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公开(公告)号:AU7624474A
公开(公告)日:1976-06-10
申请号:AU7624474
申请日:1974-12-10
Applicant: CIBA GEIGY AG
Inventor: STURM ELMAR , BERNASCONI RAYMOND , ZIMMERMANN MARKUS
IPC: C07D495/04 , C07D495/08 , C07D99/06 , A61K27/00
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公开(公告)号:AU4609072A
公开(公告)日:1974-03-07
申请号:AU4609072
申请日:1972-08-29
Applicant: CIBA GEIGY
Inventor: BADER JORG , HAMBOCK HEINZ , STURM ELMAR , WEISS ANTON GEORG
IPC: A01N43/836 , A01N43/832 , C07D285/08 , C07D91/60 , A01N9/14
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公开(公告)号:FI83776C
公开(公告)日:1991-08-26
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
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公开(公告)号:FI83776B
公开(公告)日:1991-05-15
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
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.
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公开(公告)号:DK159774C
公开(公告)日:1991-05-06
申请号:DK528382
申请日:1982-11-26
Applicant: CIBA GEIGY AG
Inventor: NYFELER ROBERT , MEYER ALFRED , STURM ELMAR
IPC: A01N43/50 , A01N43/64 , A01N43/653 , C07D233/60 , C07D249/08 , C07D521/00
Abstract: Novel substituted azolyl-ethyl ethers of the general formula I wherein R1 is phenyl, phenyl mono- to trisubstituted by halogen, C1-C3- haloalkyl, nitro, C1-C3-alkoxy, C1-C8-alkyl and/or cyano, or phenyl substituted by phenyl or phenoxy, naphthyl, or naphthyl mono- or -disubstituted by halogen, nitro and/or C1-C3-alkyl, benzyl, or benzyl mono- or disubstituted by halogen, nitro and/or C1-C3-alkyl; R2 is phenyl, phenyl mono- to trisubstituted by halogen, C1-C3-haloalkyl, nitro, C1-C3-alkoxy, C1-C8-alkyl and/or cyano, or phenyl substituted by phenyl or phenoxy, or it is C1-C10-alkyl, C3-C8-cycloalkyl or C3-C8- cycloalkyl-(C1-C4-alkyl); R3 is C1-C12-alkyl, C2-C4-alkenyl, C3-C4-alkynyl, benzyl, or benzyl mono- or disubstituted by halogen, nitro and/or C1-C3-alkyl; and R4 is an azolyl group; including acid addition salts thereof, quaternary azolium salts and metal complexes, are used in agrochemical compositions for the preventive and curative combating of harmful microorganisms.
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公开(公告)号:AU602913B2
公开(公告)日:1990-11-01
申请号:AU7741287
申请日:1987-08-25
Applicant: CIBA GEIGY AG
Inventor: KRISTIANSEN ODD , LANG ROBERT WERNER , STURM ELMAR
IPC: A01N47/34 , C07D239/34
Abstract: The invention relates to novel N-benzoyl-N,-4-(5-phenylpyrimid-2-yloxy)phenylureas of formula +TR wherein X1 is hydrogen, halogen, C1-C3alkoxy or C1-C3alkylthio, X2 is halogen, methyl, C1-C3alkoxy or C1-C3alkylthio, Y1, Y2, Y3 and Y4 are each independently hydrogen, halogen, methyl, trifluoromethyl or methoxy, Z is methyl, halomethyl containing 1 to 3 halogen atoms or pentafluoroethyl; and R1, R2 and R3 are each independently hydrogen, halogen, C1-C3alkyl, trifluoromethyl or C1-C3alkoxy, to the preparation thereof and to intermediates for the synthesis of these compounds, as well as to compositions containing them for use in pest control, especially for controlling representatives of the order Acarina that attack plants and animals and for controlling insects. The novel compounds exhibit especially pronounced activity against plant-destructive mites.
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公开(公告)号:AU584000B2
公开(公告)日:1989-05-11
申请号:AU1069288
申请日:1988-01-21
Applicant: CIBA GEIGY
Inventor: STURM ELMAR , KUNZ WALTER
IPC: A01N43/50 , A01N43/653 , A61K31/4164 , A61K31/4196 , A61P31/10 , C07C45/61 , C07C45/68 , C07C45/71 , C07D233/60 , C07D249/08 , C07D303/22 , C07D303/32 , C07D405/06 , C07D407/04 , C07D407/06 , C07D521/00 , C07D301/19 , A61K31/335 , A01N43/20
Abstract: Novel 1-carbonyl-1-phenoxyphenyl-2-azolylethanol derivatives of the general formula I wherein R1 and R2 are each independently hydrogen, halogen C1-C4 alkyl or CF3, and Rn denotes one to three alkyl, alkoxy, haloalkoxy, haloalkyl, halogen and/or cyano groups, R4 is hydrogen, C1-C10 alkyl, C3-C6 cycloalkyl or unsubstituted or substituted phenyl, X is -CH= or -N=, R5 is hydrogen, C1-C12 alkyl, C2-C4 alkenyl, C2-C4 alkynyl, or unsubstituted or substituted benzyl; and A is the radical wherein R6 and R7 are each independently C1-C12 alkyl, unsubstituted or substituted phenyl, or both together form a C2-C4 alkylene bridge which is unsubstituted or substituted by one or more identical or different members selected from the group consisting of C1-C4 alkyl, C2-C4 alkenyloxymethyl or C1-C3 alkoxymethyl; and to the acid addition salts, quaternary azolium salts and metal complexes thereof, are useful for controlling phytopathogenic microorganisms and/or regulating plant growth.
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公开(公告)号:NO161256B
公开(公告)日:1989-04-17
申请号:NO834592
申请日:1983-12-13
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
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.
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59.
公开(公告)号:HU196693B
公开(公告)日:1989-01-30
申请号:HU192684
申请日:1984-05-18
Applicant: CIBA GEIGY AG
Inventor: NYFEREL ROBERT , ZONDLER HELMUT , STURM ELMAR
IPC: A01N31/04 , C07D249/08 , A01N31/14 , A01N43/64 , A01N43/653 , B01J27/10 , B01J31/10 , B01J31/22 , C07B61/00 , C07C20060101 , C07C33/20 , C07C41/00 , C07C41/03 , C07C43/13 , C07C43/178 , C07C43/23 , C07C43/295 , C07C43/315 , C07C67/00 , C07C201/00 , C07C201/12 , C07C205/34 , C07C253/00 , C07C253/30 , C07C255/54 , C07D253/00 , C07D521/00
Abstract: Essentially, a process is described for the preparation of the 1-triazolylethyl ether derivatives, defined in claim 1, of the general formula I (I) which consists in (a) reacting an oxirane of the formula II (II) at temperatures of -20 DEG to +100 DEG C., in the presence of an acid catalyst or an acid condensation agent, with an alcohol of the formula III R3-OH (III) to give a glycol monoether of the formula IV (IV) and (b) subsequently reacting the glycol monoether of the formula IV or one of its esters, in the presence of an acid-binding agent or condensation agent, at temperatures of 0 DEG to 150 DEG C., with a triazole of the formula V (V) the substituents R1, R2 ; amd R3 in the formula II to IV being as defined under formula I and M in formula V being hydrogen or a metal atom. The novel compounds within the scope of formula I and their use are also described.
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公开(公告)号:AU1550488A
公开(公告)日:1988-07-21
申请号:AU1550488
申请日:1988-05-02
Applicant: CIBA GEIGY AG
Inventor: NYFELER ROBERT , ZONDLER HELMUT , STURM ELMAR
IPC: C07D249/08 , A01N31/04 , A01N31/14 , A01N43/64 , A01N43/653 , B01J27/10 , B01J31/10 , B01J31/22 , C07B61/00 , C07C20060101 , C07C33/20 , C07C41/00 , C07C41/03 , C07C43/13 , C07C43/178 , C07C43/23 , C07C43/295 , C07C43/315 , C07C67/00 , C07C201/00 , C07C201/12 , C07C205/34 , C07C253/00 , C07C253/30 , C07C255/54 , C07D253/00 , C07D521/00
Abstract: Essentially, a process is described for the preparation of the 1-triazolylethyl ether derivatives, defined in claim 1, of the general formula I (I) which consists in (a) reacting an oxirane of the formula II (II) at temperatures of -20 DEG to +100 DEG C., in the presence of an acid catalyst or an acid condensation agent, with an alcohol of the formula III R3-OH (III) to give a glycol monoether of the formula IV (IV) and (b) subsequently reacting the glycol monoether of the formula IV or one of its esters, in the presence of an acid-binding agent or condensation agent, at temperatures of 0 DEG to 150 DEG C., with a triazole of the formula V (V) the substituents R1, R2 ; amd R3 in the formula II to IV being as defined under formula I and M in formula V being hydrogen or a metal atom. The novel compounds within the scope of formula I and their use are also described.
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