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81. 发明授权

US4700891A Electromagnetically actuatable fuel injection valve 失效
标题翻译：电磁致动燃油喷射阀
公开(公告)号：US4700891A
公开(公告)日：1987-10-20
申请号：US912469
申请日：1986-09-29
申请人： Waldemar Hans , Wilhelm Kind , Heinrich Knapp , Wolfgang Kramer , Rudolf Sauer
发明人： Waldemar Hans , Wilhelm Kind , Heinrich Knapp , Wolfgang Kramer , Rudolf Sauer
IPC分类号： F02M51/06 , F02M51/08 , F02M53/04
CPC分类号： F02M53/04 , F02M51/0678 , F02M2051/08
摘要： A magnetic injection valve for injecting fuel into the intake tract of internal combustion machines, which is distinguished by particularly good internal cooling. A magnetic coil wound onto a coil carrier is located in the valve, being introduced into a valve housing and surrounds a ferromagnetic core. The core acts upon an armature which is connected to a movable valve needle. A bushing in the core and a sleeve located outside the core are arranged such that the fuel, emerging from an inflow tract of a supply device flows via the sleeve serving as a fuel line and reaches the interior of the valve housing that receives the magnetic coil; after flowing virtually completely around the magnetic coil, the fuel leaves this interior via a bore and flows back between the bushing and the core as far as the end of the bushing, and then flows on through the bushing to reach the armature to flow on to the valve seat. For better cooling of the magnetic coil, flow conduits are machined into the coil holder such that the fuel flow virtually surrounds the coil.
摘要翻译：一种用于将燃料喷射到内燃机的进气道中的磁性注射阀，其特征在于内部冷却特别好。缠绕在线圈架上的磁性线圈位于阀中，被引入阀壳体并围绕铁磁芯。铁芯作用在与可动阀针连接的电枢上。芯部中的衬套和位于芯部外部的套筒布置成使得从供给装置的流入管道出来的燃料经由用作燃料管线的套筒流动并到达接收电磁线圈的阀壳体的内部 ; 在几乎完全绕电磁线圈完全流动之后，燃料经由孔离开该内部，并且在衬套和芯之间回流至衬套的端部，然后通过衬套流到电枢以流到阀座。为了更好地冷却磁性线圈，将流动管道加工到线圈架中，使得燃料流动实际上围绕线圈。

82. 发明授权

US4628060A Fungicidal tetrahydrothiopyran-3,5-dione derivatives, intermediate derivatives, compositions, and method of use therefor 失效
标题翻译：杀真菌四氢噻喃-3,5-二酮衍生物，中间体衍生物，组合物及其用途
公开(公告)号：US4628060A
公开(公告)日：1986-12-09
申请号：US606316
申请日：1984-05-02
申请人： Herbert Gayer , Wolfgang Kramer , Wilhelm Brandes , Gerd Hanssler , Paul Reinecke
发明人： Herbert Gayer , Wolfgang Kramer , Wilhelm Brandes , Gerd Hanssler , Paul Reinecke
IPC分类号： A01N43/14 , A01N43/18 , C07D335/02 , A61K31/38
CPC分类号： A01N43/18 , C07D335/02
摘要： Novel substituted tetrahydrothiopyran-3,5-dione-4-carboxamide fungicides of the formula ##STR1## in which R is alkyl, cycloalkyl, optionally substituted aralkyl or optionally substituted aryl,R.sup.1, R.sup.2 and R.sup.3 each independently is hydrogen or alkyl, andR.sup.4 is alkyl,excepting the compounds in whichR.sup.1 and R.sup.3 are hydrogenR.sup.4 is methyl,R is alkyl, phenyl or phenyl which is substituted by halogen and/or methyl, andR.sup.2 is hydrogen, or methyl.Many of the intermediates are also new.
摘要翻译：式中：R为烷基，环烷基，任选取代的芳烷基或任选取代的芳基的新型取代的四氢噻喃-3,5-二酮-4-甲酰胺杀真菌剂，其中R 1，R 2和R 3各自独立地为氢或烷基，R 4 除烷基外，R 1和R 3为氢的化合物R 4为甲基，R为烷基，苯基或被卤素和/或甲基取代的苯基，R 2为氢或甲基。许多中间体也是新的。

83. 发明授权

US4549900A Combating fungi with substituted 1-azolyl-butan-2-ones and -2-ols 失效
标题翻译：用真菌与取代的1-噻唑基 - 丁-2-酮和-2-ols进行灭菌
公开(公告)号：US4549900A
公开(公告)日：1985-10-29
申请号：US481615
申请日：1983-04-04
申请人： Wolfgang Kramer , Karl H. Buchel , Hans-Ludwig Elbe , Udo Kraatz , Erik Regel , Paul-Ernst Frohberger , Wilhelm Brandes , Klaus Lurssen
发明人： Wolfgang Kramer , Karl H. Buchel , Hans-Ludwig Elbe , Udo Kraatz , Erik Regel , Paul-Ernst Frohberger , Wilhelm Brandes , Klaus Lurssen
IPC分类号： A01N43/50 , A01N43/64 , A01N43/653 , A01N47/02 , C07C45/63 , C07C45/67 , C07C45/71 , C07C45/75 , C07D249/08 , C07D521/00 , C07D233/60
CPC分类号： C07D231/12 , A01N43/50 , A01N43/64 , A01N47/02 , C07C323/00 , C07C45/63 , C07C45/673 , C07C45/71 , C07C45/75 , C07D233/56 , C07D249/08
摘要： Substituted 1-azolyl-but-2-ones and -2-ols of the formula ##STR1## in which B is --CO-- or --CH(OH)--Az represents a 1,2,4-triazol-1-yl or -4-yl or imidazol-1-yl radical,R.sup.1 represents a hydrogen atom, an alkyl, alkenyl, alkinyl, optionally substituted cycloalkyl, optionally substituted cycloalkylalkyl, optionally substituted phenoxyalkyl or optionally substituted aralkyl radical,n is 0 or 1,R.sup.2 represents a cyano radical or a grouping of the general formula --X--R.sup.3 or --CO--NR.sup.4 R.sup.5, or, if n does not represent O at the same time as R.sup.1 represents a hydrogen atom and Az represents a 1,2,4-triazolyl radical,R.sup.2 also additionally represents an optionally substituted aryl or alkoxycarbonyl radical,and whereinX represents an oxygen or sulphur atom or an SO or SO.sub.2 group,R.sup.3 represents an alkyl, halogenoalkyl, optionally substituted aryl or optionally substituted aralkyl radical,R.sup.4 represents a hydrogen atom or an alkyl or optionally substituted aryl radical, andR.sup.5 represents a hydrogen atom or an alkyl radical, or acid addition salts or metal salt complexes thereof which possess fungicidal activity and plant growth regulatory and which can be reduced to the corresponding alcohols which are also fungicidally active.
摘要翻译：其中B为-CO-或-CH（OH）的取代的1-噻唑基 - 但-2-酮和2-取代的式“IMAGE”为Az代表1,2,4-三唑-1-基或 R 1表示氢原子，烷基，烯基，炔基，任选取代的环烷基，任选取代的环烷基烷基，任选取代的苯氧基烷基或任选取代的芳烷基，n为0或1，R 2表示氰基或通式-X-R3或-CO-NR4R5的基团，或者如果在R1表示氢原子的同时不表示O，并且Az表示1,2,4-三唑基 R2还另外表示任选取代的芳基或烷氧基羰基，并且其中X表示氧或硫原子或SO或SO 2基团，R 3表示烷基，卤代烷基，任选取代的芳基或任选取代的芳烷基，R 4表示氢原子或烷基或任选取代的芳基，R 5表示氢原子或烷基或其酸加成盐或金属盐络合物，其具有杀真菌活性和植物生长调节，并且可以还原成也是杀真菌活性的相应的醇。

84. 发明授权

US4542130A 5-Aminomethyl-1,3-oxathiolane microbicides, compositions and use 失效
标题翻译： 5-氨基甲基-1,3-氧硫杂环戊烷杀微生物剂，组合物和用途
公开(公告)号：US4542130A
公开(公告)日：1985-09-17
申请号：US624889
申请日：1984-06-27
申请人： Joachim Weissmuller , Wolfgang Kramer , Dieter Berg , Paul Reinecke , Wilhelm Brandes , Gerd Hanssler
发明人： Joachim Weissmuller , Wolfgang Kramer , Dieter Berg , Paul Reinecke , Wilhelm Brandes , Gerd Hanssler
IPC分类号： A01N43/28 , A01N43/46 , A01N43/60 , A01N43/84 , C07D327/00 , C07D327/04 , C07D411/06 , C07D413/06
CPC分类号： C07D411/06 , A01N43/28 , C07D327/04
摘要： MIcrobicidally active 5-aminomethyl-1,3-oxathiolanes of the formula ##STR1## in which R.sup.1 is tetrahydronaphthyl, decahydronaphthyl or optionally substituted naphthyl, optionally substituted cycloalkyl or cycloalkenyl, optionally substituted phenyl, or alkyl which is substituted by phenyl, phenoxy, phenylthio, cyclohexyl, cyclohexyloxy or cyclohexylthio, each of which is optionally substituted,R.sup.2 is hydrogen or methyl,R.sup.3 is alkyl, andR.sup.4 is alkyl, alkenyl or optionally substituted aralkyl, orR.sup.3 and R.sup.4, together with the nitrogen atom to which they are bonded, form an optionally substituted saturated heterocyclic structure which can contain further heteroatoms,or a plant-tolerated addition product thereof with an acid or metal salt.
摘要翻译：其中R 1为四氢萘基，十氢萘基或任选取代的萘基，任选取代的环烷基或环烯基，任选取代的苯基，或被苯基，苯氧基，苯硫基取代的烷基的除草活性的5-氨基甲基-1,3-氧硫杂环戊烷环己基，环己氧基或环己基硫基，其各自任选被取代，R 2是氢或甲基，R 3是烷基，R 4是烷基，烯基或任选被取代的芳烷基，或者R 3和R 4与它们所键合的氮原子一起形成可以含有其它杂原子的任选取代的饱和杂环结构，或其含有酸或金属盐的植物耐受的加成产物。

85. 发明授权

US4505922A Triazolealkynol fungicidal agents 失效
标题翻译：三唑烷醇杀真菌剂
公开(公告)号：US4505922A
公开(公告)日：1985-03-19
申请号：US385354
申请日：1982-06-07
申请人： Gerhard Jager , Karl H. Buchel , Wolfgang Kramer , Paul-Ernst Frohberger , Wilhelm Brandes
发明人： Gerhard Jager , Karl H. Buchel , Wolfgang Kramer , Paul-Ernst Frohberger , Wilhelm Brandes
IPC分类号： A01N43/50 , A01N43/653 , C07D233/60 , C07D249/08 , C07D521/00 , A01N43/64
CPC分类号： C07D231/12 , A01N43/50 , A01N43/653 , C07D233/56 , C07D249/08
摘要： A fungicidal composition comprising a fungicidally effective amount of an alkinyl-azole derivative of the formula ##STR1## in which A is a nitrogen atom or the CH group,R.sup.1 is an optionally substituted aryl or optionally substituted aryloxy group,R.sup.2 is an alkyl group which is optionally substituted by halogen, or an optionally substituted aryl group,X is a hydrogen, bromine or iodine atom, andn is 0 or 1or an acid addition salt or metal salt complex thereof, in admixture with a diluent. Many of the compounds are new.
摘要翻译：一种杀真菌组合物，其包含杀真菌有效量的式（I）的炔基 - 唑类衍生物，其中A为氮原子或CH基团，R 1为任选取代的芳基或任选取代的芳氧基，R 2为任选被卤素或任选取代的芳基取代，X为氢，溴或碘原子，n为0或1，或其酸加成盐或金属盐络合物与稀释剂混合。许多化合物是新的。

86. 发明授权

US4495184A Morpholino propanol derivatives, fungicidal compositions and use 失效
标题翻译：吗啉代醇衍生物，杀真菌剂及用途
公开(公告)号：US4495184A
公开(公告)日：1985-01-22
申请号：US496673
申请日：1983-05-23
申请人： Hans-Joachim Knops , Wolfgang Kramer , Paul-Ernst Frohberger
发明人： Hans-Joachim Knops , Wolfgang Kramer , Paul-Ernst Frohberger
IPC分类号： C07D295/08 , A01N33/04 , A01N33/08 , A01N37/12 , A01N37/34 , A01N43/84 , A01N47/12 , A01N47/20 , A01N55/00 , A01N55/10 , C07C67/00 , C07C213/00 , C07C215/30 , C07C217/70 , C07C217/72 , C07C219/22 , C07C239/00 , C07C253/00 , C07C255/58 , C07C255/59 , C07C271/08 , C07C313/00 , C07C323/32 , C07D209/08 , C07D295/067 , C07D295/084 , C07F7/18
CPC分类号： C07D295/067 , A01N33/04 , A01N33/08 , A01N37/12 , A01N47/12 , A01N47/20 , A01N55/00 , C07D209/08 , C07D295/092 , C07F7/1856
摘要： A 1-phenyl-3-amino-propane derivative of the formula ##STR1## in which R.sup.1 and R.sup.2 independently represent alkyl radicals or R.sup.1 and R.sup.2 together with the nitrogen atom to which they are bonded complete an optionally substituted heterocyclic radical of the formula ##STR2## and or additionally, if R.sup.4 represents the radical --O--CO--R.sup.5, --O--CO--NHR.sup.6 or --O--SiR.sub.3.sup.7, complete an optionally substituted heterocyclic radical of the formula ##STR3## R.sup.3 represents a hydrogen atom or an alkyl radical, R.sup.4 represents a hydroxyl group, halogen or the radical --O--CO--R.sup.5, --O--CO--NHR.sup.6 or --O--SiR.sub.3.sup.7,R.sup.5 represents an alkyl, alkenyl or halogenoalkyl radical or an optionally substituted aryl or aralkyl radical,R.sup.6 represents an alkyl or alkenyl radical or an optionally substituted aryl radical,R.sup.7 represents an alkyl radical each Y independently represents an alkyl radical, a halogen atom or a halogenoalkyl, alkoxy, alkylthio, halogenoalkoxy, halogenoalkylthio, cycloalkyl or cyano radical andn is 0, 1, 2 or 3,or a physiologically acceptable acid addition salt thereof which possesses fungicidal activity.
摘要翻译：其中R 1和R 2独立地表示烷基或R 1和R 2与它们所键合的氮原子一起形成的式“IMAGE”的1-苯基-3-氨基 - 丙烷衍生物与式或者另外，如果R 4代表基团-O-CO-R 5，-O-CO-NHR 6或-O-SiR 37，则完成式R 3的任选取代的杂环基代表氢原子或烷基基团，R 4表示羟基，卤素或-O-CO-R 5，-O-CO-NHR 6或-O-SiR 37基团，R 5表示烷基，烯基或卤代烷基或任选取代的芳基或芳烷基，R 6 表示烷基或烯基或任选取代的芳基，R 7表示烷基，每个Y独立地表示烷基，卤素原子或卤代烷基，烷氧基，烷硫基，卤代烷氧基，卤代烷硫基，环烷基或氰基，n为0， 1,2或3，或者一个生理学家其具有杀真菌活性的其可接受的酸加成盐。

87. 发明授权

US4492795A Alkylcycloalkyl imidazolylmethyl ketones as fungicide intermediates 失效
标题翻译：烷基环烷基咪唑甲基酮作为杀真菌剂中间体
公开(公告)号：US4492795A
公开(公告)日：1985-01-08
申请号：US438087
申请日：1982-11-01
申请人： Wolfgang Kramer , Manfred Jautelat , Eckart Kranz
发明人： Wolfgang Kramer , Manfred Jautelat , Eckart Kranz
IPC分类号： A01N43/50 , C07C17/26 , C07C43/225 , C07C45/51 , C07C49/327 , C07D233/60 , C07D521/00
CPC分类号： C07D249/08 , C07C17/269 , C07C43/225 , C07C45/513 , C07C49/327 , C07D231/12 , C07D233/56
摘要： New alkylcycloalkyl imidazolylmethyl ketones of the general formula ##STR1## in which R represents an alkyl group andn is 3, 4, 5, 6 or 7,are produced as described and find use as intermediate products for the preparation of imidazolyl-vinyl-dithioacetals, which possess fungicidal properties.
摘要翻译：其中R表示烷基且n为3,4,5,6或7的通式为“IMAGE”的新的烷基环烷基咪唑基甲基酮如所述制备，可用作制备咪唑基 - 乙烯基 - 二硫代缩醛的中间产物，具有杀菌性。

88. 发明授权

US4419361A Combating fungi with 1-phenoxy -1-imidazol-1-yl-4-fluoro-butane derivatives 失效
标题翻译：抗真菌与1-苯氧基-1-咪唑-1-基-4-氟 - 丁烷衍生物
公开(公告)号：US4419361A
公开(公告)日：1983-12-06
申请号：US321642
申请日：1981-11-16
申请人： Wolfgang Kramer , Karl H. Buchel , Jorg Stetter , Paul-Ernst Frohberger , Wilhelm Brandes , Hans Scheinpflug
发明人： Wolfgang Kramer , Karl H. Buchel , Jorg Stetter , Paul-Ernst Frohberger , Wilhelm Brandes , Hans Scheinpflug
IPC分类号： A01N43/50 , C07C45/63 , C07C45/67 , C07C45/71 , C07C49/16 , C07C49/167 , C07D233/60 , C07D521/00
CPC分类号： C07D231/12 , A01N43/50 , C07C45/63 , C07C45/673 , C07C45/71 , C07C49/16 , C07C49/167 , C07D233/56 , C07D249/08
摘要： 1-Phenoxy-1-imidazol-1-yl-4-fluoro-butane derivatives of the formula ##STR1## in which B is --CO- or --CH(OH)--,X is hydrogen or fluorine,Z each independently is halogen, alkyl, nitro, cyano, alkoxy-carbonyl or optionally substituted phenyl, andn is 0, 1, 2 or 3,or an acid or metal salt adduct thereof, which possess fungicidal properties.
摘要翻译：其中B为-CO-或-CH（OH） - 的式为“IMAGE”的1-苯氧基-1-咪唑-1-基-4-氟 - 丁烷衍生物，X为氢或氟，Z各自独立地为卤素，烷基，硝基，氰基，烷氧基 - 羰基或任选取代的苯基，n为0,1,2或3，或其酸或金属盐加合物，具有杀真菌性质。

89. 发明授权

US4309434A Combating fungi with 1-(2-chlorophenyl)-1-(2-chlorobenzyloximino)-2-(1,2,4-triazol-1-yl)-etha ne 失效
标题翻译：用1-（2-氯苯基）-1-（2-氯苄肟基）-2-（1,2,4-三唑-1-基） - 乙烷
公开(公告)号：US4309434A
公开(公告)日：1982-01-05
申请号：US135380
申请日：1980-03-28
申请人： Wolfgang Kramer , Karl H. Buchel , Helmut Timmler , Wilhelm Brandes , Paul-Ernst Frohberger
发明人： Wolfgang Kramer , Karl H. Buchel , Helmut Timmler , Wilhelm Brandes , Paul-Ernst Frohberger
IPC分类号： A01N43/653 , A61K31/41 , A61P31/04 , C07D249/08 , C07D521/00 , A01N43/64
CPC分类号： C07D231/12 , C07D233/56 , C07D249/08
摘要： A 1-(2-chlorophenyl)-1-((di)-halogenbenzyloximino)-2-(1,2,4-triazol-1-yl)-ethane of the formula ##STR1## in which X is hydrogen or halogen or a salt thereof with a physiologically acceptable acid or a metal salt complex thereof which possesses fungicidal properties.
摘要翻译：具有式“IMAGE”的1-（2-氯苯基）-1 - （（二） - 卤代苯甲酰肟基）-2-（1,2,4-三唑-1-基） - 乙烷，其中X是氢或卤素或其盐与具有杀真菌性质的生理上可接受的酸或其金属盐络合物。

90. 发明授权

US4239767A Antimycotic diaryloxy-imidazolyl-O,N-acetals 失效
标题翻译：抗真菌的二芳氧基 - 咪唑基-O，N-缩醛
公开(公告)号：US4239767A
公开(公告)日：1980-12-16
申请号：US629215
申请日：1975-11-06
申请人： Karl H. Buchel , Wolfgang Kramer , Manfred Plempel
发明人： Karl H. Buchel , Wolfgang Kramer , Manfred Plempel
IPC分类号： A01N43/50 , A01P3/00 , C07D233/60 , C07D521/00 , A61K31/415
CPC分类号： C07D231/12 , C07C317/00 , C07D233/56 , C07D249/08
摘要： Diaryloxy-imidazolyl-O,N-acetals of the formula ##STR1## or pharmaceutically-acceptable, nontoxic salts thereof wherein X and Y are each halo, alkyl, alkoxy, haloalkylthio, nitro, amino, alkylamino or dialkylamino;Z is a direct bond, methylene, oxygen, sulphur, sulphonyl, alkoxymethylene or a keto moiety;A is a keto moiety or a moiety of the formula C(OH)R, wherein R is hydrogen or alkyl; anda and b are each integers from 0 to 3;are useful for their antimycotic activity and their sporocidal action.
摘要翻译：式（I）的二芳氧基 - 咪唑基-O，N-缩醛或其药学上可接受的无毒盐，其中X和Y各自为卤素，烷基，烷氧基，卤代烷硫基，硝基，氨基，烷基氨基或二烷基氨基; Z是直接键，亚甲基，氧，硫，磺酰基，烷氧基亚甲基或酮基部分; A是酮基部分或式C（OH）R的部分，其中R是氢或烷基; a和b各自为0至3的整数; 对于它们的抗真菌活性及其杀孢子作用是有用的。

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