Abstract:
Triazolopyrimidine der Formel (I), in der der Index und die Substituenten folgende Bedeutung haben: R 1 C 1 -C 10 -Alkyl, C 2 -C 10 -Alkenyl, C 2 -C 10 -Alkinyl, C 3 -C 10 -Cycloalkyl, C 3 -C 10 -Cycloalkenyl, Phenyl, Naphthyl, oder ein fünf- bis zehngliedriger gesättigter, partiell ungesättigter oder aromatischer Heterocyclus, der über Kohlenstoff mit dem Triazolopyrimidin verbunden ist und ein bis vier Heteroatome aus der Gruppe O, N oder S enthält, R 2 C1-C 4 -Alkyl, das durch Halogen, Cyano, Nitro oder C 1 -C 2 -Alkoxy substituiert sein kann; n 0 oder eine ganze Zahl von 1 bis 4; R wie in der Beschreibung definiert ist; X SO m -R x , NR x R y oder NR x -(C=O)-R y ; m 0 oder eine ganze Zahl 1 bis 3; sowieVerfahren zur Herstellung dieser Verbindungen, sie enthaltende Mittel sowie ihre Verwendung zur Bekämpfung von Schadpilzen.
Abstract:
Verfahren zur Herstellung dieser Verbindungen, sie enthaltende Mittel sowie ihre Verwendung zur Bekämpfung von Schadpilzen. Triazolopyrimidine der Formel (I), in die Substituenten folgende Bedeutung haben: L 1 Alkyl; L 2 Halogen; L 3 Wasserstoff oder Halogen; X Halogen, Cyano, Alkyl, Alkoxy oder Halogenalkoxy; R 1 ,R 2 Wasserstoff, Alkyl, Halogenalkyl, Cycloalkyl, Alkenyl, Alkadienyl, Alkinyl oder Cycloalkinyl, Phenyl, Naphthyl, oder ein fünf- bis zehngliedriger gesättigter, partiell ungesättigter oder aromatischer Heterocyclus, enthaltend ein bis vier Heteroatome aus der Gruppe O, N oder S, R 1 und R 2 können auch zusammen mit dem Stickstoffatom, an das sie gebunden sind, einen fünf- oder sechsgliedrigen Ring bilden, der durch ein Atom aus der Gruppe O, N und S unterbrochen sein und/oder substituiert sein; wobei R 1 und/oder R 2 gemäss der Beschreibung substituiert sein können; Verfahren und Zwischenprodukte zur Herstellung dieser Verbindungen, sie enthaltende Mittel sowie ihre Verwendung zur Bekämpfung von Schadpilzen.
Abstract:
Triazolopyrimidines of formula (I), wherein the index and substituents have the following meaning: n = 0 or a whole number of 1 - 5; R = halogen, cyano, hydroxy, cyanate, alkyl, alkenyl, alkinyl, halogenalkyl, halogenalkenyl, alkoxy, alkenyloxy, alkinyloxy, halogenalkoxy, cycloalkyl, cycloalkenyl, cycloalkoxy, alkoxycarbonyl, alkenyloxycarbonyl, alkinyloxycarbonyl, aminocarbonyl, alkylaminocarbonyl, dialkylaminocarbonyl, alkoximinoalkyl, alkenyloximinocarbonyl, alkinyloximinoalkyl, alkylcarbonyl, alkenylcarbonyl, alkinylcarbonyl, cycloalkylcarbonyl or a five to ten membered saturated, partially unsaturated or aromatic heterocycle, containing one to four heteroatoms from the group O, N or S; R = alkyl, alkenyl, alkinyl, cycloalkyl, cycloalkenyl, phenyl, naphthyl or a five to ten membered saturated, partially unsaturated or aromatic heterocycle, containing one to four heteroatoms from the group O, N or S, R and/or R being able to be substituted according to the description; R = alkyl, alkenyl or alkinyl which can be substituted by halogen, cyano, nitro, alkoxy or alkoxycarbonyl. The invention also relates to a method for the production of said compounds, agents containing same, and the use thereof in controlling noxious fungi.
Abstract:
The invention relates to substituted phenyl carbamates of formula (I), wherein E represents a group A or B, # characterises the bond with the phenyl ring, and R , R , Y, n, T, and Z have the meanings given in the description.
Abstract:
2-(O-[pyrimidin-4-yl] methylene oxy)phenyl acetic acid derivatives of general formula (I) and their salts and N oxides, in which R is halogen, alkyl or alkyl halide; R is hydrogen, amino, hydroxy, mercapto, halogen, possibly phenyl-substituted alkyl, alkyl halide, alkoxy alkyl, alkoxy, monoalkyl amino, dialkyl amino, alkylthio, alkyl sulphoxyl, alkylsulphonyl, cycloalkyl, trialkyl silyloxy or phenyl, phenoxy, phenoxy methyl, benzyloxy or heteroaryl possibly substituted in the aromatic ring, R being different from R ; R is hydrogen, cyano, halogen, C1-C4 alkyl, C1-C4 alkyl halide or C1-C4 alkoxy, and Q is C(=CHCH3)-COOCH3 or C(=CHOCH3)-COOCH3, and their use in combatting noxious fungi and animal pests.
Abstract:
The invention pertains to phenylcarbamates of formula (I), wherein X is a direct bond, O or NR ; Z is O, S or NR ; R is hydrogen, alkyl or alkyl halide; R is substituted methyl or optionally substituted alkyl, alkenyl, alkinyl or cycloalkyl; R is optionally substituted alkyl, alkenyl or alkinyl; R is alkyl, alkenyl or alkinyl and, if X is NR , hydrogen also; R is hydrogen or optionally substituted alkyl, alkenyl, alkinyl, alkyl carbonyl or alkoxy carbonyl. The invention also pertains to methods for their preparation and agents containing them.
Abstract:
Disclosed are azinooximethers of formula (I) in which X stands for NOCH3, CHOCH3, CHCH3, Y stands for O, NZ, Z being H or alkyl, R stands for H, alkyl, R stands for cyano, nitro, trifluoromethyl, halogen, alkyl, alkoxy, m is 0, 1 or 2, (the R rests can be different if m is 2), R is H, cyano, alkyl, alkyl halide, alkoxy, cycloalkyl, R , R and R independently of one another stand for H or optionally substituted alkyl, alkenyl, alkinyl, cycloalkyl, cycloalkenyl, heterocyclyl. Also disclosed are the salts of these compounds and process and intermediate products for manufacturing them, and the uses thereof in combating harmful fungi and pests.
Abstract:
2-[4-biphenyl-oxymethylene]-anilides have the formula (I), in which the indices and substituents have the following meanings: R, R , R stand for cyano, nitro, halogen, alkyl, alkyl halide, alkoxy, alkoxy halide, alkylthio, alkylthio halide, alkylamino, dialkylamino, alkylcarbonyl, alkoxycarbonyl, alkylaminocarbonyl, di-alkylaminocarbonyl, alkylcarbonylamino, alkylcarbonyl-(alkylamino), alkenyl, alkenyloxy, alkinyl, alkinyloxy, cycloalkyl or C(R )=NOR ; R , R stand for hydrogen, alkyl, alkenyl, alkinyl, cycloalkyl or cycloalkenyl; m equals 1, 2, 3, 4 or 5; n equals 0, 1 or 2; R equals nitro, cyano, halogen, optionally substituted alkyl, alkenyl, alkinyl, alkoxy, alkenyloxy, alkinyloxy or alkylcarbonyl, alkoxycarbonyl, alkylaminocarbonyl, dialkylaminocarbonyl, alkylcarbonylamino, alkylcarbonyl-(alkylamino) or C(R )=NOR ; o equals 0, 1, 2, 3 or 4; R stands for hydrogen, optionally substituted alkyl, alkenyl, alkinyl, cycloalkyl, cycloalkenyl, alkylcarbonyl or alkoxycarbonyl; X stands for a direct bond or CH2, O or NR ; R stands for hydrogen, alkyl, alkenyl, alkinyl, cycloalkyl or cycloalkenyl; R stands for alkyl, alkenyl, alkinyl, cycloalkyl or cycloalkenyl and when X stands for NR it may also stand for hydrogen. Also disclosed are a process and intermediate products for preparing the same and their use.
Abstract:
The invention pertains to phenylacetic acid alkyl esters of formula I, wherein the index and substituents are as follows: R' is formyl, alkyl carbonyl or alkyl; R'' is alkyl; U is -O-, -S-, -NH- or -NHO-; V is -O-, -S-, or -NH-; X is cyano, nitro, halogen, alkyl, alkyl halide, alkoxy, alkoxy halide, alkyl thio or, if n is > 1, optionally substituted alkylene, alkenylene, oxyalkylene, oxyalkylenoxy, oxyalkenylene, oxyalkenylenoxy or butadiendiyl; n is 0, 1, 2 or 3; R is halogen, hydroxy, mercapto, amino, carboxyl, carbonylamino or an organic radical which is bonded directly or via an oxy, mercapto, amino, carboxyl or carbonylamino group, or, together with an X group and the phenyl ring to which they are bonded, an optionally substituted, bicyclic, partially or completely unsaturated system. The invention also pertains to methods and intermediate products for their preparation and to their use.