Classifications

• • A—HUMAN NECESSITIES
  • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
  • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
  • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
  • A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
  • A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
• • A—HUMAN NECESSITIES
  • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
  • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
  • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
  • A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
  • A01N43/04—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom
  • A01N43/06—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings
  • A01N43/10—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings with sulfur as the ring hetero atom
• • A—HUMAN NECESSITIES
  • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
  • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
  • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
  • A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
  • A01N43/04—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom
  • A01N43/14—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom six-membered rings
  • A01N43/18—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom six-membered rings with sulfur as the ring hetero atom
• • A—HUMAN NECESSITIES
  • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
  • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
  • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
  • A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
  • A01N43/80—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,2

Definitions

• the present invention concerns a novel method to control certain insect pests, specifically those that have developed resistance to one or more classes of insecticides, through the use of N-substituted sulfoximines.
• Predicting whether or not a resistance mechanism that has conferred resistance to an existing insecticide will confer resistance to a novel insecticide is not necessarily a simple matter.
• a novel insecticide that acts at a different target site is unlikely to be affected by the resistance mechanism.
• the target site at which a novel chemistry acts is known and the resistance mechanism of concern involves a modification to a different target site, one could predict with some confidence that the resistance mechanism would not confer resistance to the novel chemistry.
• neonicotinoids One of the newer and more successful classes of insecticides to be introduced in past 25 years is the neonicotinoids.
• the introduction of neonicotinoid insecticides has provided growers with invaluable new tools for managing some of the world's most destructive crop pests, including species with a long history of developing resistance to earlier-used products.
• Imidacloprid was the first major active ingredient of the neonicotinoid class to reach the market.
• the substitution of the chloropyridinyl moiety by a chlorothiazolyl group resulted in a second subgroup of neonicotinoid insecticides including clothianidin and thiamethoxam.
• Neonicotinoid insecticides remain valuable and effective tools for the management of insect pests in most areas in spite of the limited development of resistance. Control of neonicotinoid-resistant insect pest populations, or for that matter other insecticide-resistant insect pest populations, will rely on the availability of insecticides that are effective on the resistant populations. Preventing or delaying the development of insecticide-resistant insect pest populations also relies on the rotation of insecticides that are not affected by the same resistance mechanisms. In either case, new insecticides that lack cross-resistance to currently available insecticides are imminently needed.
• This invention concerns the discovery of lack of cross-resistance for N-substituted sulfoximine compounds on insect pests that have developed resistance to one or more classes of insecticides including imidacloprid and other neonicotinoids. More particularly, this invention concerns a method to control certain insect pests that have developed resistance to one or more classes of insecticides, including neonicotinoids, organophosphates, carbamates and pyrethroids, which comprises applying to a locus where control is desired an insect-inactivating amount of a compound of the formula (I)
• X represents NO 2 , CN or COOR 4 ;
• L represents a single bond or R 1 , S and L taken together represent a 5- or 6-membered ring;
• R 1 represents methyl or ethyl
• R 2 and R 3 independently represent hydrogen, methyl, ethyl, fluoro, chloro or bromo;
• n is an integer from 0-3;
• R 4 represents C 1 -C 3 alkyl.
• Preferred compounds of formula (I) include the following classes:
• alkyl include straight chain, branched chain, and cyclic groups.
• typical alkyl groups are methyl, ethyl, 1-methylethyl, propyl, 1,1-dimethylethyl, and cyclopropyl.
• halogen includes fluorine, chlorine, bromine, and iodine.
• haloalkyl and haloalkoxy includes alkyl and alkoxy groups substituted with from one to the maximum possible number of halogen atoms, preferably fluorine atoms.
• the compounds of this invention can exist as one or more stereoisomers.
• the various stereoisomers include geometric isomers, diastereomers and enantiomers.
• the compounds of the present invention include racemic mixtures, individual stereoisomers and optically active mixtures. It will be appreciated by those skilled in the art that one stereoisomer may be more active than the others.
• Individual stereoisomers and optically active mixtures may be obtained by selective synthetic procedures, by conventional synthetic procedures using resolved starting materials or by conventional resolution procedures.
• step a of Scheme A sulfide of formula (A) is oxidized with meta-chloroperoxybenzoic acid (mCPBA) in a polar solvent below 0° C. to provide sulfoxide of formula (B).
• mCPBA meta-chloroperoxybenzoic acid
• dichloromethane is the preferred solvent for oxidation.
• step b of Scheme A sulfoxide (B) is iminated with sodium azide in the presence of concentrated sulfuric acid in an aprotic solvent under heating to provide sulfoximine of formula (C). In most cases, chloroform is the preferred solvent for this reaction.
• the nitrogen of sulfoximine (C) can be either cyanated with cyanogen bromide in the presence of a base, or nitrated with nitric acid in the presence of acetic anhydride under mildly elevated temperature, or carboxylated with alkyl (R 4 ) chloroformate in the presence of base such as 4-dimethylaminopyridine (DMAP) to provide N-substituted sulfoximine (Ia).
• base is required for efficient cyanation and carboxylation and the preferred base is DMAP, whereas sulfuric acid is used as catalyst for efficient nitration reaction.
• step a of Scheme B sulfide is oxidized with iodobenzene diacetate in the presence of cyanamide at 0° C. to give sulfilimine (F).
• the reaction can be carried out in a polar aprotic solvent like dichloromethane.
• the sulfilimine (F) is oxidized with mCPBA.
• a base such as potassium carbonate is employed to neutralize the acidity of mCPBA.
• Protic polar solvents such as ethanol and water are used to increase the solubility of the sulfilimine starting material and the base employed.
• the sulfilimine (F) can also be oxidized with aqueous sodium or potassium periodinate solution in the presence of catalyst ruthenium trichloride hydrate or similar catalyst.
• the organic solvent for this catalysis can be polar aprotic solvent such as dichloromethane, chloroform, or acetonitrile.
• KHMDS potassium hexamethyldisilamide
• base such as potassium tert-butoxide
• the corresponding appropriately substituted chloromethyl pyridine is treated with thiourea, hydrolyzed and subsequently alkylated with 1-bromo-3-chloropropane under aqueous base conditions, and cyclized in the presence of a base like potassium tert-butoxide in a polar aprotic solvent such as tetrahydrofuran (THF).
• a base like potassium tert-butoxide
• a polar aprotic solvent such as tetrahydrofuran (THF).
• step a of Scheme J which is similar to step b of Scheme A, sulfoxide is iminated with sodium azide in the presence of concentrated sulfuric acid or with O-mesitylsulfonylhydroxylamine in a polar aprotic solvent to provide sulfoximine.
• Chloroform or dichloromethane are the preferred solvents.
• step b of Scheme J similar to step c of Scheme A, the nitrogen of sulfoximine can be either cyanated with cyanogen bromide, or nitrated with nitric acid followed by treatment with acetic anhydride under refluxing conditions, or carboxylated with methyl chloroformate in the presence of base such as DMAP to provide N-substituted cyclic sulfoximine.
• Base is required for efficient cyanation and carboxylation and the preferred base is DMAP, whereas sulfuric acid is used as catalyst for efficient nitration reaction.
• the ⁇ -carbon of N-substituted sulfoximine can be alkylated with a heteroaromatic methyl halide in the presence of a base such as KHMDS or butyl lithium (BuLi) to give the desired N-substituted sulfoximines.
• a base such as KHMDS or butyl lithium (BuLi)
• the preferred halide can be bromide, chloride or iodide.
• the compounds of formula (Ib) can be prepared by a first ⁇ -alkylation of sulfoxides to give ⁇ -substituted sulfoxides and then an imination of the sulfoxide followed by N-substitution of the resulting sulfoximine by using the steps c, a and b respectively as described above for Scheme J.
• sulfoximine (1) 50 mg, 0.19 mmol
• HMPA hexamethyl-phosphoramide
• THF tetrahydrofuran
• KHMDS potassium hexamethyldisilazane
• 2-(6-Chloropyridin-3-yl)-1-oxido-tetrahydro-1H-1 ⁇ 4 -thien-1-ylidenecyanamide (8) was prepared from 3-chloromethyl-6-chloropyridine according to the same five step sequence described in Example III. Product was a colorless gum and a 1:1 ratio of diastereomers.
• Diastereomer 1 IR (film) 3439, 3006, 2949, 2194 cm ⁇ 1 ; 1 H NMR (300 MHz, CDCl 3 ): ⁇ 8.4 (d, 1H), 7.8 (dd, 1H), 7.4 (d, 1H), 4.6 (dd, 1H), 3.6 (m, 2H), 2.4-2.7 (m, 4H); GC-MS: mass calcd for C 10 H 11 ClN 3 OS [M+H] + 256. Found 256.
• Diastereomer 2 IR (film) 3040, 2926, 2191 cm ⁇ 1 ; 1 H NMR (300 MHz, CDCl 3 ): ⁇ 8.4 (d, 1H), 7.8 (dd, 1H), 7.4 (d, 1H), 4.7 (dd, 1H), 3.8 (ddd, 1H), 3.4 (m, 1H), 2.8 (m, 1H), 2.6 (m, 2H), 2.3 (m, 1H); GC-MS: mass calcd for C 10 H 11 ClN 3 OS [M+H] + 256. Found 256.
• the common name associated with the Q-biotype of B. tabaci is the sweetpotato whitefly.
• the SUD-S strain of B. tabaci was the reference strain used in these tests and is a laboratory strain that is fully susceptible to all insecticide groups.
• Resistance ⁇ ⁇ Ratio LC 50 ⁇ ⁇ on ⁇ ⁇ Resistant ⁇ ⁇ Population LC 50 ⁇ ⁇ on ⁇ ⁇ Susceptible ⁇ ⁇ Population
• the insecticidal activity of Compound 7 on adults from an insecticide-resistant, B-biotype Bemisia tabaci strain was assessed.
• the activity of commercial, neonicotinoid insecticides was also assessed and served as the basis for comparisons of relative efficacy on this insecticide-resistant whitefly strain.
• the common name associated with the B-biotype of B. tabaci is the silverleaf whitefly.
• the strain used in these tests, “GUA-MIX”, was collected from a variety of crops situated in the Zacapa Valley of Guatemala in January of 2004. This strain exhibits strong resistance to imidacloprid with the majority of adults being largely unaffected by concentrations of 1000 ppm.
• the SUD-S strain of B. tabaci was the reference strain used in these tests and is a laboratory strain that is fully susceptible to all insecticide groups.
• Compound 7 was initially dissolved in 90% acetone in distilled water (containing 0.01% Agral) to obtain a 5000 ppm stock solution. Subsequent dilutions were made by using 0.9% acetone in distilled water (containing 0.01% Agral) as the diluent.
• Commercial formulations of imidacloprid (Confidor, 200SL), thiamethoxam (Actara, 25WG) and acetamiprid (Mospilan, 20SP) were diluted using distilled water containing 0.01% Agral.
• the common name associated with the Q-biotype of B. tabaci is the sweetpotato whitefly.
• the resistant strain used in these tests, “CHLORAKA” was collected from cucumbers in Cyprus in 2003 and has exhibited stable and strong resistance to pyrethroids, organophosphates, and neonicotinoids in repeated laboratory testing. Adults from this strain are largely unaffected by exposure to imidacloprid at 1000 ppm.
• the SUD-S strain of B. tabaci was the reference strain used in these tests and is a laboratory strain that is fully susceptible to all insecticide groups.
• the common name associated with Myzus persicae is the green peach aphid.
• the “US1L” strain of M. persicae was the reference strain used in these tests. US1L is fully susceptible to all insecticide groups,
• deltamethrin (Decis, 25 g/litre ⁇ 1 EC), dimethoate (Danadim, 400 g/litre ⁇ 1 EC), profenofos (Curacron 500 g/litre ⁇ 1 EC), pirimicarb (Aphox 500 g/litre ⁇ 1 DG) and imidacloprid (Confidor, 200 g/litre ⁇ 1 SL) were obtained by diluting formulated material in distilled water containing a 0.01% concentration of the non-ionic wetter Agral®.
• LC 50 , S strain LC 50 , R strain Compound (US1L) (4013A) Resistance Ratio 2 4.13 ppm 1.52 ppm 0.4 4 146 ppm 103 ppm 0.7 5 62.3 ppm 12.5 ppm 0.2 Deltamethrin 1.5 ppm 92 ppm 60 Dimethoate 46 ppm 293 ppm 6.3 Pirimicarb 14.8 ppm >1000 ppm* >60** Imidacloprid 0.9 15.3 17 *Accurate calculation of LC 50 was not possible because doses as high as 1000 ppm caused ⁇ 10% mortality on the R strain (4013A). **Value represents a conservative estimate of the Resistance Ratio calculated using the highest concentration tested as the numerator in the equation.
• the compounds of the invention are useful for the control of insects. Therefore, the present invention also is directed to a method for inhibiting an insect which comprises applying an insect-inhibiting amount of a compound of formula (I) to a locus of the inset, to the area to be protected, or directly on the insect to be controlled.
• the compounds of the invention may also be used to control other invertebrate pests such as mites, ticks, lice, and nematodes.
• insects which eat, damage or contact edible, commodity, ornamental, turf or pasture plants can be controlled by applying the active compounds to the seed of the plant before planting, to the seedling, or cutting which is planted, the leaves, stems, fruits, grain, and/or roots, or to the soil or other growth medium before or after the crop is planted. Protection of these plants against virus, fungus or bacterium diseases may also be achieved indirectly through controlling sap-feeding pests such as whitefly, plant hopper, aphid and spider mite. Such plants include those which are bred through conventional approaches and which are genetically modified using modern biotechnology to gain insect-resistant, herbicide-resistant, nutrition-enhancement, and/or any other beneficial traits.
• the compounds might also be useful to protect textiles, paper, stored grain, seeds and other foodstuffs, houses and other buildings which may be occupied by humans and/or companion, farm, ranch, zoo, or other animals, by applying an active compound to or near such objects.
• domesticated animals, buildings or human beings might be protected with the compounds by controlling invertebrate and/or nematode pests that are parasitic or are capable of transmitting infectious diseases.
• pests include, for example, chiggers, ticks, lice, mosquitoes, flies, fleas and heartworms.
• Nonagronomic applications also include invertebrate pest control in forests, in yards, along road sides and railroad right of way.
• insects and other pests which can be inhibited include, but are not limited to:
• compositions which are important embodiments of the invention, and which comprise a compound of this invention and a phytologically-acceptable inert carrier. Control of the pests is achieved by applying compounds of the invention in forms of sprays, topical treatment, gels, seed coatings, microcapsulations, systemic uptake, baits, eartags, boluses, foggers, fumigants aerosols, dusts and many others.
• the compositions are either concentrated solid or liquid formulations which are dispersed in water for application, or are dust or granular formulations which are applied without further treatment.
• the compositions are prepared according to procedures and formulae which are conventional in the agricultural chemical art, but which are novel and important because of the presence therein of the compounds of this invention. Some description of the formulation of the compositions will be given, however, to assure that agricultural chemists can readily prepare any desired composition.
• the dispersions in which the compounds are applied are most often aqueous suspensions or emulsions prepared from concentrated formulations of the compounds.
• Such water-soluble, water-suspendable or emulsifiable formulations are either solids, usually known as wettable powders, or liquids usually known as emulsifiable concentrates or aqueous suspensions.
• Wettable powders which may be compacted to form water dispersible granules, comprise an intimate mixture of the active compound, an inert carrier, and surfactants.
• the concentration of the active compound is usually from about 10% to about 90% by weight.
• the inert carrier is usually chosen from among the attapulgite clays, the montmorillonite clays, the diatomaceous earths, or the purified silicates.
• Effective surfactants comprising from about 0.5% to about 10% of the wettable powder, are found among the sulfonated lignins, the condensed naphthalenesulfonates, the naphthalenesulfonates, the alkylbenzenesulfonates, the alkyl sulfates, and nonionic surfactants such as ethylene oxide adducts of alkyl phenols.
• Emulsifiable concentrates of the compounds comprise a convenient concentration of a compound, such as from about 50 to about 500 grams per liter of liquid, equivalent to about 10% to about 50%, dissolved in an inert carrier which is either a water miscible solvent or a mixture of water-immiscible organic solvent and emulsifiers.
• Useful organic solvents include aromatics, especially the xylenes, and the petroleum fractions, especially the high-boiling naphthalenic and olefinic portions of petroleum such as heavy aromatic naphtha.
• Other organic solvents may also be used, such as the terpenic solvents including rosin derivatives, aliphatic ketones such as cyclohexanone, and complex alcohols such as 2-ethoxyethanol.
• Suitable emulsifiers for emulsifiable concentrates are chosen from conventional nonionic surfactants, such as those discussed above.
• Aqueous suspensions comprise suspensions of water-insoluble compounds of this invention, dispersed in an aqueous vehicle at a concentration in the range from about 5% to about 50% by weight.
• Suspensions are prepared by finely grinding the compound, and vigorously mixing it into a vehicle comprised of water and surfactants chosen from the same types discussed above.
• Inert ingredients such as inorganic salts and synthetic or natural gums, may also be added, to increase the density and viscosity of the aqueous vehicle. It is often most effective to grind and mix the compound at the same time by preparing the aqueous mixture, and homogenizing it in an implement such as a sand mill, ball mill, or piston-type homogenizer.
• the compounds may also be applied as granular compositions, which are particularly useful for applications to the soil.
• Granular compositions usually contain from about 0.5% to about 10% by weight of the compound, dispersed in an inert carrier which consists entirely or in large part of clay or a similar inexpensive substance.
• Such compositions are usually prepared by dissolving the compound in a suitable solvent and applying it to a granular carrier which has been pre-formed to the appropriate particle size, in the range of from about 0.5 to 3 mm.
• Such compositions may also be formulated by making a dough or paste of the carrier and compound and crushing and drying to obtain the desired granular particle size.
• Dusts containing the compounds are prepared simply by intimately mixing the compound in powdered form with a suitable dusty agricultural carrier, such as kaolin clay, ground volcanic rock, and the like. Dusts can suitably contain from about 1% to about 10% of the compound.
• Insecticides and acaricides are generally applied in the form of a dispersion of the active ingredient in a liquid carrier. It is conventional to refer to application rates in terms of the concentration of active ingredient in the carrier. The most widely used carrier is water.
• the compounds of the invention can also be applied in the form of an aerosol composition.
• the active compound is dissolved or dispersed in an inert carrier, which is a pressure-generating propellant mixture.
• the aerosol composition is packaged in a container from which the mixture is dispensed through an atomizing valve.
• Propellant mixtures comprise either low-boiling halocarbons, which may be mixed with organic solvents, or aqueous suspensions pressurized with inert gases or gaseous hydrocarbons.
• the actual amount of compound to be applied to loci of insects and mites is not critical and can readily be determined by those skilled in the art in view of the examples above. In general, concentrations from 10 ppm to 5000 ppm by weight of compound are expected to provide good control. With many of the compounds, concentrations from 100 to 1500 ppm will suffice.
• the locus to which a compound is applied can be any locus inhabited by an insect or mite, for example, vegetable crops, fruit and nut trees, grape vines, ornamental plants, domesticated animals, the interior or exterior surfaces of buildings, and the soil around buildings.
• Systemic movement of compounds of the invention in plants may be utilized to control pests on one portion of the plant by applying the compounds to a different portion of it.
• control of foliar-feeding insects can be controlled by drip irrigation or furrow application, or by treating the seed before planting.
• Seed treatment can be applied to all types of seeds, including those from which plants genetically transformed to express specialized traits will germinate.
• Representative examples include those expressing proteins toxic to invertebrate pests, such as Bacillus thuringiensis or other insecticidal toxins, those expressing herbicide resistance, such as “Roundup Ready®” seed , or those with “stacked” foreign genes expressing insecticidal toxins, herbicide resistance, nutrition-enhancement and/or other beneficial traits.
• An insecticidal bait composition consisting of compounds of the present invention and attractants and/or feeding stimulants may be used to increase efficacy of the insecticides against insect pest in a device such as trap, bait station, and the like.
• the bait composition is usually a solid, semi-solid (including gel) or liquid bait matrix including the stimulants and one or more non-microencapsulated or microencapsulated insecticides in an amount effective to act as kill agents.
• the compounds of the present invention are often applied in conjunction with one or more other insecticides or fungicides or herbicides to obtain control of a wider variety of pests diseases and weeds.
• the presently claimed compounds can be formulated with the other insecticides or fungicides or herbicide, tank mixed with the other insecticides or fungicides or herbicides, or applied sequentially with the other insecticides or fungicides or herbicides.
• antibiotic insecticides such as
• lilacinus Photorhabdus luminescens, Spodoptera exigua NPV, trypsin modulating oostatic factor, Xenorhabdus nematophilus, and X. bovienii, plant incorporated protectant insecticides such as Cry1Ab, Cry1Ac, Cry1F, Cry1A.105, Cry2Ab2, Cry3A, mir Cry3A, Cry3Bb1, Cry34, Cry35, and VIP3A; botanical insecticides such as anabasine, azadirachtin, d-limonene, nicotine, pyrethrins, cinerins, cinerin I, cinerin II, jasmolin I, jasmolin II, pyrethrin I, pyrethrin II, quassia, rotenone, ryania and sabadilla; carbamate insecticides such as bendiocarb and carbaryl; benzofuranyl methylcarbamate
• fungicides that can be employed beneficially in combination with the compounds of the present invention include: 2-(thiocyanatomethylthio)-benzothiazole, 2-phenylphenol, 8-hydroxyquinoline sulfate, Ampelomyces, quisqualis, azaconazole, azoxystrobin, Bacillus subtilis, benalaxyl, benomyl, benthiavalicarb-isopropyl, benzylaminobenzene-sulfonate (BABS) salt, bicarbonates, biphenyl, bismerthiazol, bitertanol, blasticidin-S, borax, Bordeaux mixture, boscalid, bromuconazole, bupirimate, calcium polysulfide, captafol, captan, carbendazim, carboxin, carpropamid, carvone, chloroneb, chlorothalonil, chlozolinate, Coniothyrium minitans, copper hydro
• Some of the herbicides that can be employed in conjunction with the compounds of the present invention include: amide herbicides such as allidochlor, beflubutamid, benzadox, benzipram, bromobutide, cafenstrole, CDEA, chlorthiamid, cyprazole, dimethenamid, dimethenamid-P, diphenamid, epronaz, etnipromid, fentrazamide, flupoxam, fomesafen, halosafen, isocarbamid, isoxaben, napropamide, naptalam, pethoxamid, propyzamide, quinonamid and tebutam; anilide herbicides such as chloranocryl, cisanilide, clomeprop, cypromid, diflufenican, etobenzanid, fenasulam, flufenacet, flufenican, mefenacet, mefluid

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