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    101.
    发明专利
    未知

    公开(公告)号：BR8306862A

    公开(公告)日：1984-07-24

    申请号：BR8306862

    申请日：1983-12-13

    Applicant: CIBA GEIGY AG

    Inventor： STURM ELMAR ,  MUELLER URS ,  TOBLER HANS

    IPC: A01N43/50 ,  A01N43/64 ,  A01N43/653 ,  C07D233/60 ,  C07D249/08 ,  C07D303/22 ,  C07D303/34 ,  C07D521/00 ,  C07D303/18

    Abstract: The compounds described are those of the general formula I (I) in which R1 is an azolyl group; R2 is C1-C12-alkyl; R3 is hydrogen, C1-C12-alkyl, C2-C4-alkenyl or C2-C4-alkinyl, or benzyl which is unsubstituted or substituted by C1-C6-alkyl, C1-C6-alkoxy, C1-C6-haloalkyl, halogen and/or cyano; R4 is hydrogen, fluorine or C1-C6-alkyl; R5 is an unsubstituted or substituted radical chosen from the series comprising phenyl, naphthyl, biphenyl, benzylphenyl and benzyloxyphenyl, the substituents being chosen from the series comprising halogen, cyano, C1-C6-alkyl, C1-C6-alkoxy C1-C6-haloalkyl, C1-C6-alkylthio, C1-C6-haloalkoxy, C1-C3-haloalkylthio, nitro and/or thiocyano; and X is oxygen or sulfur; including the acid addition salts, quaternary azolium salts and metal complexes. Methods for the preparation of these products are also disclosed, as well as agrochemical compositions containing one of these compounds as the active substance. A method of controlling phytopathogenic microorganisms and/or of regulating plant growth with the aid of these substances is furthermore described.

    1-FLURO-1-ARYLOXY-2-AZOLYLMETHYL-2-ALKANOLS
    102.
    发明专利
    1-FLURO-1-ARYLOXY-2-AZOLYLMETHYL-2-ALKANOLS 未知

    公开(公告)号：AU2231083A

    公开(公告)日：1984-06-21

    申请号：AU2231083

    申请日：1983-12-12

    Applicant: CIBA GEIGY AG

    Inventor： STURM ELMAR ,  MULLER URS ,  TOBLER HANS

    IPC: A01N43/50 ,  A01N43/64 ,  A01N43/653 ,  C07D233/60 ,  C07D249/08 ,  C07D303/22 ,  C07D303/34 ,  C07D521/00

    Abstract: The compounds described are those of the general formula I (I) in which R1 is an azolyl group; R2 is C1-C12-alkyl; R3 is hydrogen, C1-C12-alkyl, C2-C4-alkenyl or C2-C4-alkinyl, or benzyl which is unsubstituted or substituted by C1-C6-alkyl, C1-C6-alkoxy, C1-C6-haloalkyl, halogen and/or cyano; R4 is hydrogen, fluorine or C1-C6-alkyl; R5 is an unsubstituted or substituted radical chosen from the series comprising phenyl, naphthyl, biphenyl, benzylphenyl and benzyloxyphenyl, the substituents being chosen from the series comprising halogen, cyano, C1-C6-alkyl, C1-C6-alkoxy C1-C6-haloalkyl, C1-C6-alkylthio, C1-C6-haloalkoxy, C1-C3-haloalkylthio, nitro and/or thiocyano; and X is oxygen or sulfur; including the acid addition salts, quaternary azolium salts and metal complexes. Methods for the preparation of these products are also disclosed, as well as agrochemical compositions containing one of these compounds as the active substance. A method of controlling phytopathogenic microorganisms and/or of regulating plant growth with the aid of these substances is furthermore described.

    104.
    发明专利
    未知

    公开(公告)号：FI834522A

    公开(公告)日：1984-06-15

    申请号：FI834522

    申请日：1983-12-09

    Applicant: CIBA GEIGY AG

    Inventor： STURM ELMAR ,  MEYER ALFRED

    IPC: A01N43/50 ,  A01N43/653 ,  A01P3/00 ,  C07C39/00 ,  C07C45/63 ,  C07C45/71 ,  C07D233/60 ,  C07D233/64 ,  C07D249/08 ,  C07D303/08 ,  C07D303/22 ,  C07D303/34 ,  C07D521/00 ,  C07D

    Abstract: 1-Azolyl-2-aryl-3-fluoro-alkan-2- ols of the general formula I in which Az is 1H-1,2,4-triazole, 4H-1,2,4-triazole or 1H-imidazole; Ar is an unsubstituted or substituted aromatic radical from the series comprising phenyl, biphenyl, phenoxyphenyl and naphthyl; R1 is hydrogen, C1-C4-alkyl, C3-C5-alkenyl or benzyl; R2 is hydrogen, fluorine or C1-C6-alkyl and R3 is hydrogen, fluorine, C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-alkoxy, C1-C6-alkylthio, phenyl, phenoxy, phenylthio or C3-C7-cycloalkyl, and each aromatic substituent or aromatic moiety of a substituent is unsubstituted or mono- or poly-substituted by halogen, C1-C4-alkyl, C1-C4-alkoxy, C1-C4-haloalkyl, nitro and/or cyano; including the acid addition salts, quaternary azolium salts and metal complexes, are useful for controlling phytopathogenic microorganisms.

    105.
    发明专利
    未知

    公开(公告)号：DK380682A

    公开(公告)日：1984-02-26

    申请号：DK380682

    申请日：1982-08-25

    Applicant: CIBA GEIGY AG

    Inventor： FANKHAUSER ERNST ,  STURM ELMAR

    IPC: A01N20060101 ,  A01N41/10 ,  A01N53/00 ,  C07C20060101 ,  C07C317/22 ,  A01N ,  C07C

    Abstract: A gametocidal agent which contains a nitroaryl- alkylsulphone derivative of the formula in which R1 is alkyl, R2 and R3 are separately H, alkyl, alkoxy, halogenoalkyl, halogen, cyano, nitro or amino, or, in the ortho position, together denote a group -(CH=CH)2-, which, together with the benzene ring, forms a naphthalene ring, R4 is H, a cation or the group -COR5, where R5 is alkyl, alkoxy, halogenoalkyloxy, alkenyl, halogenoalkenyl, alkynyl, cycloalkyl, phenyl, benzyl, furyl or tetrahydrofuryl, and where each of the cyclic substituents is unsubstituted or monosubstituted or polysubstituted by alkyl, alkoxy, halogenoalkyl, halogen, cyano and/or nitro, is used for stimulating flower formation in plants and for forming hybrid seed.

    PROCESS FOR THE PREPARATION OF 1H-AZOLE DERIVATIVES
    107.
    发明专利
    PROCESS FOR THE PREPARATION OF 1H-AZOLE DERIVATIVES 未知

    公开(公告)号：CA1154773A

    公开(公告)日：1983-10-04

    申请号：CA367087

    申请日：1980-12-18

    Applicant: CIBA GEIGY AG

    Inventor： STURM ELMAR ,  ECKHARDT WOLFGANG ,  GLOOR BERNHARD ,  NYFELER ROBERT

    IPC: C07D405/06 ,  A61K31/41 ,  A61P31/04 ,  C07D521/00 ,  C07D317/08

    Abstract: An improved process for the preparation of 2-tert.-butyl-2-(1-phenoxy-1-(1H-azol-1-yl)!-methyl-ketales of the formula wherein X represents -CH= or -N=; R1, R2 and R3 are each independently selected from the group consisting of hydrogen, halogen, lower alkyl, cyano, methoxy, phenyl and nitro; A represents -CH(R4)-CH(R5)- or -CH2-C(R6)(R7)-CH2-; R4 and R5 are each independently selected from the group consisting of hydrogen, C12-C6-alkyl, C1-C6-alkoxymethyl and phenoxymethyl or said substituents R4 and R5 form together a tetramethylene group; and R6 and R7 are each independently selected from the group consisting of hydrogen and lower alkyl, which process comprises reacting a 2-tert.-butyl-2-¢1-phenoxy-1-halo!-methyl-ketale with a quaternary ammonium or phosphonium salt of an azole. The azoles used are 1H-1,2,4-triazole or 1H-imidazole.

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