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公开(公告)号:AT135885T
公开(公告)日:1996-04-15
申请号:AT92114812
申请日:1992-08-29
Applicant: BASF AG
Inventor: SAUTER HUBERT , SCHELBERGER KLAUS , SAUR REINHOLD DR , LORENZ GISELA DR , AMMERMANN EBERHARD DR
IPC: A01N43/653 , A01N37/50 , A01N55/00 , A01N47/38
Abstract: Fungicidal mixtures of a) methyl a-methoximino-2[(2-methylphenoxy)methyl]phenyl acetate and b) an azole active compound selected from the following group: (Z)-2-(1,2,4-triazol-1-yl-ethyl)-2-(4-fluorophenyl)-3-(2-chloro- phenyl)-oxirane of the formula 1-butyl-1-(2,4-dichlorophenyl)-2-(1,2,4-triazol-1-yl) ethanol (common name hexaconazole), 1-[(2-chlorophenyl)methyl]-1-(1,1-dimethyl)-2-(1,2,4-triazol-1-yl) ethanol 1-(4-fluorophenyl)-1-(2-fluorophenyl)-2-(1,2,4-triazol-1-yl)ethanol (common name flutriafol) (RS)-4-(4-chlorphenyl)-2-phenyl-2-(1H-1,2,4-triazol-1-yl-methyl)- butyronitril, 1-[2 RS, 4RS; 2 RS, 4 SR)-4-brom-2-(2,4-dichlorphenyl)-tetrahydrofurfuryl]-1H-1,2,4-triazol, 3-(2,4-dichlorphenyl-2-(1H-1,2,4-triazol-1-yl)-quinazolin-4(3H)-on, (RS)-2,2-dimethyl-3-(2-chlorbenzyl)-4-(1H-1,2,4-triazol-1-yl)- butan-3-ol, bitertanol, triadimefon, triadimenol, cyproconazole, dichlobutrazol difenoconazole, diniconazole, etaconazole, propiconazole, flunsilazole, tebuconazole, imazalil, penconazole, prochloraz, tetraconazole or a salt of such an azole active compound and process for combating fungi using this mixture of compounds.
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公开(公告)号:ES2082090T3
公开(公告)日:1996-03-16
申请号:ES91117801
申请日:1991-10-18
Applicant: BASF AG
Inventor: SEELE RAINER DR , GOETZ NORBERT DR , LORENZ GISELA DR , AMMERMANN EBERHARD DR
IPC: A01N43/50 , A01N43/653 , C07D233/60 , C07D249/08 , C07D303/04 , C07D303/08 , C07D303/12 , C07D405/06 , C07D405/08 , C07D493/10 , C07D521/00
Abstract: Azolylmethylspiro(2.5)octanols of the formula (* CHEMICAL STRUCTURE *) where A and R are each hydrogen or alkyl; D is alkyl, cycloalkyl, cycloalkenyl, biphenylyl, naphthyl, hetaryl or phenyl, it being possible for each of these radicals to be substituted; Z is CH2 or O, X is CH or N, and the plant-compatible acid addition salts and metal complexes thereof are used as or in fungicides.
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公开(公告)号:DE59107100D1
公开(公告)日:1996-02-01
申请号:DE59107100
申请日:1991-04-20
Applicant: BASF AG
Inventor: REUTHER WOLFGANG DR , BAUS ULF DR , LORENZ GISELA DR
IPC: A01N43/50 , A01N43/52 , A01N43/56 , A01N43/647 , A01N43/653 , A01N47/48 , C07D231/10 , C07D231/12 , C07D231/56 , C07D233/54 , C07D233/56 , C07D235/22 , C07D249/04 , C07D249/08 , C07D249/18 , C07D521/00
Abstract: N-Thiocyanatomethoxyazaheterocycles of the general formula I NCS-CH2-O-Het (where Het is pyrazolyl, imidazolyl or triazolyl, each of which may be substituted, or is indazolyl, benzoimidazolyl or benzotriazolyl, where each of the fused benzene rings may furthermore be substituted, and the salts and metal complexes thereof, with the exception of 1-[(thiocyanato)methoxy]-pyrazole, and biocides containing them.
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公开(公告)号:GR3017716T3
公开(公告)日:1996-01-31
申请号:GR950402825
申请日:1995-10-11
Applicant: BASF AG
Inventor: SAUTER HUBERT DR , BAYER HERBERT DR , OBERDORF KLAUS DR , WINGERT HORST DR , VON DEYN WOLFGANG DR , GRAMMENOS WASSILIOS DR , KOENIG HARTMANN DR , RANG HARALD DR , ROEHL FRANZ DR , LORENZ GISELA DR , AMMERMANN EBERHARD DR
IPC: A01N37/36 , A01N37/38 , A01N37/44 , A01N37/48 , A01N43/08 , A01N43/10 , A01N43/36 , A01N43/56 , A01N43/74 , A01N43/78 , A01N43/80 , A01N43/82 , C07C69/618 , A61K31/21 , A61K31/40 , A61K31/505 , C07C67/343 , C07C69/65 , C07C69/734 , C07C69/736 , C07C69/738 , C07C69/75 , C07C69/76 , C07C69/84 , C07C69/86 , C07C69/92 , C07C69/94 , C07C205/34 , C07C205/38 , C07C205/56 , C07C229/40 , C07C229/44 , C07C233/11 , C07C235/32 , C07C235/34 , C07C251/38 , C07C251/48 , C07C251/52 , C07C251/60 , C07C251/66 , C07C255/57 , C07C255/64 , C07C275/64 , C07C309/66 , C07C309/73 , C07C311/09 , C07C311/21 , C07C311/29 , C07C313/04 , C07C313/06 , C07C317/44 , C07C317/46 , C07C323/56 , C07C323/62 , C07C327/22 , C07C327/48 , C07D207/32 , C07D207/335 , C07D207/337 , C07D213/53 , C07D213/64 , C07D213/643 , C07D213/66 , C07D213/68 , C07D213/70 , C07D215/22 , C07D215/227 , C07D215/233 , C07D215/36 , C07D231/12 , C07D233/84 , C07D235/28 , C07D239/52 , C07D249/12 , C07D257/04 , C07D261/08 , C07D263/32 , C07D263/34 , C07D263/58 , C07D271/06 , C07D271/10 , C07D271/113 , C07D277/28 , C07D277/30 , C07D277/36 , C07D277/68 , C07D277/74 , C07D285/12 , C07D285/125 , C07D307/46 , C07D307/52 , C07D307/54 , C07D309/06 , C07D333/24 , C07D409/04 , C07D413/04 , C07D513/04 , C07D521/00 , C07F7/08
Abstract: Derivatives of beta -substituted cinnamic acid of the general formula 1 in which R denotes optionally substituted alkyl, alkenyl, alkynyl, cycloalkyl or cycloalkenyl, and in which R can also denote chlorine or bromine, -X- represents the groups -O-, -S-, m denotes 0 or 1, -Y represents the groups -OR , -O-N=CR R , -NR R , -N(OR )R or -Sr , where the abovementioned substituents R to R denote optionally substituted alkyl, alkenyl, alkynyl, cycloalkyl or cycloalkenyl, and for the radicals R , R and R to R can also denote hydrogen, Z denotes halogen, nitro, cyano, optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted aralkyl, optionally substituted aryloxyalkyl, optionally substituted arylthioalkyl, optionally substituted heteroarylalkyl, optionally substituted heteroaryloxyalkyl, optionally substituted heteroarylthioalkyl, optionally substituted alkenyl, optionally substituted aralkenyl, optionally substituted aryloxyalkenyl, optionally substituted arylthioalkenyl, optionally substituted heteroarylalkenyl, optionally substituted heteroaryloxyalkenyl, optionally substituted heteroarylthioalkenyl, optionally substituted alkynyl, optionally substituted arylalkynyl, optionally substituted heteroarylalkynyl, optionally substituted aryl, optionally substituted heteroaryl, optionally substituted arylazo, optionally substituted acylamino, -OR , -SR ,-SOR , -SO2R , -COOR , -CONR R , -COR , -CR =NR , -N=CR R , -CR =N-OR , -CR R -O-N=CR R , -CH2-OCOR or -NR R , where the groups R to R , and R and R denote hydrogen, optionally substituted alkyl, optionally substituted alkenyl, optionally substituted alkynyl, optionally substituted cycloalkyl, optionally substituted cycloalkylalkyl, optionally substituted aryl, optionally substituted heteroaryl, optionally substituted aralkyl, optionally substituted heteroarylalkyl, optionally substituted aryloxyalkyl, optionally substituted arylthioalkyl, optionally substituted heteroaryloxyalkyl or optionally substituted heteroarylthioalkyl and R denotes hydrogen or C1-C4-alkyl and in which U, V, W denote hydrogen or have one of the meanings mentioned for Z or in which two of the groups Z, U, V or W in adjacent positions of the phenyl ring optionally together form an optionally substituted five- or six-membered, aromatic or aliphatic ring fused to the phenyl ring, which can optionally contain one to three heteroatoms (N, S, O).
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公开(公告)号:DK0483616T3
公开(公告)日:1996-01-29
申请号:DK91117801
申请日:1991-10-18
Applicant: BASF AG
Inventor: SEELE RAINER DR , AMMERMANN EBERHARD DR , LORENZ GISELA DR , GOETZ NORBERT DR
IPC: A01N43/50 , A01N43/653 , C07D233/60 , C07D249/08 , C07D303/04 , C07D303/08 , C07D303/12 , C07D405/06 , C07D405/08 , C07D493/10 , C07D521/00
Abstract: Azolylmethylspiro(2.5)octanols of the formula (* CHEMICAL STRUCTURE *) where A and R are each hydrogen or alkyl; D is alkyl, cycloalkyl, cycloalkenyl, biphenylyl, naphthyl, hetaryl or phenyl, it being possible for each of these radicals to be substituted; Z is CH2 or O, X is CH or N, and the plant-compatible acid addition salts and metal complexes thereof are used as or in fungicides.
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公开(公告)号:CZ47590A3
公开(公告)日:1996-01-17
申请号:CS47590
申请日:1990-02-01
Applicant: BASF AG
Inventor: SCHUETZ FRANZ DR , SAUTER HUBERT DR , HARREUS ALBRECHT DR , ROHR WOLFGANG DR , HEPP MICHAEL DR , BRAND SIEGBERT DR , WENDEROTH BERND DR , LORENZ GISELA DR , AMMERMANN EBERHARD DR
IPC: A01N37/10 , A01N37/50 , A01N37/52 , C07C251/38 , C07C251/48 , C07C251/50 , C07C251/52 , C07C251/54 , C07C251/60 , C07C255/62
Abstract: Substituted oxime ethers of the general formula where R1 is alkyl, alkenyl, alkynyl, haloalkyl, haloalkenyl, alkoxyalkyl, cycloalkyl, cycloalkylalkyl, cyanoalkyl, alkoxycarbonylalkyl, arylalkyl, heteroarylalkyl, arylalkenyl or aryloxyalkyl, the aromatic or heteroaromatic ring being substituted or unsubstituted, R2 and R3 are hydrogen, alkyl, haloalkyl, alkoxy, haloalkoxy, halogen, cyano or nitro, R4 is hydrogen, alkyl or aryl, the aromatic ring being substituted or unsubstituted, and X is CH or N, and fungicides containing these compounds.
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公开(公告)号:ES2078602T3
公开(公告)日:1995-12-16
申请号:ES92112086
申请日:1992-07-15
Applicant: BASF AG
Inventor: SAUTER HUBERT DR , BAYER HERBERT DR , OBERDORF KLAUS DR , WINGERT HORST DR , VON DEYN WOLFGANG DR , GRAMMENOS WASSILIOS DR , KOENIG HARTMANN DR , RANG HARALD DR , ROEHL FRANZ DR , LORENZ GISELA DR , AMMERMANN EBERHARD DR
IPC: A01N37/36 , A01N37/38 , A01N37/44 , A01N37/48 , A01N43/08 , A01N43/10 , A01N43/36 , A01N43/56 , A01N43/74 , A01N43/78 , A01N43/80 , A01N43/82 , C07C69/618 , A61K31/21 , A61K31/40 , A61K31/505 , C07C67/343 , C07C69/65 , C07C69/734 , C07C69/736 , C07C69/738 , C07C69/75 , C07C69/76 , C07C69/84 , C07C69/86 , C07C69/92 , C07C69/94 , C07C205/34 , C07C205/38 , C07C205/56 , C07C229/40 , C07C229/44 , C07C233/11 , C07C235/32 , C07C235/34 , C07C251/38 , C07C251/48 , C07C251/52 , C07C251/60 , C07C251/66 , C07C255/57 , C07C255/64 , C07C275/64 , C07C309/66 , C07C309/73 , C07C311/09 , C07C311/21 , C07C311/29 , C07C313/04 , C07C313/06 , C07C317/44 , C07C317/46 , C07C323/56 , C07C323/62 , C07C327/22 , C07C327/48 , C07D207/32 , C07D207/335 , C07D207/337 , C07D213/53 , C07D213/64 , C07D213/643 , C07D213/66 , C07D213/68 , C07D213/70 , C07D215/22 , C07D215/227 , C07D215/233 , C07D215/36 , C07D231/12 , C07D233/84 , C07D235/28 , C07D239/52 , C07D249/12 , C07D257/04 , C07D261/08 , C07D263/32 , C07D263/34 , C07D263/58 , C07D271/06 , C07D271/10 , C07D271/113 , C07D277/28 , C07D277/30 , C07D277/36 , C07D277/68 , C07D277/74 , C07D285/12 , C07D285/125 , C07D307/46 , C07D307/52 , C07D307/54 , C07D309/06 , C07D333/24 , C07D409/04 , C07D413/04 , C07D513/04 , C07D521/00 , C07F7/08
Abstract: Derivatives of beta -substituted cinnamic acid of the general formula 1 in which R denotes optionally substituted alkyl, alkenyl, alkynyl, cycloalkyl or cycloalkenyl, and in which R can also denote chlorine or bromine, -X- represents the groups -O-, -S-, m denotes 0 or 1, -Y represents the groups -OR , -O-N=CR R , -NR R , -N(OR )R or -Sr , where the abovementioned substituents R to R denote optionally substituted alkyl, alkenyl, alkynyl, cycloalkyl or cycloalkenyl, and for the radicals R , R and R to R can also denote hydrogen, Z denotes halogen, nitro, cyano, optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted aralkyl, optionally substituted aryloxyalkyl, optionally substituted arylthioalkyl, optionally substituted heteroarylalkyl, optionally substituted heteroaryloxyalkyl, optionally substituted heteroarylthioalkyl, optionally substituted alkenyl, optionally substituted aralkenyl, optionally substituted aryloxyalkenyl, optionally substituted arylthioalkenyl, optionally substituted heteroarylalkenyl, optionally substituted heteroaryloxyalkenyl, optionally substituted heteroarylthioalkenyl, optionally substituted alkynyl, optionally substituted arylalkynyl, optionally substituted heteroarylalkynyl, optionally substituted aryl, optionally substituted heteroaryl, optionally substituted arylazo, optionally substituted acylamino, -OR , -SR ,-SOR , -SO2R , -COOR , -CONR R , -COR , -CR =NR , -N=CR R , -CR =N-OR , -CR R -O-N=CR R , -CH2-OCOR or -NR R , where the groups R to R , and R and R denote hydrogen, optionally substituted alkyl, optionally substituted alkenyl, optionally substituted alkynyl, optionally substituted cycloalkyl, optionally substituted cycloalkylalkyl, optionally substituted aryl, optionally substituted heteroaryl, optionally substituted aralkyl, optionally substituted heteroarylalkyl, optionally substituted aryloxyalkyl, optionally substituted arylthioalkyl, optionally substituted heteroaryloxyalkyl or optionally substituted heteroarylthioalkyl and R denotes hydrogen or C1-C4-alkyl and in which U, V, W denote hydrogen or have one of the meanings mentioned for Z or in which two of the groups Z, U, V or W in adjacent positions of the phenyl ring optionally together form an optionally substituted five- or six-membered, aromatic or aliphatic ring fused to the phenyl ring, which can optionally contain one to three heteroatoms (N, S, O).
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公开(公告)号:DE4420277A1
公开(公告)日:1995-12-14
申请号:DE4420277
申请日:1994-06-10
Applicant: BASF AG
Inventor: AMMERMANN EBERHARD DR , LORENZ GISELA DR , MAPPES DIETRICH DR , SCHELBERGER KLAUS , HAMPEL MANFRED DR
Abstract: Described are fungicidal mixtures containing: a) the oxime ether carboxylic acid ester of formula (I) and (b) a dithiocarbamate (II) selected from the group: manganese ethylene-bis(dithiocarbamate) (zinc complex) (IIa); manganese ethylene-bis(dithiocarbamate) (IIb); zinc ammoniate ethylene-bis(dithiocarbamate) (IIc) and zinc ethylene-bis(dithiocarbamate) (IId) in a synergistically effective amount.
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公开(公告)号:ES2077935T3
公开(公告)日:1995-12-01
申请号:ES92111670
申请日:1992-07-09
Applicant: BASF AG
Inventor: SAUTER HUBERT DR , SCHELBERGER KLAUS , SAUR REINHOLD DR , LORENZ GISELA DR , AMMERMANN EBERHARD DR
Abstract: Fungicidal mixture composed of …… a) methyl alpha -methoximino-2-[(2-methylphenoxy)-methyl]-phenyl acetate … … and … b) 4-(2-methyl-3-[4-tertiary butylphenyl]-propyl)- 2,6-dimethylmorpholine (fenpropimorph) … … or the active substance tridemorph or the active substance fenpropidine, … and process for the control of fungi using this mixture.
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公开(公告)号:DE59203812D1
公开(公告)日:1995-11-02
申请号:DE59203812
申请日:1992-07-15
Applicant: BASF AG
Inventor: SAUTER HUBERT DR , BAYER HERBERT W- LUDWIGSHAFEN , OBERDORF KLAUS DR , WINGERT HORST DR , VON DEYN WOLFGANG DR , GRAMMENOS WASSILIOS DR , KOENIG HARTMANN DR , RANG HARALD DR , ROEHL FRANZ DR , LORENZ GISELA DR , AMMERMANN EBERHARD DR
IPC: A01N37/36 , A01N37/38 , A01N37/44 , A01N37/48 , A01N43/08 , A01N43/10 , A01N43/36 , A01N43/56 , A01N43/74 , A01N43/78 , A01N43/80 , A01N43/82 , C07C69/618 , A61K31/21 , A61K31/40 , A61K31/505 , C07C67/343 , C07C69/65 , C07C69/734 , C07C69/736 , C07C69/738 , C07C69/75 , C07C69/76 , C07C69/84 , C07C69/86 , C07C69/92 , C07C69/94 , C07C205/34 , C07C205/38 , C07C205/56 , C07C229/40 , C07C229/44 , C07C233/11 , C07C235/32 , C07C235/34 , C07C251/38 , C07C251/48 , C07C251/52 , C07C251/60 , C07C251/66 , C07C255/57 , C07C255/64 , C07C275/64 , C07C309/66 , C07C309/73 , C07C311/09 , C07C311/21 , C07C311/29 , C07C313/04 , C07C313/06 , C07C317/44 , C07C317/46 , C07C323/56 , C07C323/62 , C07C327/22 , C07C327/48 , C07D207/32 , C07D207/335 , C07D207/337 , C07D213/53 , C07D213/64 , C07D213/643 , C07D213/66 , C07D213/68 , C07D213/70 , C07D215/22 , C07D215/227 , C07D215/233 , C07D215/36 , C07D231/12 , C07D233/84 , C07D235/28 , C07D239/52 , C07D249/12 , C07D257/04 , C07D261/08 , C07D263/32 , C07D263/34 , C07D263/58 , C07D271/06 , C07D271/10 , C07D271/113 , C07D277/28 , C07D277/30 , C07D277/36 , C07D277/68 , C07D277/74 , C07D285/12 , C07D285/125 , C07D307/46 , C07D307/52 , C07D307/54 , C07D309/06 , C07D333/24 , C07D409/04 , C07D413/04 , C07D513/04 , C07D521/00 , C07F7/08
Abstract: Derivatives of beta -substituted cinnamic acid of the general formula 1 in which R denotes optionally substituted alkyl, alkenyl, alkynyl, cycloalkyl or cycloalkenyl, and in which R can also denote chlorine or bromine, -X- represents the groups -O-, -S-, m denotes 0 or 1, -Y represents the groups -OR , -O-N=CR R , -NR R , -N(OR )R or -Sr , where the abovementioned substituents R to R denote optionally substituted alkyl, alkenyl, alkynyl, cycloalkyl or cycloalkenyl, and for the radicals R , R and R to R can also denote hydrogen, Z denotes halogen, nitro, cyano, optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted aralkyl, optionally substituted aryloxyalkyl, optionally substituted arylthioalkyl, optionally substituted heteroarylalkyl, optionally substituted heteroaryloxyalkyl, optionally substituted heteroarylthioalkyl, optionally substituted alkenyl, optionally substituted aralkenyl, optionally substituted aryloxyalkenyl, optionally substituted arylthioalkenyl, optionally substituted heteroarylalkenyl, optionally substituted heteroaryloxyalkenyl, optionally substituted heteroarylthioalkenyl, optionally substituted alkynyl, optionally substituted arylalkynyl, optionally substituted heteroarylalkynyl, optionally substituted aryl, optionally substituted heteroaryl, optionally substituted arylazo, optionally substituted acylamino, -OR , -SR ,-SOR , -SO2R , -COOR , -CONR R , -COR , -CR =NR , -N=CR R , -CR =N-OR , -CR R -O-N=CR R , -CH2-OCOR or -NR R , where the groups R to R , and R and R denote hydrogen, optionally substituted alkyl, optionally substituted alkenyl, optionally substituted alkynyl, optionally substituted cycloalkyl, optionally substituted cycloalkylalkyl, optionally substituted aryl, optionally substituted heteroaryl, optionally substituted aralkyl, optionally substituted heteroarylalkyl, optionally substituted aryloxyalkyl, optionally substituted arylthioalkyl, optionally substituted heteroaryloxyalkyl or optionally substituted heteroarylthioalkyl and R denotes hydrogen or C1-C4-alkyl and in which U, V, W denote hydrogen or have one of the meanings mentioned for Z or in which two of the groups Z, U, V or W in adjacent positions of the phenyl ring optionally together form an optionally substituted five- or six-membered, aromatic or aliphatic ring fused to the phenyl ring, which can optionally contain one to three heteroatoms (N, S, O).
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