WO2008074418A2 - Bisoxime als fungizide und arthropodizide - Google Patents
Bisoxime als fungizide und arthropodizide Download PDFInfo
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- WO2008074418A2 WO2008074418A2 PCT/EP2007/010798 EP2007010798W WO2008074418A2 WO 2008074418 A2 WO2008074418 A2 WO 2008074418A2 EP 2007010798 W EP2007010798 W EP 2007010798W WO 2008074418 A2 WO2008074418 A2 WO 2008074418A2
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- 0 CC(*)=NO*ON=C(*)* Chemical compound CC(*)=NO*ON=C(*)* 0.000 description 38
- NLCJZEXGBUTWJR-SFQUDFHCSA-N C/C(/c1nc(C)c(C)cc1)=N\OCC1(CON)CC1 Chemical compound C/C(/c1nc(C)c(C)cc1)=N\OCC1(CON)CC1 NLCJZEXGBUTWJR-SFQUDFHCSA-N 0.000 description 1
Classifications
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/34—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
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
- A01N43/36—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom five-membered rings
- A01N43/38—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom five-membered rings condensed with carbocyclic rings
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/34—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
- A01N43/42—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 condensed with carbocyclic rings
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/50—1,3-Diazoles; Hydrogenated 1,3-diazoles
- A01N43/52—1,3-Diazoles; Hydrogenated 1,3-diazoles condensed with carbocyclic rings, e.g. benzimidazoles
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/54—1,3-Diazines; Hydrogenated 1,3-diazines
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/58—1,2-Diazines; Hydrogenated 1,2-diazines
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/72—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
- A01N43/74—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 1,3
- A01N43/78—1,3-Thiazoles; Hydrogenated 1,3-thiazoles
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/72—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
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/90—Biocides, 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
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/26—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
Definitions
- the invention relates to the novel use of partially known bisoximes for controlling unwanted microorganisms and to processes for their preparation, and to novel bisoximes, processes for their preparation and their use for controlling unwanted microorganisms and insects in crop protection and material protection.
- DE-A 4204205 describes the use of cyclohexenone oxime ethers as herbicides.
- DE-A 2820 361 alkanyl-azolyl-oximcarbamate and in DE-A 42 13 149 (hetero) -aryl-alkyl-ketone oxime O-ethers are each described as insecticidal, acaricidal or nematocidal agents.
- pvrimidine derivatives which may be substituted by two oximes, as MLR (mixed lymphocyte reaction) inhibitors is described in WO 03/091223.
- MLR mixed lymphocyte reaction
- R 1 and R 2 are each independently hydrogen, halogen, Ci-Cg-alkyl, C 3 -C 8 cycloalkyl, C 8 - haloalkyl, OH, C 1 -C 8 alkoxy, (Ci-C 6 alkoxy ) carbonyl, SH, Cj-Cg-alkylthio, C, -C 8 alkyl sulfinyl, C, -C 8 alkylsulfonyl, C r C 4 alkoxy-C 1 -C 4 alkyl, (C, -C 4 alkyl) thio (C 1 -C 4 alkyl), (C, - C 4 alkyl) sulfinyl (C, -C 4 alkyl), Amino, di (C] -C8 alkyl) - amino, (Ci-C 8 alkyl) amino, C 2 -C 8 alkenyl
- a 1 and A 2 are not simultaneously optionally substituted phenyl, Y 1 is N or CR 6 ,
- Y 2 is N or CR 7 ,
- Y 3 is N or CR 8 ,
- Y 4 stands for N or CR 9 ,
- Y 5 is N or CR 10
- R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 and R 10 are independently hydrogen, halogen, cyano, nitro, OR 11 , SR 11 , SOR 11 , SO 2 R 11 , SO 2 N (R ⁇ ) 2 , COR 11 , NR 11 CO 2 R 12 , N (R ⁇ ) 2 , NR 11 COR 11 , NR 11 SO 2 R ", OCON (R ⁇ ) 2 , 0 (CO) R 11 , CON (R 1 '), CO 2 R 11 , (CH 2 ) m OR n , (CH 2 ) m SR n , (CH 1 tR 11 ), (CH 2 ) m CO 2 R 12 , (CH 2 ) m NR ⁇ CO 2 R 12 , C 1 -C 6 -alkyl, C 2 -C 8 -alkenyl, C 2 -C
- R 5 , R 10 or R 4 , R 10 together with the carbon atoms to which they are attached form an unsubstituted or substituted, unsaturated or fully or partially saturated heterocyclic or carbocyclic 5- to 7-membered ring,
- R 11 is hydrogen, unsubstituted or substituted Q-C 6 -alkyl, C 2 -C 8 -alkenyl, C 2 -C 8 -AL-nyl, C 1 -C 9 -halogenoalkyl, C 3 -C 8 -cycloalkyl, tri-Ci- C 4 -alkyl-silyl, in each case substituted or unsubstituted aryl, -CH 2 -aryl, hetaryl or -CH 2 -hetaryl, furthermore represents C 3 -C 8 -cycloalkyl-C 1 -C 4 -alkyl, where in the case of that two R 11 radicals are bonded to a carbon or nitrogen atom, these R 11 radicals may be the same or different, and in the case where two R 11 radicals are bonded to a nitrogen atom, these two
- R 11 radicals together with the nitrogen atom to which they are attached form a 3- to 7-membered, unsubstituted or substituted, saturated or unsaturated cycle which, depending on the ring size, contains up to 3 further nitrogen atoms or alternatively up to 2 further heteroatoms , selected from among N, O and S, wherein two oxygen atoms are not adjacent, also the two radicals R 11 in the group NR 11 COR 11 together with this group to which they are attached, a 4- to 7-membered, form an unsubstituted or substituted, saturated or unsaturated cycle which, depending on the ring size, may contain up to 3 further nitrogen atoms or alternatively up to 2 further heteroatoms selected from N, O and S, where two oxygen atoms are not adjacent, R 12 is hydrogen, unsubstituted or substituted C 1 -C 6 -alkyl, C 1 -C 8 -haloalkyl, - (CH 2 ) n OR u , m stands for the numbers 1,
- X is one of the following groupings X-1 to X-10,
- Z 1 is CR 13 R 14 or SiR 15 R 16 , wherein each two radicals R 13 , R 14 or R 15 , R l ⁇ together with the carbon or silicon atom to which they are attached, an unsubstituted or substituted, unsaturated or may be wholly or partially saturated heterocyclic or carbocyclic 3- to 8-membered ring, which may contain up to 3 further nitrogen atoms or alternatively up to 2 further heteroatoms selected from N, O and S depending on the ring size, wherein two oxygen atoms are not adjacent .
- Z 11 and Z 15 are independently CR 13 R 14 or SiR 15 R 16 and Z 12 , Z 13 and Z 14 independently of one another CR 13 R 14 , SiR 15 R 16 , O or NR 17 , but two silicon or two ,
- Z 22 and Z 28 independently of one another are CR 13 R 14 or SiR 15 R 16 and Z 23 , Z 24 , Z 25 , Z 26 and Z 27 are each independently CR 13 R 14 , SiR 15 R 15 , O or NR 17 but two silicon or two oxygen atoms are not adjacent, or each two adjacent radicals Z 22 , Z 23 or
- R 13 , R 14 , R ls , R 16 and R 17 independently of one another are hydrogen, halogen, cyano, hydroxyl, nitro, OR 11 , SR 11 , SOR 11 , SO 2 R 11 , SO 2 N (R ⁇ ) 2 , COR 11 , NR 11 CO 2 R 12 , N (R ⁇ ) 2 , NR 11 COR 11 , NR 11 SO 2 R 11 , OCON (R U ) 2> 0 (CO) R 11 , CON (R U ) 2 , CO 2 R 11 , (CH 2 ) m OR n , (CH 2 ) m SR n , (CH 2) m CO 2 R 12, (CH 2) JSIR 11 CO 2 R 12, unsubstituted or substituted C 1 -C 8 - alkyl, C 2 -C 8 alkenyl, C 2 -C 8 -AIkUIyI, Ci- C 8 haloalkyl, C 3 -C
- R 18, R 19 and R 20 are independently hydrogen, unsubstituted or substituted C] -C 8 - alkyl, CRCS haloalkyl, C 2 -C 8 alkenyl, C 2 -C 8 alkynyl, C 3 -C 8 - Cycloalkyl, substituted or unsubstituted phenyl or hetaryl,
- R 18 and R 19 also together with the carbon atom to which they are attached form an unsubstituted or substituted, unsaturated or fully or partially saturated heterocyclic or carbocyclic 3- to 8-membered ring, which may be up to 3 further, depending on the ring size Nitrogen atoms or, alternatively, up to 2 further heteroatoms selected from N, O and S, with two oxygen atoms not adjacent, for controlling undesirable microorganisms in crop protection and material protection.
- LG 1 is halogen or sulfonate, where the two LG 1 may be the same or different, and
- X has the abovementioned meanings, if appropriate in the presence of a catalyst, if appropriate in the presence of an acid binder and if appropriate in the presence of a diluent (cf., Scheme 2), or
- LG 1 is halogen or sulfonate, where the two LG 1 may be the same or different, and
- X has the abovementioned meanings, if appropriate in the presence of a catalyst, if appropriate in the presence of an acid binder and optionally in the presence of a diluent (compare Monatsh ⁇ eßr Chemie 1959, 90, 799, J. Org. Chem. 1977, 42, 3952) and so on the intermediates of the formula (VT)
- R 2 , A 2 , X and LG 1 have the meanings given above, which then subsequently with a free oxime of the formula (Va) or (V) optionally in the presence of a catalyst, optionally in the presence of an acid binder and optionally in the presence of a diluent (see Scheme 3).
- X a is one of the above-mentioned groups X-3 to X-IO, with the proviso that exactly one of Z 5 , Z 8 , Z 9 , Z 12 to Z 14 , Z 17 to Z 20 , Z 23 to Z 27 , Z 30 to Z 3S , Z 38 to Z 44 , Z 47 to Z 54 is, wherein R 20 has the meanings given above, obtained in which Scheme 4
- a 1 , R 1 , R 2 and A 2 have the meanings given above,
- X b is one of the above-mentioned groups X-3 to X-IO, with the proviso that exactly one of the radicals Z 5 , Z 8 , Z 9 , Z 12 to Z 14 , Z 17 to Z 20 , Z 23 bis Z 27 , Z 30 to Z 35 , Z 38 to Z 44 , Z 47 to Z S4 , where R 18 and R 19 are those indicated above
- a 1 , R 1 , R 2 and A 2 have the meanings given above,
- X 0 is one of the groups X-3 to X-IO given above, with the proviso that exactly one of the radicals Z 5 , Z 8 , Z 9 , Z 12 to Z 14 , Z 17 to Z 20 , Z 23 to Z 27 , Z 30 to Z 35 , Z 38 to Z 44 , Z 47 to Z 54 is * , with a free oxime (or its hydrohalide) of the formula (VH) H 2 N-OR 20 (VII) in which R 20 has the meanings given above, optionally in the presence of a catalyst, if appropriate in the presence of an acid binder and if appropriate in the presence of a diluent (cf., Scheme 4).
- a free oxime (or its hydrohalide) of the formula (VH) H 2 N-OR 20 (VII) in which R 20 has the meanings given above, optionally in the presence of a catalyst, if appropriate in the presence of an acid binder and if appropriate in the presence of a diluent (
- a 1 , R 1 , R 2 and A 2 have the meanings given above, X " 1 represents one of the groups X-3 to X-IO given above, with the proviso that at least one of the radicals Z 5 , Z 8 , Z 9 , Z 12 to Z 14 , Z 17 to Z 20 , Z 23 to Z 27 , Z 30 to Z 35 , Z 38 to Z 44 , R 21
- R 18 and R 19 have the meanings given above, and
- R 21 is hydrogen, Q-Cg-alkyl, C 2 -C 8 -alkenyl, C 2 -C 8 -AlHiIyI, in each case optionally substituted phenyl, benzyl, heterocyclyl or hetaryl, in which
- X 6 represents one of the groups X-3 to X-IO given above, with the proviso that at least one of Z 5 , Z 8 , Z 9 , Z 12 to Z 14 , Z 17 to Z 20 , Z 23 to Z 27 , Z 30 to Z 35 , Z 38 to Z 44 ,
- the bisoximes which can be used according to the invention can be used as mixtures of various possible isomeric forms, in particular of stereoisomers, such as, for example, B. E and Z, threo and erythro, and optical isomers, but optionally also of tautomers. Both the E and the Z isomers, as well as the threo and erythro, and the optical isomers, any mixtures of these isomers, as well as the possible tautomeric forms claimed.
- the compounds of the formula (I) can be present in the form of (E / E), (E / Z), (Z / E) and (ZJZ) isomers or mixtures thereof, for example according to the following formulas: (EZE) - (I) (E / Z) - (I) (ZfE) - (X) (27Z) - (I)
- the bisoximes of the formula (T) have acidic or basic properties and can form salts with inorganic or organic acids or with inorganic or organic bases or with metal ions, optionally also internal salts or adducts.
- the metal ions are, in particular, the ions of the elements of the second main group, in particular calcium and magnesium, the third and fourth main groups, in particular aluminum, tin and lead, and the first to eighth transition groups, in particular chromium, manganese, iron, cobalt, nickel, copper, Zinc and others into consideration. Particularly preferred are the metal ions of the elements of the fourth period.
- the metals can be present in the various valences that belong to them.
- Suitable bases are, for example, hydroxides, carbonates, bicarbonates of alkali and alkaline earth metals, in particular those of sodium, potassium, magnesium and calcium, furthermore ammonia, primary, secondary and tertiary amines with Q -C 4 - alkyl, mono-, di- and trialkanolamines of C] -C 4 alkanols, choline and chlorocholine.
- the bisoximes of the formula (I) bear amino, alkylamino or other basic-property-inducing groups, these compounds can be reacted with acids to form salts.
- inorganic acids are hydrohalic acids such as hydrogen fluoride, hydrogen chloride, hydrogen bromide and hydrogen iodide, sulfuric acid, phosphoric acid and nitric acid and acid salts such as NaHSO 4 and KHSO 4 .
- Suitable organic acids are, for example, formic acid, carbonic acid and alkanoic acids such as acetic acid, trifluoroacetic acid, trichloroacetic acid and propionic acid and glycolic acid, thiocyanic acid, lactic acid, succinic acid, citric acid, benzoic acid, cinnamic acid, oxalic acid, alkylsulfonic acids (sulfonic acids having straight-chain or branched alkyl radicals having 1 to 20 carbon atoms ), Arylsulfonic acids or -disulfonic acids (aromatic radicals such as phenyl and naphthyl which carry one or two sulfonic acid groups), alkylphosphonic acids (phosphonic acids having straight-chain or branched alkyl radicals having 1 to 20 carbon atoms), arylphosphonic acids or diphosphonic acids (aromatic radicals such as phenyl and naphthyl which contain an or two phosphonic acid bear radicals), where
- the salts thus obtainable also have fungicidal properties.
- the bisoximes which can be used according to the invention are generally defined by the formula (I). Preferred radical definitions of the above and below formulas are given below. These definitions apply equally to the end products of formula (T) as well as to all intermediates.
- R 1 and R 2 independently of one another preferably represent hydrogen, chlorine, bromine, iodine, C 1 -C 6 -alkyl,
- Ci-C 6 haloalkyl having 1 to 13 fluorine, chlorine and / or bromine atoms, OH,
- Halogenoalkyl having 1 to 9 fluorine, chlorine and / or bromine atoms, Ci-C 4 alkyl, C 2 -C 4 alkenyl,
- R 1 and R 2 independently of one another particularly preferably represent hydrogen, chlorine, bromine, C 1 -C 4 -alkyl, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, C 1 -C 4 -haloalkyl having 1 to 9
- R 1 and R 2 independently of one another very particularly preferably represent hydrogen, chlorine, methyl,
- R 1 and R 2 independently of one another are particularly preferably chlorine, methyl, ethyl, n-propyl, isopropyl, isobutyl, cyclopropyl, trifluoromethyl, difluoromethyl, trichloromethyl, methoxycarbonyl, ethoxycarbonyl, methoxymethyl, methylthiomethyl, methylsulfonylmethyl, amino , 3-Buten-1-yl, phenyl, benzyl, thienyl, 4-methylpiperazinyl or morpholinyl.
- R 1 and R 2 are each methyl, ethyl, n-propyl or amino, in particular methyl or ethyl.
- a 1 and A 2 independently of one another are preferably one of the following cycles A 1 to A-43:
- a 1 and A 2 independently of one another particularly preferably represent one of the cycles AI, A-2, A-4, A-5, A-6, A-7, A-8, A-9, A-IO, Al 1 , A-12, A-13, A-14, A-15, A-16, A-17, A-18, A-19, A-20, A-21, A-22, A-23, A -24, A-25, A-26, A-27, A-28, A-29, A-30, A-31, A-32, A-33 or A-34, wherein A 1 and A 2 are not simultaneously stand for the cycle AI.
- a 1 and A 2 independently of one another very particularly preferably represent one of the cycles AI, A-2, A-4, A-5, A-6, A-7, A-8, A-9, A-IO, AI 1, A-14, A-15, A-16, A-18, A-20, A-21, A-24, A-26, A-30 or A-33, wherein A 1 and A 2 are not simultaneously stand for the cycle AI.
- a 1 and A 2 independently of one another particularly preferably represent one of the cycles AI, A-2, A-4, A-5, A-6, A-7, A-8, A-9 or A-IO, where A 1 and A 2 are not the same for the cycle AI.
- a 1 and A 2 are highlighted respectively for A-2.
- R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 and R 10 independently of one another preferably represent hydrogen, fluorine, chlorine, bromine, iodine, cyano, nitro, OR 11 , SR 11 , SOR 11 , SO 2 R 11 , SO 2 N (R n ) 2 , COR 11 , NR 11 CO 2 R 12 , N (R ⁇ ) 2 , NR 11 COR 11 , NR 11 SO 2 R 11 , OCON (R n ) 2 , 0 (CO) R 11 , C0N (R n ) 2 , CO 2 R 11 , (CH 2 ) ra OR n ,
- Pyrrolylmethyl in each case monosubstituted or polysubstituted, identically or differently, by fluorine, chlorine, bromine, C 1 -C 4 -alkyl, C 1 -C 4 -alkoxy, Q-Cr-haloalkyl having in each case 1 to 9 fluorine, chlorine and / or bromine atoms substituted phenyl, benzyl, pyridinyl, pyridinyl, thienyl, thenyl, furyl, furfuryl, pyrrolyl, pyrrolylmethyl.
- R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 and R 10 are moreover each independently of the other preferably C 1 -C 4 -alkoxy-C 2 -C 6 -alkenyl, C 1 -C 4 - alkoxy-C 2 -C 6 -alldnyl, (C 1 -C 4 -alkyl) carbonyloxy-C 2 -C 6 alkenyl or (Ci-C 4 -alkyl) carbonyloxy-C 2 -C 6 alkynyl.
- R 11 is preferably hydrogen, C 1 -C 6 -alkyl, vinyl, allyl, ethynyl, propargyl, C 1 -C 6 -haloalkyl having in each case 1 to 13 fluorine, chlorine and / or bromine atoms, C 3 -C 6 -Cycloalkyl, Tn-C r C 4 -alkyl-silyl, hydroxy-C r C 4 -alkyl, C r C 4 -alkoxy-Ci-C 4 -alkyl ; alkyl), phenyl, benzyl, pyridinyl, pyridinylmethyl, in each case mono- or polysubstituted by identical or different fluorine, chlorine, bromine, C 1 -C 4 -alkyl, Ci-Q-alkoxy, Ci-C 4 haloalkyl, each having 1 to 9 fluorine, chlorine and / or bromine atoms substituted phenyl,
- these two R 11 together preferably with the nitrogen atom to which they are attached form a 3- to 6-membered, unsubstituted or substituted, saturated or unsaturated cycle which, depending on the ring size, may contain up to 3 further nitrogen atoms or alternatively up to 2 further heteroatoms selected from N, O and S, with two oxygen atoms not adjacent.
- R 11 in the grouping NR 11 COR 11 together with this grouping to which they are attached preferably form a 4- to 6-membered, unsubstituted or substituted, saturated or unsaturated cycle which, depending on the ring size, up to 3 further nitrogen atoms or alternatively up to 2 further heteroatoms selected from N, O and S may contain, wherein two oxygen atoms are not adjacent.
- R 12 is preferably hydrogen, C 1 -C 6 -alkyl, Q-Q 1 -haloalkyl having in each case 1 to 13 fluorine, chlorine and / or bromine atoms, - (CH 2 ) "OR n , tri-C r C 4 - alkyl-silyl.
- m is preferably the numbers 1, 2, 3, 4, 5 or 6.
- n is preferably the numbers 1, 2, 3 or 4.
- R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 and R 10 independently of one another particularly preferably represent hydrogen, fluorine, chlorine, bromine, cyano, hydroxyl, methoxy, ethoxy, n-propoxy, i -Propoxy, n-, i-, s-, t-butoxy, -O (CH 2 ) 2 OH, -O (CH 2 ) 2 OCH 3 , -O (CH 2 ) 3 OH, -O (CHz) 3 OCH 3 , trifluoromethoxy, tri- chloromethoxy, SH, S-Me, S-Et, S-Pr, S-iPr, S-Bu, S-secBu, S-woBu, S-tBu, SCF 3, SO-Me, SO-Et, SO-Pr , SO-iPr, SO-Bu, SO-secBu, SO-woBu, SO-fBu, SO 2 -
- OCONiPr 2 OCONBu 2 , OCON ⁇ cBu 2 , OCONISOBU 2 , OCONHfBu 2 , OCOR 11 , OCOMe, OCOEt, OCOPr, OCOiPr, OCOBu, OCOsecBu, OCOwoBu, OCOfBu, CON (R ⁇ ) 2 , CONHEt, CONEt 2 , CONHMe, CONMe 2 , CONHPr, CONPr 2 , CONHBu, CONHsecBu, CONffiraBu, CONHfBu, CONHCH (CH 3 ) CH 2 OH, CONHCH (CH 3 ) CH 2 OCH 3 , CONHCH (C 2 H 5 ) CH 2 OH, CONHCH (C 2 H 5 ) CH 2 OCH 3 , CONH (CH 2 ) 2 OCH 3; CONH (CH 2 ) 2 OH, CONH (CH 2 ) 3 OCH 3 ,
- R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 and R 10 are moreover each independently particularly preferably iodine, vinyl, allyl, prop-1-en-1-yl, ethynyl, propargyl, Vinyloxy, allyloxy, propargyloxy, methoxy-prop-1-en-1-yl, methoxy-prop-1-yn-1-yl, acetyloxy-prop-1-en-1-yl, acetyloxy-prop-1-yne 1 -yl and pyrrolidin-1-yl.
- each two adjacent radicals R 6 , R 7 or R 7 , R ⁇ or R 8 , R 3 or R 3 , R 9 or R 4 , R 5 or R 5 , R 10 or R 4 , R 10 together are particularly preferred an unsubstituted or substituted, unsaturated or fully or partially saturated heterocyclic or carbocyclic 5- to 7-membered ring
- R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 and R 10 independently of one another very particularly preferably represent hydrogen, fluorine, chlorine, bromine, cyano, hydroxyl, methoxy, ethoxy, n-propoxy, i-propoxy, n-, i-, s-, t-butoxy, -O (CH 2 ) 2 OH, -O (CH 2 , hOCH 3 , trifluoromethoxy, trichloromethoxy, SH, S-Me, S-Et, S -Pr, S-zPr, S-Bu, S-secBu, S-JJOBU, S-iBu, SCF 3 , SO-Me, SO-Et, SO-iBu, SO 2 -Me, SO 2 -Et, SO 2 -Pr, SO 2 -JPr, SONHMe, SONMe 2 , SONHEt, SONEt 2 ,
- OCOzPr OCOBu, OCOsecBu, OCOwoBu, OCOiBu, CONHEt, CONEt 2 , CONHMe, CONMe 2 , CONHPr, CONPr 2 , CONHBu, CONHsecBu, CONHzSoBu, CONHiBu, CO 2 Me, CO 2 Et, CO 2 Pr, CO 2 zPr, CO 2 Bu, C0 2 secBu, C0 2 z 's ⁇ Bu, CO 2 iBu, CO 2 (CH 2) 2 OH, CO 2 (CH 2) 2 OCH 3, CH 2 OH, (CH 2) 2 OH, CH 2 OMe , (CH 2 ) 2 OMe, (CH 2 ) m N (R 12 ) 2 , CH 2 NH 2 , CH 2 NAc 2 , CH 2 N (COCF 3 ) 2 , CH 2 NHAc, CH 2 NHCOCF 3 , (CH 2) 2 NH 2) (CH 2) 3 NH 2, CH 2 NMe 2,
- R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 and R 10 are also each independently Ranz particularly preferred for iodine, vinyl, allyl, prop-1-en-l-yl, ethynyl, propargyl , Vinyloxy, allyloxy, propargyloxy, methoxy-prop-1-yn-1-yl, acetyloxy- ⁇ rop-1-yn-1-yl and pyrrolidin-1-yl.
- each two adjacent radicals R 6 , R 7 or R 7 , R 8 or R 8 , R 3 or R 3 , R 9 or R 4 , R 5 or R 5 , R 10 or R 4 , R 10 together form very particularly preferably an unsubstituted or substituted, unsaturated or fully or partially saturated heterocyclic or carbocyclic 5- or 6-membered ring.
- a 1 and A 2 can therefore independently of one another also represent the following in each case optionally methyl-substituted rings: tetrahydroquinazolinyl (preferably 5,6,7,8-tetrahydroquinazolin-2-yl), tetrahydroquinolinyl (preferably 5,6,7,8 Tetramethylquinolin-2-yl), quinolinyl (preferably quinolin-2-yl), 6,7-dihydro-5H-cyclopenta [b] pyridin-2-yl, 2,3-dihydro-1-benzofuran-5-yl, Naphthyl (preferably 2-naphthyl), benzimidazolyl (preferably 1H-benzimidazol-2-yl), 6,7,8,9-tetrahydro-5H-cyclohepta [b] pyridin-2-yl.
- tetrahydroquinazolinyl preferably 5,6,7,8-tetrahydroquin
- X preferably represents one of the groups X-I, X-2, X-3, X-4, X-5, X-6, X-7 or X-IO.
- X is particularly preferably one of the groupings X-I, X-3, X-5, X-6 or X-IO.
- X very particularly preferably represents one of the groups X-3.
- X is particularly preferably one of the groups X-3, X-5 or X-6.
- X is highlighted for grouping X-3.
- Z 1 is preferably CR 13 R 14 or SiR 15 R 16 , or each is unsubstituted or substituted oxetane-3,3-diyl, cyclopropane-1, 1-diyl, cyclobutane-1, 1-diyl, cyclopentane-1, l -diyl, cyclohexane-1, 1-diyl. ⁇ J -.
- Z 1 particularly preferably represents CR 13 R 14 or SiR 15 R 16 , or represents oxetane-3,3-diyl, oxirane-2,2-diyl,
- Z 1 is very particularly preferably -CH 2 -, -CH (Me) -, -CH (OH) -, -C (Me 2 ) - or -Si (Me 2 ) -.
- Z 1 is particularly preferably -CH 2 - or -CH (Me) -.
- Z 2 and Z 3 independently of one another preferably represent CR 13 R 14 or SiR 15 R 16 , but two
- Silicon atoms are not adjacent, or for each unsubstituted or substituted oxetane-3,3-diyl, cyclopropane-l, l-diyl, cyclobutane-l, l-diyl, cyclopentane-l, l-diyl, cyclohexane
- Z 2 and Z 3 independently of one another particularly preferably represent CR 13 R 14 or SiR 15 R 16, or etan-3,3-diyl Ox-, cyclopropane-l, l-diyl, cyclobutane-l, l-diyl, cyclopentane -l, l-diyl, cyclohexane
- X-2 contains at most one spiro group.
- X-2 very particularly preferably represents - (CH 2 V, -CH 2 C (O) -, -CH (Me) CH 2 -, -CH (Me) CH (Me) -,
- X-2 particularly preferably represents - ⁇ CH 2 ) 2 - or -CH 2 C (O) -.
- Z 4 , Z 5 and Z 6 independently of one another are preferably CR 13 R 14 or SiR 15 R 16 , but where two silicon atoms are not adjacent, or Z 4 and Z 6 are each independently of the other preferably unsubstituted or substituted oxetan-3, 3-diyl, cyclopropane-1, 1-diyl, cyclobutane-1, 1-diyl, cyclopentane-1, 1-diyl, cyclohexane-1, 1-diyl, 4,5-dihydroisoxazole-5,5-diyl, and Z 5 is independently of this preferably each unsubstituted or substituted oxetane-2,2-diyl, oxetane-3,3-diyl, oxirane-2,2-diyl, cyclopropane-1, 1-diyl, cyclobutane-1, diyl, cyclopentane-1, 1-diy
- Z 4 , Z 5 or Z 5 , Z 6 are furthermore preferably cyclopentane or cyclohexane, or X-3 is optionally halogen or C 3 alkyl substituted Pyrimidindiyl, or X-3 is also preferably cyclopentane-1,3-diyl or cyclohexane-l, 3-diyl, wherein X-3 may contain at most such a group or such a cycle.
- Z 5 is preferably CR 13 R 14 or NR 17 .
- Z 4 , Z 5 and Z 6 independently of one another particularly preferably represent CR 13 R 14 or SiR 15 R 16 , but where two silicon atoms are not adjacent, or Z 4 and Z 6 independently of one another are particularly preferably oxetane-3,3- diyl, cyclopropane-l, l-diyl, cyclobutane-l, l-diyl, cyclopentane-1,1-diyl, cyclohexane-l-diyl, 4,5-dihydroisoxazole-5,5-diyl, and Z 5 is independently especially preferred for oxetane-2,2-diyl, oxetane-3,3-diyl, oxirane-2,2-diyl, cyclopropane-1,1-diyl, cyclobutane-1,1-diyl, cyclopentane-1,1-diyl , Cyclohe
- Ci-Q-alkyl C 2 -C 6 -
- C S
- Z 5 is particularly preferably CR 13 R 14 or NR 17 .
- X-3 is particularly preferably -CH 2 -CHR 22 -CH 2 -, -CH 2 -C (R 22 R 23 ).
- R 22 is hydrogen, fluorine, chlorine, hydroxyl, methyl, ethyl, n-propyl, i-propyl, n-butyl, i-butyl, s-butyl, t-butyl, methoxy, ethoxy, phenyl or benzyl
- R 23 is fluorine, chlorine, methyl or ethyl
- R 24 is methyl, ethyl, n-propyl, i-propyl, i-butyl, t-butyl
- Z 7 , Z 8 , Z 9 and Z 10 independently of one another preferably represent CR 13 R 14 or SiR 15 R 16 , but two silicon or two oxygen atoms are not adjacent, or Z 7 and Z 10 independently of one another are preferably each unsubstituted or substituted oxetane-3,3-diyl, cyclopropane-1, 1-diyl, cyclobutane-1, 1-diyl, cyclopentane-1, 1-diyl, cyclohexane-1, 1-diyl, .
- -N CR 13 - or -O ⁇ C- or for each unsubstituted or substituted 1,3-dioxolane ⁇ , 5-diyl, l, 4-dioxane-2,3-diyl, oxirane-2,3-diyl, 1 , 2-phenylene, 2,3-pyridinediyl or 3,4-pyridinediyl, wherein X-4 may at most contain such a group or such a cycle.
- Z 7 , Z 8 , Z 9 and Z 10 independently of one another particularly preferably represent CR 13 R 14 or SiR 15 R 16 , but where two silicon or two oxygen atoms are not adjacent, or Z 7 and Z 10 are particularly preferably independently of one another
- Z 7 and Z 10 are particularly preferably independently of one another
- oxetane-3,3-diyl, cyclopropane-1,1-diyl, cyclobutane-l, l-diyl, cyclopentane-l, l-diyl, cyclohexane-l, l-diyl, and Z 8 and Z 9 are independently particularly preferred for oxetane-2,2-diyl, oxetane-3,3-diyl, oxirane
- Z 8 and Z 9 are particularly preferably CR 13 R 14 or NR 17 .
- R 25 is hydrogen or methyl.
- Z ", Z 12 , Z 14 and Z 15 independently of one another are preferably CR 13 R 14 or SiR 15 R 16 and Z 13 is independently preferably CR 13 R 14 , SiR 15 R 16 , O or NR 17 , but wherein two silicon or two oxygen atoms are not adjacent, or Z n and Z 15 are each independently preferably each unsubstituted or substituted oxetane-3,3-diyl, cyclopropane-l, l-diyl, cyclobutane-l, l-diyl, cyclopentane -l, l-diyl, cyclohexane-l, l-diyl, 4,5-
- Dihydroisoxazole-5,5-diyl, and Z 12 , Z 13 and Z 14 are each independently of the other preferably each unsubstituted or substituted oxetane-2,2-diyl, oxetane-3,3-diyl, oxirane-2,2-diyl, Cyclopropan-l, l-diyl, cyclobutan-l-diyl, cyclopentane-l, l-diyl, cyclohexane-l, l-diyl, 4,5-dihydroisoxazol-5,5-diyl, wherein X-5 contains at most one spiro group , or in each case two adjacent groups Z 11 , Z 12 or Z 12 , Z 13 or Z 13 , Z 14 or Z 14 , Z 15 are preferably for
- Z 11 and Z 15 are independently preferred for
- Z 12 and Z 14 are preferably CR 13 R 14 or NR 17 .
- Z 11 , Z 12 , Z 14 and Z 15 independently of one another are particularly preferably CR 13 R 14 or SiR 15 R 16 and Z 13 independently of this is particularly preferably CR 13 R 14 , SiR 15 R 16 , O or NR 17 ,
- ⁇ Z and Z 15 independently of one another particularly preferably represent oxetane-3,3-diyl, cyclopropane-1,1-diyl, cyclobutane-l, l-diyl, cyclopentane l, l-diyl, cyclohexane-l, l-diyl
- Z 12 , Z 13 and Z 14 are each independently particularly preferably oxetane-2,2-diyl, oxetane-3,3-diyl, oxirane-2,2 -diyl, cyclopropane-1, 1-diyl, cyclobut
- Z 12 and Z 14 are particularly preferably CR 13 R 14 or NR 17 .
- X-5 particularly preferably represents - (CH 2 ) 5 -, - (CH 2 ) 2 -O- (CH 2 ) 2 - or - (CH 2 ) 2 -CH (CH 3 ) - (CH 2 ) 2 - ,
- Z 16 , Z 17 , Z 20 and Z 21 independently of one another preferably represent CR 13 R 14 or SiR 15 R 16 and Z 18 and Z 19 independently of one another are preferably CR 13 R 14 , SiR 15 R 16 , O or Ml 17
- Z 16 and Z 21 are each independently preferably each unsubstituted or substituted, oxetane-3,3-diyl, cyclopropane-l, l-diyl, cyclobutane-l, l -diyl, cyclopentane-1, 1-diyl, cyclohexane-1, 1-diyl
- Z 17 , Z 18 , Z 19 and Z 20 are each independently of the other preferably each unsubstituted or substituted oxetane-2,2-diyl, oxetane 3,3-diyl, oxirane-2,2-diyl,
- Z 17 and Z 20 are preferably CR 13 R 14 or NR 17 .
- Z 16 , Z 17 , Z 20 and Z 21 independently of one another are particularly preferably CR 13 R 14 or SiR 15 R 16 and Z 18 and Z 19 independently of one another are particularly preferably CR 13 R 14 , SiR 15 R 16 , O or NR 17 , but where two silicon or two oxygen atoms are not adjacent, or Z 16 and Z 21 are each independently particularly preferably oxetane-3,3-diyl, cyclopropane-1, 1-diyl, cyclobutane-1, 1 -diyl, cyclopentane-1, 1-diyl, cyclohexane-1, 1-diyl, and Z 17 , Z 18 ,
- Z 17 and Z 20 are particularly preferably CR 13 R 14 or NR 17 .
- X-6 particularly preferably represents - (CHVk-.
- Z 22 , Z 23 , Z 27 and Z 2S independently of one another are preferably CR 13 R 14 or SiR 15 R 16 and Z 24 , Z 25 , and Z 26 are each, independently of one another, preferably CR 13 R 14 , SiR 15 R 16 , O or NR 17 , but where two silicon or two oxygen atoms are not adjacent, or Z 22 and Z 28 are each independently of the other preferably each unsubstituted or substituted oxetane-3,3-diyl, cyclopropane-1, 1-diyl, cyclobutane l, l-diyl, cyclo-pentane-l, l-diyl, cyclohexane-l, l-diyl, 4,5-dihydroisoxazol-5,5-diyl, and Z 23 , Z 24 , Z 25 , Z 26 and Z 27 independently of one another are preferably each unsubstituted or substituted
- Z 27 is preferred for CR 13 R 14 or NR 17 .
- Z 22 , Z 23 , Z 27 and Z 28 independently of one another are particularly preferably CR 13 R 14 or SiR 15 R 16 and Z 24 , Z 25 , and Z 26 independently of one another are particularly preferably CR 13 R 14 ,
- SiR 15 R 16 , O or NR 17 wherein, however, two silicon or two oxygen atoms are not adjacent, or Z 22 and Z 28 independently of one another particularly preferably represent oxetane-3,3-diyl, cyclopropane-1, 1-diyl, Cyclobutane-1, 1-diyl, cyclopentane-1, 1-diyl, cyclohexane-1, 1-diyl, 4,5-dihydroisoxazol-5,5-diyl, and Z 23 , Z 24 , Z 25 , Z 26 and Z 27 independently of one another particularly preferably represent oxetane-2,2-diyl, oxetane-3,3-diyl, oxirane-2,2-diyl,
- X-7 is particularly preferably - (CH 2 ) 7 - or ⁇ CH 2 ) 2 -O-CH 2 -O- (CH 2 ) 2 -.
- Z 29 , Z 30 , Z 35 and Z 36 are each independently preferably CR 13 R 14 or SiR 15 R 16 , Z 30 and Z 35 are furthermore preferably NR 17 , and Z 31 , Z 32 , Z 33 , and Z 34 are, independently of one another preferably represent CR 13 R 14, SiR 15 R 16, O or NR 17, but where two silicon or two oxygen atoms are not adjacent, or Z 29 and Z 36 are, independently of one another preferably in each case unsubstituted or substituted oxetane 3,3-diyl, cyclopropane-1, 1-diyl, cyclobutane-1, 1-diyl, cyclopentane-1, 1-diyl, cyclohexane-1, 1-diyl, and Z 30 , Z 31 , Z 32 , Z 33 , Z 34 and Z 35 are each independently preferably unsubstituted or substituted
- Z 29 , Z 30 , Z 35 and Z 36 independently of one another are particularly preferably CR 13 R 14 or SiR 15 R 16 , Z 30 and Z 35 are furthermore particularly preferably NR 17 , and Z 31 , Z 32 , Z 33 , and Z 34 independently of one another particularly preferably represent CR 13 R 14 , SiR 15 R 16 , O or NR 17 , but where two silicon or two oxygen atoms are not adjacent, or Z 29 and Z 36 independently of one another are particularly preferably oxetanes 3,3-diyl, cyclopropane-1, 1-diyl,
- Cyclobutane-1, 1-diyl, cyclopentane-1, 1-diyl, cyclohexane-1, 1-diyl, and Z 30 , Z 31 , Z 32 , Z 33 , Z 34 or Z 35 independently of one another are particularly preferably oxetanes.
- Z 30 and Z 35 are particularly preferably CR 13 R 14 or NR 17 .
- X-8 is particularly preferably - (CH 2 ) g -.
- Z 37 , Z 38 , Z 44 and Z 45 are each independently preferably CR 13 R 14 or SiR 15 R 16 , Z 38 and Z 44 are furthermore preferably NR 17 , and Z 39 , Z 40 , Z 41 , Z 42 and Z 43 are each independently preferably CR 13 R 14 , SiR 15 R 16 , O or NR 17 , but with two silicon or two oxygen atoms not adjacent, or Z 37 and Z 45 are each independently preferably unsubstituted or substituted substituted oxetane-3,3-diyl, cyclopropane-1,1-diyl, cyclobutane-U-diyl, cyclopentane-1, 1-diyl, cyclohexane-1, 1-diyl, or Z 38 , Z 39 , Z 40 , Z 41 , Z 42 , Z 43 , or Z 44 are each independently of the other preferably each unsubstituted or substituted oxetane-2,
- Z 38 and Z 44 are preferably CR 13 R 14 or NR 17 .
- Z 37 , Z 38 , Z 44 and Z 45 independently of one another are particularly preferred for CR 13 R 14 or SiR 15 R 16 , Z 38 and Z 44 are furthermore particularly preferably NR 17 , and Z 39 , Z 40 , Z 41 ,
- Z 42 and Z 43 are particularly preferably CR 13 R 14 , SiR 15 R 16 , O or NR 17 , but two silicon or two oxygen atoms are not adjacent, or
- Z 37 and Z 45 are each independently particularly preferred for oxetane-3,3-diyl, cyclopropane-1,1-diyl, cyclobutane-1, 1-diyl, cyclopentane-1, 1-diyl, cyclohexane-1, 1-diyl, or Z 3S , Z 39 , Z 40 ,
- Z 42 , Z 43 and Z 44 independently of one another particularly preferably represent oxetane-2,2-diyl, oxetane-3,3-diyl, oxirane-2,2-diyl, cyclopropane-1,1,2-diyl, cyclobutane-1, l-diyl, cyclopentane-1,1- Diyl, cyclohexane-l, l-diyl, or represents optionally mono- or polysubstituted by C r C 4 alkyl, C 2 -C 6 alkenyl, phenyl or halophenyl-substituted 4,5-dihydroisoxazol-5,5-diyl "wherein X- 9 contains a maximum of one spiro group, or two adjacent radicals Z 38 , Z 39 or Z 39 , Z 40 or Z 40 , Z 41 or Z 41 , Z 42 or Z 42 , Z 43 or Z
- X-9 particularly preferably represents - (CH? V.
- Z 46 , Z 47 , Z 54 and Z 55 independently of one another preferably represent CR 13 R 14 or SiR 15 R 16 and Z 48 , Z 49 , Z 50 , Z 51 , Z 52 , and Z 53 independently of one another are preferably CR 13 R 14 , SiR 15 R 16 , O or NR 17 , but where two silicon or two oxygen atoms are not adjacent, or Z 46 and Z 55 are each independently preferably unsubstituted or substituted oxetane-3,3-diyl, cyclopropane -l, 1-diyl, cyclobutane-1, 1-diyl, cyclopentane-1, 1-diyl, cyclohexane-U-diyl, or Z 47 , Z 48 , Z 49 , Z 50 , Z 51 , Z 52 , Z 53 , or Z 54 are each independently of the other unsubstituted or substituted oxetane-2,2-diyl,
- Z 46 , Z 47 , Z 54 and Z 55 independently of one another are particularly preferably CR 13 R 14 or SiR 15 R 16 and Z 48 , Z 49 , Z 50 , Z 51 , Z 52 , and Z 53 are each independently particularly preferred For
- CR 13 R 14 SiR 15 R 16 , O or NR 17 , but with two silicon or two oxygen atoms not adjacent, or Z 46 and Z 55 are more preferably independently ,
- Oxetane-3,3-diyl, cyclopropane-1, 1-diyl, cyclobutaQ-1, 1-diyl, cyclopentan-11-diyl, cyclohexane-1, 1-diyl, or Z 47 , Z 48 , Z 49 , Z 50 , Z 51 , Z 52 , Z 53 , or Z 54 are each independently particularly preferably oxetane-2,2-diyl, oxetane-3,3-diyl, oxirane-2,2-diyl, cyclopropane-1,1 - Diyl, cyclobutane-l, l-diyl, cyclopentane-l, l-diyl, cyclohexane-l, l-diyl, or optionally mono- or polysubstituted, identically or differently by Ci-C 4 alkyl, C 2 -C 6 Alkenyl,
- Z 47 and Z 54 are particularly preferably CR 13 R 14 or NR 17 .
- R 13 , R 14 , R 15 , R 16 and R 17 independently of one another preferably represent hydrogen, fluorine, chlorine, bromine, iodine, cyano, hydroxyl, OR 11 , SR 11 , SOR 11 , SO 2 R 11 , SO 2 N (R n ) 2 , COR 11 , NR 11 CO 2 R 12 , N (R U ) 2 , NR 11 COR 11 , NR 11 SO 2 R 11 , OCON (R 11 ⁇ , O (CO) R 11 , CON ( R U ) 2) CO 2 R 11 , (CH 2 ) m OR u , (CH 2 ) m SR n , (CH 2 ) m N (R ⁇ ) 2 , (CH 2 ) m CO 2 R 12 , (CH 2 ) Jm 11 CO 2 R 12 , C r C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C]
- Pyridinylmethyl, thienyl, thenyl, furyl, furfuryl, pyrrolyl, Pyrrolyhnethyl in each case mono- or polysubstituted by identical or different fluorine, chlorine, bromine, QQ-alkyl, QC 4 -alkoxy, Ci-C4-haloalkyl having in each case 1 to 9 fluorine -, chlorine and / or bromine atoms substituted phenyl, benzyl, pyridinyl, pyridinylmethyl, thienyl, thenyl, furyl, furfuryl, pyrrolyl, pyrrolyhnethyl.
- R 18, R 19 and R 20 are each independently preferably represents hydrogen, Ci-C 6 alkyl, C] -C 6 - haloalkyl having 1 to 13 fluorine, chlorine and / or bromine atoms, C 2 -C 6 alkenyl , C 2 -C 6 -alkynyl, C 3 -C 6 -cycloalkyl, phenyl, benzyl, pyridinyl, pyridinylmethyl, thienyl, thenyl, furyl, furfuryl, pyrrolyl, pyrrolylmethyl, in each case mono- or polysubstituted, identically or differently, by fluorine, chlorine, bromine, Ci-C4-alkyl, Ci-C 4 alkoxy, C 1 -C 4 -haloalkyl having in each case 1 to 9 ,
- Fluorine, chlorine and / or bromine atoms substituted phenyl, benzyl, pyridinyl, pyridinylmethyl, thienyl, thenyl, furyl, furfuryl, pyrrolyl, pyrrolylmethyl.
- R 18 and R 19 together with the carbon atom to which they are attached also preferably form an unsubstituted or substituted, unsaturated or fully or partially saturated heterocyclic or carbocyclic 3- to 8-membered ring, as appropriate
- Ring size may contain up to 3 further nitrogen atoms or alternatively up to 2 further heteroatoms selected from N, O and S, wherein two oxygen atoms are not adjacent.
- R 13 , R 14 , R 15 , R 16 and R 17 are each independently particularly preferably hydrogen, fluorine, chlorine, bromine, hydroxyl, methoxy, ethoxy, n-propoxy, i-propoxy, n-, i-, s- , t-butoxy,
- R 13 and R 14 are also more preferably independently of each other vinyloxymethyl
- R 18 , R 19 and R 20 independently of one another particularly preferably represent hydrogen, methyl, ethyl, n-propyl, i-propyl, n-, i-, s-, t-butyl, trifluoromethyl, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl , Phenyl, benzyl, pyridinyl, pyridinylmethyl, thienyl, thenyl, furyl, furfuryl, pyrrolyl, pyrrolylmethyl, in each case monosubstituted or polysubstituted, identically or differently, by fluorine, chlorine, bromine, methyl, ethyl, n-propyl,
- R 13 , R 14 , R 15 , R 16 and R 17 are very particularly preferably each independently hydrogen, fluorine, chlorine, bromine, hydroxyl, methoxy, ethoxy, n-propoxy, i-propoxy, n-, i-, s -, t-butoxy, -O (CH 2 ) 2 OH, -O (CH 2 ) 2 OCH 3 , trifluoromethoxy, trichloromethoxy, SH, S-Me, S-Et, S-Pr, S-iPr, S-Bu , S-jecBu, S-isoBu, S-iBu, SCF 3 , SO-Me, SO-Et, SO-fBu, SO 2 -Me, SO 2 -Et 1 SO 2 -Pr,
- R 13 and R 14 independently of one another very particularly preferably represent allyloxymethyl and propargyloxymethyl.
- R 18 , R 19 and R 20 independently of one another very particularly preferably represent hydrogen, methyl,
- R 21 is preferably hydrogen, C r C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, each optionally substituted by halogen, cyano, Ci-C 4 alkyl, Ci-C 4 alkoxy substituted phenyl, benzyl, heterocyclyl or hetaryl.
- R 21 particularly preferably represents hydrogen, methyl, ethyl, n-propyl, i-propyl, n-, i-, s-, t-butyl, vinyl, allyl, 1-butenyl, 2-butenyl, 2-methyl-propene -l -yl, each optionally mono- or polysubstituted, identically or differently, by fluorine, chlorine, bromine, cyano, methyl, ethyl, n-propyl, i-propyl, methoxy, substituted phenyl or benzyl.
- R la and R 23 independently represents halogen, Ci-Cg-alkyl, C3 -CG-cycloalkyl, Ci-C8 haloalkyl,
- Heterocyclyl or hetaryl independently represent one of the following cycles
- a la and A ⁇ 2a are not the same for optionally substituted, substituted phenyl, Y 1 , Y 2 , Y 3 , Y 4 and Y 5 have the meanings given above,
- Y 5a is N or CR 10a , where at least one substituent R 4a or R 5a or R 10a does not stand for hydrogen when Y 5a is CR 10a ,
- R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 and R 10 have the meanings given above,
- R 4a , R 5a and R IOa have the abovementioned meanings of R 4 , R 5 and R 10 , wherein at least one
- Substituent R 4a or R 5a or R 10a is not hydrogen
- X 1 has the meanings of X given above, with the proviso that X 1 does not represent pyrimidine-2,4-diyl or pyrimidine-4,6-diyl.
- novel compounds of formula (1-1) can be used to control undesirable microorganisms and insects in crop protection and material protection.
- R la and R 23 are each independently preferably represents chlorine, bromine, iodine, Ci-C ⁇ -alkyl, Cs-C ⁇ -cyclo- alkyl, QQ-halogenoalkyl having 1 to 13 fluorine, chlorine and / or bromine, OH, C 1 CE
- R a and R 2a independently of one another particularly preferably represents chlorine, bromine, Ci-C 4 alkyl, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, C r C 4 -haloalkyl having 1 to 9 fluorine, chlorine and / or bromine, OH, Ci-C4 alkoxy, (Ci-C 4 alkoxy) carbonyl, SH, C 1 -C 4 -AUCyItMo, C 1 - C 4 -Alkylsufinyl, CrC 4 -A] kylsulfonyl, d-CrAUcoxy- Ci-Cralkyl, (C 1 -C 2 -AUCyI) UIiO (C 1 -C 2 - alkyl, (C 1 -C 2 -AUCyI) UIiO (C 1 -C 2 - alkyl, (C 1 -C 2 -AUCy
- R 1a and R 28 independently of one another very particularly preferably represent chlorine, methyl, ethyl, n-propyl, i-propyl, n-, i-, s- or t-butyl, cyclopropyl, cyclopentyl, cyclohexyl, trifluoromethyl, difluoromethyl, trichloromethyl , Pentafluoroethyl, heptafluoro-n-propyl, heptafluoro-i-propyl, OH, methoxy, ethoxy, n-propoxy, i-propoxy, n-, i-, s- or t-butoxy.
- R 1a and R 2a independently of one another are particularly preferably chlorine, methyl, ethyl, n-propyl, i-propyl, i-butyl, cyclopropyl, trifluoromethyl, difluoromethyl, trichloromethyl, methoxycarbonyl, ethoxycarbonyl, methoxymethyl, methylthiomethyl, methylsulfonyhnethyl, amino, 3 Butylene-1-yl, phenyl, benzyl, thienyl, 4-methylpiperazinyl or morpholinyl.
- R 1a and R 2 " 1 are each methyl, ethyl, n-propyl or amino, in particular methyl or ethyl.
- a and A independently of one another preferably represent one of the following cycles A-I to A-43:
- A-41 A-42 A-43 wherein A la and A ⁇ are not the same for the cycle AI and wherein in A-18 a , A-19 a , A-24 a and A-25 a at least one substituent R 4a or R 5a or R 10a does not stand for hydrogen.
- a la and A ⁇ independently of one another particularly preferably represent one of the cycles AI, A-2, A-4, A-5, A-6, A-7, A-8, A-9, A-IO, A- Il, A-12, A-13, A-14, A-15, A-16, A-17, A-18 a, A-19 a,
- a la and A 2a independently of one another very particularly preferably represent one of the cycles AI, A-2, A-4, A-5, A-6, A-7, A-8, A-9, A-IO, AI l, A-14, A-15, A-16, A-18 a, A-20, A-21, A-24 a, A-26, A-30 or A-33, wherein A la and A 23 are not the same for the cycle AI and wherein in A-18 a and A-24 a at least one substituent R 4a or R 5a or R 10a is not hydrogen.
- a Ia and A 28 independently of one another particularly preferably represent one of the cycles AI, A-2, A-4, A-5, A-6, A-7, A-8, A-9 or A-IO, where A la and A 1 "do not simultaneously stand for the cycle AI.
- a la and A 2a are highlighted respectively for A-2.
- Cyclus A-2 stand. Preference is furthermore given to compounds of the formula (I-1) in which A 1a and A 2a are each selected for cycle A-
- Methyl and A 1 and A 2 are each for cycle A-2.
- Halogen fluorine, chlorine, bromine and iodine
- Alkyl saturated, straight-chain or branched hydrocarbon radicals having 1 to 8 carbon atoms, for example C 1 -C 6 -alkyl, such as methyl, ethyl, propyl, 1-methylethyl, butyl, 1-methylpropyl, 2-methylpropyl, 1,1-dimethylethyl, pentyl, 1 Methylbutyl, 2-methylbutyl, 3-methylbutyl, 2,2-dimethylpropyl, 1-ethylpropyl, hexyl, 1,1-dimethylpropyl, 1,2-dimethylpropyl, 1-methylpentyl, 2-methylpentyl, 3-methylpentyl, 4-methylpentyl 1,1-dimethylbutyl, 1,2-dimethylbutyl, 1,3-dimethylbutyl, 2,2-dimethylbutyl, 2,3-dimethylbutyl, 3,3-d
- Haloalkyl straight-chain or branched alkyl groups having 1 to 8 carbon atoms (as mentioned above), wherein in these groups partially or completely the hydrogen atoms may be replaced by halogen atoms as mentioned above, for example Ci-C 3 haloalkyl such as chloromethyl, bromomethyl, dichloromethyl, trichloromethyl , Fluoromethyl, difluoromethyl, trifluoromethyl, chlorofluoromethyl, dichlorofluoromethyl, chlorodifluoromethyl, 1-chloroethyl, 1-bromoethyl, 1-fluoroethyl, 2-fluoroethyl, 2,2-difluoroethyl, 2,2,2-trifluoroethyl, 2-chloro-2 -fluoroethyl, 2-chloro-2-difluoroethyl, 2,2-dichloro-2-fluoroethyl, 2 ⁇ , 2-trichloroethyl
- Alkenyl unsaturated, straight-chain or branched hydrocarbon radicals having 2 to 8 carbon atoms and one double bond in any position, for example C 2 -C 6 -alkenyl, such as ethenyl, 1-propenyl, 2-propenyl, 1-methylethenyl, 1-butenyl, 2-butenyl, 3-butenyl, 1-methyl-1-propenyl, 2-methyl-1-propenyl, 1-methyl-2-propenyl, 2-methyl-2-propenyl, 1-pentenyl, 2-pentenyl, 3 Pentenyl, 4-pentenyl, 1-methyl-1-butenyl, 2-methyl-1-butenyl, 3-methyl-1-butenyl, 1-methyl-2-butenyl, 2-methyl-2-butenyl, 3-methyl 2-butenyl, 1-methyl-3-butenyl, 2-methyl-3-butenyl, 3-methyl-3-butenyl, 1,1-dimethyl-2-propenyl, 1,2-di
- Alkynyl straight-chain or branched hydrocarbon groups having 2 to 8 carbon atoms and a triple bond in any position, for example C 2 -C 6 -alkynyl, such as ethynyl, 1-propynyl, 2 _ _
- Cydoalkyl monocyclic saturated hydrocarbon groups having 3 to 8 carbon atoms, such as cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl and cyclooctyl.
- Cycloalkenyl monocyclic, non-aromatic hydrocarbon groups having 3 to 8 carbon ring members having at least one double bond, such as cyclo-penten-1-yl, cyclohexen-1-yl, cyclohepta-1,3-dien-1-yl.
- Alkoxycarbonyl an alkoxy group having 1 to 6 carbon atoms (as mentioned above), which is bonded to the skeleton via a carbonyl group (-CO-).
- Oxyalkylenoxy divalent unbranched chains of 1 to 3 CH 2 groups, wherein both valences are bonded to the skeleton via an oxygen atom, eg OCH 2 O, OCH 2 CH 2 O and OCH 2 CH 2 CH 2 O.
- heterocyclyl / hetaryl unsubstituted or substituted, unsaturated or completely or partially saturated heterocyclic 5- to 7-membered ring, or unsaturated or fully or partially saturated heterocyclic 3- to 8-membered ring containing up to 4 nitrogen atoms or alternatively 1 nitrogen atom and up to 2 further Heteroatoms selected from N, O and S: eg oxiranyl, aziridinyl, 2-tetrahydrofuranyl, 3-tetrahydrofuranyl, 2-tetrahydrothienyl, 3-tetrahydrothienyl, 2-pyrrolidinyl, 3-pyrrolidinyl, 3-isoxazolidinyl, 4-isoxazolidinyl, 5-isoxazolidinyl , 3-isothiazolidinyl, 4-isothiazolidinyl, 5-isothiazolidinyl, 3-pyrazolidinyl, 4-pyrazolidinyl, 5-pyrazolidinyl
- acyl (het) aryls required as starting materials in carrying out the processes (AI) and (A-2) according to the invention are generally defined by the formulas ( ⁇ ) and (HA).
- a 1 , R 1 , R 2 and A 2 are preferred, particularly preferably, very particularly preferably or particularly preferably for those meanings which have already been described in connection with the description of the substances of the formula (I) which can be used according to the invention preferably, etc. are given for these radicals.
- acyl (het) aryls of the formulas (II) and (Ha) are either commercially available or described in the literature or accessible according to literature-analog regulations.
- the synthesis of acyl (het) aryls of the formulas (IT) or (IIa) by the Grignard method by reaction of appropriately substituted aromatic or heteroaromatic nitriles with the corresponding Grignard reagents R 1 MgHaI or R 2 MgHaI, wherein R 1 and R 2 have the meanings given above and Hal is halogen (preferably chlorine or bromine) (see J. Am Chem Chem 1956, 78, 2141). p ⁇ o ⁇ JU-Jizi /
- the acyl (het) aryls of formulas (H) and (Ha) may be obtained by Friedel-Crafts acylation of (hetero) aromatics (eg, J. Am. Chem. Soc., 1947, 69, 3018) or from carboxylic acid derivatives (Ester, amides, acids) (eg iron-catalyzed addition of methylgrignard to carbonic acid chlorides: J. Org. Chem. 2004, 69, 3943; Addition of methylgrignard to Weinreb amides: Synlett 1999, 1091: addition of malonic ester to carboxylic acid chlorides followed by double decarboxylation: Tetrahedron 1992, 48, 9233).
- Friedel-Crafts acylation of (hetero) aromatics eg, J. Am. Chem. Soc., 1947, 69, 3018
- carboxylic acid derivatives eg iron-catalyzed addition of methylgrignard to carbon
- the bishydroxylamines which are furthermore required as starting materials when carrying out the processes (A-I) and (A-2) according to the invention are generally defined by the formula (DI).
- X has preferably, more preferably, very particularly preferably or particularly preferably for those meanings, which already in connection with the description of the inventively usable substances of the formula (I) as preferred, particularly preferred, etc. for this rest were.
- the bishydrohalides of the bishydroxylamines of the formula (HI) as starting materials.
- bishydrochlorides or bishydrobromides are suitable.
- Bishydroxylamines of the formula (HT) are known in part. New and thus likewise part of this invention are bishydroxylamines of the formula (Ma)
- X f has the meanings of X except compounds of the formula (IIIa) in which
- X f is a saturated or unsaturated aliphatic, linear or branched hydrocarbon radical of 2 to 12 carbon atoms, which may be interrupted by 1 to 3 non-adjacent oxygen atoms, is [in particular -CH 2 - - (CH 2 V, - (CH 2 V, - (CH 2 V, - (CH 2 V, - (GHz) 6 -, - (CH 2 ) S-, -CCH 2) 10 -, - (CH 2 VO- (CH 2 V, - (CH 2 ) 2 -O- (CH 2 ) 2 -O- (CH 2 ) 2 -], or for -SiMe 2 -, -SiZBu 2 -, -Si (Me) ZBu-, -SiH 2 -, -C (O) - C (O) -, (1-phenyl) ethane-1, 2-diyl, -CH (CO 2 Et) -CH 2 -,
- Bishydroxylamine of the formulas (HT) or (HIa) can be prepared by
- LG 2 is halogen, sulfonate or hydroxy
- X has the abovementioned meanings, to bishydroxyphthaUmid derivatives of the formula (XI)
- hydroxylamines of the formula (XH) according to the invention may optionally be used as mixtures of various possible isomeric forms, in particular stereoisomers, such as. B. E- and Z-, threo- and erythro-, as well as optical isomers, but optionally also of tautomers vorhegen. Both the E and the Z isomers, as well as the threo and erythro, and the optical isomers, any mixtures of these isomers, as well as the possible tautomeric forms claimed.
- the compounds of formula (XII) may be in the form of E, or Z isomers or mixtures thereof, e.g. according to the following formulas:
- R lg , A lg and X 8 each have the meanings given above for R 1 , A 1 and X, where a) A lg is not phenyl, 4-fluorophenyl, 4-chlorophenyl or 2,4-dichlorophenyl, when R l ⁇ is hydrogen and X 8 is - (CH 2 V or b) A lB is not phenyl, 4-fluorophenyl, 4-chlorophenyl, 2,4-dichlorophenyl, 3,4-dichlorophenyl, 2-hydroxyphenyl, 2-hydroxy 5-bromophenyl, 3 - ⁇ [(2S) -2-hydroxypropyl] oxy ⁇ phenyl ) 2-hydroxy-3,5-bis-tert-butylphenyl, 2-hydroxy-3-methylthiophenyl, 2-hydroxy-3- methoxyphenyl or 4-nitrophenyl, when R lg is hydrogen and X 8 is - (CH 2 ) 2
- Preferred, particularly preferred, very particularly preferred and particularly preferred are compounds of the formula (XIIa) in which the radicals R 18 , A lg and X g are each those preferred, particularly preferred, very particularly preferred or especially preferred meanings of the radicals R 1 , A 1 and X have already been mentioned in connection with the description of the substances of the formula (I) which can be used according to the invention as being preferred, particularly preferred etc.
- a lg is not suitable for Phenyl, 4-fluorophenyl, 4-chlorophenyl or 2,4-dichlorophenyl, when R lg is hydrogen and X 8 is - (CH 2 ) 4 -, or b) A lg is not phenyl, 4-fluorophenyl, 4- Chlorophenyl, 2,4-dichlorophenyl, 3,4-dichlorophenyl, 2-hydroxyphenyl, 2-hydroxy-5-bromophenyl, 3 - ⁇ [(2S) -2-hydroxypropyl] oxy ⁇ phenyl, 2-hydroxy-3, 5-bis-tert-butylphenyl, 2-hydroxy-3-methylthiophenyl, 2-hydroxy-3-methoxyphenyl or 4-nitrophenyl, when R lg is Wa and X g is - (CH 2 ) 2 -.
- the bifunctional compounds required as starting materials in carrying out the processes (B) and (C) according to the invention are generally defined by the formula (IV).
- X has preferably, more preferably, very particularly preferably or particularly preferably for those meanings which have already been mentioned in connection with the description of the substances of the formula (I) which can be used according to the invention as being preferred, particularly preferred etc. for this radical.
- LG 1 is preferably chlorine, bromine, iodine, mesylate or tosylate, particularly preferably chlorine or bromine.
- Bifunctional compounds of the formula (JV) are either commercially available or are described in the literature or accessible according to literature-analogous rules.
- bischlorides can be obtained by reacting diols with thionyl chloride / pyridine (for example, analogously to Journal of Organic Chemistry 1995, 60, 4666), while bisbromides are obtainable by reaction of diols with glacial acetic acid / hydrobromic acid (for example, analogously to Journal of Organic Chemistry 1995, 60 , 4946).
- Bissulfonates of the formula (IV) are likewise either commercially available or described in the literature or accessible by literature-analogous methods (for example synthesis of bismesylates analogous to Chem. Pharm. Bull. 2006, 54, 141; bistrifluoromethanesulfonates analogously to Journal of Organic Chemistry 2006, 71 , 5423; bistosylates analogous to Carbohydrate Research 2005, 340, 2494).
- the free oximes which are furthermore required as starting materials for carrying out the processes (B) and (C) according to the invention are generally defined by the formulas (V) or (Va).
- a 1 , R 1 , R 2 and A 2 are preferred, particularly preferably, very particularly preferably or particularly preferably for those meanings which have already been mentioned as preferred in connection with the description of the substances of the formula (I) which can be used according to the invention. particularly preferably, etc. have been given for these radicals.
- the free oximes of the formulas (V) or (Va) are accessible by condensation reactions of the acyl (het) aryls of the formulas (E) or (IIa) with hydroxylamine (eg analogous Journal of Organic Chemistry 2003, 68, 3546) or leave obtained by reaction of aromatic or heteroaromatic nitriles with hydroxylamine (eg synthesis of amidoximes analogous to EP-A 0490 188).
- a 1 , R 1 , R 2 , A 2 and X are preferred, particularly preferably, very particularly preferably or particularly preferably for those meanings which have already been described in connection with the description of the substances of the formula (I ) were given as preferred, particularly preferred, etc. for these radicals.
- LG 1 is preferably chlorine, bromine, iodine, mesylate or tosylate, particularly preferably chlorine or bromine.
- the intermediates of the formulas (VI) or (VIa) according to the invention may be used as mixtures of various possible isomeric forms, in particular of stereoisomers, such as, for example, B. E and Z, threo and erythro, and optical isomers, but optionally also of tautomers.
- stereoisomers such as, for example, B. E and Z, threo and erythro, and optical isomers, but optionally also of tautomers.
- E and the Z isomers as well as the threo- and erythro-, and the r> uu- in
- the intermediates of the formulas (VT) or (VIa) may be in the form of E or Z isomers or mixtures thereof, e.g. according to the following formulas:
- Process (B) represents the one-pot variant (tandem reaction) of process (C).
- the bisoximes required as starting materials in the implementation of the process (D) or occurring as intermediates are generally defined by the formulas (Ib) and (Ic).
- a 1 , R 1 , R 2 and A 2 are preferred, particularly preferred, very particularly preferred or particularly preferred for those meanings which are already preferred in connection with the description of the substances of the formula (I) which can be used according to the invention. particularly preferably, etc. have been given for these radicals.
- X.sup.b has preferably, more preferably, very particularly preferably or particularly preferably those meanings which have already been mentioned in connection with the description of the substances of the formula (I) which can be used according to the invention as being preferred, particularly preferred etc. for the radical X.
- the above definition of X b is equivalent to this.
- X 0 has preferably, more preferably, very particularly preferably or particularly preferably those meanings which have already been mentioned in connection with the description of the substances of the formula (I) which can be used according to the invention as being preferred, particularly preferred etc.
- Bisoximes of the formulas (Ib) and (Ic) are likewise compounds according to the invention and represent a subset of the bisoximes of the formula (I).
- R 20 has preferred Particularly preferably, very particularly preferably or particularly preferably those meanings which have already been mentioned in connection with the description of the substances of the formula (T) which can be used according to the invention as being preferred, particularly preferred etc. for this radical.
- Free oximes of the formula (VH) are known or can be obtained by known methods.
- R 21 has preferred, particularly preferred, very particularly preferred or particularly preferred those meanings already in connection with Description of the substances of the formula (I) which can be used according to the invention are given as being preferred, more preferably etc., for this radical.
- N-hydroxyphthalimide of the formula (DC) used in carrying out the process (G) according to the invention is a known synthesis chemical.
- the compounds which are furthermore required as starting materials for carrying out the process (G) according to the invention are generally defined by the formula (X).
- X preferably, more preferably, very particularly preferably or particularly preferably has those meanings which have already been described in connection with the description of the substances of the formula (I) which can be used according to the invention have been given as being preferred, more preferably etc., for this radical.
- LG 2 is preferably chlorine, bromine, iodine, mesylate, tosylate or hydroxy, particularly preferably chlorine, bromine or hydroxyl
- the bishydroxyphthalimide derivatives which continue to be used as intermediates in carrying out the process (G) according to the invention are generally defined by the formula (XI).
- X has, particularly preferably, very particularly preferably or particularly preferably those which have already been described in In connection with the description of the substances of the formula (T) which can be used according to the invention are given as preferred, particularly preferred etc. for this radical.
- Bishydroxyphthalimide derivatives of the formula (XT) are known in part. New and thus also part of this invention are bishydroxyphthalimide derivatives of the formula (XIa)
- BishydroxyphthaUmid derivatives of the formula (XIa) can be prepared by process (G). - 53 -
- Suitable diluents are virtually all inert organic solvents. These include preferably aliphatic and aromatic, optionally halogenated hydrocarbons such as pentane, hexane, heptane, cyclohexane, petroleum ether, gasoline, ligroin, benzene, toluene, xylene, methylene chloride, ethylene chloride, chloroform, carbon tetrachloride, chlorobenzene and o-dichlorobenzene, ethers such as diethyl and Dibutyl ether, glycol dimethyl ether and diglycol dimethyl ether, tetrahydrofuran and dioxane, ketones such as acetone, methyl ethyl, methyl isopropyl or methyl isobutyl ketone, esters, adiluents, ethers such as diethyl and Dibutyl ether, glycol dimethyl ether and diglycol
- alcohols such as Methanol, ethanol, propanol, i-propanol, butanol, i-butanol, 2-methoxyethanol can be used.
- ethanol and methanol or mixtures thereof with dichloromethane can be used.
- Suitable diluents are virtually all inert organic solvents. These include preferably aliphatic and aromatic, optionally halogenated hydrocarbons such as pentane, hexane, heptane, cyclohexane, petroleum ether, gasoline, ligroin, benzene, toluene, xylene, methylene chloride, ethylene chloride, chloroform, carbon tetrachloride, chlorobenzene and o-dichlorobenzene, ethers such as diethyl and dibutyl ether, glycol dimethyl ether and diglycol dimethyl ether, tetrahydrofuran and dioxane, ketones such as acetone, methyl ethyl, methyl isopropyl or methyl isobutyl ketone, esters such as
- acetonitrile, diethyl ether or tetrahydrofuran can be used.
- reaction temperatures can be varied within a substantial range. In general, one works at temperatures between 0 0 C and 250 0 C, preferably at temperatures between 0 0 C and 100 0 C.
- reaction temperatures can be varied within a substantial range. In general, temperatures between -78 ° C and 25 ° C, preferably at temperatures between -40 ° C and 0 0 C. - 54 -
- AIs catalyst in carrying out the process (A-I), (A-2) and (D) are optionally the usual inorganic or organic acids into consideration. These preferably include para-toluenesulfonic acid, methanesulfonic acid, hydrochloric acid or sulfuric acid.
- Suitable reaction auxiliaries when carrying out the processes (B) and (C) according to the invention are, if appropriate, the usual inorganic or organic bases or acid binders.
- These preferably include alkali metal or alkaline earth metal acetates, amides, carbonates, hydrogen carbonates, hydrides, hydroxides or alkoxides, such as, for example, sodium, potassium or calcium acetate, lithium, sodium , Potassium or calcium amide, sodium, potassium, calcium or cesium carbonate, sodium, potassium or calcium bicarbonate, lithium, sodium, potassium or calcium hydride, lithium, sodium, potassium or calcium hydroxide, sodium or potassium methoxide, ethanolate, n- or i-propanolate, n-, -i-, -s- or -t-butanolate; furthermore also basic organic nitrogen compounds, such as trimethylamine, triethylamine, tripropylamine, tributylamine, ethyldiisopropylamine, N
- the process (F) according to the invention is optionally carried out in the presence of a catalyst.
- a catalyst As such, all catalysts which are commonly used for hydrogenations are suitable. Examples include: Raney nickel, palladium or platinum, optionally on a support material, such as activated carbon.
- suitable reaction auxiliaries when carrying out the first step of process (G) according to the invention are the customary inorganic or organic bases or acid binders.
- These include, preferably, alkali metal or alkaline earth metal acetates, amides, carbonates, bicarbonates, hydrides, hydroxides or alkoxides, such as, for example, sodium, potassium or calcium acetate, lithium, sodium, potassium or Calcium amide, sodium, potassium or calcium carbonate, sodium, potassium or calcium bicarbonate, lithium, sodium, potassium or calcium hydride, lithium, sodium, potassium or calcium hydroxide, sodium or potassium methoxide, ethanolate, n- or -propanolate, n-, -is-, -s, or -t-butanolate; furthermore also basic organic nitrogen compounds, such as, for example, trimethylamine, triethylamine, tripropylamine, tributylamine, e
- DBU 1,8-diazabicyclo [5.4.0] undec-7-ene
- DBU undec-7-ene
- l, 8-diazabicyclo [5.4.0] undec-7-ene (DBU) is used.
- suitable reaction auxiliaries when carrying out process (G) according to the invention are a combination of trialkyl- or triarylphosphines and azodicarboxylates. These preferably include triphenyl phosphine and diethyl azodicarboxylate (DEAD) or diisopropyl azodicarboxylate (DIAD).
- DEAD diethyl azodicarboxylate
- DIAD diisopropyl azodicarboxylate
- either hydrazine hydrate or a mixture of organic and inorganic acids is suitable.
- these preferably include glacial acetic acid, hydrochloric acid, hydrobromic acid. Preference is given to using a mixture of glacial acetic acid and hydrobromic acid.
- inventive methods are generally carried out under atmospheric pressure. However, it is also possible to work under elevated or reduced pressure, generally between 0, 1 bar and 10 bar.
- acyl (het) aryl of the formula (IT) is generally 1 mole of acyl (het) aryl of the formula (Ha) and between 0.9 and 1, 1 mol , Preferably 1 mol, of bishydroxylamine of the formula (HI) and 0.1 mol of a catalyst. If a bishydrohalide of bishydroxylamine of the formula (HI) is used, 0.1 to 0.5 mol of catalyst are used. However, it is also possible to use the reaction components in other proportions.
- the workup is carried out by conventional methods. In general, the procedure is that the reaction mixture is mixed with water, the organic phase is separated off and concentrated after drying under reduced pressure. If desired, the remaining residue can be freed of impurities which may still be present by customary methods, such as chromatography or recrystallization.
- the organic phase is separated and concentrated after drying under reduced pressure. If desired, the remaining residue can be freed of impurities which may still be present by customary methods, such as chromatography or recrystallization.
- the second step of the process (A-2) according to the invention is set to 1 mol of the hydroxylamine of the formula (XH) between 0.9 and 1.1 mol, preferably 1 mol, of acyl (het) aryl of the formula (Da) and 0.1 Mol of a catalyst.
- the workup is carried out by conventional methods. In general, the procedure is that the reaction mixture is mixed with water, the organic phase is separated off and concentrated after drying under reduced pressure. If desired, the remaining residue can be freed of impurities which may still be present by customary methods, such as chromatography or recrystallization.
- the amount of ozone used in the first step for 1 mol of bisoximes of the formula (Ib) is such that the reaction to form the bisoximes of the formula (Ic) is complete by thin-layer chromatography.
- 1 mol of bisoximes of the formula (Ic) IMoI of hydroxylamine of the formula (VH).
- the reaction components in other proportions.
- the workup is carried out according to customary D ⁇ ⁇ - u on
- the procedure is that the reaction mixture is mixed with water, the precipitate is separated off and dried. If desired, the remaining residue can be freed of impurities which may still be present by customary methods, such as chromatography or recrystallization.
- the procedure in the first step in such a way that the reaction mixture is mixed with water, the precipitate separated and dried.
- the second step is generally followed by filtering the reaction mixture and concentrating the filtrate under reduced pressure. If desired, the remaining residue can be freed of impurities which may still be present by customary methods, such as chromatography or recrystallization.
- the erf ⁇ ndungswen substances have a strong microbicidal activity and can be used for controlling unwanted microorganisms, such as fungi and bacteria, in crop protection and in the protection of materials. > o, -
- Fungjzide can be plant protection used to combat Plasmodiophoromycetes, Oomycetes, Chytridiomycetes, Zygomycetes, Ascomycetes, Basidiomycetes and Deuteromycetes.
- Bactericides can be used in crop protection for controlling Pseudomonadaceae, Rhizobiaceae, Enterobacteriaceae, Corynebacteriaceae and Streptomycetaceae.
- Diseases caused by powdery mildews such as e.g. Blumeria species, e.g. Blumeria graminis; Podosphaera species, e.g. Podosphaera leucotricha; Sphaerotheca species, e.g. Sphaerotheca fuliginea; Uncinula species, e.g. Uncinula necator; Diseases caused by causative agents of rust diseases, such as Gymnosporangium species, e.g. Gymnosporangium sabinae; Hemileia species, e.g. Hemileia vastatrix; Phakopsora species, e.g.
- powdery mildews such as e.g. Blumeria species, e.g. Blumeria graminis; Podosphaera species, e.g. Podosphaera leucotricha; Sphaerotheca species, e.g. Sphaer
- Phakopsora pachyrhizi and Phakopsora meibomiae Puccinia species, e.g. Puccinia recondita or Puccinia graminis; Uromyces species, e.g. Uromyces appendiculatus; Diseases caused by pathogens of the group of Oomycetes, e.g. Bremia species, e.g. Bremia lactucae; Peronospora species, e.g. Peronospora pisi or P. brassicae; Phytophthora species, e.g. Phytophthora infestans; Plasmopara species, e.g.
- Plasmopara viticola Pseudoperonospora species, such as e.g. Pseudoperonospora humuli or Pseudoperonospora cubensis; Pythium species, e.g. Pythium ultimum;
- Mycosphaerella graminicola and Mycosphaerella f ⁇ jiensis Phaeosphaeria species, e.g. Phaeosphaeria nodorum
- Pyrenophora species e.g. Pyrenophora teres
- Ramularia species e.g. Ramularia collo-cygni
- Rhynchosporium species e.g. Rhynchosporium secalis
- Septoria species e.g. Septoria apii
- Typhula species such as e.g. Typhula incarnata
- Venturia species e.g. Venturia inaequalis
- Root and stem diseases caused by eg Corticium species such as Corticium gramineanim; Fusarium species, such as Fusarium oxysporum; Gaeumannomyces species, such as p ⁇ - iua
- Gaeumannomyces graminis e.g. Rhizoctonia solani
- Tapesia species e.g.
- Tapesia acuformis or Tapesia yallundae Thielaviopsis species, e.g. TTiielaviopsis basicola;
- Ear and panicle diseases caused by e.g. Alternaria species, e.g. Alternaria spp .; Aspergillus species, e.g. Aspergillus flavus; Cladosporium species, e.g. Cladosporium cladosporioides; Claviceps species, e.g. Claviceps purpurea; Fusarium species, e.g. Fusarium culmorum; Gibberella species, e.g. Gibberella zeae; Monographella species, e.g.
- Sphacelotheca species e.g. Sphacelotheca reiliana
- Tületia species e.g. Tilletia caries
- Urocystis species e.g. Urocystis occulta
- Ustilago species e.g. Ustilago nuda
- Aspergillus species e.g. Aspergillus flavus
- Botrytis species e.g. Botrytis cinerea
- Penicillium species e.g. Penicillium expansum and penicillium purpurogenum
- Sclerotinia species e.g. Sclerotinia sclerotiorum
- Verticilium species such as e
- Fusarium species e.g. Fusarium culmorum
- Phytophthora species e.g. Phytophthora cactorum
- Pythium species e.g. Pythium ultimum
- Rhizoctonia species e.g. Rhizoctonia solani
- Sclerotium species such as e.g. Sclerotium rolfsii
- Nectria species e.g. Nectria galligena
- Botrytis species e.g. Botrytis cinerea
- Rhizoctonia species e.g. Rhizoctonia solani
- Helminthosporium species e.g. Helminthosporium solani
- Xanthomonas species e.g. Xanthomonas campestris pv. Oryzae
- Pseudomonas species e.g. Pseudomonas syringae pv. Lachrymans
- Erwinia species e.g. Erwinia amylovora
- the following diseases of soybean beans can be controlled:
- Anthracnose (Colletotrichum gloeosporoides dematium var. Truncatum), Brown spot (Septoria glycines), Cercospora leaf spot and blight (Cercospora kikuchii), Choan ⁇ hora leaf blight (Choanephora infundibulifera trispora (Syn.)) , Dactuliophora leaf spot (Dactuliophora glycines), Downy Mildew (Peronospora manshurica), Drechslera blight - 60 -
- Black Root Red (Calonectria crotalariae), Charcoal Red (Macrophomina phaseoüna), Fusarium Blight or Wiit, Root Red, and Pod and Collar Red (Fusarium oxysporum, Fusarium orthoceras, Fusarium semitectum, Fusarium equiseti), Mycoleptodiscus Root Red (Mycoleptodiscus terrestris), Neocosmospora (Neocosmopspora vasinfecta), Pod and Stem Blight (Diaporthe phaseolorum), Stem Canker (Diaporthe phaseolorum var.
- Phytophthora red (Phytophthora megaspe ⁇ na), Brown Stem red (Phialophora gregata), Pythium red (Pythium aphanidermatum, Pythium irregular , Pythium debaryanum, Pythium myriotylum, Pythium ultimum), Rhizoctonia Root Red, Stem Decay, and Damping Off (Rhizoctonia solani), Sclerotinia Stem Decay (Sclerotinia sclerotiorum), Sclerotinia Southern Blight (Sclerotinia rolfsii), Thielaviopsis Root Red (Thielaviopsis basicola) ,
- the active compounds according to the invention also have a strong tonic effect in plants. They are therefore suitable for mobilizing plant-own defenses against attack by unwanted microorganisms.
- plant-strengthening (resistance-inducing) substances are to be understood as meaning those substances which are capable of stimulating the defense system of plants in such a way that the treated plants exhibit extensive resistance to these microorganisms with subsequent inoculation with undesired microorganisms.
- Undesirable microorganisms in the present case are phytopathogenic fungi, bacteria and viruses.
- the substances according to the invention can therefore be used to protect plants within a certain period of time after the treatment against attack by said pests.
- the period within which protection is provided generally extends from 1 to 10 days, preferably 1 to 7 days after the treatment of the plants with the active ingredients.
- the active compounds according to the invention can be used with particularly good success for controlling cereal diseases, such as, for example, against Puccinia species and Pyrenophora species and diseases in wine, fruit and vegetable crops, such as e.g. against Botrytis, Venturia or Alternaria species.
- the active compounds according to the invention are also suitable for increasing crop yield. They are also low toxicity and have good plant tolerance.
- the active compounds according to the invention may optionally also be used in certain concentrations and application rates as herbicides, for influencing plant growth and for controlling animal pests. If appropriate, they can also be used as intermediates and precursors for the synthesis of other active ingredients.
- plants are to be understood as meaning all plants and plant populations, such as desired and unwanted plants or crop plants (including naturally occurring crop plants).
- Crop plants can be plants which 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 the plant varieties which can or can not be protected by plant breeders' rights.
- Plant parts are to be understood as meaning all aboveground and subterranean parts and organs of the 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 crops and vegetative and generative propagation material, such as cuttings, tubers, rhizomes, offshoots and seeds.
- the treatment according to the invention of the plants and plant parts with the active ingredients is carried out directly or by acting on their environment, habitat or storage space according to the usual treatment methods, e.g. by dipping, spraying, vaporizing, atomizing, spreading, spreading and in propagation material, in particular in seeds, further by single or multi-layer wrapping.
- the substances according to the invention can be used to protect industrial materials against infestation and destruction by undesired microorganisms.
- Technical materials as used herein mean non-living materials that have been prepared for use in the art.
- technical materials to be protected from microbial alteration or destruction by the active compounds of the present invention may be adhesives, glues, paper and board, textiles, leather, wood, paints and plastics, coolants and other materials used by microorganisms. .
- microorganisms that can cause degradation or a change in the technical materials, for example, bacteria, fungi, yeasts, algae and mucus organisms may be mentioned.
- the active compounds according to the invention preferably act against fungi, in particular molds, wood-discolouring and wood-destroying fungi (Basidiomycetes) and against slime organisms and algae.
- microorganisms of the following genera There may be mentioned, for example, microorganisms of the following genera:
- Alternaria such as Alternaria tenuis, Aspergillus such as Aspergillus niger, Chaetomium such as Chaetomium globosum, Coniophora such as Coniophora puetana, Lentinus such as Lentinus tigrinus, Penicillium such as Penicillium glaucum, Polyporus such as Polyporus versicolor, Aureobasidium such as Aureobasidium pullulans, Sclerophoma, such as Sclerophoma pityophila, Trichoderma such as Trichoderma viride, Escherichia such as Escherichia coli, Pseudomonas such as Pseudomonas aeruginosa, Staphylococcus such as Staphylococcus aureus.
- Coniophora such as Coniophora puetana
- Lentinus such as Lentinus tigrinus
- the active compounds according to the invention are suitable for plant tolerance, favorable warm-blood toxicity and good environmental compatibility for the protection of plants and plant organs, for increasing crop yields, improving the quality of the emetic and for controlling animal pests, in particular insects, arachnids, helminths, nematodes and molluscs which are found in agriculture, horticulture, livestock, forests, gardens and recreational facilities, in the protection of materials and materials and in the hygiene sector. They can preferably be used as crop protection agents. They are effective against normally sensitive and resistant species as well as against all or individual stages of development.
- the above mentioned pests include:
- Anoplura e.g. Damalinia spp., Haematopinus spp., Linognathus spp., Pediculus spp., Trichodectes spp.
- Epitrimerus pyri Eutetranychus spp., Eriophyes spp., Hemitarsonemus spp., Hyalomma spp., Ixodes spp., Latrodectus mactans, Metatetranychus spp., Oligonychus spp., Ornithodoros spp., Panonychus spp., Phyllocoptruta oleivora, Polyphagotarsonemus Latus, Psoroptes spp., Rhipicephalus spp., Rhizoglyphus spp., Sarcoptes spp., Sco ⁇ io maurus, Stenotarsonemus spp., Tarsonemus spp, Tetranychus spp, Vasates lycopersici.
- Diptera e.g. Aedes spp., Anopheles spp, Bibio hortulanus, Calliphora erythrocephala, Ceratitis capitata, Chrysomyia spp., Cochhomyia spp., Cordylobia anthropophaga, Culex spp, Cuterebra spp., Dacus oleae, Dermatobia hominis, Drosophila spp., Fannia spp., Gastrophus spp , Hylemyia spp., Hyppobosca spp., Hypoderma spp, Liriomyza spp.
- Gastropoda eg A ⁇ on spp., Biomphala ⁇ a spp, Bulinus spp., Deroceras spp., Galba spp., Lymnaea spp, Oncomelama spp., Succinea spp.
- helminths from the class of helminths, for example, Ancylostoma duodenale, Ancylostoma ceylanicum, Acylostoma braziliensis, Ancylostoma spp., Ascaris lubricoides, Ascans spp, Brugia malayi, Brugia timon, Bunostomum spp., Chabertia spp., Clonorchis spp, Copperia spp., Dicrocoehum spp, Dictyocaulus filaria, Diphyllobothrium latum, Dracunculus medinensis, Echinococcus granulosus, Echinococcus multilocularis, Enterobius vermicularis, Faciola spp., Haemonchus spp, Heterakis spp., Hymenolepis nana, Hyostrongulus spp., Loa Loa, Ne
- Trichinella nativa Trichinella britovi, Trichinella nelsoni, Trichinella pseudopsiralis, Trichostrongulus spp., Trichuris trichuria, Wuchereria bancrofti. Furthermore, protozoa, such as Eimeria, can be combated.
- Heliopeltis spp. Horcias nobilellus, Leptocorisa spp., Leptoglossus phyllopus, Lygus spp., Macropes excavatus, Miridae, Nezara spp., Oebalus spp., Pentomidae, Piesma quadrata, Piezodorus spp., Psallus seriatus, Pseudacysta persea, Rhodnius spp. Sahlbergella singularis, Scotinophora spp., Stephanitis nashi, Tibraca spp., Triatoma spp.
- Psylla spp. Pteromalus spp., Pyrilla spp., Quadraspidiotus spp., Quesada gigas, Rastrococcus spp., Rhopalosiphum spp., Saissetia spp., Scaphoides titanus, Schizaphis graminum, Selenaspidus articulatus, Sogata spp., Sogatella furcifera, Sogatodes spp.
- Stictocephala festina Tenalaphara malayensis, Tinocallis caryaefoliae, Tomaspis spp., Toxoptera spp., Trialeurodes vaporariorum, Trioza spp., Typhlocyba spp., Unaspis spp., Viteus v. Chr itifolii.
- Hymenoptera e.g. Diprion spp., Hoplocampa spp., Lasius spp., Monomorium pharaonis, Vespa spp.
- isopods e.g. Armadillidium vulgaris, Oniscus asellus, Porcellio scaber.
- Isoptera e.g. Reticulitermes spp., Odontotermes spp.
- Pectinophora gossypiella Phyllocnistis citrella, Pieris spp., Plutella xylostella, Prodenia spp., Pseudodia spp., Pseudoplusia includens, Pyrausta nubilalis, Spodoptera spp., Thermesia gemmatalis, Tinea pellionella, Tineola bisselliella, Tortrix viridana, Trichoplusia spp. From the order of Orthoptera e.g. Acheta domesticus, Blatta orientalis, Blattella germanica,
- Gryllotalpa spp. Leucophaea maderae, Locusta spp., Melanoplus spp., Periplaneta americana,
- siphonaptera e.g. Ceratophyllus spp., Xenopsylla cheopis.
- Symphyla e.g. Scutigerella immaculata.
- Thysanoptera e.g. Basothrips biformis, Enneothrips flavens, Frankliniella spp.
- Heliothrips spp. Hercinothrips femoralis, Kakothrips spp., Rhipiphorothrips cruentatus, Scirtotbxips spp., Taeniothrips cardamoni, Thrips spp.
- Thysanura e.g. Lepisma saccharina.
- the plant parasitic nematodes include e.g. Anguina spp., Aphelenchoides spp., Belonoaimus spp., Bursaphelenchus spp., Ditylenchus dipsaci, Globodera spp., Heliocotylenchus spp., Heterodera spp., Longidorus spp., Meloidogyne spp., Pratylenchus spp., Radopholus similis, Rotylenchus spp.
- Trichodorus spp. Tylenchorhynchus spp., Tylenchulus spp., Tylenchulus semipenetrans, Xiphinema spp.
- the compounds according to the invention may optionally also be used in certain concentrations or herbicides as herbicides, safeners, growth regulators or agents for improving plant properties, or as microbiologicals, for example as fungicides, antimycotics, bactericides, viricides (including anti-viral agents) or as agents MLO (Mycoplasma-like-organism) and RLO (Rickettsia-like-organism) are used. If appropriate, they can also be used as intermediates or precursors for the synthesis of further active ingredients.
- the active compounds can be converted into the customary formulations, such as solutions, emulsions, suspensions, powders, foams, pastes, granules, aerosols, ultrafine encapsulations in polymeric substances and in seed coating compositions, as well as ULV -KaIt- and warm mist formulations.
- customary formulations such as solutions, emulsions, suspensions, powders, foams, pastes, granules, aerosols, ultrafine encapsulations in polymeric substances and in seed coating compositions, as well as ULV -KaIt- and warm mist formulations.
- the active compounds can be used as such, in the form of their formulations or prepared therefrom ca ⁇ o- i us
- Use forms such as ready-to-use solutions, emulsions, water- or oil-based suspensions, powders, wettable powders, pastes, soluble powders, dusts, soluble granules, scattering granules, suspension emulsion concentrates, active substance-impregnated natural substances, active substance-impregnated synthetic substances, fertilizers and ultrafine encapsulations be used in polymeric materials.
- the application is done in the usual way, e.g. by pouring, spraying, spraying, scattering, dusting, foaming, brushing, etc. It is also possible to apply the active ingredients by the ultra-low-volume method or to inject the active ingredient preparation or the active ingredient itself into the soil. It can also be the seed of the plants to be treated.
- formulations are prepared in a known manner, e.g. by mixing the active compounds with extenders, ie liquid solvents and / or solid carriers, if appropriate using surface-active agents, ie emulsifiers and / or dispersants and / or foam-forming agents.
- extenders ie liquid solvents and / or solid carriers
- surface-active agents ie emulsifiers and / or dispersants and / or foam-forming agents.
- Excipients which can be used are those which are suitable for imparting special properties to the composition itself and / or preparations derived therefrom (for example spray liquor, seed dressing), such as certain technical properties and / or specific biological properties.
- Typical auxiliaries are: extenders, solvents and carriers.
- polar and non-polar organic chemical liquids e.g. 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), 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 dimethyl sulfoxide).
- aromatic and non-aromatic hydrocarbons such as paraffins, alkylbenzenes, alkylnaphthalenes, chlorobenzenes
- alcohols and polyols which may also be substituted, etherified and / or esterified
- ketones such
- 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, e.g.
- Petroleum fractions such as butanol or glycol, and their ethers and esters, ketones, such as acetone, methyl ethyl ketone, methyl isobutyl ketone or cyclohexanone, strongly polar solvents, such as dimethylformamide and dimethyl sulfoxide, and water.
- alcohols such as butanol or glycol
- ketones such as acetone, methyl ethyl ketone, methyl isobutyl ketone or cyclohexanone
- strongly polar solvents such as dimethylformamide and dimethyl sulfoxide
- liquefied gaseous extenders or carriers liquids which are gaseous at normal temperature and under atmospheric pressure, for example aerosol propellants, such as - 67 - Halogenated hydrocarbons as well as butane, propane, nitrogen and carbon dioxide.
- aerosol propellants such as - 67 - Halogenated hydrocarbons as well as butane, propane, nitrogen and carbon dioxide.
- Suitable solid carriers are: e.g. Ammonium salts and ground natural minerals, such as kaolins, clays, talc, chalk, quartz, attapulgite, montmorulonite or diatomaceous earth, and ground synthetic minerals, such as fumed silica, alumina and silicates, as solid carriers for granules are suitable: e.g. crushed 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 paper, sawdust, coconut shells, corn cobs and tobacco stalks; suitable emulsifiers and / or foam formers are: e.g.
- nonionic and anionic emulsifiers such as polyoxyethylene fatty acid esters, polyoxyethylene fatty alcohol ethers, e.g. Alkylaryl polyglycol ethers, alkylsulfonates, alkyl sulfates, arylsulfonates and protein hydrolysates;
- suitable dispersants are non-ionic and / or ionic substances, e.g.
- adhesives such as carboxymethylcellulose, natural and synthetic powdery, gromige or latex-shaped polymers, such as gum arabic, polyvinyl alcohol, polyvinyl acetate, and natural phospholipids, such as cephalins and lecithins, and synthetic phospholipids.
- Other additives may be mineral and vegetable oils.
- Dyes such as inorganic pigments, e.g. Iron oxide, titanium oxide, ferrocyan blue and organic dyes such as alizarin, azo and metal phthalocyanine dyes and trace nutrients such as salts of iron, manganese, boron, copper, cobalt, molybdenum and zinc.
- inorganic pigments e.g. Iron oxide, titanium oxide, ferrocyan blue and organic dyes such as alizarin, azo and metal phthalocyanine dyes and trace nutrients such as salts of iron, manganese, boron, copper, cobalt, molybdenum and zinc.
- additives may be fragrances, mineral or vegetable optionally modified oils, waxes and nutrients (also trace nutrients), such as salts of iron, manganese, boron, copper, cobalt, molybdenum and zinc.
- the formulations generally contain between 0.01 and 98% by weight, preferably between 0.1 and 95% by weight, more preferably between 0.5 and 90% of active ingredient.
- the active compounds according to the invention can also be used in admixture with known fungicides, bactericides, acaricides, nematicides or insecticides, so as to obtain e.g. to broaden the spectrum of action or to prevent development of resistance.
- known fungicides bactericides, acaricides, nematicides or insecticides, so as to obtain e.g. to broaden the spectrum of action or to prevent development of resistance.
- the following compounds are suitable as mixed partners: Fungicides:
- Inhibitors of nucleic acid synthesis e.g. Benalaxyl, Benalaxyl M, Bupirimate, Clozylacone, Dimethirimol, Ethirimol, Furalaxyl, Hymexazole, Mefenoxam, Metalaxyl, Metalaxyl-M, Ofurace,
- inhibitors of mitosis and cell division e.g. Benomyl, carbendazim, diethofencarb, ethaboxam, fuberidazole, pencycuron, thiabendazole, thiophanate-methyl, zoxamide;
- respiratory inhibitors 3.1) inhibitors of complex I of the respiratory chain: e.g. diflumetorim;
- inhibitors at the complex II of the respiratory chain e.g. Boscalid, carboxin, fenfuram, flutolanil, furametpyr, furmecyclox, myronil, oxycarboxin, penthiopyrad, thifluzamide;
- inhibitors at the complex IE of the respiratory chain e.g. Amisulbrom, azoxystrobin, cyazofamide, dimoxystrobin, enestrobin, famoxadone, fenamidone, fluoxastrobin, kresoxim-methyl, metomino-strobin, orysastrobin, picoxystrobin, pyraclostrobin, trifloxystrobin;
- decoupler e.g. Dinocap, fluazinam, meptyldinocap;
- Inhibitors of ATP production e.g. Fentin acetate, Fentin Chloride, Fentin hydroxide, Silthiofam;
- Inhibitors of amino acid and protein biosynthesis e.g. Andoprim, blasticidin-S, cyprodinil, kasugamycin, kasugamycin hydrochloride hydrate, mepanipyrim, pyrimethanil;
- Signal transduction inhibitors e.g. Fenpiclonil, fludioxonil, quinoxyfen;
- Inhibitors of lipid and membrane synthesis e.g. Biphenyl, chlozolinates, edifenphos, etridiazoles, iodocarb, Iprobenfos, iprodione, isoprothiolanes, procymidones, propamocarb, propamocarb hydrochloride, pyrazophos, tolclofos-methyl, vinclozolin;
- inhibitors of ergosterol biosynthesis for example aldimorph, azaconazole, bitertanol, bromuconazoles, cyproconazole, diclobutrazoles, difenoconazole, diniconazole, diniconazole-M, dodemorph, dodemorph acetate, epoxiconazole, etaconazole, fenarimol, fenbuconazole, fenhexamide, fenpropidin, fenpropimorph, Fluquinconazole, flurprimidol, flusilazole, flutriafol, furconazole, furconazole-cis, hexaconazole, imazalil, hitiazalil sulfate, imibenconazole, ipconazole, metconazole, myclobutanil, naftifine, nuarimol, oxpoconazole, paclobutrazole
- inhibitors of cell wall synthesis e.g. Benthiavalicarb, dimethomorph, flumorph, iprovalicarb, mandipropamide, polyoxins, polyoxorim, validamycin A;
- Inhibitors of melanin biosynthesis e.g. Carpropamide, diclocymet, fenoxanil, phthalides,
- 1 l carbamates eg alanycarb, aldicarb, aldoxycarb, allyxycarb, aminocarb, azamethiphos,
- Pyrethroids eg acrinathrin, allethrin (d-cis-trans, d-trans), beta-cyfluthrin, bifenthrin, biotethrin, bioallethrin-S-cyclopentylisomer, bioethanomethrin, biopermethrin, bioresmethrin, chlovapethrin, cis-cypermethrin , Cis-resmethrin, cis-permetlirine, clocthrin, cycloprothrin, cyfluthrin, cyhalothrin, cypermethrin (alpha-, beta-, theta-, zeta-), cyphenothrin, DDT, deltamethrin, empenthrin (IR isomer), esfenvalerate, etofenprox, fenfluthrin ,
- Oxadiazines e.g., Indoxacarb
- chloronicotinyls / neonicotinoids e.g., acetamiprid, clothianidin, dinotefiran, imidacloprid, nitenpyram, nithiazines, thiacloprid, thiamethoxam
- Nicotine Bensultap, Cartap
- Fiproles e.g., acetoprole, ethiprole, fipronil, vaniliprole 6 chloride channel activators
- Mectins e.g., abamectin, avermectin, emamectin, emamectin benzoate, ivermectin, milbemectin,
- Diacylhydrazines e.g., chromafenozides, halofenozides, methoxyfenozides, tebufenozides
- Inhibitors of chitin biosynthesis e.g., chromafenozides, halofenozides, methoxyfenozides, tebufenozides
- Benzoylneas eg, bistrifluron, chlorofluazuron, diflubenzuron, fluazuron, flucycloxuron, fenphenoxuron, hexaflumuron, lufenuron, novaluron, noviflumuron, penfluron, teflubenzuron, tri .
- Organotin e.g., azocyclotin, cyhexatin, fenbutatin oxides
- Dirritrophenols e.g., binapacyrl, dinobutone, dinocap, DNOQ 12.
- Side-1 electron-transport inhibitors e.g., side-1 electron-transport inhibitors
- METI's e.g., Fenazaquin, Fenpyroximate, Pyrimidifen, Pyridaben, Tebufenpyrad, Tolfenpyrad
- Tetronic acids e.g., spirodiclofen, spiromesifen
- 16.2 tetramic acids [e.g. 3- (2,5-Dimethylphenyl) -8-methoxy-2-oxo-1-azaspiro [4.5] dec-3-en-4-yl ethyl carbonate (also known as: Carbonic acid, 3- (2,5-dimethylphenyl) -8-methoxy-2-oxo-1-azaspiro [4.5] dec-3-en-4-yl ethyl ester, CAS Reg.
- C ⁇ rbox ⁇ mide e.g., flonicamid
- Octopa-Miner agonists e.g., Amitraz
- Inhibitors of magnesium-stimulated ATPase e.g., propargites
- Agonists of the ryanodine receptor e.g., Amitraz
- fumigants e.g., aluminum phosphides, methyl bromides, sulfuryl fluorides
- mite growth inhibitors eg clofentezine, etoxazole, hexythiazox 23.4 amidoflumet, benclothiazole, benzoximate, bifenazate, bromopropylate, buprofezin, quinomethionate, chlordimeform, chlorobenzilate, chloropicrin, clothiazoben, cycloprene, cyflumetofen, dicyanil, fenoxacrim, fentrifanil, flubenzimine, flufenerim , Flutenzin, Gossyplure, Hydramethylnone, Japonilure, Metoxadiazone, Petroleum, Piperonyl butoxide, Potassium oleate, Pyrafluprole, Pyridalyl, Pyriprole, Sulfluramid, Tetradifene, Tetrasul, Triarathene, Verbutin, furthermore the compound 3-methyl-phenyl-propylc
- the compounds of the formula (I) according to the invention also have very good antifungal effects. They have a very broad antimycotic spectrum of activity, in particular against dermatophytes and yeasts, mold and diphasic fungi (eg against Candida species such as Candida albicans, Candida glabrata) and Epidermophyton floccosum, Aspergillus species such as Aspergillus niger and Aspergillus fumigatus, Trichophyton species such as Trichophyton mentagrophytes, Microsporon species such as Microsporon canis and audouinii.
- Candida species such as Candida albicans, Candida glabrata
- Epidermophyton floccosum Aspergillus species such as Aspergillus niger and Aspergillus fumigatus
- Trichophyton species such as Trichophyton mentagrophytes
- Microsporon species such as Microsporon canis and audouinii.
- the list of these fungi is by no means
- the application rate of the active compounds according to the invention is the same as the active compounds according to the invention.
- seed treatment from 2 to 200 g per 100 kg of seed, preferably from 3 to 150 g per 100 kg of seed, more preferably from 2.5 to 25 g per 100 kg of seed, most preferably from 2.5 to 12, 5 g per 100 kg of seed;
- the active compounds or compositions according to the invention can therefore be used to protect plants against the infestation by the named pests within a certain period of time after the treatment.
- the period within which protection is provided generally extends from 1 to 28 days, preferably 1 to 14 days after the treatment of the plants with the active ingredients or up to 200 days after a seed treatment.
- DON Deoxynivalenol
- Nivalenol Nivalenol
- 15-Ac-DON 3-Ac-DON
- T2- and HT2-toxin Fumonisins
- Zearalenone Monilifolinin
- Fusarin Diaceotoxyscirpenol
- DAS Diaceotoxyscirpenol
- mycotoxins Beauvericin, enniatine, fusaroproliferin, fusarenol, ochratoxins, patulin, ergot alkaloids and aflatoxins, which may be caused, for example, by the following fungi: Fusarium spec., Such as Fusarium acuminatum, F.
- the present invention therefore more particularly relates to a method of protecting seeds and germinating plants from the infestation of phytopathogenic fungi by treating the seed with an agent according to the invention.
- the invention also relates to the use of the seed treatment agents of the invention for protecting the seed and the germinating plant from phytopathogenic fungi.
- the invention relates to seed which has been treated with an agent according to the invention for protection against phytopathogenic fungi.
- One of the advantages of the present invention is that because of the particular systemic properties of the compositions of the invention, treatment of the seed with these agents not only protects the seed itself, but also the resulting plants after emergence from phytopathogenic fungi. In this way, the immediate treatment of the culture at the time of sowing or shortly afterwards can be omitted.
- mixtures according to the invention can also be used in particular in the case of transgenic seed.
- compositions according to the invention are suitable for the protection of seeds of any plant variety used in agriculture, in the greenhouse, in forests or in horticulture.
- these are seeds of cereals (such as wheat, barley, rye, millet and oats), corn, cotton, soy, rice, potatoes, sunflower, bean, coffee, turnip (eg sugarbeet and fodder), peanut, vegetables ( like tomato, cucumber, onions and lettuce), lawn and ornamental plants.
- cereals such as wheat, barley, rye, millet and oats
- corn such as wheat, barley, rye, millet and oats
- peanut like tomato, cucumber, onions and lettuce
- the agent according to the invention is applied to the seed alone or in a suitable formulation.
- the seed is treated in a condition that is so stable that no damage occurs during the treatment.
- the treatment of the seed can be done at any time between harvesting and sowing.
- seed may be used which has been harvested, cleaned and dried to a moisture content below 15% by weight.
- seed can also be used which has been treated with water after drying, for example, and then dried again.
- the agents according to the invention can be applied directly, ie without containing further components and without being diluted.
- suitable formulations and methods for seed treatment are known to those skilled in the art and are described e.g. in the following documents: US 4,272,417 A, US 4,245,432 A, US 4,808,430 A, US 5,876,739 A, US 2003/0176428 A1, WO 2002/080675 A1, WO 2002/028186 A2.
- the active compound combinations that can be used according to the invention can be converted into the customary seed dressing formulations, such as solutions, emulsions, suspensions, powders, foams, slurries or other seed coating compositions, as well as ULV formulations.
- formulations are prepared in a known manner by mixing the active ingredients or combinations of active ingredients with conventional additives, such as conventional extenders and solvents or diluents, dyes, wetting agents, dispersants, emulsifiers, defoamers, preservatives, secondary thickeners, adhesives, gibberellins and also Water.
- conventional additives such as conventional extenders and solvents or diluents, dyes, wetting agents, dispersants, emulsifiers, defoamers, preservatives, secondary thickeners, adhesives, gibberellins and also Water.
- Dyes which may be present in the seed dressing formulations which can be used according to the invention are all dyes customary for such purposes. Both water-insoluble pigments and water-soluble dyes are useful in this case. Examples which may be mentioned under the names rhodamine B, CI. Pigment Red 112 and CI. Solvent Red 1 known dyes.
- Suitable wetting agents which may be present in the seed dressing formulations which can be used according to the invention are all wetting-promoting substances customary for the formulation of agrochemical active compounds.
- usable are alkylhaphthalene sulfonates such as diisopropyl or dnsobutyl naphthalene sulfonates.
- Suitable dispersants and / or emulsifiers which may be present in the seed dressing formulations which can be used according to the invention are all nonionic, anionic and cationic dispersants customary for the formulation of agrochemical active compounds.
- nonionic or anionic dispersants or mixtures of nonionic or anionic dispersants.
- Particularly suitable nonionic dispersants are, in particular, ethylene oxide-propylene oxide, block polymers, alkylphenol polyglycol ethers and tristryrylphenol polyglycol ethers and their phosphated or sulfated derivatives.
- Suitable anionic dispersants are in particular lignosulfonates, polyacrylic acid salts and arylsulfonate-formaldehyde condensates.
- Defoamers which may be present in the seed-dressing formulations which can be used according to the invention are all foam-inhibiting substances customary for the formulation of agrochemical active compounds.
- Preferably usable are silicone defoamers and magnesium stearate.
- Preservatives which may be present in the seed dressing formulations which can be used according to the invention are all substances which can be used for such purposes in agrochemical compositions. Examples include dichlorophen and Benzylalkoholhemiformal.
- Suitable secondary thickeners which may be present in the seed dressing formulations which can be used according to the invention are all substances which can be used for such purposes in agrochemical compositions. Preference is given to cellulose derivatives, acrylic acid derivatives, xanthan, modified clays and finely divided silica.
- Suitable adhesives which may be present in the seed dressing formulations which can be used according to the invention are all customary binders which can be used in pickling agents.
- Preferably mentioned are polyvinylpyrrolidone, polyvinyl acetate, polyvinyl alcohol and Tylose.
- the gibberellins are known (see R. Wegler "Chemie der convinced- und SwdUngsbelampfungsstoff", Vol. 2, Springer Verlag, 1970, pp. 401-412).
- the seed dressing formulations which can be used according to the invention can be used either directly or after prior dilution with water for the treatment of seed of various kinds.
- the concentrates or the preparations obtainable therefrom by dilution with water can be used for dressing the seeds of cereals such as wheat, barley, rye, oats and triticale, as well as the seeds of corn, rice, rape, peas, beans, cotton, sunflowers and beets or even vegetable seeds of various nature.
- the seed dressing formulations which can be used according to the invention or their diluted preparations can also be used for pickling seeds - 78 - transgenic plants are used. In this case, additional synergistic effects may occur in interaction with the substances formed by expression.
- Beizung usable mixers into consideration. Specifically, in the pickling procedure, the seed is placed in a mixer which adds the desired amount of seed dressing formulations, either as such or after prior dilution with water, and until uniform
- the application rate of the seed dressing formulations which can be used according to the invention can be varied within a relatively wide range. It depends on the respective content of the active ingredients in the formulations and on the seed.
- the application rates of active ingredient combination are generally between 0.001 and 50 g per kilogram of seed, preferably between 0.01 and 15 g per kilogram of seed.
- the active compounds according to the invention may furthermore, when used as insecticides in their commercial formulations and in the forms of use prepared from these formulations, be present in mixtures with inhibitors which reduce degradation of the active ingredient after application in the environment of the plant, on the surface of plant parts or in plant tissues ,
- the active substance content of the application forms prepared from the commercial formulations can vary within wide ranges.
- the active ingredient concentration of the use forms may be from 0.00000001 up to 95% by weight of active compound, preferably between 0.00001 and 1% by weight.
- the application is done in a custom forms adapted to the application.
- plants and their parts can be treated.
- wild species or plant species obtained by conventional biological breeding methods such as crossing or protoplast fusion
- plant varieties and their parts are treated.
- transgenic plants and plant cultivars which have been obtained by genetic engineering methods, 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.
- Plant varieties are understood to be plants with new properties ("traits”), which can be obtained either by conventional breeding, by mutagenesis or by - 79 - recombinant DNA techniques have been bred. These may be varieties, breeds, biotypes and genotypes.
- the treatment according to the invention may also give rise to superadditive ("synergistic") effects, for example reduced application rates and / or extensions of the activity spectrum and / or a Strengthening of the effect of the substances and agents which can be used according to the invention, better plant growth, more developed root system, higher resistance of the plant species or plant variety, increased growth of the shoots, higher plant vitality, increased tolerance to high or low temperatures, increased tolerance to drought or to water or water Soil salinity, increased flowering efficiency, easier harvesting, acceleration of ripeness, higher crop yields, larger fruits, higher plant size, greener leaf color, earlier flowering, higher quality and / or higher nutritional value of the encearies, higher sugar concentration in the fruits, higher shelf life and / or workability of the harvested products possible, which go beyond the expected effects actually.
- superadditive superadditive
- the preferred plants or plant cultivars to be treated according to the invention include all plants which have obtained genetic material by the genetic engineering modification 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, increased flowering efficiency, easier harvest, acceleration of ripeness, higher crop yields, higher quality and / or higher nutritional value of the cured products, higher shelf life and / or workability of the product Further and particularly emphasized examples of such properties are an increased defense of the plants against animal and microbial pests, such as insects, mites, phytopathogenic fungi, bacteria and / or vire n as well as an increased tolerance of the plants against certain herbicidal active substances.
- microbial pests such as insects, mites, phytopathogenic fungi, bacteria and / or vire n as well as an increased tolerance of the plants against certain herbicidal active substances.
- transgenic plants include the important crops such as cereals (wheat, rice), corn, soybean, potato, cotton, tobacco, oilseed rape and fruit plants (with the fruits apple, pear, citrus and grape), with corn, soy, potato , Cotton, tobacco and oilseed rape.
- Traits which are particularly emphasized are the increased defense of the plants against insects, arachnids, nematodes and snails by toxins which are formed in the plants, in particular those which are produced by the genetic material from Bacillus thuringiensis (for example by the genes CryIA (a) , CryIA (b), CryIA (c), CryUA, CryfflA, CrymB2, Cry9c Cry2Ab, Cry3Bb, and CrylF, and combinations thereof) in the plants (hereafter, "3t plants”).
- the increased defense of plants against fungi, bacteria and viruses by systemic acquired resistance are also particularly emphasized - 80 -
- SAR systemin
- phytoalexins elicitors
- resistance genes correspondingly expressed proteins and toxins.
- Traits which are also particularly emphasized are the increased tolerance of the plants to certain herbicidally active compounds, for example imidazolinones, sulfonylureas, glyphosate or phosphinotricin (eg "P AT” gene), which confer the desired properties ("traits") in each case
- Planticidally active compounds for example imidazolinones, sulfonylureas, glyphosate or phosphinotricin (eg "P AT” gene), which confer the desired properties ("traits") in each case
- P AT phosphinotricin
- JBt plants include maize varieties, cotton varieties, soybean varieties and potato varieties sold under the trade names YlELD GARD® (eg maize, cotton, soya), KnockOut® (eg maize), StarLink® (eg maize), Bollgard® ( Cotton), Nucoton® (cotton) and NewLeaf® (potato)
- herbicide-tolerant plants include maize varieties, cotton varieties and soybean varieties sold under the trade names Roundup Ready® (tolerance to glyphosate eg corn, cotton, soy), Liberty Link® (tolerance to phosphinotricin, eg rapeseed), IMI® (tolerance to imidazolinone) and STS® (tolerance to sulfonylureas eg maize) are also marketed as herbicide-resistant (conventionally grown on herbicide tolerance) plants Of course, these statements also apply to future developed or future marketed products Plant varieties with these or future developed genetic traits.
- the active compounds of the invention not only act against plant, hygiene and storage pests, but also in the veterinary sector against animal parasites (ecto- and
- Endoparasites such as ticks, leather ticks, turnip bees, running mites, flies (stinging and licking), parasitic fly larvae, lice, hair-pieces, feathers and fleas.
- ticks such as ticks, leather ticks, turnip bees, running mites, flies (stinging and licking), parasitic fly larvae, lice, hair-pieces, feathers and fleas.
- Anoplurida e.g. Haematopinus spp., Linognathus spp., Pediculus spp., Phtirus spp., Solenopotes spp.
- Trimenopon spp. Menopon spp., Trinoton spp., Bovicola spp., Werneckiella spp., Lepikentron spp.
- Nematocerina and Brachycerina e.g. Aedes spp., Anopheles spp., Culex spp., Simulium spp., Eusimulium spp., Phlebotomus spp., Lutzomyia spp.,
- Philipomyia spp. Braula spp., Musca spp., Hydrotaea spp., Stomoxys spp., Haematobia spp., Morellia spp., Fannia spp., Glossina spp., Calliphora spp., Lucilia spp., Chrysomyia spp., Wohlfahrtia spp .,
- Sarcophaga spp. Oestrus spp., Hypoderma spp., Gasterophilus spp., Hippobosca spp., Lipoptena spp., Melophagus spp.
- siphonaptrida e.g. Pulex spp., Ctenocephalides spp., Xenopsylla spp.
- Actinedida Prostigmata
- Acaridida e.g. Acarapis spp., Cheyletiella spp., Ornitrocheyletia spp., Myobia spp., Psorergates spp., Demodex spp., Trombicula spp., Listrophorus spp., Acarus spp., Tyrophagus spp., Caloglyphus spp., Hypodectes spp., Pterolichus spp , Psoroptes spp., Chorioptes spp., Otodectes spp., Sarcoptes spp., Notoedres spp., Knemidocoptes spp., Cytodites spp., Laminosioptes spp.
- the active compounds of the formula (I) according to the invention are also suitable for controlling arthropods which are farm animals, such as e.g. Cattle, sheep, goats, horses, pigs, donkeys, camels, buffaloes, rabbits, chickens, turkeys, ducks, geese, bees, other pets such as e.g. Dogs, cats, caged birds, aquarium fish and so-called experimental animals, such. Hamsters, guinea pigs, rats and mice.
- arthropods are farm animals, such as e.g. Cattle, sheep, goats, horses, pigs, donkeys, camels, buffaloes, rabbits, chickens, turkeys, ducks, geese, bees, other pets such as e.g. Dogs, cats, caged birds, aquarium fish and so-called experimental animals, such. Hamsters, guinea pigs, rats and mice.
- the use of the active compounds according to the invention takes place in the veterinary sector and in animal husbandry in a known manner by enteral administration in the form of, for example, tablets, capsules, infusions, drenches, granules, pastes, boilies, the feed-through process, suppositories, by parenteral administration, as by injections (intramuscular, subcutaneous, intravenous, intraperitoneal, etc.), implants, by nasal application, by dermal application in the form of, for example, diving or bathing (dipping), spraying, pouring (pour-on and spot-on ), washing, powdering and with the aid of active substance-containing shaped articles, such as shark bands, ear tags, tail tags, limb bands, holsters, marking devices, etc.
- enteral administration in the form of, for example, tablets, capsules, infusions, drenches, granules, pastes, boilies, the feed-through process, suppositories
- parenteral administration as by injections (
- the active ingredients of the formula (T) can be used as formulations (for example powders, emulsions, flowable compositions) containing the active ingredients in an amount of from 1 to 80% by weight, directly or apply after 100 to 10,000 times dilution or use as a chemical bath.
- the compounds of the invention have a high insecticidal activity , - -
- insects such as Hylotrupes bajulus, Chlorophorus pilosis, Anobium punctatum, Xestobium rufovulius, Ptilinus pecticornis, Dendrobium pertinex, Ernobius mollis, Priobium ca ⁇ ini, Lyctus brunneus, Lyctus africanus, Lyctus planicollis, Lyctus ünearis, Lyctus pubescens, Trogoxylon aequale, Minthes rugicollis, Xyleborus spec. Tryptodendron spec.
- Non-living materials such as preferably plastics, adhesives, glues, papers and cardboard, leather, wood, wood processing products and paints.
- the ready-to-use agents may optionally contain further insecticides and optionally one or more fungicides.
- the compounds according to the invention can be used to protect against fouling of objects, in particular hulls, sieves, nets, structures, quay systems and signal systems, which come into contact with seawater or brackish water.
- the compounds according to the invention can be used alone or in combinations with other active substances as antifouling agents.
- the active compounds are also suitable for controlling animal pests in household, hygiene and storage protection, in particular of insects, arachnids and mites, which occur in enclosed spaces, such as apartments, factories, offices, vehicle cabs, etc. They can be used to control these pests, alone or in combination with other active ingredients and adjuvants in household insecticide products. They are effective against sensitive and resistant species and against all stages of development.
- These pests include: From the order of Scorpionidea eg Buthus occitanus. From the order of Acarina, for example, Argas persicus, Argas reflexus, Bryobia ssp., Dermanyssus gallinae, - 83 -
- Glyciphagus domesticus Ornithodorus moubat, Rhipicephalus sanguineus, Trombicula alfreddugesi,
- Opiliones e.g. Pseudoscorpiones chelifer, Pseudoscorpiones cheiridium, Opiliones phalangium.
- Sitophilus zeamais, Stegobium paniceum From the order of Diptera e.g. Aedes aegypti, Aedes albopictus, Aedes taeniorhynchus, Anopheles spp., Calliphora erythrocephala, Chrysozona pluvialis, Culex quinquefasciatus, Culex pipiens, Culex tarsalis, Drosophila spp., Fannia canicularis, Musca domestica, Phlebotomus spp., Sarcophaga carnaria,
- Lepidoptera e.g. Achroia grisella, Galleria mellonella, Plodia interpunctella, Tinea cloacella, Tinea pellionella, Tineola bisselliella.
- Ctenocephalides canis Ctenocephalides felis, Pulex irritans,
- Hymenoptera e.g. Camponotus herculeanus, Lasius fuliginosus, Lasius niger,
- Heteroptera e.g. Cimex hemipterus, Cimex lectularius, Rhodinus prolixus
- the application is carried out in aerosols, dry sprays, e.g. Pump and atomizer sprays, misting machines, foggers, foams, gels, evaporator products with cellulose or plastic evaporator plates, liquid evaporators, gel and membrane evaporators, propeller driven evaporators, energyless or passive evaporation systems, moth papers, moth cakes and moth gels, as granules or dusts, in litter or bait stations.
- aerosols dry sprays
- dry sprays e.g. Pump and atomizer sprays, misting machines, foggers, foams, gels, evaporator products with cellulose or plastic evaporator plates, liquid evaporators, gel and membrane evaporators, propeller driven evaporators, energyless or passive evaporation systems, moth papers, moth cakes and moth gels, as granules or dusts, in litter or bait stations.
- the listed plants can be treated particularly advantageously according to the invention with the compounds of general formula (T) or the active substance mixtures according to the invention.
- T general formula
- the preferred ranges given above for the active compounds or mixtures also apply to the treatment of these plants. Particularly emphasized is the plant treatment with the compounds or mixtures specifically mentioned in the present text.
- reaction mixture was stirred at room temperature for 12 hours and then admixed with 10 ml of water.
- the organic phase was separated off via a phase separation cartridge, concentrated and chromatographed on a silica gel cartridge (cyclohexane / ethyl acetate, vol. 2: 1).
- the specified logP values are determined according to EEC Directive 79/831 Annex V.A8 by HPLC (High Performance Liquid Chromatography) on a phase reversal column (C 18). Temperature: 43 ° C.
- the calibration is carried out with unbranched alkan-2-ones (having 3 to 16 carbon atoms) whose logP values are known (determination of the logP values by means of the retention times by linear interpolation between two consecutive alkanones).
- the lambda max values were determined on the basis of the UV spectra from 200 to 400 nm in the maxima of the chromatographic signals.
- dimethylacetamide emulsifier 1 part by weight of alkyl-aryl-polyglycol ether
- 0% means an efficiency which corresponds to that of the control, while an efficiency of 100% means that no infestation is observed.
- the compounds of the invention show 73, 141, 350, 420, 477, 499, 9, 182, 186, 188, 189, 1, 639, 14, 593, 88, 90, 91, 116, 112, 118, 134 , 174, 175, 180, 239, 240, 311, 292, 225, 224, 235, 236, 262, 277, 276, 281, 280, 304, 15, 62, 270, 264, 67, 70, 177, 202 , 204, 219, 248, 265, 295, 294, 296, 297, 298, 310, 313, 315, 316, 317, 321, 322, 519, 556, 555, 559, 562, 553, 557 and 558, as well as 364, 370, 372, 460, 474, 487, 501, 502, 697, 694, 6
- dimethylacetamide emulsifier 1 part by weight of alkyl-aryl-polyglycol ether
- compounds of the invention show 73, 141, 350, 420, 499, 9, 72, 81, 14, 212, 90, 91, 116, 112, 118, 134, 131, 136, 173, 174, 175, 239 , 292, 301, 225, 224, 235, 236, 280, 302, 303, 1, 15, 23, 270, 289, 67, 70, 181, 219, 251, 254, 266, 295, 294, 296, 297 , 298, 313, 315, 316, 317, 318, 319, 320, 322, 519, 550, 556, 555, 559, 554, 562, 553, 552, 557 and 558, as well as 364, 370, 372, 460, 474, 487, 501, 502, 699, 697, 694, 695, 570, 571, 572, 683, 592, 743, 659, 561, 677, 678, 587, 588, 589, 763
- a suitable preparation of active compound 1 part by weight of active compound is mixed with the indicated amounts of solvent and emulsifier, and the concentrate is diluted with water to the desired concentration.
- young wheat plants are sprayed with the preparation of active compound in the stated application rate. 1 day after the treatment, the plants are inoculated with a spore suspension of Puccinia recondita and then stand for 48 h at 100% relative humidity and 20 0 C then the plants are at 80% relative humidity and a temperature of 20 ° C. 8-10 days after inoculation, the evaluation is performed. In this case, 0% means an efficiency which corresponds to that of the control, while an efficiency of 100% means that no infestation is observed.
- compounds of the invention 250, 141, 538, 373, 375, 428, 460, 474, 487, 491, 499, 502, 9, 570, 571, 572, 14, 90, 91, 116, 112, 118 show , 239, 292, 225, 224, 235, 236, 277, 276, 280, 303, 304, 1, 15, 17, 18, 289, 248, 296, 298, 315, 316, 318, 319, 320, 556 , 555, 559, 554, 562, 553, 552, 557 and 558, and 772, 777, 699, XII-8, 697, 694, 695, 683, 743, 698, 14, 706, 269, 267, 561, 583, 582, 587, 589, 763, 679, 681 and 682, and also 880, 798, 364, 835, 786, 782, 785, 787, 806, 799, X ⁇ -14, 834
- Emulsifier 1 part by weight of alkylaryl polyglycol ether
- compounds of the invention show 250, 73, 141, 538, 364, 367, 370, 372, 420, 423, 427, 428, 429, 460, 487, 491, 499, 502, 504, 571, 572, 573 , 14, 32, 112, 97, 118, 134, 174,
- Emulsifier 1 part by weight of alkylaryl polyglycol ether
- a suitable active ingredient preparation 1 part by weight of active compound is mixed with the indicated amounts of solvent and emulsifier, and the concentrate is diluted with water to the desired concentration.
- To test for protective activity young plants are sprayed with the Wirkstoffzubereirung in the specified rate. After the spray coating has dried on, the plants are sprayed with a conidia suspension of Pyrenophora teres. The plants remain 48 hours at 20 0 C and 100% relative humidity in an incubation cabin. The plants are then placed in a greenhouse at a temperature of about 2O 0 C and relative humidity of about 80%. 8 days after the inoculation the evaluation takes place. In this case, 0% means an efficiency which corresponds to that of the control, while an efficiency of 100% means that no infestation is observed.
- compounds of the invention show 73, 141, 502, 9, 188, 1, 12, 16, 72, 14, 115, 88, 90, 91, 116, 112, 118, 164, 167, 180, 179, 239 , 240, 311, 301, 300, 225, 224, 235, 236, 276, 281, 303, 304, 312, 15, 11, 18, 62, 269, 270, 289, 67, 75, 70, 117, 181 , 204, 217, 216, 219, 254, 295, 294, 296, 297, 298 and 213, and XH-4, 672, 690, 359, 364, 370, 372, 420, 460, 474, 487, 491, 499, 501, 243, 244, 570, 571, 572, 683, 743, 637, 292, 277, 278, 264, 290, 248, 561, 315, 316, 321, 322, 519, 556, 555, 554,
- Emulsifier 0.5 part by weight of alkylaryl polyglycol ether
- 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 emulsifier-containing water to the desired concentration.
- Chinese cabbage leaf discs (Brassica pekinensis) infested with all stages of the green peach aphid (Myzus persicae) are sprayed with an active compound preparation of the desired concentration. After the desired time, the
- the compound of the invention indicates 600 (after 5 days) at a concentration
- dimemylformamide emulsifier 1.5 parts by weight of dimemylformamide emulsifier: 0.5 part by weight of alkylaryl polyglycol ether
- a suitable preparation of active compound 1 part by weight of active compound is mixed with the indicated amounts of solvent and emulsifier, and the concentrate is diluted with emulsifier-containing water to the desired concentration.
- Chinese cabbage leaf discs (Brassica pekinensis) are sprayed with a preparation of active compound of the desired concentration and, after drying, are populated with larvae of the horseradish leaf beetle (Phaedon cochleariae). After the desired time, the effect is determined in%. 100% means that all beetle larvae have been killed; 0% means that no beetle larvae have been killed. In this test, the compound 618 of the invention shows (after 7 days) at an active ingredient concentration of 500 ppm, an efficiency of 100%.
- a suitable preparation of active compound 1 part by weight of active compound is mixed with the indicated amounts of solvent and emulsifier, and the concentrate is diluted with water to the desired concentration.
- young plants are sprayed with the preparation of active compound in the stated application rate. After the spray coating has dried on, the plants are sprayed with a spore suspension of Leptosphaeria nodorum.
- the plants remain 48 hours at 2O 0 C and 100% relative humidity in an incubation cabin.
- the plants are placed in a greenhouse at a temperature of about 20 ° C and a relative humidity of 80%. 10 days after the inoculation the evaluation takes place. In this case, 0% means an efficiency which corresponds to that of the control, while an efficiency of 100% means that no infestation is observed.
- the application of the active ingredients is carried out as a liquid dressing, wherein 1 part by weight of the active ingredient is mixed with 10 parts by weight of a solvent. For each concentration tested, the appropriate volume is pipetted from the mixture. For pickling, shake the seed for 3 minutes after the pickling agent has been pipetted onto the seed in a sealed glass bottle. Seeds are sown in pots of 2 x 5 grains in a mixture of soil and sand. Perlites overgrown with Leptosphaeria maculans are sprinkled between the seeds and then covered 3 cm high with the soil and sand mixture. The pots are first incubated for 14 days at 10 c C and then cultivated for a further 7 days in a greenhouse at a temperature of about 18 ° C and 15 hours daily light. After approx. 3 weeks the evaluation takes place. In this case, 0% means an efficiency which corresponds to that of the control, while an efficiency of 100% means that no infestation is observed.
- compounds 118, 1 and 289 according to the invention show an efficacy of 70% or more at a concentration of active ingredient of 50 g / 100 kg of seed.
- the application of the active ingredients is carried out as a liquid dressing, wherein 1 part by weight of the active ingredient is mixed with 10 parts by weight of a solvent. For each concentration tested, the appropriate volume is pipetted from the mixture. For dressing, shake the seeds in a sealed glass bottle for 3 minutes after pipetting the preparation. Seeds are sown in pots of 3 * 12 seeds in a mixture of soil and sand. The pots are first incubated for 14 days at 5 0 C in the dark and then cultivated for 14 days in the greenhouse at a temperature of about 10 0 C and 15 hours daily light. The plants are then sprayed with a spore suspension of Septoria tritici and then placed for 21 days at a temperature of about 15 0 C and a relative humidity of 80%. 10 days after the inoculation the evaluation takes place. In this case, 0% means an efficiency which corresponds to that of the control, while an efficiency of 100% means that no infestation is observed. In this - 149 -
- Test show the inventive compounds 90, 91, 116 and 562 at an active ingredient concentration of 50 g / 100 kg of seed efficiency of 70% or more.
- the application of the active ingredients is carried out as a liquid dressing, wherein 1 part by weight of the active ingredient is mixed with 10 parts by weight of a solvent. For each concentration tested, the appropriate volume is pipetted from the mixture. For dressing, shake the seeds in a sealed glass bottle for 3 minutes after pipetting the preparation. The seeds are sown in pots of 3 x 12 grain in a soil / sand mixture. The pots are first incubated for 14 days at 5 ° C in the dark and then cultivated for a further 14 days in a greenhouse at a temperature of about 10 ° C and 15 hours daily light.
- the plants are then sprayed with a spore suspension of Puccinia recondita and then placed for 48 hours at 18 ° C and 100% relative humidity in an incubation booth.
- the plants are then placed in a greenhouse at a temperature of about 18 0 C and a relative humidity of 80%.
- 0% means an efficiency which corresponds to that of the control, while an efficiency of 100% means that no infestation is observed.
- the compound of the invention 141 shows an efficacy of 70% or more at a concentration of active ingredient of 50 g / 100 kg of seed.
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Abstract
Description
Claims
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
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JP2009541829A JP2010513343A (ja) | 2006-12-19 | 2007-12-11 | 殺真菌剤としてのビスオキシム |
US12/520,211 US20100022559A1 (en) | 2006-12-19 | 2007-12-11 | Bisoximes as fungicides |
EP07847062A EP2106214A2 (de) | 2006-12-19 | 2007-12-11 | Bisoxime als fungizide und arthropodizide |
BRPI0721274-7A BRPI0721274A2 (pt) | 2006-12-19 | 2007-12-11 | Bisoximas como fungicidas |
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DE102006059970 | 2006-12-19 | ||
DE102006059970.5 | 2006-12-19 | ||
DE102007023102.6 | 2007-05-16 | ||
DE102007023102A DE102007023102A1 (de) | 2006-12-19 | 2007-05-16 | Bisoxime als Fungizide |
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WO2008074418A2 true WO2008074418A2 (de) | 2008-06-26 |
WO2008074418A3 WO2008074418A3 (de) | 2009-08-06 |
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US (1) | US20100022559A1 (de) |
EP (1) | EP2106214A2 (de) |
JP (1) | JP2010513343A (de) |
AR (1) | AR064386A1 (de) |
BR (1) | BRPI0721274A2 (de) |
CL (1) | CL2007003704A1 (de) |
DE (1) | DE102007023102A1 (de) |
TW (1) | TW200833248A (de) |
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Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
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WO2012001040A1 (en) | 2010-07-02 | 2012-01-05 | Syngenta Participations Ag | Novel microbiocidal dioxime ether derivatives |
WO2012013754A1 (en) | 2010-07-29 | 2012-02-02 | Syngenta Participations Ag | Novel microbiocidal dioxime ether derivatives |
WO2012038521A1 (en) | 2010-09-23 | 2012-03-29 | Syngenta Participations Ag | Novel microbiocides |
WO2012062844A1 (en) | 2010-11-12 | 2012-05-18 | Syngenta Participations Ag | Novel microbiocides |
WO2012117021A2 (en) | 2011-03-03 | 2012-09-07 | Syngenta Participations Ag | Novel microbiocidal oxime ethers |
WO2013092460A1 (en) | 2011-12-20 | 2013-06-27 | Syngenta Participations Ag | Cyclic bisoxime microbicides |
EP2641901A1 (de) | 2012-03-22 | 2013-09-25 | Syngenta Participations AG. | Neue bisoxim mikrobiozide |
Families Citing this family (1)
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CN114773284B (zh) * | 2022-05-21 | 2024-03-29 | 河南大学 | 可见光介导的二氢异噁唑的合成方法 |
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2007
- 2007-05-16 DE DE102007023102A patent/DE102007023102A1/de not_active Withdrawn
- 2007-12-11 WO PCT/EP2007/010798 patent/WO2008074418A2/de active Application Filing
- 2007-12-11 BR BRPI0721274-7A patent/BRPI0721274A2/pt not_active Application Discontinuation
- 2007-12-11 US US12/520,211 patent/US20100022559A1/en not_active Abandoned
- 2007-12-11 EP EP07847062A patent/EP2106214A2/de not_active Withdrawn
- 2007-12-11 JP JP2009541829A patent/JP2010513343A/ja not_active Withdrawn
- 2007-12-17 AR ARP070105661A patent/AR064386A1/es unknown
- 2007-12-18 TW TW096148350A patent/TW200833248A/zh unknown
- 2007-12-19 CL CL200703704A patent/CL2007003704A1/es unknown
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WO1993016063A1 (de) * | 1992-02-13 | 1993-08-19 | Basf Aktiengesellschaft | Cyclohexenonoximether, verfahren zu ihrer herstellung und ihre verwendung als herbizide |
EP1362850A1 (de) * | 2001-02-20 | 2003-11-19 | Nippon Soda Co., Ltd. | Oximetherverbindung und bakterizid zum einsatz in der landwirtschaft bzw. im gartenbau |
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Cited By (9)
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WO2012001040A1 (en) | 2010-07-02 | 2012-01-05 | Syngenta Participations Ag | Novel microbiocidal dioxime ether derivatives |
US20130102631A1 (en) * | 2010-07-02 | 2013-04-25 | Syngenta Crop Protection Llc | Novel microbiocidal dioxime ether derivatives |
WO2012013754A1 (en) | 2010-07-29 | 2012-02-02 | Syngenta Participations Ag | Novel microbiocidal dioxime ether derivatives |
WO2012038521A1 (en) | 2010-09-23 | 2012-03-29 | Syngenta Participations Ag | Novel microbiocides |
WO2012062844A1 (en) | 2010-11-12 | 2012-05-18 | Syngenta Participations Ag | Novel microbiocides |
WO2012117021A2 (en) | 2011-03-03 | 2012-09-07 | Syngenta Participations Ag | Novel microbiocidal oxime ethers |
WO2013092460A1 (en) | 2011-12-20 | 2013-06-27 | Syngenta Participations Ag | Cyclic bisoxime microbicides |
EP2641901A1 (de) | 2012-03-22 | 2013-09-25 | Syngenta Participations AG. | Neue bisoxim mikrobiozide |
WO2013139822A1 (en) | 2012-03-22 | 2013-09-26 | Syngenta Participations Ag | Novel bisoxime microbiocides |
Also Published As
Publication number | Publication date |
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CL2007003704A1 (es) | 2008-07-04 |
TW200833248A (en) | 2008-08-16 |
WO2008074418A3 (de) | 2009-08-06 |
JP2010513343A (ja) | 2010-04-30 |
AR064386A1 (es) | 2009-04-01 |
EP2106214A2 (de) | 2009-10-07 |
US20100022559A1 (en) | 2010-01-28 |
DE102007023102A1 (de) | 2008-06-26 |
BRPI0721274A2 (pt) | 2014-04-01 |
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