AR067523A1 - SYNERGIC COMBINATIONS OF FUNGICIDAL ACTIVE COMPOUNDS - Google Patents

SYNERGIC COMBINATIONS OF FUNGICIDAL ACTIVE COMPOUNDS

Info

Publication number
AR067523A1
AR067523A1 ARP080103172A AR067523A1 AR 067523 A1 AR067523 A1 AR 067523A1 AR P080103172 A ARP080103172 A AR P080103172A AR 067523 A1 AR067523 A1 AR 067523A1
Authority
AR
Argentina
Prior art keywords
alkyl
group
chlorine
methyl
hydrogen
Prior art date
Application number
Other languages
Spanish (es)
Original Assignee
Bayer Cropscience Ag
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Bayer Cropscience Ag filed Critical Bayer Cropscience Ag
Publication of AR067523A1 publication Critical patent/AR067523A1/en

Links

Classifications

    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION 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
    • A01N43/00Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/02Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
    • A01N43/04Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom
    • A01N43/14Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom six-membered rings
    • A01N43/16Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom six-membered rings with oxygen as the ring hetero atom

Abstract

Reivindicacion 1: Combinaciones de compuestos activos, que comprenden genisteína de formula (1) y por lo menos un compuesto activo seleccionado entre los Grupos [2] a [24] que aparecen a continuacion: Grupo [2] Estrobilurinas de la formula general (2) en la cual A1 representa uno de los radicales del grupo de formulas (3); A2 representa NH u O; A3 representa N o CH; L representa uno de los radicales del grupo de formulas (4), donde el enlace marcado con un asterisco (*) está unido al anillo de fenilo; R11 representa fenilo, fenoxi o piridinilo, cada uno de los cuales está opcionalmente mono- o disustituido con sustituyentes idénticos o diferentes del grupo formado por cloro, ciano, metilo y trifluorometilo, o representa 1-(4-clorofenil)-pirazol-3-ilo o representa 1,2-propanodiona-bis(O-metiloxima)-1-ilo; R12 representa hidrogeno o fluor; Grupo [3] Triazoles de la formula general (5) en la cual Q representa hidrogeno o SH; m representa 0 o 1; R13 representa hidrogeno, fluor, cloro, fenilo o 4-clorofenoxi; R14 representa hidrogeno o cloro; A4 representa un enlace directo, -CH2-, -(CH2)2- u -O-; A4 representa adicionalmente *-CH2-CHR17- o *-CH=CR17- donde el enlace marcado con * está unido al anillo de fenilo, en cuyo caso y en conjunto representan -CH2-CH2-CH[CH(CH3)2]- o -CH2-CH2-C(CH3)2-; A5 representa C o Si (silicio); A4 representa adicionalmente -N(R17)- y A5 adicionalmente en conjunto con R15 y R16 representa el grupo C=N-R18, en cuyo caso y R18 en conjunto representan el radical de formula (6) donde el enlace marcado con * está unido a R17; R15 representa hidrogeno, hidroxilo o ciano; R16 representa 1-ciclopropiletilo, 1-clorociclopropilo, alquilo C1-4, hidroxialquilo C1-6, alquilcarbonilo C1-4, haloalcoxi C1-2-alquilo C1-2, trimetilsilil-alquilo C1-2, monofluorofenilo o fenilo; R15 y R16 en conjunto representan adicionalmente -O-CH2-CH(R18)-O-, -O-CH2-CH(R18)-CH2-, u -O-CH-(2-clorofenil)-; R18 representa hidrogeno, alquilo C1-4 o bromo; Grupo [4] Sulfenamidas de la formula general (7) en la cual R19 representa hidrogeno o metilo; Grupo [5] Valinamidas seleccionadas entre (5-1) iprovalicarb; (5-2) N1-[2-(4-{[3-(4-clorofenil)-2-propinil]oxi}-3-metoxifenil)etil]-N2-(metilsulfonil)-D-valinamida; (5-3) bentiavalicarb; Grupo [6] Carboxamidas de la formula general: X-CO-NH-Y-Z en la cual X representa 2-cloro-3-piridinilo, representa 1-metilpirazol-4-ilo el cual está sustituido en la posicion 3 con metilo o trifluorometilo y en la posicion 5 con hidrogeno o cloro, representa 4-etil-2-etilamino-1,3-tiazol-5-ilo, representa 1-metil-ciclohexilo, representa 2,2-dicloro-1-etil-3-metilciclopropilo, representa 2-fluor-2-propilo o representa fenilo el cual está mono- a trisustituido con sustituyentes idénticos o diferentes del grupo formado por cloro, metilo y trifluorometilo; X representa adicionalmente 3,4-dicloroisotiazol-5-ilo, 5,6-dihidro-2-metil-1,4-oxatiin-3-ilo, 4-metil-1,2,3-tiadiazol-5-ilo, 4,5-dimetil-2-trimetilsililtiofen-3-ilo, 1-metilpirrol-3-ilo el cual está sustituido en la posicion 4 con metilo o trifluorometilo y en la posicion 5 con hidrogeno o cloro; Y representa un enlace directo, alcandiilo C1-6 (alquileno) el cual está opcionalmente sustituido con cloro, ciano u oxo o representa tiofendiilo; Y representa adicionalmente alquendiilo C2-6 (alquenileno); Z representa hidrogeno o el radical de formula (8); Z representa adicionalmente alquilo C1-6; A6 representa CH o N; R20 representa hidrogeno, cloro, fenilo el cual está opcionalmente mono disustituido con sustituyentes idénticos o diferentes del grupo formado por cloro y di(alquil C1-3)aminocarbonilo; R20 representa adicionalmente ciano o alquilo C1-6; R21 representa hidrogeno, cloro o 1-metiletoxi; R22 representa hidrogeno, cloro, hidroxilo, metilo o trifluorometilo; R22 representa adicionalmente di(alquil C1-3)aminocarbonilo; R20 y R21 en conjunto representan adicionalmente *-CH(CH3)-CH2- o *-CH(CH3)-O-C(CH3)2- donde el enlace marcado con * está unido a R20; o la formula general (9) en la cual R1 representa hidrogeno, halogeno, alquilo C1-3 o haloalquilo C1-3 que tiene de 1 a 7 átomos de fluor, cloro y/o bromo; a representa uno de los radicales A1 a A8 del grupo de formulas (10); R2 representa alquilo C1-3; R3 representa hidrogeno, halogeno, alquilo C1-3 o haloalquilo C1-3 que tiene de 1 a 7 átomos de fluor, cloro y/o bromo; R4 representa hidrogeno, halogeno o alquilo C1-3; R5 representa halogeno, alquilo C1-3 o haloalquilo C1-3 que tiene de 1 a 7 átomos de fluor, cloro y/o bromo; R6 representa hidrogeno, halogeno, alquilo C1-3, amino, mono- o di(alquil C1-3)amino; R7 representa hidrogeno, halogeno, alquilo C1-3 o haloalquilo C1-3 que tiene de 1 a 7 átomos de fluor, cloro y/o bromo; R8 representa halogeno, alquilo C1-3 o haloalquilo C1-3 que tiene de 1 a 7 átomos de fluor, cloro y/o bromo; R9 representa halogeno, alquilo C1-3 o haloalquilo C1-3 que tiene de 1 a 7 átomos de fluor, cloro y/o bromo; R10 representa hidrogeno, halogeno, alquilo C1-3 o haloalquilo C1-3 que tiene de 1 a 7 átomos de fluor, cloro y/o bromo; Grupo [7] Ditiocarbamatos seleccionados entre: (7-1) mancozeb; (7-2) maneb; (7-3) metiram; (7-4) propineb; (7-5) tiram; (7-6) zineb; (7-7) ziram; Grupo [8] Acilalaninas de la formula general (11) en la cual * marca un átomo en la configuracion R o S, preferentemente en la configuracion S; R23 representa bencilo, furilo o metoximetilo; Grupo [9] Anilinopirimidinas de la formula general (12) en la cual R24 representa metilo, ciclopropilo o 1-propinilo; Grupo [10] Benzimidazoles de la formula general (13) en la cual R25 y R26 cada uno representa hidrogeno o en conjunto representan -O-CF2-O-; R27 representa hidrogeno, alquil C1-4-aminocarboniIo o representa 3,5-dimetilisoxazol-4-ilsulfonilo; R28 representa cloro, metoxicarbonilamino, clorofenilo, furilo o tiazolilo; Grupo [11] Carbamatos de la formula general R29-O-CO-NH-R30 en la cual R29 representa n- o isopropilo; R30 representa di(alquil C1-2)amino-alquilo C2-4 o dietoxifenilo, se incluyen las sales de estos compuestos; Grupo [12] Dicarboximidas seleccionadas entre: (12-1) captafol; (12-2) captan; (12-3) folpet; (12-4) iprodiona; (12-5); procimidona; (12-6) vinclozolin; Grupo [13] Guanidinas seleccionadas entre: (3-1) dodina; (13-2) guazatina; (13-3) triacetato de iminoctadina; (13-4) tris(albesilato) de iminoctadina; Grupo [14] Imidazoles seleccionados entre: (14-1) ciazofamida; (14-2) procloraz; (14-3) triazoxido; (14-4) pefurazoato; Grupo [15] Morfolinas de la formula general (14) en la cual R31 y R32 independientemente uno del otro representan hidrogeno o metilo; R33 representa alquilo C1-14 (preferentemente alquilo C12-14), cicloalquilo C5-12 (preferentemente cicloalquilo C10-12), fenil-alquilo C1-4, el cual puede estar sustituido en la porcion fenilo con halogeno o alquilo C1-4 o representa acrililo el cual está sustituido con clorofenilo y dimetoxifenilo; Grupo [16] Pirroles de la formula general (15) en la cual R34 representa cloro o ciano; R35 representa cloro o nitro; R36 representa cloro; R35 y R36 en conjunto representan adicionalmente -O-CF2-O-; Grupo [17] Fosfonatos seleccionados entre: (17-1) fosetil-Al; (17-2) ácido fosfonico; Grupo [18] Feniletanamidas de la formula general (16) en la cual R37 representa fenilo no sustituido o sustituido con fluor, cloro, bromo, metilo o etilo, 2-naftilo, 1,2,3,4-tetrahidronaftilo o indanilo; Grupo [19] Fungicidas seleccionados entre: (19-1) acibenzolar-S-metilo; (19-2) clorotalonil; (19-3) cimoxanilo; (19-4) edifenfos; (19-5) famoxadona; (19-6) fluazinam; (19-7) oxicloruro de cobre; (19-8) hidroxido de cobre; (19-9) oxadixil; (19-10) espiroxamina; (19-11) ditianon; (19-12) metrafenona; (19-13) fenamidona; (19-14) 2,3-dibutil-6-clorotieno[2,3-d]pirimidin-4(3H)-ona; (19-15) probenazol; (19-16) isoprotiolano; (19-17) kasugamicina; (19-18) ftalida; (19-19) ferimzona; (19-20) triciclazol; (19-21) N-({4-[(ciclopropilamino)carbonil]fenil}suIfoniI)-2-metoxibenzamida; (19-22) 2-(4-clorofenfl)-N-{2-[3-metoxi-4-(prop-2-in-1-iloxi)fenil]etil}-2-(prop-2-in-1-iloxi)acetamida; (19-23) Diclomezina; (19-24) Himexazol; (19-25) Iprobenfos; (19-26) Triflumizol; Grupo [20] Derivados de (tio)urea seleccionados entre: (20-1) pencicuron; (20-2) tiofanato-metilo; (20-3) tiofanato-etilo; Grupo [21] Amidas de la formula general (17) en la cual A7 representa un enlace directo u -O-; A8 representa -C(=O)NH- o -NHC(=O)-; A38 representa hidrogeno o alquilo C1-4; R39 representa alquilo C1-6; Grupo [22] Triazolopirimidinas de la formula general (18) en la cual R40 representa alquilo C1-6 o alquenilo C2-6; R41 representa alquilo C1-6; R40 y R41 en conjunto representan adicionalmente alcandiilo C4-5 (alquileno) el cual está mono- o disustituido con alquilo C1-6; R42 representa bromo o cloro; R43 y R47 independientemente uno del otro representan hidrogeno, fluor, cloro o metilo; R44 y R46 independientemente uno del otro representan hidrogeno o fluor; R45 representa hidrogeno, fluor o metilo; Grupo [23] Yodocromonas de la formula general (19) en la cual R48 representa alquilo C1-6; R49 representa alquilo C1-6, alquenilo C2-6 o alquinilo C2-6; Grupo [24] Bifenilcarboxamidas de la formula general (20) en la cual R50 representa hidrogeno o fluor; R51 representa fluor, cloro, bromo, metilo, trifluorometilo, trifluorometoxi, -CH=N-OMe o -C(Me)=N-OMe; R52 representa hidrogeno, fluor, cloro, bromo, metilo o trifluorometilo; Het representa uno de los radicales Het1 a Het7 que aparecen en el grupo de formulas (21); R53 representa yodo, metilo, difluorometilo o trifluorometilo; R54 representa hidrogeno, fluor, cloro o metilo; R55 representa metilo, difluorometilo o trifluorometilo; R56 representa cloro, bromo, yodo, metilo, difluorometilo o trifluorometilo; R57 representa metilo o trifluorometilo. Reivindicacion 3: Uso de las combinaciones de compuestos activos de acuerdo con la reivindicacion 1 o con la reivindicacion 2 para controlar hongos fitopatogenos no deseados. ReivindicacioClaim 1: Combinations of active compounds, comprising genistein of formula (1) and at least one active compound selected from Groups [2] to [24] which appear below: Group [2] Estrobilurins of the general formula (2 ) in which A1 represents one of the radicals in the group of formulas (3); A2 represents NH or O; A3 represents N or CH; L represents one of the radicals of the group of formulas (4), where the link marked with an asterisk (*) is attached to the phenyl ring; R11 represents phenyl, phenoxy or pyridinyl, each of which is optionally mono- or disubstituted with identical or different substituents of the group consisting of chloro, cyano, methyl and trifluoromethyl, or represents 1- (4-chlorophenyl) -pyrazol-3- ilo or represents 1,2-propanedione-bis (O-methyloxime) -1-yl; R12 represents hydrogen or fluorine; Group [3] Triazoles of the general formula (5) in which Q represents hydrogen or SH; m represents 0 or 1; R13 represents hydrogen, fluorine, chlorine, phenyl or 4-chlorophenoxy; R14 represents hydrogen or chlorine; A4 represents a direct link, -CH2-, - (CH2) 2- or -O-; A4 additionally represents * -CH2-CHR17- or * -CH = CR17- where the link marked with * is attached to the phenyl ring, in which case and together they represent -CH2-CH2-CH [CH (CH3) 2] - or -CH2-CH2-C (CH3) 2-; A5 represents C or Si (silicon); A4 additionally represents -N (R17) - and A5 additionally in conjunction with R15 and R16 represents the group C = N-R18, in which case and R18 together represent the radical of formula (6) where the bond marked with * is attached to R17; R15 represents hydrogen, hydroxyl or cyano; R16 represents 1-cyclopropylethyl, 1-chlorocyclopropyl, C1-4 alkyl, hydroxy C1-6 alkyl, C1-4 alkylcarbonyl, C1-2 haloalkoxy C1-2 alkyl, trimethylsilyl C1-2 alkyl, monofluorophenyl or phenyl; R15 and R16 together represent additionally -O-CH2-CH (R18) -O-, -O-CH2-CH (R18) -CH2-, or -O-CH- (2-chlorophenyl) -; R18 represents hydrogen, C1-4 alkyl or bromine; Group [4] Sulfenamides of the general formula (7) in which R19 represents hydrogen or methyl; Group [5] Valinamides selected from (5-1) iprovalicarb; (5-2) N1- [2- (4 - {[3- (4-chlorophenyl) -2-propynyl] oxy} -3-methoxyphenyl) ethyl] -N2- (methylsulfonyl) -D-valinamide; (5-3) bentiavalicarb; Group [6] Carboxamides of the general formula: X-CO-NH-YZ in which X represents 2-chloro-3-pyridinyl, represents 1-methylpyrazol-4-yl which is substituted at position 3 with methyl or trifluoromethyl and in position 5 with hydrogen or chlorine, it represents 4-ethyl-2-ethylamino-1,3-thiazol-5-yl, represents 1-methyl-cyclohexyl, represents 2,2-dichloro-1-ethyl-3-methylcyclopropyl , represents 2-fluor-2-propyl or represents phenyl which is mono- to trisubstituted with identical or different substituents of the group consisting of chlorine, methyl and trifluoromethyl; X additionally represents 3,4-dichloroisothiazol-5-yl, 5,6-dihydro-2-methyl-1,4-oxatiin-3-yl, 4-methyl-1,2,3-thiadiazol-5-yl, 4 , 5-dimethyl-2-trimethylsilylthiophene-3-yl, 1-methylpyrrol-3-yl which is substituted in position 4 with methyl or trifluoromethyl and in position 5 with hydrogen or chlorine; Y represents a direct bond, C1-6 alkanyl (alkylene) which is optionally substituted with chlorine, cyano or oxo or represents thiophenedyl; Y additionally represents C2-6 alkenyl (alkenylene); Z represents hydrogen or the radical of formula (8); Z additionally represents C1-6 alkyl; A6 represents CH or N; R20 represents hydrogen, chlorine, phenyl which is optionally mono disubstituted with identical or different substituents of the group consisting of chlorine and di (C1-3 alkyl) aminocarbonyl; R20 additionally represents cyano or C1-6 alkyl; R21 represents hydrogen, chlorine or 1-methylethoxy; R22 represents hydrogen, chlorine, hydroxyl, methyl or trifluoromethyl; R22 additionally represents di (C1-3 alkyl) aminocarbonyl; R20 and R21 together represent additionally * -CH (CH3) -CH2- or * -CH (CH3) -O-C (CH3) 2- where the link marked with * is attached to R20; or the general formula (9) in which R1 represents hydrogen, halogen, C1-3 alkyl or C1-3 haloalkyl having 1 to 7 fluorine, chlorine and / or bromine atoms; a represents one of the radicals A1 to A8 of the group of formulas (10); R2 represents C1-3 alkyl; R3 represents hydrogen, halogen, C1-3 alkyl or C1-3 haloalkyl having 1 to 7 fluorine, chlorine and / or bromine atoms; R4 represents hydrogen, halogen or C1-3 alkyl; R5 represents halogen, C1-3 alkyl or C1-3 haloalkyl having 1 to 7 fluorine, chlorine and / or bromine atoms; R 6 represents hydrogen, halogen, C 1-3 alkyl, amino, mono- or di (C 1-3 alkyl) amino; R7 represents hydrogen, halogen, C1-3 alkyl or C1-3 haloalkyl having 1 to 7 fluorine, chlorine and / or bromine atoms; R8 represents halogen, C1-3 alkyl or C1-3 haloalkyl having 1 to 7 fluorine, chlorine and / or bromine atoms; R9 represents halogen, C1-3 alkyl or C1-3 haloalkyl having 1 to 7 fluorine, chlorine and / or bromine atoms; R10 represents hydrogen, halogen, C1-3 alkyl or C1-3 haloalkyl having 1 to 7 fluorine, chlorine and / or bromine atoms; Group [7] Dithiocarbamates selected from: (7-1) mancozeb; (7-2) maneb; (7-3) metiram; (7-4) propineb; (7-5) tiram; (7-6) zineb; (7-7) ziram; Group [8] Acylalanines of the general formula (11) in which * marks an atom in the R or S configuration, preferably in the S configuration; R23 represents benzyl, furyl or methoxymethyl; Group [9] Anilinopyrimidines of the general formula (12) in which R24 represents methyl, cyclopropyl or 1-propynyl; Group [10] Benzimidazoles of the general formula (13) in which R25 and R26 each represent hydrogen or together represent -O-CF2-O-; R27 represents hydrogen, C1-4alkylcarbonyl or represents 3,5-dimethylisoxazol-4-ylsulfonyl; R28 represents chlorine, methoxycarbonylamino, chlorophenyl, furyl or thiazolyl; Group [11] Carbamates of the general formula R29-O-CO-NH-R30 in which R29 represents n- or isopropyl; R30 represents di (C1-2 alkyl) aminoC2-4 alkyl or diethoxyphenyl, salts of these compounds are included; Group [12] Dicarboximides selected from: (12-1) captafol; (12-2) get; (12-3) folpet; (12-4) iprodione; (12-5); procimidone; (12-6) vinclozolin; Group [13] Guanidines selected from: (3-1) dodine; (13-2) guazatina; (13-3) iminoctadine triacetate; (13-4) iminoctadine tris (albesylate); Group [14] Imidazoles selected from: (14-1) ciazofamide; (14-2) prochloraz; (14-3) triazoxide; (14-4) pefurazoate; Group [15] Morpholines of the general formula (14) in which R31 and R32 independently of each other represent hydrogen or methyl; R33 represents C1-14 alkyl (preferably C12-14 alkyl), C5-12 cycloalkyl (preferably C10-12 cycloalkyl), phenyl-C1-4 alkyl, which may be substituted in the phenyl portion with halogen or C1-4 alkyl or represents acryl which is substituted with chlorophenyl and dimethoxyphenyl; Group [16] Pyrroles of the general formula (15) in which R34 represents chlorine or cyano; R35 represents chlorine or nitro; R36 represents chlorine; R35 and R36 together represent additionally -O-CF2-O-; Group [17] Phosphonates selected from: (17-1) fosetil-Al; (17-2) phosphonic acid; Group [18] Phenylethanamides of the general formula (16) in which R37 represents phenyl unsubstituted or substituted with fluorine, chlorine, bromine, methyl or ethyl, 2-naphthyl, 1,2,3,4-tetrahydronaphthyl or indanyl; Group [19] Fungicides selected from: (19-1) acibenzolar-S-methyl; (19-2) chlorothalonil; (19-3) cymoxanyl; (19-4) edifenfos; (19-5) famoxadone; (19-6) fluazinam; (19-7) copper oxychloride; (19-8) copper hydroxide; (19-9) oxadixil; (19-10) spiroxamine; (19-11) ditianon; (19-12) metrafenone; (19-13) fenamidone; (19-14) 2,3-dibutyl-6-chlorothiene [2,3-d] pyrimidin-4 (3H) -one; (19-15) probenazole; (19-16) isoprotiolane; (19-17) kasugamycin; (19-18) phthalic; (19-19) ferimzone; (19-20) triciclazole; (19-21) N - ({4 - [(cyclopropylamino) carbonyl] phenyl} suIfoniI) -2-methoxybenzamide; (19-22) 2- (4-chlorophenfl) -N- {2- [3-methoxy-4- (prop-2-in-1-yloxy) phenyl] ethyl} -2- (prop-2-in- 1-yloxy) acetamide; (19-23) Diclomezine; (19-24) Himexazole; (19-25) Iprobenfos; (19-26) Triflumizol; Group [20] Derivatives of (uncle) urea selected from: (20-1) pencicuron; (20-2) thiophanate-methyl; (20-3) thiophanate-ethyl; Group [21] Amides of the general formula (17) in which A7 represents a direct bond or -O-; A8 represents -C (= O) NH- or -NHC (= O) -; A38 represents hydrogen or C1-4 alkyl; R39 represents C1-6 alkyl; Group [22] Triazolopyrimidines of the general formula (18) in which R40 represents C1-6 alkyl or C2-6 alkenyl; R41 represents C1-6 alkyl; R40 and R41 together represent additionally C4-5 alkylenyl (alkylene) which is mono- or disubstituted with C1-6 alkyl; R42 represents bromine or chlorine; R43 and R47 independently of each other represent hydrogen, fluorine, chlorine or methyl; R44 and R46 independently of each other represent hydrogen or fluorine; R45 represents hydrogen, fluorine or methyl; Group [23] Yodocromonas of the general formula (19) in which R48 represents C1-6 alkyl; R49 represents C1-6 alkyl, C2-6 alkenyl or C2-6 alkynyl; Group [24] Biphenylcarboxamides of the general formula (20) in which R50 represents hydrogen or fluorine; R51 represents fluorine, chlorine, bromine, methyl, trifluoromethyl, trifluoromethoxy, -CH = N-OMe or -C (Me) = N-OMe; R52 represents hydrogen, fluorine, chlorine, bromine, methyl or trifluoromethyl; Het represents one of the radicals Het1 to Het7 that appear in the group of formulas (21); R53 represents iodine, methyl, difluoromethyl or trifluoromethyl; R54 represents hydrogen, fluorine, chlorine or methyl; R55 represents methyl, difluoromethyl or trifluoromethyl; R56 represents chlorine, bromine, iodine, methyl, difluoromethyl or trifluoromethyl; R57 represents methyl or trifluoromethyl. Claim 3: Use of the combinations of active compounds according to claim 1 or claim 2 to control unwanted phytopathogenic fungi. Claim

ARP080103172 2007-07-23 2008-07-22 SYNERGIC COMBINATIONS OF FUNGICIDAL ACTIVE COMPOUNDS AR067523A1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
EP07112966 2007-07-23

Publications (1)

Publication Number Publication Date
AR067523A1 true AR067523A1 (en) 2009-10-14

Family

ID=39967942

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP080103172 AR067523A1 (en) 2007-07-23 2008-07-22 SYNERGIC COMBINATIONS OF FUNGICIDAL ACTIVE COMPOUNDS

Country Status (2)

Country Link
AR (1) AR067523A1 (en)
WO (1) WO2009012907A1 (en)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2272346A1 (en) 2009-07-08 2011-01-12 LANXESS Deutschland GmbH Penthiopyrad for protecting wood
AU2012323970A1 (en) * 2011-10-14 2014-03-20 Sapphire Energy, Inc. Use of fungicides in liquid systems
CA2891888C (en) * 2012-11-19 2021-06-29 Arch Wood Protection, Inc. Succinate dehydrogenase inhibitor containing compositions
CN105028417A (en) * 2015-06-08 2015-11-11 柳州市天姿园艺有限公司 Composition for preventing and treating phytophthora root rot of cymbidium kanran

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES2547924T3 (en) * 2004-03-18 2015-10-09 Novozymes Bioag A/S Isoflavonoid compounds and their use
EA018627B1 (en) * 2007-01-16 2013-09-30 Зингента Партисипейшнс Аг Pesticidal combinations
BRPI0807066A8 (en) * 2007-02-02 2018-06-05 Bayer Cropscience Ag SYNERGISTIC COMBINATIONS OF FUNGICIDAL ACTIVE COMPOUNDS

Also Published As

Publication number Publication date
WO2009012907A1 (en) 2009-01-29

Similar Documents

Publication Publication Date Title
AR046144A1 (en) SYNERGIC COMBINATIONS OF FUNGICIDE ACTIVE PRODUCTS
AR065031A1 (en) SYNERGIC COMBINATIONS OF FUNGICIDAL ACTIVE COMPOUNDS. APPLICATIONS. PROCEDURES TO PREPARE SUCH COMBINATIONS. SEEDS TREATED WITH THE COMBINATION
AR046051A1 (en) SYNERGIC COMBINATIONS OF ACTIVE COMPOUNDS, FUNGICIDES
AR067523A1 (en) SYNERGIC COMBINATIONS OF FUNGICIDAL ACTIVE COMPOUNDS
AR058384A1 (en) CARBOXAMIDS AND THIOCARBOXAMIDS EMPLOYED IN THE FIGHT AGAINST INDESEABLE MICROORGANISMS AND IN THE TREATMENT OF TRANSGENIC SEEDS AND PLANTS, COMPOSITIONS THAT CONTAIN THEM AND A METHOD OF OBTAINING THE SAME AND A PROCEDURE FOR THE PREPARATION OF UNDERTAKING
AR067763A1 (en) DERIVATIVE OF OXOPIRAZINE AND HERBICIDE
AR084308A1 (en) INSECTICIDE COMPOUNDS DERIVED FROM TRIAZOL
AR086828A1 (en) FUSIONED HETEROCICLICAL COMPOUNDS AS IONIC CHANNEL MODULATORS
AR054417A1 (en) IMIDAZOL DERIVATIVES PROCESS OF OBTAINING AND PHARMACEUTICAL COMPOSITIONS.
ECSP13012526A (en) FUNGICIDE COMPOSITIONS.
RU2006141320A (en) NEW COMPOUNDS
AR085318A1 (en) TRIAZOL DERIVATIVES THAT HAVE INSECTICIATED ACTIVITY
AR072394A1 (en) FUNGICIDE COMPOSITIONS
AR052220A1 (en) FUNGICIDE COMPOSITIONS
AR094101A1 (en) ARYL SULFIDE AND ARYL SULFOXIDE DERIVATIVES AS ACARICIDES AND INSECTICIDES
AR059458A1 (en) ARILDIHYDROISOQUINOLINONES REPLACED WITH AZACICLIL, PROCEDURE FOR PREPARATION AND USE AS MEDICATIONS
ES2330313T3 (en) THIOPHENE DERIVATIVES AS ANTIVIRAL AGENTS AGAINST INFECTION WITH FLAVIVIRUS.
EA201400232A1 (en) FUNGICIDAL SUBSTITUTED 1- {2- [2-HALOGEN-4- (4-HALOGENPHENOXY) PHENYL] -2-ALKOXI-2-CYCLYLETHYL} -1H- [1,2,4] TRIASOLE COMPOUNDS
AR054184A1 (en) DERIVATIVES OF 1,5 DIFENYLPIRAZOL. PROCESSES OF OBTAINING AND PHARMACEUTICAL COMPOSITIONS.
AR099642A1 (en) FUNGICIDE COMPOSITIONS
CO6351734A2 (en) USEFUL AMIDA COMPOUNDS IN THERAPY
AR060066A1 (en) COMBINATIONS OF FUNGICIDAL ACTIVE PRINCIPLES
PE20080319A1 (en) DIHYDROTIENOPYRIMIDINES AS INHIBITING AGENTS OF PDE-4
AR080531A1 (en) TRIAZOL DERIVATIVES AS INSECTICIDES
AR047453A1 (en) N - REPLACED CYCLHEXILIMIDAZOLINONES, PROCEDURES FOR THE PREPARATION AND PHARMACEUTICAL COMPOSITIONS.

Legal Events

Date Code Title Description
FB Suspension of granting procedure