Classifications

• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D265/00—Heterocyclic compounds containing six-membered rings having one nitrogen atom and one oxygen atom as the only ring hetero atoms
  • C07D265/02—1,2-Oxazines; Hydrogenated 1,2-oxazines
• • 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
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C259/00—Compounds containing carboxyl groups, an oxygen atom of a carboxyl group being replaced by a nitrogen atom, this nitrogen atom being further bound to an oxygen atom and not being part of nitro or nitroso groups
  • C07C259/04—Compounds containing carboxyl groups, an oxygen atom of a carboxyl group being replaced by a nitrogen atom, this nitrogen atom being further bound to an oxygen atom and not being part of nitro or nitroso groups without replacement of the other oxygen atom of the carboxyl group, e.g. hydroxamic acids
  • C07C259/06—Compounds containing carboxyl groups, an oxygen atom of a carboxyl group being replaced by a nitrogen atom, this nitrogen atom being further bound to an oxygen atom and not being part of nitro or nitroso groups without replacement of the other oxygen atom of the carboxyl group, e.g. hydroxamic acids having carbon atoms of hydroxamic groups bound to hydrogen atoms or to acyclic carbon atoms

Definitions

• the present invention relates to new [1.2] -oxazin-3,5-dione derivatives and their enols, several processes for their preparation and their use as
• Microbicides, pesticides and herbicides are Microbicides, pesticides and herbicides.
• 4-phenyl-substituted [1,2] -oxazin-3,5-diones are described as herbicides for the first time in WO 01/17972. Furthermore, 4-acyl-substituted [1.2] -oxazin-3,5-diones have been used as pesticides, but especially as herbicides and growth regulators, e.g. in EP-A-39 48 89, WO 92/07837, US 5,728,831.
• W represents hydrogen, halogen, alkyl or alkoxy
• X represents halogen, alkyl, alkoxy, haloalkyl, haloalkoxy or cyano
• Y in the 4-position represents hydrogen, alkoxy, halogen, cyano or haloalkyl
• Z in the 3 or 5 position represents hydrogen or alkyl
• W also represents hydrogen, halogen or alkyl
• X also represents halogen, alkyl, alkoxy, haloalkyl, haloalkoxy or cyano
• Y in the 4-position also represents optionally substituted aryl or hetaryl
• W also represents hydrogen, halogen or alkyl
• X also represents halogen, alkyl, alkoxy, haloalkyl, haloalkoxy or cyano
• Z also stands in the 5-position for optionally substituted aryl or hetaryl
• Y in the 4-position also represents hydrogen, alkyl or halogen
• W also represents hydrogen, methyl, propyl, isopropyl or halogen
• X also represents halogen, alkyl, alkoxy, haloalkyl, haloalkoxy or cyano
• Z in the 3 or 5 position also represents hydrogen, halogen or alkyl
• Y in the 4-position also represents hydrogen, halogen, alkyl, haloalkyl, cyano or haloalkoxy,
• a for hydrogen in each case optionally substituted by halogen, alkyl, alkenyl, alkoxyalkyl, polyalkoxyalkyl, alkylthioalkyl, saturated or unsaturated saturated, optionally substituted cycloalkyl in which at least one ring atom is optionally replaced by a heteroatom
• B represents hydrogen, alkyl or alkoxyalkyl, or
• a and B together with the carbon atom to which they are attached represent a saturated or unsaturated, unsubstituted or substituted cycle optionally containing at least one heteroatom,
• D represents hydrogen or an optionally substituted radical from the series
• Alkyl alkenyl, alkoxyalkyl, polyalkoxyalkyl, alkylthioalkyl, saturated or unsaturated cycloalkyl, in which one or more ring members are optionally replaced by heteroatoms,
• E represents a metal ion equivalent or an ammonium ion
• L represents oxygen or sulfur
• M represents oxygen or sulfur
• Rl for each optionally substituted by halogen substituted alkyl, alkenyl, alkoxyalkyl, alkylthioalkyl, polyalkoxyalkyl or optionally substituted by halogen, alkyl or alkoxy cycloalkyl, which can be interrupted by at least one heteroatom, each optionally substituted phenyl, phenylalkyl, hetaryl, phenoxyalkyl or hetaryloxyalkyl stands,
• R ⁇ represents alkyl, alkenyl, alkoxyalkyl, polyalkoxyalkyl, optionally substituted by halogen, or cycloalkyl, phenyl or beryl, optionally substituted,
• R ⁇ , R4 and Rß independently of one another each represent optionally substituted by halogen alkyl, alkoxy, alkylamino, dialkylamino, alkylthio, alkenylthio, cycloalkylthio and optionally substituted phenyl, benzyl, phenoxy or phenylthio,
• Ro and R ⁇ independently of one another for hydrogen, in each case optionally substituted by halogen alkyl, cycloalkyl, alkenyl, alkoxy,
• Alkoxyalkyl for optionally substituted phenyl, for optionally substituted benzyl, or together with the nitrogen atom to which they are attached, for a cycle which may be interrupted by oxygen or sulfur.
• the compounds of the formula (I) can be present in different compositions as geometric and / or optical isomers or isomer mixtures, which can optionally be separated in a customary manner. Both the pure isomers and the isomer mixtures, their preparation and use, and agents containing them are the subject of the present invention. For the sake of simplicity, the following always refers to compounds of the formula (I), though both the pure compounds and optionally mixtures with different proportions of isomeric compounds are meant.
• the compounds of the formula (I) can exist in the two isomeric forms of the formulas (I-A) and (I-B),
• the compounds of the formulas (I-A) and (I-B) can be present both as mixtures and in the form of their pure isomers. Mixtures of the compounds of the formulas (I-A) and (I-B) can optionally be separated in a manner known per se by physical methods, for example by chromatographic methods.
• A, B, D, W, X, Y and Z have the meanings given above,
• A, B, D, W, X, Y and Z have the meanings given above, and
• R 8 represents alkyl (preferably C 1 -C 6 -alkyl)
• Rl has the meaning given above and
• R2 and M have the meanings given above,
• a mono- or divalent metal preferably an alkali or alkaline earth metal such as lithium, sodium, potassium, magnesium or
• R i O, RI I ⁇ R12 independently of one another represent hydrogen or alkyl (preferably Cj-Cg-alkyl),
• the new compounds of the formula (I) have very good activity as pesticides, preferably as insecticides, acaricides and herbicides.
• the compounds according to the invention are generally defined by the formula (I).
• W preferably represents hydrogen, halogen, C 1 -C 6 -alkyl or C 1 -C 6 -alkoxy
• X preferably represents halogen, Cj-Cg-alkyl, Cj-Cg-alkoxy, Ci-C-i-haloalkyl, C1-C4 -halogenalkoxy or cyano,
• Y is preferably in the 4-position for hydrogen, Ci-Cg-alkoxy, halogen, cyano or
• Z is preferably in the 3- or 5-position for hydrogen or Ci-Cg-alkyl
• W also preferably represents hydrogen, halogen or C 1 -C 6 -alkyl
• X also preferably represents halogen, C 1 -C 6 -alkyl, C 1 -C 6 -alkoxy, C 1 -C 4 -haloalkyl, C 1 -C 6 -haloalkoxy or cyano,
• Y is also preferably in the 4-position for the radicals
• Z also preferably represents hydrogen
• V 1 also preferably represents hydrogen, halogen, C r C 12 alkyl, C r C 6 alkoxy, C r C 6 alkylthio, C r C 6 alkyl sulfmyl, C r C 6 alkyl sulfonyl, C r C 4 - Halogen- alkyl, -C-C4-haloalkoxy, nitro, cyano or phenyl which is optionally mono- or polysubstituted by halogen, Ci-Cg-alkyl, Ci-Cg-alkoxy, C1-C4-haloalkyl, C ⁇ -C4-haloalkoxy, nitro or cyano, Phenoxy, phenoxy-C 1 -C 4 -alkyl, phenyl-C 1 -C 4 -alkoxy, phenylthio-C 1 -C 4 -alkyl or phenyl-C 1 -C 4 -alkylthio,
• V 2 and V 3 are independently of each other preferably represents hydrogen, halogen, C j -Cg- alkyl, Ci-Cg-alkoxy, C 1 -C 4 haloalkyl or C ⁇ haloalkoxy,
• V 1 and V 2 together preferably also represent C 3 -C 4 -alkanediyl, which can optionally be substituted by halogen and / or C 1 -C 2 -alkyl and which can optionally be interrupted by one or two oxygen atoms,
• W also preferably represents hydrogen, halogen or C1-C ⁇ -alkyl
• X also preferably represents halogen, Ci-Cg-alkyl, -CC-alkoxy, C1-C4-haloalkyl, Ci-Q ⁇ -haloalkoxy or cyano,
• Z is also preferably in the 5-position for the radicals
• Y is likewise preferably in the 4-position is hydrogen, C j -Cö-alkyl or halogen,
• V 1 also preferably represents hydrogen, halogen, C j -Cg alkoxy, C r C 6 alkylthio, C r C 6 alkylsulfmyl, C r C 6 alkylsulfonyl, C r C 4 - haloalkyl, C; [- C4-haloalkoxy, nitro, cyano or in each case optionally simple or phenyl, phenoxy, phenoxy-C 1 -C -alkyl, phenyl-C 1, which are substituted several times by halogen, C 1 -C 6 -alkyl, C 1 -C 6 -alkoxy, C ⁇ -C 4 -haloalkyl, C 1 -C 4 -haloalkoxy, nitro or cyano -C -alkoxy, phenylthio-C!
• V 2 and V 3 are also preferred, independently, hydrogen, halogen, C j -CG alkyl, C j -CG alkoxy, C 1 -C 4 haloalkyl or -C4- haloalkoxy,
• V 1 and V 2 together preferably also represent C 3 -C 4 alkanediyl ; , which can optionally be substituted by halogen and / or C1-C2-alkyl and which can optionally be interrupted by one or two oxygen atoms,
• W also preferably represents hydrogen, methyl, propyl, or isopropyl
• X also preferably represents halogen, Ci-Cg-alkyl, Ci-Cg-alkoxy, C1-C4-
• Haloalkyl C 1-4 haloalkoxy or cyano
• Z is also preferably in the 3 or 5 position for hydrogen, halogen or C r C 6 alkyl
• Y furthermore preferably in the 4-position hydrogen, halogen, C j -C 6 - alkyl, C 1 -C 4 haloalkyl, cyano or C 1 -C 4 haloalkoxy,
• A preferably represents hydrogen or in each case optionally substituted by halogen -C 1 -C 2 -alkyl, C 3 -C 6 -alkenyl, C 1 -C 8 -alkoxy-C 1 -C 6 -alkyl, poly-C 1 -C 6 -alkoxy-C 1 -C 6 -alkyl, Ci -Cio-Alfcyltliio-Ci -Cö-alkyl, optionally substituted by halogen, Ci-Cg-alkyl or Ci-Cg-alkoxy C3-
• B preferably represents hydrogen, Ci-C ⁇ -alk l or Ci-Cg-alkoxy-Ci-Cg-alkyl or A, B and the carbon atom to which they are attached are preferably saturated C 3 -C 10 cycloalkyl or unsaturated C 5 -C ⁇ o cycloalkyl, in which a ring member is optionally replaced by oxygen or sulfur and which, if appropriate, is mono- or disubstituted by Cj -Cg-alkyl, C3-C10-
• D preferably represents hydrogen, in each case optionally substituted by halogen -C 1 -C 2 -alkyl, C3-Cg-alkenyl, C ⁇ -C ⁇ o-alkoxy-C2-Cg-alkyl, poly-
• G preferably represents hydrogen (a) or one of the groups
• E represents a metal ion equivalent or an ammonium ion
• L represents oxygen or sulfur
• M represents oxygen or sulfur
• R preferably represents in each case optionally substituted by halogen C ⁇ - C20-alkyl, C 2 -C20-alkenyl, Cj-Cg-alkoxy-Ci-Cg-alkyl, Ci-Cg-alkylthio-Ci-Cg-alkyl, poly-C ⁇ ⁇ Cg-alkoxy-C -C-alkyl or optionally substituted by halogen, Ci-Cg-alkyl or Cj-Cg-alkoxy substituted C3-Cg-cycloalkyl, in which one or more (preferably not more than two) ring members not directly adjacent are replaced by oxygen and / or sulfur,
• hetaryl optionally substituted by halogen or C 1 -C 6 -alkyl (for example pyrazolyl, thiazolyl, pyridyl, pyrimidyl,
• hetaryloxy-Ci-Cg-alkyl optionally substituted by halogen, amino or Ci-Cg-alkyl (for example pyridyloxy-C ⁇ Cg-alkyl, pyrimidyloxy-Ci-Cg-alkyl or thiazolyloxy-Ci-Cg-alkyl alkyl),
• R2 preferably represents in each case optionally substituted by halogen substitatechnisches C ⁇ - C 2 o alkyl, C 2 -C 2 -alkenyl, C 1 -CG-alkoxy-C 2 -CG-alkyl, poly-Ci-Cg-alk- oxy -C2-Cg-alkyl, for C3-Cg-cycloalkyl optionally substituted by halogen, Cj-Cö-alkyl or Ci-Cg-alkoxy or
• Ci-Cg-alkyl for each optionally substituted by halogen, cyano, nitro, Ci-Cg-alkyl, C-Cg-alkoxy, Ci-Cg-haloalkyl or Ci-Cg-haloalkoxy
• R3 preferably represents C 1 -C 6 -alkyl which is optionally substituted by halogen or is in each case optionally substituted by halogen, C 1 -C 6 -alkyl, C 1 -C 4 -alkoxy, C 1 -C 4 -haloalkyl, C 1 -C 4 -haloalkoxy, cyano or nitro
• R 4 and R ⁇ independently of one another preferably each represent C 1 -C 6 -alkyl, C 1 -C 6 -alkoxy, C 1 -C 6 -alkylamino, optionally substituted by halogen, C2-Cg-alkenylthio, C3-
• R6 and R ⁇ independently of one another preferably represent hydrogen, in each case optionally substituted by halogen Ci-Cg-alkyl, C3-Cg-cycloalkyl, Ci-Cg-alkoxy, C3-Cg-alkenyl, Ci-Cg-alkoxy-Ci-Cg -alkyl, for phenyl optionally substituted by halogen, Ci-Cg-haloalkyl, C ⁇ -Cg-alkyl or Ci-Cg-alkoxy, optionally substituted by halogen, Ci-Cg-alkyl, C ⁇ -Cg-
• halogen represents fluorine, chlorine, bromine and iodine, in particular fluorine, chlorine and bromine.
• W particularly preferably represents hydrogen, chlorine, bromine, C 1 -C 4 -alkyl or C 1 -C 4 -alkoxy,
• X particularly preferably represents chlorine, bromine, C ⁇ 4-alkyl, C ⁇ -C4 alkoxy, C - C 2 haloalkyl, -C-C2-haloalkoxy or cyano,
• Y particularly preferably in the 4-position represents hydrogen, C1-C4-alkoxy,
• Z particularly preferably in the 3- or 5-position represents hydrogen or C ⁇ -
• W also particularly preferably represents hydrogen, chlorine, bromine or C1-C4-alkyl
• X also particularly preferably represents chlorine, bromine, C ⁇ -C4-alkyl, C1-C4 alkoxy, Cj ⁇ -C haloalkyl, C ⁇ haloalkoxy or cyano,
• Y is also particularly preferably in the 4-position for the radicals
• Z also particularly preferably represents hydrogen
• V 1 also particularly preferably represents hydrogen, fluorine, chlorine, bromine, Cj-Cg-alkyl, C1-C4-alkoxy, C ⁇ -C2-haloalkyl, Ci ⁇ -haloalkoxy, nitro,
• V 2 and V 3 are independently of one another particularly preferably represent hydrogen, fluorine, chlorine, bromine, C r C 4 alkyl, C r C 4 alkoxy, C 1 -C 2 haloalkyl or C 1 -C 2 haloalkoxy,
• V 1 and V 2 together also particularly preferably represent -O-CH 2 -O- and -O-CF2-O-,
• W also particularly preferably represents hydrogen, chlorine, bromine or C 1 -C 4 -alkyl
• X is also particularly preferably chlorine, C r C 4 - alkyl or C1-C2
• Z is also particularly preferably in the 5-position for the radicals
• Y is also particularly preferably in the 4-position for hydrogen, C1-C4-alkyl or chlorine,
• V 1 is likewise particularly preferably hydrogen, fluorine, chlorine, bromine, C r Cg-alkyl, C ⁇ -C4-alkoxy, C ⁇ -C2-haloalkyl, C ⁇ -C2-haloalkoxy, nitro, cyano or optionally mono- or disubstituted by fluorine, Chlorine, bromine, C 1 -C 4 -alk l, C 1 -C 4 -alkoxy, Oj ⁇ -haloalkyl, C -C 2 -haloalkoxy, nitro or cyano-substituted phenyl,
• V 2 and V 3 also independently of one another particularly preferably represent hydrogen, fluorine, chlorine, bromine, C r C 4 alkyl, C r C 4 alkoxy, C r C 2 - haloalkyl or C 1 -C 2 haloalkoxy,
• V 1 and V 2 together also particularly preferably represent -O-CH 2 -O- or
• W also particularly preferably represents hydrogen, methyl, chlorine or bromine
• X also particularly preferably represents chlorine, bromine, C 1 -C 4 -alkyl, C1-C4-alkoxy, C 1 -C 2 -haloalkyl, C 1 -C 2 -haloalkoxy or cyano
• Z is also particularly preferably in the 3 or 5 position for hydrogen
• Y is also particularly preferably in the 4-position for hydrogen, chlorine, bromine, C 1 -C 4 alkyl, C 1 -C 2 haloalkyl, cyano or C 1 -C 2 haloalkoxy,
• Ci-Cg-alkyl optionally single to double by fluorine, chlorine, C1-C4-
• B particularly preferably represents hydrogen or C j -Cg- alkyl or
• A, B and the carbon atom to which they are attached are particularly preferably saturated or unsaturated C 5 -C 7 cycloalkyl, in which a ring member is optionally replaced by oxygen or sulfur and which is optionally simply substituted by C 1 -C 6 -alkyl, C 5 -Cg-cycloalkyl, C1-C3 -haloalkyl or Ci-Cg-alkoxy is substituted or
• D particularly preferably represents hydrogen, each optionally mono- to trisubstituted by fluorine or chlorine -CC-o-alkyl, C3-C6-alkenyl, -C-C6-alkoxy-C2-C -alkyl or C ⁇ -C4-alkylthio- C2-C 4- alkyl, for optionally substituted by fluorine, chlorine, -C-C4-alk l, C1-C4-alkoxy or C1-C2-haloalkyl C3-C7-cycloalkyl, in which a methylene group is optionally replaced by oxygen or sulfur .
• G particularly preferably represents hydrogen (a) or one of the groups
• E represents a metal ion equivalent or an ammonium ion
• L represents oxygen or sulfur
• M oxygen or sulfur
• R particularly preferably represents in each case mono- to trisubstituted by fluorine or chlorine-substituted C 1 -C 4 -alkyl, C 2 -C 6 -alkenyl, C 1 -C 6 -alkoxy-C 1 -C 6 -alkyl, C 1 -C 4 -alkyl thio-C 1 - C4-alkyl, Pofy-C ⁇ -C4-alkoxy-
• phenoxy-C 1 -C 3 -alkyl which is optionally mono- to disubstituted by fluorine, chlorine, bromine or C 1 -C 4 -alkyl,
• R2 particularly preferably represents in each case mono- to trisubstituted by fluorine-substituted C 1 -C 6 -alkyl, C2-C ig-alkenyl, C 1 -C 6 -alkoxy-C2-C6-alkyl or poly-C 1 -C 6 -alkoxy-C2-C6- alkyl,
• C3 to C7-cycloalkyl which is optionally monosubstituted or disubstituted by fluorine, chlorine, C1-C4-alkyl or -C-C4-alkoxy or
• R3 particularly preferably represents Ci-Cg-alkyl which is optionally monosubstituted to trisubstituted by fluorine or represents in each case optionally monosubstituted to twice by fluorine, chlorine, bromine, C 1 -C 4 -alkyl, C 1 -C -alkoxy, C1-C3-
• Haloalkyl C1-C3-haloalkoxy, cyano or nitro-substituted phenyl or benzyl,
• R 4 particularly preferably represents Ci-Cg-alky !, Ci-Cg-alkoxy, Ci-Cg-alkylamino, di- (-C-C 6 -alkyl) amino, Ci-Cg-alkylthio, C3-C4-alkenylthio, C3-Cg-Cycloalkylthio or for each optionally single to double by fluorine, chlorine, bromine, nitro, cyano, -C-C3-Alko y, C1 -C3 -haloalkoxy, -C-C3-alkylthio, C -C 3 -haloalkylthio, C ⁇ -C3 alkyl or C1-C3 haloalkyl substituted phenyl, phenoxy or phenylthio,
• R 5 particularly preferably represents C 1 -C 4 -alkoxy or C 1 -C 4 -alkylthio
• R6 particularly preferably represents Ci-Cg-alkyl, C3-Cg-cycloalkyl, C ⁇ ⁇ Cg-alkoxy, C3-Cg-alkenyl, Ci-Cg-alkoxy-Ci-Cg-alkyl, for optionally one to two times by fluorine, chlorine , Bromine, -CC 3 haloalkyl, C1-C4-
• R 7 particularly preferably represents hydrogen, C j -CG alkyl or C 3 -C 6 -alkenyl
• R 6 and R 7 together with the nitrogen atom to which they are attached are particularly preferably C5-C6-cycloalkyl which is optionally mono- or disubstituted by methyl or ethyl and in which a methylene group is optionally replaced by oxygen or sulfur.
• halogen represents fluorine, chlorine and bromine, in particular fluorine and chlorine.
• W very particularly preferably represents hydrogen, chlorine, methyl, ethyl or
• X very particularly preferably represents chlorine, bromine, methyl, ethyl, propyl, methoxy, trifluoromethyl, difluoromethoxy, trifluoroethoxy or cyano
• Y very particularly preferably in the 4-position represents hydrogen, methoxy, chlorine, bromine or trifluoromethyl
• Z very particularly preferably in the 3- or 5-position represents hydrogen or methyl
• W also very particularly preferably represents hydrogen, chlorine, bromine or methyl
• X also very particularly preferably represents chlorine, bromine, methyl, ethyl, propyl,
• Y also very particularly preferably stands in the 4-position for the rest
• Z also very particularly preferably represents hydrogen
• V 1 also very particularly preferably represents hydrogen, fluorine, chlorine, bromine, methyl, ethyl, n-propyl, iso-propyl, tert-butyl, methoxy, ethoxy, n-propoxy, iso-propoxy, trifluoromethyl or trifluoromethoxy,
• V 2 also very particularly preferably represents hydrogen, fluorine, chlorine, methyl, ethyl, n-propyl, isopropyl, methoxy, ethoxy or trifluoromethyl,
• W also very particularly preferably represents hydrogen, chlorine or methyl
• X also very particularly preferably represents chlorine, methyl or trifluoromethyl
• Z is also very particularly preferably in the 5-position for the rest
• Y is also very particularly preferably in the 4-position for hydrogen or methyl
• V 1 also very particularly preferably represents hydrogen, fluorine, chlorine, bromine, methyl, ethyl, n-propyl, iso-propyl, tert-butyl, methoxy, ethoxy, n-propoxy, iso-propoxy, trifluoromethyl or trifluoromethoxy,
• V 2 also very particularly preferably represents hydrogen, fluorine, chlorine, methyl, ethyl, n-propyl, isopropyl, methoxy, ethoxy or trifluoromethyl,
• W also very particularly preferably represents hydrogen, methyl, chlorine or bromine
• X also very particularly preferably represents chlorine, bromine, methyl, methoxy, trifluoromethyl, difluoromethoxy, trifluoroethoxy or cyano,
• Z is also very particularly preferably in the 3- or 5-position for
• Y is also very particularly preferably in the 4-position for hydrogen
• B very particularly preferably represents hydrogen, methyl or ethyl or
• A, B and the carbon atom to which they are attached very particularly preferably represent saturated Cs-Cg-cycloalkyl, in which one is optionally present
• Ring member is replaced by oxygen and which is optionally simply substituted by methyl, ethyl, propyl, isopropyl, butyl, trifluoromethyl, methoxy, ethoxy, propoxy, butoxy or iso-butoxy,
• D very particularly preferably represents hydrogen, each optionally mono- to trisubstituted by fluorine-substituted C 1 -C 6 -alkyl, C 3 -C 4 -alkenyl, C 1 -C 6 -alkoxy-C2-C4-alkyl, C 1 -C 4 -alkylthio-C2-C4 -alkyl or C3-C - cycloalkyl,
• G very particularly preferably represents hydrogen (a) or one of the groups
• E represents a metal ion equivalent or an ammonium ion
• L represents oxygen or sulfur
• M represents oxygen or sulfur
• Rl very particularly preferably represents in each case mono- to trisubstituted by fluorine or chlorine-substituted C 1 -C 8 -alkyl, C2-C10 "alkenyl, C 1 -C 2 -alkoxy-C] ⁇ C 2 -alkyl, C 1 -C 2 -alkylttao- C 1 -C 2 -alkyl, or if necessary simply to twice by fluorine, chlorine, methyl, ethyl, propyl, i-propyl,
• benzyl optionally substituted once or twice by fluorine, chlorine, bromine, methyl, methoxy, trifluoromethyl or trifluoromethoxy,
• furanyl, thienyl, pyridyl, pyrimidyl, thiazolyl or pyrazolyl optionally substituted by fluorine, chlorine, bromine, methyl or ethyl,
• R ⁇ is very particularly preferably represents in each case optionally mono- to trisubstituted by fluorine C1 -C10- alkyl, C2-C1 Q-alkenyl or Ci- C4-alkoxy-C2-C3-alkyl,
• C3-Cg-cycloalkyl which is optionally simply substituted by fluorine, chlorine, methyl, ethyl or methoxy,
• R3 very particularly preferably represents methyl, ethyl, n-propyl or phenyl optionally substituted by fluorine, chlorine, bromine, methyl, tert-butyl, methoxy, trifluoromethyl, trifluoromethoxy, cyano or nitro,
• R 4 very particularly preferably represents C1-C4-alkyl, C1-C4-alkoxy, C1-C4-alkylamino, di- (-C-C4-alkyl) amino, C ⁇ -C4-alkylthio or each optionally simply by fluorine, chlorine , Bromine, nitro, cyano, -C-C2-Alko y, -CC-C2-fluoroalkoxy, -C-C2-alkylithio, -C-C2-fluoroarkylthio or C1 -C3 alkyl substituted phenoxy or phenylthio,
• R 5 very particularly preferably represents methoxy, ethoxy, methylthio or ethylthio
• R ⁇ very particularly preferably represents C1-C4-alkyl, C3-Cg-cycloalkyl, C1-C4-alkoxy, C3-C4-alkenyl, C ⁇ ⁇ C4-alkoxy-C ⁇ ⁇ C4-alkyl, for optionally single to double by fluorine , Chlorine, bromine, trifluoromethyl, methyl or
• Methoxy substituted phenyl for optionally simply by fluorine, chlorine,
• R 7 very particularly preferably represents hydrogen, methyl, ethyl, propyl,
• R 6 and R 7 together with the nitrogen atom to which they are attached very particularly preferably represent C5-C6-cycloalkyl which is monosubstituted or disubstituted by methyl and in which a methylene group is optionally replaced by oxygen.
• W particularly preferably represents hydrogen, methyl, ethyl or chlorine
• X particularly preferably represents methyl or chlorine
• Y is particularly preferably in the 4-position for methoxy, chlorine, bromine or trifluoromethyl
• Z particularly preferably in the 5-position represents hydrogen or methyl
• B particularly preferably represents methyl
• D particularly preferably represents methyl or hydrogen, emphasized methyl
• G particularly preferably represents hydrogen
• W also particularly preferably represents hydrogen
• X likewise particularly preferably represents methyl or chlorine
• Z is also particularly preferably in the 5-position for
• Y also particularly preferably represents hydrogen
• A also particularly preferably represents methyl
• B also particularly preferably represents methyl, A and B together also particularly preferably represent - (CH2) 3 -,
• D also particularly preferably represents methyl
• G also particularly preferably represents hydrogen (a) or one of the groups
• R 1 is also particularly preferably C 1 -C 6 -alkyl
• R 2 also particularly preferably represents C 1 -C 6 -alkyl
• W also particularly preferably represents hydrogen or methyl
• X also particularly preferably represents methyl or bromine
• Z is also particularly preferably in the 3 or 5 position for hydrogen or methyl
• Y is also particularly preferably in the 4-position for methyl
• A also particularly preferably represents methyl
• B also particularly preferably represents methyl
• a and B together also particularly preferably stand for - (QH ⁇ -,
• D also particularly preferably represents methyl
• G also particularly preferably represents hydrogen (a) or one of the groups
• R 1 also particularly preferably represents C 1 -C 6 -alkyl
• R 2 also particularly preferably represents Ci-Cg-alkyl.
• Saturated or unsaturated hydrocarbon radicals such as alkyl or alkenyl can also be used in connection with heteroatoms, e.g. in alkoxy, where possible, be straight-chain or branched.
• optionally substituted radicals can be mono- or polysubstituted, and the substituents can be the same or different in the case of multiple substitutions.
• reaction curve can be represented by the following reaction scheme:
• A, B, D, W, X, Y, Z and R ⁇ have the meanings given above,
• acylhydroxylamino acid esters of Fo ⁇ nel are obtained, for example, if amino acid derivatives of the formula (XIII)
• W, X, Y and Z have the meanings given above and
• A, B, and R 8 have the meaning given above, some of which are new and can be prepared by known processes (NA Porter et. Al. J. Org. Chem. 63 5547 (1998)).
• A, B and R 8 have the meaning given above if N-hydroxyphthalimide of the formula (XV)
• A, B and R 8 have the meaning given above,
• Shark is fluorine, chlorine, bromine preferably chlorine
• A, B, D, W, X, Y, Z and R 8 have the meaning given above
• A, B and R 8 have the meaning given above
• LG stands for an escape group such as chlorine, bromine, iodine, mesylate, tosylate or triflate
• Carboxylic acid anhydrides of the formula (TV), chloroformic acid esters or chloroformic acid thioesters of the formula (V), chloronothio formic acid esters or chlorodithioic acid esters of the formula (VI), sulfonic acid chlorides of the formula (VII), phosphorus compounds of the formula (VIH) and metal hydroxides, metal alkoxides or amines of the formula (IX) and (X) and isocyanates of the formula (XI) and carbamic acid chlorides of the formula (XII) are generally known compounds of organic or inorganic chemistry.
• Process (A) is characterized in that compounds of the formula (II), in which A, B, D, W, X, Y, Z and R ° have the meanings given above, are subjected to intramolecular condensation in the presence of a base ,
• All inert organic solvents can be used as diluents in process (A) according to the invention.
• Hydrocarbons such as toluene and xylene, furthermore ethers such as dibutyl ether, tetrahydrofuran, dioxane, glycol dimethyl ether and diglycol dimethyl ether, and also polar solvents such as dimethyl sulfoxide, sulfolane, dimethylformamide and N-methyl-prrolidone, and alcohols such as methanol, ethanol are preferably usable , Propanol, iso-propanol, butanol, iso-butanol and tert-butanol.
• All the usual proton acceptors can be used as the base (deprotonating agent) when carrying out process (A) according to the invention.
• Alkali metal and alkaline earth metal oxides, hydroxides and carbonates such as sodium hydroxide, potassium hydroxide, magnesium oxide, calcium oxide, sodium carbonate, potassium carbonate and calcium carbonate, which can also be used in the presence of
• Alkali metals such as sodium or potassium can also be used.
• Alkali metal and alkaline earth metal amides and hydrides, such as sodium amide, sodium hydride and calcium hydride, and also alkali metal alcoholates, such as sodium methylate, sodium ethylate and potassium tert-butoxide, can also be used.
• reaction temperatures can be varied within a relatively wide range. In general, temperatures between -78 ° C and 250 ° C, preferably between 0 ° C and 150 o C.
• Process (A) according to the invention is generally carried out under normal pressure.
• reaction components of the formula (II) and the deprotonating bases are generally employed in approximately double equimolar amounts. However, it is also possible to use one or the other component in a larger excess (up to 3 moles).
• the process (B- ⁇ ) is characterized in that compounds of the formula (Ia) are in each case reacted with carboxylic acid halides of the formula (HI), if appropriate in the presence of a diluent and if appropriate in the presence of an acid binder.
• Diluents which can be used in process (B- ⁇ ) according to the invention are all solvents which are inert to the acid halides.
• Hydrocarbons, such as gasoline, benzene, toluene, xylene and tetralin, and furthermore halogenated hydrocarbons, such as methylene chloride, chloroform, are preferably usable.
• Suitable acid binders for the reaction according to the process (B- ⁇ ) according to the invention are all customary acid acceptors.
• Tertiary amines such as triethylamine, pyridine, diazabicyclooctane (DABCO) can preferably be used,
• Diazabicycloundecene DBU
• diazabicyclonones DBN
• Hünig base Hünig base and N
• N-dimethylaniline also alkaline earth metal oxides, such as magnesium and calcium oxide
• alkali and alkaline earth metal carbonates such as sodium carbonate, potassium carbonate and calcium carbonate
• alkali metal hydroxides such as sodium hydroxide and potassium hydroxide.
• reaction temperatures can be varied within a substantial range in process (B- ⁇ ) according to the invention. In general, temperatures between -20 ° C and + 150 ° C, preferably between 0 ° C and 100 ° C.
• the starting materials of the formula (Ia) and the carboxylic acid halide of the formula (HI) are generally in each case used in approximately equivalent amounts. However, it is also possible to use the carboxylic acid halide in a larger excess (up to 5 mol).
• the processing takes place according to usual methods.
• the process (B- ⁇ ) is characterized in that compounds of the formula (Ia) are reacted with carboxylic anhydrides of the formula (IV), if appropriate in the presence of a diluent and if appropriate in the presence of an acid binder.
• the diluents which can be used in the process (B- ⁇ ) according to the invention are preferably those diluents which are also preferred when using acid halides. Otherwise, an excess of carboxylic acid anhydride can also act as a diluent.
• the acid binders which are optionally added in process (B- ⁇ ) are preferably those acid binders which are also preferred when using acid halides.
• reaction temperatures can be varied within a substantial range in the process (B- ⁇ ) according to the invention. In general, temperatures between -20 ° C and + 150 ° C, preferably between 0 ° C and 100 ° C.
• the starting materials of the formula (I-a) and the carboxylic anhydride of the formula (TV) are generally used in approximately equivalent amounts in each case. However, it is also possible to use the carboxylic anhydride in a larger excess (up to 5 mol). The processing takes place according to usual methods.
• Process (C) is characterized in that compounds of the formula (Ia) are in each case reacted with chloroformic acid esters or chloroformic acid amethiol esters of the formula (V), if appropriate in the presence of a diluent and, if appropriate, in the presence of a seed binder.
• Suitable acid binders for the reaction according to process (C) according to the invention are all customary acid acceptors.
• Tertiary amines such as triethylamine, pyridine, DABCO, DBU, DBA, Hunig base and N, N-dimethylaniline, and also alkaline earth metal oxides, such as magnesium and
• Calcium oxide also alkali and alkaline earth metal carbonates, such as sodium carbonate, potassium carbonate and calcium carbonate, and alkali hydroxides, such as sodium hydroxide and potassium hydroxide.
• Diluents which can be used in process (C) according to the invention are all solvents which are inert to the chloroformates or chloroformates.
• Hydrocarbons such as gasoline, benzene, toluene, xylene and tetralin are preferably usable, furthermore halogenated hydrocarbons such as methylene chloride, chloroform, carbon tetrachloride, chlorobenzene and o-dichlorobenzene, and also ketones such as acetone and methylisopropyl ketone
• Ethers such as diethyl ether, tetrahydrofuran and dioxane, in addition carboxylic acid esters, such as ethyl acetate, and also strongly polar solvents, such as dimethyl sulfoxide and sulfolane.
• reaction temperatures can be carried out when carrying out the process according to the invention.
• Process (C) can be varied within a wide range. If one works in the presence of a diluent and an acid binder, the reaction temperatures are generally between -20 ° C and + 100 ° C, preferably between 0 ° C and 50 ° C. Process (C) according to the invention is generally carried out under normal pressure.
• the starting materials of the formula (I-a) and the corresponding chloroformic acid ester or chloroformic acid thiolester of the formula (V) are generally in each case used in approximately equivalent amounts. However, it is also possible to use one or the other component in a larger excess (up to 2 mol).
• the processing takes place according to usual metiods. The general procedure is to remove precipitated salts and to concentrate the remaining reaction mixture by stripping off the diluent.
• Process (D) according to the invention is characterized in that compounds of the formula (I-a) are each reacted with compounds of the formula (VI) in the presence of a diluent and, if appropriate, in the presence of an acid binder.
• Possible diluents added are all inert polar organic solvents, such as ethers, aniides, sulfones, sulfoxides, but also haloalkanes.
• Dimethyl sulfoxide, tetrahydrofuran, dimethylformamide or methylene chloride are preferably used.
• the enolate salt is prepared by adding strong deprotonating agents such as sodium hydride or potassium tertiary butoxide Compounds (Ia), the further addition of acid binders can be dispensed with.
• customary inorganic or organic bases are suitable, for example sodium hydroxide, sodium carbonate, potassium carbonate, pyridine, triethylamine.
• the reaction can be carried out under normal pressure or under elevated pressure, preferably under normal pressure.
• the processing takes place according to usual methods.
• Process (E) according to the invention is characterized in that compounds of the formula (I-a) are in each case reacted with sulfonyl chlorides of the formula (VII), if appropriate in the presence of a diluent and if appropriate in the presence of an acid binder.
• Possible diluents added are all inert polar organic solvents such as ethers, amides, nitriles, sulfones, sulfoxides or halogenated hydrocarbons such as methylene chloride.
• the enolate salt is prepared by adding strong deprotonating agents (such as sodium hydride or potassium tertiary butoxide) of the compounds (Ia), the further addition of acid binders can be dispensed with.
• strong deprotonating agents such as sodium hydride or potassium tertiary butoxide
• customary inorganic or organic bases are suitable, for example sodium hydroxide, sodium carbonate, potassium carbonate, pyridine, triethylamine.
• the reaction can be carried out at normal pressure or under elevated pressure, preferably at normal pressure.
• the processing takes place according to usual methods.
• Process (F) according to the invention is characterized in that compounds of the formula (I-a) are each reacted with phosphorus compounds of the formula (VIH), if appropriate in the presence of a diluent and if appropriate in the presence of an acid binder.
• Possible diluents added are all inert, polar organic solvents such as ethers, amides, nitriles, alcohols, sulfides, sulfones, sulfoxides etc.
• Acetonitrile, dimethyl sulfoxide, tetrahydrofuran, dimethylformamide, methylene chloride are preferably used.
• Possible inorganic binders which may be added are conventional inorganic or organic bases, such as hydroxides, carbonates or amines. Be exemplary Sodium hydroxide, sodium carbonate, potassium carbonate, pyridine, triethylamine listed.
• the reaction can be carried out under normal pressure or under elevated pressure, preferably under normal pressure.
• the processing takes place according to the usual methods of organic chemistry.
• the end products obtained are preferably purified by crystallization, chromatographic purification or by so-called “distillation", i.e. Removal of volatiles in vacuo.
• Process (G) is characterized in that compounds of the formula (I-a) are reacted with metal hydroxides or metal alkoxides of the formula (IX) or amines of the formula (X), if appropriate in the presence of a diluent.
• Diluents which can be used in process (G) according to the invention are preferably ethers such as tetrahydrofuran, dioxane, diethyl ether or alcohols such as methanol, ethanol, isopropanol, but also water.
• Process (G) according to the invention is generally carried out under normal pressure.
• the reaction temperatures are generally between -20 ° C and 100 ° C, preferably between 0 ° C and 50 ° C.
• Process (H) is characterized in that compounds of the formula (Ia) in each case with (H- ⁇ ) compounds of the formula (XI) optionally in the presence of a diluent and optionally in the presence of a catalyst or (H- ⁇ ) with compounds of the formula (XII) if appropriate in the presence of a diluent and if appropriate in the presence of an acid binder.
• H- ⁇ about 1 mol of isocyanate of the formula (XI) is reacted at 0 to 100 ° C., preferably at 20 to 50 ° C., per mole of starting compound of the formula (Ia).
• Possible diluents added are all inert organic solvents, such as ethers, amides, nitriles, sulfones, sulfoxides.
• catalysts can be added to accelerate the reaction.
• Organic tin compounds such as e.g. Dibutyltin dilaurate can be used. It is preferably carried out at normal pressure.
• any inert polar organic solvents such as ethers, amides, sulfones, sulfoxides or halogenated hydrocarbons are suitable as diluents which may be added.
• Dimethyl sulfoxide, tetrahydrofuran, dimethylformamide or methylene chloride are preferably used.
• the enolate salt of the compound (Ia) is represented by the addition of strong deprotonating agents (such as sodium hydride or potassium tertiary butoxide)
• strong deprotonating agents such as sodium hydride or potassium tertiary butoxide
• acid binders can be dispensed with.
• customary inorganic or organic bases are suitable, for example sodium hydroxide, sodium carbonate, potassium carbonate, triethylamine or pyridine.
• the reaction can be carried out at normal pressure or under elevated pressure, preferably carried out under normal pressure.
• the processing takes place according to usual methods.
• the active ingredients are suitable for protecting plants and plant organs, for increasing crop yields, improving the quality of the crop and for combating animal pests, in particular insects, arachnids and nematodes, which are used in agriculture , occur in forests, in gardens and leisure facilities, in forest and material protection as well as in the hygiene sector. They can preferably be used as pesticides. They are effective against normally sensitive and resistant species as well as against all or individual stages of development.
• the pests mentioned above include:
• Isopoda e.g. Oniscus asellus, Armadillidium vulgare, Porcellio scaber.
• Thysanura e.g. Lepisma saccharina.
• Phthiraptera e.g. Pediculus humanus corporis, Haematopinus spp., Linognathus spp., Trichodectes spp., Damalinia spp.
• Thysanoptera e.g. Hercinothrips femoralis, Thrips tabaci
• Homoptera e.g. Aleurodes brassicae, Bemisia tabaci, Trialeurodes vaporariorum, Aphis gossypii, Brevicoryne brassicae, Cryptomyzus ribis, Aphis fabae, Aphis pomi, Eriosoma lanigerum, Hyalopterus arundinis, Phylloxera vastatrix, Pemphigus sppe, Phros
• Anthrenus spp. Attagenus spp., Lyctus spp., Meligethes aeneus, Ptinus spp., Niptus hololeucus, Gibbium psylloides, Tribolium spp., Tenebrio molitor, Agriotes spp., Conoderus spp., Melolontha melolontha, Costimelyontronica oryzophilus.
• Hymenoptera e.g. Diprion spp., Hoplocampa spp., Lasius spp., Monomorium pharaonis, Vespa spp.
• Hyalomma spp. Ixodes spp., Psoroptes spp., Chorioptes spp., Sarcoptes spp., Tarsonemus spp., Bryobia praetiosa, Panonychus spp., Tetranychus spp., Hemitarsonemus spp., Brevipalpus spp.
• Plant-parasitic nematodes include e.g. Pratylenchus spp., Radopholus similis, Ditylenchus dipsaci, Tylenchulus semipenetrans, Heterodera spp., Globodera spp., Meloidogyne spp., Aphelenchoides spp., Longidorus spp., Xiphinema spp., Trichodorus spp., Bursaph.
• the compounds according to the invention can optionally be used in certain aspects.
• Concentrations or application rates can also be used as herbicides and microbicides, for example as fungicides, antifungals and bactericides. If appropriate, they can also be used as intermediates or precursors for the synthesis of further active compounds.
• plants and parts of plants can be treated.
• Plants are understood here to mean all plants and plant populations, such as desired and unwanted wild plants or crop plants (including naturally occurring crop plants).
• Cultivated 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 cultivars which can or cannot be protected by plant breeders' rights.
• Plant parts are to be understood to mean all above-ground and underground parts and organs of plants, such as shoots, leaves, flowers and roots, by way of example Leaves, needles, stems, stems, flowers, fruiting bodies, fruits and seeds as well as roots, tubers and rhizomes are listed.
• the plant parts also include crops and vegetative and generative propagation material, for example cuttings, tubers, rhizomes, offshoots and seeds.
• the treatment of the plants and parts of plants with the active compounds according to the invention is carried out directly or by acting on their environment, habitat or location according to the usual treatment methods, e.g. by dipping, spraying, vaporizing, atomizing, scattering, spreading, injecting and, in the case of propagation material, in particular in the case of seeds, furthermore by means of single- or multi-layer coating.
• the active ingredients can be converted into the customary formulations, such as solutions, emulsions, wettable powders, suspensions, powders, dusts, pastes, soluble powders, granules, suspension emulsion concentrates, impregnated with active ingredients
• formulations are made in a known manner, e.g. by mixing the active ingredients with extenders, that is to say liquid solvents and / or solid carriers, optionally using surface-active agents, that is to say emulsifiers and / or dispersants and / or foam-generating agents.
• extenders that is to say liquid solvents and / or solid carriers
• surface-active agents that is to say emulsifiers and / or dispersants and / or foam-generating agents.
• organic solvents can, for example, also be used as auxiliary solvents.
• auxiliary solvents include aromatics, such as xylene, toluene, or alkylnaphthalenes, chlorinated aromatics and chlorinated aliphatic hydrocarbons, such as chlorobenzenes, chlorethylenes or methylene chloride, aliphatic hydrocarbons, such as cyclohexane or paraffins, for example petroleum fractions, mineral and vegetable oils , Alcohols such as butanol or glycol and their ethers and esters, ketones such as Acetone, methyl ethyl ketone, methyl isobutyl ketone or cyclohexanone, strongly polar solvents such as dimethylformamide and dimethyl sulfoxide, and water.
• aromatics such as xylene, toluene, or alkylnaphthalenes
• chlorinated aromatics and chlorinated aliphatic hydrocarbons such as chlorobenzenes
• e.g. Ammonium salts and natural rock powders such as kaolins, clays, talc, chalk, quartz, attapulgite, montmorillonite or diatomaceous earth and synthetic rock powders such as highly disperse silica, aluminum oxide and silicates are suitable as solid carriers for granules: e.g. broken and fractionated natural rocks such as calcite, marble, pumice, sepiolite, dolomite and synthetic granules from inorganic and organic flours as well as granules from organic material such as sawdust, coconut shells, corn cobs and tobacco stems; as emulsifying and / or foaming agents are possible: e.g. nonionic and anionic emulsifiers such as polyoxyethylene fatty acid esters, polyoxyethylene fatty alcohol ethers, e.g. Alkylaryl polyglycol ethers, alkyl sulfonates,
• Alkyl sulfates, aryl sulfonates and protein hydrolyzates Possible dispersants are: e.g. Lignin sulfite liquor and methyl cellulose.
• Adhesives such as carboxymethyl cellulose, natural and synthetic powdery, granular or latex-shaped polymers, such as gum arabic, polyvinyl alcohol, polyvinyl acetate, and natural phospholipids such as cephalins and lecithins and synthetic phospholipids can be used in the formulations.
• Other additives can be mineral and vegetable oils.
• colorants such as inorganic pigments, for example iron oxide, "titanium oxide, Ferco- dyes Blue, and organic dyestuffs, such as alizarin dyestuffs, azo dyestuffs and metal phthalocyanine and trace nutrients such as salts of iron used, manganese, boron, copper, cobalt, molybdenum and zinc ,
• the formulations generally contain between 0.1 and 95% by weight of active compound, preferably between 0.5 and 90%.
• the active compounds according to the invention can also be used in a mixture with known fungicides, bactericides, acaricides, nematicides or insecticides, for example to to broaden the spectrum or to prevent the development of resistance, in many cases synergistic effects are obtained, i.e. the effectiveness of the mixture is greater than the effectiveness of the individual components.
• Debacarb dichlorophene, diclobutrazole, diclofluanide, diclomezin, dicloran, diethofencarb, difenoconazole, dimethirimol, dimethomorph, diniconazole, diniconazole- M, dinocap, diphenylamine, dipyrithione, ditalimfos, dorphianolodin, dithianonodon, dithianonodonone Ediphenphos, Epoxiconazole, Etaconazole, Ethirimol, Etridiazole,
• Mancopper Mancozeb, Maneb, Meferimzone, Mepanipyrim, Mepronil, Metalaxyl, Metconazol, Methasulfocarb, Methfuroxam, Metiram, Metomeclam, Metsulfovax, Mildiomycin, Myclobutanil, Myclozolin,
• Tebuconazole Tebuconazole, tecloftalam, tecnazen, tetcyclacis, tetraconazole, thiabendazole,
• Thicyofen Thifluzamide, Thiophanate-methyl, Thiram, Tioxymid, Tolclofos-methyl, Tolylfluanid, Triadimefon, Triadimenol, Triazbutil, Triazoxid, Trichlamid, Tricyclazol, Tridemorph, Trifloxystrobin, Triflumizol, Trifazolin, Trifazorin, Trifazorin
• Cadusafos Carbaryl, Carbofuran, Carbophenothion, Carbosulfan, Cartap, Chloethocarb, Chlorethoxyfos, Chlorfenapyr, Chlorfenvinphos, Chlorfluazuron,
• Chlormephos Chlorpyrifos, Chlorpyrifos M, Chlovaportlirin, Chromafenozide, Cis- Resmethrin, Cispermethrin, Clocythrin, Cloethocarb, Clofentezine, Clothianidine, Cyanophos, Cycloprene, Cycloprothrin, Cyfluthrin, Cyhalothrin, Cyethrin, Cyhexatin Deltamethrin, Demeton M, Demeton S, Demeton-S-methyl, Diafenthiuron, Diazinon, Dichlorvos, Dicofol, Diflubenzuron, Dimethoat, Dimethylvinphos, Dinetofuran, Diofenolan, Disulfoton, Docusat-sodium, Dofenapyn,
• Fenamiphos Fenazaquin, Fenbutatin oxide, Fenitrothion, Fenothiocarb, Fenoxacrim, Fenoxycarb, Fenpropathrin, Fenpyrad, Fenpyrithrin, Fenpyroximate, Fenthion ,,
• Fenvalerate Fipronil, Fluazinam, Fluazuron, Flubrocythrinate, Flucycloxuron, Flucythrinate, Flufenoxuron, Flumethrin, Flupyrazofos, Flutenzine, Fluvalinate, Fonophos, Fosmethilan, Fosthiazate, Fubfenprox, Furathiocarb
• Halofenozide HCH, Heptenophos, Hexaflumuron, Hexythiazox, Hydroprene,
• Metharhilicium flavoviride methidathione, methiocarb, methoprene, methomyl, methoxyfenozide, metolcarb, metoxadiazone, mevinphos, milbemectin, milbemycin, monocrotophos,
• Paecilomyces fumosoroseus Parathion A, Parathion M, Permethrin, Phenthoat, Phorat, Phosalone, Phosmet, Phosphamidon, Phoxim, Pirimicarb, Pirimiphos A,
• Pirimiphos M Profenofos, Promecarb, Propargite, Propoxur, Prothiofos, Prothoat, Pymetrozine, Pyraclofos, Pyresmethrin, Pyrethrum, Pyridaben, Pyridathion, Pyrimidifen, Pyriproxyfen,
• Fertilizers and growth regulators, safeners and semichemicals are possible.
• the active compounds according to the invention can also be present in their commercially available formulations and in the use forms prepared from these formulations in a mixture with synergists.
• Synergists are compounds that increase the effectiveness of the active ingredients without the added synergist itself having to be active.
• the active compounds according to the invention can also be present in their commercially available formulations and in the use forms prepared from these formulations in mixtures with inhibitors which reduce degradation of the active compound after use in the environment of the plant, on the surface of parts of plants or in plant tissues ,
• the active substance content of the use forms prepared from the commercially available formulations can vary within wide ranges.
• the active substance concentration of the use forms can be from 0.0000001 to 95% by weight of active substance, preferably between 0.0001 and 1% by weight.
• the application takes place in a customary manner adapted to the application forms
• the active compound When used against hygiene pests and pests of stored products, the active compound is distinguished by an outstanding residual action on wood and clay and by a good stability to alkali on limed substrates.
• all plants and their parts can be treated according to the invention.
• plant species and plant cultivars and their parts which occur wildly or are obtained by conventional organic breeding methods, such as crossing or protoplast fusion, are treated.
• transgenic plants and plant cultivars which have been obtained by genetic engineering methods, if appropriate in combination with conventional methods (genetic modified organisms) and their parts are treated.
• the term “parts” or "parts of plants" or "plant parts” was explained above.
• Plants of the plant varieties which are in each case commercially available or in use are particularly preferably treated according to the invention.
• Plant cultivars are understood to mean plants with new properties (“traits”) which have been grown both by conventional breeding, by mutagenesis or by recombinant DNA techniques. These can be varieties, bio and genotypes.
• the treatment according to the invention can also cause superadditive (“synergistic") effects. For example, reduced application rates and / or extensions of the
• Wirl ⁇ mgspektrum and / or an enhancement of the effect of the substances and agents that can be used according to the invention better plant growth, increased tolerance to high or low temperatures, increased tolerance to drought or to water or soil salt content, increased flowering output, easier harvesting, acceleration of ripening, higher crop yields , higher quality and / or higher nutritional value of the harvested products, higher storability and / or workability of the harvested products possible, which go beyond the effects to be actually expected.
• transgenic plants or plant cultivars to be treated according to the invention include all plants which are characterized by the Genetic engineering modification received genetic material which gives these plants particularly advantageous valuable properties ("traits"). Examples of such properties are better plant growth, increased tolerance to high or low temperatures, increased tolerance to dryness or to water or soil salt content, increased flowering performance, easier harvesting,
• transgenic plants Bacteria and / or viruses and an increased tolerance of the plants to certain herbicidal active ingredients.
• transgenic plants are the important crop plants, such as cereals (wheat, rice), corn, soybeans, potatoes, cotton, tobacco, rapeseed and fruit plants (with the fruits apples, pears, citrus fruits and grapes), with corn, soybeans, potatoes , Cotton, tobacco and rapeseed are highlighted.
• the traits that are particularly emphasized are the plants' increased defense against insects, arachnids, nematodes and snails due to toxins produced in the plants, in particular those which are caused by the genetic material from Bacillus thuringiensis (for example by the genes Cry ⁇ A (a) , CryIA (b), Cry ⁇ A (c), CryllA, CrylflA, CryIIIB2, Cry9c Cry2Ab,
• Bt plants The properties (“traits”) also particularly emphasize the increased defense of plants against fungi, bacteria and viruses by systemic acquired resistance (SAR), systemin, phytoalexins, elicitors and resistance genes and correspondingly expressed proteins and toxins.
• SAR systemic acquired resistance
• the properties (“traits”) which are particularly emphasized are the increased tolerance of the plants to certain herbicidal active compounds, for example imidazolinones, sulfonylureas, glyphosate or phosphinotricin (for example “PAT” gene).
• the genes imparting the desired properties (“traits”) can also occur in combinations with one another in the transgenic plants.
• Bt plants are corn varieties, cotton varieties, soy varieties and potato varieties which are marketed under the trade names YIELD GARD® (e.g. corn, cotton, soy), KnockOut® (e.g. corn), StarLink® (e.g. corn), Bollgard® (cotton ), Nucotn® (cotton) and NewLeaf® (potato).
• YIELD GARD® e.g. corn, cotton, soy
• KnockOut® e.g. corn
• StarLink® e.g. corn
• Bollgard® cotton
• Nucotn® cotton
• NewLeaf® NewLeaf®
• Soybean varieties named under the trade names Roundup Ready® tolerance to glyphosate e.g. corn, cotton, soy
• Liberty Link® tolerance to phosphinotricin, e.g. rapeseed
• IMI® tolerance to hnidazolinone
• STS® tolerance to sulfonylureas e.g. corn
• the herbicide-resistant plants include the varieties sold under the name Clearfield® (e.g. maize).
• Clearfield® e.g. maize
• plants listed can be treated particularly advantageously according to the invention with the compounds of the general formula I or the active compound mixtures according to the invention.
• the preferred ranges given above for the active substances or mixtures also apply to the treatment of these plants.
• Plant treatment with the compounds or mixtures specifically listed in the present text should be particularly emphasized.
• the active compounds according to the invention act not only against plant, hygiene and stored-product pests, but also in the veterinary sector against animal parasites (ectoparasites) such as tick ticks, leather ticks, and mite mites,
• parasites include:
• Anoplurida for example Haematopinus spp., Linognathus spp., Pediculus spp., Phtirus spp., Solenopotes spp.
• Mallophagida and the subordinates Amblycerina and Ischnocerina for example Trimenopon spp., Menopon spp., Trinoton spp., Bovicola spp., Werneckiella spp., Lepikentron spp., Damalina spp., Trichodectes spp., Felicola spp.
• Nematocerina and Brachycerina e.g. Aedes spp., Anopheles spp., Culex spp., Simulium spp., Eusimulium spp., Phlebotomus spp., Lutzomyia spp., Culicoides spp., Chrysops spp., Hybomitra spp., Atylotas spp., Tabanus spp., Haematopota ., Philipomyia spp., Braula spp., Musca spp., Hydrotaea spp., Stomoxys spp., Haematobia spp., Morellia spp., Fannia spp., Glossina spp., Calliphora spp., Glossina spp., Chrysomyia spp.
• Amblyomma spp. Boophilus spp., Dermacentor spp., Haemophysalis spp., Hyalomma spp., Rhipicephalus spp., De ⁇ nanyssus spp., Raillietia spp., Pneumonyssus spp., Stemostoma spp., Va ⁇ oa spp.
• Actinedida Prostigmata
• Acaridida Acaridida
• Acarapis spp. Cheyletiella spp., Ornitrocheyletia spp., Myobia spp., Psorergates spp., Demodex spp., Trombicula spp., Listrophoms 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 used in agricultural animals, e.g. Cattle, sheep, goats, horses, pigs, donkeys, camels, buffalo, rabbits, chickens, turkeys, ducks, geese,
• the active compounds according to the invention are used in the veterinary sector in a known manner by enteral administration in the form of, for example, tablets, capsules, drinkers, drenches, granules, pastes, boluses, the feed-through method, suppositories, by parenteral administration, for example by Injections (intramuscular, subcutaneous, intravenous, intraperitonal, etc.), implants, by nasal application, by dermal application in the form of, for example, diving or bathing (dipping), spraying (spray), pouring on (pour-on and spot-on), washing , the Einpudems and with the help of active ingredient-containing shaped bodies, such as
• the active compounds of the formula (I) can be used as formulations (for example powders, emulsions, flowables) Agents), which contain the active substances in an amount of 1 to 80% by weight, directly or after 100 to 10,000-fold dilution or use them as a chemical bath.
• formulations for example powders, emulsions, flowables
• Agents which contain the active substances in an amount of 1 to 80% by weight, directly or after 100 to 10,000-fold dilution or use them as a chemical bath.
• Chlorophorus pilosis Anobium punctatum, Xestobium rufovillosum, Ptilinus pecticornis, Dendrobium pertinex, Emobius mollis, Priobium carpini, Lyctus brunneus, Lyctus africanus, Lyctus planicollis, Lyctus linearis, Lyctus pubesceesxes, Troagoxylonyle, Troagoxylon spec. Tryptodendron spec. Apate monachus, Bostrychus capucins, Heterobostrychus brunneus, Sinoxylon spec. Dinoderus minutas.
• Hymenoptera such as Sirex juvencus, Uroceras gigas, Urocerus gigas taignus, Urocerus augur.
• Kalotermes flavicollis Cryptotermes brevis, Heterotermes indicola, Reticulitermes flavipes, Reticulitermes santonensis, Reticulitermes lucifugus, Mastotermes darwiniensis, Zootermopsis nevadensis, Coptotermes formosanus.
• Bristle tails such as Lepisma saccharina.
• technical materials are to be understood as non-living materials, such as preferably plastics, adhesives, glues, papers and cartons, leather, wood, wood processing products and paints.
• the one to be protected against insect attack is very particularly preferably
• Wood and wood processing products which can be protected by the agent according to the invention or mixtures containing it are to be understood as examples:
• the active substances can be used as such, in the form of concentrates or generally customary formulations such as powders, granules, solutions, suspensions, emulsions or pastes.
• the formulations mentioned can be prepared in a manner known per se, e.g. by mixing the active ingredients with at least one solvent or diluent, emulsifier, dispersant and / or binder or fixative, water repellent, optionally siccatives and UV stabilizers and, if appropriate, dyes and pigments and further processing aids.
• the insecticidal compositions or concentrates used to protect wood and wood-based materials contain the active compound according to the invention in a concentration of 0.0001 to 95% by weight, in particular 0.001 to 60% by weight.
• the amount of the agents or concentrates used depends on the type and occurrence of the insects and on the medium. The optimal amount can be determined in each case by test series. In general, however, it is sufficient to use 0.0001 to 20% by weight, preferably 0.001 to 10% by weight, of the active compound, based on the material to be protected.
• organic-chemical solvent or solvent mixture and / or an oily or oily or low-volatility organic-chemical solvent or solvent mixture and / or a polar organic-chemical solvent or solvent mixture and / or water and optionally an emulsifier and / or wetting agents.
• the organic chemical solvents used are preferably oily or oily solvents with an evaporation number above 35 and a flash point above 30 ° C., preferably above 45 ° C.
• Corresponding mineral oils or their aromatic fractions or mineral oil-containing solvent mixtures, preferably white spirit, petroleum and / or alkylbenzene, are used as such low-volatility, water-insoluble, oily and oily solvents.
• Mineral oils with a boiling range of 170 to 220 ° C, white spirit with a boiling range of 170 to 220 ° C, spindle oil with a boiling range of 250 to 350 ° C, petroleum or aromatics with a boiling range of 160 to 280 ° C, turpentine oil and Like. Used.
• liquid aliphatic hydrocarbons with a boiling range from 180 to 210 ° C. or high-boiling mixtures of aromatic and aliphatic hydrocarbons with a boiling range from 180 to 220 ° C. and / or locker oil and / or monochlomaphthalene, preferably ⁇ -monochlomaphthalene, are used.
• organic low-volatility oily or oily solvents with an evaporation number above 35 and a flash point above 30 ° C, preferably above 45 ° C can be partially replaced by slightly or medium-volatile organic chemical solvents, with the proviso that the solvent mixture is also a Evaporation number over 35 and a flash point above 30 ° C, preferably above 45 ° C, and that the insecticide-fungicide mixture is soluble or emulsifiable in this solvent mixture.
• part of the organic chemical solvent or solvent mixture or an aliphatic polar organic chemical solvent or solvent mixture is replaced.
• Aliphatic organic chemical solvents containing hydroxyl and / or ester and / or ether groups, such as, for example, glycol ethers, esters or the like, are preferably used.
• organic water-borne synthetic resins and / or synthetic resins which are soluble or dispersible or emulsifiable in the organic chemical solvents used and / or binding drying oils, in particular binders consisting of or containing an acrylate resin, are used as organic-chemical binders.
• a vinyl resin e.g. polyvinyl acetate
• Polyester resin polycondensation or polyaddition resin, polyurethane resin, alkyd resin or modified alkyd resin, phenolic resin, hydrocarbon resin such as indene-coumarone resin, silicone resin, drying vegetable and / or drying oils and / or physically drying binders based on a natural and / or synthetic resin used.
• the synthetic resin used as a binder can be used in the form of an emulsion, dispersion or solution. Bitumen or bituminous substances up to 10% by weight can also be used as binders. In addition, in itself Known dyes, pigments, water-repellent agents, odorants and inhibitors or anti-corrosion agents and the like can be used.
• Alkyd resins with an oil content of more than 45% by weight, preferably 50 to 68% by weight, are preferably used according to the invention.
• binder mentioned can be replaced by a fixing agent (mixture) or a plasticizer (mixture). These additives are intended to prevent volatilization of the active ingredients and crystallization or precipitation. They preferably replace 0.01 to 30% of the binder (based on 100% of the binder used).
• the plasticizers come from the chemical classes of phthalic acid esters such as dibutyl, dioctyl or benzyl butyl phthalate, phosphoric acid esters such as tributyl phosphate, adipic acid esters such as di- (2-ethylhexyl) adipate, stearates such as butyl stearate or amyl stearate, oleates such as butyl oleate, higher glycerol glycerol or glycerol ether - Kolether, glycerol ester and p-toluenesulfonic acid ester.
• phthalic acid esters such as dibutyl, dioctyl or benzyl butyl phthalate
• phosphoric acid esters such as tributyl phosphate
• adipic acid esters such as di- (2-ethylhexyl) adipate
• Fixatives are chemically based on polyvinyl alkyl ethers such as e.g. Polyvinyl methyl ether or ketones such as benzophenone, ethylene benzophenone.
• Water is also particularly suitable as a solvent or diluent, if appropriate in a mixture with one or more of the above-mentioned organic chemical solvents or diluents, emulsifiers and dispersants.
• a particularly effective wood protection is achieved by industrial impregnation processes, e.g. vacuum, double vacuum or pressure processes.
• the ready-to-use compositions may optionally contain further insecticides and, if appropriate, one or more fungicides.
• insecticides and fungicides mentioned in WO 94/29 268 are preferably suitable as additional admixing partners.
• the compounds mentioned in this document are an integral part of the present application.
• Insecticides such as chlorpyriphos, phoxime, silafluofin, alphamethrin, cyfluthrin, cypermethrin, deltamethrin,
• fungicides such as epoxyconazole, hexaconazole, azaconazole, propiconazole, tebuconazole, cyproconazole, metconazole, imazalil, dichlorfluanide, tolylfluanid,
• the compounds according to the invention can be used to protect objects, in particular hulls, sieves, nets, structures,
• Scalpellum species or by species from the group Balanomorpha (barnacles), such as Baianus or Pollicipes species, increases the frictional resistance of ships and consequently leads to a significant increase in operating costs due to increased energy consumption and, moreover, frequent dry dock stays.
• algae for example Ectocarpus sp. and Ceramium sp.
• sessile Entomostraken groups which are grouped under the name Cirripedia (barnacles) is of particular importance.
• heavy metals such as e.g. in bis (trialkyltin) sulfides, tri-n-butyltin laurate, tri-n-butyltin chloride, copper (I) oxide, triethyltin chloride, tri-butyl (2-phenyl-4-chlorophenoxy) tin, tributyltin oxide, molybdenum disulfide , Antimony oxide, polymeric butyl titanate, phenyl- (bispyridine) bismuth chloride, tri-ft-butyltin fluoride, manganese ethylene bisthiocarbamate, zihkdimethyldrthiocarbamate, zinc ethylene bisthiocarbamate, zinc and copper salts of 2-pyridinethiol-1-oxydimide oxychloride, bis (iodide) bis (iodide) bis (iodide) oxydimi
• the ready-to-use antifouling paints may also contain other active ingredients, preferably algicides, fungicides, herbicides, molluscicides or other antifouling active ingredients.
• Suitable combination partners for the anti-fouling agents according to the invention are preferably:
• Algicides such as 2-tert-butylanino-4-cyclopropylamino-6-methylthio-l, 3,5-triazine, dichlorophen, Diuron, endothal, fentin acetate, isoprotarone, methabenzthiazuron, oxyfluorfen, quinoclamine and terbutryn;
• Fungicides such as benzo [ö] thiophenecarboxylic acid cyclohexylamide-S, S-dioxide, dichlofluanide, fluorofolpet, 3-iodo-2-propynyl butyl carbamate, tolyl fluanide and azoles such as
• the antifouling agents used contain the active compound according to the invention of the compounds according to the invention in a concentration of 0.001 to 50% by weight, in particular of 0.01 to 20% by weight.
• the antifouling agents according to the invention furthermore contain the usual constituents, e.g. in Ungerer, Chem. Ind. 1985, 37, 730-732 and Williams, Antifouling Marine Coatings, Noyes, Park Ridge, 1973.
• Antifouling paints contain algicidal, fungicidal, molluscicides and insecticidal active substances according to the invention, in particular binders.
• Examples of recognized binders are polyvinyl chloride in a solvent system, chlorinated rubber in a solvent system, acrylic resins in a solvent system, in particular in an aqueous system, vinyl chloride / vinyl acetate copolymer systems in the form of aqueous dispersions or in the form of organic solvent systems, butadiene / styrene / acrylonitrile Rubbers, drying oils such as linseed oil, resin esters or modified hard resins in combination with tar or Bitlirnina, asphalt as well as epoxy compounds, small amounts of chlorinated rubber, chlorinated polypropylene and vinyl resins.
• Paints may also contain inorganic pigments, organic pigments or dyes, which are preferably insoluble in sea water. Paints may also contain materials such as rosin to enable controlled release of the active ingredients. The paints may also contain plasticizers, modifiers that affect the rheological properties, and other conventional ingredients. The compounds according to the invention or the abovementioned mixtures can also be incorporated into self-polishing antifouling systems.
• the active ingredients are also suitable for controlling animal pests, in particular insects, arachnids and mites, which live in closed spaces such as apartments, factory halls, offices, vehicle cabins, etc. occurrence. To control these pests, they can be used alone or in combination with other active ingredients and auxiliaries in household insecticide products.
• Scorpionidea for example Buthus occitanus.
• Acarina e.g. Argas persicus, Argas reflexus, Bryobia ssp., Dermanyssus gallinae, Glyciphagus domesticus, O ⁇ iithodorus moubat, Rhipicephalus sanguineus, Trombicula alfreddugesi, Neutrombicula autumnalis, Dermatophagoides pteronissimus, Dermatophagoides pteronissimus.
• Opiliones e.g. Pseudoscorpiones chelifer, Pseudoscorpiones chemdium, Opiliones phalangium.
• Lepidoptera e.g. Achroia grisella, Galleria mellonella, Plodia interpunctella, Tinea cloacella, Tinea pellionella, Tineola bisselhella.
• Ctenocephalides canis Ctenocephalides felis, Pulex irritans, Tunga penetrans, Xenopsylla cheopis.
• Hymenoptera e.g. Camponotus herculeanus, Lasius fuliginosus, Lasius niger, Lasius umbratas, Monomorium pharaonis, Paravespula spp., Tetramorium caespitam.
• sprayless spray agents e.g. Pump and atomizer sprays, fog machines, foggels, foams, gels, vaporizer products with vaporizer platelets made of cellulose or plastic, liquid vaporizers, gel and membrane vaporizers, propeller-driven vaporizers, energy-free or passive evaporation systems, moth papers, moth bags and moth gels, as granules or dust, in scattered dust or bait stations.
• Pump and atomizer sprays fog machines, foggels, foams, gels, vaporizer products with vaporizer platelets made of cellulose or plastic, liquid vaporizers, gel and membrane vaporizers, propeller-driven vaporizers, energy-free or passive evaporation systems, moth papers, moth bags and moth gels, as granules or dust, in scattered dust or bait stations.
• the active compounds according to the invention can also be used as defoliants, desiccants, haulm killers and in particular as weed killers. Weeds in the broadest sense are all plants that grow in places where they are undesirable. Whether the substances according to the invention act as total or selective herbicides depends essentially on the amount used.
• the active compounds according to the invention can e.g. can be used in the following plants:
• Apera Avena, Brachiaria, Bromus, Cenchrus, Commelina, Cynodon, Cyperus, Dactyloctenium, Digitaria, Echinochloa, Eleocharis, Eleusine, Eragrostis, Eriochloa, Festuca, Fimbristyhs, Heteranthera, Imperata, Ischaemum, Leptochloa, Lolium, Monochoria, Panicum, Paspalum, Phalaris, Phleum, Poa, Rottboellia, Sagittaria, Scirpus, Setaria, Sorghum.
• the active compounds according to the invention are suitable for combating total weeds, e.g. on industrial and track systems and on
• the active compounds according to the invention for weed control in permanent crops e.g. Forest, ornamental wood, fruit, wine, citrus, nut, banana, coffee, tea, rubber, oil palm, cocoa, berry fruit and hop plants, on ornamental and sports turf and pasture areas as well for selective weed control in annual crops.
• the compounds of formula (I) according to the invention show strong herbicidal activity and a broad spectrum of activity when used on the soil and on above-ground parts of plants. To a certain extent, they are also suitable for selective use Control of monocotyledon and dicotyledon weeds in monocotyledon and dicotyledon crops, both pre- and post-emergence.
• the active compounds according to the invention can also be used in certain concentrations or application rates for controlling animal pests and fungal or bacterial plant diseases. If appropriate, they can also be used as intermediates or precursors for the synthesis of further active compounds.
• the active ingredients can be converted into the usual formulations, such as
• Solutions, emulsions, wettable powders, suspensions, powders, dusts, pastes, soluble powders, granules, suspension emulsion concentrates, active ingredient-impregnated natars and synthetic substances as well as very fine encapsulations in polymeric substances.
• formulations are prepared in a known manner, e.g. B. by mixing the active ingredients with extenders, that is liquid solvents and / or solid carriers, optionally using surface-active agents, ie emulsifiers and / or dispersants and / or foam-generating agents.
• extenders that is liquid solvents and / or solid carriers
• surface-active agents ie emulsifiers and / or dispersants and / or foam-generating agents.
• organic solvents can also be used as auxiliary solvents.
• auxiliary solvents e.g. organic solvents.
• aromatics such as xylene, toluene, or alkylnaphthalenes
• chlorinated aromatics and chlorinated aliphatic hydrocarbons such as
• Chlorobenzenes chlorethylenes or methylene chloride, aliphatic hydrocarbons, such as cyclohexane or paraffins, for example petroleum fractions, mineral and vegetable oils, alcohols, such as butanol or glycol and their ethers and esters, ketones such as acetone, methyl ethyl ketone, methyl isobutyl ketone or cyclohexanone, strongly polar solvents such as dimethylformamide and dimethyl sulfoxide, and water.
• aliphatic hydrocarbons such as cyclohexane or paraffins, for example petroleum fractions, mineral and vegetable oils
• alcohols such as butanol or glycol and their ethers and esters
• ketones such as acetone, methyl ethyl ketone, methyl isobutyl ketone or cyclohexanone
• strongly polar solvents such as dimethylformamide and dimethyl sulfoxide, and water.
• ammonium salts and natural rock powders such as kaolins, clays, talc, chalk, quartz, attapulgite, montmorillonite or diatomaceous earth
• synthetic rock powders such as highly disperse silica, aluminum oxide and silicates
• granules in question eg broken and fractionated natural rocks such as calcite, marble, pumice, sepiolite, dolomite as well as synthetic granules from inorganic and organic flours as well as granules from organic material such as sawdust, coconut shells, corn cobs and tobacco stalks
• suitable emulsifiers and / or foam-generating agents are: for example nonionic and anionic emulsifiers, such as polyoxyethylene fatty acid esters, polyoxyethylene fatty alcohol ethers, for example alkylaryl polyglycol ethers, alkyl sulfonates, alkyl sulf
• Adhesives such as carboxymethyl cellulose, natural and synthetic powdery, granular or latex-shaped polymers, such as gum arabic, polyvinyl alcohol, polyvinyl acetate, and natural phospholipids such as cephalins and lecithins and synthetic phospholipids can be used in the formulations.
• Other additives can 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 can be used.
• the formulations generally contain between 0.1 and 95 percent by weight of active compound, preferably between 0.5 and 90%.
• active compounds according to the invention can also be used in a mixture with known herbicides and / or with substances which improve crop tolerance (“safeners”) for combating weeds, finished formulations or tank mixes being possible Mixtures with weed control agents possible, which contain one or more known herbicides and a safener.
• Cycloxydim Cyhalofop (-butyl), 2,4-D, 2,4-DB, Desmedipham, Diallate, Dicamba, Dichlorprop (-P), Diclofop (-methyl), Diclosulam, Diethatyl (-ethyl), Difenzoquat, Diflufenican, Diflufenzopyr, Dimefuron, Dimepiperate, Dimethachlor, Dimethametryn, Dimethenamid, Dimexyflam, Dinitramine, Diphenamid, Diquat, Dithiopyr, Diuron, Dymron, Epropodan, EPTC, Esprocarb, Ethalfluralin, Ethametsulfururon (Ethylfulfur) Etobenzanid, Fenoxaprop (-P-ethyl), Fentrazamide, Flamprop (-isopropyl, -isopropyl-L, -methyl), Flazasulfuron, Florasulam
• Imazethapyr Imazosulfuron, Iodosulfuron (-methyl, -sodium), Ioxynil, Isopropalin, Isoproturon, Isouron, Isoxaben, Isoxachlortole, Isoxaflutole, Isoxapyrifop, Lactofen, Lenacil, Linuron, MCPA, Mecoprop, Motrioneacetametha , Metobenzuron, metobromuron, (alpha-) metolachlor, metosulam, metoxuron, metribuzin, metsulfuron (-methyl), molinate, monolinuron,
• Prostyzamides prosulfocarb, prosulfuron, pyraflufen (-ethyl), pyrazogyl, pyrazolates, pyrazosulfuron (-ethyl), pyrazoxyfen, pyribenzoxime, pyributicarb, pyridate, pyridodol, pyriftalid, pyriminobac (-methyl), pyrithiobac (-sodium), pyrithiobac (-sodium) Quinmerac, Quinoclamine, Quizalofop (-P-ethyl, -P-tefuryl), Rimsulfuron, Sethoxydim, Simazine, Simetryn, Sulcotrione, Sulfentrazone, Sulfometuron (-methyl), Sulfosate,
• Known safeners are also suitable for the mixtures, for example: AD-67, BAS-145138, Benoxacor, Cloquintocet (-mexyl), Cyometrinil, 2,4-D, DKA-24, dichlormid, Dymron, Fenclorim, Fenchlorazol (-ethyl ), Flurazole, fluxofenim, Furilazole, Isoxadifen (-ethyl), MCPA, Mecoprop (-P), Mefenpyr (-diethyl), MG-191, Oxabetrinil, PPG-1292, R-29148.
• a mixture with other known active compounds such as fungicides, insecticides, acaricides, nematicides, bird repellants, plant nutrients and agents which improve soil structure, is also possible.
• the active compounds can be used as such, in the form of their formulations or in the use forms prepared therefrom by further dilution, such as ready-to-use solutions, suspensions, emulsions, powders, pastes and granules. They are used in the usual way, e.g. by pouring, spraying, spraying, sprinkling.
• the active substances according to the invention can be applied both before and after emergence of the plants. They can also be worked into the soil before sowing.
• the amount of active ingredient used can vary over a wide range. It essentially depends on the type of effect desired. In general, the application rates are between 1 g and 10 kg of active ingredient per hectare of soil, preferably between 5 g and 5 kg per ha.
• the substances according to the invention have a strong microbicidal action and can be used to control unwanted microorganisms, such as fungi and bacteria, in crop protection and in material protection.
• Fungicides can be used to protect plants against Plasmodiophoromycetes, Oomycetes, Chytridiomycetes, Zygomycetes, Ascomycetes, Basidiomycetes and Deuteromycetes.
• Bactericides can be used in crop protection to combat Pseudomonadaceae, Rhizobiaceae, Enterobacteriaceae, Corynebacteriaceae and Streptomycetaceae.
• pathogens of fungal and bacterial are exemplary but not limiting
• Xanthomonas species such as, for example, Xanthomonas campestris pv. Oryzae;
• Pseudomonas species such as. for example Pseudomonas syringae pv. lachrymans;
• Erwinia species such as, for example, Erwinia .amylovora;
• Pythium species such as, for example, Pythium ultimum
• Phytophthora species such as, for example, Phytophthora infestans
• Pseudoperonospora species such as, for example, Pseudoperonospora humuli or
• Plasmopara species such as, for example, Plasmopara viticola
• Bremia species such as, for example, Bremia lactucae
• Peronospora species such as, for example, Peronospora pisi or P. brassicae;
• Erysiphe species such as, for example, Erysiphe graminis
• Sphaerotheca species such as, for example, Sphaerotheca fuliginea
• Podosphaera species such as, for example, Podosphaera leucotricha
• Venturia species such as, for example, Venturia inaequalis
• Pyrenophora species such as, for example, Pyrenophora teres or P. graminea
• Cochliobolus species such as, for example, Cochliobolus sativus
• Drechslera (Conidial form: Drechslera, Syn: Helminthosporium);
• Uromyces species such as, for example, Uromyces appendiculatus
• Puccinia species such as, for example, Puccinia recondita
• Sclerotinia species such as, for example, Sclerotinia sclerotiorum
• Tilletia species such as, for example, Tilletia caries
• Ustilago species such as, for example, Ustilago nuda or Ustilago avenae;
• Pellicularia species such as, for example, Pellicularia sasakii;
• Pyricularia species such as, for example, Pyricularia oryzae
• Fusarium species such as, for example, Fusarium culmorum
• Botrytis species such as, for example, Botrytis cinerea; Septoria species, such as, for example, Septoria nodorum;
• Leptosphaeria species such as, for example, Leptosphaeria nodorum;
• Cercospora species such as, for example, Cercospora canescens
• Altemaria species such as, for example, Altemaria brassicae;
• Pseudocercosporella species such as, for example, Pseudocercosporella herpotrichoides.
• the active compounds according to the invention also have a strong strengthening effect in plants. They are therefore suitable for mobilizing the plant's own defenses against attack by unwanted microorganisms.
• Plant-strengthening (resistance-inducing) substances are to be understood in the present context as those substances which are able to stimulate the defense system of plants in such a way that the treated plants develop extensive resistance to these microorganisms when subsequently inoculated with undesirable microorganisms.
• Undesired microorganisms are to be understood in the present case as phytopathogenic fungi, bacteria and viruses.
• the substances according to the invention can therefore be used to protect plants from attack by the said harmful agents within a certain period of time after the treatment.
• the period of time during which protection is brought about generally ranges from 1 to 10 days, preferably 1 to 7 days, after the treatment of the plants with the active compounds.
• the fact that the active compounds are well tolerated by plants in the concentrations required to combat plant diseases permits treatment of above-ground parts of plants, of propagation stock and seeds, and of the soil.
• the active compounds according to the invention are also suitable for increasing the crop yield.
• the active substances according to the invention can 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 further active compounds.
• the substances according to the invention can be used to protect technical materials against attack and destruction by undesired microorganisms.
• technical materials are to be understood as non-living materials that have been prepared for use in technology.
• technical materials that are to be protected against microbial change or destruction by active substances according to the invention can be adhesives, glues, paper and cardboard, textiles, leather, wood, paints and plastic articles, cooling lubricants and other materials that can be attacked or decomposed by microorganisms .
• parts of production plants for example cooling water circuits, are also mentioned which can be impaired by the multiplication of microorganisms.
• technical materials are preferably adhesives, glues, papers and cartons, leather, wood, paints, cooling lubricants and heat transfer fluids, particularly preferably wood.
• Bacteria, fungi, yeasts, algae and mucilaginous organisms may be mentioned as microorganisms which can break down or alter the technical materials.
• the active compounds according to the invention preferably act against fungi, in particular mold, wood-discoloring and wood-destroying fungi
• Altemaria such as Altemaria tenuis
• Altemaria tenuis such as Altemaria tenuis
• Aspergillus such as Aspergillus niger
• Chaetomium like 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 like Trichoderma vhide
• Escherichia such as Escherichia coli
• Pseudomonas such as Pseudomonas aeruginosa
• Staphylococcus such as Staphylococcus aureus.
• the active ingredients can be converted into the customary formulations, such as solutions, emulsions, suspensions, powders, foams, pastes, granules, aerosols, very fine encapsulations in polymeric substances and in coating compositions for seeds, and ULV -Cold and warm mist formulations.
• formulations are made in a known manner, e.g. by mixing the additives with extenders, that is to say liquid solvents, pressurized liquefied gases and / or solid carriers, if appropriate using surface-active agents, that is to say emulsifiers and / or dispersants and / or foam-generating agents. If water is used as an extender, e.g. organic solvents can also be used as auxiliary solvents.
• extenders that is to say liquid solvents, pressurized liquefied gases and / or solid carriers, if appropriate using surface-active agents, that is to say emulsifiers and / or dispersants and / or foam-generating agents.
• surface-active agents that is to say emulsifiers and / or dispersants and / or foam-generating agents.
• water e.g. organic solvents can also be used as auxiliary solvents.
• aromatics such as xylene, toluene or alkylnaphthalenes
• chlorinated aromatics or chlorinated aliphatic hydrocarbons such as chlorobenzenes, chlorethylenes or methylene chloride
• aliphatic hydrocarbons such as cyclohexane or paraffins, e.g. Petroleum fractions
• Alcohols 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.
• Liquefied gaseous extenders or carriers mean liquids which are gaseous at normal temperature and pressure, e.g. aerosol
• Propellants such as halogenated hydrocarbons, butane, propane, nitrogen and carbon dioxide.
• the following are suitable as solid carriers: for example, natural rock powders, such as kaolins, clays, talc, chalk, quartz, attapulgite, montmorillonite or diatomaceous earth, and synthetic rock powders, such as highly disperse silica, aluminum oxide and silicates.
• Possible solid carriers for granules are: eg broken and fractionated natural rocks such as calcite, marble, pumice, sepiolite, dolomite and synthetic granules from inorganic and organic flours as well as granules from organic material such as sawdust, coconut shells, corn cobs and tobacco stems.
• Suitable emulsifiers and / or foaming agents are: for example nonionic and anionic emulsifiers, such as polyoxyethylene fatty acid esters, polyoxyethylene fatty alcohol ethers, for example alkylaryl polyglycol ethers, alkyl sulfonates, alkyl sulfates, aryl sulfonates and protein hydrolyzates.
• Possible dispersants are, for example, lignin sulfite liquor and methyl cellulose.
• Adhesives such as carboxymethyl cellulose, natural and synthetic powdery, granular or latex-shaped polymers, such as gum arabic, polyvinyl alcohol, polyvinyl acetate, and natural phospholipids, such as cephalins and lecithins, and synthetic phospholipids can be used in the formulations.
• Other additives can be mineral and vegetable oils.
• Dyes such as inorganic pigments, e.g. Iron oxide, titanium oxide, Fe ⁇ ocyanblau 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 can be used.
• the formulations generally contain between 0.1 and 95 percent by weight of active compound, preferably between 0.5 and 90%.
• the active compounds according to the invention can also be used in a mixture with known fungicides, bactericides, acaricides, nematicides or insecticides, in order to, for example, broaden the spectrum of activity or to prevent the development of resistance; in many cases, synergistic effects, ie the effectiveness, are obtained the mixture is greater than the effectiveness of the individual components.
• the following connections can be considered as mixed partners:
• 2-phenylphenol 8-hydroxyquinoline sulfates; Acibenzolar-S-methyl; aldimorph; amidoflumet; Ampropylfos; Ampropylfos-potassium; andoprim; anilazine;
• azaconazole azoxystrobin; benalaxyl; Benodanil; benomyl; Benthiavalicarbisopropyl; Benzamacril; Benzamacril-isobutyl; bilanafos; binapacryl; biphenyl;
• bitertanol Blasticidin-S; bromuconazole; Bupirimate; Buthiobate; butylamine;
• chloroneb chlorothalonil; chlozolinate; Clozylacon; cyazofamid; cyflufenamid;
• diethofencarb Difenoconazole; Diflmnetorim; dimethirimol; dimethomorph; dimoxystrobin; diniconazole; Diniconazole-M; Dinöcap; diphenylamines;
• epoxiconazole ethaboxam; ethirimol; etridiazole; famoxadone; fenamidone;
• fenoxanil fenpiclonil; fenpropidin; fenpropimorph; ferbam; fluazinam; Flubenzimine; fludioxonil; flumetover; Flumo h; fluoromides; fluoxastrobin;
• fluquinconazole flurprimidol
• flusilazole flusulfamide
• flutolanil flutriafol
• folpet Fosetyl-Al; Fosetyl-sodium; fuberidazole; furalaxyl; furametpyr;
• Furcarbanil Furmecyclox; guazatine; Hexachlorobenzene; hexaconazole;
• hymexazol imazalil; hnibenconazole; Iminoctadine triacetate; Iminoctadine tris (albesil; lodocarb; Ipconazole; Iprobefos; Iprodione; Iprovalicarb; Irmnamycin;
• isoprothiolane isoprothiolane; Isovaledione; kasugamycin; Kresoxim-methyl; mancozeb; maneb;
• Meferimzone mepanipyrim; mepronil; metalaxyl; Metalaxyl-M; metconazole;
• methasulfocarb MetMuroxam; metiram; metominostrobin; Metsulfovax;
• Polyoxorim Probenazole; prochloraz; procymidone; propamocarb; Propanosine sodium; propiconazole; propineb; proquinazid; prothioconazole; pyraclostrobin; Pyrazohos; pyrifenox; pyrimethanil; pyroquilon; Pyroxyfur; Py ⁇ olnitrine;
• Thicyofen Thifluzamide; Thiöphanate-methyl; Thirani; Tioxymid; Tolclofos-methyl;
• Copper naphthenate Copper oxychloride; Copper sulfate; Cufraneb; Cuprous oxide;
• Chlorobenzilate Chloropicrin, Chlo ⁇ roxyfen, Chlo ⁇ yrifos-methyl, Chlorpyrifos (-ethyl), Chlovaporthrin, Chromafenozide, Cis-Cypermethrin, Cis-Resmethrin, Cis- Permethrin, Clocytlirin, Cloethocarb, Clofentezine, Coxosphosphos, Cosylosone, Clothianidin, Clothianidin, Clothianidin, Clothianidine, Cycloprene, Cycloprothrin, Cydia pomonella, Cyfluthrin, Cyhalothrin, Cyhexatin, Cypermethrin, Cyphenothrin
• DDT Deltamethrin, Demeton-S-methyl, Demeton-S-methylsulphone, Diafenthiuron, Dialifos, Diazinon, Dichlofenthion, Dichlorvos, Dicofol, Dicrotophos, Dicyclanil, Diflubenzuron, Dimethoate, Dimethylvinphos, Dinobuton, Dinocap, Dinotefuran, Diofenolan, Disulfoton, Docusat-sodium, Dofenapyn, DOWCO-439,
• Fenamiphos Fenazaquin, Fenbutatin oxide, Fenfluthrin, Fenitrothion, Fenobucarb, Fenothiocarb, Fenoxacrim, Fenoxycarb, Fenpropathrin, Fenpyrad, Fenpyrithrin, Fenpyroximate, Fensulfothion, Fenthion, Fentrifanil, Fenronilerate, Fenronilate,
• Fluacrypyrim Fluazuron, Flubenzimine, Flubrocytlirinate, Flucycloxuron, Flucythrinate, Flufenerim, Flufenoxuron, Flufenprox, Flumethrin, Flupyrazo- fos, Flutenzin (Flufenzine), Fluvalinate, Fofofosuphonofan, Fofofoffenuphane, ), Furathiocarb,
• Halofenozide HCH, HCN-801, Heptenophos, Hexaflumuron, Hexythiazox, Hydramethylnone, Hydroprene,
• IKA-2002 Imidacloprid, Imiprothrin, Indoxacarb, Iodofenphos, Iprobefos, Isazofos, Isofenphos, Isoprocarb, Isoxathion, Ivermectin,
• NC-104 NC-170, NC-184, NC-194, NC-196, Niclosamide, Nicotine, Nitenpyram, Nithiazine, NNI-0001, NNI-0101, NNI-0250, NNI-9768, Novaluron, Noviflumuron,
• Paecilomyces fumosoroseus Parathion-methyl, Parathion (-ethyl), Permethrin (eis, trans-), Petroleum, PH-6045, Phenothrin (IR-trans isomer), Phenthoate, Phorate,
• the compounds of formula (I) according to the invention also have very good antifungal effects. They have a very broad anti mycoticumblesspelctrum, in particular against dermatophytes and yeasts, molds and diphasic fungi (for example against Candida species such as Candida albicans, Candida glabrata) and also 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 in no way a limitation of the detectable mycotic spectrum, but is only of an explanatory nature.
• the active compounds can be used as such, in the form of their formulations or the use forms prepared therefrom, such as ready-to-use solutions, suspensions, wettable powders, pastes, soluble powders, dusts and granules. They are used in the usual way, e.g. by pouring, spraying, atomizing, scattering, dusting, foaming, brushing, etc. It is possible for him
• the application rates can be varied within a substantial range, depending on the type of application.
• the active compound application rates are generally between 0.1 and 10,000 g / ha, preferably between 10 and 1,000 g ha.
• the active compound application rates are generally between 0.001 and 50 g per kilogram of seed, preferably between 0.01 and
• the active compound application rates are generally between 0.1 and 10,000 g / ha, preferably between 1 and 5,000 g / ha.
• the preparation and use of the active compounds according to the invention can be seen from the examples below.
• Solvent 7 parts by weight of dimethylformamide emulsifier: 2 parts 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 to the desired concentration with water containing emulsifier.
• Cabbage leaves (Brassica oleracea), which are heavily infested with peach aphids (Myzus persicae), are treated by immersing them in the active ingredient preparation of the desired concentration.
• the kill is determined in%. 100% means that all aphids have been killed; 0% means that no aphids have been killed.
• Solvent 7 parts by weight of dimethylformamide emulsifier: 2 parts 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 to the desired concentration with water containing emulsifier.
• Cabbage leaves (Brassica oleracea) are treated by being dipped into the preparation of active compound of the desired concentration and populated with larvae of the horseradish leaf beetle (Phaedon cochleariae) while the leaves are still moist.
• the kill is determined in%. 100% means that all beetle larvae have been killed; 0% means that no beetle larvae have been killed.

Landscapes

• Chemical & Material Sciences (AREA)
• Organic Chemistry (AREA)
• Life Sciences & Earth Sciences (AREA)
• Wood Science & Technology (AREA)
• Environmental Sciences (AREA)
• Plant Pathology (AREA)
• Health & Medical Sciences (AREA)
• Engineering & Computer Science (AREA)
• Dentistry (AREA)
• General Health & Medical Sciences (AREA)
• Agronomy & Crop Science (AREA)
• Zoology (AREA)
• Pest Control & Pesticides (AREA)
• Agricultural Chemicals And Associated Chemicals (AREA)
• Plural Heterocyclic Compounds (AREA)
• Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
• Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
• Indole Compounds (AREA)
• Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
• Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)

Applications Claiming Priority (3)

Publications (1)

Family

ID=7708295

Family Applications (1)

Country Status (14)

Families Citing this family (9)

Family Cites Families (23)

• 2001
  • 2001-12-06 DE DE10160007A patent/DE10160007A1/de not_active Withdrawn
• 2002
  • 2002-11-27 CN CN02827658.2A patent/CN100506806C/zh not_active Expired - Fee Related
  • 2002-11-27 KR KR1020047007909A patent/KR100861483B1/ko not_active IP Right Cessation
  • 2002-11-27 BR BR0214759-9A patent/BR0214759A/pt not_active Application Discontinuation
  • 2002-11-27 US US10/497,479 patent/US7183238B2/en not_active Expired - Fee Related
  • 2002-11-27 WO PCT/EP2002/013382 patent/WO2003048138A1/de active Application Filing
  • 2002-11-27 AU AU2002358053A patent/AU2002358053B2/en not_active Ceased
  • 2002-11-27 RU RU2004120559/04A patent/RU2004120559A/ru not_active Application Discontinuation
  • 2002-11-27 EP EP02791728A patent/EP1456185A1/de not_active Withdrawn
  • 2002-11-27 PL PL02370715A patent/PL370715A1/xx unknown
  • 2002-11-27 JP JP2003549330A patent/JP4542340B2/ja not_active Expired - Fee Related
  • 2002-11-27 MX MXPA04005371A patent/MXPA04005371A/es active IP Right Grant
  • 2002-11-27 CA CA2469191A patent/CA2469191C/en not_active Expired - Fee Related
• 2004
  • 2004-06-01 ZA ZA200404286A patent/ZA200404286B/en unknown

Non-Patent Citations (1)

Also Published As

Similar Documents

Legal Events