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公开(公告)号:AT143657T
公开(公告)日:1996-10-15
申请号:AT93112327
申请日:1993-07-31
Applicant: BASF AG
Inventor: WINGERT HORST DR , HELLENDAHL BEATE DR , KIRSTGEN REINHARD DR , SAUTER HUBERT DR , AMMERMANN EBERHARD DR , LORENZ GISELA DR
IPC: A01N37/42 , A01N37/10 , A01N37/34 , A01N37/36 , A01N37/50 , A01N43/10 , A01N43/40 , A01N43/78 , A01N43/80 , A01N43/84 , A01N55/00 , C07C69/618 , C07C69/734 , C07C69/738 , C07C69/76 , C07C205/56 , C07C233/31 , C07C233/54 , C07C251/48 , C07C255/23 , C07C255/62 , C07C323/57 , C07C323/60 , C07D213/54 , C07D213/55 , C07D213/56 , C07D215/12 , C07D217/16 , C07D231/12 , C07D233/92 , C07D261/08 , C07D271/10 , C07D271/107 , C07D277/20 , C07D277/22 , C07D277/58 , C07D277/66 , C07D285/12 , C07D307/54 , C07D307/71 , C07D317/60 , C07D319/18 , C07D333/24 , C07D333/28 , C07D333/38 , C07D333/42 , C07D413/12 , C07D521/00 , C07F7/10 , C07F7/22
Abstract: Acetylene derivatives of the general formula I in which U, V and W denote hydrogen, halogen, nitro, cyano, alkyl and alkoxy, A denotes alkylidene, alkoxymethylidene, alkylthiomethylidene and alkoximino, B denotes OH, alkoxy and alkylamino and R denotes hydrogen, halogen, cyano, CF3, alkyl, cycloalkyl, haloalkyl, aryl, alkenyl, alkinyl, heterocyclyl, heteroaryl, arylalkyl, arylalkenyl, arylethinyl, heteroaryl-C1-C4-alkyl, C1-C4-alkoxy-C1-C4-alkyl, aryloxyalkyl, heteroaryloxyalkyl, arylamino-alkyl, arylthiomethyl, heteroarylthiomethyl, C(O)R , C(O)NR R , C(S)NR R , C(O)SR , C(S)OR , C(S)SR , CH(OH)R )R , SiR R R , SnR R R , C(OR)R , C(=N-OR )R , and the radicals R -R , R and R denote hydrogen, alkyl, aryl, heteroaryl, arylalkyl and heteroarylalkyl, and fungicides containing these compounds.
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公开(公告)号:DE59206443D1
公开(公告)日:1996-07-11
申请号:DE59206443
申请日:1992-01-24
Applicant: BASF AG
Inventor: GRAMMENOS WASSILIOS DR , HARREUS ALBRECHT DR , SAUTER HUBERT DR , HELLENDAHL BEATE DR , DOETZER REINHARD DR , AMMERMANN EBERHARD DR , LORENZ GISELA DR
IPC: A01N37/50 , A01N43/54 , A01N43/58 , A01N43/76 , A01N43/836 , C07C69/65 , C07C69/653 , C07C69/734 , C07C69/738 , C07C251/48 , C07C251/50 , C07C251/52 , C07C251/54 , C07C251/56 , C07C251/58 , C07C251/60 , C07C251/86 , C07C255/15 , C07C255/57 , C07C255/58 , C07C255/62 , C07D213/77 , C07D239/42 , C07D241/20 , C07D263/32 , C07D333/28
Abstract: Iminoalkyl-phenylacrylic acid derivs. (I) ar new: R = H or 1-6C alkyl; R = H; 1-4C alkyl opt. substd. by halo; or opt. substd. aryl; Z ,Z = H; halo; CN; NO2;etc.;Y = O; NH; or NR ; and R = H; 1-4C alkoxycarbonyl-1-4C alkyl; or opt. substd. alkyl, cycloalkyl, etc.; or Y+R form a ring which is opt. substd. when Y = NH or NR ; R = 1-6C alkyl; X = CH-1-4C alkoxy or CH-1-4C alkylthio (also 1-4C alkylidene and 1-4C alkoxyimino in the description).
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公开(公告)号:ES2085812T3
公开(公告)日:1996-06-01
申请号:ES94114505
申请日:1994-09-15
Applicant: BASF AG
Inventor: WINGERT HORST DR , SAUTER HUBERT DR , AMMERMANN EBERHARD DR , LORENZ GISELA DR , SAUR REINHOLD DR , SCHELBERGER KLAUS
IPC: A01N37/50 , A01N43/653 , A01N47/38 , A01N55/00 , A01N55/10
Abstract: Fungicidal mixture comprising a) the oxime ether carboxamide of the formula I and b) an azole derivative II selected from the group consisting of the compounds II.1 to II.16 - 1-[(2RS,4RS; 2RS,4SR)-4-bromo-2-(2,4-dichlorophenyl)tetrahydrofuryl]-1H-1,2,4-triaz ole (II.1) - 2-(4-chlorophenyl)-3-cyclopropyl-1-(1H-1,2,4-triazol-1-yl)-butan-2-ol (II.2) - (+/-)-4-chloro-4-[4-methyl-2-(1H-1,2,4-triazol-1-ylmethyl)-1,3-dioxolan- 2-yl]-phenyl 4-chlorophenyl ether (II.3) - (E)-(RS)-1-(2,4-dichlorophenyl)-4,4-dimethyl-2-(1H-1,2,4-triazol-1-yl) pent-1-ene-3-ol (II.4) - (Z)-2-(1H-1,2,4-triazol-1-ylmethyl)-2-(4-fluorophenyl)-3-(2-chlorophen yl)-oxiran (II.5) - 4-(4-chlorophenyl)-2-phenyl-2-(1H-1,2,4-triazolylmethyl)-butyronitrile (II.6) - 3-(2,4-dichlorophenyl)-6-fluoro-2-(1H-1,2,4-triazol-1-yl)quinazolin-4( 3H)-one (II.7) - bis(4-fluorophenyl)(methyl)(1H-1,2,4-triazol-1-ylmethyl)silane (II.8) - (R,S)-2-(2,4-dichlorophenyl)-1-(1H-1,2,4-triazol-1-yl)-hexan-2-ol (II.9) - (1RS,5RS;1RS,5SR)-5-(4-chlorobenzyl)-2,2-dimethyl-1-(1H- 1,2,4-triazol-1-ylmethyl)cyclopentanol (II.10) - N-propyl-N-[2-(2,4,6-trichlorophenoxy)ethyl]imidazole-1-carboxamide (II.11) - (+/-)-1-[2-(2,4-dichlorophenyl)-4-propyl-1,3-dioxolan-2-ylmethyl]-1H-1,2 ,4-triazole (II.12) - (R,S)-1-(4-chlorophenyl)-4,4-dimethyl-3-(1H-1,2,4-triazol-1-ylmethyl)- pentan-3-ol (II.13) - (+/-)-2-(2,4-dichlorophenyl)-3-(1H-1,2,4-triazolyl)-propyl 1,1,2,2-tetrafluoroethyl ether (II.14) - (E)-1-[1-[[4-chloro-2-(trifluoromethyl)-phenyl]imino]-2-propoxyethyl]- 1H-imidazole (II.15) and - (RS)-2,4'-difluoro- alpha -(1H-1,2,4-triazol-1-ylmethyl)-benzhydryl-alcohol (II.16) in a synergistically active amount.)
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公开(公告)号:DE4441676A1
公开(公告)日:1996-05-30
申请号:DE4441676
申请日:1994-11-23
Applicant: BASF AG
Inventor: MUELLER BERND DR , SAUTER HUBERT DR , ROEHL FRANZ DR , AMMERMANN EBERHARD DR , LORENZ GISELA DR , GOETZ NORBERT DR
IPC: A01N47/24 , A01N47/30 , C07C271/60 , C07D209/48 , C07D239/30 , C07D239/34 , C07D401/04 , C07D403/04 , C07D405/04 , C07D239/32 , A01N43/48 , A01N43/64 , A01N43/90 , A01N47/10 , C07C271/28 , C07D213/84 , C07D237/14 , C07D241/18
Abstract: Iminooxymethylene anilides have the formula (I), in which the indices and substituents have the following meanings: n equals 0, 1, 2, 3 or 4; R stands for nitro, cyano, halogen, optionally substituted alkyl, alkenyl, alkinyl, alkoxy, alkenyloxy, alkinyloxy or an optionally substituted bridge bound to two adjacent ring atoms; X stands for a direct bond, CH2, O or NR ; R stands for hydrogen, alkyl, alkenyl, alkinyl, cycloalkyl or cycloalkenyl; R stands for hydrogen, optionally substituted alkyl, alkenyl, alkinyl, cycloalkyl, cycloalkenyl, alkylcarbonyl or alkoxycarbonyl; R stands for alkyl, alkenyl, alkinyl, cycloalkyl or cycloalkenyl and when X stands for NR it may also stand for hydrogen; R stands for hydrogen, cyano, halogen, alkyl, alkylhalide, alkoxy, alkoxyhalide, alkylthio, alkylthiohalide or cycloalkyl; R stands for a substituted 6 to 10-membered monocyclic or bicyclic heteroaromatic ring system. Also disclosed are a process and intermediate products for preparing these compounds and their use.
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公开(公告)号:AT136732T
公开(公告)日:1996-05-15
申请号:AT94114507
申请日:1994-09-15
Applicant: BASF AG
Inventor: WINGERT HORST DR , SAUTER HUBERT DR , AMMERMANN EBERHARD DR , LORENZ GISELA DR , SAUR REINHOLD DR , SCHELBERGER KLAUS , HAMPEL MANFRED DR
Abstract: Fungicidal mixture comprising a) the oxime ether carboxamide of the formula I and b) 1-(2-cyano-2-methoxyiminoacetyl)-3-ethylurea (II> H3CCH2-NHCONH-C(CN)=NOCH3 II in a synergistically active amount.i
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公开(公告)号:DK0645090T3
公开(公告)日:1996-05-13
申请号:DK94114507
申请日:1994-09-15
Applicant: BASF AG
Inventor: SAUTER HUBERT DR , LORENZ GISELA DR , AMMERMANN EBERHARD DR , HAMPEL MANFRED DR , SAUR REINHOLD DR , SCHELBERGER KLAUS , WINGERT HORST DR
Abstract: Fungicidal mixture comprising a) the oxime ether carboxamide of the formula I and b) 1-(2-cyano-2-methoxyiminoacetyl)-3-ethylurea (II> H3CCH2-NHCONH-C(CN)=NOCH3 II in a synergistically active amount.i
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公开(公告)号:DE59205825D1
公开(公告)日:1996-05-02
申请号:DE59205825
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
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:DE59205797D1
公开(公告)日:1996-05-02
申请号:DE59205797
申请日:1992-01-17
Applicant: BASF AG
Inventor: BENOIT REMY DR , SAUTER HUBERT DR , KIRSTGEN REINHARD DR , LORENZ GISELA DR , AMMERMANN EBERHARD DR
IPC: A01N35/10 , A01N37/12 , A01N37/34 , A01N37/50 , A01N43/10 , A01N53/10 , C07C251/48 , C07C251/50 , C07C251/58 , C07C251/60 , C07C251/80 , C07C255/61 , C07C255/62 , C07D239/52
Abstract: alpha -Imino oxime cpds, described as oxime ethers, of formula (I) are new: R = CR2R3R4 or opt. substd. 3-8C cycloalkyl, 2-8C alkenyl, 2-8C alkynyl, phenyl or heteroaryl; R1 = H or 1-8C alkyl; R2 = H, 1-8C alkyl, aralkyl, heteroarylalkyl, alkoxyalkyl, aryloxyalkyl, aryl or heteroaryl; R3 = H, Me, CN, COOH or 2-9C alkoxycarbonyl; R4 = a gp. as defined for R2; or CR2R3 is a 5- to 8-membered lactone ring or CR2R4 is a 3-8C cycloalkane ring; R5 = H, 1-8C alkyl, aralkyl, 3-6C cycloalkyl, OH, 1-4C alkoxy, NH2, 1-4C alkylamino or dialkylamino; Y = a gp. stated to be an opt. substd. 1-8C alkyl, opt. substd. 2-8C alkenyl, 2-8C alkynyl, O, S(O)m (m = 0-2), N substd. by opt. substd. 1-8C alkyl, oxycarbonyl, carbonyloxy, oxycarbonyl (1-8C) alkyl, carbonyloxy (1-8C) alkyl, 2-8C oxyalkyloxy, 2-8C oxyalkenyl, 1-8C alkoxy, 1-4C oxyalkyl, 1-8C thioalkyl, azo, opt. 1-8C alkyl-substd. -carbonylamino, -aminocarbonyl or -aminocarbonyloxy, oxyimino or opt. substd. imino oxyalkyl; Z = (a) 1-18C alkyl, 2-18C alkenyl, 3-18C alkynyl, aryl, aryl (1-10C) alkyl, aryl (2-10C) alkenyl, aryloxy (1-10C) alkyl, (1-4C) alkoxy (1-10C) alkyl, 1-10C haloalkyl, 2-5C alkoxycarbonyl or heteroaryl; (b) aryloxy, aryloxy (1-10C) alkoxy, aryl (1-10C) alkoxy, 1-10C alkoxy or heteroaryloxy when Y is not oxyalkyl, oxyalkyloxy, thialkyl (sic), -O-N=C- (sic), -N=N-, oxycarbonyl, oxycarbonyloxy, O or S; or (c) 1-18C alkylthio or arylthio when Y is not oxyalkyl, oxyalkyloxy, -O-N=C- (sic), -N=N-, oxycarbonyl, oxycarbonyloxy or O, and Z is opt. substd. by halogen, CN, NO2, 1-4C alkyl, 2-4C alkenyl, 1-4C alkoxy, 1-4C haloalkyl, (1-4C) alkoxy (1-4C) alkyl, di(1-4C) alkoxy (1-4C) alkyl, opt. substd. 1-10C alkoxyimino, opt. substd. 2-10C alkenyloxyimino, opt. substd. aralkoxyimino, opt. substd. 2-10C alkanoyl, opt. substd. formyl, 2-4C haloalkenyl, 2-5C alkoxycarbonyl, opt. substd. phenyl, or opt. substd. 5-membered heterocyclyl which contains 1-4 heteroatoms (N, O and/or S) and is opt. fused with an opt. substd. aromatic or heteroaromatic ring; X = H, halogen, NO2 and/or opt. substd. 1-4C alkyl, 1-4C alkoxy and/or 1-4C haloalkyl; m = 1-4.
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公开(公告)号:DK0531837T3
公开(公告)日:1996-04-22
申请号:DK92114812
申请日:1992-08-29
Applicant: BASF AG
Inventor: LORENZ GISELA DR , SAUR REINHOLD DR , AMMERMANN EBERHARD DR , SCHELBERGER KLAUS , SAUTER HUBERT
IPC: A01N43/653 , A01N37/50
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:DK0498188T3
公开(公告)日:1996-04-22
申请号:DK92100713
申请日:1992-01-17
Applicant: BASF AG
Inventor: SAUTER HUBERT DR , AMMERMANN EBERHARD DR , LORENZ GISELA DR , KIRSTGEN REINHARD DR , BENOIT REMY DR
IPC: A01N35/10 , A01N37/12 , A01N37/34 , A01N37/50 , A01N43/10 , A01N53/10 , C07C251/48 , C07C251/50 , C07C251/58 , C07C251/60 , C07C251/80 , C07C255/61 , C07C255/62 , C07D239/52
Abstract: alpha -Imino oxime cpds, described as oxime ethers, of formula (I) are new: R = CR2R3R4 or opt. substd. 3-8C cycloalkyl, 2-8C alkenyl, 2-8C alkynyl, phenyl or heteroaryl; R1 = H or 1-8C alkyl; R2 = H, 1-8C alkyl, aralkyl, heteroarylalkyl, alkoxyalkyl, aryloxyalkyl, aryl or heteroaryl; R3 = H, Me, CN, COOH or 2-9C alkoxycarbonyl; R4 = a gp. as defined for R2; or CR2R3 is a 5- to 8-membered lactone ring or CR2R4 is a 3-8C cycloalkane ring; R5 = H, 1-8C alkyl, aralkyl, 3-6C cycloalkyl, OH, 1-4C alkoxy, NH2, 1-4C alkylamino or dialkylamino; Y = a gp. stated to be an opt. substd. 1-8C alkyl, opt. substd. 2-8C alkenyl, 2-8C alkynyl, O, S(O)m (m = 0-2), N substd. by opt. substd. 1-8C alkyl, oxycarbonyl, carbonyloxy, oxycarbonyl (1-8C) alkyl, carbonyloxy (1-8C) alkyl, 2-8C oxyalkyloxy, 2-8C oxyalkenyl, 1-8C alkoxy, 1-4C oxyalkyl, 1-8C thioalkyl, azo, opt. 1-8C alkyl-substd. -carbonylamino, -aminocarbonyl or -aminocarbonyloxy, oxyimino or opt. substd. imino oxyalkyl; Z = (a) 1-18C alkyl, 2-18C alkenyl, 3-18C alkynyl, aryl, aryl (1-10C) alkyl, aryl (2-10C) alkenyl, aryloxy (1-10C) alkyl, (1-4C) alkoxy (1-10C) alkyl, 1-10C haloalkyl, 2-5C alkoxycarbonyl or heteroaryl; (b) aryloxy, aryloxy (1-10C) alkoxy, aryl (1-10C) alkoxy, 1-10C alkoxy or heteroaryloxy when Y is not oxyalkyl, oxyalkyloxy, thialkyl (sic), -O-N=C- (sic), -N=N-, oxycarbonyl, oxycarbonyloxy, O or S; or (c) 1-18C alkylthio or arylthio when Y is not oxyalkyl, oxyalkyloxy, -O-N=C- (sic), -N=N-, oxycarbonyl, oxycarbonyloxy or O, and Z is opt. substd. by halogen, CN, NO2, 1-4C alkyl, 2-4C alkenyl, 1-4C alkoxy, 1-4C haloalkyl, (1-4C) alkoxy (1-4C) alkyl, di(1-4C) alkoxy (1-4C) alkyl, opt. substd. 1-10C alkoxyimino, opt. substd. 2-10C alkenyloxyimino, opt. substd. aralkoxyimino, opt. substd. 2-10C alkanoyl, opt. substd. formyl, 2-4C haloalkenyl, 2-5C alkoxycarbonyl, opt. substd. phenyl, or opt. substd. 5-membered heterocyclyl which contains 1-4 heteroatoms (N, O and/or S) and is opt. fused with an opt. substd. aromatic or heteroaromatic ring; X = H, halogen, NO2 and/or opt. substd. 1-4C alkyl, 1-4C alkoxy and/or 1-4C haloalkyl; m = 1-4.
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