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1. 发明授权

US5700831A Pesticidal hydrazide derivatives 失效
标题翻译：杀虫酰肼衍生物
公开(公告)号：US5700831A
公开(公告)日：1997-12-23
申请号：US614291
申请日：1996-03-12
申请人： Mark Achiel Dekeyser , Paul Thomas McDonald
发明人： Mark Achiel Dekeyser , Paul Thomas McDonald
IPC分类号： C07D333/38 , A01N37/28 , A01N37/40 , A01N37/44 , A01N37/48 , C07C243/28 , C07C243/38 , C07C281/06 , C07D213/81 , C07D213/87 , C07D307/68 , C07D335/02 , C07C243/14 , A61K31/16
CPC分类号： C07D213/87 , A01N37/28 , A01N37/40 , A01N37/44 , A01N37/48 , C07C243/28 , C07C243/38
摘要： A compound of the formula ##STR1## wherein R is a) phenyl; phenyl(C.sub.1 -C.sub.4 alkoxy); phenoxy; or benzyl; the phenyl ring of each substituent being optionally substituted with one or more of halogen, nitro, C.sub.1 -C.sub.8 alkyl, C.sub.1 -C.sub.8 alkoxy, C.sub.1 -C.sub.8 haloalkyl, C.sub.1 -C.sub.8 haloalkoxy, di(C.sub.1 -C.sub.8 alkyl)amino, phenyl or phenoxy; or b) a 5- or 6-membered heterocyclic group comprising 1-3 heteroatoms selected from the group consisting of N, O or S, optionally substituted with one or more of halogen, nitro, C.sub.1 -C.sub.8 alkyl, C.sub.1 -C.sub.8 alkoxy, C.sub.1 -C.sub.8 haloalkyl, C.sub.1 -C.sub.8 haloalkoxy, or di-(C.sub.1 -C.sub.8 alkyl)amino. These compounds and pesticidal compositions prepared therefrom, are useful as plant protecting agents for the control of insects, nematodes, and mites.
摘要翻译：式IMA的化合物，其中R是a）苯基; 苯基（C 1 -C 4烷氧基）; 苯氧基或苄基; 每个取代基的苯环任选被一个或多个卤素，硝基，C 1 -C 8烷基，C 1 -C 8烷氧基，C 1 -C 8卤代烷基，C 1 -C 8卤代烷氧基，二（C 1 -C 8烷基）氨基，苯基或苯氧基 ; 或b）包含1-3个选自N，O或S的杂原子的5-或6-元杂环基，任选被一个或多个卤素，硝基，C 1 -C 8烷基，C 1 -C 8烷氧基， C1-C8卤代烷基，C1-C8卤代烷氧基或二（C1-C8烷基）氨基。这些化合物和由其制备的杀虫组合物可用作防治昆虫，线虫和螨虫的植物保护剂。

2. 发明授权

US5567723A Miticidal hydrazine compounds and their intermediates 失效
标题翻译：杀螨肼化合物及其中间体
公开(公告)号：US5567723A
公开(公告)日：1996-10-22
申请号：US498102
申请日：1995-07-05
申请人： Mark A. Dekeyser , Derek J. McPhee , Paul T. McDonald
发明人： Mark A. Dekeyser , Derek J. McPhee , Paul T. McDonald
IPC分类号： A01N37/28 , A01N47/24 , C07C243/28 , C07C245/06 , C07C281/00 , C07C281/02 , C07D213/42 , C07D277/28 , C07D333/20 , C07D213/02 , A01N33/26 , A01N43/40 , C07C243/24
CPC分类号： C07D213/42 , A01N47/24 , C07C281/00 , C07C281/02 , C07D277/28 , C07D333/20 , C07C2103/18
摘要： Compounds having the structural formula ##STR1## wherein R is C.sub.1 -C.sub.6 alkoxy or C.sub.1 -C.sub.6 alkyl; R.sup.1 is fluorenyl, thienyl, pyridyl or thiazolyl, unsubstituted or substituted by one or more substituents selected from C.sub.1 -C.sub.4 alkoxy, C.sub.1 -C.sub.4 alkyl, C.sub.1 -C.sub.4 alkylthio, halogen, C.sub.1 -C.sub.4 haloalkyl and nitro; and R.sup.2 is C.sub.1 -C.sub.6 alkyl, C.sub.3 -C.sub.6 cycloalkyl, C.sub.1 -C.sub.6 haloalkyl, C.sub.2 -C.sub.6 alkenyl, or C.sub.2 -C.sub.6 alkoxyalkyl. The compounds of this invention are effective for controlling mites and nematodes.
摘要翻译：具有结构式（I）或（II）的化合物，其中R是C 1 -C 6烷氧基或C 1 -C 6烷基; R1是未取代的或被一个或多个选自C 1 -C 4烷氧基，C 1 -C 4烷基，C 1 -C 4烷硫基，卤素，C 1 -C 4卤代烷基和硝基的取代基取代的芴基，噻吩基，吡啶基或噻唑基。和R 2是C 1 -C 6烷基，C 3 -C 6环烷基，C 1 -C 6卤代烷基，C 2 -C 6烯基或C 2 -C 6烷氧基烷基。本发明的化合物可有效控制螨虫和线虫。

3. 发明授权

US5543404A Pesticidal phenylhydrazinephosphates 失效
标题翻译：杀虫剂苯基肼基磷酸盐
公开(公告)号：US5543404A
公开(公告)日：1996-08-06
申请号：US498556
申请日：1995-07-05
申请人： Mark A. Dekeyser , Paul T. McDonald
发明人： Mark A. Dekeyser , Paul T. McDonald
IPC分类号： A01N57/30 , C07F9/24 , C07C243/10 , C07C245/02
CPC分类号： C07F9/2491 , A01N57/30
摘要： Compounds having the formula: ##STR1## wherein R is C.sub.1 -C.sub.4 alkoxy, C.sub.1 -C.sub.4 alkyl, hydrogen, halogen, or C.sub.1 -C.sub.4 alkylthio; R.sup.1 is phenyl, phenoxy, or benzyl, the phenyl ring of each substituent being optionally substituted with one or more of halogen, nitro, C.sub.1 -C.sub.4 alkyl, C.sub.1 -C.sub.4 alkoxy, C.sub.1 -C.sub.4 haloalkyl or di(C.sub.1 -C.sub.4 alkyl)amino; and R.sup.2 is branched or straight-chained, C.sub.1 -C.sub.6 alkyl, C.sub.1 -C.sub.6 alkoxy, C.sub.3 -C.sub.6 cycloalkoxy, C.sub.1 -C.sub.6 haloalkyl, alkoxyalkyl, C.sub.1 -C.sub.6 alkenyl, C.sub.1 -C.sub.6 alkylthio, (C.sub.1 -C.sub.6 alkoxy)carbonyl, C.sub.1 -C.sub.6 alkylamino, C.sub.1 -C.sub.6 haloalkoxy, or C.sub.3 -C.sub.6 cycloalkyl. These compounds are effective for controlling mites.
摘要翻译：具有下式的化合物：其中R是C 1 -C 4烷氧基，C 1 -C 4烷基，氢，卤素或C 1 -C 4烷硫基; R1是苯基，苯氧基或苄基，每个取代基的苯环任选被一个或多个卤素，硝基，C 1 -C 4烷基，C 1 -C 4烷氧基，C 1 -C 4卤代烷基或二（C 1 -C 4烷基）氨基 ; C1-C6烷氧基，C3-C6环烷氧基，C1-C6卤代烷基，烷氧基烷基，C1-C6烯基，C1-C6烷硫基，（C1-C6烷氧基）羰基，C1 -C6烷基氨基，C1-C6卤代烷氧基或C3-C6环烷基。这些化合物对控制螨有效。

4. 发明授权

US5486533A Fungicidal substituted azole derivatives 失效
标题翻译：杀真菌剂取代唑衍生物
公开(公告)号：US5486533A
公开(公告)日：1996-01-23
申请号：US443632
申请日：1995-05-18
申请人： Anupama Mishra , Robert A. Davis
发明人： Anupama Mishra , Robert A. Davis
IPC分类号： A01N43/50 , A01N43/653 , C07C15/44 , C07C17/16 , C07C22/04 , C07C25/24 , C07C43/166 , C07C43/215 , C07C205/06 , C07C321/28 , C07C323/07 , C07C323/12 , C07C323/16 , C07D233/60 , C07D249/08 , C07D521/00
CPC分类号： C07D231/12 , A01N43/50 , A01N43/653 , C07C15/44 , C07C17/16 , C07C205/06 , C07C22/04 , C07C25/24 , C07C321/28 , C07C323/07 , C07C323/12 , C07C323/16 , C07C43/166 , C07C43/215 , C07D233/56 , C07D249/08
摘要： Compounds having the structural formula ##STR1## wherein: R can be the same or different and is halogen, hydrogen, C.sub.1 -C.sub.8 alkyl, C.sub.1 -C.sub.8 haloalkyl, C.sub.3 -C.sub.6 cycloalkyl, C.sub.7 -C.sub.9 aralkyl, phenyl, nitro, C.sub.1 -C.sub.6 alkoxy, C.sub.1 -C.sub.6 alkylthio, C.sub.1 -C.sub.6 alkylsulfinyl, C.sub.1 -C.sub.6 alkylsulfonyl, C.sub.7 -C.sub.9 aralkoxy, phenoxy, phenylthio, phenylsulfinyl, or phenylsulfonyl;m is an integer from 0 to 5;Y is CH.sub.2, oxygen, or sulfur;n is an integer from 0 to 5;R.sub.1 is C.sub.1 -C.sub.5 alkyl, phenyl, C.sub.1 -C.sub.5 alkyl substituted phenyl, or halogenated phenyl;X is N or CH; or physiologically acceptable salts thereof are disclosed which have fungicidal activity. Fungicidal compositions comprising the compounds and a carrier are also disclosed, as are methods for controlling the growth of phytopathogenic fungi utilizing the compounds. Methods for the preparation of such compounds are also disclosed.
摘要翻译：具有结构式的化合物其中：R可以相同或不同，为卤素，氢，C1-C8烷基，C1-C8卤代烷基，C3-C6环烷基，C7-C9芳烷基，苯基，硝基，C1- C 1 -C 6烷氧基，C 1 -C 6烷硫基，C 1 -C 6烷基亚磺酰基，C 1 -C 6烷基磺酰基，C 7 -C 9芳烷氧基，苯氧基，苯硫基，苯基亚磺酰基或苯磺酰基; m是0至5的整数; Y是CH 2，氧或硫; n为0〜5的整数， R 1是C 1 -C 5烷基，苯基，C 1 -C 5烷基取代的苯基或卤代苯基; X为N或CH; 或其生理上可接受的盐，其具有杀真菌活性。还公开了包含化合物和载体的杀真菌组合物，以及利用该化合物控制植物病原真菌生长的方法。还公开了制备这些化合物的方法。

5. 发明授权

US5134145A Pesticidal pyrimidinyl benzoic acids and esters 失效
标题翻译：杀虫剂吡咯烷酮苯甲酸和酯
公开(公告)号：US5134145A
公开(公告)日：1992-07-28
申请号：US438913
申请日：1989-11-17
申请人： Walter G. Brouwer , Ethel E. Felauer , Paul T. McDonald
发明人： Walter G. Brouwer , Ethel E. Felauer , Paul T. McDonald
IPC分类号： A01N43/54 , C07D239/54 , C07D239/553 , C07D239/56
CPC分类号： C07D239/54 , A01N43/54 , C07D239/56
摘要： This invention is related to a novel class of aryl pyrimidine derivatives having insecticidal, miticidal and nematocidal activity at low concentration. The class of compounds is represented by formula (I): ##STR1## wherein R.sup.1, R.sup.2, R.sup.3, R.sup.4, R.sup.5, R.sup.6, X and Z have the significance given in the description.Pesticidal compositions, methods of controlling pests and methods for preparing the compounds are within the scope of the invention.
摘要翻译：本发明涉及一种新型的具有低浓度杀虫，杀螨和杀线虫活性的芳基嘧啶衍生物。化合物的类别由式（I）表示：其中R 1，R 2，R 3，R 4，R 5，R 6，X和Z具有在说明书中给出的含义。杀虫剂组合物，防治害虫的方法和制备化合物的方法在本发明的范围内。

6. 发明授权

US5134144A Pesticidal 3-arylpyrimidinyl ethers and thioethers 失效
标题翻译：杀虫剂3-ARYLPYRIMIDINYLETHERS和THIOETHERS
公开(公告)号：US5134144A
公开(公告)日：1992-07-28
申请号：US439732
申请日：1989-11-20
申请人： Walter G. Brouwer , Ethel E. Felauer , Paul T. McDonald , James A. McGuinness , Anupama Mishra
发明人： Walter G. Brouwer , Ethel E. Felauer , Paul T. McDonald , James A. McGuinness , Anupama Mishra
IPC分类号： A01N43/54 , C07D239/54 , C07D239/56
CPC分类号： C07D239/54 , A01N43/54 , C07D239/56
摘要： This invention is related to a novel class of 3-arylpyrimidine ethers and thioethers having insecticidal, miticidal and nematocidal activity at low concentration. The class of compounds is represented by formula (I): ##STR1## wherein R.sup.1, R.sup.2, R.sup.3, R.sup.4, R.sup.5, R.sup.6, R.sup.7, X and Y have the significance given in the description.Pesticidal compositions, methods of controlling pests and methods for preparing the compounds are within the scope of the invention.
摘要翻译：本发明涉及一种新型的3-芳基嘧啶醚和硫醚，其具有低浓度的杀虫，杀螨和杀线虫活性。化合物类由式（I）表示：其中R 1，R 2，R 3，R 4，R 5，R 6，R 7，X和Y具有在说明书中给出的含义。杀虫剂组合物，防治害虫的方法和制备化合物的方法在本发明的范围内。

7. 发明授权

US5010068A Oxadiazinyl organophosphorus pesticides 失效
标题翻译：恶二嗪基有机磷杀虫剂
公开(公告)号：US5010068A
公开(公告)日：1991-04-23
申请号：US454668
申请日：1989-12-21
申请人： Mark A. Dekeyser , Richard C. Moore
发明人： Mark A. Dekeyser , Richard C. Moore
IPC分类号： A01N57/16 , A01N57/24 , C07D273/04 , C07F9/6533
CPC分类号： A01N57/24 , A01N57/16 , C07D273/04 , C07F9/6533
摘要： Organophosphorus-substituted oxadiazines are disclosed which exhibit insecticidal, acaricidal and nematicidal activity, as well as compositions including such compounds, and methods for controlling insects, acarids or nematodes employing such compounds and/or compositions. Also disclosed are novel intermediates useful in the preparation of such compounds.
摘要翻译：公开了显示杀虫，杀螨和杀线虫活性的有机磷取代的恶二嗪，以及包含这些化合物的组合物，以及使用这种化合物和/或组合物来控制昆虫，螨虫或线虫的方法。还公开了可用于制备这些化合物的新型中间体。

8. 发明授权

US4950671A Substituted 2-propenyl derivatives of pyridine 失效
标题翻译：吡啶的取代的2-丙烯基衍生物
公开(公告)号：US4950671A
公开(公告)日：1990-08-21
申请号：US321028
申请日：1989-03-09
申请人： Hoi Kiong Lai , Robert A. Davis
发明人： Hoi Kiong Lai , Robert A. Davis
IPC分类号： C07D209/08 , A01N43/36 , A01N43/38 , A01N43/40 , A01N43/42 , A01N43/84 , C07D207/06 , C07D211/14 , C07D211/18 , C07D211/22 , C07D215/06 , C07D217/02 , C07D265/30 , C07D295/02 , C07D295/03 , C07D295/06 , C07D295/073 , C07D295/08 , C07D295/096
CPC分类号： C07D295/03 , A01N43/38 , A01N43/40 , A01N43/42 , A01N43/84 , C07D209/08 , C07D215/06 , C07D295/073 , C07D295/096
摘要： A heterocyclic compound having the structural formula ##STR1## where R is C.sub.1 -C.sub.8 alkyl, C.sub.3 -C.sub.6 cycloalkyl, trifluoromethyl, phenyl, substituted phenyl, phenoxy, substituted phenoxy, benzyl or substituted benzyl; and R.sup.1 is at least a partially saturated monocyclic or bicyclic heterocycle of nitrogen which may be substituted with lower alkyl and physiologically acceptable salts thereof is disclosed. A process for forming this compound which involves the reaction of an amine of the formula HR.sup.1 where R.sup.1 has the meanings given above with a substituted 2-propenyl halide having the structural formula ##STR2## where R has the meanings given above; and X is a halogen atom is described. The invention embodies the above-mentioned novel 2-propenyl halide utilized as an intermediate in the formation of the heterocyclic compound of this invention. A method ofcontrolling phytopathogenic fungi by applying a fungicidally effective amount of the heterocyclic compound of the present invention to the locus under attack by said fungi is also taught. Finally, a fungicidally composition comprising the heterocyclic compound of the present invention and a suitable carrier therefor is set forth.
摘要翻译：其中R是C1-C8烷基，C3-C6环烷基，三氟甲基，苯基，取代的苯基，苯氧基，取代的苯氧基，苄基或取代的苄基的结构式的杂环化合物。并且R 1是至少部分饱和的单环或双环氮杂环，其可被低级烷基和其生理上可接受的盐所取代。形成该化合物的方法，其涉及式为HR1的胺，其中R1具有上述含义的结构式为：其中R具有上述含义的取代的2-丙烯基卤化物; 并且X是卤素原子。本发明体现了用作本发明的杂环化合物形成中间体的上述新型2-丙烯基卤化物。还教导了通过将杀真菌有效量的本发明的杂环化合物施用于被所述真菌攻击的场所来控制植物致病真菌的方法。最后，提出了包含本发明的杂环化合物和其合适的载体的杀真菌组合物。

9. 发明授权

US5693827A Treatment of HIV infections and compounds useful therein 失效
标题翻译：治疗艾滋病毒感染及其中有用的化合物
公开(公告)号：US5693827A
公开(公告)日：1997-12-02
申请号：US485291
申请日：1995-06-07
申请人： William Ashley Harrison , Gary Edward Jewell , Ethel Ellen Felauer , Mark Achiel Dekeyser , Dong Dao-Cong , James Anthony McGuiness , Anupama Mishra , Walter Gerhard Brouwer , Derek James McPhee
发明人： William Ashley Harrison , Gary Edward Jewell , Ethel Ellen Felauer , Mark Achiel Dekeyser , Dong Dao-Cong , James Anthony McGuiness , Anupama Mishra , Walter Gerhard Brouwer , Derek James McPhee
IPC分类号： A61K31/075 , A61K31/00 , A61K31/05 , A61K31/10 , A61K31/11 , A61K31/12 , A61K31/13 , A61K31/15 , A61K31/18 , A61K31/215 , A61K31/255 , A61K31/33 , A61K31/335 , A61K31/341 , A61K31/351 , A61K31/38 , A61K31/382 , A61K31/39 , A61K31/40 , A61K31/41 , A61K31/42 , A61K31/421 , A61K31/4245 , A61K31/66 , A61P31/12 , A61P31/18 , C07C229/54 , C07C233/54 , C07C233/55 , C07C233/63 , C07C233/64 , C07C233/65 , C07C233/80 , C07C233/81 , C07C233/87 , C07C257/10 , C07C261/04 , C07C271/06 , C07C271/28 , C07C271/38 , C07C275/28 , C07C281/06 , C07C281/16 , C07C311/51 , C07C311/57 , C07C327/16 , C07C327/22 , C07C333/08 , C07C337/06 , C07D207/34 , C07D209/42 , C07D261/18 , C07D263/34 , C07D271/02 , C07D277/06 , C07D279/12 , C07D305/06 , C07D307/12 , C07D307/36 , C07D307/42 , C07D307/68 , C07D309/20 , C07D309/28 , C07D319/12 , C07D327/06 , C07D333/28 , C07D333/38 , C07D339/08 , C07D413/12 , C07F9/24 , C07F9/38 , C07F9/40 , C07F9/655 , C07F9/6553
CPC分类号： C07D263/34 , A61K31/00 , A61K31/33 , C07C233/54 , C07C233/55 , C07C233/63 , C07C233/81 , C07C271/28 , C07C271/38 , C07C327/22 , C07D209/42 , C07D277/06 , C07D305/06 , C07D307/12 , C07D307/42 , C07D307/68 , C07D309/28 , C07D319/12 , C07D327/06 , C07D333/28 , C07D339/08 , C07F9/2475 , C07F9/3808 , C07F9/4006 , C07F9/6552 , C07C2101/14
摘要： A method of inhibiting the growth or replication of viruses of the HIV group is disclosed. Also disclosed are compounds useful in the method and pharmaceutical formulations incorporating such compounds. The method involves the use of compounds having the general formula: ##STR1## wherein the substituent groups are as defined in the specification.
摘要翻译：公开了抑制HIV组病毒生长或复制的方法。还公开了可用于该方法的化合物和掺入这种化合物的药物制剂。该方法包括使用具有以下通式的化合物：其中取代基如说明书中所定义。

10. 发明授权

US5656169A Biodegradation process for de-toxifying liquid streams 失效
标题翻译：用于去除液体流的生物降解过程
公开(公告)号：US5656169A
公开(公告)日：1997-08-12
申请号：US693692
申请日：1996-08-06
申请人： Andrew Jerry Lugowski , Garry Allen Palmateer , Timothy Richard Boose , Jeffrey Edward Merriman
发明人： Andrew Jerry Lugowski , Garry Allen Palmateer , Timothy Richard Boose , Jeffrey Edward Merriman
IPC分类号： C02F3/34
CPC分类号： C02F3/34 , Y10S210/908 , Y10S210/909 , Y10S435/874
摘要： A biological degradation process is disclosed. The biological gradation process utilizes a unique thermophilic aerobic bacterial mixture capable of converting, biologically or via oxidation, aqueous and other liquid streams containing substances that are ordinarily considered toxic to conventional biological systems. Substances ordinarily considered toxic to conventional biological systems, but which nevertheless are converted by the thermophilic aerobic bacterial mixture, include aniline; benzothiazole; 5,6-dihydro-2-methyl-N-phenyl-1,4-oxathiin-3-carboxamide; lindane (technically known as 1.alpha.,2.alpha.,3.beta.,4.alpha.,5.alpha.,6.beta.-hexachlorocyclohexane); 2-mercaptobenzothiazole; toluene; and combinations thereof. The unique thermophilic aerobic bacterial mixture comprises relative effective amounts of Pseudomonas stutzeri, Pseudomonas aeruginosa, Pseudomonas fluorescens, Pseudomonas mendocina and Alcaligenes denitrificans subsp. xylosoxydans. A biological degradation process for treating the liquid stream containing substances ordinarily considered toxic comprises contacting the stream with the thermophilic aerobic bacterial mixture, for an amount of time that is effective for de-toxifying the stream.
摘要翻译：公开了生物降解过程。生物分级过程利用独特的嗜热好氧细菌混合物，其能够生物地或通过氧化，水性和其它液体流转化，其含有通常被认为对常规生物系统有毒的物质。通常认为对常规生物系统有毒的物质，但是由嗜热好氧细菌混合物转化的物质包括苯胺; 苯并噻唑; 5,6-二氢-2-甲基-N-苯基-1,4-氧硫杂环己烯-3-甲酰胺; 林丹（技术上称为1α，2α，3β，4α，5α，6β-六氯环己烷）; 2-巯基苯并噻唑; 甲苯; 及其组合。独特的嗜热好氧细菌混合物包括相对有效量的铜绿假单胞菌，铜绿假单胞菌，荧光假单胞菌，门氏假单胞菌和产碱假单胞菌亚硝酸盐亚种。 xylosoxydans。用于处理含有通常被认为是毒性的物质的液体物流的生物降解方法包括使该物流与嗜热好氧细菌混合物接触一段有效去除毒素流的时间。

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