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:
New fungicidal mixtures contain dithianon (I) and at least one 1,2,4-triazole derivative (II) in synergistic amounts, where (II) is metconazole, epoxiconazole, fluquinconazole, tebuconazole (IIa), tetraconazole, difenconazole and/or prothioconazole (preferably metconazole, epoxiconazole or (IIa)). Independent claims are included for: (1) a fungicidal composition comprising the (I)/(II) mixture plus a solid or liquid carrier; and (2) a method for controlling harmful fungi, by applying (I) and (II) to the fungi, their habitat or plants, seeds, soil, surfaces, materials or regions to be protected. ACTIVITY : Fungicide. In tests against Botrytis cinerea in paprika seedlings, (I) at 16 ppm or (IIa) at 4 ppm gave no control, whereas a combination of 16 ppm (I) and 4 ppm (IIa) gave 59% control. MECHANISM OF ACTION : Synergist.
Abstract:
FUNGICIDAL MIXTURES, COMPRISING (A) AT LEAST ONE ACTIVE STROBILURIN COMPOUND SELECTED FROM (A1) CARBAMATES OF THE FORMULA I IN WHICH T IS CH OR N, n IS O, 1 OR 2 AND R IS HALOGEN, ALKYL OR HALOALKYL, WHERE THE RADICALS R MAY BE DIFFERENT IF N IS 2, AND/OR (A2)THE PHENYL ACETIC ACID DERIVATIVES OF THE FORMULAE IIA TO IIF AND (B) THE COMPOUND OF THE FORMULA III IN A SYNERGISTICALLY EFFECTIVE AMOUNT, AND METHODS FOR CONTROLLING HARMFUL FUNGI USING THESE MIXTURES ARE DESCRIBED.
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.