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121. 发明授权

US5371065A Substituted azolylmethyloxiranes 失效
标题翻译：取代的唑基甲基环氧乙烷
公开(公告)号：US5371065A
公开(公告)日：1994-12-06
申请号：US305836
申请日：1989-02-02
申请人： Hans-Ludwig Elbe , Karl H. Buchel , Wilhelm Brandes , Stefan Dutzmann , Klaus Lurssen
发明人： Hans-Ludwig Elbe , Karl H. Buchel , Wilhelm Brandes , Stefan Dutzmann , Klaus Lurssen
IPC分类号： C07D405/06 , A01N43/50 , A01N43/653 , C07D233/60 , C07D249/08 , C07D521/00
CPC分类号： C07D249/08 , A01N43/50 , A01N43/653 , C07D231/12 , C07D233/56
摘要： Fungicidal and plant growth-regulating substituted azolylmethyloxiranes of the formula ##STR1## in which R.sup.1 stands for alkyl,R.sup.2 stands for alkyl,X stands for a nitrogen atom or the CH group,Y stands (or halogen, alkyl, cycloalkyl, alkoxy, alkylthio, halogenoalkyl, halogenoalkoxy, halogenoalkylthio, optionally substituted phenyl, optionally substituted phenoxy, optionally substituted phenylalkyl and/or optionally substituted phenylalkoxy andm stands for the numbers 0, 1, 2 or 3,and addition products thereof with acids and metal salts.
摘要翻译： R 1代表烷基，R 2代表烷基，X代表氮原子或CH基团，Y代表（或卤素，烷基，环烷基，环烷基，环烷基或芳烷基）的杀真菌和植物生长调节取代的吡唑基甲基环氧烷，烷氧基，烷硫基，卤代烷基，卤代烷氧基，卤代烷硫基，任选取代的苯基，任选取代的苯氧基，任选取代的苯基烷基和/或任选取代的苯基烷氧基，m代表数字0,1,2或3，其加成产物与酸和金属盐。

122. 发明授权

US4894382A Substituted 1,3-diazolyl-2-propanols and their use as antimycotic agents 失效
标题翻译：取代的1,3-二唑基-2-丙醇及其作为抗真菌剂的用途
公开(公告)号：US4894382A
公开(公告)日：1990-01-16
申请号：US924658
申请日：1986-10-29
申请人： Hans-Ludwig Elbe , Graham Holmwood , Erik Regel , Karl H. Buchel , Klaus Schaller , Manfred Plempel
发明人： Hans-Ludwig Elbe , Graham Holmwood , Erik Regel , Karl H. Buchel , Klaus Schaller , Manfred Plempel
IPC分类号： A61K31/41 , A61K31/415 , A61P31/04 , C07C45/63 , C07C45/68 , C07D233/60 , C07D249/08 , C07D403/06 , C07D405/06 , C07D521/00
CPC分类号： C07D231/12 , C07C45/63 , C07C45/68 , C07D233/56 , C07D249/08
摘要： The invention provides substituted 1,3-diazolyl-2-propanols defined herein generically by formula (I), useful as antimycotic agents. Also included in the invention are methods for the procurement of said substituted 1,3-diazolyl-2-propanols, compositions containing said antimycotic compounds and methods for the use of said compounds and compositions for treatment of mycoses.
摘要翻译：本发明提供了通式（I）定义的取代的1,3-二唑基-2-丙醇，其可用作抗真菌剂。本发明还包括采购所述取代的1,3-二唑基-2-丙醇的方法，含有所述抗霉菌化合物的组合物以及用于所述化合物和组合物治疗霉菌病的方法。

123. 发明授权

US4879385A Substituted hydroxyalkyl-azoles and their use as antimycotics 失效
标题翻译：取代的羟基烷基 - 唑类及其作为抗霉菌剂的用途
公开(公告)号：US4879385A
公开(公告)日：1989-11-07
申请号：US62251
申请日：1987-06-15
申请人： Hans-Ludwig Elbe , Karl H. Buchel , Klaus Schaller , Manfred Plempel
发明人： Hans-Ludwig Elbe , Karl H. Buchel , Klaus Schaller , Manfred Plempel
IPC分类号： A61K31/415 , A61P31/04 , C07C45/63 , C07C45/68 , C07C45/71 , C07D233/60 , C07D249/08 , C07D303/08 , C07D303/22 , C07D521/00
CPC分类号： C07D303/22 , C07C45/63 , C07C45/68 , C07C45/71 , C07D231/12 , C07D233/56 , C07D249/08 , C07D303/08
摘要： The invention relates to substituted hydroxyalkylazoles defined herein by formula (I), which compounds are useful as antimycotic agents. Also included in the invention are compositions containing said compounds and methods for the use of said compounds and compositions. In addition, the invention includes methods for the manufacture of the compounds of formula (I).
摘要翻译：本发明涉及由式（I）定义的取代羟基烷基唑，该化合物可用作抗真菌剂。本发明还包括含有所述化合物的组合物和使用所述化合物和组合物的方法。此外，本发明包括制备式（I）化合物的方法。

124. 发明授权

US4877446A Pesticides based on pyrimidine derivatives 失效
标题翻译：基于嘧啶衍生物的农药
公开(公告)号：US4877446A
公开(公告)日：1989-10-31
申请号：US146996
申请日：1988-01-22
申请人： Hans-Ludwig Elbe , Stefan Dutzmann , Paul Reinecke
发明人： Hans-Ludwig Elbe , Stefan Dutzmann , Paul Reinecke
IPC分类号： A01N43/54 , C07D239/26 , C07D405/12
CPC分类号： C07D239/26 , A01N43/54 , C07D405/12
摘要： A method of combating fungi which comprises applying to such fungi or to a fungus habitat a fungicidally effective amount of a substituted pyrimidine of the formula ##STR1## in which Ar represents optionally substituted phenyl,X represents oxygen, sulphur, sulphinyl, sulphonyl or one of the groups--CH.sub.2 --; --O--CH.sub.2 --; --CHhd 2--O----O--CH.sub.2 --CH.sub.2 --; --S(O).sub.n --CH.sub.2 --; --CH.sub.2 --S(O).sub.n --or --S(O).sub.n --CH.sub.2 --CH.sub.2 --, andY represents on eof the groups ##STR2## where R represents hydrogen, alkyl, alkenyl, alkinyl or optionally substituted aralkyl, andn represents a number 0, 1 or 2,or an acid-additonal salt or metal-salt complex thereof. Most of the compounds are new.
摘要翻译：一种对抗真菌的方法，其包括将杀真菌有效量的下式的取代嘧啶应用于真菌或真菌栖息地，其中Ar表示任选取代的苯基，X表示氧，硫，亚磺酰基，磺酰基或其中之一基团-CH 2 - ; -O-CH 2 - ; -CH 2 O-O-CH 2 -CH 2 - ; -S（O）n -CH 2 - ; -CH 2 -S（O）n - 或-S（O）n -CH 2 -CH 2 - ，Y表示基团，其中R表示氢，烷基，烯基，炔基或任选取代的芳烷基，n表示数字0,1或2，或其酸加成盐或金属盐络合物。大多数化合物是新的。

125. 发明授权

US4845288A Process for the preparation of hydroxybenzaldoxime O-ethers 失效
标题翻译：制备羟基苯甲醛肟O-醚的方法
公开(公告)号：US4845288A
公开(公告)日：1989-07-04
申请号：US147417
申请日：1988-01-25
申请人： Reinhard Lantzsch , Heinz Ziemann , Hans-Ludwig Elbe
发明人： Reinhard Lantzsch , Heinz Ziemann , Hans-Ludwig Elbe
IPC分类号： C07C251/48 , A01N43/653 , A61K31/41 , C07B61/00 , C07C67/00 , C07C239/00 , C07C249/12 , C07C251/32 , C07D249/08
CPC分类号： C07C239/20
摘要： A process for the preparation of a hydroxybenzaldoxime O-ether of the formula ##STR1## in which R.sup.1 represents alkyl, comprising(a) in a first step, hydrogenating a nitro-benzaldoxime O-ether of the formula ##STR2## using the calculated amount of hydrogen in the presence of a catalyst and in the presence of a diluent, and(b) in a second step, reacting the amino-benzaldoxime O-ether of the formula ##STR3## thus obtained with a diazotizing agent in acidic, aqueous solution, and, without isolation, thermally hydrolyzing the resultant diazonium salt of the formula ##STR4## in which X.crclbar. represents an equivalent of an inorganic anion, in acidic, aqueous solution.
摘要翻译：制备式（I）的羟基苯甲醛肟O-醚的方法，其中R 1表示烷基，包括（a）在第一步骤中氢化式IMAGE的硝基苯甲醛肟O-醚 II）在催化剂存在下和稀释剂存在下使用计算量的氢，和（b）在第二步中，使由此得到的式（III）的氨基 - 苯甲醛肟O-醚反应用酸性水溶液中的重氮化试剂，并且在不分离的情况下，在酸性水溶液中热解所得到的其中X（ - ）代表无机阴离子的式Ⅺ（Ⅳ）的重氮盐。

126. 发明授权

US4845287A Hydroxybenzaldoxime O-ethers 失效
标题翻译：羟基苯甲醛肟O-醚
公开(公告)号：US4845287A
公开(公告)日：1989-07-04
申请号：US43662
申请日：1987-04-28
申请人： Hans-Ludwig Elbe , Reinhard Lantzsch
发明人： Hans-Ludwig Elbe , Reinhard Lantzsch
IPC分类号： C07C251/48 , A01N33/24 , C07C67/00 , C07C239/00 , C07C249/12 , C07D249/08
CPC分类号： C07C249/12 , C07C251/48
摘要： A process for the preparation of a hydroxybenzaldoxime O-ether of the formula ##STR1## in which R.sup.1 is alkyl, alkenyl or alkinyl, comprising reacting an aminobenzaldoxime O-ether of the formula ##STR2## in which R.sup.1 has the abovementioned meaning, with a diazotizing agent in acidic, aqueous solution, and thermally hydrolyzing the resulting diazonium salt of the formula ##STR3## in which X.crclbar. in an equivalent of an inorganic anion andR.sup.1 has the abovementioned meaning,in acidic, aqueous solution without intermediate isolation.The products are intermediates for agricultural and pharmaceutical chemicals.Novel amino-benzaldoxime O-ethers of the formula ##STR4## wherein R.sup.1 has the above-mentioned meaning.
摘要翻译：制备式（I）的羟基苯甲醛肟O-醚的方法，其中R 1是烷基，链烯基或炔基，包括使式（II）的氨基苯甲醛肟O-醚与其中R1具有上述含义，在酸性水溶液中用重氮化剂，并热解水解所得的式（III）的重氮盐，其中X（ - ）的当量无机阴离子和R1具有上述含义，在酸性水溶液中，无需中间隔离。该产品是农药和化学药品的中间体。新颖的式（Ia）的氨基 - 苯甲醛肟O-醚，其中R1具有上述含义。

127. 发明授权

US4747869A Substituted azolyl-ketones and -alcohols 失效
标题翻译：取代的唑基酮和醇
公开(公告)号：US4747869A
公开(公告)日：1988-05-31
申请号：US724375
申请日：1985-04-18
申请人： Wolfgang Kramer , Karl H. Buchel , Klaus Ditgens , Hans-Ludwig Elbe , Gerhard Jager , Manfred Jautelat , Klaus Lurssen , Paul Reinecke
发明人： Wolfgang Kramer , Karl H. Buchel , Klaus Ditgens , Hans-Ludwig Elbe , Gerhard Jager , Manfred Jautelat , Klaus Lurssen , Paul Reinecke
IPC分类号： A01N43/50 , A01N43/653 , C07C17/269 , C07C43/225 , C07C45/51 , C07C45/59 , C07C49/16 , C07C49/185 , C07D233/60 , C07D249/08 , C07D317/26 , C07D521/00 , A61K31/41
CPC分类号： C07D231/12 , A01N43/50 , A01N43/653 , C07C17/269 , C07C43/225 , C07C45/513 , C07C45/59 , C07C49/16 , C07C49/185 , C07D233/56 , C07D249/08 , C07D317/26
摘要： Substituted azoyl-ketones and -alcohols of the formula ##STR1## in which A is a nitrogen atom or the CH group,B is CO or CH(OH),R.sup.1 is alkyl, alkenyl, alkinyl, optionally substituted phenylalkyl, optionally substituted cycloalkyl or optionally substituted cycloalkylalkyl,R.sup.2 is optionally substituted cycloalkyl or the grouping --C(CH.sub.3).sub.2 R.sup.3, andR.sup.3 is alkyl having more than 2 carbon atoms, alkenyl, alkinyl or the --CH.dbd.O group or a derivative thereof,or addition products thereof with acids or metal salts, exhibit plant growth regulating and fungicidal properties, several intermediates therefor are new.
摘要翻译：取代的式（IMAGE）的芳基酮和醇，其中A是氮原子或CH基团，B是CO或CH（OH），R 1是烷基，烯基，炔基，任选取代的苯基烷基，任选取代的环烷基或任选取代的环烷基烷基，R 2是任选取代的环烷基或基团-C（CH 3）2 R 3，并且R 3是具有多于2个碳原子的烷基，烯基，炔基或-CH = O基团或其衍生物，或其加成产物与酸或金属盐，表现出植物生长调节和杀真菌性能，其中几个是新的。

128. 发明授权

US4472395A Combating fungi with novel 2-azolylmethyl-1,3-dioxolane and -dioxane derivatives 失效
标题翻译：用新型2-吡唑基甲基-1,3-二氧戊环和二恶烷衍生物灭菌
公开(公告)号：US4472395A
公开(公告)日：1984-09-18
申请号：US343054
申请日：1982-01-27
申请人： Wolfgang Kramer , Karl H. Buchel , Hans-Ludwig Elbe , Udo Kraatz , Wolf Reiser , Andreas Schulze , Erik Regel , Wilhelm Brandes , Paul-Ernest Frohberger
发明人： Wolfgang Kramer , Karl H. Buchel , Hans-Ludwig Elbe , Udo Kraatz , Wolf Reiser , Andreas Schulze , Erik Regel , Wilhelm Brandes , Paul-Ernest Frohberger
IPC分类号： C07D405/06 , A61K31/41 , A61P31/04 , C07D521/00 , A01N43/50 , A01N43/64 , C07D405/14
CPC分类号： C07D231/12 , C07D233/56 , C07D249/08
摘要： A 2-azolylmethyl-1,3-dioxolane or -dioxane derivative of the formula ##STR1## in which Az is imidazol-1-yl or 1,2,4-triazol-1-yl,R.sup.1, R.sup.2, R.sup.3 and R.sup.5 each independently is hydrogen or alkyl, orR.sup.1 and R.sup.3 together are an optionally substituted multi-membered methylene bridge,R.sup.4 is hydrogen, optionally substituted alkyl, optionally substituted aryl or optionally substituted aralykyl,m is 0 or 1,R.sup.6 is hydrogen, halogen, cyano, alkyl, optionally substituted aryl, --X--R.sup.7, --COOR.sup.8 or --CONHR.sup.9,X is oxygen, sulphur, SO, or SO.sub.2,R.sup.7 is alkyl, halogenoalkyl, cyano, optionally substituted aralkyl or optionally substituted aryl,R.sup.8 is alkyl,R.sup.9 is alkyl or optionally substituted aryl, andn is 0 or 1, or a plant-tolerated acid addition salt or metal salt complex thereof which possesses fungicidal activity.
摘要翻译：其中Az为咪唑-1-基或1,2,4-三唑-1-基的式（Ⅰ）的2-吡唑基甲基-1,3-二氧戊环或二恶烷衍生物，R1，R2，R3 R 5和R 5各自独立地为氢或烷基，或者R 1和R 3一起为任选取代的多元亚甲基桥，R 4为氢，任选取代的烷基，任选取代的芳基或任选取代的芳烷基，m为0或1，R 6为氢，卤素，氰基，烷基，任选取代的芳基，-X-R7，-COOR8或-CONHR9，X是氧，硫，SO或SO2，R7是烷基，卤代烷基，氰基，任选取代的芳烷基或任选取代的芳基，烷基，R9为烷基或任选取代的芳基，n为0或1，或其具有杀真菌活性的植物耐受酸加成盐或金属盐络合物。

129. 发明授权

US4406909A Combating fungi with 4-substituted 1-azolyl-1-phenoxy-3,3-dimethyl-butan-2-ones and -ols 失效
标题翻译：用4-取代的1-噻唑基-1-苯氧基-3,3-二甲基 - 丁-2-酮和醇灭菌
公开(公告)号：US4406909A
公开(公告)日：1983-09-27
申请号：US265050
申请日：1981-05-19
申请人： Wolfgang Kramer , Hans-Ludwig Elbe , Karl H. Buchel , Wilhelm Brandes , Paul-Ernst Frohberger
发明人： Wolfgang Kramer , Hans-Ludwig Elbe , Karl H. Buchel , Wilhelm Brandes , Paul-Ernst Frohberger
IPC分类号： A01N43/48 , A01N43/50 , A01N43/64 , A01N43/653 , C07C45/63 , C07C45/71 , C07C49/16 , C07C49/255 , C07D233/60 , C07D249/08 , C07D521/00
CPC分类号： C07D231/12 , A01N43/50 , A01N43/653 , C07C323/00 , C07C45/63 , C07C45/71 , C07C49/16 , C07C49/255 , C07D233/56 , C07D249/08
摘要： A fungicidally active 4-substituted-1-azolyl-1-phenoxy-3,3-dimethyl-butan-2-one or -ol of the formula ##STR1## in which A is a nitrogen atom or CH,B is --CO-- or CH(OH),R is cyano or X--R.sup.1,R.sup.1 is alkyl, optionally substituted aryl or optionally substituted aralkyl,X is oxygen, sulphur, SO or SO.sub.2,Z each independently is halogen, alkyl, halogenoalkyl, alkoxy, alkylthio, alkylsulphonyl, nitro, cyano, alkoxycarbonyl or optionally substituted phenyl, andn is 0, 1, 2 or 3,or an addition product thereof with a physiologically acceptable acid or with a metal salt. Intermediates therefor of the formula ##STR2## are also new.
摘要翻译： A为氮原子或CH的杀真菌活性的4-取代-1-吡唑基-1-苯氧基-3,3-二甲基 - 丁-2-酮或其结构式为“IMAGE”的醇，B为-CO- 或CH（OH），R是氰基或X-R 1，R 1是烷基，任选取代的芳基或任选取代的芳烷基，X是氧，硫，SO或SO 2，Z各自独立地是卤素，烷基，卤代烷基，烷氧基，烷硫基，烷基磺酰基，硝基，氰基，烷氧基羰基或任选取代的苯基，n为0,1,2或3，或其与生理上可接受的酸或金属盐的加成产物。具有公式“IMAGE”和“IMAGE”的中间体也是新的。

130. 发明授权

US09155302B2 Active substance combinations 有权
标题翻译：活性物质组合
公开(公告)号：US09155302B2
公开(公告)日：2015-10-13
申请号：US11912773
申请日：2006-04-15
申请人： Anne Suty-Heinze , Heike Hungenberg , Wolfgang Thielert , Hans-Ludwig Elbe
发明人： Anne Suty-Heinze , Heike Hungenberg , Wolfgang Thielert , Hans-Ludwig Elbe
IPC分类号： A01N43/56
CPC分类号： A01N43/56 , A01N51/00 , A01N47/24 , A01N47/22 , A01N47/02 , A01N43/22 , A01N2300/00
摘要： The present invention relates to novel active compound combinations comprising, firstly, known carboxamides and, secondly, insecticidally active compounds, which active compound combinations are highly suitable for controlling unwanted animal pests, such as insects or acarids, and also unwanted phytopathogenic fungi.
摘要翻译：本发明涉及新的活性化合物组合，其包括首先是已知的羧酰胺，其次是杀虫活性化合物，其活性化合物组合高度适用于防治不想要的动物害虫，例如昆虫或螨虫，以及不想要的植物病原性真菌。

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