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1. 发明授权

US11564394B2 Distorted gold (I)-phosphine complexes and and methods for use as antifungal agents 有权
公开(公告)号：US11564394B2
公开(公告)日：2023-01-31
申请号：US17118328
申请日：2020-12-10
申请人： University of Kentucky Research Foundation
发明人： Sylvie Garneau-Tsodikova , Emily K Dennis , Jong Hyun Kim , Samuel G. Awuah
IPC分类号： A01N57/36 , C07F9/50 , C07F9/6568
摘要： The presently-disclosed subject matter describes distorted gold (I) phosphine compounds. The presently-disclosed subject matter also describes a method for killing fungus comprising contacting fungus with distorted gold (I) phosphine compounds. The presently-disclosed subject matter further describes a method of preventing or disrupting a biofilm on a surface comprising contacting a surface with distorted gold (I) phosphine compounds.

2. 发明申请

US20140171644A1 SUBSTITUTED PHENOXYETHYL (ISOPROPYL) ACYLOXYALKYL PHOSPHONATE COMPRISING PHOSPHORUSHETEROCYCLIC RING AND HAVING HERBICIDAL ACTIVITY, AND PREPARATION THEREFOR 有权
标题翻译：取代的含有磷杂环戊烯的环氧乙烷（异丙基）乙酰氧基磷酸酯，并具有除草活性及其制备方法
公开(公告)号：US20140171644A1
公开(公告)日：2014-06-19
申请号：US14185721
申请日：2014-02-20
申请人： CENTRAL CHINA NORMAL UNIVERSITY
发明人： Hongwu He , Wei Wang , Na Zuo , Xijun Sheng , Hao Peng , Xiaosong Tan
IPC分类号： A01N57/36
CPC分类号： A01N57/36 , C07F9/657118 , C07F9/65742 , C07F9/65748
摘要： A substituted phenoxyethyl(isopropyl)acyloxyalkyl phosphonate having phosphorusheterocyclic ring and having herbicidal activity, with a general formula of I, wherein R represents 5,5-dimethyl-1,3,2-dioxaphosphorinan-2-one-2-yl, or 1-oxo-1-phospha-2,6,7-trioxabicyclo[2,2,2]octan-4-yl, or 1-sulfo-1-phospha-2,6,7-trioxabicyclo 2,6,7-trioxabicyclo[2,2,2]octan-4-yl; R1 represents H, C1-C4 alkyl, phenyl, furyl, pyridyl, or phenyl substituted with methyl, methoxyl, nitro or chloro; R2 represents H, methyl, and methyl only if R in the general formula I is 1-sulfo-1-phospha-2,6,7-trioxabicyclo[2,2,2]octan-4-yl as phosphorusheterocyclic ring; X and Y represent H, halogen, C1-C4 alkyl or trifluoromethyl, and X and Y are the same or different. The compounds according to the present invention may be used as active component of dicotyledonous broadleaf weed herbicides.
摘要翻译：具有磷杂环并具有除草活性的取代的苯氧基乙基（异丙基）酰氧基烷基膦酸酯，具有通式I，其中R表示5,5-二甲基-1,3,2-二氧杂磷杂环己烷-2-酮-2-基或1 - 氧代-1-磷杂-2,6,7-三氧杂双环[2,2,2]辛-4-基或1-磺基-1-磷杂-2,6,7-三氧杂双环2,6,7-三氧杂双环 [2,2,2]辛-4-基; R 1表示H，C 1 -C 4烷基，苯基，呋喃基，吡啶基或被甲基，甲氧基，硝基或氯取代的苯基; 只有通式Ⅰ中的R是作为磷杂环的1-磺基-1-磷杂-2,6,7-三氧杂双环[2,2,2]辛-4-基，R2表示H，甲基和甲基。 X和Y表示H，卤素，C 1 -C 4烷基或三氟甲基，X和Y相同或不同。根据本发明的化合物可以用作双子叶阔叶杂草除草剂的活性组分。

3. 发明申请

US20100168066A1 NOVEL INSECTICIDES 有权
标题翻译：新型杀虫剂
公开(公告)号：US20100168066A1
公开(公告)日：2010-07-01
申请号：US12160794
申请日：2007-01-15
申请人： Michel Muehlebach , Andre Jeanguenat , Roger Graham Hall
发明人： Michel Muehlebach , Andre Jeanguenat , Roger Graham Hall
IPC分类号： A01N43/56 , C07D409/14 , C07D401/14 , C07D405/14 , C07D401/04 , A01N57/36 , C07F9/6584 , A01P7/02
CPC分类号： A01N43/56 , C07D331/04 , C07D401/12 , C07D401/14 , C07D403/12 , C07D403/14 , C07D405/12 , C07D405/14 , C07D409/12 , C07D409/14 , C07F9/65681
摘要： Compounds of formula (I) wherein the substituents are as defined in claim (1), and the agrochemically acceptable salts and all stereoisomers and tautomeric forms of the compounds of formula (I) can be used as agrochemical active ingredients and can be prepared in a manner known per se.
摘要翻译：式（I）化合物，其中取代基如权利要求（1）中所定义，以及式（I）化合物的农业化学上可接受的盐和所有立体异构体和互变异构体形式可以用作农业化学活性成分，并且可以在本身已知的方式。

4. 发明授权

US07326695B2 Anti-bacterial agents based upon oxoanion binding 失效
标题翻译：基于氧阴离子结合的抗菌剂
公开(公告)号：US07326695B2
公开(公告)日：2008-02-05
申请号：US11435978
申请日：2006-05-17
申请人： Stephen R. Cooper , Kraig M. Yager
发明人： Stephen R. Cooper , Kraig M. Yager
IPC分类号： A01N55/08 , A01N57/36 , A01N43/82 , A01N43/78 , A01N43/80 , A01N43/06 , A01N43/26
CPC分类号： A61K31/381 , A01N43/26 , A01N43/82 , A01N43/90 , A01N55/00 , A01N57/36 , A61K31/38 , A61K31/425 , A61K31/66 , A61K31/69
摘要： Compounds of the structure I: are useful for treating bacterial growth, wherein E is selected from the group consisting of B, P, and S, T1 and T2 are each independently selected from the group consisting of O, NR, and CH2, where R=H or C1-C8 alkyl, or C1-C8 oxoalkyl, and L is selected from the group consisting of ethylene, propylene, and four to six-membered alicyclic and aromatic rings, provided that structure I does not include AI-2-borate. The compounds may be used to treat bacterial infections in human beings and to regulate biofilm formation. Pharmaceutical compositions comprising one or more such compounds are useful for treating bacterial infections in human beings.
摘要翻译：结构I的化合物可用于治疗细菌生长，其中E选自B，P和S，T 1和T 2各自为独立地选自O，NR和CH 2，其中R = H或C 1 -C 8烷基，或C 1个C 1 -C 8氧代烷基，L选自乙烯，丙烯和四至六元脂环和芳环，条件是结构I不包括AI-2-硼酸盐。该化合物可用于治疗人类的细菌感染并调节生物膜形成。包含一种或多种这样的化合物的药物组合物可用于治疗人类的细菌感染。

5. 发明授权

US5922644A Triazole phosphonic acid derivatives and their use as herbicides 失效
标题翻译：三唑膦酸衍生物及其作为除草剂的用途
公开(公告)号：US5922644A
公开(公告)日：1999-07-13
申请号：US314481
申请日：1994-09-28
申请人： John Michael Cox , Peter Bellini , Roger Barrett , Russell Martin Ellis , Timothy Robert Hawkes
发明人： John Michael Cox , Peter Bellini , Roger Barrett , Russell Martin Ellis , Timothy Robert Hawkes
IPC分类号： A01N57/24 , A01N57/36 , C07D249/08 , C07F9/40 , C07F9/6518 , C07F9/6571
CPC分类号： C07D249/08 , A01N57/24 , C07F9/4015 , C07F9/65182 , C07F9/657181
摘要： A herbicidal compound of formula (I) ##STR1## or a salt, tautomer or cyclic derivative thereof; where R.sup.1 and R.sup.2 are hydrogen and A is an optionally substituted saturated or unsaturated chain or ring of three carbon atoms.Methods for preparing these compounds, intermediates used in the preparation and herbicidal compositions containing them are also described and claimed.
摘要翻译：式（I）的除草化合物或其盐，互变异构体或环状衍生物; 其中R 1和R 2是氢并且A是任选取代的具有三个碳原子的饱和或不饱和链或环。还描述和要求保护制备这些化合物的方法，用于制备的中间体和含有它们的除草组合物。

6. 发明授权

US5162327A Pyrimidinetrione derivatives, agents containing them and their use as agents for combating pests 失效
标题翻译：衍生物衍生物，包含它们的试剂及其用作组合物的试剂
公开(公告)号：US5162327A
公开(公告)日：1992-11-10
申请号：US474379
申请日：1990-02-02
申请人： Gunter Kratt , Gerhard Salbeck , Werner Bonin , Dieter Duwel
发明人： Gunter Kratt , Gerhard Salbeck , Werner Bonin , Dieter Duwel
IPC分类号： C07D239/557 , A01N43/54 , A01N57/36 , C07C217/84 , C07C265/12 , C07C323/36 , C07D239/54 , C07D239/545 , C07D239/553 , C07D239/60 , C07D239/62 , C07D319/12 , C07D401/12 , C07D403/12 , C07D405/12 , C07F9/6584
CPC分类号： C07D239/545 , A01N43/54 , C07C217/84 , C07C265/12 , C07C323/36 , C07D239/62 , C07D401/12
摘要： Pyrimidinetrione derivatives, processes for their preparation, agents containing them and their use as agents for combating pests.Compounds of the formula I, tautomeric forms thereof of the formula Ia, stereoisomers thereof and the mixtures of these forms ##STR1## wherein R.sup.1 and R.sup.2 denote unsubstituted or substituted alkyl, alkenyl, alkynyl; alkoxy, alkylsulfonyl, alkylcarbonyl or cyano or optionally substituted phenyl, phenylsulfonyl or phenylcarbonyl,R.sup.3 denotes hydrogen, alkyl or optionally substituted phenyl,R.sup.4 denote H, OH, unsubstituted or substituted alkyl, alkenyl, alkynyl, phenylsulfonyl, phenylcarbonyl, phenylcarbamoyl or phenyl; alkylsulfonyl or alkylcarbonyl, which can be halogenated, alkylcarbamoyl or cyano,R.sup.5 and R.sup.6 denote halogen, alkoxy, alkylcarbonyl, alkoxycarbonyl, alkylsulfenyl, -sulfinyl or -sulfonyl, haloalkoxy, alkylamino, cyano, sulfo or nitro,A,X,Z and L denote oxygen, sulfur, sulfinyl, sulfonyl or nitrogen, which can be substituted by alkyl, or L denotes a double bond,M,D,E,Q and G denote carbon or nitrogen,V denotes carbon or substituted phosphorus,W denotes alkylene or haloalkylene, both of which can be substituted,Y.sup.1 denotes H, halogen, alkyl, alkylamino or hydroxyl,Y.sup.2 denotes oxygen, sulfur or nitrogen which is optionally substituted by alkyl andn amd m denote 0-4, and salts thereof which can be employed in agriculture or are physiologically tolerated, have advantageous actions against a broad spectrum or animal pests in agriculture and animal breeding.
摘要翻译：嘧啶四酮衍生物，其制备方法，含有它们的试剂及其作为防治害虫的试剂的用途。（Ⅰ）的化合物，式Ia的互变异构体，其立体异构体和这些形式的混合物，其中R 1和R 2表示未取代或取代的烷基，烯基，炔基; 烷氧基，烷基磺酰基，烷基羰基或氰基或任选取代的苯基，苯基磺酰基或苯基羰基，R 3表示氢，烷基或任选取代的苯基，R 4表示H，OH，未取代或取代的烷基，烯基，炔基，苯基磺酰基，苯基羰基，苯基氨基甲酰基或苯基; 烷基磺酰基或烷基羰基，其可以被卤化，烷基氨基甲酰基或氰基，R5和R6表示卤素，烷氧基，烷基羰基，烷氧基羰基，烷基亚磺酰基， - 亚磺酰基或 - 磺酰基，卤代烷氧基，烷基氨基，氰基，磺基或硝基，A，X，Z和L 表示可被烷基取代的氧，硫，亚磺酰基，磺酰基或氮，或L表示双键，M，D，E，Q和G表示碳或氮，V表示碳或取代的磷，W表示亚烷基或卤代亚烷基，它们都可以被取代，Y1表示H，卤素，烷基，烷基氨基或羟基，Y2表示氧，硫或氮，任选被烷基取代，n表示0-4，可以使用其盐在农业中或具有生理上的耐受性，对农业和动物育种中的广谱或动物害虫具有有利的作用。

7. 发明授权

US5082832A Novel cyclopropane carboxylates 失效
标题翻译：新型环丙基羧酸酯
公开(公告)号：US5082832A
公开(公告)日：1992-01-21
申请号：US423803
申请日：1989-10-18
申请人： Joseph Cadiergue , Jean-Pierre Demoute , Jean Tessier
发明人： Joseph Cadiergue , Jean-Pierre Demoute , Jean Tessier
IPC分类号： C07C69/74 , A01N53/00 , A01N53/02 , A01N53/04 , A01N53/06 , A01N53/08 , A01N55/00 , A01N57/12 , A01N57/14 , A01N57/36 , A23K1/16 , A61K31/215 , A61K31/23 , C07C51/377 , C07C61/40 , C07C62/02 , C07C67/00 , C07C67/317 , C07C69/63 , C07C69/65 , C07C69/743 , C07C69/757 , C07C69/76 , C07C253/00 , C07C253/30 , C07C255/10 , C07C255/31 , C07C255/53 , C07C301/00 , C07C303/28 , C07C303/30 , C07C309/63 , C07C309/64 , C07C309/65 , C07C309/66 , C07C309/70 , C07C309/72 , C07C309/73 , C07C317/04 , C07C317/14 , C07D209/48 , C07D209/49 , C07D213/30 , C07D213/57 , C07D213/64 , C07D213/647 , C07D213/65 , C07D213/68 , C07D233/64 , C07D233/72 , C07D307/42 , C07D307/45 , C07D309/38 , C07D317/24 , C07F9/09 , C07F9/117 , C07F9/177 , C07F9/38 , C07F9/40 , C07F9/58 , C07F9/655 , C07F9/6574
CPC分类号： C07D213/647 , A01N53/00 , A01N55/00 , A01N57/14 , A01N57/36 , A23K20/00 , C07C309/00 , C07C309/65 , C07C309/66 , C07C309/72 , C07C61/40 , C07C69/757 , C07D317/24 , C07F9/117 , C07F9/177 , C07F9/581 , C07F9/65502 , C07F9/65742 , C07C2101/02
摘要： Novel 2,2-dimethyl-cyclopropane carboxylic acid derivatives of the formula ##STR1## wherein X.sub.1 and X.sub.2 are individually halogen, R.sub.1 is selected from the group consisting of halogen, alkyl of 1 to 8 carbon atoms, optionally substituted aryl of 6 to 14 carbon atoms, perfluoroalkyl of 1 to 8 carbon atoms, --CN and ##STR2## R' is alkyl of 1 to 8 carbon atoms, Y is selected from the group consisting of ##STR3## Alk.sub.1 is optionally unsaturated alkyl of 1 to 8 carbon atoms no substituted or substituted with at least one functional group, Ar is aryl of 6 to 14 carbon atoms no substituted or substituted with at least one functional group, Alk.sub.2 and Alk.sub.3 and Alk.sub.2 ' and Alk.sub.3 ' are optionally unsaturated alkyl of 1 to 8 carbon atoms no substituted or substituted with at least one functional group or together with ##STR4## form the rings ##STR5## wherein A is optionally unsaturated alkyl of 1 to 6 carbon atoms optionally substituted with at least one functional group, R" is alkyl of 1 to 6 carbon atoms no substituted or substituted with at least one functional group or aryl of 6 to 14 carbon atoms no substituted or substituted with at least one functional group and R is selected from the group consisting of hydrogen, alkyl of 1 to 8 carbon atoms and residue of an alcohol used in pyrethrinoid esters having pestioidal activity.

8. 发明授权

US4889906A Amine salts of 1,4,2-oxazaphospholidine-4-acetic acid, 2-alkoxy-2-oxides 失效
标题翻译： 1,4-二氧杂磷杂环丁烷-4-乙酸，2-烷氧基-2-氧化物的胺盐
公开(公告)号：US4889906A
公开(公告)日：1989-12-26
申请号：US276009
申请日：1988-11-25
申请人： Donald L. Fields, Jr. , Raymond C. Grabiak
发明人： Donald L. Fields, Jr. , Raymond C. Grabiak
IPC分类号： A01N57/36 , C07F9/6584
CPC分类号： A01N57/36 , C07F9/6584
摘要： The compounds 1,4,2-oxazaphospholidine-4-acetic acid, 2-alkoxy-2-oxides and their trialkylamine salts represented by the formula ##STR1## wherein R.sup.1, R.sup.2, R.sup.3 and R.sup.4 are individually selected from the group consisting of alkyl having from one to about four carbon atoms are useful as post emergent, selective herbicides and plant growth regulators.

9. 发明授权

US4797484A Process for the preparation of N'-sulphonyl- and N',N"-bis-sulphonyl-guanidine derivatives 失效
标题翻译：制备N'-磺酰基和N'，N“ - 双磺酰基 - 胍衍生物的方法
公开(公告)号：US4797484A
公开(公告)日：1989-01-10
申请号：US5800
申请日：1987-01-16
申请人： Koichi Moriya , Theodor Pfister , Hans-Jochem Riebel , Ludwig Eue , Robert R. Schmidt , Klaus Lurssen
发明人： Koichi Moriya , Theodor Pfister , Hans-Jochem Riebel , Ludwig Eue , Robert R. Schmidt , Klaus Lurssen
IPC分类号： A01N43/48 , A01N47/44 , A01N51/00 , A01N55/10 , A01N57/26 , A01N57/32 , A01N57/36 , C07D213/75 , C07D239/42 , C07D239/46 , C07D239/47 , C07D239/69 , C07D251/18 , C07D251/26 , C07D251/46 , C07D405/12 , C07D409/12 , C07D413/12 , C07D521/00 , C07D213/62 , C07D215/16
CPC分类号： C07D239/42 , A01N47/44 , A01N51/00 , C07C309/00 , C07D239/47 , C07D251/46 , C07D409/12 , C07D521/00
摘要： A process for the preparation of a guanidine derivative of the formula ##STR1## in which R.sup.1 represents hydrogen or the radical R.sup.5 --S(O).sub.m --,m represents the numbers zero, 1 or 2 andR.sup.5 represents an optionally substituted radical from the series comprising alkyl, aralkyl, aryl and heteroaryl,R.sup.2 represents a six-membered aromatic heterocyclic structure which contains at least one nitrogen atom and is substituted, andR.sup.8 represents an optionally substituted radical from the series comprising C.sub.1 -C.sub.6 -alkyl, alkenyl, alkinyl, cycloalkyl, phenylalkyl and aryl,which comprises reacting a guanidine derivative of the formula ##STR2## with one or two molar equivalent(s), respectively, of a halogen/sulphur compound of the formulaR.sup.5 --S(O).sub.m --X.sup.1in whichX.sup.1 represents fluorine, chlorine or bromine.The compounds are herbicidally active.
摘要翻译：制备式“IMAGE”的胍衍生物的方法，其中R 1表示氢或基团R 5 -S（O）m - ，m表示数字0,1或2，R 5表示任选取代的基团，包含烷基，芳烷基，芳基和杂芳基的R 2代表含有至少一个氮原子并且被取代的六元芳族杂环结构，并且R 8代表包含C 1 -C 6 - 烷基，链烯基，炔基，环烷基，苯基烷基和芳基，其包括使式IMA图的胍衍生物分别与一个或两个摩尔当量的式R 5 -S（O）m -X 1的卤素/硫化合物反应，其中X1表示氟，氯或溴。这些化合物是除草活性的。

10. 依法登记的发明

USH563H Use of sulfur-containing compounds for controlling plant parasitic nematodes 失效
标题翻译：使用含硫化合物控制植物寄生线虫
公开(公告)号：USH563H
公开(公告)日：1989-01-03
申请号：US808199
申请日：1985-12-12
申请人： Terrence L. Kirkpatrick , Henry S. Yang
发明人： Terrence L. Kirkpatrick , Henry S. Yang
IPC分类号： A01N47/24 , A01N57/36
CPC分类号： A01N47/24 , A01N57/36
摘要： This invention relates to the use of sulfur-containing compounds for the control of plant parasitic nematodes by application of the compounds directly to seeds, seed pieces or root systems.

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