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    Substituted maleimides and their use as fungicides for plant-pathogenic fungi
    4.
    发明授权
    Substituted maleimides and their use as fungicides for plant-pathogenic fungi 失效
    取代的马来酰亚胺及其作为植物致病真菌的杀真菌剂的用途

    公开(公告)号：US4666935A

    公开(公告)日：1987-05-19

    申请号：US578231

    申请日：1984-02-08

    申请人： Gerhard Marzolph ,  Heinz U. Blank ,  Paul Reinecke ,  Wilhelm Brandes ,  Gerd Hanssler

    发明人： Gerhard Marzolph ,  Heinz U. Blank ,  Paul Reinecke ,  Wilhelm Brandes ,  Gerd Hanssler

    IPC分类号： C07D207/416 ,  A01N37/32 ,  C07D207/44 ,  C07D207/456 ,  C07D207/448

    CPC分类号： C07D207/456 ,  A01N37/32

    摘要： Substituted maleimides of the formula in whichX represents hydrogen, chlorine or bromine,X.sup.1 represents chlorine or bromine,n represents 2, 3, 4 or 5 andR represents halogen, alkyl, optionally substituted aryl, aryloxy or cycloalkyl, halogenoalkyl, hydroxyalkyl, alkoxyalkyl, acyloxyalkyl, nitro, cyano, alkoxycarbonyl, alkylcarbonyl, carboxyl, carbonylamino, hydroxyl, alkoxy, halogenoalkoxy, acyloxy, sulphonylamino, alkylsulphonyl, alkylmercapto, marcapto, acylmercapto, halogenoalkylmercapto, amino, mono- or di-alkylamino or acylamino andm represents 1, 2, 3, 4 or 5,which possess fungicidal activity.

    摘要翻译： 取代的式“IMAGE”的马来酰亚胺，其中X表示氢，氯或溴，X1表示氯或溴，n表示2,3,4或5，R表示卤素，烷基，任选取代的芳基，芳氧基或环烷基，卤代烷基， 羟基烷基，烷氧基烷基，酰氧基烷基，硝基，氰基，烷氧基羰基，烷基羰基，羧基，羰基氨基，羟基，烷氧基，卤代烷氧基，酰氧基，磺酰基氨基，烷基磺酰基，烷基巯基，巯基，酰巯基，卤代烷基巯基，氨基，单 - 或二 - 烷基氨基或酰氨基 代表1,2,3,4或5，具有杀真菌活性。

    Fungicidal N-substituted maleic acid imides
    5.
    发明授权
    Fungicidal N-substituted maleic acid imides 失效
    杀真菌剂N-取代马来酰亚胺

    公开(公告)号：US4582849A

    公开(公告)日：1986-04-15

    申请号：US498610

    申请日：1983-05-27

    申请人： Gerhard Marzolph ,  Heinz U. Blank ,  Paul Reinecke ,  Wilhelm Brandes ,  Hans Scheinpflug

    发明人： Gerhard Marzolph ,  Heinz U. Blank ,  Paul Reinecke ,  Wilhelm Brandes ,  Hans Scheinpflug

    IPC分类号： A01N37/32 ,  C04B18/14 ,  C07D207/44 ,  C07D207/456 ,  C07D207/452 ,  A61K31/40

    CPC分类号： C07D207/456 ,  A01N37/32 ,  C04B18/141 ,  Y02W30/94

    摘要： Fungicidally active substituted maleic acid amides of the formula ##STR1## in which X is hydrogen, chlorine or bromine,X.sup.1 is chlorine or bromine,R is alkyl, optionally substituted aryl or optionally substituted aralkyl,R.sup.1 to R.sup.5 each independently is hydrogen, alkyl, optionally substituted aryl or optionally substituted aralkyl,R.sup.6 each independently is halogen, alkyl, optionally substituted aryl, optionally substituted cycloalkyl, alkoxy, sulphonylamine, halogenoalkyl, nitro, cyano, alkoxycarbonyl, alkylsulphonyl or carboxylamine,n is 0, 1, 2 or 3,m is 0, 1, 2 or 3,m+n is 0, 1, 2 or 3, andy is 0, 1, 2, 3, 4 or 5,with the exception of the compound in whichX and X.sup.1 are chlorine,m and y are 0,n is 1,R.sup.1, R.sup.4 and R.sup.5 are hydrogen, andR is methyl,and the compound in whichX and X.sup.1 are chlorine,m, n and y are 0,R.sup.1 is hydrogen, andR is phenyl.

    摘要翻译： 式中：X为氢，氯或溴，X为氯或溴，R为烷基，任选取代的芳基或任选取代的芳烷基，R 1至R 5各自独立地为氢，烷基， 任选取代的芳基或任选取代的芳烷基，R 6各自独立地为卤素，烷基，任选取代的芳基，任选取代的环烷基，烷氧基，磺酰胺，卤代烷基，硝基，氰基，烷氧基羰基，烷基磺酰基或羧基胺，n为0,1,2或3， m为0,1,2或3，m + n为0,1,2或3，y为0,1,2,3,4或5，其中X和X 1为氯的化合物除外 ，m和y是0，n是1，R1，R4和R5是氢，R是甲基，X和X1是氯，m，n和y的化合物是0，R1是氢，R是 苯基。

    Combating fungi with 1-phenoxy-2-pyridinyl-alkanols
    9.
    发明授权
    Combating fungi with 1-phenoxy-2-pyridinyl-alkanols 失效
    抗真菌与1-苯氧基-2-吡啶基 - 链烷醇

    公开(公告)号：US4438122A

    公开(公告)日：1984-03-20

    申请号：US391749

    申请日：1982-06-24

    申请人： Graham Holmwood ,  Paul-Ernst Frohberger ,  Wilhelm Brandes ,  Volker Paul

    发明人： Graham Holmwood ,  Paul-Ernst Frohberger ,  Wilhelm Brandes ,  Volker Paul

    IPC分类号： A01N43/40 ,  A01N43/54 ,  C04B35/565 ,  C07D213/30 ,  C07D239/26 ,  A61K31/44

    CPC分类号： C07D213/30 ,  A01N43/40 ,  A01N43/54 ,  C04B35/565 ,  C07D239/26

    摘要： 1-Phenoxy-2-pyridinyl(pyrimidinyl)-alkanols of the formula ##STR1## in which R represents alkyl, optionally substituted aryl or optionally substituted aralkyl,X represents a nitrogen atom or the CH group,Y represents halogen, alkyl, cycloalkyl, alkoxy, halogenoalkyl, alkylthio, or an optionally substituted phenyl, phenoxy, phenylalkoxy or phenylalkyl radical, andn represents 0 or an integer from 1 to 5, the Y's being selected independently of one another when n is 2, 3, 4 or 5,in the form of the free base, a salt or a metal salt complex thereof, which possess fungicidal properties.

    摘要翻译： 式“IMAGE”的1-苯氧基-2-吡啶基（嘧啶基） - 链烷醇，其中R表示烷基，任选取代的芳基或任选取代的芳烷基，X表示氮原子或CH基团，Y表示卤素，烷基，环烷基， 烷氧基，卤代烷基，烷硫基或任选取代的苯基，苯氧基，苯基烷氧基或苯基烷基，n表示0或1至5的整数，当n为2,3,4或5时，Y彼此独立地选择， 以游离碱的形式，其盐或金属盐络合物具有杀真菌性能。

    Combating fungi with 2-methylene-3-substituted-4,5-bis-trifluoromethyl-imino-thiazolidines
    10.
    发明授权
    Combating fungi with 2-methylene-3-substituted-4,5-bis-trifluoromethyl-imino-thiazolidines 失效
    与2-亚甲基-3-取代-4,5-双 - 三氟甲基 - 亚氨基 - 噻唑烷的抗真菌

    公开(公告)号：US4382933A

    公开(公告)日：1983-05-10

    申请号：US267830

    申请日：1981-05-28

    申请人： Klaus Grohe ,  Hans-Joachim Scholl ,  Volker Paul ,  Wilhelm Brandes ,  Paul-Ernst Frohberger

    发明人： Klaus Grohe ,  Hans-Joachim Scholl ,  Volker Paul ,  Wilhelm Brandes ,  Paul-Ernst Frohberger

    IPC分类号： A01N43/78 ,  A01N47/08 ,  C07D277/20 ,  C07D277/38 ,  C07D277/40 ,  C07D277/42 ,  C07D277/04 ,  A61K31/425

    CPC分类号： C07D277/20 ,  A01N47/08

    摘要： 2-Methylene-3-substituted-4,5-bis-trifluoromethyl-imino-thiazolidines of the formula ##STR1## in which R.sup.1 represents optionally substituted alkyl, optionally substituted alkenyl, optionally substituted alkynyl, optionally substituted cycloalkyl, optionally substituted aryl, aralkyl, it being possible for the last-mentioned group to be substituted on the alkyl radical, or an amino group --NR.sup.4 R.sup.5, whereinR.sup.4 and R.sup.5 may be identical or different, each represent optionally substituted alkyl, or R.sup.4 and R.sup.5 together with the connecting nitrogen atom and optionally one or more further hetero-atoms, form a 4-membered to 12-membered heterocyclic ring,R.sup.2 represents cyano, alkoxycarbonyl, acyl, alkylsulphonyl or arylsulphonyl, the four last-mentioned groups being optionally substituted, or represents an amide or thioamide group, comprising the radical CO--NR.sup.6 R.sup.7 or CS--NR.sup.6 R.sup.7,whereinR.sup.6 represents hydrogen or alkyl andR.sup.7 represents alkyl, cycloalkyl or optionally substituted phenyl, orR.sup.2 and R.sup.3, together with the connecting carbon atom, represent an .alpha.-cycloalkanone ring system with 5 to 7 carbon atoms, which can be optionally substituted, which possess fungicidal properties.

    摘要翻译： 其中R 1表示任选取代的烷基，任选取代的烯基，任选取代的炔基，任选取代的环烷基，任选取代的芳基，芳烷基（取代或未取代的芳基），亚烷基 最后提到的基团可以被烷基取代，或氨基-NR4R5，其中R4和R5可以相同或不同，各自表示任选取代的烷基，或者R4和R5连同连接的氮 原子和任选的一个或多个另外的杂原子形成4元至12元杂环，R 2表示氰基，烷氧基羰基，酰基，烷基磺酰基或芳基磺酰基，四个最后提及的基团任选被取代，或表示酰胺或 硫代酰胺基团，其包含基团CO-NR 6 R 7或CS-NR 6 R 7，其中R 6表示氢或烷基，R 7表示烷基，环烷基或任选取代的苯基，或R 2和R 3， 与连接碳原子一起表示具有5至7个碳原子的α-环烷酮环系，其可任选被取代，其具有杀真菌性质。