026) (IR, 2S, 5S) -5 - (4-chlorobenzyl ) -2- (chloromethyl) -2-methyl-1- (1H-1,2,4-triazol-1-ylmethyl) cyclopentanol, (1.027) (IS, 2R, 5R) -5- (4-chlorobenzyl) -2- (chloromethyl) -2-methyl-1- (1H-l, 2,4-triazol-1-ylmethyl) cyclopentanol, (1.028) (2R) -2- (1-chlorocyclopropyl) -4 - [(lR 2,2,2-dichlorocyclopropyl] -1- (1H-1,2,4-triazol-1-yl) butan-2-ol, (1029) (2R) -2- (1-chlorocyclopropyl) -4- [(1S) -2,2-dichloro cyclopropyl] - 1 - (1H-1,2,4-triazol-1-yl) butan-2-ol, (1.030) (2R) -2- [4- (4-chlorophenoxy) -2- (trifluoro- methyl) phenyl] -1- (1H-1,2,4-triazol-1-yl) -propan-2-ol, (1.031) (2S) -2- (1-chlorocyclopropyl) -4 - [(1R ) -2,2-dichlorocyclopropyl] -1 - (1H-1,2,4-triazol-1-yl) butan-2-ol, (1032) (2S) -2- (1-chlorocyclopropyl) -4- [(1S) -2,2-dichlorocyclopropyl] -1- (1H-1,2,4-triazol-1-yl) butan-2-ol, (1033) (2S) -2- [4- (4 -Chlorphenoxy) -2-
(trifluormethyl)phenyl] - 1 -( 1 H- 1 ,2,4-triazol- 1 -yl)propan-2-ol, ( 1.034) (R)- [3-(4-Chlor-2-fluorphenyl)-5 - (2,4-difluorphenyl)-l,2-oxazol-4-yl](pyridin-3-yl)methanol, (1.035) (S)-[3-(4-Chlor-2-fluorphenyl)-5- (2,4-difluorphenyl)-l,2-oxazol-4-yl](pyridin-3-yl)methanol, (1.036) [3-(4-Chlor-2-fluorphenyl)-5-(2,4- difluorphenyl)- 1 ,2-oxazol-4-yl] (pyridin-3-yl)methanol, ( 1.037) 1 -( { (2R,4S)-2-[2-Chlor-4-(4- chlorphenoxy)phenyl] -4-methyl- 1 ,3-dioxolan-2-yl Jmethyl)- 1 H- 1 ,2,4-triazol, ( 1.038) 1 -( { (2S,4S)-2- [2- Chlor-4-(4-chlorphenoxy)phenyl] -4-methyl- 1 ,3-dioxolan-2-yl } methyl)- 1 H- 1 ,2,4-triazol, ( 1.039) 1 - { [3- (2-Chlorphenyl)-2-(2,4-difluorphenyl)oxiran-2-yl] methyl } - 1 H- 1 ,2,4-triazol -5 -ylthiocyanat, ( 1.040) 1 - { [rel(2R,3R)-3-(2-Chlorphenyl)-2-(2,4-difluorphenyl)oxiran-2-yl]methyl}-lH-l,2,4-triazol-5- ylthiocyanat, ( 1.041 ) 1 - { [rel(2R,3S)-3-(2-Chlorphenyl)-2-(2,4-difluorphenyl)oxiran-2-yl] methyl } - 1 H- 1 ,2,4-triazol -5 -ylthiocyanat, ( 1.042) 2- [(2R,4R,5R)- 1 -(2,4-Dichlorphenyl)-5 -hydroxy-2,6,6- trimethylheptan-4-yl]-2,4-dihydro-3H-l,2,4-triazol-3-thion, (1.043) 2-[(2R,4R,5S)-l-(2,4-(trifluoromethyl) phenyl] -1- (1H-1,2,4-triazol-1-yl) propan-2-ol, (1034) (R) - [3- (4-Chloro-2-fluorophenyl) - 5 - (2,4-difluorophenyl) -1,2-oxazol-4-yl] (pyridin-3-yl) methanol, (1.035) (S) - [3- (4-chloro-2-fluorophenyl) -5 - (2,4-difluorophenyl) -1,2-oxazol-4-yl] (pyridin-3-yl) methanol, (1.036) [3- (4-chloro-2-fluorophenyl) -5- (2,4 (difluorophenyl) -1,2-oxazol-4-yl] (pyridin-3-yl) methanol, (1.037) 1 - ({(2R, 4S) -2- [2-chloro-4- (4-chlorophenoxy) phenyl] -4-methyl-1,3-dioxolan-2-yl-methyl) -1 H -1, 2,4-triazole, (1038) 1 - ({(2S, 4S) -2- [2-chloro 4- (4-chlorophenoxy) phenyl] -4-methyl-1,3-dioxolan-2-yl} methyl) -1 H -1, 2,4-triazole, (1.039) 1 - {[3- (2- Chlorophenyl) -2- (2,4-difluorophenyl) oxiran-2-yl] methyl} -1H-1,2,4-triazole-5-thyl-thiocyanate, (1040) 1 - {[rel (2R, 3R) - 3- (2-chlorophenyl) -2- (2,4-difluorophenyl) oxiran-2-yl] methyl} -1H-l, 2,4-triazol-5-ylthiocyanate, (1.041) 1 - {[rel (2R , 3S) -3- (2-chlorophenyl) -2- (2,4-difluorophenyl) oxiran-2-yl] methyl} -1H-1,2,4-triazole-5-thyl-thiocyanate, (1.04 2) 2- [(2R, 4R, 5R) -1- (2,4-dichlorophenyl) -5-hydroxy-2,6,6-trimethylheptan-4-yl] -2,4-dihydro-3H-1, 2,4-triazole-3-thione, (1043) 2 - [(2R, 4R, 5S) -l- (2,4-)
Dichlorphenyl)-5-hydroxy-2,6,6-trimethylheptan-4-yl]-2,4-dihydro-3H-l,2,4-triazol-3-thion, (1.044) 2- [(2R,4S,5R)-l-(2,4-Dichlorphenyl)-5-hydroxy-2,6,6-trimethylheptan-4-yl]-2,4-dihydro-3H-l,2,4-triazol- 3-thion, (1.045) 2-[(2R,4S,5S)-l-(2,4-Dichlorphenyl)-5-hydroxy-2,6,6-trimethylheptan-4-yl]-2,4- dihydro-3H-l,2,4-triazol-3-thion, (1.046) 2-[(2S,4R,5R)-l-(2,4-Dichlorphenyl)-5-hydroxy-2,6,6- trimethylheptan-4-yl] -2,4-dihydro-3H- 1 ,2,4-triazol-3-thion, ( 1.047) 2- [(2S,4R,5S)- 1 -(2,4-Dichlorophenyl) -5-hydroxy-2,6,6-trimethylheptan-4-yl] -2,4-dihydro-3H-l, 2,4-triazole-3-thione, (1.044) 2- [(2R, 4S , 5R) -1- (2,4-dichlorophenyl) -5-hydroxy-2,6,6-trimethylheptan-4-yl] -2,4-dihydro-3H-1,2,4-triazole-3-thione , (1.045) 2 - [(2R, 4S, 5S) -1- (2,4-dichlorophenyl) -5-hydroxy-2,6,6-trimethylheptan-4-yl] -2,4-dihydro-3H- l, 2,4-triazole-3-thione, (1.046) 2 - [(2S, 4R, 5R) -1- (2,4-dichlorophenyl) -5-hydroxy-2,6,6- trimethylheptan-4-yl] -2,4-dihydro-3H-1,2,4-triazole-3-thione, (1047) 2- [(2S, 4R, 5S) -1- (2,4-)
Dichlorphenyl)-5-hydroxy-2,6,6-trimethylheptan-4-yl]-2,4-dihydro-3H-l,2,4-triazol-3-thion, (1.048) 2- [(2S,4S,5R)-l-(2,4-Dichlorphenyl)-5-hydroxy-2,6,6-trimethylheptan-4-yl]-2,4-dihydro-3H-l,2,4-triazol-Dichlorophenyl) -5-hydroxy-2,6,6-trimethylheptan-4-yl] -2,4-dihydro-3H-l, 2,4-triazole-3-thione, (1048) 2- [(2S, 4S , 5R) -l- (2,4-dichlorophenyl) -5-hydroxy-2,6,6-trimethylheptane-4-yl] -2,4-dihydro-3H-l, 2,4-triazol-
3-thion, (1.049) 2-[(2S,4S,5S)-l-(2,4-Dichlorphenyl)-5-hydroxy-2,6,6-trimethylheptan-4-yl]-2,4- dihydro-3H-l,2,4-triazol-3-thion, (1.050) 2-[l-(2,4-Dichlorphenyl)-5-hydroxy-2,6,6-trimethylheptan-4- yl] -2,4-dihydro-3H- 1 ,2,4-triazol-3-thion, ( 1.051 ) 2-[2-Chlor-4-(2,4-dichlorphenoxy)phenyl] - 1 -( 1 H-3-thione, (1.049) 2 - [(2S, 4S, 5S) -1- (2,4-dichlorophenyl) -5-hydroxy-2,6,6-trimethylheptan-4-yl] -2,4-dihydro -3H-l, 2,4-triazole-3-thione, (1050) 2- [1- (2,4-dichlorophenyl) -5-hydroxy-2,6,6-trimethylheptan-4-yl] -2, 4-dihydro-3H-1,2,4-triazole-3-thione, (1.051) 2- [2-chloro-4- (2,4-dichlorophenoxy) phenyl] -1 - (1H-
1.2.4-triazol- 1 -yl)propan-2-ol, ( 1.052) 2-[2-Chlor-4-(4-chlorphenoxy)phenyl] - 1 -( 1 H- 1 ,2,4-triazol- 1 - yl)butan-2-ol, ( 1.053) 2- [4-(4-Chlorphenoxy)-2-(trifluormethyl)phenyl] - 1 -( 1 H- 1 ,2,4-triazol- 1 -yl)butan- 2-ol, ( 1.054) 2-[4-(4-Chlorphenoxy)-2-(trifluormethyl)phenyl] - 1 -( 1 H- 1 ,2,4-triazol- 1 -yl)pentan-2-ol, ( 1.055) 2- [4-(4-Chlorphenoxy)-2-(trifluormethyl)phenyl] - 1 -( 1 H- 1 ,2,4-triazol- 1 -yl)propan-2-ol, ( 1.056)1,2,4-triazol-1-yl) propan-2-ol, (1.052) 2- [2-chloro-4- (4-chlorophenoxy) phenyl] -1- (1H-1, 2,4-triazole) 1-yl) butan-2-ol, (1.053) 2- [4- (4-chlorophenoxy) -2- (trifluoromethyl) phenyl] -1- (1H-1,2,4-triazol-1-yl) butan-2-ol, (1.054) 2- [4- (4-chlorophenoxy) -2- (trifluoromethyl) phenyl] -1- (1H-1,2,4-triazol-1-yl) pentan-2-one ol, (1.055) 2- [4- (4-chlorophenoxy) -2- (trifluoromethyl) phenyl] -1- (1H-1,2,4-triazol-1-yl) propan-2-ol, (1.056 )
2-{ [3-(2-Chlorphenyl)-2-(2,4-difluorphenyl)oxiran-2-yl]methyl}-2,4-dihydro-3H-l,2,4-triazol-3-thion, (1.057) 2-{ [rel(2R,3R)-3-(2-Chlorphenyl)-2-(2,4-difluorphenyl)oxiran-2-yl]methyl}-2,4-dihydro-3H-2- {[3- (2-chlorophenyl) -2- (2,4-difluorophenyl) oxiran-2-yl] methyl} -2,4-dihydro-3H-l, 2,4-triazole-3-thione, (1.057) 2- {[rel (2R, 3R) -3- (2-chlorophenyl) -2- (2,4-difluorophenyl) oxiran-2-yl] methyl} -2,4-dihydro-3H-
1.2.4-triazol-3-thion, (1.058) 2-{ [rel(2R,3S)-3-(2-Chlorphenyl)-2-(2,4-difluorphenyl)oxiran-2- yl]methyl}-2,4-dihydro-3H-l,2,4-triazol-3-thion, (1.059) 5-(4-Chlorbenzyl)-2-(chlormethyl)-2-methyl-l- ( 1 H- 1 ,2,4-triazol- 1 -ylmethyl)cyclopentanol, ( 1.060) 5-( Allylsulfanyl)- 1 - { [3-(2-chlorphenyl)-2-(2,4- difluorphenyl)oxiran-2-yl] methyl } - 1H- 1 ,2,4-triazol, ( 1.061) 5-(Allylsulfanyl)- 1 - { [rel(2R,3R)-3-(2- chlorphenyl)-2-(2,4-difluorphenyl)oxiran-2-yl]methyl } - 1 H- 1 ,2,4-triazol, ( 1.062) 5 -(Allylsulfanyl)- 1 - { [rel(2R,3S)-3-(2-chlorphenyl)-2-(2,4-difluorphenyl)oxiran-2-yl]methyl}-lH-l,2,4-triazol, (1.063) N'- (2,5-Dimethyl-4-{ [3-(l,l,2,2-tetrafluorethoxy)phenyl]sulfanyl}phenyl)-N-ethyl-N-methylimidoform- amid, (1.064) N'-(2,5-Dimethyl-4-{ [3-(2,2,2-trifluorethoxy)phenyl]sulfanyl}phenyl)-N-ethyl-N- methylimidoformamid, (1.065) N'-(2,5-Dimethyl-4-{ [3-(2,2,3,3-tetrafluorpropoxy)phenyl]- sulfanyl}phenyl)-N-ethyl-N-methylimidoformamid, (1.066) N'-(2,5-Dimethyl-4-{ [3-(pentafluorethoxy)- phenyl] sulfanyl } phenyl) -N-ethyl-N-methylimidoformamid, ( 1.067) N'-(2,5 -Dimethyl-4- { 3- [( 1 , 1 ,2,2- tetrafluorethyl)sulfanyl]phenoxy }phenyl)-N-ethyl-N-methylimidoformamid, (1.068) N'-(2,5-Dimethyl-1,2,4-triazole-3-thione, (1.058) 2- {[rel (2R, 3S) -3- (2-chlorophenyl) -2- (2,4-difluorophenyl) oxiran-2-yl] methyl} - 2,4-dihydro-3H-l, 2,4-triazole-3-thione, (1.059) 5- (4-chlorobenzyl) -2- (chloromethyl) -2-methyl-1- (1H-1,2-dione) , 4-triazol-1-ylmethyl) cyclopentanol, (1.060) 5- (allylsulfanyl) -1 - {[3- (2-chlorophenyl) -2- (2,4-difluorophenyl) oxiran-2-yl] methyl} - 1H-1,2,4-triazole, (1.061) 5- (allylsulfanyl) -1 - {[rel (2R, 3R) -3- (2-chlorophenyl) -2- (2,4-difluorophenyl) oxirane-2 -yl] methyl} -1 H -1, 2,4-triazole, (1.062) 5 - (allylsulfanyl) -1 - {[rel (2R, 3S) -3- (2-chlorophenyl) -2- (2, 4-difluorophenyl) oxiran-2-yl] methyl} -1H-l, 2,4-triazole, (1.063) N '- (2,5-dimethyl-4- {[3- (1,1,2,2 tetrafluoroethoxy) phenyl] sulfanyl} phenyl) -N-ethyl-N-methylimidoformamide, (1.064) N '- (2,5-dimethyl-4- {[3- (2,2,2-trifluoroethoxy) phenyl] sulfanyl} phenyl) -N-ethyl-N-methylimidoformamide, (1.065) N '- (2,5-dimethyl-4- {[3- (2,2,3,3-tetrafluoropropoxy) phenyl] sulfanyl} phenyl) -N-ethyl-N-methylimidoformamide, (1.066) N '- (2,5-dimethyl-4- {[3- (pe ntafluoroethoxy) - phenyl] sulfanyl} phenyl) -N-ethyl-N-methylimidoformamide, (1.067) N '- (2,5-dimethyl-4- {3- [(1,1,2,2-tetrafluoroethyl) sulfanyl] phenoxy} phenyl) -N-ethyl-N-methylimidoformamide, (1.068) N '- (2,5-dimethyl-
4-{3-[(2,2,2-trifluorethyl)sulfanyl]phenoxy}phenyl)-N-ethyl-N-methylimidoformamid, (1.069) N'-(2,5-4- {3 - [(2,2,2-trifluoroethyl) sulfanyl] phenoxy} phenyl) -N-ethyl-N-methylimidoformamide, (1.069) N '- (2.5-
Dimethyl-4-{3-[(2,2,3,3-tetrafluorpropyl)sulfanyl]phenoxy}phenyl)-N-ethyl-N-methylimidoformamid, (1.070) N'-(2,5-Dimethyl-4-{3-[(pentafluorethyl)sulfanyl]phenoxy}phenyl)-N-ethyl-N- methylimidoformamid, (1.071) N'-(2,5-Dimethyl-4-phenoxyphenyl)-N-ethyl-N-methylimidoformamid, ( 1.072) N'-(4- { [3-(Difluormethoxy)phenyl] sulfanyl } -2,5-dimethylphenyl)-N-ethyl-N- methylimidoformamid, (1.073) N'-(4-{3-[(Difluormethyl)sulfanyl]phenoxy}-2,5-dimethylphenyl)-N- ethyl-N-methylimidoformamid, (1.074) N'-[5-Brom-6-(2,3-dihydro-lH-inden-2-yloxy)-2-methylpyridin-Dimethyl 4- {3 - [(2,2,3,3-tetrafluoropropyl) sulfanyl] phenoxy} phenyl) -N-ethyl-N-methylimidoformamide, (1.070) N '- (2,5-dimethyl-4- { 3 - [(pentafluoroethyl) sulfanyl] phenoxy} phenyl) -N-ethyl-N-methylimidoformamide, (1.071) N '- (2,5-dimethyl-4-phenoxyphenyl) -N-ethyl-N-methylimidoformamide, (1.072) N '- (4- {[3- (Difluoromethoxy) phenyl] sulfanyl} -2,5-dimethylphenyl) -N-ethyl-N-methylimidoformamide, (1.073) N' - (4- {3 - [(Difluoromethyl) sulfanyl ] phenoxy} -2,5-dimethylphenyl) -N-ethyl-N-methylimidoformamide, (1.074) N '- [5-bromo-6- (2,3-dihydro-1H-inden-2-yloxy) -2- methylpyridine
3-yl]-N-ethyl-N-methylimidoformamid, (1.075) N'-{4-[(4,5-Dichlor-l,3-thiazol-2-yl)oxy]-2,5- dimethylphenyl} -N-ethyl-N-methylimidoformamid, (1.076) N'-{5-Brom-6-[(lR)-l-(3,5-difluorphenyl)- ethoxy] -2-methylpyridin-3-yl } -N-ethyl-N-methylimidoformamid, ( 1.077) N'- { 5 -Brom-6-[( 1 S)-l-(3,5- difluorphenyl)ethoxy]-2-methylpyridin-3-yl }-N-ethyl-N-methylimidoformamid, ( 1.078) N'- {5-Brom-6- [(cis-4-isopropylcyclohexyl)oxy]-2-methylpyridin-3-yl}-N-ethyl-N-methylimidoformamid, (1.079) N'- {5-Brom-6-[(trans-4-isopropylcyclohexyl)oxy]-2-methylpyridin-3-yl}-N-ethyl-N- methylimidoformamid, ( 1.080) N'- { 5-Brom-6-[ 1 -(3,5-difluorphenyl)ethoxy]-2-methylpyridin-3-yl}-N- ethyl-N-methylimidoformamid, (1.081) Mefentrifluconazol, (1.082) Ipfentrifluconazol. 3-yl] -N-ethyl-N-methylimidoformamide, (1.075) N '- {4 - [(4,5-dichloro-l, 3-thiazol-2-yl) oxy] -2,5-dimethylphenyl} - N-ethyl-N-methylimidoformamide, (1.076) N '- {5-bromo-6 - [(1R) -l- (3,5-difluorophenyl) -ethoxy] -2-methylpyridin-3-yl} -N- ethyl N -methylimidoformamide, (1.077) N '- {5-bromo-6 - [(1S) -1- (3,5-difluorophenyl) ethoxy] -2-methylpyridin-3-yl} -N-ethyl- N-methylimidoformamide, (1.078) N '- {5-bromo-6- [(cis-4-isopropylcyclohexyl) oxy] -2-methylpyridin-3-yl} -N-ethyl-N-methylimidoformamide, (1.079) N' - {5-bromo-6 - [(trans-4-isopropylcyclohexyl) oxy] -2-methylpyridin-3-yl} -N-ethyl-N- methylimidoformamide, (1080) N '- {5-bromo-6- [1- (3,5-difluorophenyl) ethoxy] -2-methylpyridin-3-yl} -N-ethyl-N-methylimidoformamide, (1,081) mefentrifluconazole, (1,082) Ipfentrifluconazole.
2) Inhibitoren der Atmungskette an Komplex I oder P, zum Beispiel (2.001) Benzovindiflupyr, (2.002) Bixafen, (2.003) Boscalid, (2.004) Carboxin, (2.005) Fluopyram, (2.006) Flutolanil, (2.007) Fluxapyroxad, (2.008) Furametpyr, (2.009) Isofetamid, (2.010) Isopyrazam (anti-epimeres Enantiomer 1R,4S,9S), (2.011) Isopyrazam (anti-epimeres Enantiomer 1S,4R,9R), (2.012) Isopyrazam (anti epimeres Racemat 1RS,4SR,9SR), (2.013) Isopyrazam (Mischung von syn-epimerem Racemat 1RS,4SR,9RS und anti-epimerem Racemat 1RS,4SR,9SR), (2.014) Isopyrazam (syn-epimeres Enantiomer 1R,4S,9R), (2.015) Isopyrazam (syn-epimeres Enantiomer 1S,4R,9S), (2.016) Isopyrazam (syn-epimeres Racemat 1RS,4SR,9RS), (2.017) Penflufen, (2.018) Penthiopyrad, (2.019)2) respiratory chain inhibitors on complex I or P, for example (2,001) benzovindiflupyr, (2,002) bixafen, (2,003) boscalid, (2,004) carboxin, (2,005) fluopyram, (2,006) flutolanil, (2,007) fluxapyroxad, (2,008 ) Furametpyr, (2.009) isofetamide, (2.010) isopyrazam (anti-epimeric enantiomer 1R, 4S, 9S), (2.011) isopyrazam (anti-epimeric enantiomer 1S, 4R, 9R), (2.012) isopyrazam (anti-epimeric racemate 1RS, 4SR, 9SR), (2.013) isopyrazam (mixture of syn-epimeric racemate 1RS, 4SR, 9RS and anti-epimeric racemate 1RS, 4SR, 9SR), (2.014) isopyrazam (syn-epimeric enantiomer 1R, 4S, 9R), ( 2.015) isopyrazam (syn-epimeric enantiomer 1S, 4R, 9S), (2.016) isopyrazam (syn-epimeric racemate 1RS, 4SR, 9RS), (2.017) penflufen, (2.018) penthiopyrad, (2.019)
Pydiflumetofen, (2.020) Pyraziflumid, (2.021) Sedaxan, (2.022) l,3-Dimethyl-N-(l,l,3-trimethyl-2,3- dihydro-lH-inden-4-yl)-lH-pyrazol-4-carboxamid, (2.023) l,3-Dimethyl-N-[(3R)-l,l,3-trimethyl-2,3- dihydro-lH-inden-4-yl]-lH-pyrazol-4-carboxamid, (2.024) l,3-Dimethyl-N-[(3S)-l,l,3-trimethyl-2,3- dihydro-lH-inden-4-yl]-lH-pyrazol-4-carboxamid, (2.025) l-Methyl-3-(trifluormethyl)-N-[2'- (trifluormethyl)biphenyl-2-yl] - lH-pyrazol-4-carboxamid, (2.026) 2-Fluor-6-(trifluormethyl)-N-(l , 1 ,3- trimethyl-2,3-dihydro-lH-inden-4-yl)benzamid, (2.027) 3-(Difluormethyl)-l-methyl-N-(l,l,3-trimethyl-Pydiflumetofen, (2,020) pyrazolium, (2,021) sedaxane, (2,022) 1,3-dimethyl-N- (1,1,3-trimethyl-2,3-dihydro-1H-inden-4-yl) -1H-pyrazole 4-carboxamide, (2.023) l, 3-dimethyl-N - [(3R) -l, l, 3-trimethyl-2,3-dihydro-1H-inden-4-yl] -1H-pyrazole-4 carboxamide, (2.024) 1,3-dimethyl-N - [(3S) -1,1,3-trimethyl-2,3-dihydro-1H-inden-4-yl] -1H-pyrazole-4-carboxamide, ( 2.025) 1-methyl-3- (trifluoromethyl) -N- [2'- (trifluoromethyl) biphenyl-2-yl] -1H-pyrazole-4-carboxamide, (2.026) 2-fluoro-6- (trifluoromethyl) -N (l, 1, 3-trimethyl-2,3-dihydro-1H-inden-4-yl) benzamide, (2.027) 3- (difluoromethyl) -1-methyl-N- (1, 1, 3-trimethyl-
2.3-dihydro-lH-inden-4-yl)-lH-pyrazol-4-carboxamid, (2.028) 3-(Difluormethyl)-l-methyl-N-[(3R)-2,3-dihydro-1H-inden-4-yl) -1H-pyrazole-4-carboxamide, (2.028) 3- (difluoromethyl) -1-methyl-N - [(3R) -
1.1.3-trimethyl-2,3 -dihydro- 1 H-inden-4-yl] - 1 H-pyrazol-4-carboxamid, (2.029) 3 -(Difluormethyl) - 1 - methyl-N-[(3S)-l,l,3-trimethyl-2,3-dihydro-lH-inden-4-yl]-lH-pyrazol-4-carboxamid, (2.030) 3-1,1,3-trimethyl-2,3-dihydro-1H-inden-4-yl] - 1H-pyrazole-4-carboxamide, (2.029) 3 - (difluoromethyl) -1-methyl-N - [(3S) -l, l, 3-trimethyl-2,3-dihydro-1H-inden-4-yl] -1H-pyrazole-4-carboxamide, (2.030) 3-
(Difluormethyl)-N-(7-fluor-l,l,3-trimethyl-2,3-dihydro-lH-inden-4-yl)-l-methyl-lH-pyrazol-4- carboxamid, (2.031) 3-(Difluormethyl)-N-[(3R)-7-fluor-l,l,3-trimethyl-2,3-dihydro-lH-inden-4-yl]-l- methyl-lH-pyrazol-4-carboxamid, (2.032) 3-(Difluormethyl)-N-[(3S)-7-fluor-l,l,3-trimethyl-2,3- dihydro-lH-inden-4-yl]-l-methyl-lH-pyrazol-4-carboxamid, (2.033) 5,8-Difluor-N-[2-(2-fluor-4-{ [4- (trifluormethyl)pyridin-2-yl]oxy}phenyl)ethyl]chinazolin-4-amin, (2.034) N-(2-Cyclopentyl-5- fluorbenzyl)-N-cyclopropyl-3-(difluormethyl)-5-fluor-l-methyl-lH-pyrazol-4-carboxamid, (2.035) N- (2-tert.-Butyl-5-methylbenzyl)-N-cyclopropyl-3-(difluormethyl)-5-fluor-l-methyl-lH-pyrazol-4- carboxamid, (2.036) N-(2-tert.-Butylbenzyl)-N-cyclopropyl-3-(difluormethyl)-5-fluor-l-methyl-lH- pyrazol-4-carboxamid, (2.037) N-(5-Chlor-2-ethylbenzyl)-N-cyclopropyl-3-(difluormethyl)-5-fluor-l- methyl-lH-pyrazol-4-carboxamid, (2.038) N-(5-Chlor-2-isopropylbenzyl)-N-cyclopropyl-3-(difluor- methyl)-5-fluor-l-methyl-lH-pyrazol-4-carboxamid, (2.039) N-[(lR,4S)-9-(Dichlormethylen)-l,2,3,4- tetrahydro-l,4-methanonaphthalin-5-yl]-3-(difluormethyl)-l-methyl-lH-pyrazol-4-carboxamid, (2.040) N-[(lS,4R)-9-(Dichlormethylen)-l,2,3,4-tetrahydro-l,4-methanonaphthalin-5-yl]-3-(difluormethyl)-l- methyl- lH-pyrazol-4-carboxamid, (2.041) N-[l -(2,4-Dichlorphenyl)- 1 -methoxypropan-2-yl] -3-(Difluoromethyl) -N- (7-fluoro-1,1,3-trimethyl-2,3-dihydro-1H-inden-4-yl) -1-methyl-1H-pyrazole-4-carboxamide, (2.031) 3 - (Difluoromethyl) - N - [(3R) -7-fluoro-1,1,3-trimethyl-2,3-dihydro-1H-inden-4-yl] -1-methyl-1H-pyrazole-4-carboxamide , (2.032) 3- (difluoromethyl) -N - [(3S) -7-fluoro-1,1,3-trimethyl-2,3-dihydro-1H-inden-4-yl] -l-methyl-1H pyrazole-4-carboxamide, (2.033) 5,8-difluoro-N- [2- (2-fluoro-4- {[4- (trifluoromethyl) pyridin-2-yl] oxy} phenyl) ethyl] quinazoline-4 amine, (2.034) N- (2-cyclopentyl-5-fluorobenzyl) -N-cyclopropyl-3- (difluoromethyl) -5-fluoro-1-methyl-1H-pyrazole-4-carboxamide, (2.035) N- (2 tert -butyl-5-methylbenzyl) -N-cyclopropyl-3- (difluoromethyl) -5-fluoro-1-methyl-1H-pyrazole-4-carboxamide, (2.036) N- (2-tert-butylbenzyl) -N-cyclopropyl-3- (difluoromethyl) -5-fluoro-1-methyl-1H-pyrazole-4-carboxamide, (2.037) N- (5-chloro-2-ethylbenzyl) -N-cyclopropyl-3- (difluoromethyl ) -5-fluoro-1-methyl-1H-pyrazole-4-carboxamide, (2.038) N- (5-chloro-2-isopropylbenzyl) -N-cyclopropyl-3- (difluoro-methyl) -5-fluoro-1 methyl-lH-pyrazol- 4-carboxamide, (2.039) N - [(IR, 4S) -9- (dichloromethylene) -l, 2,3,4-tetrahydro-1,4-methanonaphthalen-5-yl] -3- (difluoromethyl) -l -methyl-1H-pyrazole-4-carboxamide, (2.040) N - [(IS, 4R) -9- (dichloromethylene) -1,3,3,4-tetrahydro-1,4-methanonaphthalen-5-yl] - 3- (difluoromethyl) -1-methyl-1H-pyrazole-4-carboxamide, (2.041) N- [1- (2,4-dichlorophenyl) -1-methoxypropan-2-yl] -3-
(difluormethyl)-l-methyl-lH-pyrazol-4-carboxamid, (2.042) N-[2-Chlor-6-(trifluormethyl)benzyl]-N- cyclopropyl-3-(difluormethyl)-5-fluor-l-methyl-lH-pyrazol-4-carboxamid, (2.043) N-[3-Chlor-2-fluor- 6-(trifluormethyl)benzyl]-N-cyclopropyl-3-(difluormethyl)-5-fluor-l-methyl-lH-pyrazol-4-carboxamid, (2.044) N-[5-Chlor-2-(trifluormethyl)benzyl]-N-cyclopropyl-3-(difluormethyl)-5-fluor-l-methyl-lH- pyrazol-4-carboxamid, (2.045) N-Cyclopropyl-3-(difluormethyl)-5-fluor-l-methyl-N-[5-methyl-2- (trifluormethyl)benzyl]-lH-pyrazol-4-carboxamid, (2.046) N-Cyclopropyl-3-(difluormethyl)-5-fluor-N- (2-fluor-6-isopropylbenzyl) - 1 -methyl- 1 H-pyrazol-4-carboxamid, (2.047) N -Cyclopropyl-3 -(difluoromethyl) -1-methyl-1H-pyrazole-4-carboxamide, (2.042) N- [2-chloro-6- (trifluoromethyl) benzyl] -N-cyclopropyl-3- (difluoromethyl) -5-fluoro-1-one methyl-1H-pyrazole-4-carboxamide, (2.043) N- [3-chloro-2-fluoro-6- (trifluoromethyl) benzyl] -N-cyclopropyl-3- (difluoromethyl) -5-fluoro-1-methyl- 1H-pyrazole-4-carboxamide, (2.044) N- [5-chloro-2- (trifluoromethyl) benzyl] -N-cyclopropyl-3- (difluoromethyl) -5-fluoro-1-methyl-1H- pyrazole-4-carboxamide, (2.045) N-cyclopropyl-3- (difluoromethyl) -5-fluoro-1-methyl-N- [5-methyl-2- (trifluoromethyl) benzyl] -1H-pyrazole-4-carboxamide, (2.046) N-Cyclopropyl-3- (difluoromethyl) -5-fluoro-N- (2-fluoro-6-isopropylbenzyl) -1-methyl-1H-pyrazole-4-carboxamide, (2.047) N -cyclopropyl-3 -
(difluormethyl)-5-fluor-N-(2-isopropyl-5-methylbenzyl)-l-methyl-lH-pyrazol-4-carboxamid, (2.048) N- Cyclopropyl-3-(difluormethyl)-5-fluor-N-(2-isopropylbenzyl)-l-methyl-lH-pyrazol-4-carbothioamid, (2.049) N-Cyclopropyl-3-(difluormethyl)-5-fluor-N-(2-isopropylbenzyl)-l-methyl-lH-pyrazol-4- carboxamid, (2.050) N-Cyclopropyl-3-(difluormethyl)-5-fluor-N-(5-fluor-2-isoprc>pylbenzyl)-l -methyl- lH-pyrazol-4-carboxamid, (2.051) N-Cyclopropyl-3-(difluormethyl)-N-(2-ethyl-4,5-dimethylbenzyl)-5- fluor-1 -methyl- lH-pyrazol-4-carboxamid, (2.052) N-Cyclopropyl-3-(difluormethyl)-N-(2-ethyl-5- fluorbenzyl)-5-fluor-l-methyl-lH-pyrazol-4-carboxamid, (2.053) N-Cyclopropyl-3-(difluormethyl)-N- (2-ethyl-5-methylbenzyl)-5-fluor-l-methyl-lH-pyrazol-4-carboxamid, (2.054) N-Cyclopropyl-N-(2- cyclopropyl-5-fluorbenzyl)-3-(difluormethyl)-5-fluor-l-methyl-lH-pyrazol-4-carboxamid, (2.055) N- Cyclopropyl-N-(2-cyclopropyl-5-methylbenzyl)-3-(difluormethyl)-5-fluor-l -methyl- lH-pyrazol-4- carboxamid, (2.056) N-Cyclopropyl-N-(2-cyclopropylbenzyl)-3-(difluormethyl)-5-fluor-l-methyl-lH- pyrazol-4-carboxamid. (difluoromethyl) -5-fluoro-N- (2-isopropyl-5-methylbenzyl) -l-methyl-1H-pyrazole-4-carboxamide, (2.048) N-cyclopropyl-3- (difluoromethyl) -5-fluoro-N - (2-isopropylbenzyl) -1-methyl-1H-pyrazole-4-carbothioamide, (2.049) N-cyclopropyl-3- (difluoromethyl) -5-fluoro-N- (2-isopropylbenzyl) -l-methyl-1H- pyrazole-4-carboxamide, (2.050) N-cyclopropyl-3- (difluoromethyl) -5-fluoro-N- (5-fluoro-2-isopropylbenzyl) -1-methyl-1H-pyrazole-4-carboxamide, ( 2.051) N-Cyclopropyl-3- (difluoromethyl) -N- (2-ethyl-4,5-dimethylbenzyl) -5-fluoro-1-methyl-1H-pyrazole-4-carboxamide, (2.052) N-cyclopropyl-3 - (difluoromethyl) - N - (2-ethyl-5-fluorobenzyl) -5-fluoro-1-methyl-1H-pyrazole-4-carboxamide, (2.053) N-cyclopropyl-3- (difluoromethyl) -N- (2 -ethyl-5-methylbenzyl) -5-fluoro-1-methyl-1H-pyrazole-4-carboxamide, (2.054) N-cyclopropyl-N- (2-cyclopropyl-5-fluorobenzyl) -3- (difluoromethyl) -5 fluoro-1-methyl-1H-pyrazole-4-carboxamide, (2.055) N-cyclopropyl-N- (2-cyclopropyl-5-methylbenzyl) -3- (difluoromethyl) -5-fluoro-1-methyl-1H- pyrazole-4-carboxamide, (2.056) N-cycl O-propyl N- (2-cyclopropylbenzyl) -3- (difluoromethyl) -5-fluoro-1-methyl-1H-pyrazole-4-carboxamide.
3) Inhibitoren der Atmungskette an Komplex PI, zum Beispiel (3.001) Ametoctradin, (3.002)3) respiratory chain inhibitors on complex PI, for example (3,001) ametoctradine, (3,002)
Amisulbrom, (3.003) Azoxystrobin, (3.004) Coumethoxystrobin, (3.005) Coumoxystrobin, (3.006) Cyazofamid, (3.007) Dimoxystrobin, (3.008) Enoxastrobin, (3.009) Famoxadon, (3.010) Fenamidon, (3.011) Flufenoxystrobin, (3.012) Fluoxastrobin, (3.013) Kresoxim-methyl, (3.014) Metominostrobin, (3.015) Orysastrobin, (3.016) Picoxystrobin, (3.017) Pyraclostrobin, (3.018) Pyrametostrobin, (3.019) Pyraoxystrobin, (3.020) Trifloxystrobin, (3.021) (2E)-2-{2-[({ [(lE)-l-(3-{ [(E)-l-Fluor-2- phenylvinyl]oxy}phenyl)ethyliden]amino}oxy)methyl]phenyl}-2-(methoxyimino)-N-methylacetamid, (3.022) (2E,3Z)-5-{ [l-(4-Chlorphenyl)-lH-pyrazol-3-yl]oxy}-2-(methoxyimino)-N,3-dimethylpent-3- enamid, (3.023) (2R)-2-{2-[(2,5-Dimethylphenoxy)methyl]phenyl}-2-methoxy-N-methylacetamid, (3.024) (2S)-2-{2-[(2,5-Dimethylphenoxy)methyl]phenyl}-2-methoxy-N-methylacetamid, (3.025) (3S,6S,7R,8R)-2-Methylpropansäure-8-benzyl-3-[({3-[(isobutyryloxy)methoxy] -4-methoxypyridin-2- yl}carbonyl)amino]-6-methyl-4,9-dioxo-l,5-dioxonan-7-ylester, (3.026) 2-{2-[(2,5-Dimethylphenoxy)- methyl]phenyl}-2-methoxy-N-methylacetamid, (3.027) N-(3-Ethyl-3,5,5-trimethylcyclohexyl)-3- formamido-2-hydroxybenzamid, (3.028) (2E,3Z)-5 - { [ 1 -(4-Chlor-2-fluorphenyl)- lH-pyrazol-3-yl] oxy } - 2-(methoxyimino)-N,3-dimethylpent-3-enamid, (3.029) {5-[3-(2,4-Dimethylphenyl)-lH-pyrazol-l-yl]-2- methylbenzyljcarbamidsäuremethylester. Amisulbrom, (3.003) Azoxystrobin, (3.004) Coumethoxystrobin, (3.005) Coumoxystrobin, (3.006) Cyazofamide, (3.007) Dimoxystrobin, (3.008) Enoxastrobin, (3.009) Famoxadone, (3.010) Fenamidon, (3.011) Flufenoxystrobin, (3.012) Fluoxastrobin, (3.013) kresoxim-methyl, (3.014) metominostrobin, (3.015) orysastrobin, (3.016) picoxystrobin, (3.017) pyraclostrobin, (3.018) pyrametostrobin, (3.019) pyraoxystrobin, (3.020) trifloxystrobin, (3.021) (2E) -2- {2 - [({[(IE) -l- (3 - {[(E) -1-Fluoro-2-phenylvinyl] oxy} phenyl) ethylidene] amino} oxy) methyl] phenyl} -2- (methoxyimino) -N-methylacetamide, (3.022) (2E, 3Z) -5- {[1- (4-chlorophenyl) -1H-pyrazol-3-yl] oxy} -2- (methoxyimino) -N, 3- dimethylpent-3-enamide, (3.023) (2R) -2- {2 - [(2,5-dimethylphenoxy) methyl] phenyl} -2-methoxy-N-methylacetamide, (3.024) (2S) -2- {2 [(2,5-dimethylphenoxy) methyl] phenyl} -2-methoxy-N-methylacetamide, (3.025) (3S, 6S, 7R, 8R) -2-methylpropanoic acid 8-benzyl-3 - [({3- [(isobutyryloxy) methoxy] -4-methoxypyridin-2-yl} carbonyl) amino] -6-methyl-4,9-dioxo-l, 5-dioxonane -7-yl ester, (3.026) 2- {2 - [(2,5-dimethylphenoxy) methyl] phenyl} -2-methoxy-N-methylacetamide, (3.027) N- (3-ethyl-3,5,5 -trimethylcyclohexyl) -3-formamido-2-hydroxybenzamide, (3.028) (2E, 3Z) -5 - {[1- (4-chloro-2-fluorophenyl) -1H-pyrazol-3-yl] oxy} -2- (methoxyimino) -N, 3-dimethylpent-3-enamide, (3.029) methyl {5- [3- (2,4-dimethylphenyl) -1H-pyrazol-1-yl] -2-methylbenzyl-carbamate.
4) Inhibitoren von Mitose und Zellteilung, zum Beispiel (4.001) Carbendazim, (4.002) Diethofencarb,4) inhibitors of mitosis and cell division, for example (4,001) carbendazim, (4,002) diethofencarb,
(4.003) Ethaboxam, (4.004) Fluopicolid, (4.005) Pencycuron, (4.006) Thiabendazol, (4.007) Thiophanat-methyl, (4.008) Zoxamid, (4.009) 3-Chlor-4-(2,6-difluorphenyl)-6-methyl-5- phenylpyridazin, (4.010) 3-Chlor-5-(4-chlorphenyl)-4-(2,6-difluorphenyl)-6-methylpyridazin, (4.011) 3- Chlor-5-(6-chlorpyridin-3-yl)-6-methyl-4-(2,4,6-trifluorphenyl)pyridazin, (4.012) 4-(2-Brom-4- fluorphenyl)-N-(2,6-difluorphenyl)-l,3-dimethyl-lH-pyrazol-5-amin, (4.013) 4-(2-Brom-4-fluorphenyl)- N-(2-brom-6-fluorphenyl)-l,3-dimethyl-lH-pyrazol-5-amin, (4.014) 4-(2-Brom-4-fluorpheriyl)-N-(2- bromphenyl)-l,3-dimethyl-lH-pyrazol-5-amin, (4.015) 4-(2-Brom-4-fluorphenyl)-N-(2-chlor-6- fluorphenyl)-l,3-dimethyl-lH-pyrazol-5-amin, (4.016) 4-(2-Brom-4-fluorphenyl)-N-(2-chlorphenyl)-(4.003) ethaboxam, (4.004) fluopicolide, (4.005) pencycuron, (4.006) thiabendazole, (4.007) thiophanate-methyl, (4.008) zoxamide, (4.009) 3-chloro-4- (2,6-difluorophenyl) -6 -methyl-5-phenylpyridazine, (4.010) 3-chloro-5- (4-chlorophenyl) -4- (2,6-difluorophenyl) -6-methylpyridazine, (4,011) 3-chloro-5- (6-chloropyridine) 3-yl) -6-methyl-4- (2,4,6-trifluorophenyl) pyridazine, (4.012) 4- (2-bromo-4- fluorophenyl) -N- (2,6-difluorophenyl) -1,3-dimethyl-1H-pyrazol-5-amine, (4.013) 4- (2-bromo-4-fluorophenyl) -N- (2-bromo-6 -fluorophenyl) -1,3-dimethyl-1H-pyrazol-5-amine, (4.014) 4- (2-bromo-4-fluoropiperiyl) -N- (2-bromophenyl) -l, 3-dimethyl-1H-pyrazole -5-amine, (4.015) 4- (2-bromo-4-fluorophenyl) -N- (2-chloro-6-fluorophenyl) -1,3-dimethyl-1H-pyrazol-5-amine, (4.016) 4 - (2-bromo-4-fluorophenyl) -N- (2-chlorophenyl) -
1.3-dimethyl- 1 H-pyrazol-5-amin, (4.017) 4-(2-Brom-4-fluorphenyl)-N-(2-fluorphenyl)- 1 ,3-dimethyl- lH-pyrazol-5-amin, (4.018) 4-(2-Chlor-4-fluorphenyl)-N-(2,6-difluorphenyl)-l,3-dimethyl-lH-pyrazol-1,3-dimethyl-1H-pyrazol-5-amine, (4.017) 4- (2-bromo-4-fluorophenyl) -N- (2-fluorophenyl) -1,3-dimethyl-1H-pyrazol-5-amine, (4.018) 4- (2-Chloro-4-fluorophenyl) -N- (2,6-difluorophenyl) -1,3-dimethyl-1H-pyrazole
5-amin, (4.019) 4-(2-Chlor-4-fluorphenyl)-N-(2-chlor-6-fluorphenyl)-l,3-dimethyl-lH-pyrazol-5-amin, (4.020) 4-(2-Chlor-4-fluorphenyl)-N-(2-chlorphenyl)-l,3-dimethyl-lH-pyrazol-5-amin, (4.021) 4-(2- Chlor-4-fluorphenyl)-N-(2-fluorphenyl)-l,3-dimethyl-lH-pyrazol-5-amin, (4.022) 4-(4-Chlorphenyl)-5- (2,6-difluorphenyl)-3,6-dimethylpyridazin, (4.023) N-(2-Brom-6-fluorphenyl)-4-(2-chlor-4- fluorphenyl)-l,3-dimethyl-lH-pyrazol-5-amin, (4.024) N-(2-Bromphenyl)-4-(2-chlor-4-fluorphenyl)-5-amine, (4.019) 4- (2-Chloro-4-fluorophenyl) -N- (2-chloro-6-fluorophenyl) -1,3-dimethyl-1H-pyrazole-5-amine, (4,020) 4- (2-chloro-4-fluorophenyl) -N- (2-chlorophenyl) -1,3-dimethyl-1H-pyrazol-5-amine, (4,021) 4- (2-chloro-4-fluorophenyl) -N- ( 2-fluorophenyl) -1,3-dimethyl-1H-pyrazol-5-amine, (4.022) 4- (4-chlorophenyl) -5- (2,6-difluorophenyl) -3,6-dimethylpyridazine, (4.023) N - (2-bromo-6-fluorophenyl) -4- (2-chloro-4-fluorophenyl) -1,3-dimethyl-1H-pyrazole-5-amine, (4,024) N- (2-bromophenyl) -4- (2-chloro-4-fluorophenyl) -
1.3-dimethyl-lH-pyrazol-5-amin, (4.025) N-(4-Chlor-2,6-difluorphenyl)-4-(2-chlor-4-fluorphenyl)-l,3- dimethyl-lH-pyrazol-5-amin. 1,3-dimethyl-1H-pyrazol-5-amine, (4.025) N- (4-chloro-2,6-difluorophenyl) -4- (2-chloro-4-fluorophenyl) -1,3-dimethyl-1H-pyrazole -5-amine.
5) Verbindungen, die an mehreren Stellen wirken können („Multisite Action“), zum Beispiel (5.001) Bordeaux-Mischung, (5.002) Captafol, (5.003) Captan, (5.004) Chlorothalonil, (5.005) Kupferhydroxid, (5.006) Kupfernaphthenat, (5.007) Kupferoxid, (5.008) Kupferoxychlorid, (5.009) Kupfer(2+)-sulfat, (5.010) Dithianon, (5.011) Dodin, (5.012) Folpet, (5.013) Mancozeb, (5.014) Maneb, (5.015) Metiram, (5.016) Metiram-Zink, (5.017) Oxine -Kupfer, (5.018) Propineb, (5.019) Schwefel und Schwefel zubereitungen einschließlich Calciumpolysulfid, (5.020) Thiram, (5.021) Zineb, (5.022) Ziram, (5.023)5) Multisite action compounds, for example (5,001) Bordeaux mixture, (5,002) captafol, (5,003) captan, (5,004) chlorothalonil, (5,005) copper hydroxide, (5,006) copper naphthenate , (5.007) copper oxide, (5.008) copper oxychloride, (5.009) copper (2+) sulfate, (5.010) dithianone, (5.011) dodin, (5.012) folpet, (5.013) mancozeb, (5.014) maneb, (5.015) Metiram, (5.016) Metiram Zinc, (5.017) Oxine Copper, (5.018) Propineb, (5.019) Sulfur and Sulfur Preparations including Calcium Polysulfide, (5.020) Thiram, (5.021) Zineb, (5.022) Ziram, (5.023)
6-Ethyl-5,7-dioxo-6,7-dihydro-5H-pyrrolo[3,,4,:5,6] [l,4]dithiino[2,3-c] [l,2]thiazol-3-carbonsäurenitril. 6-ethyl-5,7-dioxo-6,7-dihydro-5H-pyrrolo [3 , 4 , 5,6] [1,4] dithiino [2,3-c] [1,2] thiazole 3-carbonitrile.
6) Verbindungen, die dazu in der Lage sind, Abwehrreaktionen des Wirtes zu induzieren, zum Beispiel (6.001) Acibenzolar-S-methyl, (6.002) Isotianil, (6.003) Probenazol, (6.004) Tiadinil. 6) Compounds capable of inducing host defense responses, for example (6,001) acibenzolar-S-methyl, (6,002) isotianil, (6,003) probenazole, (6,004) tiadinil.
7) Inhibitoren von Aminosäure- und/oder Proteinbiosynthese, zum Beispiel (7.001) Cyprodinil, (7.002) Kasugamycin, (7.003) Kasugamycinhydrochlorid-hydrat, (7.004) Oxytetracyclin, (7.005) Pyrimethanil, (7.006) 3-(5-Fluor-3,3,4,4-tetramethyl-3,4-dihydroisochinolin-l-yl)chinolin. 7) inhibitors of amino acid and / or protein biosynthesis, for example (7,001) cyprodinil, (7,002) kasugamycin, (7,003) kasugamycin hydrochloride hydrate, (7,004) oxytetracycline, (7,005) pyrimethanil, (7,006) 3- (5-fluoro) 3,3,4,4-tetramethyl-3,4-dihydroisoquinoline-l-yl) quinoline.
8) Inhibitoren der ATP-Produktion, zum Beispiel (8.001) Silthiofam. 8) inhibitors of ATP production, for example (8,001) silthiofam.
9) Inhibitoren der Zellwandsynthese, zum Beispiel (9.001) Benthiavalicarb, (9.002) Benthiavalicarb- isopropyl, (9.003) Dimethomorph, (9.004) Flumorph, (9.005) Iprovalicarb, (9.006) Mandipropamid, (9.007) Pyrimorph, (9.008) Valifenalat, (9.009) (2E)-3-(4-tert.-Butylphenyl)-3-(2-chlorpyridin-4-yl)-l- (morpholin-4-yl)prop-2-en-l-on, (9.010) (2Z)-3-(4-tert.-Butylphenyl)-3-(2-chlorpyridin-4-yl)-l- (morpholin-4-yl)prop-2-en- 1 -on. 9) inhibitors of cell wall synthesis, for example, (9.001) benthi- avalicarb, (9.002) benthiavalicarbisopropyl, (9.003) dimethomorph, (9.004) flumorph, (9.005) iprovalicarb, (9.006) mandipropamide, (9.007) pyrimorph, (9.008) valproate, (9.009) (2E) -3- (4-tert-butylphenyl) -3- (2-chloropyridin-4-yl) -1- (morpholin-4-yl) prop-2-en-1-one, 9,010) (2Z) -3- (4-tert-butylphenyl) -3- (2-chloropyridin-4-yl) -1- (morpholin-4-yl) prop-2-en-1-one.
10) Inhibitoren der Lipid- und Membransynthese, zum Beispiel (10.001) Propamocarb, (10.002) Propamocarb-hydrochlorid, (10.003) Tolclofos-methyl. 11) Inhibitoren der Melaninbiosynthese, zum Beispiel (11.001) Tricyclazol, (11.002) [3-Methyl-l-[(4- methylbenzoyl)amino]butan-2-yl}carbamidsäure-2,2,2-trifluorethylester. 10) inhibitors of lipid and membrane synthesis, for example (10,001) propamocarb, (10,002) propamocarb hydrochloride, (10,003) tolclofos-methyl. 11) Inhibitors of melanin biosynthesis, for example, (11.001) tricyclazole, (11.002) [3-methyl-1 - [(4-methylbenzoyl) amino] butan-2-yl} carbamic acid 2,2,2-trifluoroethyl ester.
12) Inhibitoren der Nukleinsäuresynthese, zum Beispiel (12.001) Benalaxyl, (12.002) Benalaxyl-M (Kiralaxyl), (12.003) Metalaxyl, (12.004) Metalaxyl-M (Mefenoxam). 12) inhibitors of nucleic acid synthesis, for example (12.001) benalaxyl, (12.002) benalaxyl-M (kiralaxyl), (12.003) metalaxyl, (12.004) metalaxyl-M (mefenoxam).
13) Inhibitoren der Signalübertragung, zum Beispiel (13.001) Fludioxonil, (13.002) Iprodion, (13.003) Procymidon, (13.004) Proquinazid, (13.005) Quinoxyfen, (13.006) Vinclozolin. 13) inhibitors of signal transduction, for example (13.001) fludioxonil, (13.002) iprodione, (13.003) procymidone, (13.004) proquinazide, (13.005) quinoxyfen, (13.006) vinclozolin.
14) Verbindungen, die als Entkoppler wirken können, zum Beispiel (14.001) Fluazinam, (14.002) Meptyldinocap. 14) Compounds which may act as decouplers, for example (14.001) fluazinam, (14.002) meptyldinocap.
15) Weitere Verbindungen, zum Beispiel (15.001) Abscisinsäure, (15.002) Benthiazol, (15.003) Bethoxazin, (15.004) Capsimycin, (15.005) Carvon, (15.006) Chinomethionat, (15.007) Cufraneb, (15.008) Cyflufenamid, (15.009) Cymoxanil, (15.010) Cyprosulfamid, (15.011) Flutianil, (15.012) Fosetyl-Aluminium, (15.013) Fosetyl-Calcium, (15.014) Fosetyl-Natrium, (15.015) Methyl- isothiocyanat, (15.016) Metrafenon, (15.017) Mildiomycin, (15.018) Natamycin, (15.019) Nickel- dimethyldithiocarbamat, (15.020) Nitrothal-isopropyl, (15.021) Oxamocarb, (15.022) Oxathiapiprolin, (15.023) Oxyfenthiin, (15.024) Pentachlorphenol und Salze, (15.025) phosphorige Säure und deren Salze, (15.026) Propamocarb-fosetylat, (15.027) Pyriofenon (Chlazafenon), (15.028) Tebufloquin, (15.029) Tecloftalam, (15.030) Tolnifanid, (15.031) l-(4-{4-[(5R)-5-(2,6-Difluorphenyl)-4,5-dihydro-15) Further compounds, for example (15.001) abscisic acid, (15.002) benthiazole, (15.003) bethoxazine, (15.004) capsimycin, (15.005) carvone, (15.006) quinomethionate, (15.007) Cufraneb, (15.008) cyflufenamid, (15.009) Cymoxanil, (15.010) cyprosulfamide, (15.011) flutianil, (15.012) fosetyl-aluminum, (15.013) fosetyl-calcium, (15.014) fosetyl-sodium, (15.015) methyl-isothiocyanate, (15.016) metrafenone, (15.017) mildiomycin, (15.018) natamycin, (15.019) nickel dimethyldithiocarbamate, (15.020) nitrothal isopropyl, (15.021) oxamocarb, (15.022) oxathiapiproline, (15.023) oxyfenthiine, (15.024) pentachlorophenol and salts, (15.025) phosphorous acid and its salts, (15,026) propamocarb-fosetylate, (15,027) pyriofenone (Chlazafenone), (15,028) tebufloquine, (15,029) tecloftalam, (15,030) tolnifanide, (15,031) 1- (4- {4 - [(5R) -5- (2 , 6-difluorophenyl) -4,5-dihydro-
1.2-oxazol-3-yl]-l,3-thiazol-2-yl}piperidin-l-yl)-2-[5-methyl-3-(trifluormethyl)-lH-pyrazol-l-yl]- ethanon, (15.032) l-(4-[4-[(5S)-5-(2,6-Difluorphenyl)-4,5-dihydro-l,2-oxazol-3-yl]-l,3-thiazol-2-yl}- piperidin-l-yl)-2-[5-methyl-3-(trifluormethyl)-lH-pyrazol-l-yl]ethanon, (15.033) 2-(6-Benzylpyridin-2- yl)chinazolin, (15.034) 2,6-Dimethyl-lH,5H-[l,4]dithiino[2,3-c:5,6-c']dipyrrol-l,3,5,7(2H,6H)-tetron, ( 15.035) 2- [3,5 -Bis(difluormethyl)- IH-pyrazol- 1 -yl] - 1 - [4-(4- { 5-[2-(prop-2-in- 1 -yloxy)phenyl] -4,5 - dihydro- 1 ,2-oxazol-3-yl } - 1 ,3-thiazol-2-yl)piperidin- 1 -yl] ethanon, ( 15.036) 2- [3,5 -Bis(difluormethyl)- 1 H-pyrazol- 1 -yl] - 1 - [4-(4- { 5-[2-chlor-6-(prop-2-in- 1 -yloxy)phenyl] -4,5 -dihydro- 1 ,2-oxazol-3-yl } - 1 ,3- thiazol-2-yl)piperidin-l -yljethanon, (15.037) 2-[3,5-Bis(difluormethyl)-lH-pyrazol-l-yl]-l-[4-(4-{5-[2- fluor-6-(prop-2-in- 1 -yloxy)phenyl] -4,5 -dihydro- 1 ,2-oxazol-3-yl } - 1 ,3-thiazol-2-yl)piperidin- 1 -yl] - ethanon, (15.038) 2-[6-(3-Fluor-4-methoxyphenyl)-5-methylpyridin-2-yl]chinazolin, (15.039) Methansulfonsäure-2-[(5R)-3-[2-(l-{ [3,5-bis(difluormethyl)-lH-pyrazol-l-yl]acetyl}piperidin-4-yl)-1,2-oxazol-3-yl] -1,3-thiazol-2-yl} piperidin-1-yl) -2- [5-methyl-3- (trifluoromethyl) -1H-pyrazol-1-yl] ethanone, (15.032) 1- (4- [4 - [(5S) -5- (2,6-Difluorophenyl) -4,5-dihydro-1,2-oxazol-3-yl] -1,3-thiazole-2 -yl} - piperidin-1-yl) -2- [5-methyl-3- (trifluoromethyl) -1H-pyrazol-1-yl] ethanone, (15.033) 2- (6-benzylpyridin-2-yl) quinazoline, (15.034) 2,6-dimethyl-1H, 5H- [1,4] dithiino [2,3-c: 5,6-c '] dipyrrole-l, 3,5,7 (2H, 6H) -tetrone, (15.035) 2- [3,5-bis (difluoromethyl) -H-pyrazol-1-yl] - 1 - [4- (4- {5- [2- (prop-2-yn-1-yloxy) -phenyl ] -4,5-dihydro-1,2-oxazol-3-yl} -1,3-thiazol-2-yl) piperidin-1-yl] ethanone, (15,036) 2- [3,5-bis (difluoromethyl ) - 1 H -pyrazol-1-yl] - 1 - [4- (4- {5- [2-chloro-6- (prop-2-yn-1-yloxy) phenyl] -4,5-dihydro- 1,2-oxazol-3-yl} -1,3-thiazol-2-yl) piperidine-1-yl-ylanone, (15.037) 2- [3,5-bis (difluoromethyl) -1H-pyrazol-1-yl] -l- [4- (4- {5- [2- fluoro-6- (prop-2-yn-1-ynyloxy) phenyl] -4,5-dihydro-1,2-oxazol-3-yl} - 1, 3-thiazol-2-yl) piperidin-1-yl] ethanone, (15.038) 2- [6- (3-fluoro 4-methoxyphenyl) -5-methylpyridin-2-yl] quinazoline, (15.039) Methanesulfonic acid 2 - [(5R) -3- [2- (1 - {[3,5-bis (difluoromethyl) -1H-pyrazole -l-yl] acetyl} piperidin-4-yl) -
1.3-thiazol-4-yl] -4,5 -dihydro- 1 ,2-oxazol-5 -yl } -3-chlorphenylester, ( 15.040) Methansulfonsäure -2- { (5S)- 3-[2-(l-[ [3,5-bis(difluormethyl)-lH-pyrazol-l-yl]acetyl}piperidin-4-yl)-l,3-thiazol-4-yl]-4,5-dihydro-1,3-thiazol-4-yl] -4,5-dihydro-1,2-oxazol-5-yl-3-chlorophenyl ester, (15.040) methanesulfonic acid -2- {(5S) -3- [2- (1H) [[3,5-bis (difluoromethyl) -1H-pyrazol-1-yl] acetyl} piperidin-4-yl) -1,3-thiazol-4-yl] -4,5-dihydro-
1 ,2-oxazol-5 -yl } -3-chlorphenylester, ( 15.041 ) 2- { 2- [(7,8-Difluor-2-methylchinolin-3-yl)oxy] -6- fluorphenyl}propan-2-ol, (15.042) 2-{2-Fluor-6-[(8-fluor-2-methylchinolin-3-yl)oxy]phenyl}propan-2- ol, (15.043) Methansulfonsäure -2-{3-[2-(l-{ [3, 5-bis(difluormethyl)-lH-pyrazol-l-yl]acetyl]piperidin-4- yl)-l ,3-thiazol-4-yl] -4,5-dihydro- 1 ,2-oxazol-5 -yl } -3-chlorphenylester, (15.044) Methansulfonsäure -2- [3-[2-(l-[ [3,5-bis(difluormethyl)-lH-pyrazol-l-yl]acetyl}piperidin-4-yl)-l,3-thiazol-4-yl]-4,5-dihydro- l,2-oxazol-5-yl}phenylester, (15.045) 2-Phenylphenol und Salze, (15.046) 3-(4,4,5-Trifluor-3,3- dimethyl-3,4-dihydroisochinolin-l-yl)chinolin, (15.047) 3-(4,4-Difluor-3,3-dimethyl-3,4-dihydro- isochinolin-l-yl)chinolin, (15.048) 4-Amino-5-fluorpyrimidin-2-ol (tautomere Form: 4-Amino-5- fluorpyrimidin-2(lH)-on), (15.049) 4-Oxo-4-[(2-phenylethyl)amino]butansäure, (15.050) 5-Amino- 1 ,3,4-thiadiazol-2-thiol, ( 15.051 ) 5 -Chlor-N'-phenyl-N'-(prop-2-in- 1 -yl)thiophen-2-sulfonohydrazid, (15.052) 5-Fluor-2-[(4-fluorbenzyl)oxy]pyrimidin-4-amin, (15.053) 5-Fluor-2-[(4-methylbenzyl)- oxy |pyrimidiii-4-amin, (15.054) 9-Fluor-2,2-dimethyl-5-(chinolin-3-yl)-2,3-dihydro-l,4-benzoxazepin, ( 15.055) { 6- [( { [(Z)-( 1 -Methyl- 1 H-tetrazol-5 -yl)(phenyl)methylen] amino } oxy)methyl]pyridin-2-yl } - carbamidsäurebut-3-in-l-ylester, (15.056) (2Z)-3-Amino-2-cyano-3-phenylacrylsäureethylester, (15.057) Phenazin- 1 -carbonsäure, (15.058) 3,4,5-Trihydroxybenzoesäurepropylester, (15.059) Chinolin- 8-ol, (15.060) Chinolin-8-olsulfat (2: 1), (15.061) {6-[({ [(l-Methyl-lH-tetrazol-5-yl)(phenyl)methylen]- amino}oxy)methyl]pyridin-2-yl}carbamidsäure-tert.-butylester, (15.062) 5-Fluor-4-imino-3-methyl-l- [(4-methylphenyl)sulfonyl] -3,4-dihydropyrimidin-2( lH)-on. 1,2-oxazol-5-yl-3-chlorophenyl ester, (15.041) 2- {2- [(7,8-difluoro-2-methylquinolin-3-yl) oxy] -6-fluorophenyl} propan-2-yl ol, (15.042) 2- {2-Fluoro-6 - [(8-fluoro-2-methylquinolin-3-yl) oxy] phenyl} propan-2-ol, (15.043) Methanesulfonic acid -2- {3- [2 - (1 - {[3,5-bis (difluoromethyl) -1H-pyrazol-1-yl] acetyl] piperidin-4-yl) -1,3-thiazol-4-yl] -4,5-dihydro-1 , 2-oxazol-5-yl-3-chlorophenyl ester, (15.044) methanesulfonic acid -2- [3- [2- (1 - [[3,5-bis (difluoromethyl) -1H-pyrazol-1-yl] -acetyl } piperidin-4-yl) -l, 3-thiazol-4-yl] -4,5-dihydro- l, 2-oxazol-5-yl} phenyl ester, (15.045) 2-phenylphenol and salts, (15.046) 3- (4,4,5-trifluoro-3,3-dimethyl-3,4-dihydroisoquinolin-1-yl ) quinoline, (15.047) 3- (4,4-difluoro-3,3-dimethyl-3,4-dihydro-isoquinolin-1-yl) quinoline, (15.048) 4-amino-5-fluoropyrimidin-2-ol ( tautomeric form: 4-amino-5-fluoropyrimidine-2 (1H) -one), (15.049) 4-oxo-4 - [(2-phenylethyl) amino] butanoic acid, (15.050) 5-amino-1, 3,4 thiadiazole-2-thiol, (15.051) 5-chloro-N'-phenyl-N '- (prop-2-yn-1-yl) thiophene-2-sulfonohydrazide, (15.052) 5-fluoro-2 - [( 4-fluorobenzyl) oxy] pyrimidin-4-amine, (15.053) 5-fluoro-2 - [(4-methylbenzyl) oxy] pyrimidiii-4-amine, (15.054) 9-fluoro-2,2-dimethyl-5 - (quinolin-3-yl) -2,3-dihydro-l, 4-benzoxazepine, (15.055) {6- [({[(Z) - (1-methyl-1H-tetrazol-5-yl) ( phenyl) methylene] amino} oxy) methyl] pyridin-2-yl} -carbamic acid but-3-yn-1-yl ester, (15.056) (2Z) -3-amino-2-cyano-3-phenylacrylic acid ethyl ester, (15.057) phenazine - 1-carboxylic acid, (15.058) 3,4,5-trihydroxybenzoic acid propyl ester, (15.059) quinoline-8-o l, (15,060) quinoline-8-olsulfate (2: 1), (15,061) {6 - [({[(1-methyl-1H-tetrazol-5-yl) (phenyl) -methylene] -amino} oxy) -methyl ] pyridin-2-yl} -carbamic acid tert-butyl ester, (15.062) 5-Fluoro-4-imino-3-methyl-1- [(4-methylphenyl) sulfonyl] -3,4-dihydropyrimidine-2 (1H) -one.
Die hier mit ihrem“Common Name” spezifizierten Wirkstoffe sind bekannt und beispielsweise im “Pesticide Manual” (16. Aufl. British Crop Protection Council) oder im Internet recherchierbar (beispielsweise: http://www.alanwood.net/pesticides) beschrieben. The active ingredients specified here by their "common name" are known and described, for example, in the "Pesticide Manual" (16th edition British Crop Protection Council) or searchable on the Internet (for example: http://www.alanwood.net/pesticides).
Alle genannten Mischungspartner der Klassen (1) bis (15) können, wenn sie auf Grund ihrer funktionellen Gruppen dazu imstande sind, gegebenenfalls mit geeigneten Basen oder Säuren Salze bilden. Alle genannten fungiziden Mischungspartner der Klassen (1) bis (15) können gegebenenfalls tautomere Formen einschließen. All of the above-mentioned mixture partners of classes (1) to (15), if they are capable of doing so on the basis of their functional groups, may optionally form salts with suitable bases or acids. All of the mentioned fungicidal mixture partners of classes (1) to (15) may optionally include tautomeric forms.
Bevorzugt sind Wirkstoffkombinationen enthaltend Verbindungen der Formel (I), in welcher die Reste die folgende Bedeutung haben: Preference is given to active compound combinations comprising compounds of the formula (I) in which the radicals have the following meaning:
W steht bevorzugt für Methyl, W is preferably methyl,
X steht bevorzugt für Chlor oder Methyl, (hervorgehoben für Methyl), X is preferably chlorine or methyl, (highlighted for methyl),
Y steht bevorzugt für Chlor, Brom oder Methyl, Y is preferably chlorine, bromine or methyl,
D steht bevorzugt für Wasserstoff, D is preferably hydrogen,
A, B und das Kohlenstoffatom, an das sie gebunden sind, stehen bevorzugt für gesättigtes Cg- Cycloalkyl, welches mit einer Alkylendioxyl-Gruppe substituiert ist, die mit dem Kohlenstoffatom, an das sie gebunden ist, ein 5-Ring- oder 6-Ringketal bildet, A, B and the carbon atom to which they are attached are preferably saturated C 1-6 cycloalkyl which is substituted with an alkylenedioxy group having a 5-ring or 6-ring ketal with the carbon atom to which it is attached forms,
G steht bevorzugt für Wasserstoff (a) oder für eine der Gruppen
Figure imgf000011_0001
in welchen
G is preferably hydrogen (a) or one of the groups
Figure imgf000011_0001
in which
M für Sauerstoff steht, M stands for oxygen,
E für ein Metallionenäquivalent oder ein Ammoniumion steht, (hervorgehoben für Natrium oder Kalium) E is a metal ion equivalent or an ammonium ion (highlighted for sodium or potassium)
Rl steht bevorzugt für geradkettigtes oder verzweigtes C | -('q-Alkyl, steht bevorzugt für geradkettigtes oder verzweigtes C | -('q-Alkyl. Rl preferably represents geradkettigtes or branched C | - ('q-alkyl, preferably represents straight-chain or branched C | - (' q-alkyl.
Besonders bevorzugt sind die Verbindungen der Formel (I) mit G = Wasserstoff. Particularly preferred are the compounds of formula (I) with G = hydrogen.
Ganz besonders bevorzugt sind Wirkstoffkombinationen enthaltend Verbindungen der Formel (I), in welcher die Reste die folgende Bedeutung haben: Very particular preference is given to active compound combinations comprising compounds of the formula (I) in which the radicals have the following meaning:
Figure imgf000011_0002
Figure imgf000011_0002
Figure imgf000011_0003
Figure imgf000012_0001
Figure imgf000011_0003
Figure imgf000012_0001
Insbesondere bevorzugt sind Wirkstoffkombinationen enthaltend die Verbindung der Formel (1-2) und mindestens eine weitere Verbindung (B) der wie oben beschriebenen Klassen (1) bis (15). Particular preference is given to active ingredient combinations comprising the compound of the formula (I-2) and at least one further compound (B) of the classes (1) to (15) described above.
Hervorgehoben bevorzugt sind Wirkstoffkombinationen enthaltend die Verbindung der Formel (1-2) und mindestens eine weitere Verbindung (B) ausgewählt aus: Particularly preferred are combinations of active substances containing the compound of the formula (1-2) and at least one further compound (B) selected from:
(1.002) Difenoconazol, (1.010) hnazalil, (1.012) Ipconazol, (1.018) Prothioconazol, (1.020) Spiroxamin, (1.021) Tebuconazol, (1.026) (lR,2S,5S)-5-(4-Chlorbenzyl)-2-(chlormethyl)-2-methyl-l- ( 1H-1 ,2,4-triazol- 1 -ylmethyl)cyclopentanol, ( 1.027) ( lS,2R,5R)-5-(4-Chlorbenzyl)-2-(chlormethyl)-2- methyl- 1 -( 1 H- 1 ,2,4-triazol- 1 -ylmethyl)cyclopentanol, ( 1.059) 5 -(4-Chlorbenzyl)-2-(chlormethyl)-2- methyl-l-(lH-l,2,4-triazol-l-ylmethyl)cyclopentanol, (1.081) Mefentrifluconazol, (1.082) Ipfentrifluconazol, (1,002) difenoconazole, (1,010) hnazalil, (1,012) ipconazole, (1,018) prothioconazole, (1,020) spiroxamine, (1,021) tebuconazole, (1,026) (1R, 2S, 5S) -5- (4-chlorobenzyl) -2 (chloromethyl) -2-methyl-1- (1H-1,2,4-triazol-1-ylmethyl) cyclopentanol, (1.027) (IS, 2R, 5R) -5- (4-chlorobenzyl) -2- ( chloromethyl) -2-methyl-1 - (1H-1,2,4-triazol-1-ylmethyl) cyclopentanol, (1.059) 5- (4-chlorobenzyl) -2- (chloromethyl) -2-methyl-1-one (lH-l, 2,4-triazol-1-ylmethyl) cyclopentanol, (1.081) Mefentrifluconazole, (1.082) Ipfentrifluconazole,
(2.001) Benzovindiflupyr, (2.002) Bixafen, (2.005) Fluopyram, (2.007) Fluxapyroxad, (2.017) Penflufen, (2.018) Penthiopyrad, (2.019) Pydiflumetofen, (2.021) Sedaxane, (2.027) 3-(Difluormethyl)- l-methyl-N-(l,l,3-trimethyl-2,3-dihydro-lH-inden-4-yl)-lH-pyrazol-4-carboxamid, (2.030) 3-(2.001) benzovindiflupyr, (2.002) bixafen, (2.005) fluopyram, (2.007) fluxapyroxad, (2.017) penflufen, (2.018) penthiopyrad, (2.019) pydiflumetofen, (2.021) sedaxanes, (2.027) 3- (difluoromethyl) - l -methyl-N- (1,1,3-trimethyl-2,3-dihydro-1H-inden-4-yl) -1H-pyrazole-4-carboxamide, (2.030) 3-
(Difluormethyl)-N-(7-fluor-l,l,3-trimethyl-2,3-dihydro-lH-inden-4-yl)-l-methyl-lH-pyrazol-4- carboxamid, (2.038) N-(5-Chlor-2-isopropylbenzyl)-N-cyclopropyl-3-(difluormethyl)-5-fluor-l-methyl- 1 H-pyrazol-4-carboxamid, (Difluoromethyl) -N- (7-fluoro-1,1,3-trimethyl-2,3-dihydro-1H-inden-4-yl) -1-methyl-1H-pyrazole-4-carboxamide, (2.038) N - (5-chloro-2-isopropylbenzyl) -N-cyclopropyl-3- (difluoromethyl) -5-fluoro-1-methyl-1H-pyrazole-4-carboxamide,
(3.003) Azoxystrobin, (3.012) Fluoxastrobin, (3.016) Picoxystrobin, (3.017) Pyraclostrobin, (3.020) Trifloxystrobin, (3.025) (3S,6S,7R,8R)-2-Methylpropansäure-8-benzyl-3-[({3-(3.003) azoxystrobin, (3.012) fluoxastrobin, (3.016) picoxystrobin, (3.017) pyraclostrobin, (3.020) trifloxystrobin, (3.025) (3S, 6S, 7R, 8R) -2-methylpropanoic acid 8-benzyl-3 - [( {3-
[(isobutyryloxy)methoxy]-4-methoxypyridin-2-yl}carbonyl)amino]-6-methyl-4,9-dioxo-l,5-dioxonan-7- ylester, (3.026) 2-{2-[(2,5-Dimethylphenoxy)methyl]phenyl}-2-methoxy-N-methylacetamid, [(isobutyryloxy) methoxy] -4-methoxypyridin-2-yl} carbonyl) amino] -6-methyl-4,9-dioxo-l, 5-dioxonan-7-yl ester, (3.026) 2- {2 - [( 2,5-dimethylphenoxy) methyl] phenyl} -2-methoxy-N-methylacetamide,
(4.005) Pencycuron, (4.007) Thiophanat-methyl, (4.012) 4-(2-Brom-4-fluorphenyl)-N-(2,6- difluorphenyl)- 1 ,3-dimethyl- 1 H-pyrazol-5-amin, (4.015) 4-(2-Brom-4-fluorphenyl)-N-(2-chlor-6- fluorphenyl)-l,3-dimethyl-lH-pyrazol-5-amin, (4.025) N-(4-Chlor-2,6-difluorphenyl)-4-(2-chlor-4- fluorpheny 1)- 1 ,3 -dimethy 1- 1 H-pyrazol-5-amin, (4.005) Pencycuron, (4.007) thiophanate-methyl, (4.012) 4- (2-bromo-4-fluorophenyl) -N- (2,6-difluorophenyl) -1,3-dimethyl-1H-pyrazole-5- amine, (4.015) 4- (2-bromo-4-fluorophenyl) -N- (2-chloro-6-fluorophenyl) -1,3-dimethyl-1H-pyrazol-5-amine, (4.025) N- (4 -Chloro-2,6-difluorophenyl) -4- (2-chloro-4-fluorophenyl) -1,3-dimethyl-1-1H-pyrazole-5-amine,
(5.004) Chlorothalonil, (5.011) Dodine, (5.012) Folpet, (5.013) Mancozeb, (5.018) Propineb, (5.004) chlorothalonil, (5.011) dodine, (5.012) folpet, (5.013) mancozeb, (5.018) propineb,
(6.002) Isotianil, (7.005) Pyrimethanil, (6.002) Isotianil, (7.005) pyrimethanil,
(12.003) Metalaxyl, (12.004) Metalaxyl-M (Mefenoxam), (12.003) metalaxyl, (12.004) metalaxyl-M (mefenoxam),
(13.001) Fludioxonil, (13.004) Proquinazid, (13.001) fludioxonil, (13.004) proquinazide,
(14.001) Fluazinam, (14.002) Meptyldinocap, (15.008) Cyflufenamid, (15.027) Pyriofenon (Chlazafenon), (15.047) 3-(4,4-Difluor-3,3-dimethyl-3,4- dihydroisochinolin-l-yl)chinolin, (15.048) 4-Amino-5-fluoropyrimidin-2-ol (tautomere Form: 4-Amino- 5-fluorpyrimidin-2(lH)-on), (15.052) 5-Fluor-2-[(4-fluorberrzyl)oxy]pyrimidirr-4-amin, (15.053) 5- Fluor-2- [(4-methylbenzyl)oxy]pyrimidin-4-amin, (15.062) 5 -Fluor-4-imino-3-methyl- 1-[(4- methylphenyl)sulforryl]-3,4-dihydropyrimidirr-2(lH)-orr. Besonders hervorgehoben bevorzugt sind Wirkstoffkombinationen enthaltend die Verbindung der Formel (1-2) und mindestens eine weitere Verbindung (B) ausgewählt aus: (14.001) Fluazinam, (14.002) Meptyldinocap, (15.008) Cyflufenamid, (15.027) Pyriofenone (Chlazafenone), (15.047) 3- (4,4-Difluoro-3,3-dimethyl-3,4-dihydroisoquinolin-1-yl ) quinoline, (15.048) 4-amino-5-fluoropyrimidin-2-ol (tautomeric form: 4-amino-5-fluoropyrimidin-2 (1H) -one), (15.052) 5-fluoro-2 - [(4- fluorberrzyl) oxy] pyrimidirr-4-amine, (15.053) 5-fluoro-2- [(4-methylbenzyl) oxy] pyrimidin-4-amine, (15.062) 5-fluoro-4-imino-3-methyl-1 [(4-methylphenyl) sulforryl] -3,4-dihydropyrimidine-2 (1H) -orr. Particular preference is given to active compound combinations comprising the compound of the formula (I-2) and at least one further compound (B) selected from:
(1.012) Ipconazol, (1.018) Prothioconazol, (1.020) Spiroxamin, (1.021) Tebuconazol, (1,012) ipconazole, (1,018) prothioconazole, (1,020) spiroxamine, (1,021) tebuconazole,
(2.002) Bixafen, (2.005) Fluopyram, (2.017) Penflufen, (2.027) 3-(Difluormethyl)-l-methyl-N-(l,l,3- trimethyl-2,3 -dihydro- 1 H-inden-4-yl) - 1 H-pyrazol-4-carboxamid, (2.038) N-(5 -Chlor-2- isopropylbenzyl)-N-cyclopropyl-3-(difluormethyl)-5-fluor-l-methyl-lH-pyrazol-4-carboxamid, (2.002) Bixafen, (2.005) Fluopyram, (2.017) Penflufen, (2.027) 3- (difluoromethyl) -l-methyl-N- (l, l, 3-trimethyl-2,3-dihydro-1 H-indene 4-yl) -1 H -pyrazole-4-carboxamide, (2.038) N- (5-chloro-2-isopropylbenzyl) -N-cyclopropyl-3- (difluoromethyl) -5-fluoro-1-methyl-1H-pyrazole -4-carboxamide,
(3.020) Trifloxystrobin, (3.025) (3S,6S,7R,8R)-2-Methylpropansäure-8-benzyl-3-[({3- [(isobutyryloxy)methoxy]-4-methoxypyridin-2-yl}carbonyl)amino]-6-methyl-4,9-dioxo-l,5-dioxonan-7- ylester, (3.020) Trifloxystrobin, (3.025) (3S, 6S, 7R, 8R) -2-methylpropanoic acid 8-benzyl-3 - [({3- [(isobutyryloxy) methoxy] -4-methoxypyridin-2-yl} carbonyl) amino] -6-methyl-4,9-dioxo-l, 5-dioxonan-7-yl-ester,
(4.005) Pencycuron, (5.004) Chlorothalonil, (5.013) Mancozeb, (5.018) Propineb, (4.005) Pencycuron, (5.004) Chlorothalonil, (5.013) Mancozeb, (5.018) Propineb,
(12.003) Metalaxyl, (12.004) Metalaxyl-M (Mefenoxam), (12.003) metalaxyl, (12.004) metalaxyl-M (mefenoxam),
(13.001) Fludioxonil, (13.004) Proquinazid, (13.001) fludioxonil, (13.004) proquinazide,
(15.008) Cyflufenamid, (15.047) 3-(4,4-Difluor-3,3-dimethyl-3,4-dihydroisochinolin-l-yl)chinolin. (15.008) Cyflufenamide, (15.047) 3- (4,4-Difluoro-3,3-dimethyl-3,4-dihydroisoquinolin-1-yl) quinoline.
Besonders hervorgehoben sind Wirkstoffkombinationen enthaltend die Verbindung der Formel (1-2) und Isotianil. Particularly noteworthy are combinations of active substances containing the compound of formula (1-2) and isotianil.
Die erfindungsgemäßen Wirkstoffkombinationen enthalten die Verbindungen der Formel (I) und die Mischpartner (B) der wie oben beschriebenen Klassen (1) bis (15) vorzugsweise in synergistisch wirksamen Mengen. Die Gewichtsverhältnisse der Verbindungen in den Wirkstoffkombinationen können in einem relativ großen Bereich variiert werden hn allgemeinen enthalten die erfindungsgemäßen Kombinationen Verbindungen der Formel (I) und die Mischpartner (B) der wie oben beschriebenen Klassen (1) bis (15) in den folgenden Mischungsverhältnissen: The active compound combinations according to the invention contain the compounds of the formula (I) and the mixing partners (B) of the classes (1) to (15) as described above, preferably in synergistically effective amounts. The weight ratios of the compounds in the active substance combinations can be varied within a relatively wide range. In general, the combinations according to the invention contain compounds of the formula (I) and the mixing partners (B) of the classes (1) to (15) as described above in the following mixing ratios:
3000: 1 bis 1:3000, 1000: 1 bis 1: 1000, 750: 1 bis 1:750, 500: 1 bis 1:500, 250 : 1 bis 1: 250, 200 : 1 bis 1: 200, 100 : 1 bis 1: 100, 95: 1 bis 1:95, 90: 1 bis 1:90, 85: 1 bis 1:85, 80: 1 bis 1:80, 75: 1 bis 1:75, 70: 1 bis 1:70, 65: 1 bis 1:65, 60: 1 bis 1:60, 55: 1 bis 1:55, 45: 1 bis 1:45, 40: 1 bis 1:40, 35: 1 bis 1:35, 30: 1 bis 1:30, 20: 1 bis 1:20, 15: 1 bis 1: 15, 10: 1 bis 1: 10, 9: 1 bis 1:9, 8: 1 bis 1:8, 7: 1 bis 1:7, 6: 1 bis 1:6, 5: 1 bis 1:5, 4: 1 bis 1:4, 3: 1 bis 1:3, 2: 1 bis 1:2, 1: 1, 1: 1.25, 0,001: 1 bis 1:0,001. 3000: 1 to 1: 3000, 1000: 1 to 1: 1000, 750: 1 to 1: 750, 500: 1 to 1: 500, 250: 1 to 1: 250, 200: 1 to 1: 200, 100: 1 to 1: 100, 95: 1 to 1:95, 90: 1 to 1:90, 85: 1 to 1:85, 80: 1 to 1:80, 75: 1 to 1:75, 70: 1 to 1:70, 65: 1 to 1:65, 60: 1 to 1:60, 55: 1 to 1:55, 45: 1 to 1:45, 40: 1 to 1:40, 35: 1 to 1: 35, 30: 1 to 1:30, 20: 1 to 1:20, 15: 1 to 1:15, 10: 1 to 1:10, 9: 1 to 1: 9, 8: 1 to 1: 8, 7: 1 to 1: 7, 6: 1 to 1: 6, 5: 1 to 1: 5, 4: 1 to 1: 4, 3: 1 to 1: 3, 2: 1 to 1: 2, 1: 1, 1: 1.25, 0.001: 1 to 1: 0.001.
Bevorzugt sind Wirkstoffkombinationen enthaltend die Verbindung der Formel (1-2) und Isotianil in dem Mischungsverhältnis 10: 1 - 1: 10. Preference is given to active compound combinations comprising the compound of the formula (I-2) and isotianil in the mixing ratio of 10: 1 to 1:10.
Besonders bevorzugt sind Wirkstoffkombinationen enthaltend die Verbindung der Formel (1-2) und Isotianil in dem Mischungsverhältnis 5: 1 - 1:5. Particularly preferred are combinations of active ingredients containing the compound of formula (1-2) and isotianil in the mixing ratio 5: 1-1: 5.
Ganz besonders bevorzugt sind Wirkstoffkombinationen enthaltend die Verbindung der Formel (1-2) und Isotianil in dem Mischungsverhältnis 3: 1 - 1:3. Very particular preference is given to active ingredient combinations comprising the compound of the formula (I-2) and isotianil in the mixing ratio 3: 1 to 1: 3.
Hervorgehoben sind Wirkstoffkombinationen enthaltend die Verbindung der Formel (1-2) und Isotianil in dem Mischungsverhältnis 1: 1.25. hn Rahmen der vorliegenden Erfindung steht der Begriff „Wirkstoffkombination“ für verschiedene Kombinationen von Verbindungen der Formel (I) und dem Mischpartner (B) z.B. in Form einer einzelnen Fertigmischung („Ready-Mix“), in einer kombinierten Spraymischung, die zusammengesetzt ist aus getrennten Formulierungen der einzelnen Wirkstoffe, z.B. einer Tankmischung („Tank-Mix“) oder in einer kombinierten Verwendung der einzelnen Wirkstoffe, wenn diese sequentiell appliziert werden, z.B. nacheinander innerhalb eines angemessen kurzen Zeitraums, z.B. wenigen Stunden oder Tagen. Gemäß einer bevorzugten Ausführungsform ist die Reihenfolge der Applikation der Wirkstoffe der Formel (I) und dem Mischpartner (B) für die Ausführung der vorliegenden Erfindung nicht entscheidend. Highlighted are active ingredient combinations containing the compound of formula (1-2) and isotianil in the mixing ratio 1: 1.25. In the context of the present invention, the term "active ingredient combination" stands for different combinations of compounds of the formula (I) and the mixing partner (B), for example in the form of a single ready-mix, in a combined spray mixture composed of separate formulations of the individual active ingredients, e.g. a tank mix or in a combined use of the individual active ingredients when applied sequentially, e.g. successively within a reasonably short period of time, e.g. a few hours or days. According to a preferred embodiment, the order of application of the active compounds of the formula (I) and the mixing partner (B) is not critical to the practice of the present invention.
Methoden und Anwendungen Methods and applications
Die erfindungsgemäßen Wirkstoffkombinationen haben eine starke mikrobizide Wirkung und/oder ein hohes pflanzenverteidigungsmodulierendes Potenzial. Sie können zur Bekämpfung unerwünschter Mikroorganismen wie unerwünschter Pilze und Bakterien eingesetzt werden. Sie eignen sich insbesondere für den Pflanzenschutz (sie bekämpfen Mikroorganismen, die Pflanzenkrankheiten verursachen) oder für den Schutz von Materialien (z. B. technische Materialien, Nutzholz, gelagerte Güter), wie unten ausführlicher beschrieben. Genauer gesagt können die erfindungsgemäßen Wirkstoffkombinationen zum Schutz von Samen, keimenden Samen, aufgelaufenen Keimlingen, Pflanzen, Pflanzenteilen, Früchten, Erntegut und/oder dem Erdboden, in dem die Pflanzen wachsen, gegen unerwünschte Mikroorganismen eingesetzt werden. The active compound combinations according to the invention have a potent microbicidal activity and / or a high potential for plant defense modulating. They can be used to control unwanted microorganisms such as unwanted fungi and bacteria. They are particularly suitable for plant protection (they control micro-organisms that cause plant diseases) or for the protection of materials (eg technical materials, timber, stored Goods), as described in more detail below. More specifically, the active compound combinations according to the invention can be used to protect against undesired microorganisms seeds, germinating seeds, accumulated seedlings, plants, plant parts, fruits, crops and / or the soil in which the plants grow.
Die Kontrolle bzw. Bekämpfung umfasst, so wie der Begriff hier verwendet wird, die protektive, kurative und eradikative Behandlung unerwünschter Mikroorganismen. Bei den unerwünschten Mikroorganismen kann es sich um pathogene Bakterien, pathogene Viren, pathogene Oomyceten oder pathogene Pilze, spezieller phytopathogene Bakterien, phytopathogene Viren, phytopathogene Oomyceten oder phytopathogene Pilze handeln. Wie unten ausführlich beschrieben handelt es sich bei diesen phytopathogenen Mikroorganismen um die Verursacher eines breiten Spektrums an Pflanzenkrankheiten. As used herein, the control encompasses the protective, curative and eradicative treatment of undesirable microorganisms. The undesirable microorganisms may be pathogenic bacteria, pathogenic viruses, pathogenic oomycetes or pathogenic fungi, specific phytopathogenic bacteria, phytopathogenic viruses, phytopathogenic oomycetes or phytopathogenic fungi. As described in detail below, these phytopathogenic microorganisms are the causative agents of a wide variety of plant diseases.
Genauer gesagt können die erfindungsgemäßen Wirkstoffkombinationen als Fungizide eingesetzt werden. Im Rahmen der Beschreibung bezieht sich der Begriff „Fungizid“ auf eine Verbindung oder Zusammensetzung, die sich im Pflanzenschutz zur Bekämpfung unerwünschter Pilze wie Plasmodiophoromyceten, Chytridiomyceten, Zygomyceten, Ascomyceten, Basidiomyceten und Deuteromyceten und/oder zur Bekämpfung von Oomyceten verwenden lässt. More specifically, the active compound combinations according to the invention can be used as fungicides. In the description, the term "fungicide" refers to a compound or composition which can be used in crop protection for controlling undesired fungi such as Plasmodiophoromycetes, Chytridiomycetes, Zygomycetes, Ascomycetes, Basidiomycetes and Deuteromycetes and / or for controlling Oomycetes.
Die erfindungsgemäße Wirkstoffkombinationen können auch als antibakterielles Mittel eingesetzt werden. Sie können insbesondere im Pflanzenschutz zur Anwendung kommen, zum Beispiel zur Bekämpfung unerwünschter Bakterien wie Pseudomonadaceae, Rhizobiaceae, Xanthomonadaceae, Enterobacteriaceae, Corynebacteriaceae und Streptomycetaceae. The active compound combinations according to the invention can also be used as antibacterial agent. They can be used in particular in crop protection, for example for controlling undesired bacteria such as Pseudomonadaceae, Rhizobiaceae, Xanthomonadaceae, Enterobacteriaceae, Corynebacteriaceae and Streptomycetaceae.
Die erfindungsgemäßen Wirkstoffkombinationen können auch als antivirales Mittel im Pflanzenschutz eingesetzt werden. Die erfindungsgemäße Verbindung und die erfindungsgemäße Zusammensetzung können beispielsweise Wirkungen auf Krankheiten von Pflanzen viren wie dem Tabakmosaikvirus (TMV), Tobacco Rattle Virus, Tobacco Stunt Virus (TStuV), Tobacco Leaf Curl Virus (VLCV), Tobacco Nervilia Mosaic Virus (TVBMV), Tobacco Necrotic Dwarf Virus (TNDV), Tobacco Streak Virus (TSV), Potato Virus X (PVX), Potato Viruses Y, S, M, und A, Potato Acuba Mosaic Virus (PAMV), Potato Mop-Top Virus (PMTV), Potato Leaf-Roll Virus (PLRV), Alfalfa Mosaic Virus (AMV), Cucumber Mosaic Virus (CMV), Cucumber Green Mottlemosaic Virus (CGMMV), Cucumber Yellows Virus (CuYV), Watermelon Mosaic Virus (WMV), Tomato Spotted Wilt Virus (TSWV), Tomato Ringspot Virus (TomRSV), Sugarcane Mosaic Virus (SCMV), Rice Dwarf Virus, Rice Stripe Virus, Rice Black-Streaked Dwarf Virus, Strawberry Mottle Virus (SMoV), Strawberry Vein Banding Virus (SVBV), Strawberry Mild Yellow Edge Virus (SMYEV), Strawberry Crinkle Virus (SCrV), Broad Bean Wilt Virus (BBWV) und Melon Necrotic Spot Virus (MNSV) haben. Die vorliegende Erfindung betrifft außerdem ein Verfahren zur Bekämpfung unerwünschter Mikroorganismen wie unerwünschter Pilze, Oomyceten und Bakterien, welches den Schritt des Ausbringens mindestens einer erfindungsgemäßen Wirkstoffkombination auf die Mikroorganismen und/oder ihren Lebensraum (auf die Pflanzen, Pflanzenteile, Samen, Früchte oder auf den Boden, in dem die Pflanzen wachsen) umfasst. The active compound combinations according to the invention can also be used as an antiviral agent in crop protection. For example, the compound of the present invention and the composition of the present invention may have effects on diseases of plant viruses such as Tobacco Mosaic Virus (TMV), Tobacco Rattle Virus, Tobacco Stunt Virus (TStuV), Tobacco Leaf Curl Virus (VLCV), Tobacco Nervilia Mosaic Virus (TVBMV), Tobacco Necrotic Dwarf Virus (TNDV), Tobacco Streak Virus (TSV), Potato Virus X (PVX), Potato Viruses Y, S, M, and A, Potato Acuba Mosaic Virus (PAMV), Potato Mop-Top Virus (PMTV), Potato Leaf Roll Virus (PLRV), Alfalfa Mosaic Virus (AMV), Cucumber Mosaic Virus (CMV), Cucumber Green Mottlemosaic Virus (CGMMV), Cucumber Yellows Virus (CuYV), Watermelon Mosaic Virus (WMV), Tomato Spotted Wilt Virus (TSWV ), Tomato Ringspot Virus (TomRSV), Sugarcane Mosaic Virus (SCMV), Rice Dwarf Virus, Rice Stripe Virus, Rice Black-Streaked Dwarf Virus, Strawberry Mottle Virus (SMoV), Strawberry Vein Banding Virus (SVBV), Strawberry Mild Yellow Edge Virus (SMYEV), Strawberry Crinkle Virus (SCrV), Broad Bean Wil t Virus (BBWV) and Melon Necrotic Spot Virus (MNSV). The present invention also relates to a method for controlling unwanted microorganisms such as undesirable fungi, oomycetes and bacteria, which comprises the step of applying at least one active ingredient combination according to the invention to the microorganisms and / or their habitat (to the plants, plant parts, seeds, fruits or soil in which the plants grow).
Typischerweise bringt man, wenn die erfindungsgemäße Wirkstoffkombinationen in kurativen oder protektiven Verfahren zur Bekämpfung phytopathogener Pilze und/oder phytopathogener Oomyceten zur Anwendung kommen, eine wirksame und pflanzenkompatible Menge davon auf die Pflanzen, Pflanzenteile, Früchte, Samen oder auf den Boden oder Substrate, in denen die Pflanzen wachsen, aus. Geeignete Substrate, die zum Kultivieren von Pflanzen verwendet werden können, schließen Substrate auf anorganischer Basis wie Mineralwolle, insbesondere Steinwolle, Perlit, Sand oder Kiesel; organische Substrate wie Torf, Kiefernrinde oder Sägespäne; und Substrate auf Petroleumbasis wie polymere Schäume oder Kunststoffkügelchen ein. Wirksame und pflanzenkompatible Menge bedeutet eine Menge, die zur Bekämpfung oder Zerstörung der vorhandenen oder auf dem Kulturland auftretenden Pilze ausreicht und die bei den Kulturpflanzen keine nennenswerten Symptome von Phytotoxizität auslösen. Eine solche Menge kann in Abhängigkeit von dem zu bekämpfenden Pilz, dem Kulturpflanzentyp, dem Wachstumsstadium der Kulturpflanze, den klimatischen Bedingungen und der betreffenden eingesetzten erfindungsgemäßen Wirkstoffkombinationen in einem weiten Bereich schwanken. Diese Menge lässt sich durch systematische, dem Fachmann vertraute Freilandversuche bestimmen. Typically, when the drug combinations of the present invention are used in curative or protective methods for controlling phytopathogenic fungi and / or phytopathogenic oomycetes, an effective and plant compatible amount thereof is provided to the plants, plant parts, fruits, seeds or soil or substrates in which: the plants grow out. Suitable substrates that can be used to cultivate plants include inorganic based substrates such as mineral wool, especially rockwool, perlite, sand or pebbles; organic substrates such as peat, pine bark or sawdust; and petroleum-based substrates such as polymeric foams or plastic beads. Effective and plant-compatible amount means an amount sufficient to control or destroy the fungi present or occurring on the cultivated land, and which does not induce significant symptoms of phytotoxicity in the crops. Such an amount may vary widely depending on the fungus to be controlled, the crop type, the growth stage of the crop, the climatic conditions and the active compound combinations of the present invention used. This amount can be determined by systematic field trials familiar to the person skilled in the art.
Pathogene pathogens
Zu den nicht einschränkenden Beispielen für Pathogene von Pilzkrankheiten, die sich erfindungsgemäß behandeln lassen, zählen: Nonlimiting examples of pathogens of fungal diseases which can be treated according to the invention include:
Krankheiten, die durch Echter-Mehltau-Pathogene, zum Beispiel Blumeria- Arten, zum Beispiel Blumeria graminis ; Podosphaera- Arten, zum Beispiel Podosphaera leucotrichcr, Sphaerotheca-Arten, zum Beispiel Sphaerotheca fuliginecr, Uncinula- Arten, zum Beispiel Uncinula necator, verursacht werden; Diseases caused by downy mildew pathogens, for example Blumeria species, for example Blumeria graminis; Podosphaera species, for example Podosphaera leucotrichcr, Sphaerotheca species, for example Sphaerotheca fuliginecr, Uncinula species, for example Uncinula necator;
Krankheiten, die durch Rostkrankheitspathogene, zum Beispiel Gymnosporangium- Arten, zum Beispiel Gymnosporangium sabinae ; Hemileia- Arten, zum Beispiel Hemileia vastatrix ; Phakopsora- Arten, zum Beispiel Phakopsora pachyrhizi oder Phakopsora meibomiae, Puccinia- Arten, zum Beispiel Puccinia recondita, Puccinia graminis oder Puccinia striiformis ; Uromyces- Arten, zum Beispiel Uromyces appendiculatus, verursacht werden; Krankheiten, die durch Pathogene aus der Gruppe der Oomyceten, zum Beispiel Albugo-Arten, zum Beispiel Albugo candida) Bremia-Arten, zum Beispiel Bremia lactucae ; Peronospora- Arten, zum Beispiel Peronospora pisi oder P. brassicae, Phytophthora- Arten, zum Beispiel Phytophthora infestan ; Plasmopara- Arten, zum Beispiel Plasmopara viticola ; Pseudoperonospora- Arten, zum Beispiel Pseudoperonospora humuli oder Pseudoperonospora cubensis ; Pythium- Arten, zum Beispiel Pythium ultimum, verursacht werden; Diseases caused by rust pathogens, for example, Gymnosporangium species, for example, Gymnosporangium sabinae; Hemileia species, for example Hemileia vastatrix; Phakopsora species, for example Phakopsora pachyrhizi or Phakopsora meibomiae, Puccinia species, for example Puccinia recondita, Puccinia graminis or Puccinia striiformis; Uromyces species, for example Uromyces appendiculatus, are caused; Diseases caused by pathogens from the group of the Oomycetes, for example Albugo species, for example Albugo candida) Bremia species, for example Bremia lactucae; Peronospora species, for example Peronospora pisi or P. brassicae, Phytophthora species, for example Phytophthora infestan; Plasmopara species, for example Plasmopara viticola; Pseudoperonospora species, for example Pseudoperonospora humuli or Pseudoperonospora cubensis; Pythium species, for example Pythium ultimum, are caused;
Blattfleckenkrankheiten und Blattwelken, die z. B. von Alternaria- Arten, zum Beispiel Alternaria solani ; Cercospora-Arten, zum Beispiel Cercospora beticola ; Cladiosporium- Arten, zum Beispiel Cladiosporium cucumerinum ; Cochliobolus- Arten, zum Beispiel Cochliobolus sativus (Konidienform: Drechslera, Syn: Helminthosporium ) oder Cochliobolus miyabeanus ; Colletotrichum- Arten, zum Beispiel Colletotrichum lindemuthanium ; Corynespora-Arten, zum Beispiel Corynespora cassiicola ; Cycloconium-Arten, zum Beispiel Cycloconium oleaginum ; Diaporthe- Arten, zum Beispiel Diaporthe citri ; Zitanoe-Arten, zum Beispiel Elsinoe fawcettiv, Gloeosporium- Arten, zum Beispiel Gloeosporium laeticolor, Glomerella- Arten, zum Beispiel Glomerella cingulata ; Guignardia- Arten, zum Beispiel Guignardia bidwelli ; Leptosphaeria- Arten, zum Beispiel Leptosphaeria maculans ; Magnaporthe- Arten, zum Beispiel Magnaporthe grisea Microdochium-Arten, zum Beispiel Microdochium nivale ; Mycosphaerella- Arten, zum Beispiel Mycosphaerella graminicola, Mycosphaerella arachidicola oder Mycosphaerella fijiensis ; Phaeosphaeria- Arten, zum Beispiel Phaeosphaeria nodorum ; Pyrenophora- Arten, zum Beispiel Pyrenophora teres oder Pyrenophora tritici repentis ; Ramularia- Arten, zum Beispiel Ramularia collo-cygni oder Ramularia areola ; Rhynchosporium- Arten, zum Beispiel Rhynchosporium secalis ; Sepiorza-Arten, zum Beispiel Septoria apii oder Septoria lycopersici ; Stagonospora- Arten, zum Beispiel Stagonospora nodorum ; Typhula- Arten, zum Beispiel Typhula incarnata ; Gewinna-Arten, zum Beispiel Venturia inaequalis verursacht werden; Leaf spot diseases and leaf withering, the z. Alternaria species, for example Alternaria solani; Cercospora species, for example Cercospora beticola; Cladiosporium species, for example Cladiosporium cucumerinum; Cochliobolus species, for example Cochliobolus sativus (conidia form: Drechslera, Syn: Helminthosporium) or Cochliobolus miyabeanus; Colletotrichum species, for example Colletotrichum lindemuthanium; Corynespora species, for example Corynespora cassiicola; Cycloconium species, for example cycloconium oleaginum; Diaporthe species, for example Diaporthe citri; Citeranoe species, for example Elsinoe fawcettiv, Gloeosporium species, for example Gloeosporium laeticolor, Glomerella species, for example Glomerella cingulata; Guignardia species, for example Guignardia bidwelli; Leptosphaeria species, for example Leptosphaeria maculans; Magnaporthe species, for example Magnaporthe grisea Microdochium species, for example Microdochium nivale; Mycosphaerella species, for example Mycosphaerella graminicola, Mycosphaerella arachidicola or Mycosphaerella fijiensis; Phaeosphaeria species, for example Phaeosphaeria nodorum; Pyrenophora species, for example Pyrenophora teres or Pyrenophora tritici repentis; Ramularia species, for example Ramularia collo-cygni or Ramularia areola; Rhynchosporium species, for example Rhynchosporium secalis; Sepiorza species, for example Septoria apii or Septoria lycopersici; Stagonospora species, for example Stagonospora nodorum; Typhula species, for example Typhula incarnata; Profita species, for example, Venturia inaequalis are caused;
Wurzel- und Stängelkrankheiten, die z. B. von Corticium- Arten, zum Beispiel Corticium graminearum Fusarium-Arten, zum Beispiel Fusarium oxysporum ; Gaeumannomyces- Arten, zum Beispiel Gaeumannomyces graminis ; Plasmodiophora- Arten, zum Beispiel Plasmodiophora brassicae, Rhizoctonia- Arten, zum Beispiel Rhizoctonia solani ; Sarocladium- Arten, zum Beispiel Sarocladium oryzae ; Sclerotium- Alten, zum Beispiel Sclerotium oryzae ; Tapesm-Arten, zum Beispiel Tapesia acuformis ; Thielaviopsis- Arten, zum Beispiel Thielaviopsis basicola verursacht werden; Root and stem diseases, the z. Corticium species, for example Corticium graminearum Fusarium species, for example Fusarium oxysporum; Gaeumannomyces species, for example Gaeumannomyces graminis; Plasmodiophora species, for example Plasmodiophora brassicae, Rhizoctonia species, for example Rhizoctonia solani; Sarocladium species, for example Sarocladium oryzae; Sclerotium-Alten, for example Sclerotium oryzae; Tapesm species, for example Tapesia acuformis; Thielaviopsis species, for example Thielaviopsis basicola, are caused;
Ähren- und Rispenerkrankungen (einschließlich Maiskolben), die z. B. von Alternaria- Arten, zum Beispiel Alternaria spp .; Aspergillus- Arten, zum Beispiel Aspergillus flavus Cladosporium-Arten, zum Beispiel Cladosporium cladosporioides ; C/av/cepi-Arten, zum Beispiel Claviceps purpurea ; Fusarium- Arten, zum Beispiel Fusarium culmorum ; Gibberella- Arten, zum Beispiel Gibberella zeae ; Monographella- Arten, zum Beispiel Monographella nivalis, Stagnospora- Arten, zum Beispiel Stagnospora nodorum verursacht werden; Krankheiten, die von Brandpilzen, zum Beispiel Sphacelotheca- Arten, zum Beispiel Sphacelotheca reiliana ; Tilletia- Arten, zum Beispiel Tilletia caries oder Tilletia controverscr, Urocystis- Arten, zum Beispiel Urocystis occulta Ustilago- Arten, zum Beispiel Ustilago nuda verursacht werden; Ear and panicle diseases (including corncob), the z. Alternaria species, for example Alternaria spp. Aspergillus species, for example Aspergillus flavus Cladosporium species, for example Cladosporium cladosporioides; C / av / cepi species, for example Claviceps purpurea; Fusarium species, for example Fusarium culmorum; Gibberella species, for example Gibberella zeae; Monographella species, for example Monographella nivalis, Stagnospora species, for example Stagnospora nodorum are caused; Diseases caused by gangrenous fungi, for example sphacelotheca species, for example Sphacelotheca reiliana; Tilletia species, for example Tilletia caries or Tilletia controverscr, Urocystis species, for example Urocystis occulta Ustilago species, for example Ustilago nuda;
Fruchtfäule, die z. B. von Aspergillus- Arten, zum Beispiel Aspergillus flavus Botrytis- Arten, zum Beispiel Botrytis cinerea ; Monilinia- Arten, zum Beispiel Monilinia laxa Penicillium- Arten, zum Beispiel Penicillium expansum oder Penicillium purpurogenum ; Rhizopus- Arten, zum Beispiel Rhizopus stolonifer, Sclerotinia- Arten, zum Beispiel Sclerotinia sclerotiorum ; Verticilium- Arten, zum Beispiel Verticilium alboatrum verursacht wird; samen- und bodenbürtige Fäulen und Welken sowie Auflauferkrankungen, die z. B. Alternaria- Arten, zum Beispiel Alternaria brassicicola ; Aphanomyces- Arten, zum Beispiel Aphanomyces euteiches ; Ascochyta- Arten, zum Beispiel Ascochyta lentis ; Aspergillus- Arten, zum Beispiel Aspergillus flavus, Cladosporium- Arten, zum Beispiel Cladosporium herbarum ; Cochliobolus- Arten, zum Beispiel Cochliobolus sativus (Konidienform: Drechslera, Bipolaris Syn: Helminthosporium ); Colletotrichum- Arten, zum Beispiel Colletotrichum coccodes ; Fusarium- Arten, zum Beispiel Fusarium culmorum ; Gibberella- Arten, zum Beispiel Gibberella zeae ; Macrophomina- Arten, zum Beispiel Macrophomina phaseolina ; Microdochium- Arten, zum Beispiel Microdochium nivale ; Monographella- Arten, zum Beispiel Monographella nivalis, Penicillium- Arten, zum Beispiel Penicillium expansum ; Phoma- Arten, zum Beispiel Phoma Ungarn ; Phomopsis- Arten, zum Beispiel Phomopsis sojae Phytophthora- lten, zum Beispiel Phytophthora cactorum ; Pyrenophora- Arten, zum Beispiel Pyrenophora graminea ; Pyricularia- Arten, zum Beispiel Pyricularia oryzae ; Pythium- Arten, zum Beispiel Pythium ultimum, Rhizoctonia- Arten, zum Beispiel Rhizoctonia solani ; Rhizopus-Arten, zum Beispiel Rhizopus oryzae ; Sclerotium- Arten, zum Beispiel Sclerotium rolfsii, Septoria- Arten, zum Beispiel Septoria nodorum ; Typhula-Arten, zum Beispiel Typhula incarnata ; Verticillium- Arten, zum Beispiel Verticillium dahliae verursacht werden; Fruit rot, the z. Aspergillus species, for example Aspergillus flavus Botrytis species, for example Botrytis cinerea; Monilinia species, for example Monilinia laxa Penicillium species, for example Penicillium expansum or Penicillium purpurogenum; Rhizopus species, for example Rhizopus stolonifer, Sclerotinia species, for example Sclerotinia sclerotiorum; Verticilium species, for example Verticilium alboatrum is caused; seed- and soil-borne rots and wilting as well as casserole diseases, the z. Alternaria species, for example Alternaria brassicicola; Aphanomyces species, for example Aphanomyces euteiches; Ascochyta species, for example Ascochyta lentis; Aspergillus species, for example Aspergillus flavus, Cladosporium species, for example Cladosporium herbarum; Cochliobolus species, for example Cochliobolus sativus (conidia form: Drechslera, Bipolaris Syn: Helminthosporium); Colletotrichum species, for example Colletotrichum coccodes; Fusarium species, for example Fusarium culmorum; Gibberella species, for example Gibberella zeae; Macrophomina species, for example Macrophomina phaseolina; Microdochium species, for example Microdochium nivale; Monographella species, for example Monographella nivalis, Penicillium species, for example Penicillium expansum; Phoma species, for example Phoma Hungary; Phomopsis species, for example Phomopsis soyae phytophthora lals, for example Phytophthora cactorum; Pyrenophora species, for example Pyrenophora graminea; Pyricularia species, for example Pyricularia oryzae; Pythium species, for example Pythium ultimum, Rhizoctonia species, for example Rhizoctonia solani; Rhizopus species, for example Rhizopus oryzae; Sclerotium species, for example Sclerotium rolfsii, Septoria species, for example Septoria nodorum; Typhula species, for example Typhula incarnata; Verticillium species, for example Verticillium dahliae are caused;
Krebserkrankungen, Gallen und Hexenbesen, die z. B. von Nectria- Arten, zum Beispiel Nectria galligena verursacht werden; Cancers, galls and witches brooms, the z. Caused by Nectria species, for example Nectria galligena;
Welkeerkrankungen, die z.B. von Verticillium- Arten, zum Beispiel Verticillium longisporum; Fusarium- Arten, zum Beispiel Fusarium oxysporum verursacht werden; Wilting diseases, e.g. Verticillium species, for example Verticillium longisporum; Fusarium species, for example Fusarium oxysporum are caused;
Deformationen von Blättern, Blüten und Früchten, die z. B. von Exobasidium- Arten, zum Beispiel Exobasidium vexans ; Taphrina- Arten, zum Beispiel Taphrina deformans verursacht werden; Deformations of leaves, flowers and fruits, the z. B. Exobasidium species, for example Exobasidium vexans; Taphrina species, for example, Taphrina deformans are caused;
Degenerationserkrankungen holziger Pflanzen, die z. B. von foca-Arten, zum Beispiel Phaeomoniella chlamydospora, Phaeoacremonium aleophilum oder Fomitiporia mediterranea ; Ganoderma- Arten, zum Beispiel Ganoderma boninense verursacht werden; Krankheiten von Pflanzenknollen, die z. B. von Rhizoctonia- Arten, zum Beispiel Rhizoctonia solani ; Helminthosporium- Arten, zum Beispiel Helminthosporium solani verursacht werden; Degenerative diseases of woody plants, the z. From foca species, for example Phaeomoniella chlamydospora, Phaeoacremonium aleophilum or Fomitiporia mediterranea; Ganoderma species, for example Ganoderma boninense be caused; Diseases of plant tubers, the z. From Rhizoctonia species, for example Rhizoctonia solani; Helminthosporium species, for example Helminthosporium solani;
Krankheiten, die von bakteriellen Erregern, z. B. Xanthomonas- Arten, zum Beispiel Xanthomonas campestris pv. oryzae Pseudomonas- Arten, zum Beispiel Pseudomonas syringae pv. lachryman ; Erwinia- Arten, zum Beispiel Erwinia amylovora ; Liberibacter- Arten, zum Beispiel Liberibacter asiaticu ; Xyella-Arten, zum Beispiel Xylella fastidiosa Ralstonia-Arten, zum Beispiel Ralstonia solanacearum ; Dickeya- Arten, zum Beispiel Dickeya solani ; Clavibacter- Arten, zum Beispiel Clavibacter michiganensis ; Streptomyces- Arten, zum Beispiel Streptomyces scabies verursacht werden. Diseases caused by bacterial agents, eg. Xanthomonas species, for example Xanthomonas campestris pv. Oryzae Pseudomonas species, for example Pseudomonas syringae pv. Lachryman; Erwinia species, for example Erwinia amylovora; Liberibacter species, for example Liberibacter asiaticu; Xyella species, for example Xylella fastidiosa Ralstonia species, for example Ralstonia solanacearum; Dickeya species, for example Dickeya solani; Clavibacter species, for example Clavibacter michiganensis; Streptomyces species, for example Streptomyces scabies are caused.
Krankheiten von Sojabohnen: Diseases of soybeans:
Pilzkrankheiten an Blättern, Stängeln, Schoten und Samen, die z. B. durch A/ieraana-Blattflecken ( Altemaria spec. atrans tenuissima), Anthracnose (Colletotrichum gloeosporoides dematium var. truncatuni), Braunfleckenkrankheit ( Septoria glycines), Cercoipora-Purpurfleckenkrankheit ( Cercospora kikuchii), Choanephora- Leaf-Blight (Choanephora infundibulifera trispora (Syn.j), Dactuliophora-heuf-Spot (Dactuliophora glycines), Falscher Mehltau ( Peronospora manshurica), Drechslera- Blight ( Drechslern glycini), Cen ospora-R\ attll ecken k ran k hei t ( Cercospora sojina), Feptosphaerulina-Blattüeckenkrankheit (Leptosphaerulina trifolii), P/ry/Zorf/ca-Blattfleckenkrankheit ( Phyllosticta sojaecola), Pod and Stern Blight ( Phomopsis sojae), Echter Mehltau (Microsphaera diffusa), Pyrenoc/iaeta-Blattfleckenkrankheit (Pyrenochaeta glycines), Rhizoctonia Aerial, Foliage and Web Blight (Rhizoctonia solani), Rost (Phakopsora pachyrhizi, Phakopsora meibomiae), Schorf (Sphaceloma glycines), stemphylium Leaf Blight (Stemphylium botryosum), Sudden Death Syndrome (Fusarium virguliforme), Target Spot (Corynespora cassiicola) verursacht werden; Fungal diseases on leaves, stems, pods and seeds, the z. Anthracnose (Colletotrichum gloeosporoides dematium var. Truncatuni), brown spot disease (Septoria glycines), Cercoipora purple spot disease (Cercospora kikuchii), Choanephora leaf-blight (Choanephora infundibulifera trispora (Choanephora infundibulifera trispora). Syn.j), Dactuliophora-heuf-Spot (Dactuliophora glycines), downy mildew (Peronospora manshurica), Drechslera blight (Drechsler glycini), Cen ospora shrimp (Cercospora sojina), Feptosphaerulina leaf vascular disease (Leptosphaerulina trifolii), P / ry / Zorf / ca-blotch disease (Phyllosticta sojaecola), Pod and Star Blight (Phomopsis sojae), Powdery mildew (Microsphaera diffusa), Pyrenoc / iaeta leaf spot disease (Pyrenochaeta glycines), Rhizoctonia Aerial, Foliage and Web Blight (Rhizoctonia solani), rust (Phakopsora pachyrhizi, Phakopsora meibomiae), scab (Sphaceloma glycines), stemphyllium Leaf Blight (Stemphylium botryosum), Sudden Death Syndrome (Fusarium virguliforme), target spot (Corynespora cassiicola) are caused;
Pilzkrankheiten an Wurzeln und der Stängelbasis, die z. B. durch Black Root Rot (Calonectria crotalariae), Schwarzfäule (Macrophomina phaseolina), Fusarium Blight or Wilt, Root Rot, und Pod and Collar Rot (Fusarium oxysporum, Fusarium orthoceras, Fusarium semitectum, Fusarium equiseti), Mycoleptodiscus Root Rot (Mycoleptodiscus terrestris), Neocosmospora (Neocosmospora vasinfecta), Pod and Stern Blight (Diaporthe phaseolorum), Stängelkrebs (Diaporthe phaseolorum var. caulivora), Phytophthora-Fäule. (Phytophthora megasperma), Brown Stern Rot (Phialophora gregata), Pythium-Fäule (Pythium aphanidermatum, Pythium irreguläre, Pythium debaryanum, Pythium myriotylum, Pythium ultimum), Rhizoctonia Root Rot, Stern Decay and Damping-off (Rhizoctonia solani), Sclerotinia Stern Decay (Sclerotinia sclerotiorum), Sclerotinia Southern Blight (Sclerotinia rolfsii), Thielaviopsis- Wurzelfäule (Thielaviopsis basicola) verursacht werden. Mykotoxine Fungal diseases on roots and the stem base, the z. Black Root Red (Calonectria crotalariae), Black Rot (Macrophomina phaseolina), Fusarium Blight or Wilt, Root Red, and Pod and Collar Red (Fusarium oxysporum, Fusarium orthoceras, Fusarium semitectum, Fusarium equiseti), Mycoleptodiscus Root Red (Mycoleptodiscus terrestris ), Neocosmospora (Neocosmospora vasinfecta), Pod and Star Blight (Diaporthe phaseolorum), Stem Crab (Diaporthe phaseolorum var. Caulivora), Phytophthora rot. (Phytophthora megasperma), Brown Star Red (Phialophora gregata), Pythium rot (Pythium aphanidermatum, Pythium irregular, Pythium debaryanum, Pythium myriotylum, Pythium ultimum), Rhizoctonia Root Red, Star Decay and Damping off (Rhizoctonia solani), Sclerotinia star Decay (Sclerotinia sclerotiorum), Sclerotinia Southern Blight (Sclerotinia rolfsii), Thielaviopsis root rot (Thielaviopsis basicola). mycotoxins
Darüber hinaus können die erfindungsgemäßen Wirkstoffkombinationen den Mykotoxingehalt im Erntegut und den daraus hergestellten Nahrungs- und Futtermitteln reduzieren. Zu den Mykotoxinen zählen insbesondere, wobei dies nicht ausschließend ist, die folgenden: Desoxynivalenol (DON), Nivalenol, 15-Ac-DON, 3-Ac-DON, T2- und HT2-Toxin, Fumonisine, Zearalenon, Moniliformin, Fusarin, Diaceotoxyscirpenol (DAS), Beauvericin, Enniatin, Fusaroproliferin, Fusarenol, Ochratoxine, Patulin, Ergotalkaloide und Aflatoxine, die zum Beispiel durch die folgenden Pilze produziert werden können: Fusarium spec., wie F. acuminatum, F. asiaticum, F. avenaceum, F. crookwellense, F. culmorum, F. graminearum (Gibberella zeae), F. equiseti, F. fujikoroi, F. musarum, F. oxysporum, F. proliferatum, F. poae, F. pseudograminearum, F. sambucinum, F. scirpi, F. semitectum, F. solani, F. sporotrichoide , F. langsethiae, F. subglutinans, F. tricinctum, F. verticillioides usw., und außerdem durch Aspergillus spec. wie A. flavus, A. parasiticus, A. nomius, A. ochraceus, A. clavatus, A. terreus, A. versicolor, Penicillium spec. wie P. verrucosum, P. viridicatum, P. citrinum, P. expansum, P. claviforme, P. roqueforti, Claviceps spec. wie C. purpurea, C. fusiformis, C. paspali, C. africana, Stachybotrys spec. und andere. In addition, the active compound combinations according to the invention can reduce the mycotoxin content in the crop and the food and feed produced therefrom. Specifically, mycotoxins include, but are not limited to, the following: desoxynivalenol (DON), nivalenol, 15-Ac-DON, 3-Ac-DON, T2 and HT2 toxin, fumonisins, zearalenone, moniliformin, fusarin, diaceotoxyscirpenol (DAS), beauvericin, enniatine, fusaroproliferin, fusarenol, ochratoxins, patulin, ergot alkaloids and aflatoxins, which can be produced, for example, by the following fungi: Fusarium spec., Such as F. acuminatum, F. asiaticum, F. avenaceum, F. crookwellense, F. culmorum, F. graminearum (Gibberella zeae), F. equiseti, F. fujikoroi, F. musarum, F. oxysporum, F. proliferatum, F. poae, F. pseudograminearum, F. sambucinum, F. scirpi, F. semitectum, F. solani, F. sporotrichoid, F. langsethiae, F. subglutinans, F. tricinctum, F. verticillioides, etc., and also by Aspergillus spec. such as A. flavus, A. parasiticus, A. nomius, A. ochraceus, A. clavatus, A. terreus, A. versicolor, Penicillium spec. as P. verrucosum, P. viridicatum, P. citrinum, P. expansum, P. claviforme, P. roqueforti, Claviceps spec. as C. purpurea, C. fusiformis, C. paspali, C. africana, Stachybotrys spec. and other.
Verfahren und Verwendungen Methods and uses
Die Erfindung betrifft auch Verfahren zur Bekämpfung von tierischen Schädlingen, bei dem man die erfindungsgemäßen Wirkstoffkombinationen auf tierische Schädlinge und/oder ihren Eebensraum einwirken lässt. Bevorzugt wird die Bekämpfung der tierischen Schädlinge in der Fand- und Forstwirtschaft und im Materialschutz durchgeführt. Hierunter vorzugsweise ausgeschlossen sind Verfahren zur chirurgischen oder therapeutischen Behandlung des menschlichen oder tierischen Körpers und Diagnostizierverfahren, die am menschlichen oder tierischen Körper vorgenommen werden. The invention also relates to methods for controlling animal pests, in which the active ingredient combinations according to the invention are allowed to act on animal pests and / or their Eebensraum. The control of animal pests is preferably carried out in forestry and material protection. Excluded therefor are preferably methods for the surgical or therapeutic treatment of the human or animal body and diagnostic methods that are performed on the human or animal body.
Die Erfindung betrifft ferner die Verwendung der erfindungsgemäßen Wirkstoffkombinationen als Schädlingsbekämpfungsmittel, insbesondere Pflanzenschutzmittel. The invention further relates to the use of the active compound combinations according to the invention as pesticides, in particular crop protection agents.
Im Rahmen der vorliegenden Anmeldung umfasst der Begriff Schädlingsbekämpfungsmittel jeweils immer auch den Begriff Pflanzenschutzmittel. In the context of the present application, the term pest control always always includes the term pesticides.
Die erfindungsgemäßen Wirkstoffkombinationen eignen sich bei guter Pflanzenverträglichkeit, günstiger Warmblütertoxizität und guter Umweltverträglichkeit zum Schutz von Pflanzen und Pflanzenorganen vor biotischen und abiotischen Stressfaktoren, zur Steigerung der Ernteerträge, Verbesserung der Qualität des Erntegutes und zur Bekämpfung von tierischen Schädlingen, insbesondere Insekten, Spinnentieren, Helminthen, insbesondere Nematoden, und Mollusken, die in der Landwirtschaft, im Gartenbau, in Forsten, in Gärten und Freizeiteinrichtungen Vorkommen. Die erfindungsgemäßen Wirkstoffkombinationen können vorzugsweise als The active compound combinations according to the invention are suitable for plant protection, favorable warm-blooded toxicity and good environmental compatibility for the protection of plants and plant organs against biotic and abiotic stress factors, for increasing crop yields, improving the quality of the crop and for controlling animal pests, in particular insects, arachnids, helminths, especially nematodes, and mollusks that occur in agriculture, horticulture, forests, gardens and recreational facilities. The active compound combinations according to the invention can preferably be used as
Schädlingsbekämpfungsmittel eingesetzt werden. Sie sind gegen normal sensible und resistente Arten sowie gegen alle oder einzelne Entwicklungsstadien wirksam. Zu den oben erwähnten Schädlingen gehören:  Pesticides are used. They are effective against normally sensitive and resistant species as well as against all or individual stages of development. The above mentioned pests include:
Schädlinge aus dem Stamm der Arthropoda, insbesondere aus der Klasse der Arachnida z. B. Acarus spp., z. B. Acarus siro, Aceria kuko, Aceria sheldoni, Aculops spp., Aculus spp., z. B. Aculus fockeui, Aculus schlechtendali, Amblyomma spp., Amphitetranychus viennensis, Argas spp., Boophilus spp., Brevipalpus spp., z. B. Brevipalpus phoenicis, Bryobia graminum, Bryobia praetiosa, Centruroides spp., Chorioptes spp., Dermanyssus gallinae, Dermatophagoides pteronyssinus, Dermatophagoides farinae, Dermacentor spp., Eotetranychus spp., z. B. Eotetranychus hicoriae, Epitrimerus pyri, Eutetranychus spp., z. B. Eutetranychus banksi, Eriophyes spp., z. B. Eriophyes pyri, Glycyphagus domesticus, Halotydeus destructor, Hemitarsonemus spp., z. B. Hemitarsonemus latus (=Polyphagotarsonemus latus), Hyalomma spp., Ixodes spp., Latrodectus spp., Loxosceles spp., Neutrombicula autumnalis, Nuphersa spp., Oligonychus spp., z. B. Oligonychus coffeae, Oligonychus coniferarum, Oligonychus ilicis, Oligonychus indicus, Oligonychus mangiferus, Oligonychus pratensis, Oligonychus punicae, Oligonychus yothersi, Ornithodorus spp., Ornithonyssus spp., Panonychus spp., z. B. Panonychus citri (=Metatetranychus citri), Panonychus ulmi (=Metatetranychus ulmi), Phyllocoptruta oleivora, Platytetranychus multidigituli, Polyphagotarsonemus latus, Psoroptes spp., Rhipicephalus spp., Rhizoglyphus spp., Sarcoptes spp., Scorpio maurus, Steneotarsonemus spp., Steneotarsonemus spinki, Tarsonemus spp., z. B. Tarsonemus confusus, Tarsonemus pallidus, Tetranychus spp., z. B. Tetranychus canadensis, Tetranychus cinnabarinus, Tetranychus turkestani, Tetranychus urticae, Trombicula alfreddugesi, Vaejovis spp., Vasates lycopersici; aus der Klasse der Chilopoda z. B. Geophilus spp., Scutigera spp.; aus der Ordnung oder der Klasse der Collembola z. B. Onychiurus armatus; Sminthurus viridis; aus der Klasse der Diplopoda z. B. Blaniulus guttulatus; aus der Klasse der Insecta, z. B. aus der Ordnung der Blattodea z. B. Blatta orientalis, Blattella asahinai, Blattella germanica, Leucophaea maderae, Loboptera decipiens, Neostylopyga rhombifolia, Panchlora spp., Parcoblatta spp., Periplaneta spp., z. B. Periplaneta americana, Periplaneta australasiae, Pycnoscelus surinamensis, Supella longipalpa; aus der Ordnung der Coleoptera z. B. Acalymma vittatum, Acanthoscelides obtectus, Adoretus spp., Aethina tumida, Agelastica alni, Agrilus spp., z. B. Agrilus planipennis, Agrilus coxalis, Agrilus bilineatus, Agrilus anxius, Agriotes spp., z. B. Agriotes linneatus, Agriotes mancus, Alphitobius diaperinus, Amphimallon solstitialis, Anobium punctatum, Anoplophora spp., z. B. Anoplophora glabripennis, Anthonomus spp., z. B. Anthonomus grandis, Anthrenus spp., Apion spp., Apogonia spp., Atomaria spp., z. B. Atomaria linearis, Attagenus spp., Baris caerulescens, Bruchidius obtectus, Bruchus spp., z. B. Bruchus pisorum, Bruchus rufimanus, Cassida spp., Cerotoma trifurcata, Ceutorrhynchus spp., z. B. Ceutorrhynchus assimilis, Ceutorrhynchus quadridens, Ceutorrhynchus rapae, Chaetocnema spp., z. B. Chaetocnema confinis, Chaetocnema denticulata, Chaetocnema ectypa, Cleonus mendicus, Conoderus spp., Cosmopolites spp., z. B. Cosmopolites sordidus, Costelytra zealandica, Ctenicera spp., Curculio spp., z. B. Curculio caryae, Curculio caryatrypes, Curculio obtusus, Curculio sayi, Cryptolestes ferrugineus, Cryptolestes pusillus, Cryptorhynchus lapathi, Cryptorhynchus mangiferae, Cylindrocopturus spp., Cylindrocopturus adspersus, Cylindrocopturus furnissi, Dendroctonus spp., z. B. Dendroctonus ponderosae, Dermestes spp., Diabrotica spp., z. B. Diabrotica balteata, Diabrotica barberi, Diabrotica undecimpunctata howardi, Diabrotica undecimpunctata undecimpunctata, Diabrotica virgifera virgifera, Diabrotica virgifera zeae, Dichocrocis spp., Dicladispa armigera, Diloboderus spp., Epicaerus spp., Epilachna spp., z. B. Epilachna borealis, Epilachna varivestis, Epitrix spp., z. B. Epitrix cucumeris, Epitrix fuscula, Epitrix hirtipennis, Epitrix subcrinita, Epitrix tuberis, Faustinus spp., Gibbium psylloides, Gnathocerus cornutus, Hellula undalis, Heteronychus arator, Heteronyx spp., Hylamorpha elegans, Hylotrupes bajulus, Hypera postica, Hypomeces squamosus, Hypothenemus spp., z. B. Hypothenemus hampei, Hypothenemus obscurus, Hypothenemus pubescens, Lachnosterna consanguinea, Lasioderma serricorne, Latheticus oryzae, Lathridius spp., Lema spp., Leptinotarsa decemlineata, Leucoptera spp., z. B. Leucoptera coffeella, Limonius ectypus, Lissorhoptrus oryzophilus, Listronotus (=Hyperodes) spp., Lixus spp., Luperodes spp., Luperomorpha xanthodera, Lyctus spp., Megacyllene spp., z. B. Megacyllene robiniae, Megascelis spp., Melanotus spp., z. B. Melanotus longulus oregonensis, Meligethes aeneus, Melolontha spp., z. B. Melolontha melolontha, Migdolus spp., Monochamus spp., Naupactus xanthographus, Necrobia spp., Neogalerucella spp., Niptus hololeucus, Oryctes rhinoceros, Oryzaephilus surinamensis, Oryzaphagus oryzae, Otiorhynchus spp., z. B. Otiorhynchus cribricollis, Otiorhynchus ligustici, Otiorhynchus ovatus, Otiorhynchus rugosostriarus, Otiorhynchus sulcatus, Oulema spp., z. B. Oulema melanopus, Oulema oryzae, Oxycetonia jucunda, Phaedon cochleariae, Phyllophaga spp., Phyllophaga helleri, Phyllotreta spp., z. B. Phyllotreta armoraciae, Phyllotreta pusilla, Phyllotreta ramosa, Phyllotreta striolata, Popillia japonica, Premnotrypes spp., Prostephanus truncatus, Psylliodes spp., z. B. Psylliodes affinis, Psylliodes chrysocephala, Psylliodes punctulata, Ptinus spp., Rhizobius ventralis, Rhizopertha dominica, Rhynchophorus spp., Rhynchophorus ferrugineus, Rhynchophorus palmarum, Scolytus spp., z. B. Scolytus multistriatus, Sinoxylon perforans, Sitophilus spp., z. B. Sitophilus granarius, Sitophilus linearis, Sitophilus oryzae, Sitophilus zeamais, Sphenophorus spp., Stegobium paniceum, Sternechus spp., z. B. Sternechus paludatus, Symphyletes spp., Tanymecus spp., z. B. Tanymecus dilaticollis, Tanymecus indicus, Tanymecus palliatus, Tenebrio molitor, Tenebrioides mauretanicus, Tribolium spp., z. B. Tribolium audax, Tribolium castaneum, Tribolium confusum, Trogoderma spp., Tychius spp., Xylotrechus spp., Zabrus spp., z. B. Zabrus tenebrioides; aus der Ordnung der Dermaptera z. B. Anisolabis maritime, Forficula auricularia, Labidura riparia; aus der Ordnung der Diptera z. B. Aedes spp., z. B. Aedes aegypti, Aedes albopictus, Aedes sticticus, Aedes vexans, Agromyza spp., z. B. Agromyza frontella, Agromyza parvicornis, Anastrepha spp., Anopheles spp., z. B. Anopheles quadrimaculatus, Anopheles gambiae, Asphondylia spp., Bactrocera spp., z. B. Bactrocera Cucurbitae, Bactrocera dorsalis, Bactrocera oleae, Bibio hortulanus, Calliphora erythrocephala, Calliphora vicina, Ceratitis capitata, Chironomus spp., Chrysomya spp., Chrysops spp., Chrysozona pluvialis, Cochliomya spp., Contarinia spp., z. B. Contarinia johnsoni, Contarinia nasturtii, Contarinia pyrivora, Contarinia schulzi, Contarinia sorghicola, Contarinia tritici, Cordylobia anthropophaga, Cricotopus sylvestris, Culex spp., z. B. Culex pipiens, Culex quinquefasciatus, Culicoides spp., Culiseta spp., Cuterebra spp., Dacus oleae, Dasineura spp., z. B. Dasineura brassicae, Delia spp., z. B. Delia antiqua, Delia coarctata, Delia florilega, Delia platura, Delia radicum, Dermatobia hominis, Drosophila spp., z. B. Drosphila melanogaster, Drosophila suzukii, Echinocnemus spp., Euleia heraclei, Fannia spp., Gasterophilus spp., Glossina spp., Haematopota spp., Hydrellia spp., Hydrellia griseola, Hylemya spp., Hippobosca spp., Hypoderma spp., Liriomyza spp., z. B. Liriomyza brassicae, Liriomyza huidobrensis, Liriomyza sativae, Lucilia spp., z. B. Lucilia cuprina, Lutzomyia spp., Mansonia spp., Musca spp., z. B. Musca domestica, Musca domestica vicina, Oestrus spp., Oscinella frit, Paratanytarsus spp., Paralauterborniella subcincta, Pegomya oder Pegomyia spp., z. B. Pegomya betae, Pegomya hyoscyami, Pegomya rubivora, Phlebotomus spp., Phorbia spp., Phormia spp., Piophila casei, Platyparea poeciloptera, Prodiplosis spp., Psila rosae, Rhagoletis spp., z. B. Rhagoletis cingulata, Rhagoletis completa, Rhagoletis fausta, Rhagoletis indifferens, Rhagoletis mendax, Rhagoletis pomonella, Sarcophaga spp., Simulium spp., z. B. Simulium meridionale, Stomoxys spp., Tabanus spp., Tetanops spp., Tipula spp., z. B. Tipula paludosa, Tipula simplex, Toxotrypana curvicauda; aus der Ordnung der Hemiptera z. B. Acizzia acaciaebaileyanae, Acizzia dodonaeae, Acizzia uncatoides, Acrida turrita, Acyrthosipon spp., z. B. Acyrthosiphon pisum, Acrogonia spp., Aeneolamia spp., Agonoscena spp., Aleurocanthus spp., Aleyrodes proletella, Aleurolobus barodensis, Aleurothrixus floccosus, Allocaridara malayensis, Amrasca spp., z. B. Amrasca bigutulla, Amrasca devastans, Anuraphis cardui, Aonidiella spp., z. B. Aonidiella aurantii, Aonidiella citrina, Aonidiella inornata, Aphanostigma piri, Aphis spp., z. B. Aphis citricola, Aphis craccivora, Aphis fabae, Aphis forbesi, Aphis glycines, Aphis gossypii, Aphis hederae, Aphis illinoisensis, Aphis middletoni, Aphis nasturtii, Aphis nerii, Aphis pomi, Aphis spiraecola, Aphis viburniphila, Arboridia apicalis, Arytainilla spp., Aspidiella spp., Aspidiotus spp., z. B. Aspidiotus nerii, Atanus spp., Aulacorthum solani, Bemisia tabaci, Blastopsylla occidentalis, Boreioglycaspis melaleucae, Brachycaudus helichrysi, Brachycolus spp., Brevicoryne brassicae, Cacopsylla spp., z. B. Cacopsylla pyricola, Calligypona marginata, Capulinia spp., Carneocephala fulgida, Ceratovacuna lanigera, Cercopidae, Ceroplastes spp., Chaetosiphon fragaefolii, Chionaspis tegalensis, Chlorita onukii, Chondracris rosea, Chromaphis juglandicola, Chrysomphalus aonidum, Chrysomphalus ficus, Cicadulina mbila, Coccomytilus halb, Coccus spp., z. B. Coccus hesperidum, Coccus longulus, Coccus pseudomagnoliarum, Coccus viridis, Cryptomyzus ribis, Cryptoneossa spp., Ctenarytaina spp., Dalbulus spp., Dialeurodes chittendeni, Dialeurodes citri, Diaphorina citri, Diaspis spp., Diuraphis spp., Doralis spp., Drosicha spp., Dysaphis spp., z. B. Dysaphis apiifolia, Dysaphis plantaginea, Dysaphis tulipae, Dysmicoccus spp., Empoasca spp., z. B. Empoasca abrupta, Empoasca fabae, Empoasca maligna, Empoasca solana, Empoasca stevensi, Eriosoma spp., z. B. Eriosoma americanum, Eriosoma lanigerum, Eriosoma pyricola, Erythroneura spp., Eucalyptolyma spp., Euphyllura spp., Euscelis bilobatus, Ferrisia spp., Fiorinia spp., Furcaspis oceanica, Geococcus coffeae, Glycaspis spp., Heteropsylla cubana, Heteropsylla spinulosa, Homalodisca coagulata, Hyalopterus arundinis, Hyalopterus pruni, Icerya spp., z. B. Icerya purchasi, Idiocerus spp., Idioscopus spp., Laodelphax striatellus, Lecanium spp., z. B. Lecanium corni (=Parthenolecanium corni), Lepidosaphes spp., z. B. Lepidosaphes ulmi, Lipaphis erysimi, Lopholeucaspis japonica, Lycorma delicatula, Macrosiphum spp., z. B. Macrosiphum euphorbiae, Macrosiphum lilii, Macrosiphum rosae, Macrosteies facifrons, Mahanarva spp., Melanaphis sacchari, Metcalfiella spp., Metcalfa pruinosa, Metopolophium dirhodum, Monellia costalis, Monelliopsis pecanis, Myzus spp., z. B. Myzus ascalonicus, Myzus cerasi, Myzus ligustri, Myzus ornatus, Myzus persicae, Myzus nicotianae, Nasonovia ribisnigri, Neomaskellia spp., Nephotettix spp., z. B. Nephotettix cincticeps, Nephotettix nigropictus, Nettigoniclla spectra, Nilaparvata lugens, Oncometopia spp., Orthezia praelonga, Oxya chinensis, Pachypsylla spp., Parabemisia myricae, Paratrioza spp., z. B. Paratrioza cockerelli, Parlatoria spp., Pemphigus spp., z. B. Pemphigus bursarius, Pemphigus populivenae, Peregrinus maidis, Perkinsiella spp., Phenacoccus spp., z. B. Phenacoccus madeirensis, Phloeomyzus passerinii, Phorodon humuli, Phylloxera spp., z. B. Phylloxera devastatrix, Phylloxera notabilis, Pinnaspis aspidistrae, Planococcus spp., z. B. Planococcus citri, Prosopidopsylla flava, Protopulvinaria pyriformis, Pseudaulacaspis pentagona, Pseudococcus spp., z. B. Pseudococcus calceolariae, Pseudococcus comstocki, Pseudococcus longispinus, Pseudococcus maritimus, Pseudococcus viburni, Psyllopsis spp., Psylla spp., z. B. Psylla buxi, Psylla mali, Psylla pyri, Pteromalus spp., Pulvinaria spp., Pyrilla spp., Quadraspidiotus spp., z. B. Quadraspidiotus juglansregiae, Quadraspidiotus ostreaeformis, Quadraspidiotus perniciosus, Quesada gigas, Rastrococcus spp., Rhopalosiphum spp., z. B. Rhopalosiphum maidis, Rhopalosiphum oxyacanthae, Rhopalosiphum padi, Rhopalosiphum rufiabdominale, Saissetia spp., z. B. Saissetia coffeae, Saissetia miranda, Saissetia neglecta, Saissetia oleae, Scaphoideus titanus, Schizaphis graminum, Selenaspidus articulatus, Sipha flava, Sitobion avenae, Sogata spp., Sogatella furcifera, Sogatodes spp., Stictocephala festina, Siphoninus phillyreae, Tenalaphara malayensis, Tetragonocephela spp., Tinocallis caryaefoliae, Tomaspis spp., Toxoptera spp., z. B. Toxoptera aurantii, Toxoptera citricidus, Trialeurodes vaporariorum, Trioza spp., z. B. Trioza diospyri, Typhlocyba spp., Unaspis spp., Viteus vitifolii, Zygina spp.; aus der Unterordnung der Heteroptera z. B. Aelia spp., Anasa tristis, Antestiopsis spp., Boisea spp., Blissus spp., Calocoris spp., Campylomma livida, Cavelerius spp., Cimex spp., z. B. Cimex adjunctus, Cimex hemipterus, Cimex lectularius, Cimex pilosellus, Collaria spp., Creontiades dilutus, Dasynus piperis, Dichelops furcatus, Diconocoris hewetti, Dysdercus spp., Euschistus spp., z. B. Euschistus heros, Euschistus servus, Euschistus tristigmus, Euschistus variolarius, Eurydema spp., Eurygaster spp., Halyomorpha halys, Heliopeltis spp., Horcias nobilellus, Leptocorisa spp., Leptocorisa varicornis, Leptoglossus occidentalis, Leptoglossus phyllopus, Lygocoris spp., z. B. Lygocoris pabulinus, Lygus spp., z. B. Lygus elisus, Lygus hesperus, Lygus lineolaris, Macropes excavatus, Megacopta cribraria, Miridae, Monalonion atratum, Nezara spp., z. B. Nezara viridula, Nysius spp., Oebalus spp., Pentomidae, Piesma quadrata, Piezodorus spp., z. B. Piezodorus guildinii, Psallus spp., Pseudacysta persea, Rhodnius spp., Sahlbergella singularis, Scaptocoris castanea, Scotinophora spp., Stephanitis nashi, Tibraca spp., Triatoma spp.; aus der Ordnung der Hymenoptera z. B. Acromyrmex spp., Athalia spp., z. B. Athalia rosae, Atta spp., Camponotus spp., Dolichovespula spp., Diprion spp., z. B. Diprion similis, Hoplocampa spp., z. B. Hoplocampa cookei, Hoplocampa testudinea, Lasius spp., Linepithema (Iridiomyrmex) humile, Monomorium pharaonis, Paratrechina spp., Paravespula spp., Plagiolepis spp., Sirex spp., z. B. Sirex noctilio, Solenopsis invicta, Tapinoma spp., Technomyrmex albipes, Urocerus spp., Vespa spp., z. B. Vespa crabro, Wasmannia auropunctata, Xeris spp.; aus der Ordnung der Isopoda z. B. Armadillidium vulgare, Oniscus asellus, Porcellio scaber; aus der Ordnung der Isoptera z. B. Coptotermes spp., z. B. Coptotermes formosanus, Cornitermes cumulans, Cryptotermes spp., Incisitermes spp., Kalotermes spp., Microtermes obesi, Nasutitermis spp., Odontotermes spp., Porotermes spp., Reticulitermes spp., z. B. Reticulitermes flavipes, Reticulitermes hesperus; aus der Ordnung der Lepidoptera z. B. Achroia grisella, Acronicta major, Adoxophyes spp., z. B. Adoxophyes orana, Aedia leucomelas, Agrotis spp., z. B. Agrotis segetum, Agrotis ipsilon, Alabama spp., z. B. Alabama argillacea, Amyelois transitella, Anarsia spp., Anticarsia spp., z. B. Anticarsia gemmatalis, Argyroploce spp., Autographa spp., Barathra brassicae, Blastodacna atra, Borbo cinnara, Bucculatrix thurberiella, Bupalus piniarius, Busseola spp., Cacoecia spp., Caloptilia theivora, Capua reticulana, Carpocapsa pomonella, Carposina niponensis, Cheimatobia brumata, Chilo spp., z. B. Chilo plejadellus, Chilo suppressalis, Choreutis pariana, Choristoneura spp., Chrysodeixis chalcites, Clysia ambiguella, Cnaphalocerus spp., Cnaphalocrocis medinalis, Cnephasia spp., Conopomorpha spp., Conotrachelus spp., Copitarsia spp., Cydia spp., z. B. Cydia nigricana, Cydia pomonella, Dalaca noctuides, Diaphania spp., Diparopsis spp., Diatraea saccharalis, Dioryctria spp., z. B. Dioryctria zimmermani, Earias spp., Ecdytolopha aurantium, Elasmopalpus lignosellus, Eldana saccharina, Ephestia spp., z. B. Ephestia elutella, Ephestia kuehniella, Epinotia spp., Epiphyas postvittana, Erannis spp., Erschoviella musculana, Etiella spp., Eudocima spp., Eulia spp., Eupoecilia ambiguella, Euproctis spp., z. B. Euproctis chrysorrhoea, Euxoa spp., Feltia spp., Galleria mellonella, Gracillaria spp., Grapholitha spp., z. B. Grapholita molesta, Grapholita prunivora, Hedylepta spp., Helicoverpa spp., z. B. Helicoverpa armigera, Helicoverpa zea, Heliothis spp., z. B. Heliothis virescens , Hofmannophila pseudospretella, Homoeosoma spp., Homona spp., Hyponomeuta padella, Kakivoria flavofasciata, Lampides spp., Laphygma spp., Laspeyresia molesta, Leucinodes orbonalis, Leucoptera spp., z. B. Leucoptera coffeella, Lithocolletis spp., z. B. Lithocolletis blancardella, Lithophane antennata, Lobesia spp., z. B. Lobesia botrana, Loxagrotis albicosta, Lymantria spp., z. B. Lymantria dispar, Lyonetia spp., z. B. Lyonetia clerkella, Malacosoma neustria, Maruca testulalis, Mamestra brassicae, Melanitis leda, Mocis spp., Monopis obviella, Mythimna separata, Nemapogon cloacellus, Nymphula spp., Oiketicus spp., Omphisa spp., Operophtera spp., Oria spp., Orthaga spp., Ostrinia spp., z. B. Ostrinia nubilalis, Panolis flammea, Parnara spp., Pectinophora spp., z. B. Pectinophora gossypiella, Perileucoptera spp., Phthorimaea spp., z. B. Phthorimaea operculella, Phyllocnistis citrella, Phyllonorycter spp., z. B. Phyllonorycter blancardella, Phyllonorycter crataegella, Pieris spp., z. B. Pieris rapae, Platynota stultana, Plodia interpunctella, Plusia spp., Plutella xylostella (=Plutella maculipennis), Podesia spp., z. B. Podesia syringae, Prays spp., Prodenia spp., Protoparce spp., Pseudaletia spp., z. B. Pseudaletia unipuncta, Pseudoplusia includens, Pyrausta nubilalis, Rachiplusia nu, Schoenobius spp., z. B. Schoenobius bipunctifer, Scirpophaga spp., z. B. Scirpophaga innotata, Scotia segetum, Sesamia spp., z. B. Sesamia inferens, Sparganothis spp., Spodoptera spp., z. B. Spodoptera eradiana, Spodoptera exigua, Spodoptera frugiperda, Spodoptera praefica, Stathmopoda spp., Stenoma spp., Stomopteryx subsecivella, Synanthedon spp., Tecia solanivora, Thaumetopoea spp., Thermesia gemmatalis, Tinea cloacella, Tinea pellionella, Tineola bisselliella, Tortrix spp., Trichophaga tapetzella, Trichoplusia spp., z. B. Trichoplusia ni, Tryporyza incertulas, Tuta absoluta, Virachola spp.; aus der Ordnung der Orthoptera oder Saltatoria z. B. Acheta domesticus, Dichroplus spp., Gryllotalpa spp., z. B. Gryllotalpa gryllotalpa, Hieroglyphus spp., Locusta spp., z. B. Locusta migratoria, Melanoplus spp., z. B. Melanoplus devastator, Paratlanticus ussuriensis, Schistocerca gregaria; aus der Ordnung der Phthiraptera z. B. Damalinia spp., Haematopinus spp., Linognathus spp., Pediculus spp., Phylloxera vastatrix, Phthirus pubis, Trichodectes spp.; aus der Ordnung der Psocoptera z. B. Lepinotus spp., Liposcelis spp.; aus der Ordnung der Siphonaptera z. B. Ceratophyllus spp., Ctenocephalides spp., z. B. Ctenocephalides canis, Ctenocephalides felis, Pulex irritans, Tunga penetrans, Xenopsylla cheopis; aus der Ordnung der Thysanoptera z. B. Anaphothrips obscurus, Baliothrips biformis, Chaetanaphothrips leeuweni, Drepanothrips reuteri, Enneothrips flavens, Frankliniella spp., z. B. Frankliniella fusca, Frankliniella occidentalis, Frankliniella schultzei, Frankliniella tritici, Frankliniella vaccinii, Frankliniella williamsi, Haplothrips spp., Heliothrips spp., Hercinothrips femoralis, Kakothrips spp., Rhipiphorothrips cruentatus, Scirtothrips spp., Taeniothrips cardamomi, Thrips spp., z. B. Thrips palmi, Thrips tabaci; aus der Ordnung der Zygentoma (= Thysanura), z. B. Ctenolepisma spp., Lepisma saccharina, Lepismodes inquilinus, Thermobia domestica; aus der Klasse der Symphyla z. B. Scutigerella spp., z. B. Scutigerella immaculata; Pests from the strain of Arthropoda, in particular from the class of Arachnida z. Acarus spp., E.g. Acarus siro, Aceria kuko, Aceria sheldoni, Aculops spp., Aculus spp., E.g. Aculus fockeui, Aculus badendali, Amblyomma spp., Amphitetranychus viennensis, Argas spp., Boophilus spp., Brevipalpus spp., E.g. B. Brevipalpus phenicis, Bryobia graminum, Bryobia praetiosa, Centruroides spp., Chorioptes spp., Dermanyssus gallinae, Dermatophagoides pteronyssinus, Dermatophagoides farinae, Dermacentor spp., Eotetranychus spp. Eotetranychus hicoriae, Epitrimerus pyri, Eutetranychus spp., E.g. Eutetranychus banksi, Eriophyes spp., E.g. B. Eriophyes pyri, Glycyphagus domesticus, Halotydeus destructor, Hemitarsonemus spp., Z. B. Hemitarsonemus latus (= Polyphagotarsonemus latus), Hyalomma spp., Ixodes spp., Latrodectus spp., Loxosceles spp., Neutrombicula autumnalis, Nuphersa spp., Oligonychus spp., Z. Oligonychus coffeae, Oligonychus coniferarum, Oligonychus ilicis, Oligonychus indicus, Oligonychus mangiferus, Oligonychus pratensis, Oligonychus punicae, Oligonychus yothersi, Ornithodorus spp., Ornithonyssus spp., Panonychus spp., E.g. Panonychus citri (= Metatetranychus citri), Panonychus ulmi (= Metatetranychus ulmi), Phyllocoptruta oleivora, Platytetranychus multidigituli, Polyphagotarsonemus latus, Psoroptes spp., Rhipicephalus spp., Rhizoglyphus spp., Sarcoptes spp., Scorpio maurus, Steneotarsonemus spp. Steneotarsonemus spinki, Tarsonemus spp. Tarsonemus confusus, Tarsonemus pallidus, Tetranychus spp., E.g. Tetranychus canadensis, Tetranychus cinnabarinus, Tetranychus turkestani, Tetranychus urticae, Trombicula alfreddugesi, Vaejovis spp., Vasates lycopersici; from the class of Chilopoda z. Geophilus spp., Scutigera spp .; from the order or class of Collembola z. B. Onychiurus armatus; Sminthurus viridis; from the class of Diplopoda z. B. Blaniulus guttulatus; from the class of the Insecta, z. B. from the order of Blattodea z. Blatta orientalis, Blattella asahinai, Blattella germanica, Leucophaea maderae, Loboptera decipiens, Neostylopyga rhombifolia, Panchlora spp., Parcoblatta spp., Periplaneta spp., E.g. Periplaneta americana, Periplaneta australasiae, Pycnoscelus surinamensis, Supella longipalpa; from the order of Coleoptera z. Acalymma vittatum, Acanthoscelides obtectus, Adoretus spp., Aethina tumida, Agelastica alni, Agrilus spp., E.g. Agrilus planipennis, Agrilus coxalis, Agrilus bilineatus, Agrilus anxius, Agriotes spp., E.g. B. Agriotes linneatus, Agriotes mancus, Alphitobius diaperinus, Amphimallon solstitialis, Anobium punctatum, Anoplophora spp., Z. B. Anoplophora glabripennis, Anthonomus spp., e.g. Anthonomus grandis, Anthrenus spp., Apion spp., Apogonia spp., Atomaria spp., E.g. Eg Atomaria linearis, Attagenus spp., Baris caerulescens, Bruchidius obtectus, Bruchus spp., E.g. Bruchus pisorum, Bruchus rufimanus, Cassida spp., Cerotoma trifurcata, Ceutorrhynchus spp. Ceutorrhynchus assimilis, Ceutorrhynchus quadridens, Ceutorrhynchus rapae, Chaetocnema spp., E.g. Chaetocnema confinis, Chaetocnema denticulata, Chaetocnema ectypa, Cleonus mendicus, Conoderus spp., Cosmopolites spp., E.g. Cosmopolites sordidus, Costelytra zealandica, Ctenicera spp., Curculio spp., E.g. Curculio caryae, Curculio caryatrypes, Curculio obtusus, Curculio sayi, Cryptolestes ferrugineus, Cryptolestes pusillus, Cryptorhynchus lapathi, Cryptorhynchus mangiferae, Cylindrocopturus spp., Cylindrocopturus adspersus, Cylindrocopturus furnissi, Dendroctonus spp., E.g. Dendroctonus ponderosae, Dermestes spp., Diabrotica spp., E.g. Diabrotica balteata, Diabrotica barberi, Diabrotica undecimpunctata howardi, Diabrotica undecimpunctata undecimpunctata, Diabrotica virgifera virgifera, Diabrotica virgifera zeae, Dichocrocis spp., Dicladispa armigera, Diloboderus spp., Epicaerus spp., Epilachna spp., E.g. Epilachna borealis, Epilachna varivestis, Epitrix spp., E.g. Epitrix cucumeris, Epitrix fuscula, Epitrix hirtipennis, Epitrix subcrinita, Epitrix tuberis, Faustinus spp., Gibbium psylloides, Gnathocerus cornutus, Hellula and alis, Heteronychus arator, Heteronyx spp., Hylamorpha elegans, Hylotrupes bajulus, Hypera postica, Hypomeces squamosus, Hypothenemus spp., z. Hypothenemus hampei, Hypothenemus obscurus, Hypothenemus pubescens, Lachnosterna consanguinea, Lasioderma serricorne, Latheticus oryzae, Lathridius spp., Lema spp., Leptinotarsa decemlineata, Leucoptera spp., E.g. Luperoptera spp., Luperodes spp., Luperomorpha xanthodera, Lyctus spp., Megacyllene spp., E.g. Megacyllene robiniae, Megascelis spp., Melanotus spp., E.g. Melanotus longulus oregonensis, Meligethes aeneus, Melolontha spp., E.g. Melolontha melolontha, Migdolus spp., Monochamus spp., Naupactus xanthographus, Necrobia spp., Neogalerucella spp., Niptus hololeucus, Oryctes rhinoceros, Oryzaephilus surinamensis, Oryzaphagus oryzae, Otiorhynchus spp., E.g. Otiorhynchus cribricollis, Otiorhynchus ligustici, Otiorhynchus ovatus, Otiorhynchus rugosostriarus, Otiorhynchus sulcatus, Oulema spp., E.g. Oulema melanopus, Oulema oryzae, Oxycetonia jucunda, Phaedon cochleariae, Phyllophaga spp., Phyllophaga helleri, Phyllotreta spp., E.g. Phyllotreta armoraciae, Phyllotreta pusilla, Phyllotreta ramosa, Phyllotreta striolata, Popillia japonica, Premnotrypes spp., Prostephanus truncatus, Psylliodes spp., E.g. Psylliodes affinis, Psylliodes chrysocephala, Psylliodes punctulata, Ptinus spp., Rhizobius ventralis, Rhizopertha dominica, Rhynchophorus spp., Rhynchophorus ferruginus, Rhynchophorus palmarum, Scolytus spp. Scolytus multistriatus, Sinoxylon perforans, Sitophilus spp., E.g. Sitophilus granarius, Sitophilus linearis, Sitophilus oryzae, Sitophilus zeamais, Sphenophorus spp., Stegobium paniceum, Stemus spp., E.g. Starchus paludatus, Symphyletes spp., Tanymecus spp., E.g. Tanymecus dilaticollis, Tanymecus indicus, Tanymecus palliatus, Tenebrio molitor, Tenebrioides mauretanicus, Tribolium spp., E.g. Tribolium audax, Tribolium castaneum, Tribolium confusum, Trogoderma spp., Tychius spp., Xylotrechus spp., Zabrus spp., E.g. Zabrus tenebrioides; from the order of Dermaptera z. B. Anisolabis maritime, Forficula auricularia, Labidura riparia; from the order of Diptera z. B. Aedes spp., Z. Aedes aegypti, Aedes albopictus, Aedes sticticus, Aedes vexans, Agromyza spp., E.g. Agromyza frontella, Agromyza parvicornis, Anastrepha spp., Anopheles spp., E.g. Anopheles quadrimaculatus, Anopheles gambiae, Asphondylia spp., Bactrocera spp., E.g. Bactrocera cucurbitae, Bactrocera dorsalis, Bactrocera oleae, Bibio hortulanus, Calliphora erythrocephala, Calliphora vicina, Ceratitis capitata, Chironomus spp., Chrysomya spp., Chrysops spp., Chrysozona pluvialis, Cochliomya spp., Contarinia spp., E.g. Contarinia johnsoni, Contarina nasturtii, Contarina pyrivora, Contarinia schulzi, Contarina sorghicola, Contarinia tritici, Cordylobia anthropophaga, Cricotopus sylvestris, Culex spp. Culex pipiens, Culex quinquefasciatus, Culicoides spp., Culiseta spp., Cuterebra spp., Dacus oleae, Dasineura spp., E.g. B. Dasineura brassicae, Delia spp. Delia antiqua, Delia coarctata, Delia florilega, Delia platura, Delia radicum, Dermatobia hominis, Drosophila spp., E.g. Drosophila melanogaster, Drosophila suzukii, Echinocnemus spp., Euleia heraclei, Fannia spp., Gasterophilus spp., Glossina spp., Haematopota spp., Hydrellia spp., Hydrellia griseola, Hylemya spp., Hippobosca spp., Hypoderma spp. Liriomyza spp., E.g. Liriomyza brassicae, Liriomyza huidobrensis, Liriomyza sativae, Lucilia spp., E.g. Lucilia cuprina, Lutzomyia spp., Mansonia spp., Musca spp., E.g. Musca domestica, Musca domestica vicina, Oestrus spp., Oscinella frit, Paratanytarsus spp., Paralauterborniella subcincta, Pegomya or Pegomyia spp., E.g. Pegomya betae, Pegomya hyoscyami, Pegomya rubivora, Phlebotomus spp., Phorbia spp., Phormia spp., Piophila casei, Platyparea poeciloptera, Prodiplosis spp., Psila rosae, Rhagoletis spp., E.g. Rhagoletis cingulata, Rhagoletis completa, Rhagoletis fausta, Rhagoletis indifferens, Rhagoletis mendax, Rhagoletis pomonella, Sarcophaga spp., Simulium spp., E.g. B. Simulium meridionale, Stomoxys spp., Tabanus spp., Tetanops spp., Tipula spp., Z. B. Tipula paludosa, Tipula simplex, Toxotrypana curvicauda; from the order of Hemiptera z. Acizzia acaciaebaileyanae, Acizzia dodonaeae, Acizzia uncatoides, Acrida turrita, Acyrthosipon spp., E.g. Acyrthosiphon pisum, Acrogonia spp., Aeneolamia spp., Agonoscena spp., Aleurocanthus spp., Aleyrodes proletella, Aleurolobus barodensis, Aleurothrixus floccosus, Allocaridara malayensis, Amrasca spp., E.g. Amrasca bigutulla, Amrasca devastans, Anuraphis cardui, Aonidiella spp. Aonidiella aurantii, Aonidiella citrina, Aonidiella inornata, Aphanostigma piri, Aphis spp., E.g. Aphis citricola, Aphis craccivora, Aphis fabae, Aphis forbesi, Aphis glycines, Aphis gossypii, Aphis hederae, Aphis illinoisensis, Aphis middletoni, Aphis nasturtii, Aphis nerii, Aphis pomi, Aphis spiraecola, Aphis viburniphila, Arboridia apicalis, Arytainilla spp. , Aspidiella spp., Aspidiotus spp., E.g. Aspidiotus nerii, Atanus spp., Aulacorthum solani, Bemisia tabaci, Blastopsylla occidentalis, Boreioglycaspis melaleucae, Brachycaudus helichrysi, Brachycolus spp., Brevicoryne brassicae, Cacopsylla spp., E.g. Cacopsylla pyricola, Calligypona marginata, Capulinia spp., Carneocephala fulgida, Ceratovacuna lanigera, Cercopidae, Ceroplastes spp., Chaetosiphon fragaefolii, Chionaspis tegalensis, Chlorita onukii, Chondracris rosea, Chromaphis juglandicola, Chrysomphalus aonidum, Chrysomphalus ficus, Cicadulina mbila, Coccomytilus half, Coccus spp., e.g. Coccus hesperidum, Coccus longulus, Coccus pseudomagnoliarum, Coccus viridis, Cryptomyzus ribis, Cryptoneossa spp., Ctenarytaina spp., Dalbulus spp., Dialeurodes chittendeni, Dialeurodes citri, Diaphorina citri, Diaspis spp., Diuraphis spp., Doralis spp. Drosicha spp., Dysaphis spp., Z. Dysaphis apiifolia, Dysaphis plantaginea, Dysaphis tulipae, Dysmicoccus spp., Empoasca spp., E.g. Empaasca abrupta, Empoasca fabae, Empoasca maligna, Empoasca solana, Empoasca stevensi, Eriosoma spp. Eriosoma americanum, Eriosoma lanigerum, Eriosoma pyricola, Erythroneura spp., Eucalyptolyma spp., Euphyllura spp., Euscelis bilobatus, Ferrisia spp., Fiorinia spp., Furcaspis oceanica, Geococcus coffeae, Glycaspis spp., Heteropsylla cubana, Heteropsylla spinulosa, Homalodisca coagulata, Hyalopterus arundinis, Hyalopterus pruni, Icerya spp., E.g. Icerya purchasi, Idiocerus spp., Idioscopus spp., Laodelphax striatellus, Lecanium spp., E.g. B. Lecanium corni (= Parthenolecanium corni), Lepidosaphes spp., Z. Lepidosaphes ulmi, Lipaphis erysimi, Lopholeucaspis japonica, Lycorma delicatula, Macrosiphum spp., E.g. Macrosiphum euphorbiae, Macrosiphum lilii, Macrosiphum rosae, Macrosteies facifrons, Mahanarva spp., Melanaphis sacchari, Metcalfiella spp., Metcalfa pruinosa, Metopolophium dirhodum, Monellia costalis, Monelliopsis pecanis, Myzus spp., E.g. Myzus ascalonicus, Myzus cerasi, Myzus ligustri, Myzus ornatus, Myzus persicae, Myzus nicotianae, Nasonovia ribisnigri, Neomaskellia spp., Nephotettix spp., E.g. Nephotettix cincticeps, Nephotettix nigropictus, Nettigoniclla spectra, Nilaparvata lugens, Oncometopia spp., Orthezia praelonga, Oxya chinensis, Pachypsylla spp., Parabemisia myricae, Paratrioza spp., E.g. Paratrioza cockerelli, Parlatoria spp., Pemphigus spp., E.g. B. Pemphigus bursarius, Pemphigus populivenae, Peregrinus maidis, Perkinsiella spp., Phenacoccus spp., Z. Phenacoccus madeirensis, Phloeomyzus passerinii, Phorodon humuli, Phylloxera spp., E.g. Phylloxera devastatrix, Phylloxera notabilis, Pinnaspis aspidistrae, Planococcus spp., E.g. B. Planococcus citri, Prosopidopsylla flava, Protopulvinaria pyriformis, Pseudaulacaspis pentagona, Pseudococcus spp., Z. Pseudococcus calceolariae, Pseudococcus comstocki, Pseudococcus longispinus, Pseudococcus maritimus, Pseudococcus viburni, Psyllopsis spp., Psylla spp., E.g. Psylla buxi, Psylla mali, Psylla pyri, Pteromalus spp., Pulvinaria spp., Pyrilla spp., Quadraspidiotus spp., E.g. Quadraspidiotus juglansregiae, Quadraspidiotus ostreaeformis, Quadraspidiotus perniciosus, Quesada gigas, Rastrococcus spp., Rhopalosiphum spp., E.g. Rhopalosiphum maidis, Rhopalosiphum oxyacanthae, Rhopalosiphum padi, Rhopalosiphum rufiabdominal, Saissetia spp., E.g. Saissetia coffeae, Saissetia miranda, Saissetia neglecta, Saissetia oleae, Scaphoidus titanus, Schizaphis graminum, Selenaspidus articulatus, Sipha flava, Sitobion avenae, Sogata spp., Sogatella furcifera, Sogatodes spp., Stictocephala festina, Siphoninus phillyreae, Tenalaphara malayensis, Tetragonocephela spp., Tinocallis caryaefoliae, Tomaspis spp., Toxoptera spp., e.g. Toxoptera aurantii, Toxoptera citricidus, Trialeurodes vaporariorum, Trioza spp., E.g. Trioza diospyri, Typhlocyba spp., Unaspis spp., Viteus vitifolii, Zygina spp .; from the subordination of Heteroptera z. Aelia spp., Anasa tristis, Antestiopsis spp., Boisea spp., Blissus spp., Calocoris spp., Campylomma livida, Cavelerius spp., Cimex spp., E.g. Cimex adjunctus, Cimex hemipterus, Cimex lectularius, Cimex pilosellus, Collaria spp., Creontiades dilutus, Dasynus piperis, Dichelops furcatus, Diconocoris hewetti, Dysdercus spp., Euschistus spp., E.g. Eustistus heros, Euschistus servus, Eustistus tristigmus, Euschistus variolarius, Eurydema spp., Eurygaster spp., Halyomorpha halys, Heliopeltis spp., Horcias nobilellus, Leptocorisa spp., Leptocorisa varicornis, Leptoglossus occidentalis, Leptoglossus phyllopus, Lygocoris spp , Lygocoris pabulinus, Lygus spp., E.g. B. Lygus elisus, Lygus hesperus, Lygus lineolaris, Macropes excavatus, Megacopta cribraria, Miridae, Monalonion atratum, Nezara spp., Z. Nezara viridula, Nysius spp., Oebalus spp., Pentomidae, Piesma quadrata, Piezodorus spp., E.g. Pseudacysta persea, Rhodnius spp., Sahlbergella singularis, Scaptocoris castanea, Scotinophora spp., Stephanitis nashi, Tibraca spp., Triatoma spp .; from the order of Hymenoptera z. Acromyrmex spp., Athalia spp., E.g. B. Athalia rosae, Atta spp., Camponotus spp., Dolichovespula spp., Diprion spp., Z. B. Diprion similis, Hoplocampa spp., Z. Hoplocampa cookei, Hoplocampa testudinea, Lasius spp., Linepithema (Iridiomyrmex) humile, Monomorium pharaonis, Paratrechina spp., Paravespula spp., Plagiolepis spp., Sirex spp., E.g. Sirex noctilio, Solenopsis invicta, Tapinoma spp., Technomyrmex albipes, Urocerus spp., Vespa spp., E.g. Vespa crabro, Wasmannia auropunctata, Xeris spp .; from the order of Isopoda z. Armadillidium vulgare, Oniscus asellus, Porcellio scaber; from the order of Isoptera z. B. Coptotermes spp., Z. B. Coptotermes formosanus, Cornitermes cumulans, Cryptotermes spp., Incisitermes spp., Kalotermes spp., Microtermes obesi, Nasutitermis spp., Odontotermes spp., Porotermes spp., Reticulitermes spp., E.g. B. Reticulitermes flavipes, Reticulitermes hesperus; from the order of Lepidoptera z. Achroia grisella, Acronica major, Adoxophyes spp., E.g. Adoxophytes orana, Aedia leucomelas, Agrotis spp., E.g. B. Agrotis segetum, Agrotis ipsilon, Alabama spp., Z. Alabama argillacea, Amyelois transitella, Anarsia spp., Anticarsia spp., E.g. Anticarsia gemmatalis, Argyroploce spp., Autographa spp., Barathra brassicae, Blastodacna atra, Borbo cinnara, Bucculatrix thurberiella, Bupalus piniarius, Busseola spp., Cacoecia spp., Caloptilia theivora, Capua reticulana, Carpocapsa pomonella, Carposina niponensis, Cheimatobia brumata , Chilo spp., Z. Chilo plejadellus, Chilo suppressalis, Choreutis pariana, Choristoneura spp., Chrysodixis chalcites, Clysia ambiguella, Cnaphalocerus spp., Cnaphalocrocis medinalis, Cnephasia spp., Conopomorpha spp., Conotrachelus spp., Copitarsia spp., Cydia spp., E.g. Cydia nigricana, Cydia pomonella, Dalaca noctuides, Diaphania spp., Diparopsis spp., Diatraea saccharalis, Dioryctria spp., E.g. B. Dioryctria zimmermani, Earias spp., Ecdytolopha aurantium, Elasmopalpus lignosellus, Eldana saccharina, Ephestia spp., E.g. Ephestia elutella, Ephestia kuehniella, Epinotia spp., Epiphyas postvittana, Erannis spp., Efciella musculana, Etiella spp., Eudocima spp., Eulia spp., Eupoecilia ambiguella, Euproctis spp. Euproctis chrysorrhoea, Euxoa spp., Feltia spp., Galleria mellonella, Gracillaria spp., Grapholitha spp., E.g. B. Grapholita molesta, Grapholita prunivora, Hedylepta spp., Helicoverpa spp., Z. Helicoverpa armigera, Helicoverpa zea, Heliothis spp. Homo. Spp., Hyponomeuta padella, Kakivoria flavofasciata, Lampides spp., Laphygma spp., Laspeyresia molesta, Leucinodes orbonalis, Leucoptera spp., E.g. B. Leucoptera coffeella, Lithocolletis spp., Z. B. Lithocolletis blancardella, Lithophane antennata, Lobesia spp., Z. Lobesia botrana, Loxagrotis albicosta, Lymantria spp., E.g. B. Lymantria dispar, Lyonetia spp., Z. B. Lyonetia clerkella, Malacosoma neustria, Maruca testulalis, Mamestra brassicae, Melanitis leda, Mocis spp., Monopis obviella, Mythimna separata, Nemapogon cloacellus, Nymphula spp., Oiketicus spp., Omphisa spp., Operophtera spp., Oria spp. Orthaga spp., Ostrinia spp. Ostrinia nubilalis, Panolis flammea, Parnara spp., Pectinophora spp., E.g. B. Pectinophora gossypiella, Perileucoptera spp., Phthorimaea spp., Z. Phthorimaea operculella, Phyllocnistis citrella, Phyllonorycter spp., E.g. Phyllonorycter blancardella, Phyllonorycter crataegella, Pieris spp., E.g. Pieris rapae, Platynota stultana, Plodia interpunctella, Plusia spp., Plutella xylostella (= Plutella maculipennis), Podesia spp., E.g. Podesia syringae, Prays spp., Prodenia spp., Protoparce spp., Pseudaletia spp., E.g. B. Pseudaletia unipuncta, Pseudoplusia includens, Pyrausta nubilalis, Rachiplusia nu, Schoenobius spp., Z. Schoenobius bipunctifer, Scirpophaga spp., E.g. Scirpophaga innotata, Scotia segetum, Sesamia spp., E.g. Sesamia inferens, Sparganothis spp., Spodoptera spp., E.g. Spodoptera eradiana, Spodoptera exigua, Spodoptera frugiperda, Spodoptera praefica, Stathmopoda spp., Stenoma spp., Stomopteryx subsecivella, Synanthedon spp., Tecia solanivora, Thaumetopoea spp., Thermesia gemmatalis, Tinea cloacella, Tinea pellionella, Tineola bisselliella, Tortrix spp ., Trichophaga tapetzella, Trichoplusia spp. Trichoplusia ni, Tryporyza incertulas, Tuta absoluta, Virachola spp .; from the order of Orthoptera or Saltatoria z. B. Acheta domesticus, Dichroplus spp., Gryllotalpa spp., Z. Gryllotalpa gryllotalpa, Hieroglyphus spp., Locusta spp., E.g. Locusta migratoria, melanoplus spp., E.g. Melanoplus devastator, Paratlanticus ussuriensis, Schistocerca gregaria; from the order of Phthiraptera z. Damalinia spp., Haematopinus spp., Linognathus spp., Pediculus spp., Phylloxera vastatrix, Phthirus pubis, Trichodectes spp .; from the order of Psocoptera z. Lepinotus spp., Liposcelis spp .; from the order of Siphonaptera z. Ceratophyllus spp., Ctenocephalides spp., E.g. Ctenocephalides canis, Ctenocephalides felis, Pulex irritans, Tunga penetrans, Xenopsylla cheopis; from the order of Thysanoptera z. B. Anaphothrips obscurus, Baliothrips biformis, Chaetanaphothrips leeuweni, Drepanothrips reuteri, Enneothrips flavens, Frankliniella spp. Frankliniella fusca, Frankliniella occidentalis, Frankliniella schultzei, Frankliniella tritici, Frankliniella vaccinii, Frankliniella williamsi, Haplothrips spp., Heliothrips spp., Hercinothrips femoralis, Kakothrips spp., Rhipiphorothrips cruentatus, Scirtothrips spp., Taeniothrips cardamomi, Thrips spp., e.g. B. Thrips palmi, Thrips tabaci; from the order of Zygentoma (= Thysanura), z. Ctenolepisma spp., Lepisma saccharina, Lepismodes inquilinus, Thermobia domestica; from the class of Symphyla z. B. Scutigerella spp., Z. B. Scutigerella immaculata;
Schädlinge aus dem Stamm der Mollusca, z. B. aus der Klasse der Bivalvia, z. B. Dreissena spp.; sowie aus der Klasse der Gastropoda z. B. Arion spp., z. B. Arion ater rufus, Biomphalaria spp., Bulinus spp., Deroceras spp., z. B. Deroceras laeve, Galba spp., Lymnaea spp., Oncomelania spp., Pomacea spp., Succinea spp.; Pests of the strain of Mollusca, z. B. from the class of Bivalvia, z. B. Dreissena spp .; and from the class of Gastropoda z. B. Arion spp., Z. B. Arion ater rufus, Biomphalaria spp., Bulinus spp., Deroceras spp., Z. B. Deroceras laeve, Galba spp., Lymnaea spp., Oncomelania spp., Pomacea spp., Succinea spp .;
Pflanzenschädlinge aus dem Stamm der Nematoda, d. h. pflanzenparasitäre Nematoden, insbesondere Aglenchus spp., z. B. Aglenchus agricola, Anguina spp., z. B. Anguina tritici, Aphelenchoides spp., z. B. Aphelenchoides arachidis, Aphelenchoides fragariae, Belonolaimus spp., z. B. Belonolaimus gracilis, Belonolaimus longicaudatus, Belonolaimus nortoni, Bursaphelenchus spp., z. B. Bursaphelenchus cocophilus, Bursaphelenchus eremus, Bursaphelenchus xylophilus, Cacopaurus spp., z. B. Cacopaurus pestis, Criconemella spp., z. B. Criconemella curvata, Criconemella onoensis, Criconemella ornata, Criconemella rusium, Criconemella xenoplax (= Mesocriconema xenoplax), Criconemoides spp., z. B. Criconemoides ferniae, Criconemoides onoense, Criconemoides ornatum, Ditylenchus spp., z. B. Ditylenchus dipsaci, Dolichodorus spp., Globodera spp., z. B. Globodera pallida, Globodera rostochiensis, Helicotylenchus spp., z. B. Helicotylenchus dihystera, Hemicriconemoides spp., Hemicycliophora spp., Heterodera spp., z. B. Heterodera avenae, Heterodera glycines, Heterodera schachtii, Hirschmaniella spp., Hoplolaimus spp., Longidorus spp., z. B. Longidorus africanus, Meloidogyne spp., z. B. Meloidogyne chitwoodi, Meloidogyne fallax, Meloidogyne hapla, Meloidogyne incognita, Meloinema spp., Nacobbus spp., Neotylenchus spp., Paralongidorus spp., Paraphelenchus spp., Paratrichodorus spp., z. B. Paratrichodorus minor, Paratylenchus spp., Pratylenchus spp., z. B. Pratylenchus penetrans, Pseudohalenchus spp., Psilenchus spp., Punctodera spp., Quinisulcius spp., Radopholus spp., z. B. Radopholus citrophilus, Radopholus similis, Rotylenchulus spp., Rotylenchus spp., Scutellonema spp., Subanguina spp., Trichodorus spp., z. B. Trichodorus obtusus, Trichodorus primitivus, Tylenchorhynchus spp., z. B. Tylenchorhynchus annulatus, Tylenchulus spp., z. B. Tylenchulus semipenetrans, Xiphinema spp., z. B. Xiphinema index. Plant pests from the strain of Nematoda, d. H. plant parasitic nematodes, especially Aglenchus spp., e.g. Aglenchus agricola, Anguina spp., E.g. Anguina tritici, Aphelenchoides spp., E.g. Aphelenchoides arachidis, Aphelenchoides fragariae, Belonolaimus spp., E.g. Belonolaimus gracilis, Belonolaimus longicaudatus, Belonolaimus nortoni, Bursaphelenchus spp. Bursaphelenchus cocophilus, Bursaphelenchus eremus, Bursaphelenchus xylophilus, Cacopaurus spp., E.g. Cacopaurus pestis, Criconemella spp., E.g. Criconemella curvata, Criconemella onoensis, Criconemella ornata, Criconemella rusium, Criconemella xenoplax (= Mesocriconema xenoplax), Criconemoides spp., E.g. Criconemoides ferniae, Criconemoides onoense, Criconemoides ornatum, Ditylenchus spp., E.g. Ditylenchus dipsaci, Dolichodorus spp., Globodera spp., E.g. B. Globodera pallida, Globodera rostochiensis, Helicotylenchus spp., Z. Helicotylenchus dihystera, Hemicriconemoides spp., Hemicycliophora spp., Heterodera spp., E.g. Heterodera avenae, Heterodera glycines, Heterodera schachtii, Hirschmaniella spp., Hoplolaimus spp., Longidorus spp., E.g. Longidorus africanus, Meloidogyne spp., E.g. Meloidogyne chitwoodi, Meloidogyne fallax, Meloidogyne hapla, Meloidogyne incognita, Meloinema spp., Nacobbus spp., Neotylenchus spp., Paralongidorus spp., Paraphelenchus spp., Paratrichodorus spp., E.g. Paratrichodorus minor, Paratylenchus spp., Pratylenchus spp., E.g. Pratylenchus penetrans, Pseudohalenchus spp., Psilenchus spp., Punctodera spp., Quinisulcius spp., Radopholus spp., E.g. Radopholus citrophilus, Radopholus similis, Rotylenchulus spp., Rotylenchus spp., Scutellonema spp., Subanguina spp., Trichodorus spp., E.g. Trichodorus obtusus, Trichodorus primitivus, Tylenchorhynchus spp., E.g. Tylenchorhynchus annulatus, Tylenchulus spp., E.g. B. Tylenchulus semipenetrans, Xiphinema spp., Z. B. Xiphinema index.
Die erfindungsgemäßen Wirkstoffkombinationen können gegebenenfalls in bestimmten Kon zentrationen bzw. Aufwandmengen auch als Herbizide, Safener, Wachstumsregulatoren oder Mittel zur Verbesserung der Pflanzeneigenschaften, als Mikrobizide oder Gametozide, beispielsweise als Fungizide, Antimykotika, Bakterizide, Virizide (einschließlich Mittel gegen Viroide) oder als Mittel gegen MLO (Mycoplasma-like-organism) und RLO (Rickettsia-like-organism) verwendet werden. Sie lassen sich gegebenenfalls auch als Zwischen- oder Vorprodukte für die Synthese weiterer Wirkstoffe einsetzen. The active compound combinations according to the invention may optionally in certain con centrations or application rates as herbicides, safeners, growth regulators or agents for improving plant properties, as microbicides or gametocides, for example as Fungicides, antimycotics, bactericides, viricides (including anti-viral agents) or as agents against MLO (Mycoplasma-like-organism) and RLO (Rickettsia-like-organism). If appropriate, they can also be used as intermediates or precursors for the synthesis of further active ingredients.
F ormulierungen Formulations
Die vorliegende Erfindung betrifft weiterhin Formulierungen und daraus bereitete Anwendungsformen als Schädlingsbekämpfungsmittel wie z. B. Drench-, Drip- und Spritzbrühen, umfassend mindestens eine erfindungsgemäße Wirkstoffkombination. Gegebenenfalls enthalten die Anwendungsformen weitere Schädlingsbekämpfungsmittel und/oder die Wirkung verbessernde Adjuvantien wie Penetrationsförderer, z. B. pflanzliche Öle wie beispielsweise Rapsöl, Sonnenblumenöl, Mineralöle wie beispielsweise Paraffinöle, Alkylester pflanzlicher Fettsäuren wie beispielsweise Rapsöl- oder Sojaölmethylester oder Alkanol-alkoxylate und/oder Spreitmittel wie beispielsweise Alkylsiloxane und/oder Salze, z. B. organische oder anorganische Ammonium- oder Phosphoniumsalze wie beispielsweise Ammoniumsulfat oder Diammonium-hydrogenphosphat und/oder die Retention fördernde Mittel wie z. B. Dioctylsulfosuccinat oder Hydroxypropyl-guar-Polymere und/oder Humectants wie z. B. Glycerin und/oder Dünger wie beispielsweise Ammonium, Kalium oder Phosphor enthaltende Dünger. The present invention further relates to formulations and application forms prepared therefrom as pesticides such. B. drench, Drip and spray, comprising at least one active ingredient combination according to the invention. Optionally, the uses include other pesticides and / or effect-improving adjuvants such as penetration enhancers, e.g. As vegetable oils such as rapeseed oil, sunflower oil, mineral oils such as paraffin oils, alkyl esters of fatty acids such as rapeseed oil or soybean oil or alkanol alkoxylates and / or spreading agents such as alkyl siloxanes and / or salts, eg. As organic or inorganic ammonium or phosphonium salts such as ammonium sulfate or diammonium hydrogen phosphate and / or retention-promoting agents such. As dioctyl sulfosuccinate or hydroxypropyl guar polymers and / or humectants such. As glycerol and / or fertilizers such as ammonium, potassium or phosphorus-containing fertilizer.
Übliche Formulierungen sind beispielsweise wasserlösliche Flüssigkeiten (SF), Emulsionskonzentrate (EC), Emulsionen in Wasser (EW), Suspensionskonzentrate (SC, SE, FS, OD), in Wasser dispergierbare Granulate (WG), Granulate (GR) und Kapselkonzentrate (CS); diese und weitere mögliche Formuliertypen sind beispielsweise durch Crop Fife International und in Pesticide Specifications, Manual on development and use of FAO and WHO specifications for pesticides, FAO Plant Production and Protection Papers - 173, prepared by the FAO/WHO Joint Meeting on Pesticide Specifications, 2004, ISBN: 9251048576 beschrieben. Gegebenenfalls enthalten die Formulierungen neben einer oder mehreren erfindungsgemäßen Wirkstoffkombinationen weitere agrochemische Wirkstoffe. Typical formulations are, for example, water-soluble liquids (SF), emulsion concentrates (EC), emulsions in water (EW), suspension concentrates (SC, SE, FS, OD), water-dispersible granules (WG), granules (GR) and capsule concentrates (CS). ; These and other possible formulation types are described, for example, by Crop Fife International and in Pesticide Specifications, Manual on development and use of FAO and WHO specifications for pesticides, FAO Plant Production and Protection Papers - 173, prepared by the FAO / WHO Joint Meeting on Pesticide Specifications, 2004, ISBN: 9251048576. If appropriate, the formulations contain, in addition to one or more active compound combinations according to the invention, further agrochemical active substances.
Vorzugsweise handelt es sich um Formulierungen oder Anwendungsformen, welche Hilfsstoffe wie beispielsweise Streckmittel, Fösemittel, Spontanitätsförderer, Trägerstoffe, Emulgiermittel, Dispergiermittel, Frostschutzmittel, Biozide, Verdicker und/oder weitere Hilfsstoffe wie beispielsweise Adjuvantien enthalten. Ein Adjuvant in diesem Kontext ist eine Komponente, die die biologische Wirkung der Formulierung verbessert, ohne dass die Komponente selbst eine biologische Wirkung hat. Beispiele für Adjuvantien sind Mittel, die die Retention, das Spreitverhalten, das Anhaften an der Blattoberfläche oder die Penetration fördern. Diese Formulierungen werden in bekannter Weise hergestellt, z. B. durch Vermischen der erfindungsgemäßen Wirkstoffkombinationen mit Hilfsstoffen wie beispielsweise Streckmitteln, Lösemitteln und/oder festen Trägerstoffen und/oder weiteren Hilfsstoffen wie beispielsweise oberflächenaktiven Stoffen. Die Herstellung der Formulierungen erfolgt entweder in geeigneten Anlagen oder auch vor oder während der Anwendung. They are preferably formulations or use forms which contain auxiliaries, such as extenders, foaming agents, spontaneity promoters, carriers, emulsifiers, dispersants, antifreeze agents, biocides, thickeners and / or further auxiliaries, for example adjuvants. An adjuvant in this context is a component that enhances the biological effect of the formulation without the component itself having a biological effect. Examples of adjuvants are agents that promote retention, spreading behavior, adherence to the leaf surface, or penetration. These formulations are prepared in a known manner, for. Example by mixing the active compound combinations according to the invention with excipients such as extenders, solvents and / or solid carriers and / or other excipients such as surface-active substances. The preparation of the formulations is carried out either in suitable systems or before or during use.
Als Hilfsstoffe können solche Stoffe Verwendung finden, die geeignet sind, der Formulierung der erfindungsgemäßen Wirkstoffkombinationen oder den aus diesen Formulierungen bereiteten Anwendungsformen (wie z. B. gebrauchsfähigen Schädlingsbekämpfungsmitteln wie Spritzbrühen oder Saatgutbeizen) besondere Eigenschaften, wie bestimmte physikalische, technische und/oder biologische Eigenschaften zu verleihen. Excipients which can be used are those which are suitable for the formulation of the active compound combinations according to the invention or for the use forms prepared from these formulations (such as, for example, usable pesticides such as spray mixtures or seed dressing), such as certain physical, technical and / or biological properties to rent.
Als Streckmittel eignen sich z. B. Wasser, polare und unpolare organische chemische Flüssigkeiten z. B. aus den Klassen der aromatischen und nicht-aromatischen Kohlenwasserstoffe (wie Paraffine, Alkylbenzole, Alkylnaphthaline, Chlorbenzole), der Alkohole und Polyole (die ggf. auch substituiert, verethert und/oder verestert sein können), der Ketone (wie Aceton, Cyclohexanon), der Ester (auch Fette und Öle) und (Poly-)Ether, der einfachen und substituierten Amine, Amide, Lactame (wie N- Alkylpyrrolidone) und Lactone, der Sulfone und Sulfoxide (wie Dimethylsulfoxid), der Carbonate und der Nitrile. hn Falle der Benutzung von Wasser als Streckmittel können z. B. auch organische Lösemittel als Hilfslösemittel verwendet werden. Als flüssige Lösemittel kommen im Wesentlichen infrage: Aromaten wie Xylol, Toluol oder Alkylnaphthaline, chlorierte Aromaten oder chlorierte aliphatische Kohlenwasserstoffe wie Chlorbenzole, Chlorethylene oder Methylenchlorid, aliphatische Kohlenwasserstoffe, wie Cyclohexan oder Paraffine, z. B. Erdölfraktionen, mineralische und pflanzliche Öle, Alkohole wie Butanol oder Glykol sowie deren Ether und Ester, Ketone wie Aceton, Methylethylketon, Methylisobutylketon oder Cyclohexanon, stark polare Lösemittel wie Dimethylformamid oder Dimethylsulfoxid, Carbonate wie Propylencarbonat, Butylencarbonat, Diethylcarbonat oder Dibutylcarbonat, oder Nitrile wie Acetonitril oder Propannitril. Suitable extenders z. As water, polar and nonpolar organic chemical liquids such. B. from the classes of aromatic and non-aromatic hydrocarbons (such as paraffins, alkylbenzenes, alkylnaphthalenes, chlorobenzenes), alcohols and polyols (which may also be substituted, etherified and / or esterified), the ketones (such as acetone, cyclohexanone ), esters (including fats and oils) and (poly) ethers, simple and substituted amines, amides, lactams (such as N-alkylpyrrolidones) and lactones, sulfones and sulfoxides (such as dimethylsulfoxide), carbonates and nitriles. In the case of using water as an extender z. As well as organic solvents can be used as an auxiliary solvent. Suitable liquid solvents are essentially: aromatics such as xylene, toluene or alkylnaphthalenes, chlorinated aromatics or chlorinated aliphatic hydrocarbons such as chlorobenzenes, chloroethylenes or methylene chloride, aliphatic hydrocarbons such as cyclohexane or paraffins, eg. As petroleum fractions, mineral and vegetable oils, alcohols such as butanol or glycol and their ethers and esters, ketones such as acetone, methyl ethyl ketone, methyl isobutyl ketone or cyclohexanone, strong polar solvents such as dimethylformamide or dimethyl sulfoxide, carbonates such as propylene carbonate, butylene carbonate, diethyl carbonate or dibutyl carbonate, or nitriles such as acetonitrile or propanenitrile.
Grundsätzlich können alle geeigneten Lösemittel verwendet werden. Geeignete Lösemittel sind beispielsweise aromatische Kohlenwasserstoffe wie z. B. Xylol, Toluol oder Alkylnaphthaline, chlorierte aromatische oder chlorierte aliphatische Kohlenwasserstoffe wie z. B. Chlorbenzol, Chlorethylen, oder Methylenchlorid, aliphatische Kohlenwasserstoffe wie z. B. Cyclohexan, Paraffine, Erdölfraktionen, mineralische und pflanzliche Öle, Alkohole wie z. B. Methanol, Ethanol, iso-Propanol, Butanol oder Glykol sowie deren Ether und Ester, Ketone wie z. B. Aceton, Methylethylketon, Methylisobutylketon oder Cyclohexanon, stark polare Lösemittel wie Dimethylsulfoxid, Carbonate wie Propylencarbonat, Butylencarbonat, Diethylcarbonat oder Dibutylcarbonat, Nitrile wie Acetonitril oder Propannitril, sowie Wasser. Grundsätzlich können alle geeigneten Trägerstoffe eingesetzt werden. Als Trägerstoffe kommen insbesondere infrage: z. B. Ammoniumsalze und natürliche Gesteinsmehle wie Kaoline, Tonerden, Talkum, Kreide, Quarz, Attapulgit, Montmorillonit oder Diatomeenerde und synthetische Gesteinsmehle, wie hochdisperse Kieselsäure, Aluminiumoxid und natürliche oder synthetische Silikate, Harze, Wachse und/oder feste Düngemittel. Mischungen solcher Trägerstoffe können ebenfalls verwendet werden. Als Trägerstoffe für Granulate kommen infrage: z. B. gebrochene und fraktionierte natürliche Gesteine wie Calcit, Marmor, Bims, Sepiolith, Dolomit sowie synthetische Granulate aus anorganischen und organischen Mehlen sowie Granulate aus organischem Material wie Sägemehl, Papier, Kokosnussschalen, Maiskolben und Tabakstängel. In principle, all suitable solvents can be used. Suitable solvents are, for example, aromatic hydrocarbons such. As xylene, toluene or alkylnaphthalenes, chlorinated aromatic or chlorinated aliphatic hydrocarbons such. As chlorobenzene, chloroethylene, or methylene chloride, aliphatic hydrocarbons such. As cyclohexane, paraffins, petroleum fractions, mineral and vegetable oils, alcohols such. As methanol, ethanol, iso-propanol, butanol or glycol and their ethers and esters, ketones such. As acetone, methyl ethyl ketone, methyl isobutyl ketone or cyclohexanone, strong polar solvents such as dimethyl sulfoxide, carbonates such as propylene carbonate, butylene carbonate, diethyl carbonate or dibutyl carbonate, nitriles such as acetonitrile or propanenitrile, and water. In principle, all suitable carriers can be used. As carriers are in particular question: z. For example, ammonium salts and ground natural minerals such as kaolins, clays, talc, chalk, quartz, attapulgite, montmorillonite or diatomaceous earth and synthetic minerals such as finely divided silica, alumina and natural or synthetic silicates, resins, waxes and / or solid fertilizers. Mixtures of such carriers can also be used. Suitable carriers for granules are: z. As broken and fractionated natural rocks such as calcite, marble, pumice, sepiolite, dolomite and synthetic granules of inorganic and organic flours and granules of organic material such as sawdust, paper, coconut shells, corncobs and tobacco stems.
Auch verflüssigte gasförmige Streckmittel oder Lösemittel können eingesetzt werden. Insbesondere eignen sich solche Streckmittel oder Trägerstoffe, welche bei normaler Temperatur und unter Normaldruck gasförmig sind, z. B. Aerosol-Treibgase wie Halogenkohlenwasserstoffe sowie Butan, Propan, Stickstoff und Kohlendioxid. Also, liquefied gaseous diluents or solvents can be used. In particular, are such extenders or carriers which are gaseous at normal temperature and under atmospheric pressure, for. As aerosol propellants such as halogenated hydrocarbons and butane, propane, nitrogen and carbon dioxide.
Beispiele für Emulgier- und/oder Schaum erzeugende Mittel, Dispergiermittel oder Benetzungsmittel mit ionischen oder nicht-ionischen Eigenschaften oder Mischungen dieser oberflächenaktiven Stoffe sind Salze von Polyacrylsäure, Salze von Lignosulfonsäure, Salze von Phenolsulfonsäure oder Naphthalinsulfonsäure, Polykondensate von Ethylenoxid mit Fettalkoholen oder mit Fettsäuren oder mit Fettaminen, mit substituierten Phenolen (vorzugsweise Alkylphenole oder Arylphenole), Salze von Sulf obernsteinsäureestern, Taurinderivate (vorzugsweise Alkyltaurate), Isethionatderivate, Phosphorsäureester von polyethoxylierten Alkoholen oder Phenolen, Fettsäureester von Polyolen und Derivate der Verbindungen enthaltend Sulfate, Sulfonate und Phosphate, z. B. Alkylarylpolyglycolether, Alkylsulfonate, Alkylsulfate, Arylsulfonate, Eiweißhydrolysate, Lignin- Sulfitablaugen und Methylcellulose. Die Anwesenheit einer oberflächenaktiven Substanz ist vorteilhaft, wenn eine der erfindungsgemäßen Wirkstoffkombinationen und/oder einer der inerten Trägerstoffe nicht in Wasser löslich ist und wenn die Anwendung in Wasser erfolgt. Examples of emulsifying and / or foaming agents, dispersants or wetting agents having ionic or non-ionic properties or mixtures of these surfactants are salts of polyacrylic acid, salts of lignosulfonic acid, salts of phenolsulfonic acid or naphthalenesulfonic acid, polycondensates of ethylene oxide with fatty alcohols or with fatty acids or with fatty amines, with substituted phenols (preferably alkylphenols or arylphenols), salts of sulfosuccinic acid esters, taurine derivatives (preferably alkyl taurates), isethionate derivatives, phosphoric acid esters of polyethoxylated alcohols or phenols, fatty acid esters of polyols and derivatives of the compounds containing sulfates, sulfonates and phosphates, e.g. As alkylaryl polyglycol ethers, alkylsulfonates, alkyl sulfates, arylsulfonates, protein hydrolysates, lignin liquors and methylcellulose. The presence of a surface-active substance is advantageous if one of the active compound combinations according to the invention and / or one of the inert carriers is not soluble in water and if the application is carried out in water.
Als weitere Hilfsstoffe können in den Formulierungen und den daraus abgeleiteten Anwendungsformen Farbstoffe wie anorganische Pigmente, z. B. Eisenoxid, Titanoxid, Ferrocyanblau und organische Farbstoffe wie Alizarin-, Azo- und Metallphthalocyaninfarbstoffe und Nähr- und Spurennährstoffe wie Salze von Eisen, Mangan, Bor, Kupfer, Kobalt, Molybdän und Zink vorhanden sein. As further auxiliaries can in the formulations and the applications derived therefrom dyes such as inorganic pigments, eg. For example, iron oxide, titanium oxide, ferrocyan blue and organic dyes such as alizarin, azo and Metallphthalocyaninfarbstoffe and nutrient and trace nutrients such as salts of iron, manganese, boron, copper, cobalt, molybdenum and zinc may be present.
Weiterhin enthalten sein können Stabilisatoren wie Kältestabilisatoren, Konservierungsmittel, Oxidationsschutzmittel, Lichtschutzmittel oder andere die chemische und/oder physikalische Stabilität verbessernde Mittel. Weiterhin enthalten sein können schaumerzeugende Mittel oder Entschäumer. Stabilizers such as cold stabilizers, preservatives, antioxidants, light stabilizers or other chemical and / or physical stability-improving agents may also be present. It may also contain foam-forming agents or defoamers.
Ferner können die Formulierungen und daraus abgeleiteten Anwendungsformen als zusätzliche Hilfsstoffe auch Haftmittel wie Carboxymethylcellulose, natürliche und synthetische pulverige, körnige oder latexförmige Polymere enthalten wie Gummiarabikum, Polyvinylalkohol, Polyvinylacetat sowie natürliche Phospholipide wie Kephaline und Lecithine und synthetische Phospholipide. Weitere Hilfsstoffe können mineralische und pflanzliche Öle sein. Furthermore, the formulations and their derived use forms as additional auxiliaries also adhesives such as carboxymethylcellulose, natural and synthetic powdery, granular or latex-like polymers such as gum arabic, polyvinyl alcohol, polyvinyl acetate and natural phospholipids such as cephalins and lecithins and synthetic phospholipids. Other auxiliaries may be mineral and vegetable oils.
Gegebenenfalls können noch weitere Hilfsstoffe in den Formulierungen und den daraus abgeleiteten Anwendungsformen enthalten sein. Solche Zusatzstoffe sind beispielsweise Duftstoffe, schützende Kolloide, Bindemittel, Klebstoffe, Verdicker, thixotrope Stoffe, Penetrationsförderer, Retentionsförderer, Stabilisatoren, Sequestiermittel, Komplexbildner, Feuchthaltemittel, Spreitmittel hn Allgemeinen können die erfindungsgemäßen Wirkstoffkombinationen mit jedem festen oder flüssigen Zusatzstoff, welcher für Formulierungszwecke gewöhnlich verwendet wird, kombiniert werden. Optionally, further auxiliaries may be present in the formulations and in the use forms derived therefrom. Such additives include, for example, fragrances, protective colloids, binders, adhesives, thickeners, thixotropic agents, penetrants, retention promoters, stabilizers, sequestrants, chelants, humectants, spreading agents. Generally, the active compound combinations of this invention can be used with any solid or liquid additive commonly used for formulation purposes , be combined.
Als Retentionsförderer kommen alle diejenigen Substanzen in Betracht, die die dynamische Oberflächenspannung verringern wie beispielsweise Dioctylsulfosuccinat oder die die Visko-Elastizität erhöhen wie beispielsweise Hydroxypropyl-guar-Polymere. As retention promoters are all those substances which reduce the dynamic surface tension such as dioctylsulfosuccinate or increase the visco-elasticity such as hydroxypropyl guar polymers.
Als Penetrationsförderer kommen im vorliegenden Zusammenhang alle diejenigen Substanzen in Be tracht, die üblicherweise eingesetzt werden, um das Eindringen von agrochemischen Wirkstoffen in Pflanzen zu verbessern. Penetrationsförderer werden in diesem Zusammenhang dadurch definiert, dass sie aus der (in der Regel wässerigen) Applikationsbrühe und/oder aus dem Spritzbelag in die Kutikula der Pflanze eindringen und dadurch die Beweglichkeit der Wirkstoffe in der Kutikula erhöhen können. Die in der Literatur (Baur et al., 1997, Pesticide Science 51, 131-152) beschriebene Methode kann zur Bestimmung dieser Eigenschaft eingesetzt werden. Beispielhaft werden genannt Alkoholalkoxylate wie beispielsweise Kokosfettethoxylat (10) oder Isotridecylethoxylat (12), Fettsäureester wie beispielsweise Rapsöl- oder Sojaölmethylester, Fettaminalkoxylate wie beispielsweise Tallowamine-ethoxylat (15) oder Ammonium- und/oder Phosphonium-Salze wie beispielsweise Ammoniumsulfat oder Diammonium-hydrogenphosphat. In the present context, all those substances which are conventionally used to improve the penetration of agrochemical active substances into plants come into consideration as penetration promoters. Penetration promoters are in this context defined by the fact that they can penetrate from the (usually aqueous) application broth and / or from the spray coating into the cuticle of the plant and thereby increase the mobility of the active ingredients in the cuticle. The method described in the literature (Baur et al., 1997, Pesticide Science 51, 131-152) can be used to determine this property. Examples include alcohol alkoxylates such as coconut oil ethoxylate (10) or isotridecyl ethoxylate (12), fatty acid esters such as rapeseed oil or soybean oil, Fettaminalkoxylate such as tallowamine ethoxylate (15) or ammonium and / or phosphonium salts such as ammonium sulfate or diammonium hydrogen phosphate.
Die Formulierungen enthalten bevorzugt zwischen 0,00000001 und 98 Gew.-% der erfindungsgemäßen Wirkstoffkombination, besonders bevorzugt zwischen 0,01 und 95 Gew.-% der erfindungsgemäßen Wirkstoffkombination, ganz besonders bevorzugt zwischen 0,5 und 90 Gew.-% der erfindungsgemäßen Wirkstoffkombination, bezogen auf das Gewicht der Formulierung. The formulations preferably contain between 0.00000001 and 98% by weight of the active ingredient combination according to the invention, more preferably between 0.01 and 95% by weight of the active ingredient combination according to the invention, very particularly preferably between 0.5 and 90% by weight of the active ingredient combination according to the invention , based on the weight of the formulation.
Der Gehalt an der erfindungsgemäßen Wirkstoffkombination in den aus den Formulierungen bereiteten Anwendungsformen (insbesondere Schädlingsbekämpfungsmittel) kann in weiten Bereichen variieren. Die Konzentration der erfindungsgemäßen Wirkstoffkombination in den Anwendungsformen kann üblicherweise zwischen 0,00000001 und 95 Gew.-% der erfindungsgemäßen Wirkstoffkombination, vorzugsweise zwischen 0,00001 und 1 Gew.-%, bezogen auf das Gewicht der Anwendungsform, liegen. Die Anwendung geschieht in einer den Anwendungsformen angepassten üblichen Weise. Mischungen The content of the active ingredient combination according to the invention in the forms of application prepared from the formulations (in particular pesticides) can vary within wide ranges. The concentration of the active ingredient combination according to the invention in the application forms can usually be between 0.00000001 and 95% by weight of the active ingredient combination according to the invention, preferably between 0.00001 and 1% by weight, based on the weight of the application form. The application is done in a custom forms adapted to the application forms. mixtures
Die erfindungsgemäßen Wirkstoffkombinationen können auch in Mischung mit einem oder mehreren geeigneten Fungiziden, Bakteriziden, Akariziden, Molluskiziden, Nematiziden, Insektiziden, Mikrobiologika, Nützlingen, Herbiziden, Düngemitteln, Vogelrepellentien, Phytotonics, Sterilantien, Safenern, Semiochemicals und/oder Pflanzenwachstumsregulatoren verwendet werden, um so z. B. das Wirkungsspektrum zu verbreitern, die Wirkdauer zu verlängern, die Wirkgeschwindigkeit zu steigern, Repellenz zu verhindern oder Resistenzentwicklungen vorzubeugen. Des Weiteren können solche Wirkstoffkombinationen das Pflanzenwachstum und/oder die Toleranz gegenüber abiotischen Faktoren wie z. B. hohen oder niedrigen Temperaturen, gegen Trockenheit oder gegen erhöhten Wasser- bzw. Bodensalzgehalt verbessern. Auch lässt sich das Blüh- und Fruchtverhalten verbessern, die Keimfähigkeit und Bewurzelung optimieren, die Ernte erleichtern und Ernteertrag steigern, die Reife beeinflussen, die Qualität und/oder der Ernährungswert der Ernteprodukte steigern, die Lagerfähigkeit verlängern und/oder die Bearbeitbarkeit der Ernteprodukte verbessern. The active compound combinations according to the invention can also be used in admixture with one or more suitable fungicides, bactericides, acaricides, molluscicides, nematicides, insecticides, microbiologicals, beneficials, herbicides, fertilizers, avian repellents, phytotonics, sterilants, safeners, semiochemicals and / or plant growth regulators, in order to: z. B. to broaden the spectrum of action, to extend the duration of action, to increase the rate of action, to prevent repellence or to prevent development of resistance. Furthermore, such drug combinations, plant growth and / or tolerance to abiotic factors such. As high or low temperatures, improve against dryness or increased water or Bodensalzgehalt. Also, flowering and fruiting behavior can be improved, germination and rooting can be improved, harvesting and crop yields increased, maturity can be enhanced, crop quality and / or nutritional value increased, shelf life extended and / or crop productivity improved.
Weiterhin können die erfindungsgemäßen Wirkstoffkombinationen in Mischung mit weiteren Wirkstoffen oder Semiochemicals, wie Lockstoffen und/oder Vogelrepellentien und/oder Pflanzenaktivatoren und/oder Wachstumsregulatoren und/oder Düngemitteln vorliegen. Gleichfalls können die erfindungsgemäßen Wirkstoffkombinationen zur Verbesserung der Pflanzeneigenschaften wie zum Beispiel Wuchs, Ertrag und Qualität des Erntegutes eingesetzt werden. Furthermore, the active compound combinations according to the invention may be present in a mixture with other active substances or semiochemicals, such as attractants and / or avian repellents and / or plant activators and / or growth regulators and / or fertilizers. Likewise, the active compound combinations according to the invention can be used to improve the plant properties such as, for example, growth, yield and quality of the crop.
In einer besonderen erfindungsgemäßen Ausführungsform hegen die erfindungsgemäßen Wirkstoffkombinationen in Formulierungen bzw. in den aus diesen Formulierungen bereiteten Anwendungsformen in Mischung mit weiteren Verbindungen vor, vorzugsweise solchen wie nachstehend beschrieben. In a particular embodiment according to the invention, the active compound combinations according to the invention are present in formulations or in the use forms prepared from these formulations in admixture with further compounds, preferably those as described below.
Wenn eine der im Folgenden genannten Verbindungen in verschiedenen tautomeren Formen Vorkommen kann, sind auch diese Formen mit umfasst, auch wenn sie sie nicht in jedem Fall explizit genannt wurden. Alle genannten Mischungspartner können außerdem, wenn sie auf Grund ihrer funktionellen Gruppen dazu imstande sind, gegebenenfalls mit geeigneten Basen oder Säuren Salze bilden. If one of the following compounds can exist in different tautomeric forms, these forms are also included, although they were not explicitly mentioned in each case. In addition, if they are capable of doing so on the basis of their functional groups, all said mixing partners can optionally form salts with suitable bases or acids.
Insektizide/Akarizide/Nematizide Insecticides / acaricides / nematicides
Die hier mit ihrem „Common Name“ genannten Wirkstoffe sind bekannt und beispielsweise im Pestizidhandbuch („The Pesticide Manual“ 16th Ed., British Crop Protection Council 2012) beschrieben oder im Internet recherchierbar (z. B. http://www.alanwood.net/pesticides). Die Klassifizierung basiert auf dem zum Zeitpunkt der Einreichung dieser Patentanmeldung gültigen IRAC Mode of Action Classification Scheme. (1) Acetylcholinesterase(AChE)-Inhibitoren, vorzugsweise Carbamate ausgewählt aus Alanycarb, Aldicarb, Bendiocarb, Benfuracarb, Butocarboxim, Butoxycarboxim, Carbaryl, Carbofuran, Carbosulfan, Ethiofencarb, Fenobucarb, Formetanate, Furathiocarb, Isoprocarb, Methiocarb, Methomyl, Metolcarb, Oxamyl, Pirimicarb, Propoxur, Thiodicarb, Thiofanox, Triazamate, Trimethacarb, XMC und Xylylcarb, oder Organophosphate ausgewählt aus Acephat, Azamethiphos, Azinphos-ethyl, Azinphos- methyl, Cadusafos, Chlorethoxyfos, Chlorfenvinphos, Chlormephos, Chlorpyrifos-methyl, Coumaphos, Cyanophos, Demeton-S-methyl, Diazinon, Dichlorvos/DDVP, Dicrotophos, Dimethoat, Dimethylvinphos, Disulfoton, EPN, Ethion, Ethoprophos, Famphur, Fenamiphos, Fenitrothion, Fenthion, Fosthiazat, Heptenophos, Imicyafos, Isofenphos, Isopropyl-0-(methoxyaminothio- phosphoryl)salicylat, Isoxathion, Malathion, Mecarbam, Methamidophos, Methidathion, Mevinphos, Monocrotophos, Naled, Omethoate, Oxydemeton-methyl, Parathion-methyl, Phenthoat, Phorat, Phosalon, Phosmet, Phosphamidon, Phoxim, Pirimiphos-methyl, Profenofos, Propetamphos, Prothiofos, Pyraclofos, Pyridaphenthion, Quinalphos, Sulfotep, Tebupirimfos, Temephos, Terbufos, Tetrachlorvinphos, Thiometon, Triazophos, Triclorfon und Vamidothion. The active substances mentioned here by their "common name" are known and described, for example, in the Pesticide Handbook ("The Pesticide Manual" 16th ed., British Crop Protection Council 2012) or searchable on the Internet (eg http: //www.alanwood. net / pesticides). The classification is based on the IRAC Mode of Action Classification Scheme valid at the time of filing this patent application. (1) Acetylcholinesterase (AChE) inhibitors, preferably carbamates selected from alanycarb, aldicarb, bendiocarb, benfuracarb, butocarboxime, butoxycarboxime, carbaryl, carbofuran, carbosulfan, ethiofencarb, fenobucarb, formetanate, furathiocarb, isoprocarb, methiocarb, methomyl, metolcarb, oxamyl, Pirimicarb, propoxur, thiodicarb, thiofanox, triazamate, trimethacarb, XMC and xylylcarb, or organophosphates selected from acephate, azamethiphos, azinphos-ethyl, azinphos-methyl, cadusafos, chloroethoxyfos, chlorfenvinphos, chloroforms, chlorpyrifos-methyl, coumaphos, cyanophos, demeton S-methyl, diazinon, dichlorvos / DDVP, dicrotophos, dimethoate, dimethylvinphos, disulfone, EPN, ethion, ethoprophos, famphur, fenamiphos, fenitrothion, fenthione, fosthiazate, heptenophos, imicyafos, isofenphos, isopropyl-0- (methoxyaminothio-phosphoryl) salicylate , Isoxathione, Malathion, Mecarbam, Methamidophos, Methidathione, Mevinphos, Monocrotophos, Naled, Omethoate, Oxydemeton-methyl, Parathion-methyl, Phe nthoate, Phorat, Phosalon, Phosmet, Phosphamidone, Phoxim, Pirimiphos-methyl, Profenofos, Propetamphos, Prothiofos, Pyraclofos, Pyridaphenthion, Quinalphos, Sulfotep, Tebupirimfos, Temephos, Terbufos, Tetrachlorvinphos, Thiometon, Triazophos, Triclorfon and Vamidothion.
(2) GABA-gesteuerte Chlorid-Kanal-Blocker, vorzugsweise Cyclodien-organochlorine ausgewählt aus Chlordan und Endosulfan, oder Phenylpyrazole (Fiprole) ausgewählt aus Ethiprol und Fipronil. (2) GABA-controlled chloride channel blockers, preferably cyclodiene organochlorines selected from chlordane and endosulfan, or phenylpyrazoles (fiproles) selected from ethiprole and fipronil.
(3) Natrium-Kanal-Modulatoren, vorzugsweise Pyrethroide ausgewählt aus Acrinathrin, Allethrin, d- cis-trans-Allethrin, d-trans-Allethrin, Bifenthrin, Bioallethrin, Bioallethrin-S-cyclopentenyl-Isomer, Bioresmethrin, Cycloprothrin, Cyfluthrin, beta-Cyfluthrin, Cyhalothrin, lambda-Cyhalothrin, gamma- Cyhalothrin, Cypermethrin, alpha-Cypermethrin, beta-Cypermethrin, theta-Cypermethrin, zeta- Cypermethrin, Cyphenothrin [(lR)-trans-Isomer], Deltamethrin, Empenthrin [(EZ)-(IR) -Isomer], Esfenvalerat, Etofenprox, Fenpropathrin, Fenvalerat, Flucythrinat, Flumethrin, tau-Fluvalinat, Halfenprox, bniprothrin, Kadethrin, Momfluorothrin, Permethrin, Phenothrin [(lR)-trans-Isomer], Prallethrin, Pyrethrine (pyrethrum), Resmethrin, Silafluofen, Tefluthrin, Tetramethrin, Tetramethrin [(IR) -Isomer], Tralomethrin und Transfluthrin, oder DDT oder Methoxychlor. (3) Sodium channel modulators, preferably pyrethroids selected from acrinathrin, allethrin, d-cis-trans-allethrin, d-trans-allethrin, bifenthrin, bioallethrin, bioallethrin-S-cyclopentenyl isomer, bioresmethrin, cycloprothrin, cyfluthrin, beta Cyfluthrin, cyhalothrin, lambda-cyhalothrin, gamma-cyhalothrin, cypermethrin, alpha-cypermethrin, beta-cypermethrin, theta-cypermethrin, zeta-cypermethrin, cyphenothrin [(lR) -trans isomer], deltamethrin, empenthrin [(EZ) (IR) isomer], esfenvalerate, etofenprox, fenpropathrin, fenvalerate, flucythrinate, flumethrin, tau-fluvalinate, halfenprox, bniprothrin, kadethrin, momfluorothrin, permethrin, phenothrin [(lR) -trans isomer], prallethrin, pyrethrin (pyrethrum) , Resmethrin, silafluofen, tefluthrin, tetramethrin, tetramethrin [(IR) isomer], tralomethrin and transfluthrin, or DDT or methoxychlor.
(4) Kompetitive Modulatoren des nicotinischen Acetylcholin-Rezeptors (nAChR), vorzugsweise Neonicotinoide ausgewählt aus Acetamiprid, Clothianidin, Dinotefuran, bnidacloprid, Nitenpyram, Thiacloprid und Thiamethoxam, oder Nicotin, oder Sufoximine ausgewählt aus Sulfoxaflor, oder Butenolide ausgewählt aus Flupyradifurone. (4) Competitive modulators of the nicotinic acetylcholine receptor (nAChR), preferably neonicotinoids selected from acetamiprid, clothianidin, dinotefuran, bnidacloprid, nitenpyram, thiacloprid and thiamethoxam, or nicotine, or sufoximines selected from sulfoxaflor, or butenolides selected from flupyradifurone.
(5) Allosterische Modulatoren des nicotinischen Acetylcholin-Rezeptors (nAChR), vorzugsweise Spinosyne ausgewählt aus Spinetoram und Spinosad. (5) Allosteric modulators of the nicotinic acetylcholine receptor (nAChR), preferably spinosyns selected from spinetoram and spinosad.
(6) Allosterische Modulatoren des Glutamat-abhängigen Chloridkanals (GluCl), vorzugsweise Avermectine/Milbemycine ausgewählt aus Abamectin, Emamectin-benzoat, Eepimectin und Milbemectin. (7) Juvenilhormon-Mimetika, vorzugsweise Juvenilhormon-Analoge ausgewählt aus Hydropren, Kinopren und Methopren, oder Fenoxycarb oder Pyriproxyfen. (6) Allosteric modulators of the glutamate-dependent chloride channel (GluCl), preferably avermectins / milbemycins selected from abamectin, emamectin benzoate, eepimectin and milbemectin. (7) Juvenile hormone mimetics, preferably juvenile hormone analogs selected from hydroprene, kinoprene and methoprene, or fenoxycarb or pyriproxyfen.
(8) Verschiedene nicht spezifische (multi-site) Inhibitoren, vorzugsweise Alkylhalogenide ausgewählt aus Methylbromid und andere Alkylhalogenide, oder Chloropicrin oder Sulfurylfluorid oder Borax oder Brechweinstein oder Methylisocyanaterzeuger ausgewählt aus Diazomet und Metam. (8) Various non-specific (multi-site) inhibitors, preferably alkyl halides selected from methyl bromide and other alkyl halides, or chloropicrin or sulfuryl fluoride or borax or tartaric or methyl isocyanate producers selected from Diazomet and Metam.
(9) TRPV-Kanal -Modulatoren chordotonaler Organe ausgewählt aus Pymetrozin und Pyrifluquinazon. (9) TRPV channel modulators of chordotonic organs selected from pymetrozine and pyrifluquinazone.
(10) Milbenwachstumsinhibitoren ausgewählt aus Clofentezin, Hexythiazox, Diflovidazin und Etoxazol. (10) mite growth inhibitors selected from clofentezine, hexythiazox, diflovidazine and etoxazole.
(11) Mikrobielle Disruptoren der Insektendarmmembran ausgewählt aus Bacillus thuringiensis Subspezies israelensis, Bacillus sphaericus, Bacillus thuringiensis Subspezies aizawai, Bacillus thuringiensis Subspezies kurstaki, Bacillus thuringiensis Subspezies tenebrionis und B.t.- Pflanzenproteine ausgewählt aus CrylAb, CrylAc, CrylFa, CrylA.105, Cry2Ab, VIP3A, mCry3A, Cry3Ab, Cry3Bb und Cry34Ab 1/35 Abi. (11) Insect intestinal membrane microbial disruptors selected from Bacillus thuringiensis subspecies israelensis, Bacillus sphaericus, Bacillus thuringiensis subspecies aizawai, Bacillus thuringiensis subspecies kurstaki, Bacillus thuringiensis subspecies tenebrionis, and Bt plant proteins selected from CrylAb, CrylAc, CrylFa, CrylA.105, Cry2Ab, VIP3A , mCry3A, Cry3Ab, Cry3Bb and Cry34Ab 1/35 Abi.
(12) Inhibitoren der mitochondrialen ATP-Synthase, vorzugsweise ATP-Disruptoren ausgewählt aus Diafenthiuron, oder Organozinnverbindungen ausgewählt aus Azocyclotin, Cyhexatin und Fenbutatin- oxid, oder Propargit oder Tetradifon. (12) inhibitors of mitochondrial ATP synthase, preferably ATP disruptors selected from diafenthiuron, or organotin compounds selected from azocyclotine, cyhexatin and fenbutatin oxide, or propargite or tetradifone.
(13) Entkoppler der oxidativen Phoshorylierung durch Störung des Protonengradienten ausgewählt aus Chlorfenapyr, DNOC und Sulfluramid. (13) Decoupling of oxidative phosphorylation by perturbation of the proton gradient selected from chlorfenapyr, DNOC, and sulfluramide.
(14) Blocker des nicotinischen Acetylcholinrezeptorkanals ausgewählt aus Bensultap, Cartap- hydrochlorid, Thiocyclam und Thiosultap-Natrium. (14) Blocker of the nicotinic acetylcholine receptor channel selected from Bensultap, Cartap hydrochloride, thiocyclam and thiosultap sodium.
(15) Inhibitoren der Chitinbiosynthese, Typ 0, ausgewählt aus Bistrifluron, Chlorfluazuron, Diflubenzuron, Flucycloxuron, Flufenoxuron, Hexaflumuron, Lufenuron, Novaluron, Noviflumuron, Teflubenzuron und Triflumuron. (15) Inhibitors of chitin biosynthesis, type 0, selected from bistrifluron, chlorofluorazuron, diflubenzuron, flucycloxuron, flufenoxuron, hexaflumuron, lufenuron, novaluron, noviflumuron, teflubenzuron and triflumuron.
(16) Inhibitoren der Chitinbiosynthese, Typ 1 ausgewählt aus Buprofezin. (16) inhibitors of chitin biosynthesis, type 1 selected from buprofezin.
(17) Häutungsdisruptor (insbesondere bei Dipteren, d. h. Zweiflüglern) ausgewählt aus Cyromazin. (17) Skinning disruptor (especially in dipterans, i.e., two-winged) selected from cyromazine.
(18) Ecdyson-Rezeptor-Agonisten ausgewählt aus Chromafenozid, Halofenozid, Methoxyfenozid und Tebufenozid. (18) Ecdysone receptor agonists selected from chromafenozide, halofenozide, methoxyfenozide and tebufenozide.
(19) Oktopamin-Rezeptor- Agonisten ausgewählt aus Amitraz. (20) Mitochondriale Komplex-III-Elektronentransportinhibitoren ausgewählt aus Hydramethylnon, Acequinocyl und Fluacrypyrim. (19) Octopamine receptor agonists selected from Amitraz. (20) Mitochondrial complex III electron transport inhibitors selected from hydramethylnone, acequinocyl and fluacrypyrim.
(21) Mitochondriale Komplex-I-Elektronentransportinhibitoren, vorzugsweise METI- Akarizide ausgewählt aus Fenazaquin, Fenpyroximat, Pyrimidifen, Pyridaben, Tebufenpyrad und Tolfenpyrad, oder Rotenon (Derris). (21) Mitochondrial Complex I Electron Transport Inhibitors, preferably META acaricides selected from Fenazaquin, Fenpyroximate, Pyrimidifen, Pyridaben, Tebufenpyrad and Tolfenpyrad, or rotenone (Derris).
(22) Blocker des spannungsabhängigen Natriumkanals ausgewählt aus Indoxacarb und Metaflumizone. (22) Voltage-responsive sodium channel blocker selected from indoxacarb and metaflumizone.
(23) Inhibitoren der Acetyl-CoA-Carboxylase, vorzugsweise Tetron- und Tetramsäurederivate ausgewählt aus Spirodiclofen, Spiromesifen und Spirotetramat. (23) Inhibitors of acetyl-CoA carboxylase, preferably tetronic and tetramic acid derivatives selected from spirodiclofen, spiromesifen and spirotetramat.
(24) Inhibitoren des mitochondrialen Komplex-IV -Elektronentransports, vorzugsweise Phosphine ausgewählt aus Aluminiumphosphid, Calciumphosphid, Phosphin und Zinkphosphid, oder Cyanide ausgewählt aus Calciumcyanid, Kaliumcyanid und Natriumcyanid. (24) inhibitors of mitochondrial complex IV electron transport, preferably phosphines selected from aluminum phosphide, calcium phosphide, phosphine and zinc phosphide, or cyanides selected from calcium cyanide, potassium cyanide and sodium cyanide.
(25) Inhibitoren des mitochondrialen Komplex-II-Elektronentransports, vorzugsweise beta- Ketonitrilderivate ausgewählt aus Cyenopyrafen und Cyflumetofen, oder Carboxanilide ausgewählt aus Pyflubumid. (25) inhibitors of mitochondrial complex II electron transport, preferably beta-ketone nitrile derivatives selected from cyenopyrafen and Cyflumetofen, or carboxanilides selected from Pyflubumid.
(28) Ryanodinrezeptor-Modulatoren, vorzugsweise Diamide ausgewählt aus Chlorantraniliprol, Cyantraniliprol und Flubendiamid. (28) ryanodine receptor modulators, preferably diamides selected from chlorantraniliprole, cyantraniliprole and flubendiamide.
(29) Modulatoren chordotonaler Organe (mit Undefinierter Zielstruktur) ausgewählt aus Flonicamid. (29) Modulators of chordotonic organs (with undefined target structure) selected from flonicamid.
(30) weitere Wirkstoffe ausgewählt aus Afidopyropen, Afoxolaner, Azadirachtin, Benclothiaz,(30) other active substances selected from afidopyropes, afoxolans, azadirachtin, benclothiaz,
Benzoximat, Bifenazat, Broflanilid, Bromopropylat, Chinomethionat, Chloroprallethrin, Cryolit, Cyclaniliprol, Cycloxaprid, Cyhalodiamid, Dicloromezotiaz, Dicofol, epsilon-Metofluthrin, epsilon- Momfluthrin, Flometoquin, Fluazaindolizin, Fluensulfon, Flufenerim, Flufenoxystrobin, Flufiprol, Fluhexafon, Fluopyram, Fluralaner, Fluxametamid, Fufenozid, Guadipyr, Heptafluthrin, Imidaclothiz, Iprodione, kappa-Bifenthrin, kappa-Tefluthrin, Fotilaner, Meperfluthrin, Paichongding, Pyridalyl, Pyrifluquinazon, Pyriminostrobin, Spirobudiclofen, Tetramethylfluthrin, Tetraniliprol, Tetrachlorantraniliprol, Tigolaner, Tioxazafen, Thiofluoximat, Triflumezopyrim und Iodmethan; des Weiteren Präparate auf Basis von Bacillus firmus (1-1582, BioNeem, Votivo), sowie folgende Verbindungen: l-{2-Fluor-4-methyl-5-[(2,2,2-trifluorethyl)sulfmyl]phenyl}-3-(trifluormethyl)-lH- l,2,4-triazol-5-amin (bekannt aus W02006/043635) (CAS 885026-50-6), { l'-[(2E)-3-(4-Benzoximat, bifenazate, broflanilide, bromopropylate, quinomethionate, chloroprallethrine, cryolite, cyclaniliprole, cycloxapride, cyhalodiamide, dicloromezotiaz, dicofol, epsilon-metofluthrin, epsilon-momfluthrin, flometoquine, fluazaindolizine, fluensulfone, flufenerim, flufenoxystrobin, flufiprole, fluxtaxon, fluopyram, fluralan, Fluxametamid, Fufenozid, Guadipyr, Heptafluthrin, Imidaclothiz, iprodione, kappa-bifenthrin, kappa-tefluthrin, Fotilaner, Meperfluthrin, Paichongding, pyridalyl, Pyrifluquinazon, Pyriminostrobin, Spirobudiclofen, Tetramethylfluthrin, Tetraniliprol, Tetrachlorantraniliprol, Tigolaner, Tioxazafen, Thiofluoximat, Triflumezopyrim and iodomethane; furthermore preparations based on Bacillus firmus (1-1582, BioNeem, Votivo), and the following compounds: 1- {2-fluoro-4-methyl-5 - [(2,2,2-trifluoroethyl) sulfmyl] phenyl} - 3- (trifluoromethyl) -1H-l, 2,4-triazol-5-amine (known from WO02006 / 043635) (CAS 885026-50-6), {1 '- [(2E) -3- (4-
Chlorphenyl)prop-2-en- 1 -yl] -5 -fluorspiro [indol-3,4'-piperidin] - 1 (2H)-yl } (2-chlorpyridin-4-yl)methanon (bekannt aus W02003/106457) (CAS 637360-23-7), 2-Chlor-N-[2-{ l-[(2E)-3-(4-chlorphenyl)prop-2- en-l-yl]piperidin-4-yl}-4-(trifluormethyl)phenyl]isonicotinamid (bekannt aus W02006/003494) (CAS 872999-66-1), 3-(4-Chlor-2,6-dimethylphenyl)-4-hydroxy-8-methoxy-l,8-diazaspiro[4.5]dec-3-en-2-on (bekannt aus WO 2010052161) (CAS 1225292-17-0), 3-(4-Chlor-2, 6-dimethylphenyl)-8-methoxy-2- oxo-1, 8-diazaspiro[4.5]dec-3-en-4-yl-ethylcarbonat (bekannt aus EP 2647626) (CAS-1440516-42-6), 4- (But-2-in-l-yloxy)-6-(3,5-dimethylpiperidin-l-yl)-5-fluorpyrimidin (bekannt aus W02004/099160) (CAS 792914-58-0), PF1364 (bekannt aus JP2010/018586) (CAS-Reg.No. 1204776-60-2), N-[(2E)-1- [(6-Chlorpyridin-3-yl)methyl]pyridin-2(lH)-yliden]-2,2,2-trifluoracetamid (bekannt ausChlorophenyl) prop-2-en-1-yl] -5-fluorospiro [indole-3,4'-piperidine] -1 (2H) -yl} (2-chloropyridin-4-yl) -methanone (known from WO0200 / 106457 ) (CAS 637360-23-7), 2-chloro-N- [2- {1 - [(2E) -3- (4-chlorophenyl) -prop-2-en-1-yl] -piperidin-4-yl} -4- (trifluoromethyl) phenyl] isonicotinamide (known from WO 02006/003494) (CAS 872999-66-1), 3- (4-chloro-2,6-dimethylphenyl) -4-hydroxy-8-methoxy-1,8 -diazaspiro [4.5] dec-3-en-2-one (known from WO 2010052161) (CAS 1225292-17-0), 3- (4-chloro-2, 6-dimethylphenyl) -8-methoxy-2-oxo-1,8-diazaspiro [4.5] dec-3-ene 4-yl ethyl carbonate (known from EP 2647626) (CAS-1440516-42-6), 4- (but-2-yn-1-yloxy) -6- (3,5-dimethylpiperidin-1-yl) - 5-fluoropyrimidine (known from W02004 / 099160) (CAS 792914-58-0), PF1364 (known from JP2010 / 018586) (CAS Reg. No. 1204776-60-2), N - [(2E) -1- [(6-chloropyridin-3-yl) methyl] pyridine-2 (1H) -ylidene] -2,2,2-trifluoroacetamide (known from
WO2012/029672) (CAS 1363400-41-2), (3E)-3-[l-[(6-Chlor-3-pyridyl)methyl]-2-pyridyliden]-l,l,l- trifluorpropan-2-on (bekannt aus WO2013/144213) (CAS 1461743-15-6), N-[3-(Benzylcarbamoyl)-4- chlorphenyl] - 1 -methyl-3-(pentafluorethyl)-4-(trifluormethyl)- 1 H-pyrazol-5 -carboxamid (bekannt aus W02010/051926) (CAS 1226889-14-0), 5-Brom-4-chlor-N-[4-chlor-2-methyl-6-WO2012 / 029672) (CAS 1363400-41-2), (3E) -3- [l - [(6-chloro-3-pyridyl) methyl] -2-pyridylidene] -l, l, l-trifluoropropane-2 on (known from WO2013 / 144213) (CAS 1461743-15-6), N- [3- (benzylcarbamoyl) -4-chlorophenyl] -1-methyl-3- (pentafluoroethyl) -4- (trifluoromethyl) -1 H- pyrazole-5-carboxamide (known from WO2010 / 051926) (CAS 1226889-14-0), 5-bromo-4-chloro-N- [4-chloro-2-methyl-6-
(methylcarbamoyl)phenyl]-2-(3-chlor-2-pyridyl)pyrazol-3-carboxamid (bekannt aus CN103232431) (CAS 1449220-44-3), 4-[5-(3,5-Dichlorphenyl)-4,5-dihydro-5-(trifluormethyl)-3-isoxazolyl]-2-methyl- N-(cis-l-oxido-3-thietanyl)benzamid, 4-[5-(3,5-Dichlorphenyl)-4,5-dihydro-5-(trifluormethyl)-3- isoxazolyl]-2-methyl-N-(trans-l-oxido-3-thietanyl)benzamid und 4-[(5S)-5-(3,5-Dichlorphenyl)-4,5- dihydro-5-(trifluormethyl)-3-isoxazolyl]-2-methyl-N-(cis-l-oxido-3-thietanyl)benzamid (bekannt aus WO 2013/050317 Al) (CAS 1332628-83-7), N-[3-Chlor-l-(3-pyridinyl)-lH-pyrazol-4-yl]-N-ethyl-3- [(3,3,3-trifluorpropyl)sulfinyl]propanamid, (+)-N-[3-Chlor-l-(3-pyridinyl)-lH-pyrazol-4-yl]-N-ethyl-3- [(3,3,3-trifluorpropyl)sulfinyl]propanamid und (-)-N-[3-Chlor-l-(3-pyridinyl)-lH-pyrazol-4-yl]-N-ethyl- 3-[(3,3,3-trifluorpropyl)sulfinyl]propanamid (bekannt aus WO 2013/162715 A2, WO 2013/162716 A2, US 2014/0213448 Al) (CAS 1477923-37-7), 5-[[(2E)-3-Chlor-2-propen-l-yl]amino]-l-[2,6-dichlor-4- (trifluormethyl)phenyl]-4-[(trifluormethyl)sulfinyl]-lH-pyrazol-3-carbonitrile (bekannt aus CN 101337937 A) (CAS 1105672-77-2), 3-Brom-N-[4-chlor-2-methyl-6-(methylcarbamoyl) phenyl] -2- (3-chloro-2-pyridyl) pyrazole-3-carboxamide (known from CN103232431) (CAS 1449220-44-3), 4- [5- (3,5-dichlorophenyl) -4 , 5-dihydro-5- (trifluoromethyl) -3-isoxazolyl] -2-methyl-N- (cis-1-oxido-3-thietanyl) -benzamide, 4- [5- (3,5-dichlorophenyl) -4, 5-dihydro-5- (trifluoromethyl) -3-isoxazolyl] -2-methyl-N- (trans-1-oxido-3-thietanyl) benzamide and 4 - [(5S) -5- (3,5-dichlorophenyl) -4,5-dihydro-5- (trifluoromethyl) -3-isoxazolyl] -2-methyl-N- (cis-1-oxido-3-thietanyl) benzamide (known from WO 2013/050317 A1) (CAS 1332628-83 -7), N- [3-chloro-1- (3-pyridinyl) -1H-pyrazol-4-yl] -N-ethyl-3- [(3,3,3-trifluoropropyl) sulfinyl] propanamide, (+ ) -N- [3-chloro-1- (3-pyridinyl) -1H-pyrazol-4-yl] -N-ethyl-3- [(3,3,3-trifluoropropyl) sulfinyl] propanamide and (-) - N- [3-chloro-1- (3-pyridinyl) -1H-pyrazol-4-yl] -N-ethyl-3 - [(3,3,3-trifluoropropyl) sulfinyl] propanamide (known from WO 2013/162715 A2, WO 2013/162716 A2, US 2014/0213448 A1) (CAS 1477923-37-7), 5 - [[(2E) -3-chloro-2-propen-1-yl] amino] -1- [2 , 6-dichloro-4- (trifluoromethyl) phenyl l] -4 - [(trifluoromethyl) sulfinyl] -1H-pyrazole-3-carbonitrile (known from CN 101337937 A) (CAS 1105672-77-2), 3-bromo-N- [4-chloro-2-methyl 6
[(methylamino)thioxomethyl]phenyl]-l-(3-chlor-2-pyridinyl)-lH-pyrazol-5-carboxamid, [(Methylamino) thioxomethyl] phenyl] -l- (3-chloro-2-pyridinyl) -lH-pyrazole-5-carboxamide,
(Liudaibenjiaxuanan, bekannt aus CN 103109816 A) (CAS 1232543-85-9); N-[4-Chlor-2-[[(l,l- dimethylethyl)amino] carbony 1] -6-methylphenyl]- 1 -(3-chlor-2-pyridinyl)-3-(fluormethoxy)- lH-pyrazol- 5-carboxamid (bekannt aus WO 2012/034403 Al) (CAS 1268277-22-0), N-[2-(5-Amino-l,3,4- thiadiazol-2-yl)-4-chlor-6-methylphenyl]-3-brom-l-(3-chlor-2-pyridinyl)-lH-pyrazol-5-carboxamid (bekannt aus WO 2011/085575 Al) (CAS 1233882-22-8), 4-[3-[2,6-Dichlor-4-[(3,3-dichlor-2-propen-l- yl)oxy]phenoxy]propoxy]-2-methoxy-6-(trifluormethyl)pyrimidin (bekannt aus CN 101337940 A) (CAS 1108184-52-6); (2E)- und 2(Z)-2-[2-(4-Cyanophenyl)-l-[3-(trifluormethyl)phenyl]ethyliden]-N- [4-(difluormethoxy)phenyl]hydrazincarboxamid (bekannt aus CN 101715774 A) (CAS 1232543-85-9); Cyclopropancarbonsäure-3-(2,2-dichlorethenyl)-2,2-dimethyl-4-(lH-benzimidazol-2-yl)phenylester (bekannt aus CN 103524422 A) (CAS 1542271-46-4); (4aS)-7-Chlor-2,5-dihydro-2- [ [(methoxycarbonyl) [4-[(trifluormethyl)thio]phenyl] amino] carbonyl] indeno [ 1 ,2-e] [ 1 ,3,4]oxadiazin- 4a(3H)-carbonsäuremethylester (bekannt aus CN 102391261 A) (CAS 1370358-69-2); 6-Desoxy-3-0- ethyl-2,4-di-0-methyl- 1 - [N- [4- [ 1 - [4-( 1 , 1 ,2,2,2-pentafluorethoxy)phenyl] - 1 H- 1 ,2,4-triazol-3- yl]phenyl]carbamat]-a-L-mannopyranose (bekannt aus US 2014/0275503 Al) (CAS 1181213-14-8); 8- (2-Cyclopropylmethoxy-4-trifluormethylphenoxy)-3-(6-trifluormethylpyridazin-3-yl)-3- azabicyclo[3.2.1]octan (CAS 1253850-56-4), (8-anti)-8-(2-Cyclopropylmethoxy-4- trifluormethylphenoxy)-3-(6-trifluormethylpyridazin-3-yl)-3-azabicyclo[3.2.1]octan (CAS 933798-27- 7), (8-syn)-8-(2-Cyclopropylmethoxy-4-trifluormethylphenoxy)-3-(6-trifluormethylpyridazin-3-yl)-3- azabicyclo[3.2.1]octan (bekannt aus WO 2007040280 Al, WO 2007040282 Al) (CAS 934001-66-8), N-[3-Chlor-l -(3-pyridinyl)-lH-pyrazol-4-yl]-N-ethyl-3-[(3, 3, 3-trifluorpropyl)thio] -propanamid (bekannt aus WO 2015/058021 Al, WO 2015/058028 Al) (CAS 1477919-27-9) und N-[4-(Aminothioxomethyl)-(Liudaibenjiaxuanan, known from CN 103109816 A) (CAS 1232543-85-9); N- [4-chloro-2 - [[(1,1-dimethylethyl) amino] carbonyl 1] -6-methylphenyl] -1- (3-chloro-2-pyridinyl) -3- (fluoromethoxy) -1H-pyrazole 5-carboxamide (known from WO 2012/034403 A1) (CAS 1268277-22-0), N- [2- (5-amino-1, 3,4-thiadiazol-2-yl) -4-chloro-6 -methylphenyl] -3-bromo-1- (3-chloro-2-pyridinyl) -1H-pyrazole-5-carboxamide (known from WO 2011/085575 A1) (CAS 1233882-22-8), 4- [3 [2,6-dichloro-4 - [(3,3-dichloro-2-propen-1-yl) oxy] phenoxy] propoxy] -2-methoxy-6- (trifluoromethyl) pyrimidine (known from CN 101337940 A) ( CAS 1108184-52-6); (2E) - and 2 (Z) -2- [2- (4-cyanophenyl) -1- [3- (trifluoromethyl) phenyl] ethylidene] -N- [4- (difluoromethoxy) phenyl] hydrazinecarboxamide (known from CN 101715774 A) (CAS 1232543-85-9); Cyclopropanecarboxylic acid 3- (2,2-dichloroethenyl) -2,2-dimethyl-4- (1H-benzimidazol-2-yl) phenyl ester (known from CN 103524422 A) (CAS 1542271-46-4); (4aS) -7-chloro-2,5-dihydro-2- [[(methoxycarbonyl) [4 - [(trifluoromethyl) thio] phenyl] amino] carbonyl] indeno [1,2-e] [1, 3,4 ] oxadiazine-4a (3H) -carboxylic acid methyl ester (known from CN 102391261 A) (CAS 1370358-69-2); 6-Deoxy-3-0-ethyl-2,4-di-O-methyl-1 - [N- [4- [1 - [4- (1,1,2,2-pentafluoroethoxy) phenyl] - 1 H -1,2,4-triazol-3-yl] phenyl] carbamate] -AL-mannopyranose (known from US 2014/0275503 A1) (CAS 1181213-14-8); 8- (2-Cyclopropylmethoxy-4-trifluoromethylphenoxy) -3- (6-trifluoromethylpyridazin-3-yl) -3- azabicyclo [3.2.1] octane (CAS 1253850-56-4), (8-anti) -8- (2-cyclopropylmethoxy-4-trifluoromethylphenoxy) -3- (6-trifluoromethylpyridazin-3-yl) -3-azabicyclo [ 3.2.1] octane (CAS 933798-27-7), (8-syn) -8- (2-cyclopropylmethoxy-4-trifluoromethylphenoxy) -3- (6-trifluoromethylpyridazin-3-yl) -3-azabicyclo [3.2. 1] octane (known from WO 2007040280 A1, WO 2007040282 A1) (CAS 934001-66-8), N- [3-chloro-1- (3-pyridinyl) -1H-pyrazol-4-yl] -N-ethyl 3 - [(3,3,3-trifluoropropyl) thio] -propanamide (known from WO 2015/058021 A1, WO 2015/058028 A1) (CAS 1477919-27-9) and N- [4- (aminothioxomethyl) -
2-methyl-6-[(methylamino)carbonyl]phenyl]-3-bromo-l-(3-chloro-2-pyridinyl)- I //-pyrazol-5- carboxamid (bekannt aus CN 103265527 A) (CAS 1452877-50-7), 5-(l,3-Dioxan-2-yl)-4-[[4- (trifluormethyl)phenyl]methoxy] -pyrimidin (bekannt aus WO 2013/115391 Al) (CAS 1449021-97-9),2-methyl-6 - [(methylamino) carbonyl] phenyl] -3-bromo-1- (3-chloro-2-pyridinyl) -1-pyrazole-5-carboxamide (known from CN 103265527 A) (CAS 1452877 -50-7), 5- (1,3-dioxan-2-yl) -4 - [[4- (trifluoromethyl) phenyl] methoxy] -pyrimidine (known from WO 2013/115391 A1) (CAS 1449021-97- 9)
3-(4-Chlor-2,6-dimethylphenyl)-4-hydroxy-8-methoxy-l-methyl-l,8-diazaspiro[4.5]dec-3-en-2-on3- (4-chloro-2,6-dimethylphenyl) -4-hydroxy-8-methoxy-l-methyl-l, 8-diazaspiro [4.5] dec-3-en-2-one
(bekannt aus WO 2010/066780 Al, WO 2011/151146 Al) (CAS 1229023-34-0), 3-(4-Chlor-2,6- dimethylphenyl)-8-methoxy-l-methyl-l,8-diazaspiro[4.5]decane-2,4-dion (bekannt aus WO 2014/187846 Al) (CAS 1638765-58-8), 3-(4-Chlor-2,6-dimethylphenyl)-8-methoxy-l-methyl-2-oxo-l, 8-diazaspiro[4.5]dec-3-en-4-yl-carbonsäureethylester (bekannt aus WO 2010/066780 Al, WO 2011151146 Al) (CAS 1229023-00-0), N-[l-[(6-chlor-3-pyridinyl)methyl]-2(l//)-pyridinylidene]-2,2,2- trifluor-acetamide (bekannt aus DE 3639877 Al, WO 2012029672 Al) (CAS 1363400-41-2), [N(£)]-N- [l-[(6-chlor-3-pyridinyl)methyl]-2(l//)-pyridinylidene]-2,2,2-trifluor-acetamide (bekannt aus WO 2016005276 Al) (CAS 1689566-03-7), [N(Z)]-N-[l-[(6-chlor-3-pyridinyl)methyl]-2(l//)- pyridinylidene]-2,2,2-trifluor- acetamide (CAS 1702305-40-5), 3- io-3-[2-Propoxy-4-(trifluormethyl) phenoxy]-9-[[5-(trifluormethyl)-2-pyridinyl]oxy]-9-azabicyclo[3.3.1]nonan (bekannt aus WO 2011/105506 Al, WO 2016/133011 Al) (CAS 1332838-17-1). (known from WO 2010/066780 A1, WO 2011/151146 A1) (CAS 1229023-34-0), 3- (4-chloro-2,6-dimethylphenyl) -8-methoxy-1-methyl-1, 8- diazaspiro [4.5] decane-2,4-dione (known from WO 2014/187846 A1) (CAS 1638765-58-8), 3- (4-chloro-2,6-dimethylphenyl) -8-methoxy-1-methyl 2-oxo-l, 8-diazaspiro [4.5] dec-3-en-4-yl-carboxylic acid ethyl ester (known from WO 2010/066780 A1, WO 2011151146 A1) (CAS 1229023-00-0), N- [l [(6-chloro-3-pyridinyl) methyl] -2 (1 //) -pyridinylidenes] -2,2,2-trifluoroacetamides (known from DE 3639877 A1, WO 2012029672 A1) (CAS 1363400-41- 2), [N (£)] - N - [l - [(6-chloro-3-pyridinyl) methyl] -2 (1 //) pyridinylidenes] -2,2,2-trifluoroacetamides (known from WO 2016005276 A1) (CAS 1689566-03-7), [N (Z)] - N- [1- (6-chloro-3-pyridinyl) methyl] -2 (1 //) -pyridinylidenes] -2, 2,2-trifluoroacetamides (CAS 1702305-40-5), 3-io-3- [2-propoxy-4- (trifluoromethyl) phenoxy] -9 - [[5- (trifluoromethyl) -2-pyridinyl] oxy ] -9-azabicyclo [3.3.1] nonane (known from WO 2011/105506 A1, WO 2016/133011 A1) (CAS 1332838-17-1).
Biologische Schädlingsbekämpfungsmittel als Mischungskomponenten Biological pesticides as mixture components
Die erfindungsgemäßen Wirkstoffkombinationen können mit biologischen Schädlingsbekämpfungsmitteln kombiniert werden. The active compound combinations according to the invention can be combined with biological pesticides.
Biologische Schädlingsbekämpfungsmittel umfassen insbesondere Bakterien, Pilze, Hefen, Pflanzenextrakte und solche Produkte, die von Mikroorganismen gebildet wurden inklusive Proteine und sekundäre Stoffwechselprodukte. Biological pesticides include, in particular, bacteria, fungi, yeasts, plant extracts and those products formed by microorganisms, including proteins and secondary metabolites.
Biologische Schädlingsbekämpfungsmittel umfassen Bakterien wie sporenbildende Bakterien, wurzelbesiedelnde Bakterien und Bakterien, die als biologische Insektizide, Fungizide oder Nematizide wirken. Biological pesticides include bacteria such as spore-forming bacteria, root-colonizing bacteria and bacteria that act as biological insecticides, fungicides or nematicides.
Beispiele für solche Bakterien, die als biologische Schädlingsbekämpfungsmittel eingesetzt werden bzw. verwendet werden können, sind: Examples of such bacteria which can be used as biological pesticides are:
Bacillus amyloliquefaciens, Stamm FZB42 (DSM 231179), oder Bacillus cereus, insbesondere B. cereus Stamm CNCM 1-1562 oder Bacillus firmus, Stamm 1-1582 (Accession number CNCM 1-1582) oder Bacillus pumilus, insbesondere Stamm GB34 (Accession No. ATCC 700814) und Stamm QST2808 (Accession No. NRRL B-30087), oder Bacillus subtilis, insbesondere Stamm GB03 (Accession No. ATCC SD-1397), oder Bacillus subtilis Stamm QST713 (Accession No. NRRL B- 21661) oder Bacillus subtilis Stamm OST 30002 (Accession No. NRRL B-50421), Bacillus thuringiensis, insbesondere B. thuringiensis Subspezies israelensis (Serotyp H-14), Stamm AM65-52 (Accession No. ATCC 1276), oder B. thuringiensis subsp. aizawai, insbesondere Stamm ABTS-1857 (SD-1372), oder B. thuringiensis subsp. kurstaki Stamm HD-1, oder B. thuringiensis subsp. tenebrionis Stamm NB 176 (SD-5428), Pasteuria penetrans, Pasteuria spp. (Rotylenchulus reniformis nematode)- PR3 (Accession Number ATCC SD-5834), Streptomyces microflavus Stamm AQ6121 (= QRD 31.013, NRRL B-50550), Streptomyces galbus Stamm AQ 6047 (Acession Number NRRL 30232). Bacillus amyloliquefaciens, strain FZB42 (DSM 231179), or Bacillus cereus, in particular B. cereus strain CNCM 1-1562 or Bacillus firmus, strain 1-1582 (Accession number CNCM 1-1582) or Bacillus pumilus, in particular strain GB34 (Accession No. ATCC 700814) and strain QST2808 (Accession No. NRRL B-30087), or Bacillus subtilis, in particular strain GB03 (Accession No. ATCC SD-1397), or Bacillus subtilis strain QST713 (Accession No. NRRL B-21661) or Bacillus subtilis strain OST 30002 (Accession No. NRRL B-50421), Bacillus thuringiensis, in particular Thuringiensis subspecies israelensis (serotype H-14), strain AM65-52 (Accession No. ATCC 1276), or B. thuringiensis subsp. aizawai, in particular strain ABTS-1857 (SD-1372), or B. thuringiensis subsp. kurstaki strain HD-1, or B. thuringiensis subsp. tenebrionis strain NB 176 (SD-5428), Pasteuria penetrans, Pasteuria spp. (Rotylenchulus reniformis nematode) - PR3 (Accession Number ATCC SD-5834), Streptomyces microflavus strain AQ6121 (= QRD 31.013, NRRL B-50550), Streptomyces galbus strain AQ 6047 (Accession Number NRRL 30232).
Beispiele für Pilze und Hefen, die als biologische Schädlingsbekämpfungsmittel eingesetzt werden bzw. verwendet werden können, sind: Examples of fungi and yeasts which can be used as biological pesticides are:
Beauveria bassiana, insbesondere Stamm ATCC 74040, Coniothyrium minitans, insbesondere Stamm CON/M/91-8 (Accession No. DSM-9660), Lecanicillium spp., insbesondere Stamm HRO LEC 12, Lecanicillium lecanii (ehemals bekannt als Verticillium lecanii), insbesondere Stamm KV01, Metarhizium anisopliae, insbesondere Stamm F52 (DSM3884/ ATCC 90448), Metschnikowia fructicola, insbesondere Stamm NRRL Y-30752, Paecilomyces fumosoroseus (neu: Isaria fumosorosea), insbesondere Stamm IFPC 200613, oder Stamm Apopka 97 (Accesion No. ATCC 20874), Paecilomyces lilacinus, insbesondere P. lilacinus Stamm 251 (AGAL 89/030550), Talaromyces flavus, insbesondere Stamm VI 17b, Trichoderma atroviride, insbesondere Stamm SCI (Accession Number CBS 122089), Trichoderma harzianum, insbesondere T. harzianum rifai T39. (Accession Number CNCM 1-952). Beauveria bassiana, in particular strain ATCC 74040, coniothyrium minitans, in particular strain CON / M / 91-8 (Accession No. DSM-9660), Lecanicillium spp., In particular strain HRO LEC 12, Lecanicillium lecanii (formerly known as Verticillium lecanii), in particular Strain KV01, Metarhizium anisopliae, in particular strain F52 (DSM3884 / ATCC 90448), Metschnikowia fructicola, in particular strain NRRL Y-30752, Paecilomyces fumosoroseus (new: Isaria fumosorosea), in particular strain IFPC 200613, or strain Apopka 97 (Accesion No. ATCC 20874 ), Paecilomyces lilacinus, in particular P. lilacinus strain 251 (AGAL 89/030550), Talaromyces flavus, in particular strain VI 17b, Trichoderma atroviride, in particular strain SCI (Accession Number CBS 122089), Trichoderma harzianum, in particular T. harzianum rifai T39. (Accession Number CNCM 1-952).
Beispiele für Viren, die als biologische Schädlingsbekämpfungsmittel eingesetzt werden bzw. verwendet werden können, sind: Examples of viruses that can be used or used as biological pesticides are:
Adoxophyes orana (Apfelschalenwickler) Granulosevirus (GV), Cydia pomonella (Apfelwickler) Granulosevirus (GV), Helicoverpa armigera (Baumwollkapselwurm) Nuklear Polyhedrosis Virus (NPV), Spodoptera exigua (Zuckerrübeneule) mNPV, Spodoptera frugiperda (Heerwurm) mNPV, Spodoptera littoralis (Afrikanischer Baumwollwurm) NPV. Adoxophyes orana (Apple peel winder) Granulosis virus (GV), Cydia pomonella (codling moth) Granulosis virus (GV), Helicoverpa armigera (cotton bollworm) Nuclear polyhedrosis virus (NPV), Spodoptera exigua (mNPV), Spodoptera frugiperda (armyworm) mNPV, Spodoptera littoralis (African Cotton worm) NPV.
Es sind auch Bakterien und Pilze umfasst, die als ,Inokulant‘ Pflanzen oder Pflanzenteilen oder Pflanzenorganen beigegeben werden und durch ihre besonderen Eigenschaften das Pflanzenwachstum und die Pflanzengesundheit fördern. Als Beispiele sind genannt: It also includes bacteria and fungi that are added as 'inoculant' plants or parts of plants or plant organs and promote by their special properties, plant growth and plant health. Examples are:
Agrobacterium spp., Azorhizobium caulinodans , Azospirillum spp., Azotobacter spp., Bradyrhizobium spp., Burkholderia spp., insbesondere Burkholderia cepacia (ehemals bekannt als Pseudomonas cepacia), Gigaspora spp., oder Gigaspora monosporum, Glomus spp., Laccaria spp., Lactobacillus buchneri, Paraglomus spp., Pisolithus tinctorus, Pseudomonas spp., Rhizobium spp., insbesondere Rhizobium trifolii, Rhizopogon spp., Scleroderma spp., Suillus spp., Streptomyces spp.. Agrobacterium spp., Azorhizobium caulinodans, Azospirillum spp., Azotobacter spp., Bradyrhizobium Spp., Burkholderia spp., in particular Burkholderia cepacia (formerly known as Pseudomonas cepacia), Gigaspora spp., or Gigaspora monosporum, Glomus spp., Laccaria spp., Lactobacillus buchneri, Paraglomus spp., Pisolithus tinctorus, Pseudomonas spp., Rhizobium spp , in particular Rhizobium trifolii, Rhizopogon spp., Scleroderma spp., Suillus spp., Streptomyces spp.
Beispiele für Pflanzenextrakte und solche Produkte, die von Mikroorganismen gebildet wurden inklusive Proteine und sekundäre Stoffwechselprodukte, die als biologische Schädlingsbekämpfungsmittel eingesetzt werden bzw. verwendet werden können, sind: Examples of plant extracts and those products formed by microorganisms, including proteins and secondary metabolites, which can be used as biological pesticides are:
Allium sativum, Artemisia absinthium, Azadirachtin, Biokeeper WP, Cassia nigricans, Celastrus angulatus, Chenopodium anthelminticum, Chitin, Armour-Zen, Dryopteris filix-mas, Equisetum arvense, Fortune Aza, Fungastop, Heads Up (Chenopodium quinoa-Saponinextrakt), Pyrethrum/Pyrethrine, Quassia amara, Quercus, Quillaja, Regalia,„Requiem™ Insecticide“, Rotenon, Ryania/Ryanodine, Symphytum officinale, Tanacetum vulgare, Thymol, Triact 70, TriCon, Tropaeulum majus, Urtica dioica, Veratrin, Viscum album, Brassicacaeen-Extrakt, insbesondere Raps- oder Senfpulver. Allium sativum, Artemisia absinthium, Azadirachtin, Biokeeper WP, Cassia nigricans, Celastrus angulatus, Chenopodium anthelminticum, Chitin, Armor Zen, Dryopteris filix-mas, Equisetum arvense, Fortune Aza, Fungastop, Heads Up (Chenopodium quinoa saponin extract), Pyrethrum / Pyrethrins, Quassia amara, Quercus, Quillaja, Regalia, Requiem ™ Insecticide, Rotenone, Ryania / Ryanodine, Symphytum officinale, Tanacetum vulgare, Thymol, Triact 70, TriCon, Tropaeulum majus, Urtica dioica, Veratrin, Viscum album, Brassicacaeen extract , in particular rapeseed or mustard powder.
Safener als Mischungskomponenten Safener as a mixture component
Die erfindungsgemäßen Wirkstoffkombinationen können mit Safenern kombiniert werden, wie zum Beispiel Benoxacor, Cloquintocet (-mexyl), Cyometrinil, Cyprosulfamide, Dichlormid, Fenchlorazole (- ethyl), Fenclorim, Flurazole, Fluxofenim, Furilazole, Isoxadifen (-ethyl), Mefenpyr (-diethyl), Naphthalic anhydride, Oxabetrinil, 2-Methoxy-N-({4-The active compound combinations according to the invention can be combined with safeners, for example Benoxacor, Cloquintocet (-mexyl), Cyometrinil, Cyprosulfamide, Dichlormid, Fenchlorazole (- ethyl), Fenclorim, Flurazole, Fluxofenim, Furilazole, Isoxadifen (-ethyl), Mefenpyr (-diethyl ), Naphthalene anhydrides, oxabetrinil, 2-methoxy-N - ({4-
[(methylcarbamoyl)amino]phenyl}sulfonyl)benzamid (CAS 129531-12-0), 4-(Dichloracetyl)-l-oxa-4- azaspiro[4.5]decan (CAS 71526-07-3), 2,2,5-Trimethyl-3-(dichloracetyl)-l,3-oxazolidin (CAS 52836- 31-4). [(methylcarbamoyl) amino] phenyl} sulfonyl) benzamide (CAS 129531-12-0), 4- (dichloroacetyl) -1-oxa-4-azaspiro [4.5] decane (CAS 71526-07-3), 2,2, 5-trimethyl-3- (dichloroacetyl) -1,3-oxazolidine (CAS 52836- 31-4).
Pflanzen und Pflanzenteile Plants and plant parts
Erfindungsgemäß können alle Pflanzen und Pflanzenteile behandelt werden. Unter Pflanzen werden hierbei alle Pflanzen und Pflanzenpopulationen verstanden wie erwünschte und unerwünschte Wildpflanzen oder Kulturpflanzen (einschließlich natürlich vorkommender Kulturpflanzen), beispielsweise Getreide (Weizen, Reis, Triticale, Gerste, Roggen, Hafer), Mais, Soja, Kartoffel, Zuckerrüben, Zuckerrohr, Tomaten, Paprika, Gurke, Melone, Möhre, Wassermelone, Zwiebel, Salat, Spinat, Porree, Bohnen, Brassica oleracea (z. B. Kohl) und andere Gemüsesorten, Baumwolle, Tabak, Raps, sowie Obstpflanzen (mit den Früchten Äpfel, Birnen, Zitrusfrüchte und Weintrauben). Kulturpflanzen können Pflanzen sein, die durch konventionelle Züchtungs- und Optimierungsmethoden oder durch biotechnologische und gentechnologische Methoden oder Kombinationen dieser Methoden erhalten werden können, einschließlich der transgenen Pflanzen und einschließlich der durch Sortenschutzrechte schützbaren oder nicht schützbaren Pflanzensorten. Unter Pflanzen sollen alle Entwicklungsstadien wie Saatgut, Stecklinge, junge (unausgereifte) Pflanzen bis hin zu ausgereiften Pflanzen verstanden werden. Unter Pflanzenteilen sollen alle oberirdischen und unterirdischen Teile und Organe der Pflanzen wie Spross, Blatt, Blüte und Wurzel verstanden werden, wobei beispielhaft Blätter, Nadeln, Stängel, Stämme, Blüten, Fruchtkörper, Früchte und Samen sowie Wurzeln, Knollen und Rhizome aufgeführt werden. Zu den Pflanzenteilen gehören auch geerntete Pflanzen oder geerntete Pflanzenteile sowie vegetatives und generatives Vermehrungsmaterial, beispielsweise Stecklinge, Knollen, Rhizome, Ableger und Samen. According to the invention, all plants and parts of plants can be treated. Plants are understood to mean all plants and plant populations, such as desirable and unwanted wild plants or crops (including naturally occurring crops), for example cereals (wheat, rice, triticale, barley, rye, oats), corn, soybeans, potatoes, sugar beets, sugarcane, tomatoes , Paprika, cucumber, melon, carrot, watermelon, onion, lettuce, spinach, leek, beans, Brassica oleracea (eg cabbage) and other vegetables, cotton, tobacco, rapeseed, as well as fruit plants (with the fruits apples, pears, Citrus fruits and grapes). Crop plants can be plants that can be obtained by conventional breeding and optimization methods or by biotechnological and genetic engineering methods or combinations of these methods, including the transgenic plants and including by Plant variety rights protectable or non-protectable plant varieties. Plants are to be understood as meaning all stages of development, such as seeds, cuttings, young (unripe) plants and mature plants. Plant parts are understood to mean all aboveground and subterranean parts and organs of plants such as shoot, leaf, flower and root, examples of which include leaves, needles, stems, stems, flowers, fruiting bodies, fruits and seeds, and roots, tubers and rhizomes. The plant parts also include harvested plants or harvested plant parts as well as vegetative and generative propagation material, for example cuttings, tubers, rhizomes, offshoots and seeds.
Die erfindungsgemäße Behandlung der Pflanzen und Pflanzenteile mit den erfindungsgemäßen Wirkstoffkombinationen erfolgt direkt oder durch Einwirkung der Verbindungen auf die Umgebung, den Eebensraum oder den Eagerraum nach den üblichen Behandlungsmethoden, z. B. durch Eintauchen, Spritzen, Verdampfen, Vernebeln, Streuen, Aufstreichen, Injizieren und bei Vermehrungsmaterial, ins besondere bei Saatgut, weiterhin durch ein- oder mehrschichtiges Umhüllen. The treatment according to the invention of the plants and plant parts with the active compound combinations according to the invention is carried out directly or by the action of the compounds on the environment, the Eebensraum or Eagerraum after the usual treatment methods, eg. B. by immersion, spraying, evaporation, nebulization, scattering, brushing, injecting and in propagating material, in particular in seeds, further by single or multi-layer wrapping.
Wie bereits oben erwähnt, können erfindungsgemäß alle Pflanzen und deren Teile behandelt werden. In einer bevorzugten Ausführungsform werden wild vorkommende oder durch konventionelle biologische Zuchtmethoden wie Kreuzung oder Protoplastenfusion erhaltene Pflanzenarten und Pflanzensorten sowie deren Teile behandelt. In einer weiteren bevorzugten Ausführungsform werden transgene Pflanzen und Pflanzensorten, die durch gentechnologische Methoden gegebenenfalls in Kombination mit konventionellen Methoden erhalten wurden (Genetically Modified Organisms) und deren Teile behandelt. Der Begriff „Teile“ bzw.„Teile von Pflanzen“ oder„Pflanzenteile“ wurde oben erläutert. Besonders bevorzugt werden erfindungsgemäß Pflanzen der jeweils handelsüblichen oder in Gebrauch befindlichen Pflanzensorten behandelt. Unter Pflanzensorten versteht man Pflanzen mit neuen Eigenschaften („Traits“), die durch konventionelle Züchtung, durch Mutagenese oder durch rekombinante DNA-Techniken erhalten worden sind. Dies können Sorten, Rassen, Bio- und Genotypen sein. As already mentioned above, according to the invention all plants and their parts can be treated. In a preferred embodiment, wild-type or plant species and plant varieties obtained by conventional biological breeding methods such as crossing or protoplast fusion and parts thereof are treated. In a further preferred embodiment, transgenic plants and plant cultivars obtained by genetic engineering, if appropriate in combination with conventional methods (Genetically Modified Organisms), and parts thereof are treated. The term "parts" or "parts of plants" or "plant parts" has been explained above. It is particularly preferred according to the invention to treat plants of the respective commercially available or in use plant cultivars. Plant varieties are understood as meaning plants having new traits which have been obtained by conventional breeding, by mutagenesis or by recombinant DNA techniques. These may be varieties, breeds, biotypes and genotypes.
Transgene Pflanze Transgenic plant
Zu den bevorzugten erfindungsgemäß zu behandelnden transgenen (gentechnologisch erhaltenen) Pflanzen bzw. Pflanzensorten gehören alle Pflanzen, die durch die gentechnologische Modifikation genetisches Material erhielten, welches diesen Pflanzen besondere vorteilhafte wertvolle Eigenschaften ("Traits") verleiht. Beispiele für solche Eigenschaften sind besseres Pflanzenwachstum, erhöhte Toleranz gegenüber hohen oder niedrigen Temperaturen, erhöhte Toleranz gegen Trockenheit oder gegen Wasser- bzw. Bodensalzgehalt, erhöhte Blühleistung, erleichterte Ernte, Beschleunigung der Reife, höhere Ernteerträge, höhere Qualität und/oder höherer Ernährungswert der Ernteprodukte, höhere Lagerfähigkeit und/oder Bearbeitbarkeit der Ernteprodukte. Weitere und besonders hervorgehobene Beispiele für solche Eigenschaften sind eine erhöhte Abwehrfähigkeit der Pflanzen gegen tierische und mikrobielle Schädlinge, wie Insekten, Spinnentiere, Nematoden, Milben, Schnecken, bewirkt z. B. durch in den Pflanzen entstehende Toxine, insbesondere solche, die durch das genetische Material aus Bacillus Thuringiensis (z. B. durch die Gene CrylA(a), CrylA(b), CrylA(c), CryflA, CrylllA, CryfIIB2, Cry9c Cry2Ab, Cry3Bb und CrylF sowie deren Kombinationen) in den Pflanzen erzeugt werden, ferner eine erhöhte Abwehrfähigkeit der Pflanzen gegen pflanzenpathogene Pilze, Bakterien und/oder Viren, bewirkt z. B. durch Systemisch Akquirierte Resistenz (SAR), Systemin, Phytoalexine, Elicitoren sowie Resistenzgene und entsprechend exprimierte Proteine und Toxine, sowie eine erhöhte Toleranz der Pflanzen gegen bestimmte herbizide Wirkstoffe, beispielsweise Imidazolinone, Sulfonylharnstoffe, Glyphosat oder Phosphinotricin (z. B. "PAT"-Gen). Die jeweils die gewünschten Eigenschaften ("Traits") verleihenden Gene können auch in Kombinationen miteinander in den transgenen Pflanzen Vorkommen. Als Beispiele transgener Pflanzen werden die wichtigen Kulturpflanzen, wie Getreide (Weizen, Reis, Triticale, Gerste, Roggen, Hafer), Mais, Soja, Kartoffel, Zuckerrüben, Zuckerrohr, Tomaten, Erbsen und andere Gemüsesorten, Baumwolle, Tabak, Raps, sowie Obstpflanzen (mit den Früchten Äpfel, Birnen, Zitrusfrüchte und Weintrauben) erwähnt, wobei Mais, Soja, Weizen, Reis, Kartoffel, Baumwolle, Zuckerrohr, Tabak und Raps besonders hervorgehoben werden. Als Eigenschaften ("Traits") werden besonders hervorgehoben die erhöhte Abwehrfähigkeit der Pflanzen gegen Insekten, Spinnentiere, Nematoden und Schnecken. The preferred plants or plant varieties to be treated according to the invention to be treated include all plants which, as a result of the genetic engineering modification, obtained genetic material which gives these plants particularly advantageous valuable properties ("traits"). Examples of such properties are better plant growth, increased tolerance to high or low temperatures, increased tolerance to dryness or to bottoms salt, increased flowering, easier harvesting, acceleration of ripeness, higher crop yields, higher quality and / or higher nutritional value of the harvested products , higher shelf life and / or workability of the harvested products. Further and particularly emphasized examples of such properties are an increased resistance of the plants against animal and microbial pests, such as insects, arachnids, nematodes, mites, snails, causes z. By toxins produced in the plants, in particular those produced by the genetic material from Bacillus thuringiensis (eg by the genes CrylA (a), CrylA (b), CrylA (c), CryflA, CrylllA, CryfIIB2, Cry9c Cry2Ab, Cry3Bb and CrylF and their combinations) are produced in the plants, further increased resistance of the plants against plant pathogenic fungi, bacteria and / or viruses, causes z. For example, systemically acquired resistance (SAR), systemin, phytoalexins, elicitors and resistance genes and correspondingly expressed proteins and toxins, as well as an increased tolerance of the plants to certain herbicidal active compounds, for example imidazolinones, sulfonylureas, glyphosate or phosphinotricin (eg "PAT "-Gene). The genes which confer the desired properties ("traits") can also be present in combinations with one another in the transgenic plants. Examples of transgenic plants are the important crops such as cereals (wheat, rice, triticale, barley, rye, oats), corn, soy, potato, sugar beets, sugarcane, tomatoes, peas and other vegetables, cotton, tobacco, oilseed rape, and fruit plants (with the fruits apples, pears, citrus fruits and grapes), with emphasis on corn, soy, wheat, rice, potato, cotton, sugar cane, tobacco and oilseed rape. Traits that are particularly emphasized are the increased resistance of the plants to insects, arachnids, nematodes and snails.
Pflanzenschutz - Behandlungsarten Plant protection - types of treatment
Die Behandlung der Pflanzen und Pflanzenteile mit den erfindungsgemäßen Wirkstoffkombinationen erfolgt direkt oder durch Einwirkung auf deren Umgebung, Lebensraum oder Lagerraum nach den üblichen Behandlungsmethoden, z. B. durch Tauchen, Spritzen, Sprühen, Berieseln, Verdampfen, Zerstäuben, Vernebeln, Verstreuen, Verschäumen, Bestreichen, Verstreichen, Injizieren, Gießen (drenchen), Tröpfchenbewässerung und bei Vermehrungsmaterial, insbesondere bei Saatgut, weiterhin durch Trockenbeizen, Nassbeizen, Schlämmbeizen, Inkrustieren, ein- oder mehrschichtiges Umhüllen, usw. Es ist ferner möglich, die erfindungsgemäßen Wirkstoffkombinationen nach dem Ultra-Low- Volume -Verfahren auszubringen oder die Anwendungsform oder die erfindungsgemäßen Wirkstoffkombinationen selbst in den Boden zu injizieren. The treatment of the plants and plant parts with the active compound combinations according to the invention is carried out directly or by acting on their environment, habitat or storage space according to the usual treatment methods, eg. B. by dipping, spraying, spraying, sprinkling, vaporizing, atomizing, atomizing, scattering, foaming, brushing, spreading, injecting, pouring (drenchen), drip irrigation and propagating material, especially in seeds, further by dry pickling, wet pickling, slurry pickling, encrusting , single or multi-layer encasing, etc. It is also possible to apply the active compound combinations according to the invention by the ultra-low-volume method or to inject the application form or the active compound combinations according to the invention itself into the soil.
Eine bevorzugte direkte Behandlung der Pflanzen ist die Blattapplikation, d. h. die erfindungsgemäßen Wirkstoffkombinationen werden auf das Blattwerk aufgebracht, wobei die Behandlungsfrequenz und die Aufwandmenge auf den Befallsdruck des jeweiligen Schädlings abgestimmt sein sollte. A preferred direct treatment of the plants is foliar application, i. H. the active compound combinations according to the invention are applied to the foliage, wherein the treatment frequency and the application rate should be matched to the infestation pressure of the respective pest.
Formel für den Abtötungsgrad einer Kombination aus zwei Wirkstoffen Formula for the kill rate of a combination of two drugs
Die zu erwartende Wirkung für eine gegebene Kombination zweier Wirkstoffe kann nach S.R. Colby („Calculating Synergistic and Antagonistic Responses of Herbicide Combinations“, Weeds 15, 20-22, 1967) wie folgt berechnet werden: The expected effect for a given combination of two drugs can be assessed by SR Colby ("Calculating Synergistic and Antagonistic Responses of Herbicide Combinations", Weeds 15, 20-22, 1967) are calculated as follows:
Wenn X den Abtötungsgrad, ausgedrückt in % der unbehandelten Kontrolle, beim Einsatz desIf X is the kill rate, expressed in% of the untreated control, using the
Wirkstoffes A in einer Aufwandmenge von m g/ha oder in einer Konzentration von Active ingredient A at a rate of m g / ha or in a concentration of
m ppm bedeutet,  m ppm means
Y den Abtötungsgrad, ausgedrückt in % der unbehandelten Kontrolle, beim Einsatz des Wirkstoffes B in einer Aufwandmenge von n g/ha oder in einer Konzentration von n ppm bedeutet und Y means the degree of killing, expressed in% of the untreated control, when using the active ingredient B in an application rate of n g / ha or in a concentration of n ppm, and
E den Abtötungsgrad, ausgedrückt in % der unbehandelten Kontrolle, beim Einsatz der Wirkstoffe A und B in Aufwandmengen von m und n g/ha oder in einer Konzentration von m und n ppm bedeutet, E means the degree of killing, expressed in% of the untreated control, when using the active compounds A and B at application rates of m and n g / ha or in a concentration of m and n ppm,
X x Y X x Y
dann ist E = X + Y -then E = X + Y -
100 100
Ist der tatsächliche Abtötungsgrad größer als der berechnete Abtötungsgrad (E), so ist die Kombination in ihrer Abtötung überadditiv, d.h. es hegt ein synergistischer Effekt vor. If the actual kill rate is greater than the calculated kill rate (E), the combination is over-additive in its kill, ie it has a synergistic effect.
Beispiel A Example A
Aphis gossypii - Drenchtest Aphis gossypii - Drench test
Lösungsmittel: 7 Gewichtsteile Dimethylformamid Solvent: 7 parts by weight of dimethylformamide
Emulgator: 2 Gewichtsteile Alkylarylpolyglykolether Zur Herstellung einer zweckmäßigen Wirkstoffzubereitung vermischt man 1 Gewichtsteil Wirkstoff mit den angegebenen Mengen Lösungsmittel und Emulgator und verdünnt das Konzentrat mit Wasser auf die gewünschte Konzentration, wobei das Erdvolumen in das gedrencht wird, mitberücksichtigt werden muss. Es ist darauf zu achten, dass in der Erde eine Konzentration von 40 ppm Emulgator nicht überschritten wird. Zur Herstellung weiterer Testkonzentrationen wird mit Wasser verdünnt. Baumwollpflanzen ( Gossypium hirsutum) in Erdtöpfen, die stark von der Baumwollblattlaus (Aphis gossypii) befallen sind, werden mit einer Wirkstoffzubereitung der gewünschten Konzentration angegossen.  Emulsifier: 2 parts by weight of alkylaryl polyglycol ether To prepare a suitable preparation of active compound, 1 part by weight of active compound is mixed with the stated amounts of solvent and emulsifier, and the concentrate is diluted with water to the desired concentration, whereby the volume of the earth into which it is compressed must also be taken into account. It must be ensured that a concentration of 40 ppm emulsifier is not exceeded in the soil. To prepare further test concentrations, it is diluted with water. Cotton plants (Gossypium hirsutum) in soil pots which are heavily infested with the cotton aphid (Aphis gossypii) are infused with an active compound preparation of the desired concentration.
Nach der gewünschten Zeit wird die Abtötung in % bestimmt. Dabei bedeutet 100 %, dass alle Blattläuse abgetötet wurden; 0 % bedeutet, dass keine Blattläuse abgetötet wurden. Die ermittelten Abtötungs werte verrechnet man nach der Colby-Formel. After the desired time the kill is determined in%. 100% means that all aphids have been killed; 0% means that no aphids have been killed. The determined mortality values are calculated according to the Colby formula.
Bei diesem Test zeigten die folgenden Wirkstoffkombinationen gemäß vorliegender Anmeldung eine synergistisch verstärkte Wirksamkeit im Vergleich zu den einzeln angewendeten Wirkstoffen: In this test, the following active ingredient combinations according to the present application showed a synergistically enhanced effectiveness in comparison to the individually applied active ingredients:
Tabelle A: Aphis gossypii - Drenchtest Table A: Aphis gossypii - Drench test
Figure imgf000043_0001
Figure imgf000044_0001
Figure imgf000043_0001
Figure imgf000044_0001
*gef. = gefundene Wirkung, ber. = berechnete Wirkung anhand der Colby-Formel  * Found. = found effect, calc. = calculated effect on the Colby formula

Claims

Patentansprüche claims
1 Wirkstoffkombinationen enthaltend mindestens eine Verbindung der Formel (I), 1 combination of active substances containing at least one compound of the formula (I),
Figure imgf000045_0001
in welcher
Figure imgf000045_0001
in which
W und Y unabhängig voneinander für Wasserstoff, C1-C4- Alkyl, Chlor, Brom, Jod oder Fluor stehen, W and Y independently of one another represent hydrogen, C 1 -C 4 -alkyl, chlorine, bromine, iodine or fluorine,
X für C1-C4- Alkyl, C | -( ^-Alkoxy, Chlor, Brom oder Jod steht, X is C1-C4 alkyl, C | - (^) alkoxy, chlorine, bromine or iodine,
D für Wasserstoff oder Methyl steht, D is hydrogen or methyl,
A, B und das Kohlenstoffatom, an das sie gebunden sind, für Cj-C^-Cycloalkyl stehen, in welchem gegebenenfalls ein Ringglied durch Stickstoff ersetzt ist und welches gegebenenfalls einfach durch Ci-C t-Alkoxy substituiert ist oder A, B and the carbon atom to which they are attached are C j -C -cycloalkyl in which optionally one ring member is replaced by nitrogen and which is optionally monosubstituted by C t-C alkoxy, or
A, B und das Kohlenstoffatom, an das sie gebunden sind, für Cj-C^-Cycloalkyl stehen, welches durch eine gegebenenfalls durch C!-C4-Alkyl oder Ci-C4-Alkoxy-Ci-C2-alkyl-sub- stituierte Alkylendioxyl-Gruppe substituiert ist, die mit dem Kohlenstoffatom, an das sie gebunden ist, ein 5-Ring- oder 6-Ringketal bildet, A, B and the carbon atom to which they are attached are C j -C ^ -cycloalkyl which is substituted by an optionally C 1 -C 4 -alkyl or C 1 -C 4 -alkoxy-C 1 -C 2 -alkyl-sub substituted alkylenedioxy group which forms a 5-membered or 6-membered ketal with the carbon atom to which it is attached,
G für Wasserstoff (a) oder für eine der Gruppen G is hydrogen (a) or one of the groups
E (d)E (d)
Figure imgf000045_0002
stehen, in welchen
Figure imgf000045_0002
stand in which
E für ein Metallion oder ein Ammoniumion steht, E is a metal ion or an ammonium ion,
M für Sauerstoff oder Schwefel steht, M is oxygen or sulfur,
Rl für geradkettigtes oder verzweigtes C | -C^-Alkyl steht, für geradkettigtes oder verzweigtes C | -C^-Alkyl steht und mindestens eine weitere Verbindung (B) ausgewählt aus folgenden Gruppen (Klassen): R1 for straight-chain or branched C | -C ^ alkyl, for straight-chain or branched C | -C ^ alkyl and at least one further compound (B) selected from the following groups (classes):
1) Inhibitoren der Ergosterolbiosynthese, 1) inhibitors of ergosterol biosynthesis,
2) Inhibitoren der Atmungskette an Komplex I oder II, 2) inhibitors of the respiratory chain on complex I or II,
3) Inhibitoren der Atmungskette an Komplex PI, 4) Inhibitoren von Mitose und Zellteilung, 3) inhibitors of the respiratory chain on complex PI, 4) inhibitors of mitosis and cell division,
5) Verbindungen, die an mehreren Stellen wirken können („Multisite Action“), 5) compounds that can act in several places ("multisite action"),
6) Verbindungen, die dazu in der Lage sind, Abwehrreaktionen des Wirtes zu induzieren, 6) Compounds capable of inducing host defense responses
7) Inhibitoren von Aminosäure- und/oder Proteinbiosynthese, 7) inhibitors of amino acid and / or protein biosynthesis,
8) Inhibitoren der ATP-Produktion, 9) Inhibitoren der Zellwandsynthese, 8) inhibitors of ATP production, 9) inhibitors of cell wall synthesis,
10) Inhibitoren der Lipid- und Membransynthese, 10) inhibitors of lipid and membrane synthesis,
11) Inhibitoren der Melaninbiosynthese, 11) inhibitors of melanin biosynthesis,
12) Inhibitoren der Nukleinsäuresynthese, 12) inhibitors of nucleic acid synthesis,
13) Inhibitoren der Signalübertragung, 14) Verbindungen, die als Entkoppler wirken können, 13) inhibitors of signal transmission, 14) compounds which can act as decouplers,
15) weitere Lungizide. 15) other lung fungicides.
2. Wirkstoffkombinationen enthaltend mindestens eine Verbindung der Lormel (I) gemäß2. active ingredient combinations containing at least one compound of the formula (I) according to
Anspruch 1 und mindestens eine weitere Verbindung (B) ausgewählt aus folgenden Gruppen (Klassen): 1) Inhibitoren der Ergosterolbiosynthese: (1.001) Cyproconazol, (1.002) Difenoconazol, (1.003)Claim 1 and at least one further compound (B) selected from the following groups (classes): 1) inhibitors of ergosterol biosynthesis: (1.001) cyproconazole, (1.002) difenoconazole, (1.003)
Epoxiconazol, (1.004) Fenhexamid, (1.005) Fenpropidin, (1.006) Fenpropimorph, (1.007) Fenpyrazamin, (1.008) Fluquinconazol, (1.009) Flutriafol, (1.010) Imazalil, (1.011) hnazalilsulfat, (1.012) Ipconazol, (1.013) Metconazol, (1.014) Myclobutanil, (1.015)Epoxiconazole, (1.004) fenhexamid, (1.005) fenpropidin, (1.006) fenpropimorph, (1.007) fenpyrazamine, (1.008) fluquinconazole, (1.009) flutriafol, (1.010) imazalil, (1.011) hnazalilsulfate, (1.012) ipconazole, (1.013) Metconazole, (1.014) Myclobutanil, (1.015)
Paclobutrazol, (1.016) Prochloraz, (1.017) Propiconazol, (1.018) Prothioconazol, (1.019) Pyrisoxazol, (1.020) Spiroxamin, (1.021) Tebuconazol, (1.022) Tetraconazol, (1.023)Paclobutrazole, (1,016) prochlorazole, (1,017) propiconazole, (1,018) prothioconazole, (1,019) pyrisoxazole, (1,020) spiroxamine, (1,021) tebuconazole, (1,022) tetraconazole, (1,023)
Triadimenol, (1.024) Tridemorph, (1.025) Triticonazol, (1.026) (lR,2S,5S)-5-(4-Chlorbenzyl)- 2-(chlormethyl)-2-methyl- 1 -( 1 H- 1 ,2,4-triazol- 1 -ylmethyl)cyclopentanol, ( 1.027) ( 1 S,2R,5R)-5 - (4-Chlorbenzyl)-2-(chlormethyl)-2-methyl- 1 -( 1 H- 1 ,2,4-triazol- 1 -ylmethyl)cyclopentanol,Triadiophene, (1,024) tridemorph, (1,025) triticonazole, (1,026) (1R, 2S, 5S) -5- (4-chlorobenzyl) -2- (chloromethyl) -2-methyl-1 - (1H-1, 2 , 4-triazol-1-ylmethyl) cyclopentanol, (1.027) (1S, 2R, 5R) -5 - (4-chlorobenzyl) -2- (chloromethyl) -2-methyl-1- (1H-1,2,4-triazol-1-ylmethyl) cyclopentanol,
( 1.028) (2R)-2-( 1 -Chlorcyclopropyl)-4- [( lR)-2,2-dichlorcyclopropyl] - 1 -( 1 H- 1 ,2,4-triazol- 1 - yl)butan-2-ol, ( 1.029) (2R)-2-( 1 -Chlorcyclopropyl)-4-[( 1 S)-2,2-dichlorcyclopropyl] - 1 -( 1 H-(1.028) (2R) -2- (1-Chlorocyclopropyl) -4- [(1R) -2,2-dichlorocyclopropyl] -1- (1H-1,2,4-triazol-1-yl) butane-2 -ol, (1.029) (2R) -2- (1-chlorocyclopropyl) -4 - [(1S) -2,2-dichlorocyclopropyl] -1 - (1H-
1.2.4-triazol- 1 -yl)butan-2-ol, ( 1.030) (2R)-2-[4-(4-Chlorphenoxy)-2-(trifluormethyl)phenyl] - 1 -1,2,4-triazol-1-yl) butan-2-ol, (1030) (2R) -2- [4- (4-chlorophenoxy) -2- (trifluoromethyl) phenyl] - 1 -
( 1H- 1 ,2,4-triazol- 1 -yl)propan-2-ol, ( 1.031) (2S)-2-( 1 -Chlorcyclopropyl)-4-[( 1 R)-2,2- dichlorcyclopropyl] - 1 -( 1H- 1 ,2,4-triazol- 1 -yl)butan-2-ol, ( 1.032) (2S)-2-( 1 -Chlorcyclopropyl)-4- [( 1 S)-2,2-dichlorcyclopropyl] - 1 -( 1 H- 1 ,2,4-triazol- 1 -yl)butan-2-ol, (1.033) (2S)-2- [4-(4-(1H-1,2,4-triazol-1-yl) propan-2-ol, (1.031) (2S) -2- (1-chlorocyclopropyl) -4 - [(1R) -2,2-dichlorocyclopropyl] - 1 - (1H-1,2,4-triazol-1-yl) butan-2-ol, (1.032) (2S) -2- (1-chlorocyclopropyl) -4- [(1S) -2,2 dichlorocyclopropyl] -1- (1H-1,2,4-triazol-1-yl) butan-2-ol, (1033) (2S) -2- [4- (4-
Chlorphenoxy)-2-(trifluormethyl)phenyl] - 1 -( 1H- 1 ,2,4-triazol- 1 -yl)propan-2-ol, ( 1.034) (R)- [3- (4-Chlor-2-fluorphenyl)-5-(2,4-difluorphenyl)-l,2-oxazol-4-yl](pyridin-3-yl)methanol, (1.035) (S)-[3-(4-Chlor-2-fluorphenyl)-5-(2,4-difluorphenyl)-l,2-oxazol-4-yl](pyridin-3-yl)methanol, (1.036) [3-(4-Chlor-2-fluorphenyl)-5-(2,4-difluorphenyl)-l,2-oxazol-4-yl](pyridin-3- yl)methanol, ( 1.037) 1 -( { (2R,4S)-2- [2-Chlor-4-(4-chlorphenoxy)phenyl] -4-methyl- 1 ,3-dioxolan- 2-yl } methyl)- 1 H- 1 ,2,4-triazol, (1.038) l-({ (2S,4S)-2- [2-Chlor-4-(4-chlorphenoxy)phenyl] -4- methyl-l,3-dioxolan-2-yl}methyl)-lH-l,2,4-triazol, (1.039) l-{ [3-(2-Chlorphenyl)-2-(2,4- difluorphenyl)oxiran-2-yl]methyl}-lH-l,2,4-triazol-5-ylthiocyanat, (1.040) l-{ [rel(2R,3R)-3-(2- Chlorphenyl)-2-(2,4-difluorphenyl)oxiran-2-yl]methyl } - 1 H- 1 ,2,4-triazol-5 -ylthiocyanat, ( 1.041 ) 1 - { [rel(2R,3S)-3-(2-Chlorphenyl)-2-(2,4-difluorphenyl)oxiran-2-yl] methyl } - 1 H- 1 ,2,4-triazol -5 - ylthiocyanat, (1.042) 2-[(2R,4R,5R)-l-(2,4-Dichlorphenyl)-5-hydroxy-2,6,6-trimethylheptan-4- yl]-2,4-dihydro-3H-l,2,4-triazol-3-thion, (1.043) 2-[(2R,4R,5S)-l-(2,4-Dichlorphenyl)-5- hydroxy-2,6,6-trimethylheptan-4-yl]-2,4-dihydro-3H-l,2,4-triazol-3-thion, (1.044) 2-Chlorophenoxy) -2- (trifluoromethyl) phenyl] -1- (1H-1,2,4-triazol-1-yl) propan-2-ol, (1034) (R) - [3- (4-Chloro-2 -fluorophenyl) -5- (2,4-difluorophenyl) -1,2-oxazol-4-yl] (pyridin-3-yl) methanol, (1035) (S) - [3- (4-chloro-2- fluorophenyl) -5- (2,4-difluorophenyl) -1,2-oxazol-4-yl] (pyridin-3-yl) methanol, (1.036) [3- (4-chloro-2-fluorophenyl) -5- (2,4-difluorophenyl) -1,2-oxazol-4-yl] (pyridin-3-yl) methanol, (1.037) 1 - ({(2R, 4S) -2- [2-chloro-4- ( 4-chlorophenoxy) phenyl] -4-methyl-1,3-dioxolan-2-yl} methyl) -1 H -1, 2,4-triazole, (1038) 1 - ({(2S, 4S) -2- [2-chloro-4- (4-chlorophenoxy) phenyl] -4-methyl-1,3-dioxolan-2-yl} methyl) -1H-1,2,4-triazole, (1039) 1-{[3 - (2-chlorophenyl) -2- (2,4-difluorophenyl) oxiran-2-yl] methyl} -1H-l, 2,4-triazol-5-ylthiocyanate, (1040) 1- {[rel (2R, 3R) -3- (2-chlorophenyl) -2- (2,4-difluorophenyl) oxiran-2-yl] methyl} -1H-1,2,4-triazole-5-thyl-thiocyanate, (1.041) 1 - { [rel (2R, 3S) -3- (2-chlorophenyl) -2- (2,4-difluorophenyl) oxiran-2-yl] methyl} -1H-1,2,4-triazole-5-ylthiocyanate, ( 1,042) 2 - [( 2R, 4R, 5R) -l- (2,4-dichlorophenyl) -5-hydroxy-2,6,6-trimethylheptan-4-yl] -2,4-dihydro-3H-l, 2,4-triazole 3-thione, (1043) 2 - [(2R, 4R, 5S) -1- (2,4-dichlorophenyl) -5-hydroxy-2,6,6-trimethylheptan-4-yl] -2,4-dihydro -3H-l, 2,4-triazole-3-thione, (1044) 2-
[(2R,4S,5R)-l-(2,4-Dichlorphenyl)-5-hydroxy-2,6,6-trimethylheptan-4-yl]-2,4-dihydro-3H-[(2R, 4S, 5R) -l- (2,4-dichlorophenyl) -5-hydroxy-2,6,6-trimethylheptane-4-yl] -2,4-dihydro-3H-
1.2.4-triazol-3-thion, (1.045) 2-[(2R,4S,5S)-l-(2,4-Dichlorphenyl)-5-hydroxy-2,6,6- trimethylheptan-4-yl] -2,4-dihydro-3H- 1 ,2,4-triazol-3-thion, ( 1.046) 2- [(2S,4R,5R)- 1 -(2,4- Dichlorphenyl)-5-hydroxy-2,6,6-trimethylheptan-4-yl]-2,4-dihydro-3H-l,2,4-triazol-3-thion,1,2,4-triazole-3-thione, (1.045) 2 - [(2R, 4S, 5S) -1- (2,4-dichlorophenyl) -5-hydroxy-2,6,6-trimethylheptan-4-yl] -2,4-dihydro-3H-1,2,4-triazole-3-thione, (1.046) 2- [(2S, 4R, 5R) -1- (2,4-dichlorophenyl) -5-hydroxy-2 , 6,6-trimethylheptane-4-yl] -2,4-dihydro-3H-l, 2,4-triazole-3-thione,
( 1.047) 2- [(2S,4R,5S)- 1 -(2,4-Dichlorphenyl)-5 -hydroxy-2,6,6-trimethylheptan-4-yl] -2,4- dihydro-3H-l,2,4-triazol-3-thion, (1.048) 2-[(2S,4S,5R)-l-(2,4-Dichlorphenyl)-5-hydroxy-2,6,6- trimethylheptan-4-yl]-2,4-dihydro-3H-l,2,4-triazol-3-thion, (1.049) 2-[(2S,4S,5S)-l-(2,4-(1.047) 2- [(2S, 4R, 5S) -1- (2,4-dichlorophenyl) -5-hydroxy-2,6,6-trimethylheptan-4-yl] -2,4-dihydro-3H-1 , 2,4-triazole-3-thione, (1048) 2 - [(2S, 4S, 5R) -1- (2,4-dichlorophenyl) -5-hydroxy-2,6,6-trimethylheptan-4-yl ] -2,4-dihydro-3H-l, 2,4-triazole-3-thione, (1.049) 2 - [(2S, 4S, 5S) -l- (2,4-)
Dichlorphenyl)-5-hydroxy-2,6,6-trimethylheptan-4-yl] -2,4-dihydro-3H-l,2,4-triazol-3-thion,Dichlorophenyl) -5-hydroxy-2,6,6-trimethylheptan-4-yl] -2,4-dihydro-3H-1, 2,4-triazole-3-thione,
( 1.050) 2-[ 1 -(2,4-Dichlorphenyl)-5-hydroxy-2,6,6-trimethylheptan-4-yl] -2,4-dihydro-3H-l ,2,4- tiazol-3-thion, ( 1.051) 2- [2-Chlor-4-(2,4-dichlorphenoxy)phenyl] - 1 -( 1 H- 1 ,2,4-triazol- 1 - yl)propan-2-ol, ( 1.052) 2- [2-Chlor-4-(4-chlorphenoxy)phenyl] - 1 -( 1 H- 1 ,2,4-triazol- 1 -yl)butan-2- ol, ( 1.053) 2- [4-(4-Chlorphenoxy)-2-(trifluormethyl)phenyl] - 1 -( 1H- 1 ,2,4-triazol- 1 -yl)butan-2-ol, ( 1.054) 2-[4-(4-Chlorphenoxy)-2-(trifluormethyl)phenyl] - 1 -( 1 H- 1 ,2,4-triazol- 1 -yl)pentan-2-ol, ( 1.055) 2- [4-(4-Chlorphenoxy)-2-(trifluormethyl)phenyl] - 1 -( 1H- 1 ,2,4-triazol- 1 -yl)propan-2-ol,(1.050) 2- [1- (2,4-dichlorophenyl) -5-hydroxy-2,6,6-trimethylheptan-4-yl] -2,4-dihydro-3H-1,2,4-tiazole-3 -thione, (1.051) 2- [2-Chloro-4- (2,4-dichlorophenoxy) phenyl] -1- (1H-1,2,4-triazol-1-yl) -propan-2-ol, ( 1.052) 2- [2-Chloro-4- (4-chlorophenoxy) phenyl] -1- (1H-1,2,4-triazol-1-yl) butan-2-ol, (1.053) 2- [4 - (4-chlorophenoxy) -2- (trifluoromethyl) phenyl] -1- (1H-1,2,4-triazol-1-yl) butan-2-ol, (1.054) 2- [4- (4-chlorophenoxy ) -2- (trifluoromethyl) phenyl] -1- (1H-1,2,4-triazol-1-yl) pentan-2-ol, (1.055) 2- [4- (4-chlorophenoxy) -2- (trifluoromethyl) phenyl] -1- (1H-1,2,4-triazol-1-yl) propan-2-ol,
( 1.056) 2- { [3-(2-Chlorphenyl)-2-(2,4-difluorphenyl)oxiran-2-yl] methyl } -2,4-dihydro-3H- 1,2,4- triazol-3-thion, (1.057) 2-{ [rel(2R,3R)-3-(2-Chlorphenyl)-2-(2,4-difluorphenyl)oxiran-2- yl]methyl}-2,4-dihydro-3H-l,2,4-triazol-3-thion, (1.058) 2-{ [rel(2R,3S)-3-(2-Chlorphenyl)-2- (2,4-difluorphenyl)oxiran-2-yl]methyl}-2,4-dihydro-3H-l,2,4-triazol-3-thion, (1.059) 5-(4-(1.056) 2- {[3- (2-Chlorophenyl) -2- (2,4-difluorophenyl) oxiran-2-yl] methyl} -2,4-dihydro-3H-1,2,4-triazole-3 -thione, (1.057) 2- {[rel (2R, 3R) -3- (2-chlorophenyl) -2- (2,4-difluorophenyl) oxiran-2-yl] methyl} -2,4-dihydro-3H 1-l, 2,4-triazole-3-thione, (1.058) 2- {[rel (2R, 3S) -3- (2-chlorophenyl) -2-] (2,4-difluorophenyl) oxiran-2-yl] methyl} -2,4-dihydro-3H-l, 2,4-triazole-3-thione, (1.059) 5- (4-
Chlorbenzyl)-2-(chlormethyl)-2-methyl- 1 -( 1H- 1 ,2,4-triazol- 1 -ylmethyl)cyclopentanol, ( 1.060)Chlorobenzyl) -2- (chloromethyl) -2-methyl-1 - (1H-1,2,4-triazol-1-ylmethyl) cyclopentanol, (1,060)
5-(Allylsulfanyl)- 1- { [3-(2-chlorphenyl)-2-(2,4-difluorphenyl)oxiran-2-yl]methyl } - 1H- 1 ,2,4- triazol, (1.061) 5-(Allylsulfanyl)-l-{ [rel(2R,3R)-3-(2-chlorphenyl)-2-(2,4-difluorphenyl)oxiran-5- (allylsulfanyl) -1- [[3- (2-chlorophenyl) -2- (2,4-difluorophenyl) oxiran-2-yl] methyl} -1H-1,2,4-triazole, (1061) 5 - (allylsulfanyl) -l- {[rel (2R, 3R) -3- (2-chlorophenyl) -2- (2,4-difluorophenyl) oxirane
2-yl]methyl } -1H-1 ,2,4-triazol, ( 1.062) 5-(Allylsulfanyl)-l - { [rel(2R,3S)-3-(2-chlorphenyl)-2-2-yl] methyl} -1H-1, 2,4-triazole, (1.062) 5- (allylsulfanyl) -1 - {[rel (2R, 3S) -3- (2-chlorophenyl) -2-
(2,4-difluorphenyl)oxiran-2-yl]methyl}-lH-l,2,4-triazol, (1.063) N'-(2,5-Dimethyl-4-{ [3-(2,4-difluorophenyl) oxiran-2-yl] methyl} -1H-l, 2,4-triazole, (1063) N '- (2,5-dimethyl-4- {3)
(l,l,2,2-tetrafluorethoxy)phenyl]sulfanyl}phenyl)-N-ethyl-N-methylimidoformamid, (1.064) N'- (2,5-Dimethyl-4-{ [3-(2,2,2-trifluorethoxy)phenyl]sulfanyl}phenyl)-N-ethyl-N- methylimidoformamid, (1.065) N'-(2,5-Dimethyl-4-{ [3-(2,2,3,3-tetrafluorpropoxy)phenyl]- sulfanyl} phenyl) -N-ethyl-N-methylimidoformamid, (1.066) N'-(2,5-Dimethyl-4-{ [3-(pentafluor- ethoxy)phenyl]sulfanyl}phenyl)-N-ethyl-N-methylimidoformamid, (1.067) N'-(2,5-Dimethyl-4- {3-[(l,l,2,2-tetrafluorethyl)sulfanyl]phenoxy}phenyl)-N-ethyl-N-methylimidoformamid,(l, l, 2,2-tetrafluoroethoxy) phenyl] sulfanyl} phenyl) -N-ethyl-N-methylimidoformamide, (1.064) N '- (2,5-dimethyl-4- {[3- (2,2, 2-trifluoroethoxy) phenyl] sulfanyl} phenyl) -N-ethyl-N-methylimidoformamide, (1.065) N '- (2,5-dimethyl-4- {[3- (2,2,3,3-tetrafluoropropoxy) phenyl] ] - sulfanyl} phenyl) -N-ethyl-N-methylimidoformamide, (1.066) N '- (2,5-dimethyl-4- {[3- (pentafluoroethoxy) phenyl] sulfanyl} phenyl) -N-ethyl- N-methylimidoformamide, (1.067) N '- (2,5-dimethyl-4- {3 - [(1, l, 2,2-tetrafluoroethyl) sulfanyl] phenoxy} phenyl) -N-ethyl-N-methylimidoformamide,
(1.068) N'-(2,5-Dimethyl-4-{3-[(2,2,2-trifluorethyl)sulfanyl]phenoxy}phenyl)-N-ethyl-N- methylimidoformamid, (1.069) N'-(2, 5-Dimethyl-4-{3-[(2, 2,3,3- tetrafluorpropyl)sulfanyl]phenoxy }phenyl)-N-ethyl-N-methylimidoformamid, ( 1.070) N'-(2,5- Dimethyl-4-{3-[(pentafluorethyl)sulfanyl]phenoxy}phenyl)-N-ethyl-N-methylimidoformamid, (1.071) N'-(2,5-Dimethyl-4-phenoxyphenyl)-N-ethyl-N-methylimidoformamid, (1.072) N'-(4- { [3-(Difluormethoxy)phenyl]sulfanyl}-2,5-dimethylphenyl)-N-ethyl-N-methylimidoformamid, (1.073) N'-(4-{3-[(Difluormethyl)sulfanyl]phenoxy}-2,5-dimethylphenyl)-N-ethyl-N- methylimidoformamid, (1.074) N'-[5-Brom-6-(2,3-dihydro-lH-inden-2-yloxy)-2-methylpyridin-(1.068) N '- (2,5-Dimethyl-4- {3 - [(2,2,2-trifluoroethyl) sulfanyl] phenoxy} phenyl) -N-ethyl-N-methylimidoformamide, (1.069) N' - ( 2, 5-Dimethyl-4- {3 - [(2,3,3,3-tetrafluoropropyl) sulfanyl] phenoxy} phenyl) -N-ethyl-N-methylimidoformamide, (1.070) N '- (2,5-dimethyl -4- {3 - [(pentafluoroethyl) sulfanyl] phenoxy} phenyl) -N-ethyl-N-methylimidoformamide, (1.071) N '- (2,5-dimethyl-4-phenoxyphenyl) -N-ethyl-N-methylimidoformamide , (1.072) N '- (4- {[3- (Difluoromethoxy) phenyl] sulfanyl} -2,5-dimethylphenyl) -N-ethyl-N-methylimidoformamide, (1.073) N' - (4- {3- [ (Difluoromethyl) sulfanyl] phenoxy} -2,5-dimethylphenyl) -N-ethyl-N-methylimidoformamide, (1.074) N '- [5-bromo-6- (2,3-dihydro-1H-inden-2-yloxy ) -2-methylpyridine
3-yl] -N-ethyl-N-methylimidoformamid, ( 1.075) N'- { 4- [(4,5 -Dichlor- 1 ,3-thiazol-2-yl)oxy] -2,5 - dimethylphenyl } -N-ethyl-N-methylimidoformamid, ( 1.076) N'-{ 5-Brom-6-[( IR)- 1 -(3,5-difluor- phenyl)ethoxy]-2-methylpyridin-3-yl} -N-ethyl-N-methylimidoformamid, (1.077) N'-{5-Brom-6- [( 1 S)-l -(3,5-difluorphenyl)ethoxy]-2-methylpyridin-3-yl } -N-ethyl-N-methylimidoformamid,3-yl] -N-ethyl-N-methylimidoformamide, (1.075) N '- {4- [(4,5-dichloro-1,3-thiazol-2-yl) oxy] -2,5-dimethylphenyl} - N-ethyl-N-methylimidoformamide, (1.076) N '- {5-bromo-6 - [(IR) -1- (3,5-difluorophenyl) ethoxy] -2-methylpyridin-3-yl} -N ethyl N-methylimidoformamide, (1.077) N '- {5-bromo-6- [(1S) -1- (3,5-difluorophenyl) ethoxy] -2-methylpyridin-3-yl} -N-ethyl -N-methylimidoformamid,
(1.078) N'- { 5-Brom-6-[(cis-4-isopropylcyclohexyl)oxy] -2-methylpyridin-3-yl } -N-ethyl-N- methylimidoformamid, (1.079) N'-{5-Brom-6-[(trans-4-isopropylcyclohexyl)oxy]-2- methylpyridin-3-yl } -N-ethyl-N-methylimidoformamid, ( 1.080) N'- { 5-Brom-6-[l -(3,5- difluorphenyl)ethoxy] -2-methylpyridin-3-yl } -N-ethyl-N-methylimidoformamid, (1.081)(1.078) N '- {5-Bromo-6 - [(cis-4-isopropylcyclohexyl) oxy] -2-methylpyridin-3-yl} -N-ethyl-N-methylimidoformamide, (1.079) N' - {5- Bromo-6 - [(trans-4-isopropylcyclohexyl) oxy] -2-methylpyridin-3-yl} -N-ethyl-N-methylimidoformamide, (1080) N '- {5-bromo-6- [1- (3 , 5-difluorophenyl) ethoxy] -2-methylpyridin-3-yl} -N-ethyl-N-methylimidoformamide, (1.081)
Mefentrifluconazol, (1.082) Ipfentrifluconazol. Mefentrifluconazole, (1.082) Ipfentrifluconazole.
2) Inhibitoren der Atmungskette an Komplex I oder II: (2.001) Benzovindiflupyr, (2.002) Bixafen, (2.003) Boscalid, (2.004) Carboxin, (2.005) Fluopyram, (2.006) Flutolanil, (2.007) Fluxapyroxad, (2.008) Furametpyr, (2.009) Isofetamid, (2.010) Isopyrazam (anti-epimeres Enantiomer 1R,4S,9S), (2.011) Isopyrazam (anti-epimeres Enantiomer 1S,4R,9R), (2.012) Isopyrazam (anti-epimeres Racemat 1RS,4SR,9SR), (2.013) Isopyrazam (Mischung von syn- epimerem Racemat 1RS,4SR,9RS und anti-epimerem Racemat 1RS,4SR,9SR), (2.014) Isopyrazam (syn-epimeres Enantiomer 1R,4S,9R), (2.015) Isopyrazam (syn-epimeres2) respiratory chain inhibitors on complex I or II: (2.001) benzovindiflupyr, (2.002) bixafen, (2.003) boscalid, (2.004) carboxin, (2.005) fluopyram, (2.006) flutolanil, (2.007) fluxapyroxad, (2.008) furametpyr , (2.009) isofetamide, (2.010) isopyrazam (anti-epimeric enantiomer 1R, 4S, 9S), (2.011) isopyrazam (anti-epimeric enantiomer 1S, 4R, 9R), (2.012) isopyrazam (anti-epimeric racemate 1RS, 4SR , 9SR), (2.013) isopyrazam (mixture of synepimeric racemate 1RS, 4SR, 9RS and anti-epimeric racemate 1RS, 4SR, 9SR), (2.014) isopyrazam (syn-epimeric enantiomer 1R, 4S, 9R), (2.015 Isopyrazam (syn-epimeres
Enantiomer 1S,4R,9S), (2.016) Isopyrazam (syn-epimeres Racemat 1RS,4SR,9RS), (2.017) Penflufen, (2.018) Penthiopyrad, (2.019) Pydiflumetofen, (2.020) Pyraziflumid, (2.021) Sedaxan, (2.022) l,3-Dimethyl-N-(l,l,3-trimethyl-2,3-dihydro-lH-inden-4-yl)-lH-pyrazol-4- carboxamid, (2.023) l,3-Dimethyl-N-[(3R)-l,l,3-trimethyl-2,3-dihydro-lH-inden-4-yl]-lH- pyrazol-4-carboxamid, (2.024) l,3-Dimethyl-N-[(3S)-l,l,3-trimethyl-2,3-dihydro-lH-inden-4- yl]-lH-pyrazol-4-carboxamid, (2.025) l-Methyl-3-(trifluormethyl)-N-[2'-Enantiomer 1S, 4R, 9S), (2.016) isopyrazam (syn-epimeric racemate 1RS, 4SR, 9RS), (2.017) Penflufen, (2.018) Penthiopyrad, (2.019) Pydiflumetofen, (2.020) Pyracetlumide, (2.021) Sedaxane, (2.022) l, 3-Dimethyl-N- (l, l, 3-trimethyl-2,3-dihydro-lH- inden-4-yl) -1H-pyrazole-4-carboxamide, (2.023) l, 3-dimethyl-N - [(3R) -l, l, 3-trimethyl-2,3-dihydro-1H-indene-4 -yl] -1H-pyrazole-4-carboxamide, (2.024) l, 3-dimethyl-N - [(3S) -l, l, 3-trimethyl-2,3-dihydro-1H-inden-4-yl] -lH-pyrazole-4-carboxamide, (2.025) 1-methyl-3- (trifluoromethyl) -N- [2'-
(trifluormethyl)biphenyl-2-yl]-lH-pyrazol-4-carboxamid, (2.026) 2-Fluor-6-(trifluormethyl)-N- (l,l,3-trimethyl-2,3-dihydro-lH-inden-4-yl)benzamid, (2.027) 3-(Difluormethyl)-l-methyl-N- (l,l,3-trimethyl-2,3-dihydro-lH-inden-4-yl)-lH-pyrazol-4-carboxamid, (2.028) 3-(trifluoromethyl) biphenyl-2-yl] -1H-pyrazole-4-carboxamide, (2.026) 2-fluoro-6- (trifluoromethyl) -N- (1, 1, 3-trimethyl-2,3-dihydro-1H- inden-4-yl) benzamide, (2.027) 3- (difluoromethyl) -1-methyl-N- (1,1,3-trimethyl-2,3-dihydro-1H-inden-4-yl) -1H-pyrazole -4-carboxamide, (2.028) 3-
(Difluormethyl)-l -methyl-N-[(3R)- 1, 1 ,3-trimethyl-2,3-dihydro- lH-inden-4-yl]- lH-pyrazol-4- carboxamid, (2.029) 3-(Difluormethyl)-l-methyl-N-[(3S)-l,l,3-trimethyl-2,3-dihydro-lH-inden-(Difluoromethyl) -1-methyl-N - [(3R) -1,1,3-trimethyl-2,3-dihydro-1H-inden-4-yl] -1H-pyrazole-4-carboxamide, (2.029) 3 - (difluoromethyl) -l-methyl-N - [(3S) -l, l, 3-trimethyl-2,3-dihydro-lH-inden
4-yl]-lH-pyrazol-4-carboxamid, (2.030) 3-(Difluormethyl)-N-(7-fluor-l,l,3-trimethyl-2,3- dihydro-lH-inden-4-yl)-l-methyl-lH-pyrazol-4-carboxamid, (2.031) 3-(Difluormethyl)-N- [(3R)-7 -fluor- 1 , 1 ,3-trimethyl-2,3-dihydro- 1 H-inden-4-yl] - 1 -methyl- lH-pyrazol-4-carboxamid, (2.032) 3-(Difluormethyl)-N-[(3S)-7-fluor-l,l,3-trimethyl-2,3-dihydro-lH-inden-4-yl]-l- methyl-lH-pyrazol-4-carboxamid, (2.033) 5,8-Difluor-N-[2-(2-fluor-4-{ [4-(trifluormethyl)- pyridin-2-yl]oxy }phenyl)ethyl]chinazolin-4-amin, (2.034) N-(2-Cyclopentyl-5-fluorbenzyl)-N- cyclopropyl-3-(difluormethyl)-5-fluor-l-methyl-lH-pyrazol-4-carboxamid, (2.035) N-(2-tert.- Butyl-5 -methylbenzyl) -N -cyclopropyl-3 -(difluormethyl)-5 -fluor- 1 -methyl- 1 H-pyrazol-4- carboxamid, (2.036) N-(2-tert.-Butylbenzyl)-N-cyclopropyl-3-(difluormethyl)-5-fluor-l-methyl- lH-pyrazol-4-carboxamid, (2.037) N-(5-Chlor-2-ethylbenzyl)-N-cyclopropyl-3-(difluormethyl)-4-yl] -1H-pyrazole-4-carboxamide, (2.030) 3- (difluoromethyl) -N- (7-fluoro-1,1,3-trimethyl-2,3-dihydro-1H-inden-4-yl ) -l-methyl-1H-pyrazole-4-carboxamide, (2.031) 3- (difluoromethyl) -N- [(3R) -7-fluoro-1,1,3-trimethyl-2,3-dihydro-1H -inden-4-yl] - 1-methyl-1H-pyrazole-4-carboxamide, (2.032) 3- (difluoromethyl) -N - [(3S) -7-fluoro-1, 1, 3-trimethyl-2, 3-dihydro-1H-inden-4-yl] -l-methyl-1H-pyrazole-4-carboxamide, (2.033) 5,8-difluoro-N- [2- (2-fluoro-4- {4 (trifluoromethyl) pyridin-2-yl] oxy} phenyl) ethyl] quinazolin-4-amine, (2.034) N- (2-cyclopentyl-5-fluorobenzyl) -N-cyclopropyl-3- (difluoromethyl) -5-fluoro -l-methyl-1H-pyrazole-4-carboxamide, (2.035) N- (2-tert-butyl-5-methylbenzyl) -N-cyclopropyl-3 - (difluoromethyl) -5-fluoro-1-methyl-1 H-pyrazole-4-carboxamide, (2.036) N- (2-tert-butylbenzyl) -N-cyclopropyl-3- (difluoromethyl) -5-fluoro-1-methyl-1H-pyrazole-4-carboxamide, (2.037 ) N- (5-chloro-2-ethylbenzyl) -N-cyclopropyl-3- (difluoromethyl) -
5-fluor-l-methyl-lH-pyrazol-4-carboxamid, (2.038) N-(5-Chlor-2-isopropylbenzyl)-N- cyclopropyl-3-(difluormethyl)-5-fluor-l-methyl-lH-pyrazol-4-carboxamid, (2.039) N-[(1R,4S)- 9-(Dichlormethylen)- 1 ,2,3,4-tetrahydro-l ,4-methanonaphthalin-5-yl] -3-(difluormethyl)-l - methyl- lH-pyrazol-4-carboxamid, (2.040) N-[(lS,4R)-9-(Dichlormethylen)-l,2,3,4-tetrahydro- 1 ,4-methanonaphthalin-5 -yl] -3-(difluormethyl)- 1 -methyl- 1 H-pyrazol-4-carboxamid, (2.041 ) N- [ 1 -(2,4-Dichlorphenyl)- 1 -methoxypropan-2-yl] -3-(difluormethyl)- 1 -methyl- 1 H-pyrazol-4- carboxamid, (2.042) N-[2-Chlor-6-(trifluormethyl)benzyl]-N-cyclopropyl-3-(difluormethyl)-5- fluor- l-methyl-lH-pyrazol-4-carboxamid, (2.043) N-[3-Chlor-2-fluor-6-(trifluormethyl)benzyl]- N-cyclopropyl-3-(difluormethyl)-5-fluor- 1 -methyl- 1 H-pyrazol-4-carboxamid, (2.044) N-[5-5-fluoro-1-methyl-1H-pyrazole-4-carboxamide, (2.038) N- (5-chloro-2-isopropylbenzyl) -N-cyclopropyl-3- (difluoromethyl) -5-fluoro-1-methyl-1H pyrazole-4-carboxamide, (2.039) N - [(1R, 4S) -9- (dichloromethylene) -1,2,3,4-tetrahydro-1,4-methanonaphthalen-5-yl] -3- (difluoromethyl ) -l-methyl-1H-pyrazole-4-carboxamide, (2.040) N - [(IS, 4R) -9- (dichloromethylene) -l, 2,3,4-tetrahydro-1,4-methanonaphthalene-5 - yl] -3- (difluoromethyl) -1-methyl-1H-pyrazole-4-carboxamide, (2.041) N- [1- (2,4-dichlorophenyl) -1-methoxypropan-2-yl] -3- ( difluoromethyl) -1-methyl-1H-pyrazole-4-carboxamide, (2.042) N- [2-chloro-6- (trifluoromethyl) benzyl] -N-cyclopropyl-3- (difluoromethyl) -5-fluoro-1-one methyl-1H-pyrazole-4-carboxamide, (2.043) N- [3-chloro-2-fluoro-6- (trifluoromethyl) benzyl] - N -cyclopropyl-3- (difluoromethyl) -5-fluoro-1-methyl- 1 H-pyrazole-4-carboxamide, (2.044) N- [5-
Chlor-2-(trifluormethyl)benzyl]-N-cyclopropyl-3-(difluormethyl)-5-fluor-l-methyl-lH-pyrazol- 4-carboxamid, (2.045) N-Cyclopropyl-3-(difluormethyl)-5-fluor-l-methyl-N-[5-methyl-2- (trifluormethyl)benzyl]-lH-pyrazol-4-carboxamid, (2.046) N-Cyclopropyl-3-(difluormethyl)-5- fluor-N-(2-fluor-6-isopropylbenzyl)-l-methyl-lH-pyrazol-4-carboxamid, (2.047) N- Cyclopropyl-3-(difluormethyl)-5-fluor-N-(2-isopropyl-5-methylbenzyl)-l-methyl-lH-pyrazol-4- carboxamid, (2.048) N-Cyclopropyl-3-(difluormethyl)-5-fluor-N-(2-isopropylbenzyl)-l-methyl- lH-pyrazol-4-carbothioamid, (2.049) N-Cyclopropyl-3-(difluormethyl)-5-fluor-N-(2- isopropylbenzyl)-! -methyl- lH-pyrazol-4-carboxamid, (2.050) N-Cyclopropyl-3- (difluormethyl)-5-fluor-N-(5-fluor-2-isopropylbenzyl)-l-methyl-lH-pyrazol-4-carboxamid, (2.051) N-Cyclopropyl-3-(difluormethyl)-N-(2-ethyl-4,5-dimethylbenzyl)-5-fluor-l-methyl-lH- pyrazol-4-carboxamid, (2.052) N-Cyclopropyl-3-(difluormethyl)-N-(2-ethyl-5-fluorbenzyl)-5- fluor-l-methyl-lH-pyrazol-4-carboxamid, (2.053) N-Cyclopropyl-3-(difluormethyl)-N-(2-ethyl- 5-methylbenzyl)-5-fluor-l-methyl-lH-pyrazol-4-carboxamid, (2.054) N-Cyclopropyl-N-(2- cyclopropyl-5-fluorbenzyl)-3-(difluormethyl)-5-fluor-l-methyl-lH-pyrazol-4-carboxamid, (2.055) N-Cyclopropyl-N-(2-cyclopropyl-5-methylbenzyl)-3-(difluormethyl)-5-fluor-l-methyl- lH-pyrazol-4-carboxamid, (2.056) N-Cyclopropyl-N-(2-cyclopropylbenzyl)-3-(difluormethyl)- 5-fluor- 1 -methyl- 1 H-pyrazol-4-carboxamid. Chloro-2- (trifluoromethyl) benzyl] -N-cyclopropyl-3- (difluoromethyl) -5-fluoro-1-methyl-1H-pyrazole-4-carboxamide, (2.045) N-cyclopropyl-3- (difluoromethyl) -5 fluoro-1-methyl-N- [5-methyl-2- (trifluoromethyl) benzyl] -1H-pyrazole-4-carboxamide, (2.046) N-cyclopropyl-3- (difluoromethyl) -5-fluoro-N- ( 2-fluoro-6-isopropylbenzyl) -1-methyl-1H-pyrazole-4-carboxamide, (2.047) N-cyclopropyl-3- (difluoromethyl) -5-fluoro-N- (2-isopropyl-5-methylbenzyl) - 1-methyl-1H-pyrazole-4-carboxamide, (2.048) N-cyclopropyl-3- (difluoromethyl) -5-fluoro-N- (2-isopropylbenzyl) -1-methyl-1H-pyrazole-4-carbothioamide, 2.049) N-Cyclopropyl-3- (difluoromethyl) -5-fluoro-N- (2-isopropylbenzyl) -! -methyl-1H-pyrazole-4-carboxamide, (2.050) N-cyclopropyl-3- (difluoromethyl) -5-fluoro-N- (5-fluoro-2-isopropylbenzyl) -l-methyl-1H-pyrazole-4-carboxamide, (2.051) N-cyclopropyl-3- (difluoromethyl) -N- (2) ethyl-4,5-dimethylbenzyl) -5-fluoro-1-methyl-1H-pyrazole-4-carboxamide, (2.052) N-cyclopropyl-3- (difluoromethyl) -N- (2-ethyl-5-fluorobenzyl) - 5-fluoro-1-methyl-1H-pyrazole-4-carboxamide, (2.053) N-cyclopropyl-3- (difluoromethyl) -N- (2-ethyl-5-methylbenzyl) -5-fluoro-1-methyl-1H pyrazole-4-carboxamide, (2.054) N-cyclopropyl-N- (2-cyclopropyl-5-fluorobenzyl) -3- (difluoromethyl) -5-fluoro-1-methyl-1H-pyrazole-4-carboxamide, (2.055 ) N-Cyclopropyl-N- (2-cyclopropyl-5-methylbenzyl) -3- (difluoromethyl) -5-fluoro-1-methyl-1H-pyrazole-4-carboxamide, (2.056) N-cyclopropyl-N- (2 -cyclopropylbenzyl) -3- (difluoromethyl) -5-fluoro-1-methyl-1H-pyrazole-4-carboxamide.
3) Inhibitoren der Atmungskette an Komplex PI: (3.001) Ametoctradin, (3.002) Amisulbrom,3) respiratory chain inhibitors on complex PI: (3.001) ametoctradine, (3.002) amisulbrom,
(3.003) Azoxystrobin, (3.004) Coumethoxystrobin, (3.005) Coumoxystrobin, (3.006) Cyazofamid, (3.007) Dimoxystrobin, (3.008) Enoxastrobin, (3.009) Famoxadon, (3.010) Fenamidon, (3.011) Flufenoxystrobin, (3.012) Fluoxastrobin, (3.013) Kresoxim-methyl, (3.014) Metominostrobin, (3.015) Orysastrobin, (3.016) Picoxystrobin, (3.017) Pyraclostrobin, (3.018) Pyrametostrobin, (3.019) Pyraoxystrobin, (3.020) Trifloxystrobin, (3.021) (2E)-2-{2-[({ [(lE)-l- (3-{ [(E)-l-Fluor-2-phenylvinyl]oxy}phenyl)ethyliden]amino}oxy)methyl]phenyl}-2- (methoxyimino)-N-methylacetamid, (3.022) (2E,3Z)-5-{ [l-(4-Chlorphenyl)-lH-pyrazol-3- yl]oxy}-2-(methoxyimino)-N,3-dimethylpent-3-enamid, (3.023) (2R)-2-{2-[(2,5-(3.003) azoxystrobin, (3.004) coumethoxystrobin, (3.005) coumoxystrobin, (3.006) cyazofamide, (3.007) dimoxystrobin, (3.008) enoxastrobin, (3.009) famoxadone, (3.010) fenamidone, (3.011) flufenoxystrobin, (3.012) fluoxastrobin, (3.013) kresoxim-methyl, (3.014) metominostrobin, (3.015) orysastrobin, (3.016) picoxystrobin, (3.017) pyraclostrobin, (3.018) pyrametostrobin, (3.019) pyraoxystrobin, (3.020) trifloxystrobin, (3.021) (2E) -2 - {2 - [({[(IE) -l- (3- {[(E) -l-fluoro-2-phenylvinyl] oxy} phenyl) ethylidene] amino} oxy) methyl] phenyl} -2- (methoxyimino ) -N-methylacetamide, (3.022) (2E, 3Z) -5- {[1- (4-chlorophenyl) -1H-pyrazol-3-yl] oxy} -2- (methoxyimino) -N, 3-dimethylpent- 3-enamide, (3.023) (2R) -2- {2 - [(2,5-)
Dimethylphenoxy)methyl]phenyl}-2-methoxy-N-methylacetamid, (3.024) (2S)-2-{2-[(2,5-Dimethylphenoxy) methyl] phenyl} -2-methoxy-N-methylacetamide, (3.024) (2S) -2- {2 - [(2,5-)
Dimethylphenoxy)methyl]phenyl}-2-methoxy-N-methylacetamid, (3.025) (3S,6S,7R,8R)-2-Dimethylphenoxy) methyl] phenyl} -2-methoxy-N-methylacetamide, (3.025) (3S, 6S, 7R, 8R) -2-
Methylpropansäure-8-benzyl-3-[({3-[(isobutyryloxy)methoxy]-4-methoxypyridin-2- yl }carbonyl)amino] -6-methyl-4,9-dioxo- 1 ,5-dioxonan-7-ylester, (3.026) 2- { 2- [(2,5 -Dimethyl- phenoxy)methyl]phenyl}-2-methoxy-N-methylacetamid, (3.027) N-(3-Ethyl-3,5,5- trimethylcyclohexyl)-3-formamido-2-hydroxybenzamid, (3.028) (2E,3Z)-5-{ [l-(4-Chlor-2- fluorphenyl)-lH-pyrazol-3-yl]oxy}-2-(methoxyimino)-N,3-dimethylpent-3-enamid, (3.029) [5- [3-(2,4-Dimethylphenyl)-lH-pyrazol-l-yl]-2-methylbenzyl}carbamidsäuremethylester. Methylpropanoic acid 8-benzyl-3 - [({3 - [(isobutyryloxy) methoxy] -4-methoxypyridin-2-yl} carbonyl) amino] -6-methyl-4,9-dioxo-1, 5-dioxonane-7 ethyl ester, (3.026) 2- {2- [(2,5-dimethylphenoxy) methyl] phenyl} -2-methoxy-N-methylacetamide, (3.027) N- (3-ethyl-3,5,5- trimethylcyclohexyl) -3-formamido-2-hydroxybenzamide, (3.028) (2E, 3Z) -5- {[1- (4-chloro-2-fluorophenyl) -1H-pyrazol-3-yl] oxy} -2- ( methoxyimino) -N, 3-dimethylpent-3-enamide, (3.029) [5- [3- (2,4-dimethylphenyl) -1H-pyrazol-1-yl] -2-methylbenzyl} carbamic acid, methyl ester.
4) Inhibitoren von Mitose und Zellteilung: (4.001) Carbendazim, (4.002) Diethofencarb, (4.003)4) Inhibitors of Mitosis and Cell Division: (4.001) Carbendazim, (4.002) Diethofencarb, (4.003)
Ethaboxam, (4.004) Fluopicolid, (4.005) Pencycuron, (4.006) Thiabendazol, (4.007) Thiophanat-methyl, (4.008) Zoxamid, (4.009) 3-Chlor-4-(2,6-difluorphenyl)-6-methyl-5- phenylpyridazin, (4.010) 3-Chlor-5-(4-chlorphenyl)-4-(2,6-difluorphenyl)-6-methylpyridazin, (4.011) 3-Chlor-5-(6-chlorpyridin-3-yl)-6-methyl-4-(2,4,6-trifluorphenyl)pyridazin, (4.012) 4- (2-Brom-4-fluorphenyl)-N-(2,6-difluorphenyl)-l,3-dimethyl-lH-pyrazol-5-amin, (4.013) 4-(2- Brom-4-fluorphenyl)-N-(2-brom-6-fluorphenyl)-l,3-dimethyl-lH-pyrazol-5-amin, (4.014) 4-(2- Brom-4-fluorphenyl)-N-(2-bromphenyl)-l,3-dimethyl-lH-pyrazol-5-amin, (4.015) 4-(2-Brom-4- fluorphenyl)-N-(2-chlor-6-fluorphenyl)-l,3-dimethyl-lH-pyrazol-5-amin, (4.016) 4-(2-Brom-4- fluorphenyl)-N-(2-chlorphenyl)-l,3-dimethyl-lH-pyrazol-5-amin, (4.017) 4-(2-Brom-4- fluorphenyl)-N-(2-fluorphenyl)-l,3-dimethyl-lH-pyrazol-5-amin, (4.018) 4-(2-Chlor-4- fluorphenyl)-N-(2,6-difluorphenyl)-l,3-dimethyl-lH-pyrazol-5-amin, (4.019) 4-(2-Chlor-4- fluorphenyl)-N-(2-chlor-6-fluorphenyl)-l,3-dimethyl-lH-pyrazol-5-amin, (4.020) 4-(2-Chlor-4- fluorphenyl)-N-(2-chlorphenyl)-l,3-dimethyl-lH-pyrazol-5-amin, (4.021) 4-(2-Chlor-4- fluorphenyl)-N-(2-fluorphenyl)-l,3-dimethyl-lH-pyrazol-5-amin, (4.022) 4-(4-Chlorphenyl)-5- (2,6-difluorphenyl)-3,6-dimethylpyridazin, (4.023) N-(2-Brom-6-fluorphenyl)-4-(2-chlor-4- fluorphenyl)-l,3-dimethyl-lH-pyrazol-5-amin, (4.024) N-(2-Bromphenyl)-4-(2-chlor-4- fluorphenyl)-l,3-dimethyl-lH-pyrazol-5-amin, (4.025) N-(4-Chlor-2,6-difluorphenyl)-4-(2- chlor-4-fluorphenyl)- 1 ,3-dimethyl- 1 H-pyrazol-5-amin. Ethaboxam, (4.004) fluopicolide, (4.005) pencycuron, (4.006) thiabendazole, (4.007) thiophanate-methyl, (4.008) zoxamide, (4.009) 3-chloro-4- (2,6-difluorophenyl) -6-methyl- 5-phenylpyridazine, (4.010) 3-chloro-5- (4-chlorophenyl) -4- (2,6-difluorophenyl) -6-methylpyridazine, (4,011) 3-chloro-5- (6-chloropyridin-3-yl ) -6-methyl-4- (2,4,6-trifluorophenyl) pyridazine, (4.012) 4- (2-bromo-4-fluorophenyl) -N- (2,6-difluorophenyl) -1,3-dimethyl 1H-pyrazol-5-amine, (4.013) 4- (2-bromo-4-fluorophenyl) -N- (2-bromo-6-fluorophenyl) -1,3-dimethyl-1H-pyrazol-5-amine, ( 4.014) 4- (2-bromo-4-fluorophenyl) -N- (2-bromophenyl) -l, 3-dimethyl-1H-pyrazol-5-amine, (4.015) 4- (2-bromo-4-fluorophenyl) N- (2-chloro-6-fluorophenyl) -1,3-dimethyl-1H-pyrazol-5-amine, (4.016) 4- (2-bromo-4-fluorophenyl) -N- (2-chlorophenyl) - 1,3-dimethyl-1H-pyrazol-5-amine, (4.017) 4- (2-bromo-4- fluorophenyl) -N- (2-fluorophenyl) -1,3-dimethyl-1H-pyrazol-5-amine, (4,018) 4- (2-chloro-4-fluorophenyl) -N- (2,6-difluorophenyl) - l, 3-dimethyl-1H-pyrazol-5-amine, (4.019) 4- (2-chloro-4-fluorophenyl) -N- (2-chloro-6-fluorophenyl) -1,3-dimethyl-1H-pyrazole -5-amine, (4.020) 4- (2-chloro-4-fluorophenyl) -N- (2-chlorophenyl) -1,3-dimethyl-1H-pyrazole-5-amine, (4,021) 4- (2- Chloro-4-fluorophenyl) -N- (2-fluorophenyl) -1,3-dimethyl-1H-pyrazol-5-amine, (4,022) 4- (4-chlorophenyl) -5- (2,6-difluorophenyl) - 3,6-dimethylpyridazine, (4.023) N- (2-bromo-6-fluorophenyl) -4- (2-chloro-4-fluorophenyl) -1,3-dimethyl-1H-pyrazole-5-amine, (4,024) N- (2-bromophenyl) -4- (2-chloro-4-fluorophenyl) -1,3-dimethyl-1H-pyrazol-5-amine, (4,025) N- (4-chloro-2,6-difluorophenyl) -4- (2-chloro-4-fluorophenyl) -1,3-dimethyl-1H-pyrazole-5-amine.
5) Verbindungen, die an mehreren Stellen wirken können („Multisite Action“): (5.001) Bordeaux-Mischung, (5.002) Captafol, (5.003) Captan, (5.004) Chlorothalonil, (5.005) Kupferhydroxid, (5.006) Kupfernaphthenat, (5.007) Kupferoxid, (5.008) Kupferoxychlorid, (5.009) Kupfer(2+)-sulfat, (5.010) Dithianon, (5.011) Dodin, (5.012) Folpet, (5.013) Mancozeb, (5.014) Maneb, (5.015) Metiram, (5.016) Metiram-Zink, (5.017) Oxine -Kupfer, (5.018) Propineb, (5.019) Schwefel und Schwefelzubereitungen einschließlich Calciumpolysulfid, (5.020) Thiram, (5.021) Zineb, (5.022) Ziram, (5.023) 6-Ethyl-5,7-dioxo-6,7-dihydro-5H- pyrrolo [3', 4': 5,6] [ 1 ,4]dithiino [2,3-c] [ 1 ,2] thiazol-3-carbonsäurenitril. 5) Multisite Action Compounds: (5.001) Bordeaux Mixture, (5.002) Captafol, (5.003) Captan, (5.004) Chlorothalonil, (5.005) Copper Hydroxide, (5.006) Copper Napthenate, ( 5.007) copper oxide, (5.008) copper oxychloride, (5.009) copper (2+) sulfate, (5.010) dithianone, (5.011) dodin, (5.012) folpet, (5.013) mancozeb, (5.014) maneb, (5.015) metiram, (5,016) Metiram Zinc, (5,017) Oxine Copper, (5,018) Propineb, (5,019) Sulfur and Sulfur Preparations Including Calcium Polysulfide, (5,020) Thiram, (5,021) Zineb, (5,022) Ziram, (5,023) 6-Ethyl 5,7-dioxo-6,7-dihydro-5H-pyrrolo [3 ', 4': 5,6] [1,4] dithiino [2,3-c] [1,2] thiazole-3-carbonitrile.
6) Verbindungen, die dazu in der Lage sind, Abwehrreaktionen des Wirtes zu induzieren: (6.001) Acibenzolar-S-methyl, (6.002) Isotianil, (6.003) Probenazol, (6.004) Tiadinil. 6) Compounds capable of inducing host defense responses: (6,001) acibenzolar-S-methyl, (6,002) isotianil, (6,003) probenazole, (6,004) tiadinil.
7) Inhibitoren von Aminosäure- und/oder Proteinbiosynthese: (7.001) Cyprodinil, (7.002) Kasugamycin, (7.003) Kasugamycinhydrochlorid-hydrat, (7.004) Oxytetracyclin, (7.005) Pyrimethanil, (7.006) 3-(5-Fluor-3,3,4,4-tetramethyl-3,4-dihydroisochinolin-l-yl)chinolin. 7) Inhibitors of amino acid and / or protein biosynthesis: (7,001) cyprodinil, (7,002) kasugamycin, (7,003) kasugamycin hydrochloride hydrate, (7,004) oxytetracycline, (7,005) pyrimethanil, (7,006) 3- (5-fluoro-3, 3,4,4-tetramethyl-3,4-dihydroisoquinoline-l-yl) quinoline.
8) Inhibitoren der ATP-Produktion: (8.001) Silthiofam. 8) Inhibitors of ATP production: (8,001) Silthiofam.
9) Inhibitoren der Zellwandsynthese: (9.001) Benthiavalicarb, (9.002) Benthiavalicarb- isopropyl, (9.003) Dimethomorph, (9.004) Flumorph, (9.005) Iprovalicarb, (9.006) Mandipropamid, (9.007) Pyrimorph, (9.008) Valifenalat, (9.009) (2E)-3-(4-tert.-Butylphenyl)-3- (2-chlorpyridin-4-yl)-l-(morpholin-4-yl)prop-2-en-l-on, (9.010) (2Z)-3-(4-tert.-Butylphenyl)-3- (2-chlorpyridin-4-yl)- 1 -(morpholin-4-yl)prop-2-en- 1 -on. 9) Inhibitors of Cell Wall Synthesis: (9.001) Benthiavalicarb, (9.002) Benthiavalicarb-isopropyl, (9.003) Dimethomorph, (9.004) Flumorph, (9.005) Iprovalicarb, (9.006) Mandipropamide, (9.007) Pyrimorph, (9.008) Valifenalate, (9.009 ) (2E) -3- (4-tert-butylphenyl) -3- (2-chloropyridin-4-yl) -1- (morpholin-4-yl) prop-2-en-1-one, (9.010) (2Z) -3- (4-tert-butylphenyl) -3- (2-chloropyridin-4-yl) -1- (morpholin-4-yl) prop-2-en-1-one.
10) Inhibitoren der Lipid- und Membransynthese: (10.001) Propamocarb, (10.002) Propamocarb-hydrochlorid, (10.003) Tolclofos-methyl. 10) Inhibitors of Lipid and Membrane Synthesis: (10,001) Propamocarb, (10,002) Propamocarb hydrochloride, (10,003) Tolclofos-methyl.
11) Inhibitoren der Melaninbiosynthese: (11.001) Tricyclazol, (11.002) {3-Methyl-l-[(4- methylbenzoyl)amino]butan-2-yl}carbamidsäure-2,2,2-trifluorethylester. 12) Inhibitoren der Nukleinsäuresynthese: (12.001) Benalaxyl, (12.002) Benalaxyl-M (Kiralaxyl), (12.003) Metalaxyl, (12.004) Metalaxyl-M (Mefenoxam). 11) Inhibitors of melanin biosynthesis: (11.001) tricyclazole, (11.002) {3-methyl-1 - [(4-methylbenzoyl) amino] butan-2-yl} carbamic acid 2,2,2-trifluoroethyl ester. 12) Inhibitors of Nucleic Acid Synthesis: (12.001) Benalaxyl, (12.002) Benalaxyl-M (Kiralaxyl), (12.003) Metalaxyl, (12.004) Metalaxyl-M (Mefenoxam).
13) Inhibitoren der Signalübertragung: (13.001) Fludioxonil, (13.002) Iprodion, (13.003) Procymidon, (13.004) Proquinazid, (13.005) Quinoxyfen, (13.006) Vinclozolin. 13) Inhibitors of signal transduction: (13.001) fludioxonil, (13.002) iprodione, (13.003) procymidone, (13.004) proquinazide, (13.005) quinoxyfen, (13.006) vinclozolin.
14) Verbindungen, die als Entkoppler wirken können: (14.001) Fluazinam, (14.002) Meptyldinocap. 14) Compounds that may act as decouplers: (14.001) fluazinam, (14.002) meptyldinocap.
15) Weitere Verbindungen: (15.001) Abscisinsäure, (15.002) Benthiazol, (15.003) Bethoxazin,15) Further compounds: (15.001) abscisic acid, (15.002) benthiazole, (15.003) bethoxazine,
(15.004) Capsimycin, (15.005) Carvon, (15.006) Chinomethionat, (15.007) Cufraneb, (15.008) Cyflufenamid, (15.009) Cymoxanil, (15.010) Cyprosulfamid, (15.011) Flutianil, (15.012) Fosetyl-Aluminium, (15.013) Fosetyl-Calcium, (15.014) Fosetyl-Natrium, (15.015) Methyl- isothiocyanat, (15.016) Metrafenon, (15.017) Mildiomycin, (15.018) Natamycin, (15.019) Nickeldimethyldithiocarbamat, (15.020) Nitrothal-isopropyl, (15.021) Oxamocarb, (15.022) Oxathiapiprolin, (15.023) Oxyfenthiin, (15.024) Pentachlorphenol und Salze, (15.025) phosphorige Säure und deren Salze, (15.026) Propamocarb-fosetylat, (15.027) Pyriofenon (Chlazafenon), (15.028) Tebufloquin, (15.029) Tecloftalam, (15.030) Tolnifanid, (15.031) l-(4- { 4-[(5R)-5-(2,6-Difluorphenyl)-4,5 -dihydro- 1 ,2-oxazol-3-yl] - 1 ,3-thiazol-2-yl Jpiperidin- 1 -yl)-2- [5-methyl-3-(trifluormethyl)-lH-pyrazol-l-yl]ethanon, (15.032) l-(4-{4-[(5S)-5-(2,6-(15.004) Capsimycin, (15.005) Carvone, (15.006) Quinomethionate, (15.007) Cufraneb, (15.008) Cyflufenamid, (15.009) Cymoxanil, (15.010) Cyprosulfamide, (15.011) Flutianil, (15.012) Fosetyl-Aluminum, (15.013) Fosetyl calcium, (15.014) fosetyl sodium, (15.015) methyl isothiocyanate, (15.016) metrafenone, (15.017) mildiomycin, (15.018) natamycin, (15.019) nickel dimethyldithiocarbamate, (15.020) nitrothal isopropyl, (15.021) oxamocarb, (15.022) Oxathiapiproline, (15.023) Oxyfenthiine, (15.024) Pentachlorophenol and salts, (15.025) Phosphoric acid and its salts, (15.026) Propamocarb-fosetylate, (15.027) Pyriofenone (Chlazafenone), (15.028) Tebufloquine, (15.029) Tecloftalam , (15,030) Tolnifanide, (15,031) 1- (4- {4 - [(5R) -5- (2,6-difluorophenyl) -4,5-dihydro-1,2-oxazol-3-yl] -1 , 3-thiazol-2-yl, piperidine-1-yl) -2- [5-methyl-3- (trifluoromethyl) -1H-pyrazol-1-yl] ethanone, (15.032) 1- (4- {4- [. (5S) -5- (2,6-
Difluorphenyl)-4,5 -dihydro- 1 ,2-oxazol-3-yl] - 1 ,3-thiazol-2-yl Jpiperidin- 1 -yl)-2- [5-methyl-3- (trifluormethyl)-lH-pyrazol-l-yl]ethanon, (15.033) 2-(6-Benzylpyridin-2-yl)chinazolin, (15.034) 2,6-Dimethyl-lH,5H-[l,4]dithiino[2,3-c:5,6-c']dipyrrol-l,3,5,7(2H,6H)-tetron,Difluorophenyl) -4,5-dihydro-1,2-oxazol-3-yl] -1,3-thiazol-2-yl. Jipiperidin-1-yl) -2- [5-methyl-3- (trifluoromethyl) -1H pyrazol-1-yl] ethanone, (15.033) 2- (6-benzylpyridin-2-yl) quinazoline, (15.034) 2,6-dimethyl-1H, 5H- [1,4] dithiino [2,3-c : 5,6-c '] dipyrrole-l, 3,5,7 (2H, 6H) -tetrone,
(15.035) 2-[3,5-Bis(difluormethyl)-lH-pyrazol-l-yl]-l-[4-(4-{5-[2-(prop-2-in-l-yloxy)phenyl]- 4,5 -dihydro- 1 ,2-oxazol-3-yl } - 1 ,3-thiazol-2-yl)piperidin- 1 -yl] ethanon, ( 15.036) 2-[3,5-(15.035) 2- [3,5-bis (difluoromethyl) -1H-pyrazol-1-yl] -1- [4- (4- {5- [2- (prop-2-yn-1-yloxy) -phenyl ] - 4,5-dihydro-1,2-oxazol-3-yl} -1,3-thiazol-2-yl) piperidin-1-yl] ethanone, (15.036) 2- [3.5-
Bis(difluormethyl)- IH-pyrazol- 1 -yl] - 1 - [4-(4- { 5-[2-chlor-6-(prop-2-in- 1 -yloxy)phenyl] -4,5- dihydro- 1 ,2-oxazol-3-yl } - 1 ,3-thiazol-2-yl)piperidin- 1 -yl] ethanon, (15.037) 2-[3,5-Bis (difluoromethyl) -H-pyrazol-1-yl] -1- [4- (4- {5- [2-chloro-6- (prop-2-yn-1-yloxy) -phenyl] -4,5- dihydro-1,2-oxazol-3-yl} -1,3-thiazol-2-yl) piperidin-1-yl] ethanone, (15.037) 2- [3,5-
Bis(difluormethyl)- IH-pyrazol- 1 -yl] - 1 - [4-(4- { 5-[2-fluor-6-(prop-2-in- 1 -yloxy)phenyl] -4,5- dihydro- 1 ,2-oxazol-3-yl } - 1 ,3-thiazol-2-yl)piperidin- 1 -yl] ethanon, ( 15.038) 2- [6-(3-Fluor-4- methoxyphenyl)-5 -methylpyridin-2-yl] Chinazolin, ( 15.039) Methansulfonsäure-2- { (5R)-3- [2-( 1 - { [3,5 -bis(difluormethyl)- IH-pyrazol- 1 -yl] acetyl }piperidin-4-yl)- 1 ,3-thiazol-4-yl] -4,5 -dihydro-Bis (difluoromethyl) -H-pyrazol-1-yl] -1- [4- (4- {5- [2-fluoro-6- (prop-2-yn-1-yloxy) -phenyl] -4,5- dihydro-1, 2-oxazol-3-yl} -1,3-thiazol-2-yl) piperidin-1-yl] ethanone, (15.038) 2- [6- (3-fluoro-4-methoxyphenyl) -5 -methylpyridin-2-yl] quinazoline, (15.039) methanesulfonic acid 2- {(5R) -3- [2- (1 - {[3,5-bis (difluoromethyl) -H-pyrazol-1-yl] -yl] -acetyl} piperidin-4-yl) -1,3-thiazol-4-yl] -4,5-dihydro-
1 ,2-oxazol-5-yl } -3-chlorphenylester, ( 15.040) Methansulfonsäure-2- { (5S)-3- [2-( 1 - { [3,5- bis(difluormethyl)- IH-pyrazol- 1-yl] acetyl }piperidin-4-yl)-l ,3-thiazol-4-yl] -4,5-dihydro-l ,2- oxazol-5 -yl } -3-chlorphenylester, ( 15.041) 2- { 2- [(7, 8-Difluor-2-methylchinolin-3-yl)oxy] -6- fluorphenyl}propan-2-ol, (15.042) 2-{2-Fluor-6-[(8-fluor-2-methylchinolin-3- yl)oxy]phenyl }propan-2-ol, (15.043) Methansulfonsäure-2-{3-[2-(l-{ [3,5-bis(difluormethyl)- IH-pyrazol-l -yl] acetyl }piperidin-4-yl)- 1 ,3-thiazol-4-yl] -4,5-dihydro- 1 ,2-oxazol-5-yl } -3- chlorphenylester, (15.044) Methansulfonsäure -2-{3-[2-(l-{ [3,5-bis(difluormethyl)-lH-pyrazol- 1-yl]acetyl}piperidin-4-yl)-l,3-thiazol-4-yl]-4,5-dihydro-l,2-oxazol-5-yl}phenylester, (15.045)1, 2-oxazol-5-yl} -3-chlorophenyl ester, (15.040) methanesulfonic acid 2- {(5S) -3- [2- (1 - {[3,5-bis (difluoromethyl) -H-pyrazole] 1-yl] acetyl} piperidin-4-yl) -1,3-thiazol-4-yl] -4,5-dihydro-1,2-oxazol-5-yl-3-chlorophenyl ester, (15.041) 2- {2- [(7,8-Difluoro-2-methylquinolin-3-yl) oxy] -6-fluorophenyl} propan-2-ol, (15.042) 2- {2-fluoro-6 - [(8-fluoro) 2-methylquinolin-3-yl) oxy] phenyl} propan-2-ol, (15.043) methanesulfonic acid 2- {3- [2- (1-{[3,5-bis (difluoromethyl) -H-pyrazole-1 -yl] acetyl} piperidin-4-yl) -1,3-thiazol-4-yl] -4,5-dihydro-1,2-oxazol-5-yl} -3-chlorophenyl ester, (15.044) methanesulfonic acid -2 - {3- [2- (1 - {[3,5-bis (difluoromethyl) -1H-pyrazole] 1-yl] acetyl} piperidin-4-yl) -1,3-thiazol-4-yl] -4,5-dihydro-l, 2-oxazol-5-yl} phenyl ester, (15.045)
2-Phenylphenol und Salze, (15.046) 3-(4,4,5-Trifluor-3,3-dimethyl-3,4-dihydroisochinolin-l- yl)chinolin, (15.047) 3-(4,4-Difluor-3,3-dimethyl-3,4-dihydroisochinolin-l-yl)chinolin, (15.048)2-phenylphenol and salts, (15.046) 3- (4,4,5-trifluoro-3,3-dimethyl-3,4-dihydroisoquinolin-1-yl) quinoline, (15.047) 3- (4,4-difluoro- 3,3-dimethyl-3,4-dihydroisoquinolin-1-yl) quinoline, (15.048)
4-Amino-5-fluorpyrimidin-2-ol (tautomere Form: 4-Amino-5-fluorpyrimidin-2(lH)-on), (15.049) 4-Oxo-4-[(2-phenylethyl)amino]butansäure, (15.050) 5-Amino-l,3,4-thiadiazol-2-thiol, (15.051) 5-Chlor-N'-phenyl-N'-(prop-2-in-l-yl)thiophen-2-sulfonohydrazid, (15.052) 5-Fluor-2- [(4-fluorbenzyl)oxy]pyrimidin-4-amin, ( 15.053) 5 -Fluor-2- [(4-methylbenzyl)oxy]pyrimidin-4- amin, (15.054) 9-Fluor-2,2-dimethyl-5-(chinolin-3-yl)-2,3-dihydro-l,4-benzoxazepin, (15.055) {6-[({ [(Z)-(l-Methyl-lH-tetrazol-5-yl)(phenyl)methylen]amino}oxy)methyl]pyridin-2-yl}- carbamidsäurebut-3-in-l-ylester, (15.056) (2Z)-3-Amino-2-cyano-3-phenylacrylsäureethylester, (15.057) Phenazin- 1 -carbonsäure, (15.058) 3,4,5-Trihydroxybenzoesäurepropylester, (15.059) Chinolin-8-ol, (15.060) Chinolin-8-olsulfat (2: 1), (15.061) {6-[({ [(l-Methyl-lH-tetrazol-5- yl)(phenyl)methylen]amino}oxy)methyl]pyridin-2-yl}carbamidsäure-tert.-butylester, (15.062)4-amino-5-fluoropyrimidin-2-ol (tautomeric form: 4-amino-5-fluoropyrimidin-2 (1H) -one), (15.049) 4-oxo-4 - [(2-phenylethyl) amino] butanoic acid, (15,050) 5-Amino-l, 3,4-thiadiazole-2-thiol, (15,051) 5-Chloro-N'-phenyl-N '- (prop-2-yn-1-yl) thiophene-2-sulfonohydrazide , (15.052) 5-Fluoro-2- [(4-fluorobenzyl) oxy] pyrimidin-4-amine, (15.053) 5-Fluoro-2- [(4-methylbenzyl) oxy] pyrimidin-4-amine, (15.054) 9-Fluoro-2,2-dimethyl-5- (quinolin-3-yl) -2,3-dihydro-1,4-benzoxazepine, (15,055) {6 - [({[(Z) - (1-methyl -lH-tetrazol-5-yl) (phenyl) methylene] amino} oxy) methyl] pyridin-2-yl} -carbamic acid but-3-yn-1-yl ester, (15.056) (2Z) -3-amino-2- cyano-3-phenylacrylic acid ethyl ester, (15.057) phenazine-1-carboxylic acid, (15.058) propyl 3,4,5-trihydroxybenzoate, (15,059) quinolin-8-ol, (15,060) quinoline-8-olsulfate (2: 1), ( 15.061) tert-butyl {6 - [({[(1-methyl-1H-tetrazol-5-yl) (phenyl) -methylene] oxy) -methyl] -pyridin-2-yl} -carbamic acid, (15.062)
5 -Fluor-4-imino-3-methyl- 1 - [(4-methylphenyl)sulfonyl] -3,4-dihydropyrimidin-2( 1 H)-on. 5-Fluoro-4-imino-3-methyl-1 - [(4-methylphenyl) sulfonyl] -3,4-dihydropyrimidine-2 (1 H) -one.
3. Wirkstoffkombinationen gemäß Anspruch 1, in welcher W für Methyl steht, 3. active substance combinations according to claim 1, in which W is methyl,
X für Chlor oder Methyl steht, X is chlorine or methyl,
Y für Chlor, Brom oder Methyl steht, Y is chlorine, bromine or methyl,
D für Wasserstoff steht, D is hydrogen,
A, B und das Kohlenstoffatom, an das sie gebunden sind, für gesättigtes Cg-Cycloalkyl stehen, welches mit einer Alkylendioxyl-Gruppe substituiert ist, die mit dem Kohlenstoffatom, an das sie gebunden ist, ein 5-Ring- oder 6-Ringketal bildet, A, B and the carbon atom to which they are attached represent saturated C 9 -cycloalkyl which is substituted with an alkylenedioxyl group which forms a 5-membered or 6-membered ketal with the carbon atom to which it is attached .
G für Wasserstoff (a) oder für eine der Gruppen
Figure imgf000053_0001
steht, in welchen
G is hydrogen (a) or one of the groups
Figure imgf000053_0001
stands in which
M für Sauerstoff steht, M stands for oxygen,
E für ein Metallionenäquivalent oder ein Ammoniumion steht, E is a metal ion equivalent or an ammonium ion,
R1 für geradkettigtes oder verzweigtes C1-C4- Alkyl, für geradkettigtes oder verzweigtes C | -( '4-LI ky I . R 1 represents straight-chain or branched C 1 -C 4 -alkyl, for straight-chain or branched C | - ('4-LI ky I.
4. Wirkstoffkombinationen gemäß Anspruch 1, wobei die Substituenten W, X, Y, A, B, D und G die in der Tabelle angegebenen Bedeutungen haben: 4. active ingredient combinations according to claim 1, wherein the substituents W, X, Y, A, B, D and G have the meanings given in the table:
Figure imgf000054_0001
Figure imgf000054_0001
Figure imgf000054_0002
Figure imgf000054_0002
5 Wirkstoffkombinationen gemäß Anspruch 1, wobei die Verbindung der Formel (I) folgende Struktur hat:
Figure imgf000055_0001
5 drug combinations according to claim 1, wherein the compound of formula (I) has the structure:
Figure imgf000055_0001
Wirkstoffkombinationen gemäß Anspruch 1, enthaltend die Verbindung der Formel (1-2) Active substance combinations according to Claim 1, containing the compound of the formula (1-2)
Figure imgf000055_0002
und Isotianil.
Figure imgf000055_0002
and Isotianil.
7. Verwendung einer Wirkstoffkombination gemäß einem der Ansprüche 1, 2, 3, 4, 5 oder 6 zur Bekämpfung tierischer Schädlinge. 7. Use of a combination of active substances according to any one of claims 1, 2, 3, 4, 5 or 6 for controlling animal pests.
Verwendung einer Wirkstoffkombination gemäß einem der Ansprüche 1, 2, 3, 4, 5 oder 6 zur Bekämpfung unerwünschter Mikroorganismen. Use of a combination of active substances according to one of claims 1, 2, 3, 4, 5 or 6 for controlling unwanted microorganisms.
9. Verwendung einer Wirkstoffkombination gemäß einer der Ansprüche 1, 2, 3, 4, 5 oder 6 an transgenen Pflanzen. 10 Verfahren zur Bekämpfung tierischer Schädlinge, dadurch gekennzeichnet, dass man Wirkstoffkombinationen gemäß einem der Ansprüche 1, 2, 3, 4, 5 oder 6 auf tierische Schädlinge und/oder deren Lebensraum einwirken lässt. 9. Use of a combination of active substances according to any one of claims 1, 2, 3, 4, 5 or 6 of transgenic plants. 10. A method for controlling animal pests, characterized in that one allows drug combinations according to any one of claims 1, 2, 3, 4, 5 or 6 to act on animal pests and / or their habitat.
11 Verfahren zur Bekämpfung unerwünschter Mikroorganisemn, dadurch gekennzeichnet, dass man Wirkstoffkombinationen gemäß einem der Ansprüche 1, 2, 3, 4, 5 oder 6 auf unerwünschte Mikroorganismen und/oder deren Lebensraum einwirken lässt. 11. A process for controlling undesired microorganisms, which comprises allowing active substance combinations according to claim 1, 2, 3, 4, 5 or 6 to act on undesired microorganisms and / or their habitat.
12 Verfahren zur Herstellung insektizider, fungizider und/oder akarizider Mittel, dadurch gekenn zeichnet, dass man Wirkstoffkombinationen wie in einem der Ansprüche 1, 2, 3, 4, 5 oder 6 definiert, mit Streckmitteln und/oder oberflächenaktiven Stoffen vermischt. 12 A process for the preparation of insecticidal, fungicidal and / or acaricidal agents, characterized in that active compound combinations as defined in any one of claims 1, 2, 3, 4, 5 or 6, mixed with extenders and / or surface-active substances.
PCT/EP2019/059434 2018-04-13 2019-04-12 Active ingredient combinations with fungicides, insecticides and acaricidal properties WO2019197615A1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP18167236.1 2018-04-13
EP18167236 2018-04-13

Publications (1)

Publication Number Publication Date
WO2019197615A1 true WO2019197615A1 (en) 2019-10-17

Family

ID=61972455

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/EP2019/059434 WO2019197615A1 (en) 2018-04-13 2019-04-12 Active ingredient combinations with fungicides, insecticides and acaricidal properties

Country Status (1)

Country Link
WO (1) WO2019197615A1 (en)

Citations (39)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3639877A1 (en) 1986-11-21 1988-05-26 Bayer Ag HETARYLALKYL SUBSTITUTED 5- AND 6-RINGHETEROCYCLES
WO2003106457A1 (en) 2002-06-14 2003-12-24 Syngenta Limited Spiroindolinepiperidine derivatives
WO2004099160A1 (en) 2003-05-12 2004-11-18 Sumitomo Chemical Company, Limited Pyrimidine compounds and pests controlling composition containing the same
WO2006003494A2 (en) 2004-06-28 2006-01-12 Syngenta Participations Ag Piperidine derivatives and their use as insecticides, acaricides, molluscicides or nematicides
WO2006043635A1 (en) 2004-10-20 2006-04-27 Kumiai Chemical Industry Co., Ltd. 3-triazolylphenyl sulfide derivative and insecticide/acaricide/nematicide containing the same as active ingredient
WO2006089633A2 (en) 2005-02-22 2006-08-31 Bayer Cropscience Ag Spiroketal-substituted cyclic ketoenols
WO2007040280A1 (en) 2005-10-06 2007-04-12 Nippon Soda Co., Ltd. Cyclic amine compound and pest control agent
CN101337940A (en) 2008-08-12 2009-01-07 国家农药创制工程技术研究中心 Nitrogen heterocyclic ring dichlorin allyl ether compounds with insecticidal activity
CN101337937A (en) 2008-08-12 2009-01-07 国家农药创制工程技术研究中心 N-benz-3-substituted amino pyrazoles compounds with insecticidal activity
WO2009039951A2 (en) 2007-09-21 2009-04-02 Bayer Cropscience Ag Active ingredient combinations having insecticidal and acaricidal properties
JP2010018586A (en) 2008-07-14 2010-01-28 Meiji Seika Kaisha Ltd Substance pf1364, its manufacturing method, producing strain and agricultural/horticultural insecticide having the substance as active ingredient
WO2010052161A2 (en) 2008-11-06 2010-05-14 Syngenta Participations Ag Herbicidal compositions
WO2010051926A2 (en) 2008-11-05 2010-05-14 Bayer Cropscience Aktiengesellschaft New halogen-substituted bonds
CN101715774A (en) 2008-10-09 2010-06-02 浙江化工科技集团有限公司 Preparation and use of compound having insecticidal activity
WO2010066780A1 (en) 2008-12-12 2010-06-17 Syngenta Participations Ag Spiroheterocyclic n-oxypiperidines as pesticides
WO2010149274A2 (en) * 2009-06-23 2010-12-29 Bayer Cropscience Aktiengesellschaft Use of active ingredient combinations having insecticidal properties for controlling pests from the family of stink bugs
WO2011085575A1 (en) 2010-01-15 2011-07-21 江苏省农药研究所股份有限公司 Ortho-heterocyclyl formanilide compounds, their synthesis methods and use
WO2011105506A1 (en) 2010-02-25 2011-09-01 日本曹達株式会社 Cyclic amine compound and miticide
WO2011151146A1 (en) 2010-05-31 2011-12-08 Syngenta Participations Ag Method of crop enhancement
WO2012029672A1 (en) 2010-08-31 2012-03-08 Meiji Seikaファルマ株式会社 Noxious organism control agent
WO2012034403A1 (en) 2010-09-14 2012-03-22 中化蓝天集团有限公司 Fluoromethoxypyrazole anthranilamide compounds, synthesization methods and uses thereof
CN102391261A (en) 2011-10-14 2012-03-28 上海交通大学 N-substituted dioxazine compound as well as preparation method and application thereof
WO2013050317A1 (en) 2011-10-03 2013-04-11 Syngenta Limited Polymorphs of an isoxazoline derivative
CN103109816A (en) 2013-01-25 2013-05-22 青岛科技大学 Thiobenzamide compounds and application thereof
WO2013110612A1 (en) * 2012-01-26 2013-08-01 Bayer Intellectual Property Gmbh Phenyl-substituted ketoenols for controlling fish parasites
CN103232431A (en) 2013-01-25 2013-08-07 青岛科技大学 Dihalogenated pyrazole amide compound and its use
WO2013115391A1 (en) 2012-02-01 2013-08-08 日本農薬株式会社 Arylalkyloxy pyrimidine derivative, pesticide for agricultural and horticultural use containing arylalkyloxy pyrimidine derivative as active ingredient, and use of same
CN103265527A (en) 2013-06-07 2013-08-28 江苏省农用激素工程技术研究中心有限公司 Anthranilamide compound as well as preparation method and application thereof
WO2013144213A1 (en) 2012-03-30 2013-10-03 Basf Se N-substituted pyridinylidene compounds and derivatives for combating animal pests
EP2647626A1 (en) 2012-04-03 2013-10-09 Syngenta Participations AG. 1-Aza-spiro[4.5]dec-3-ene and 1,8-diaza-spiro[4.5]dec-3-ene derivatives as pesticides
WO2013162715A2 (en) 2012-04-27 2013-10-31 Dow Agrosciences Llc Pesticidal compositions and processes related thereto
CN103524422A (en) 2013-10-11 2014-01-22 中国农业科学院植物保护研究所 Benzimidazole derivative, and preparation method and purpose thereof
US20140213448A1 (en) 2012-04-27 2014-07-31 Dow Agrosciences Llc Pesticidal compositions and processes related thereto
US20140275503A1 (en) 2013-03-13 2014-09-18 Dow Agrosciences Llc Process for the preparation of certain triaryl rhamnose carbamates
WO2014187846A1 (en) 2013-05-23 2014-11-27 Syngenta Participations Ag Tank-mix formulations
WO2015058028A1 (en) 2013-10-17 2015-04-23 Dow Agrosciences Llc Processes for the preparation of pesticidal compounds
WO2015058021A1 (en) 2013-10-17 2015-04-23 Dow Agrosciences Llc Processes for the preparation of pesticidal compounds
WO2016005276A1 (en) 2014-07-07 2016-01-14 Bayer Cropscience Aktiengesellschaft Process for preparing fluorinated iminopyridine compounds
WO2016133011A1 (en) 2015-02-17 2016-08-25 日本曹達株式会社 Agrochemical composition

Patent Citations (41)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3639877A1 (en) 1986-11-21 1988-05-26 Bayer Ag HETARYLALKYL SUBSTITUTED 5- AND 6-RINGHETEROCYCLES
WO2003106457A1 (en) 2002-06-14 2003-12-24 Syngenta Limited Spiroindolinepiperidine derivatives
WO2004099160A1 (en) 2003-05-12 2004-11-18 Sumitomo Chemical Company, Limited Pyrimidine compounds and pests controlling composition containing the same
WO2006003494A2 (en) 2004-06-28 2006-01-12 Syngenta Participations Ag Piperidine derivatives and their use as insecticides, acaricides, molluscicides or nematicides
WO2006043635A1 (en) 2004-10-20 2006-04-27 Kumiai Chemical Industry Co., Ltd. 3-triazolylphenyl sulfide derivative and insecticide/acaricide/nematicide containing the same as active ingredient
WO2006089633A2 (en) 2005-02-22 2006-08-31 Bayer Cropscience Ag Spiroketal-substituted cyclic ketoenols
WO2007040280A1 (en) 2005-10-06 2007-04-12 Nippon Soda Co., Ltd. Cyclic amine compound and pest control agent
WO2007040282A1 (en) 2005-10-06 2007-04-12 Nippon Soda Co., Ltd. Bridged cyclic amine compound and pest control agent
WO2009039951A2 (en) 2007-09-21 2009-04-02 Bayer Cropscience Ag Active ingredient combinations having insecticidal and acaricidal properties
JP2010018586A (en) 2008-07-14 2010-01-28 Meiji Seika Kaisha Ltd Substance pf1364, its manufacturing method, producing strain and agricultural/horticultural insecticide having the substance as active ingredient
CN101337937A (en) 2008-08-12 2009-01-07 国家农药创制工程技术研究中心 N-benz-3-substituted amino pyrazoles compounds with insecticidal activity
CN101337940A (en) 2008-08-12 2009-01-07 国家农药创制工程技术研究中心 Nitrogen heterocyclic ring dichlorin allyl ether compounds with insecticidal activity
CN101715774A (en) 2008-10-09 2010-06-02 浙江化工科技集团有限公司 Preparation and use of compound having insecticidal activity
WO2010051926A2 (en) 2008-11-05 2010-05-14 Bayer Cropscience Aktiengesellschaft New halogen-substituted bonds
WO2010052161A2 (en) 2008-11-06 2010-05-14 Syngenta Participations Ag Herbicidal compositions
WO2010066780A1 (en) 2008-12-12 2010-06-17 Syngenta Participations Ag Spiroheterocyclic n-oxypiperidines as pesticides
WO2010149274A2 (en) * 2009-06-23 2010-12-29 Bayer Cropscience Aktiengesellschaft Use of active ingredient combinations having insecticidal properties for controlling pests from the family of stink bugs
WO2011085575A1 (en) 2010-01-15 2011-07-21 江苏省农药研究所股份有限公司 Ortho-heterocyclyl formanilide compounds, their synthesis methods and use
WO2011105506A1 (en) 2010-02-25 2011-09-01 日本曹達株式会社 Cyclic amine compound and miticide
WO2011151146A1 (en) 2010-05-31 2011-12-08 Syngenta Participations Ag Method of crop enhancement
WO2012029672A1 (en) 2010-08-31 2012-03-08 Meiji Seikaファルマ株式会社 Noxious organism control agent
WO2012034403A1 (en) 2010-09-14 2012-03-22 中化蓝天集团有限公司 Fluoromethoxypyrazole anthranilamide compounds, synthesization methods and uses thereof
WO2013050317A1 (en) 2011-10-03 2013-04-11 Syngenta Limited Polymorphs of an isoxazoline derivative
CN102391261A (en) 2011-10-14 2012-03-28 上海交通大学 N-substituted dioxazine compound as well as preparation method and application thereof
WO2013110612A1 (en) * 2012-01-26 2013-08-01 Bayer Intellectual Property Gmbh Phenyl-substituted ketoenols for controlling fish parasites
WO2013115391A1 (en) 2012-02-01 2013-08-08 日本農薬株式会社 Arylalkyloxy pyrimidine derivative, pesticide for agricultural and horticultural use containing arylalkyloxy pyrimidine derivative as active ingredient, and use of same
WO2013144213A1 (en) 2012-03-30 2013-10-03 Basf Se N-substituted pyridinylidene compounds and derivatives for combating animal pests
EP2647626A1 (en) 2012-04-03 2013-10-09 Syngenta Participations AG. 1-Aza-spiro[4.5]dec-3-ene and 1,8-diaza-spiro[4.5]dec-3-ene derivatives as pesticides
WO2013162715A2 (en) 2012-04-27 2013-10-31 Dow Agrosciences Llc Pesticidal compositions and processes related thereto
US20140213448A1 (en) 2012-04-27 2014-07-31 Dow Agrosciences Llc Pesticidal compositions and processes related thereto
WO2013162716A2 (en) 2012-04-27 2013-10-31 Dow Agrosciences Llc Pesticidal compositions and processes related thereto
CN103232431A (en) 2013-01-25 2013-08-07 青岛科技大学 Dihalogenated pyrazole amide compound and its use
CN103109816A (en) 2013-01-25 2013-05-22 青岛科技大学 Thiobenzamide compounds and application thereof
US20140275503A1 (en) 2013-03-13 2014-09-18 Dow Agrosciences Llc Process for the preparation of certain triaryl rhamnose carbamates
WO2014187846A1 (en) 2013-05-23 2014-11-27 Syngenta Participations Ag Tank-mix formulations
CN103265527A (en) 2013-06-07 2013-08-28 江苏省农用激素工程技术研究中心有限公司 Anthranilamide compound as well as preparation method and application thereof
CN103524422A (en) 2013-10-11 2014-01-22 中国农业科学院植物保护研究所 Benzimidazole derivative, and preparation method and purpose thereof
WO2015058028A1 (en) 2013-10-17 2015-04-23 Dow Agrosciences Llc Processes for the preparation of pesticidal compounds
WO2015058021A1 (en) 2013-10-17 2015-04-23 Dow Agrosciences Llc Processes for the preparation of pesticidal compounds
WO2016005276A1 (en) 2014-07-07 2016-01-14 Bayer Cropscience Aktiengesellschaft Process for preparing fluorinated iminopyridine compounds
WO2016133011A1 (en) 2015-02-17 2016-08-25 日本曹達株式会社 Agrochemical composition

Non-Patent Citations (36)

* Cited by examiner, † Cited by third party
Title
ANON.: "FRAC Code List 2017: Fungicides sorted by mode of action", 1 January 2017 (2017-01-01), pages 1 - 12, XP055486188, Retrieved from the Internet <URL:https://cpb-us-w2.wpmucdn.com/u.osu.edu/dist/b/28945/files/2017/04/frac-code-list-2017-final-1juq211.pdf> [retrieved on 20180620] *
BAUR ET AL., PESTICIDE SCIENCE, vol. 51, 1997, pages 131 - 152
CHEMICAL ABSTRACTS, Columbus, Ohio, US; abstract no. 1105672-77-2
CHEMICAL ABSTRACTS, Columbus, Ohio, US; abstract no. 1108184-52-6
CHEMICAL ABSTRACTS, Columbus, Ohio, US; abstract no. 1181213-14-8
CHEMICAL ABSTRACTS, Columbus, Ohio, US; abstract no. 1204776-60-2
CHEMICAL ABSTRACTS, Columbus, Ohio, US; abstract no. 1225292-17-0
CHEMICAL ABSTRACTS, Columbus, Ohio, US; abstract no. 1226889-14-0
CHEMICAL ABSTRACTS, Columbus, Ohio, US; abstract no. 1229023-00-0
CHEMICAL ABSTRACTS, Columbus, Ohio, US; abstract no. 1229023-34-0
CHEMICAL ABSTRACTS, Columbus, Ohio, US; abstract no. 1232543-85-9
CHEMICAL ABSTRACTS, Columbus, Ohio, US; abstract no. 1233882-22-8
CHEMICAL ABSTRACTS, Columbus, Ohio, US; abstract no. 1253850-56-4
CHEMICAL ABSTRACTS, Columbus, Ohio, US; abstract no. 1268277-22-0
CHEMICAL ABSTRACTS, Columbus, Ohio, US; abstract no. 1332628-83-7
CHEMICAL ABSTRACTS, Columbus, Ohio, US; abstract no. 1332838-17-1
CHEMICAL ABSTRACTS, Columbus, Ohio, US; abstract no. 1363400-41-2
CHEMICAL ABSTRACTS, Columbus, Ohio, US; abstract no. 1370358-69-2
CHEMICAL ABSTRACTS, Columbus, Ohio, US; abstract no. 1440516-42-6
CHEMICAL ABSTRACTS, Columbus, Ohio, US; abstract no. 1449021-97-9
CHEMICAL ABSTRACTS, Columbus, Ohio, US; abstract no. 1449220-44-3
CHEMICAL ABSTRACTS, Columbus, Ohio, US; abstract no. 1452877-50-7
CHEMICAL ABSTRACTS, Columbus, Ohio, US; abstract no. 1461743-15-6
CHEMICAL ABSTRACTS, Columbus, Ohio, US; abstract no. 1477919-27-9
CHEMICAL ABSTRACTS, Columbus, Ohio, US; abstract no. 1477923-37-7
CHEMICAL ABSTRACTS, Columbus, Ohio, US; abstract no. 1542271-46-4
CHEMICAL ABSTRACTS, Columbus, Ohio, US; abstract no. 1638765-58-8
CHEMICAL ABSTRACTS, Columbus, Ohio, US; abstract no. 1689566-03-7
CHEMICAL ABSTRACTS, Columbus, Ohio, US; abstract no. 1702305-40-5
CHEMICAL ABSTRACTS, Columbus, Ohio, US; abstract no. 637360-23-7
CHEMICAL ABSTRACTS, Columbus, Ohio, US; abstract no. 792914-58-0
CHEMICAL ABSTRACTS, Columbus, Ohio, US; abstract no. 872999-66-1
CHEMICAL ABSTRACTS, Columbus, Ohio, US; abstract no. 885026-50-6
CHEMICAL ABSTRACTS, Columbus, Ohio, US; abstract no. 933798-27-7
CHEMICAL ABSTRACTS, Columbus, Ohio, US; abstract no. 934001-66-8
S.R. COLBY: "Calculating Synergistic and Antagonistic Responses of Herbicide Combinations", WEEDS, vol. 15, 1967, pages 20 - 22, XP001112961

Similar Documents

Publication Publication Date Title
ES2818608T3 (en) Bicyclic compounds as pesticides
AU2016214502B2 (en) 2-(Het)Aryl-substituted condensed bicyclic heterocycle derivatives as pest control agents
AU2019229521A1 (en) Use of heteroaryl-triazole and heteroaryl-tetrazole compounds as pesticides in plant protection
US9554573B2 (en) Binary insecticidal or pesticidal mixture
US9775349B2 (en) Binary fungicidal or pesticidal mixture
ES2837396T3 (en) Derivatives of 2- [3- (alkylsulfonyl) -2H-indazol-2-yl] -3H-imidazo [4,5-b] pyridine and similar compounds as pesticides
WO2016001125A1 (en) Active compound combinations and methods to protect the propagation material of plants
EP3177607B1 (en) Halogen-substituted bipyrazole compounds for controlling animal pests
EP3608311A1 (en) Crystalline form a of n-[4-chloro-3-[(1-cyanocyclopropyl)carbamoyl]phenyl]-2-methyl-4-methylsulfonyl-5-(1,1,2,2,2-pentafluoroethyl)pyrazole-3-carboxamide
WO2021097162A1 (en) Beneficial combinations with paenibacillus
ES2702454T3 (en) Bipyrazole compounds substituted with halogen to control animal pests
WO2019007887A1 (en) Insecticide and fungicide active ingredient combinations
US9815792B2 (en) Method for producing carboxamides
US20170327471A1 (en) Aryl sulphide and aryl sulphoxide derivatives having C-C-attached uracils as pesticides
JP7437318B2 (en) Active ingredient combination with insecticidal, bactericidal and acaricidal properties
WO2019197615A1 (en) Active ingredient combinations with fungicides, insecticides and acaricidal properties
WO2019224143A1 (en) Active ingredient combinations with insecticidal, nematicidal and acaricidal properties
ES2857806T3 (en) 2-Alkylimidazolyl-substituted carboxamides as pesticides
WO2017174544A1 (en) Active substance combinations with insecticide and acaricide properties

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 19716427

Country of ref document: EP

Kind code of ref document: A1

NENP Non-entry into the national phase

Ref country code: DE

122 Ep: pct application non-entry in european phase

Ref document number: 19716427

Country of ref document: EP

Kind code of ref document: A1