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    • 102. 发明授权
    • Fungicidal compositions
    • 杀真菌剂
    • US5260326A
    • 1993-11-09
    • US943677
    • 1992-09-11
    • Hubert SauterKlaus SchelbergerReinhold SaurGisela LorenzEberhard Ammermann
    • Hubert SauterKlaus SchelbergerReinhold SaurGisela LorenzEberhard Ammermann
    • A01N43/653A01N37/50A01N37/34A01N43/64
    • A01N37/50
    • Fungicidal compositions consisting ofa) methyl .alpha.-methoximino-2-[2-methylphenoxy)-methyl]-phenylacetate ##STR1## and b) an azole active ingredient selected from the following group: (Z)-2-(1,2,4-triazol-1-ylmethyl)-2-(4-fluorophenyl)-3-(2-chlorophenyl)-oxirane of the formula ##STR2## 1-butyl-1-(2,4-dichlorophenyl)-2-(1,2,4-triazol-1-yl)-ethanol (common name hexaconazole), 1-[(2-chlorophenyl)methyl]-1-(1,1-dimethyl)-2- (1,2,4-triazol-1-yl-ethanol, 1-(4-fluorophenyl)- 1-(2-fluorophenyl)-2-(1,2,4-triazol-1-yl)-ethanol (common name flutriafol), (RS)-4-(4-chlorophenyl)-2-phenyl-2-(1H-1,2,4-triazol-1-yl-methyl)-butyronitrile, 1-[(2 RS, 4 RS; 2 RS, 4 SR)-4-bromo-2-(2,4-dichlorophenyl)-tetrahydrofurfuryl]-1H-1,2,4-triazole, 3-(2,4-dichlorophenyl)-2-(1H-1,2,4-triazol-1-yl)-quinazolin-4(3H)-one, (RS)-2,2-dimethyl-3-(2-chlorobenzyl)-4-(1H-1,2,4-triazol-1-yl)-butan-3-ol, bitutanol, triadimefon, triadimenol, cyproconazole, dichlobutrazol, difenoconazole, diniconazole, etaconazole, propiconazole, flusilazole, tebuconazole, imazalil, penconazole, prochloraz, tetraconazole and salts of such azole active ingredients,and methods of combating fungi with such compositions.
    • 由a)甲基α-甲氧基亚氨基-2- [2-甲基苯氧基] - 甲基] - 苯基乙酸酯组成的杀真菌组合物和b)选自以下组的唑类活性成分:(Z)-2-(1,2, 4-(4-氟苯基)-3-(2-氯苯基) - 环氧丙烷,1-丁基-1-(2,4-二氯苯基)-2-(1 ,2,4-三唑-1-基) - 乙醇(通用名六氮唑),1 - [(2-氯苯基)甲基] -1-(1,1-二甲基)-2-(1,2,4-三唑 -1-(2-氟苯基)-1-(2-氟苯基)-2-(1,2,4-三唑-1-基) - 乙醇(俗名氟替芬),(RS) - 4-(4-氯苯基)-2-苯基-2-(1H-1,2,4-三唑-1-基 - 甲基) - 丁腈,1 - [(2RS,4RS; 2RS,4RR )-4-溴-2-(2,4-二氯苯基) - 四氢糠基] -1H-1,2,4-三唑,3-(2,4-二氯苯基)-2-(1H- 三唑-1-基) - 喹唑啉-4(3H) - 酮,(RS)-2,2-二甲基-3-(2-氯苄基)-4-(1H-1,2,4-三唑-1-基 )丁烷-3-醇,bitutanol,triadimefon,triadimenol,cyproconazole,dichlobutrazol,difenoconazole,diniconazole,etaconazole,propiconazo le,氟替唑,戊唑醇,咪达唑仑,康康唑,丙氯灵,噻卡唑和这些唑类活性成分的盐,以及用这种组合物对抗真菌的方法。
    • 106. 发明授权
    • Pyridine compounds which are useful as fungicides
    • 可用作杀真菌剂的吡啶化合物
    • US5112828A
    • 1992-05-12
    • US502401
    • 1990-03-30
    • Bernhard ZippererHubert SauterEberhard AmmermannGisela Lorenz
    • Bernhard ZippererHubert SauterEberhard AmmermannGisela Lorenz
    • A01N43/10A01N43/40C07D213/30C07D213/89C07D405/06C07D409/06
    • C07D213/30A01N43/40C07D213/89C07D405/06
    • Pyridines of the formula ##STR1## where R.sup.1 is hydrogen, C.sub.1 -C.sub.6 -alkyl, C.sub.3 -C.sub.6 -alkenyl, C.sub.3 -C.sub.6 -alkynyl or an acyl radical COR.sup.2 ; R.sup.2 is C.sub.1 -C.sub.6 -alkyl, C.sub.3 -C.sub.6 -alkenyl, C.sub.3 -C.sub.6 -alkynyl, C.sub.1 -C.sub.6 -haloalkyl or substituted or unsubstituted aryl; A is one of the groups ##STR2## where R.sup.3 and R.sup.4 are identical or differ and each is C.sub.1 -C.sub.6 -alkyl, with the proviso that R.sup.3 and R.sup.4 are not simultaneously methyl; R.sup.5 is one of the groups (CH.sub.2).sub.n, CH.sub.2 OCH.sub.2, CH.sub.2 S(O).sub.m CH.sub.2, CH.sub.2 CH.sub.2 O or CH.sub.2 CH.sub.2 S(O).sub.m, n denoting 1, 2, 3, 4 or 5, and m being 0, 1 or 2; Ar is aryl which is unsubstituted or bears from one to five substituents selected from the group consisting of C.sub.1 -C.sub.6 -alkyl, phenyl, halogen, C.sub.1 -C.sub.6 -haloalkyl, C.sub.1 -C.sub.6 -alkoxy, C.sub.1 -C.sub.6 -haloalkoxy, C.sub.1 -C.sub.6 -alkoxyiminocarbyl, phenoxy, halophenoxy and benzyloxy, and the N-oxides and plant-tolerated acid addition salts thereof, and fungicides containing these compounds.
    • 其中R 1是氢,C 1 -C 6烷基,C 3 -C 6烯基,C 3 -C 6炔基或酰基COR 2; R2是C1-C6-烷基,C3-C6-烯基,C3-C6-炔基,C1-C6-卤代烷基或取代或未取代的芳基; A是其中R 3和R 4相同或不同且各自为C 1 -C 6 - 烷基的组之一,条件是R 3和R 4不同时为甲基; R5是(CH2)n,CH2OCH2,CH2S(O)mCH2,CH2CH2O或CH2CH2S(O)m中的一个,n表示1,2,3,4或5,m是0,1或2; Ar是未取代的芳基,或含1至5个选自C 1 -C 6 - 烷基,苯基,卤素,C 1 -C 6 - 卤代烷基,C 1 -C 6 - 烷氧基,C 1 -C 6 - 卤代烷氧基,C 1 -C 6 - 烷氧基亚氨基羰基,苯氧基,卤代苯氧基和苄氧基,及其N-氧化物和植物耐受的酸加成盐,以及含有这些化合物的杀真菌剂。
    • 108. 发明授权
    • Fungicidal mixture
    • 真菌混合物
    • US5064828A
    • 1991-11-12
    • US470229
    • 1990-01-25
    • Matthias ZippliesHubert SauterRandall E. GoldAlan AkersEberhard AmmermannGisela Lorenz
    • Matthias ZippliesHubert SauterRandall E. GoldAlan AkersEberhard AmmermannGisela Lorenz
    • A01N43/40A01N43/84
    • A01N43/40A01N43/84
    • A fungicidal mixture ofa) a compound of the formula I ##STR1## where R.sup.a =tridecyl or 3-(p-tert-butyl-(phenyl)-2-methylpropyl,R.sup.b =H, CH.sub.3 andX=O, CH.sub.2andb) a compound of the formula II ##STR2## where R.sup.1 is substituted or unsubstituted phenyl, naphthyl, tetrahydronaphthyl, benzothiophenyl, benzofuranyl, anthracenyl, acenaphthenyl, hexahydroindacenyl, tetrahydrophenanthrenyl, stilbenyl or benzodioxolanyl,R.sup.2 is hydrogen or methyl,R.sup.3 is hydrogen,R.sup.4 is alkyl, cyclopropyl, haloalkyl or alkenyl,W is alkenylene, fluoroalkenylene or a single bond,R.sup.5 is substituted or unsubstituted phenyl, or is naphthyl, substituted or unsubstituted alkenyl, or alkynyl, where the radical ##STR3## may denote the acenaphthenyl radical ##STR4## and the radical ##STR5## may also be part of a heterocyclic ring.
    • a)式Ⅰ化合物的杀真菌混合物,其中R a =十三烷基或3-(对叔丁基 - (苯基)-2-甲基丙基,R b = H,CH 3和X = O,CH 2和 b)式II的化合物其中R1是取代或未取代的苯基,萘基,四氢萘基,苯并噻吩基,苯并呋喃基,蒽基,苊基,六氢茚基,四氢菲基,茋基或苯并二氧杂环戊烷基,R 2是氢或甲基, R4是烷基,环丙基,卤代烷基或烯基,W是亚烯基,氟亚烷基或单键,R5是取代或未取代的苯基,或是萘基,取代或未取代的烯基或炔基,其中基团可以表示苊基 < IMAGE>和激进的也可以是杂环的一部分。