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    Process for preparing nitrobiphenylene
    52.
    发明专利
    Process for preparing nitrobiphenylene 未知

    公开(公告)号：AU1925797A

    公开(公告)日：1997-10-01

    申请号：AU1925797

    申请日：1997-03-06

    Applicant: BASF AG

    Inventor： EICKEN KARL ,  GEBHARDT JOACHIM ,  RANG HARALD ,  RACK MICHAEL ,  SCHAFER PETER

    IPC: B01J31/24 ,  C07B37/04 ,  C07B61/00 ,  C07C201/12 ,  C07C205/06 ,  C07C205/11 ,  C07C205/12 ,  C07C205/35 ,  C07C253/30

    Abstract: The invention concerns a process for preparing nitrobiphenylene of formula (I) wherein m stands for 1 or 2, R means halogen, R' or OR', R' being a C-organic group which can carry groups which are inert in the reaction conditions, n stands for 0, 1, 2 or 3 and, if n is 2 or 3, the R groups can also be different. According to the invention, a chloronitrobenzene of formula (II) is reacted in the presence of a palladium catalyst and a base in a solvent with a phenyl boric acid (IIIa), one of its alkyl esters of formula (IIIb), R meaning C1-C6 alkyl, or one of its anhydrides. The compounds (I) are suitable as initial products for biphenylamines which are in turn intermediate products for fungicidal plant-growth substances.

    N-PHENYLTETRAHYDROINDAZOLES, THEIR PREPARATION, AND THEIR USE AS CROP PROTECTION AGENTS
    56.
    发明专利
    N-PHENYLTETRAHYDROINDAZOLES, THEIR PREPARATION, AND THEIR USE AS CROP PROTECTION AGENTS 未知

    公开(公告)号：CA2197902A1

    公开(公告)日：1996-03-07

    申请号：CA2197902

    申请日：1995-08-18

    Applicant: BASF AG

    Inventor： HEISTRACHER ELISABETH ,  RUEB LOTHAR ,  VON DEM BUSSCHE-HUENNEFELD CHR ,  HAMPRECHT GERHARD ,  KLINTZ RALF ,  SCHAFER PETER ,  WESTPHALEN KARL-OTTO ,  GERBER MATTHIAS ,  WATTER HELMUT

    IPC: C07D231/56 ,  A01N43/56 ,  C07D213/56 ,  C07D401/12 ,  C07D403/12 ,  C07D405/12 ,  C07D409/12 ,  C07D413/12 ,  C07D417/12 ,  A01N43/48 ,  A01N43/64 ,  A01N43/72

    Abstract: N-Phenyltetrahydroindazoles of formula (I), where R1 is H or C1-4-alkyl; R2 is halogen, C1-4-alkyl or C1-4-haloalkyl; R3 is H or halogen; R4 is NO2, halogen, C1-4-alkyl or C1-4-haloalkyl; R5 is -XR6; X is -O-, -S-, -SO- or -SO2-; R6 is Alk-R7; Alk is a substituted or unsubstituted methylene, ethylene, propylene, butylene or pentamethylene chain, where one chain member can carry a spirolinked 2- to 5-membered C chain or where 2 ring members can be bridged via a C1-5-alkylene chain; R7 is CN, SCN, halogen or -YR11, where Y is -O-, -S-, -SO- or -SO2-; R10 is H, OH, C1-C4-alkyl, C1-C4-haloalkyl, C3-C5-cycloalkyl, C1-C4-alkoxy, C1-C4-haloalkoxy, C3-C5-cycloalkoxy, C1-C4-alkylthio, C1-C4-haloalkylthio, -NH-R12, -N(C1-C4-alkyl)-R12, -N(C3-C4-alkenyl)-R12, -N(C3-C4-alkynyl)-R12, pyrrolidin-1-yl, piperid-1-yl, morpholin-4-yl, azepan-1-yl, (i) unsubstituted or substituted phenyl, benzyl, phenoxy or benzyloxy; R11 is C1-6-alkyl, C1-6-haloalkyl or C1-6-cycloalkyl; R12 is H, OH, C1-4-alkyl, C3-4-alkenyl, C3-4-alkynyl, C3-6-cycloalkyl, C1-4-alkoxy, C3-4-alkenyloxy, C3-4-alkenyloxy, C3-4-alkynyloxy, or substituted or unsubstituted phenyl or benzyl; and the agriculturally utilizable salts of formula (I), with the provisoes that the simultaneous meaning of R6 as dihalomethyl, R2 and R4 as chlorine and R3 as halogen is excluded; the simultaneous meaning of X as oxygen and R7 as OR11 or C1-C6-alkylthio is excluded; Alk must not carry a spiro-linked threemembered ring if R7 is halogen and R11 is not C1-6-alkyl if R1 is H, R2 is C14-haloalkyl, R3 is F, R4 is halogen and R7 is -OR11. Use: as herbicides; for desiccating/defoliating plants.

    SUBSTITUTED 1-AMINO-3-PHENYLURACILS
    57.
    发明专利
    SUBSTITUTED 1-AMINO-3-PHENYLURACILS 未知

    公开(公告)号：CA2169467A1

    公开(公告)日：1995-03-09

    申请号：CA2169467

    申请日：1994-08-25

    Applicant: BASF AG

    Inventor： SCHAFER PETER ,  KLINTZ RALF ,  HAMPRECHT GERHARD ,  HEISTRACHER ELISABETH ,  WESTPHALEN KARL-OTTO ,  GERBER MATTHIAS ,  WALTER HELMUT

    IPC: A01N43/54 ,  C07D239/54 ,  C07D239/56 ,  C07D405/10 ,  C07D409/10 ,  C07D411/10

    Abstract: Substituted 1-amino-3-phenyluracils (I), where the variables have the following meanings: R1 = H, F, Cl; Y = O, S; W = -CH=N-OH, -CH=N-O-(alkyl), -CH=N-O-(alkylene)-O-(alkyl), -CH=N-O-CH2-COOH, -CH=N-O-CH(alkyl)-COOH, -CN-O-CH2-CO-O-(alkyl), -CH=N-O-CH(alkyl)-CO-O-(alkyl), -CH=N-O-CH2-CO-O-(alkylene)-O-(alkyl), -CH=N-O-CH(alkyl)-CO-O-(alkylene)-O-(alkyl), -CH=CH-CO-O-(alkyl), -CH=CH-CO-O-(alkylene)-O- (alkyl), -CH=C(Cl)-CO-O-(alkyl), -CH=C(Br)-CO-O-(alkyl), CH=C(Cl)-CO-O(alkylene)-O-(alkyl), -CH=C(Br)-CO-O-(alkylene)-O- (alkyl), -CH=C(CH3)-CO-O-(alkyl), -CH=C(CH3)-CO-O-(alkylene)-O-(alkyl), -CH¢XI-(alkyl)!!¢X2-(alkyl)! or a radical (a), (b), X1-X6 = O, S; R2-R11 = H, alkyl, vinyl, alkoxycarbonyl are described, Use: herbicides; desiccation/defoliation of plants.

    Oxazin(thi)one compounds used as fungicides
    60.
    发明专利
    Oxazin(thi)one compounds used as fungicides 未知

    公开(公告)号：AU2002304642B2

    公开(公告)日：2008-02-07

    申请号：AU2002304642

    申请日：2002-05-17

    Applicant: BASF AG

    Inventor： GYPSER ANDREAS ,  SCHAFER PETER ,  LORENZ GISELA ,  AMMERMANN EBERHARD ,  ROSE INGO ,  RHEINHEIMER JOACHIM ,  SCHIEWECK FRANK ,  SPEAKMAN JOHN-BRYAN ,  STRATHMANN SIEGFRIED ,  GROTE THOMAS

    IPC: C07D265/24 ,  A01N43/86 ,  A01N43/90 ,  C07D498/04 ,  C07D513/04

    Abstract: Oxazin(ethi)one compounds of the formula I: in which the variables Z, R 1 , R 2 , R 3 and n are as defined in claim 1 and A is a 5- or 6-membered carbocycle or a 5- or 6-membered heterocycle having 1, 2 or 3 heteroatoms selected from the group consisting of N, O and S, each of which cycles is attached via two carbon atoms to the oxazin(ethi)one ring, and the agriculturally useful salts of the oxazin(ethi)one compounds I are described. Moreover, the invention describes the use of compounds I and their salts for controlling phytopathogenic fungi, compositions which comprise the compounds I and/or their salts in a fungicidally effective amount and a method for controlling phytopathogenic fungi which comprises treating the fungi or the materials, plants, seeds or the soil threatened by fungal attack with a fungicidally effective amount of at least one compound of the formula I as claimed in claim 1 and/or a salt of I.

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