Abstract:
PCT No. PCT/EP96/04446 Sec. 371 Date Apr. 15, 1998 Sec. 102(e) Date Apr. 15, 1998 PCT Filed Oct. 11, 1996 PCT Pub. No. WO97/15552 PCT Pub. Date May 1, 1997Phenylacetic acid derivatives of the formula I where the substituents and the index have the following meanings: x is NOCH3, CHOCH3, CHCH3; Y is O, NR R1,R independently of one another are hydrogen and C1-C4-alkyl; R2 is cyano, nitro, trifluoromethyl, halogen, alkyl and alkoxy; m is 0, 1 or 2, it being possible for the radicals R2 to be different when m is 2; R3 is hydrogen, cyano, C1-C4-alkyl, C1-C4-haloalkyl, C3-C6-cycloalkyl; R4, R5 and R6 have the meanings given in claim 1, and their salts, a process and intermediates for the preparation of these compounds, and compositions comprising them for controlling animal pests and harmful fungi.
Abstract:
Fungicidal mixture comprises: (1) an amide compound of formula (I) and (2) one or more compounds (II), (III), (IV) or (V). Fungicidal mixture comprises: (1) an amide compound of formula (I); and (2) a synegistically effective amount of a second component comprising: (a) a carboxamide selected from dimethomorph (IIa) and flumetover (IIb); (b) a valinamide compound of formula (III); (c) at least one compound selected from benalaxyl (IVa), ofurace (IVb), metalaxyl (IVc), furalaxyl (IVd) and oxadixyl (IVe); and/or (d) 1-(2-cyano-2-methoxyiminoacetyl)-3-ethyl-urea (cymoxanil (V)). A = Ar or Het (both optionally substituted by 1-3 alkyl, halo, CHF2, CF3, (halo)alkoxy, alkylthio, alkylsulfinyl or alkylsulfonyl; R = H; R = phenyl (optionally substituted by 1-3 Q and optionally fused to a group M); or cycloalkyl (optionally substituted by 1-3 Q); M = a saturated 5-membered ring which may contain an O or S atom and is optionally substituted by one or more alkyl; Ar = an aryl group; Het = an aromatic or non-aromatic, 5-6 membered heterocycle which contains 1-3 N, O or S atoms; Q = alkyl, alkenyl, alkynyl, alkoxy, alkenyloxy, alkynyloxy, cycloalkyl, cycloalkenyl, cycloalkyloxy, cycloalkenyloxy, phenyl or halo; in Q, the (cyclo)aliphatic residues are optionally halogenated, the cycloaliphatic residues are optionally substituted by 1-3 alkyl, and the phenyl is optionally substituted by 1-5 halo and/or 1-3 (halo)alkyl, (halo)alkoxy or (halo)alkylthio; R = 3-4C alkyl; R = naphthyl, or phenyl (optionally substituted in the 4-position by halo, 1-4C alkyl or 1-4C alkoxy)
Abstract:
Mezcla fungicida, que contiene como componentes activos a) un compuesto de amida de la fórmula I, donde R4 representa halógeno, y R11 representa fenilo, que está substituido por halógeno, y b) un derivado de ftalimida seleccionado a partir del grupo de compuestos IIa, IIb y III y/o c) una arilsulfamida de las fórmulas IVa y IVb IVa IVb en una cantidad eficaz de manera sinérgica.
Abstract:
The present invention relates to a fungicidal mixture containing, as active components in synergistically effective amount and in weight ratio ranging from 1:50 to 50:1 an amide compound of the general formula Ib wherein Re represents a halogen and Re11 phenyl that is substituted with a halogen, and a dithiocarbamate of the general formula II being selected from the group consisting of: manganese-ethylene bis(dithiocarbamate) (zinc complex) of the general formula IIa, manganese-ethylene bis(dithiocarbamate) of the general formula IIb, zinc ammoniate-ethylene bis(dithiocarbamate) of the general formula IIc, and zinc-ethylene bis(dithiocarbamate) of the general formula IId. There is also described a method for controlling harmful fungi by making use of the above-indicated fungicidal mixture.
Abstract:
PCT No. PCT/EP97/04541 Sec. 371 Date Feb. 22, 1999 Sec. 102(e) Date Feb. 22, 1999 PCT Filed Aug. 21, 1997 PCT Pub. No. WO98/08385 PCT Pub. Date Mar. 5, 1998The present invention relates to a fungicidal mixture which comprises a) a carbamate of the formula I where X is CH and N, n is 0, 1 or 2 and R is halogen, C1-C4-alkyl and C1-C4-haloalkyl, it being possible for the radicals R to be different when n is 2, or a salt or adduct thereof, and b) an anilide of the formula II where R1 is fluorine or chlorine, or a salt or adduct thereof, in a synergistically active amount.
Abstract:
Fungicidal mixtures comprise: (1) an amide compound of formula (I) and (2) a quinoline derivative of formula (II) and/or an amine compound of formula (III). Fungicidal mixture comprises: (1) an amide compound of formula (I); and (2) a synergistically effective amount of a second component which comprises: (i) a quinoline derivative of formula (II), or an N-oxide or salt and/or; (ii) a compound of formula (III). A = Ar or Het (both optionally substituted by 1-3 alkyl, halo, CHF2, CF3, (halo)alkoxy, alkylthio, alkylsulfinyl or alkylsulfonyl; R = H; R = phenyl (optionally substituted by 1-3 Q and optionally fused to a group M); or cycloalkyl (optionally substituted by 1-3 Q); M = a saturated 5-membered ring which may contain an O or S atom and is optionally substituted by one or more alkyl; Ar = an aryl group; Het = an aromatic or non-aromatic, 5-6 membered heterocycle which contains 1-3 N, O or S atoms; Q = alkyl, alkenyl, alkynyl, alkoxy, alkenyloxy, alkynyloxy, cycloalkyl, cycloalkenyl, cycloalkyloxy, cycloalkenyloxy, phenyl or halo; in Q, the (cyclo)aliphatic residues are optionally halogenated, the cycloaliphatic residues are optionally substituted by 1-3 alkyl, and the phenyl is optionally substituted by 1-5 halo and/or 1-3 (halo)alkyl, (halo)alkoxy or (halo)alkylthio; R -R = H, OH, NO2, halo, T, TO or TS; R -R = H, OH, CN, NO2, halo, R, RO, RS, 1-7C hydroxyalkyl, 2-4C acyl, or aryl or aryloxy (both optionally substituted by 1-3 CN, NO2, halo, T, TO or TS); X -X = H, halo, T, TO, 1-4C alkylthio, 1-4C thioalkoxy, 1-4C sulfonylalkyl, NO2, NH2, N-(1-4C carboxyl)-amino or N-(1-4C alkyl)-amino; R = 1-4C alkyl, 2-4C alkenyl, 2-4C alkynyl or 1-4C alkyl-(3-7C) cycloalkyl (all optionally substituted by halo, CN or 1-4C alkoxy); R = phenyl or Het' (both optionally substituted by halo, T, TO, 1-4C alkoxy-(2-4C) alkenyl or 1-4C alkoxy-(2-4C) alkynyl; R , R = H, T, TO, 1-4C alkylthio or N-(1-4C alkyl)-amino T = 1-4C alkyl, halo(1-4C)alkyl; R = 1-7C alkyl, halo(1-7C)alkyl.
Abstract:
In the present invention, there is disclosed a fungicidal agent comprising an oxime ether carboxylic acid ester of the general formula Ia or Ib and 1-(2-cyano-2-methoxyiminoacetyl)-3-ethylurea of the general formula Hi3CCHi2-NHCONH-CO-C(CN)=NOCHi3 in a synergistically effective amount. Further disclosed is the use of said compounds as well as a method for controlling harmful fungi, which comprises treating the harmful fungi, their habitat or the plants, seeds, soil, areas materials or rooms which are to be kept free of them with an effective amount of the above indicated fungicidal agent in a synergistically effective amount, wherein the synergistically effective amount of the compound of the general formula Ia or Ib and said urea derivative is applied simultaneously together or separately or successively.