-
公开(公告)号:DE59610410D1
公开(公告)日:2003-06-05
申请号:DE59610410
申请日:1996-05-13
Applicant: BASF AG
Inventor: MUELLER DR , KIRSTGEN DR , KOENIG DR , RACK DR , OBERDORF DR , ROEHL DR , SAUTER DR , LORENZ DR , AMMERMANN DR , STRATHMANN DR , HARRIES DR
IPC: A01N43/56 , A01N43/653 , C07D231/18 , C07D231/20 , C07D231/22 , C07D249/12 , C07D401/04 , C07D401/12 , C07D403/04 , C07D403/12
Abstract: Substd. 2-phenyl-3-alkoxy-acrylate ester cpds. of formula (I) are new: n = 0-4; R = alkyl, alkenyl, alkynyl, etc.; or R+R on adjacent C = 3-4 membered bridge contg. 0-2 N, O and/or S, and the rest C (where the ring formed is opt. unsatd. or aromatic); R1, R2 = 1-4C alkyl; R3 = a pyrazolyl or triazolyl gp. of e.g. formula (a1): R4 = alkyl, alkenyl, alkynyl, etc.; Het = N, O or S; m = 0-2; R5 = CN, NO2, halo, etc..
-
公开(公告)号:DE50100210D1
公开(公告)日:2003-06-05
申请号:DE50100210
申请日:2001-11-30
Applicant: BASF AG
Inventor: EICKEN DR , AMMERMANN DR , STIERL DR , LORENZ DR , STRATHMANN DR , SCHERER MARIA , SCHELBERGER KLAUS , HAMPEL DR
Abstract: New fungicidal mixtures contain synergistic amounts of an N-(1,1'-biphenyl-2-yl)-nicotinamide derivative (I) and the spiro-dioxolan derivative spiroxamine (II). New fungicidal mixtures contain synergistic amounts of a nicotinamide derivative of formula (I) and the spiro-dioxolan derivative spiroxamine of formula (II). R1, R2 = halo, NO2, CN, 1-8C alkyl, 2-8C alkenyl, 2-8C alkynyl, 1-8C haloalkyl, 2-8C haloalkenyl, 2-8C haloalkynyl, 1-8C alkoxy, 1-8C haloalkoxy, 1-8C haloalkylthio, 1-8C alkylsulfinyl or 1-8C alkylsulfonyl; x = 1-4; and y = 1-5. An Independent claim is also included for a method for controlling fungi, involving applying (I) and (II), simultaneously (in combination or separately) or successively, to the fungi, their habitat or plants, seeds, soil, areas, material or regions to be protected.
-
公开(公告)号:DE59813084D1
公开(公告)日:2005-11-03
申请号:DE59813084
申请日:1998-12-15
Applicant: BASF AG
Inventor: SCHELBERGER KLAUS , SCHERER MARIA , EICKEN DR , HAMPEL DR , AMMERMANN DR , LORENZ DR , STRATHMANN DR
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)
-
公开(公告)号:DE59812725D1
公开(公告)日:2005-05-12
申请号:DE59812725
申请日:1998-12-15
Applicant: BASF AG
Inventor: SCHELBERGER KLAUS , SCHERER MARIA , EICKEN DR , HAMPEL DR , AMMERMANN DR , LORENZ DR , STRATHMANN DR
-
公开(公告)号:DE50100541D1
公开(公告)日:2003-10-02
申请号:DE50100541
申请日:2001-06-21
Applicant: BASF AG
Inventor: GYPSER DR , GROTE DR , RHEINHEIMER DR , ROSE DR , CULLMANN DR , GEWEHR DR , GRAMMENOS DR , TORMO I BLASCO DR , MUELLER DR , SAUTER DR , AMMERMANN DR , STRATHMANN DR , LORENZ DR , STIERL DR
IPC: C07C251/80 , A01N33/26 , A01N37/50 , C07C249/16 , C07C251/86
Abstract: Hydrazonomethyl-salicylic acid (I) derivatives are new. The hydrazonomethyl-salicylic acid derivatives are compounds of formula (I). X = halo, NO2, CN, 1-4C alkyl, or 1-4C alkoxy; m = 0-3; A = OH, 1-4C alkoxy, NH2, NHCH3, or N(CH3)2; R = phenyl, naphthyl, 3-10C cycloalkyl, 5- or 6-membered heteroaryl or heterocyclyl containing 1-3 N and/or 1 O or S or 1 or 2 O and/or S (each optionally substituted with 1-3 Ra); Ra = CN, NO2, NH2, H2NCO-, H2NCS-, halo, OH, 1-6C alkyl or 1-6C alkoxy (each optionally substituted with halo), 1-6C alkylcarbonyl, 1-6C alkylsulfonyl, 1-6C alkylsulfoxyl, 3-6C cycloalkyl, 1-6C alkoxycarbonyl, 1-6C alkylthio, NH(1-6C alkyl), N(1-6C alkyl)2, 1-6C alkyl-NH-CO-, (1-6C alkyl)2N-CO-, 1-6C alkyl-NH-CS-, (1-6C alkyl)2N-CS-, 2-6C alkenyl, 2-6C alkenyloxy, phenyl, phenoxy, benzyl, benzyloxy, 5- or 6-membered heterocyclyl, heteroaryl or heteroaryloxy, C(=NOR alpha )-OR beta , or OC(R alpha )2-C(R beta )=NOR beta , and cyclic groups are optionally substituted with 1-3 Rb; Rb = CN, NO2, NH2, H2NCO-, H2NCS-, halo, OH, 1-6C alkyl or 1-6C alkoxy (each optionally substituted with halo), 1-6C alkylcarbonyl, 1-6C alkylsulfonyl, 1-6C alkylsulfoxyl, 3-6C cycloalkyl, 1-6C alkoxycarbonyl, 1-6C alkylthio, NH(1-6C alkyl), N(1-6C alkyl)2, 1-6C alkyl-NH-CO-, (1-6C alkyl)2N-CO-, 1-6C alkyl-NH-CS-, (1-6C alkyl)2N-CS-, 2-6C alkenyl, 2-6C alkenyloxy, 3-6C cycloalkenyl, phenyl, phenoxy, phenylthio, benzyl, benzyloxy, 5- or 6-membered heterocyclyl, heteroaryl or heteroaryloxy, or C(=NOR alpha )-OR beta ; R alpha and R beta = H or 1-6C alkyl; R = H, CN, or 1-6C alkyl, 2-6C alkenyl, 2-6C alkynyl, 1-6C haloalkyl, 1-6C alkoxy or 1-6C alkylthio (each optionally substituted with 1 or more halo and/or 1-3 Rc); Rc = halo, CN, NO2, OH; 1-6C alkyl or 1-6C alkoxy (each optionally substituted with halo); 1-6C alkylcarbonyl, 3-6C cycloalkyl, 1-6C alkoxycarbonyl, 1-6C alkylthio, NH(1-6C alkyl), N(1-6C alkyl)2, 2-6C alkenyl, 3-6C alkenyloxy, 3-6C alkynyloxy, or 1-4C alkylenedioxy (optionally halogenated). An Independent claim is also included for the preparation of compounds (I).
-
公开(公告)号:DE50200390D1
公开(公告)日:2004-06-03
申请号:DE50200390
申请日:2002-10-18
Applicant: BASF AG
Inventor: ROSE DR , TORMO I BLASCO DR , GEWEHR DR , GRAMMENOS DR , MUELLER DR , RHEINHEIMER DR , SCHAEFER DR , SCHIEWECK DR , GROTE DR , GYPSER DR , AMMERMANN DR , LORENZ DR , STIERL DR , STRATHMANN DR , CARTER DR , CURTZE DR
IPC: A01N31/14 , A01N31/16 , A01N33/10 , A01N37/38 , A01N37/40 , C07B61/00 , C07C39/42 , C07C41/26 , C07C43/23 , C07C69/017 , C07C69/14 , C07C323/19 , C07C323/25
Abstract: Polysubstituted 4-methoxy-benzhydryl alcohol or thiol derivatives (I) are new. Polysubstituted 4-methoxy-benzhydryl alcohol or thiol derivatives of formula (I) are new: X = O or S; R , R = halo, CN, NO2, OH, SH, NH2, alkyl, alkenyl, alkynyl, alkoxy, alkenyloxy, alkynyloxy, alkylcarbonyloxy, OCHO, alkylthio, alkenylthio, alkynylthio, mono- or dialkylamino, alkylcarbonyl or CHO (where all hydrocarbyl moieties are optionally mono- or polyhalogenated); R = halo, CN, NO2, OH, SH, NH2, alkyl, alkoxy, haloalkyl or haloalkoxy; R = alkyl, alkenyl or alkynyl (all optionally mono- or polyhalogenated); R , R = OH, alkyl, alkenyl, haloalkyl, haloalkenyl, alkoxy, alkenyloxy, haloalkoxy, haloalkenyloxy, cycloalkyl, cycloalkyl-(1-3C) alkyl, cycloalkoxy or cycloalkyl-(1-3C) alkoxy; and n = 0-2. Unless specified otherwise alkyl moieties have 1-6C, alkenyl or alkynyl moieties 2-6C and cycloalkyl moieties 3-8C. An Independent claim is also included for the preparation of (I).
-
公开(公告)号:DE59811122D1
公开(公告)日:2004-05-06
申请号:DE59811122
申请日:1998-12-15
Applicant: BASF AG
Inventor: SCHELBERGER KLAUS , SCHERER MARIA , EICKEN DR , HAMPEL DR , AMMERMANN DR , LORENZ DR , STRATHMANN DR
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.
-
公开(公告)号:DE50100225D1
公开(公告)日:2003-06-12
申请号:DE50100225
申请日:2001-11-30
Applicant: BASF AG
Inventor: EICKEN DR , AMMERMANN DR , STIERL DR , LORENZ DR , STRATHMANN DR , SCHERER MARIA , SCHELBERGER KLAUS , HAMPEL DR
Abstract: New fungicidal mixtures contain synergistic amounts of an N-(1,1'-biphenyl-2-yl)-nicotinamide derivative (I) and O-(but-2-enoyl)-2,4-dinitro-6-alkyl- (or 2,6-dinitro-4-alkyl)-phenol derivatives (II) (i.e. dinocap). New fungicidal mixtures contain synergistic amounts of a nicotinamide derivative of formula (I) and the dinitrophenol derivatives (II) of formulae (IIa) and (IIb). R1, R2 = halo, NO2, CN, 1-8C alkyl, 2-8C alkenyl, 2-8C alkynyl, 1-8C haloalkyl, 2-8C haloalkenyl, 2-8C haloalkynyl, 1-8C alkoxy, 1-8C haloalkoxy, 1-8C haloalkylthio, 1-8C alkylsulfinyl or 1-8C alkylsulfonyl; x = 1-4; y = 1-5; and n = 0-2. An Independent claim is also included for a method for controlling fungi, involving applying (I) and (II), simultaneously (in combination or separately) or successively, to the fungi, their habitat or plants, seeds, soil, areas, material or regions to be protected.
-
-
-
-
-
-
-