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    3.
    发明专利
    未知

    公开(公告)号：DE4029192A1

    公开(公告)日：1992-03-19

    申请号：DE4029192

    申请日：1990-09-14

    Applicant: BASF AG

    Inventor： KIRSTGEN REINHARD DR ,  OTTER RAINER DR ,  KUENAST CHRISTOPH DR ,  KARDORFF UWE DR ,  STEGLICH WOLFGANG PROF DR ,  BERTRAM GUNDA

    IPC: A01N37/10 ,  A01N37/36 ,  A01N37/38 ,  A01N37/44 ,  A01N37/48 ,  A01N49/00 ,  C07C69/734

    Abstract: Use of alpha-arylacrylic acid derivatives of the general formula I in which the substituents and indices have the following meanings: X is ethylene or ethenylene; n is 0 or 1; m is 0, 1, 2, 3 or 4; R is cyano; cyanato; thiocyanato; nitro; hydroxyl; carboxyl; haloalkyl, haloalkoxy; optionally subst. cycloalkyl, cycloalkenyl, cycloalkdienyl, alkenyl, alkynyl or amino; alkylcarbonyl; alkoxycarbonyl; alkylaminocarbonyl; dialkylaminocarbonyl; optionally subst. benzyloxycarbonyl, benzoyl, phenylalkyl, phenylalkoxy or phenoxyalkyl; or R together with one of the radicals R forms an optionally subst. 1,3-butadiene-1,4-diyl group or an optionally subst. chain of carbon members and one oxygen member; R is halogen; optionally subst. alkyl, alkoxy, alkenyloxy, alkynyloxy, alkdienyloxy, benzyloxy or benzylthio for controlling pests, and processes for their use.

    Process for the preparation of bis(aminomethyl)phosphinic acid, and acidic or basic salts thereof
    7.
    发明专利
    Process for the preparation of bis(aminomethyl)phosphinic acid, and acidic or basic salts thereof 未知

    公开(公告)号：DE3824961A1

    公开(公告)日：1990-01-25

    申请号：DE3824961

    申请日：1988-07-22

    Applicant: BASF AG

    Inventor： KOBER REINER DR ,  SEELE RAINER DR ,  STEGLICH WOLFGANG PROF DR ,  SCHRADER THOMAS

    IPC: C07F9/30

    Abstract: Process for the preparation of bis(aminomethyl)phosphinic acid I or acidic or basic salts thereof by reacting an N-hydroxymethylcarboxamide of the general formula II in which R denotes an unsubstituted or substituted alkyl, cycloalkyl, aralkyl or aryl radical, with a trivalent phosphorus-halogen compound, if appropriate in the presence of an alkali bromide, alkaline earth bromide, ammonium bromide, alkali metal iodide, alkaline earth metal iodide or ammonium iodide, to give bis(aminomethyl)phosphinic acid derivatives of the general formula III and these are converted into bis(aminomethyl)phosphinic acid in the form of its acidic or basic salts by hydrolytic elimination of the acyl radicals and, if appropriate, liberating the free acid I.

    10.
    发明专利
    未知

    公开(公告)号：DE4117371A1

    公开(公告)日：1992-12-03

    申请号：DE4117371

    申请日：1991-05-28

    Applicant: BASF AG

    Inventor： SAUTER HUBERT DR ,  LORENZ GISELA DR ,  STEINER GERD DR ,  JANSSEN BERND DR ,  ANKE TIMM PROF DR ,  STEGLICH WOLFGANG PROF DR

    IPC: A61K31/165 ,  A61K31/215 ,  A61K31/415 ,  A61K31/42 ,  A61K31/44 ,  A61K31/505

    Abstract: Antimycotic compositions containing a compound of the formula in which = Y is =CH-OCH3, =CH-CH3, =CH-CH2-CH3, =CH-SCH3 or =N-OCH3 and X is oxygen, or in which X can also be NH when Y is =N-OCH3, Z is halogen, nitro, cyano, optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted aralkyl, optionally substituted aryloxyalkyl, optionally substituted arylthioalkyl, optionally substituted heteroarylalkyl, optionally substituted heretoaryloxyalkyl, 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 aryl, optionally substituted heteroaryl, optionally substituted amino, 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 , and U, V, W are hydrogen or can have one of the meanings stated for Z, or in which two of the groups Z, U, V or W in adjacent positions on the phenyl ring optionally form together an optionally substituted 5- or 6-membered, aromatic or aliphatic ring which is fused onto the phenyl ring and which can optionally contain 1 to 3 hetero atoms (N, S, O), where the groups R to R are optionally identical or different hydrogen, optionally substituted C1-C8-alkyl, optionally substituted C2-C8-alkenyl, optionally substituted C2-C8-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 their use for controlling mycoses.

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