Abstract:
The present invention relates to novel triazole compounds of the formulae I, II and IV to agricultural compositions containing them, to their use as fungicides and to intermediate compounds used in the method of producing them.
Abstract:
The present invention relates to novel triazole compounds of the formulae (I), (Il) and (IV) as defined below, to agricultural and pharmaceutical compositions containing them and to their use as fungicides, antimycotic, anticancer and antiviral agents.
Abstract:
The invention relates to fungicidal mixtures which comprise 1) azolylmethyloxiranes of general formula I, wherein the variables are defined as in the application, and 2) a fungicidal compound II as the active components, the compounds II of component 2 being selected from among the compounds described in the application. The invention also relates to the use of the fungicidal mixtures for the control of phytopathogenic fungi and to agents containing said mixtures.
Abstract:
The present invention relates to pyrimidin-4-ylmethyl-sulfonamides of formula (I) wherein Ra, n, R, A, Y and Het are as defined in the claims and to the N-oxides, and salts thereof and their use for combating harmful fungi, and also to compositions and seed comprising at least one such compound. The invention also relates to a process for preparing these compounds.
Abstract:
The present invention relates to novel pyridylmethyl-sulfonamide compounds of formula (I) where: n is 0 to 4; m is 0 to 4; R1 is halogen, CN, NO2, OH, SH, C1-C4-alkyl, C1-C4-haloalkyl, C1-C4-alkoxy, C1-C4-haloalkoxy, etc.; and/or two radicals R1 together form a fused ring; R2 is H, C1-C4-alkyl, C1-C4-haloalkyl, C2-C4-alkenyl, C2-C4-alkynyl, C3-C8-cycloalkyl, C1-C4-alkyl-C3-C8-cycloalkyl or benzyl; R3 is halogen, CN, NO2, C1-C4-alkyl, C1-C4-haloalkyl, C1-C4-alkoxy or C1-C4-haloalkoxy; Y is -O-, C1-C4-alkane- diyl, -O-CH2-, -CH2-O-, -C(NOR')-, -S-, -S(=0)-, -Sf=O)2- or -N(R')-; and the N-oxides, and salts thereof and their use for combating phytopathogenic harmful fungi, and also to compositions and seed comprising at least one such compound.
Abstract:
The present invention relates to mixtures of fungicidally active compounds comprising at least one substituted 3-hydroxyl-3-(3-pyridyl)propanoate compound of the formula (I) X 1 and X 2 are hydrogen or X 1 together with X 2 form a covalent bond; R 1 is H, CN, C 1 -C 6 -alkyl, C 2 -C 6 -alkynyl, C 1 -C 6 -alkoxy-C 1 -C 6 -alkyl, C 1 -C 6 - alkylthio-C 1 -C 6 -alkyl, C 1 -C 6 -haloalkyl, C 1 -C 6 -alkoxy, aryl-C 1 -C 4 -alkyl, ary- loxy-C 1 -C 4 -alkyl, arylthio-C 1 -C 4 -alkyl, aryl, hetaryl-C 1 -C 4 -alkyl, hetaryloxy- C 1 -C 4 -alkyl, hetarylthioC 1 -C 4 -alkyl or heteroaryl, wherein the cyclic moieties of the last eight radicals are unsubstituted or substituted with 1, 2 or 3 radicals selected from halogen, C 1 -C 4 -alkyl, C 2 -C 4 -alkynyl, C 1 -C 4 -haloalkyl, C 1 -C 4 -alkoxy, C 1 -C 4 -alkylthio, C 1 -C 4 -alkylsulfinyl, C 1 -C 4 -alkylsulfonyl, C 1 -C 4 -haloalkoxy, C 1 -C 4 -haloalkylthio, cyano and nitro; A is a covalent bond or Ci-C4-alkylen, which is unsubstituted or which may carry a substitutent selected from Ci-C4-alkyl, Ci-C4-haloalkyl, Ci-C4-alkoxy and cyano; Ar is aryl or heteroaryl, wherein the cyclic moieties of the aromatic radicals are unsubstituted or substituted with 1, 2 or 3 radicals R a , where the radicals R a are identical or different and selected from halogen, C 1 -C 4 -alkyl, C 2 -C 4 - alkenyl, C 2 -C 4 -alkynyl, C 1 -C 4 -haloalkyl, C 1 -C 4 -alkoxy, C 1 -C 4 -alkylthio, C 1 -C 4 -haloalkoxy, C 1 -C 4 -haloalkylthio, cyano, nitro, aryl, hetaryl, aryloxy, hetaryloxy, aryloxy-C 1 -C 4 -alkyl and hetaryloxy-C 1 -C 4 -alkyl, wherein the cyclic moieties of the six last mentioned radicals are unsbsubstituted or substituted with 1, 2 or 3 radicals selected from halogen, C 1 -C 4 -alkyl, C 1 -C 4 -haloalkyl, C 1 -C 4 -alkoxy, C 1 -C 4 -alkylthio, C 1 -C 4 -haloalkoxy, cyano and nitro; or a tautomer or a salt thereof. and at least one further fungicidally active compound II.
Abstract:
The present invention relates to mixtures comprising, as active components, 1) a fungicidal compound of formula (I) wherein: R1 is alkyl; alkoxyalkyl; haloalkyl; arylalkyl; aryl; or heteroaryl; R2 is alkyl; alkoxyalkyl; haloalkyl; arylalkyl; aryl; heteroaryl; 5-pyrimidinyl; or 2-or 5-thiazolyl; R3 is H; alkyl; alkoxyalkyl; haloalkyl; arylalkyl; aryloxyalkyl; arylthioalkyl; aryl; heteroaryl; or alkylsilyl; R4 is H; acyl; haloacyl, alkoxycarbonyl; aryloxycarbonyl; alkylaminocarbonyl; or dialkylaminocarbonyl; or a salt thereof; and 2) a fungicidal compound II selected from azoles, strobilurins, carboxamides, heterocylic compounds, carbamates, and other active compounds in synergistically effective amounts.
Abstract:
Azolopyrimidines of the formula (I), wherein the symbols have the meanings provided in the description, are suited to fight plant pathogenic fungi.
Abstract:
The invention relates to 2-(pyridin-2-yl)-pyrimidines of formula (I) and their use in the control of parasitic fungi and to herbicides that contain said compounds as an effective ingredient thereof. In formula (I), Q represents a condensed, saturated five-, six- or seven-membered carbocycle or five-, six- or seven-membered heterocycle which, in addition to the carbon ring members, has one or two heteroatoms selected from oxygen and sulfur as the ring members, the carbocycle and the heterocycle being unsubstituted or having 1, 2, 3 or 4 C1-C4 alkyl groups as the substituents; R1 represents hydrogen, OH, C1-C4 alkyl, C1-C4 alkoxy, C1-C4 halogenalkyl, C1-C4 halogenalkoxy or halogen; R2 represents hydrogen, NO2, halogen, C1-C6 alkyl, C3-C6 cycloalkyl, C1-C6 alkoxy, C1-C6 halogenalkyl or C1-C6 halogenalkoxy; R3 represents hydrogen, halogen, C1-C4 alkyl, C1-C4 alkoxy, C1-C4 halogenalkyl or C1-C4 halogenalkoxy; R4 has phenyl, 5-membered heteroaryl which has 1, 2, 3 or 4 nitrogen atoms or 1 heteroatom selected from oxygen and sulfur and optionally 1, 2 or 3 nitrogen atoms as the ring atoms, or 6-membered hetaryl, which has 1, 2, 3 or 4 nitrogen atoms as the ring members, wherein phenyl, 5- and 6-membered hetaryl may have 1, 2, 3 or 4 substituents Ra.
Abstract:
The invention relates to a 6-phenyl-pyrazolopyrimidine-7-ylamine of formula (I), wherein substituents are defined according to the description. Methods for producing said compounds, agents containing said compounds and the use thereof for controlling phytopathogenic parasitic fungi are also disclosed.