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公开(公告)号:CZ300571B6
公开(公告)日:2009-06-17
申请号:CZ20033153
申请日:2002-05-17
Applicant: BASF AG
Inventor: RHEINHEIMER JOACHIM , GYPSER ANDREAS , ROSE INGO , GROTE THOMAS , SCHOFER PETER , SCHIEWECK FRANK , AMMERMANN EBERHARD , SPEAKMAN JOHN-BRYAN , STRATHMANN SIEGFRIED , LORENZ GISELA
IPC: C07D265/24 , A01N43/86 , A01N43/90 , A01P3/00 , C07D498/00 , C07D498/04 , C07D513/04
Abstract: Popisují se oxazin(thi)onové slouceniny vzorce I', kde promenné Z, R.sup.1.n., R.sup.2.n., R.sup.3.n. a n mají specifický význam a zemedelsky prijatelné soli oxazin(thi)onových sloucenin vzorce I'. Dále se popisuje použití sloucenin vzorce I' a jejich solí pro kontrolu fytopatogenních hub, kompozice, které obsahují slouceniny vzorce I' a/nebo jejich soli ve fungicidne úcinném množství, a zpusob kontroly fytopatogenních hub, který zahrnuje ošetrení hub nebo materiálu, rostlin, semen nebo pudy ohrožené napadením houbami fungicidne úcinným množstvím nejméne jedné slouceniny vzorce I' a/nebo soli slouceniny I'.
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公开(公告)号:CA2356114C
公开(公告)日:2009-05-05
申请号:CA2356114
申请日:1999-12-11
Applicant: BASF AG
Inventor: SCHELBERGER KLAUS , SAUR REINHOLD , EICKEN KARL , SCHERER MARIA , GROTE THOMAS , LORENZ GISELA , AMMERMANN EBERHARD , HADEN EGON , STRATHMANN SIEGFRIED
IPC: A01N43/84 , A01N37/26 , A01N37/52 , A01N43/10 , A01N43/30 , A01N43/40 , A01N43/56 , A01N47/02 , A01P3/00
Abstract: The invention relates to fungicide mixtures containing the following as their active components: a) a morpholine or piperidine derivative (I) chosen from the following group of compounds (Ia), (Ib), (Ic) and (Id) and compounds of formula (II), the substituents X1 to X5 and R1 to R4 having the following meanings: X1 C1-C4 represents alkyl halide, C1-C4 represents halogenalkoxy or halogen; X1 to X5 represent, independently of each other, hydrogen, halogen, C1-C4-alkyl, C1-C4-alkyl halide, C1-C4-alkoxy or C1-C4-halogenalkoxy; R1 represents C1-C4-alkyl, C2-C6-alkenyl, C2-C6-alkinyl, C1-C4 alkyl-C3-C7-cycloalkyl, C1-C4-alkyl-C3-C7-cycloalkenyl, and these radicals can carry substituents chosen from the following: halogen, cyano and C1-C4-alkoxy; R2 represents a phenyl radical or a 5- or 6-membered saturated or unsaturated heterocyclyl radical with at least one hetero atom chosen from the following group: N, O and S; the cyclical radicals having one to three substituents chosen from the following group: halogen, C1-C4-alkyl, C1-C4 alkoxy, C1-C4-alkyl halide, C1-C4-halogenalkoxy, C1-C4-alkoxy-C2-C4alkenyl, C1-C4-alkoxy-C2-C4-alkinyl; R3 and R4 represent, independently of each other, C1-C4-alkyl, C1-C4-alkoxy, C1-C4-alkylthio, N-C1-C4 alkylamino, C1-C4-alkyl halide or C1-C4-halogenalkoxy in a synergistically effective quantity.
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公开(公告)号:DE50309022D1
公开(公告)日:2008-03-06
申请号:DE50309022
申请日:2003-03-19
Applicant: BASF AG
Inventor: TORMO I BLASCO JORDI , BLETTNER CARSTEN , MUELLER BERND , GEWEHR MARKUS , GRAMMENOS WASSILIOS , GROTE THOMAS , GYPSER ANDREAS , RHEINHEIMER JOACHIM , SCHAEFER PETER , SCHIEWECK FRANK , SCHWOEGLER ANJA , AMMERMANN EBERHARD , STRATHMANN SIEGFRIED , LORENZ GISELA , STIERL REINHARD , SCHOEFL ULRICH
IPC: C07D487/04 , A01N43/90 , C07C255/57 , C07C323/62
Abstract: The invention relates to triazolopyrimidines of formula (I), in which the substituents are defined as follows: L 1 represents cyano, S(-O) n A 1 or C(-O)A 2 , wherein A 1 stands for hydrogen, hydroxy, alkyl, alkylamino or dialkylamino; A 2 stands for C 1 -C 8 alkoxy, C 1 -C 6 haloalkoxy or one of the groups named in A 1 ; and n stands for 0, 1 or 2; L 2 , L 3 represent hydrogen or halogen; L 4 , L 5 represent hydrogen, halogen or alkyl; X represents halogen, cyano, alkyl, haloalkyl, alkoxy or haloalkoxy; R 1 represents alkyl, haloalkyl, cycloalkyl, halocycloalkyl, alkenyl, alkadienyl, haloalkenyl, cycloalkenyl, alkynyl, haloalkynyl or cycloalkynyl, phenyl, naphthyl, or a five to ten-membered saturated, partially unsaturated or aromatic heterocyclus containing between one and four heteroatoms from the group containing O, N or S; R 2 represents hydrogen or R 1 ; R 1 and R 2 can form, together with the nitrogen atom to which they are bonded, a five or six-membered ring, which can be interrupted and/or substituted by an atom from the group O, N and S; whereby R 1 and/or R 2 can be substituted in accordance with the description. The invention also relates to methods and intermediate products for producing said compounds, to agents containing the latter and to the use of said compounds for combating harmful fungi.
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公开(公告)号:CA2351819C
公开(公告)日:2008-01-08
申请号:CA2351819
申请日:1999-11-06
Applicant: BASF AG
Inventor: MULLER BERND , BIRNER ERICH , LEYENDECKER JOACHIM , SAUR REINHOLD , STRATHMANN SIEGFRIED , LORENZ GISELA , AMMERMANN EBERHARD , SCHERER MARIA , SCHELBERGER KLAUS , SAUTER HUBERT
Abstract: A fungicidal mixture containing a.1) a carbamate of formula (I.a), wherein X means CH and N, N is 0, 1 or 2 and R is halogen, C1-C4-alkyl and C1-C4 halogen alkane, whereby the radicals R can be differen t when n@ 2, and b) a fungicidal active substance (II) containing copper in a synergistically effective amount.
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公开(公告)号:ES2287453T3
公开(公告)日:2007-12-16
申请号:ES03712051
申请日:2003-03-19
Applicant: BASF AG
Inventor: AMMERMANN EBERHARD , STIERL REINHARD , LORENZ GISELA , SCHOFL ULRICH , STRATHMANN SIEGFRIED , SCHELBERGER KLAUS
IPC: A01N43/42 , A01N33/18 , A01N43/653 , A01N35/04 , A01N35/06 , A01N37/34 , A01N37/46 , A01N37/52 , A01N43/24 , A01N43/28 , A01N43/32 , A01N43/36 , A01N43/40 , A01N43/50 , A01N43/78 , A01N47/14 , A01N47/18 , A01N47/34 , B60Q1/50
Abstract: Mezcla fungicida que contiene (1) 2-[2-(1-clorciclopropil)-3-(2-clorfenil)-2-hidroxipropil]-2, 4-dihidro-[1, 2, 4]-triazol-3-tiona (Protioconazol) de la fórmula I o sus sales o aductos
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公开(公告)号:CA2229308C
公开(公告)日:2007-11-13
申请号:CA2229308
申请日:1996-09-04
Applicant: BASF AG
Inventor: LORENZ GISELA , REICHARDT MICHAEL , SCHELBERGER KLAUS , AMMERMANN EBERHARD , SAUR REINHOLD , STRATHMANN SIEGFRIED
IPC: A01N37/34 , A01N43/653
Abstract: A fungicide mixture contains synergistically effective amounts of (a) (2RS,3SR)-1-[3-(2-chlorophenyl)-2, 3-epoxy--2-(4-fluorophenyl)propyl]-1H-1,2,4-triazol having formula (I), one of its salts or addition products, and of (b) tetrachlorisophthalonitril having formula (II). Also disclosed is its use for controlling harmful fungi.
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公开(公告)号:SI1489906T1
公开(公告)日:2007-10-31
申请号:SI200330890
申请日:2003-03-19
Applicant: BASF AG
Inventor: AMMERMANN EBERHARD , STIERL REINHARD , LORENZ GISELA , SCHOFL ULRICH , STRATHMANN SIEGFRIED , SCHELBERGER KLAUS , CHRISTEN THOMAS
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公开(公告)号:DK1489906T3
公开(公告)日:2007-10-01
申请号:DK03712051
申请日:2003-03-19
Applicant: BASF AG
Inventor: AMMERMANN EBERHARD , STIERL REINHARD , LORENZ GISELA , SCHOEFL ULRICH , STRATHMANN SIEGFRIED , SCHELBERGER KLAUS , CHRISTEN THOMAS
IPC: A01N43/42 , A01N33/18 , A01N43/653 , A01N35/04 , A01N35/06 , A01N37/34 , A01N37/46 , A01N37/52 , A01N43/24 , A01N43/28 , A01N43/32 , A01N43/36 , A01N43/40 , A01N43/50 , A01N43/78 , A01N47/14 , A01N47/18 , A01N47/34 , B60Q1/50
Abstract: A new fungicidal mixture contains synergistic amounts of (1) prothioconazole (I) and (2) at least one of 20 other specific fungicides, e.g. boscalid, carboxine, metrafenone, quinoxyfen, fenoxanil, carbendazim, metalaxyl, prochloraz or anthraquinone. A fungicidal mixture contains synergistic amounts of the following active components: (1) prothioconazole (I) or its salt or adduct; and (2) one or more of boscalid, carboxine, metrafenone, N-(alpha -cyclopropoxyimino)-(2,3-difluoro-6-trifluoromethyl-benzyl)-phenylacetamide, N-(alpha -cyclopropoxyimino)-2,3-difluoro-6-difluoromethyl-benzyl)-phenylacetamide, quinoxyfen, dithianon, thiram, mepiquat chloride, cyazofamid, fenoxanil, 6-fluoro-2-(1-(2-(isopropoxycarbonylamino)-isovaleramido)-ethyl)-benzothiazole, thiophanate methyl, carbendazim, metalaxyl, fludioxonil, thiabendazole, quintozen, prochloraz and/or anthraquinone. Independent claims are included for: (a) a harmful fungus control method involving application of the mixture of (1) and (2) to the fungi, their habitat or plants, seeds, soil, surfaces, materials or regions to be protected ((1) and (2) being applied simultaneously, separately or successvely); and (b) a fungicidal composition comprising the (1)/(2) mixture together with a solid or liquid carrier. ACTIVITY : Fungicide. In tests for protective action against Blumeria graminis f. sp. triciti (mildew) in wheat, prothioconazole (I) at 1 ppm alone or boscalid (II) at 4 ppm alone gave no (0%) control, whereas a combination of 1 ppm (I) and 4 ppm (II) gave 92% control. MECHANISM OF ACTION : None given in the source material.
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公开(公告)号:NZ535307A
公开(公告)日:2007-09-28
申请号:NZ53530703
申请日:2003-03-19
Applicant: BASF AG
Inventor: AMMERMANN EBERHARD , STIERL REINHARD , LORENZ GISELA , SCHOFL ULRICH , STRATHMANN SIEGFRIED , SCHELBERGER KLAUS , CHRISTEN THOMAS
IPC: A01N33/18 , A01N35/04 , A01N35/06 , A01N37/34 , A01N37/46 , A01N37/52 , A01N43/24 , A01N43/28 , A01N43/32 , A01N43/36 , A01N43/40 , A01N43/50 , A01N43/653 , A01N43/78 , A01N47/14 , A01N47/18 , A01N47/34 , A01N43/42 , B60Q1/50 , A01N47/26 , A01N37/38 , A01N37/22
Abstract: Disclosed is a fungicidal mixture, comprising 2-[2-(1-chlorocyclopropyl)-3-(2-chlorophenyl)-2-hydroxypropyl]-2,4-dihydro-[1,2,4]-triazole-3-thione (prothioconazole) of the formula (I) and at least one further fungicidal compound consisting of a boscalid of formula (II) wherein the weight ratio of prothioconazole of the formula (I) to the respective fungicide of formula (II) is from 20:1 to 1:20.
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公开(公告)号:CA2313323C
公开(公告)日:2007-09-04
申请号:CA2313323
申请日:1998-12-15
Applicant: BASF AG
Inventor: STRATHMANN SIEGFRIED , LORENZ GISELA , EICKEN KARL , HAMPEL MANFRED , AMMERMANN EBERHARD , SCHERER MARIA , SCHELBERGER KLAUS
Abstract: The invention relates to fungicide mixtures containing, as active components, a) an amide compound of formula (I) A-CO-NR1R2, wherein A represents an aryl group or an aromatic or non-aromatic, 5- or 6-structured heterocyclic compound having 1 to 3 heteroatoms selected from O, N, S; whereby the aryl group or the heterocycli c compound can optionally comprise 1, 2 or 3 substituents selected independently of one another from alkyl, halogen, CHF2, CF3, alkoxy l, haloalkoxyl, alkylthio, alkyl sulfinyl and alkyl sulfonyl; R1 represents a hydrogen atom; R2 represents a phenyl group or cycloalkyl group optionally containing 1, 2 or 3 substituents selected independently of one another from alkyl, alkenyl, alkynyl, alkoxyl, alkenyloxyl, alkynyloxyl, cycloalkyl, cycloalkenyl, cycolalkyloxyl, cycloalkenyloxyl, phenyl and halogen, whereby the aliphatic and cycloaliphat ic radicals can be partially or completely halogenated and/or the cycloaliphatic radicals can be substituted by 1 to 3 alkyl groups, where by the phenyl group can contain 1 to 5 halogen atoms and/or 1 to 3 substituents selected independently of one another from alkyl, haloalky l, alkoxyl, haloxyl, alkylthio and haloalkylthio, and whereby the amidic phenyl group is optionally condensed with a saturated 5-structured ri ng which is optionally substituted by one or more alkyl groups and/or can comprise a heteroatom selected from O and S, and b) (~)-(2- chlorphenyl)(4-chlorphenyl)(pyrimidine-5-yl)methanol (a). The active components are provided in a synergistically effective quantity.
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