| 序号 | 专利名 | 申请号 | 申请日 | 公开（公告）号 | 公开（公告）日 | 发明人 |
|---|---|---|---|---|---|---|
| 21 | Catalysts containing per-ortho aryl substituted aryl or heteroaryl substituted nitrogen donors | US10990955 | 2004-11-18 | US20050090381A1 | 2005-04-28 | Leslie Moody; Peter Mackenzie; Christopher Killian; Gino Lavoie; James Ponasik; Thomas Smith; Jason Pearson; Anthony Gerard Barrett |
| Catalyst compositions useful for the polymerization of olefins are disclosed. These compositions comprise a Group 8-10 metal complex comprising a bidentate or variable denticity ligand comprising one or two nitrogen donor atom or atoms independently substituted by an aromatic or heteroaromafic ring(s), wherein the ortho positions of said ring(s) are substituted by aryl or heteroaryl groups. Also disclosed are processes for the polymerization of olefins using the catalyst compositions. | ||||||
| 22 | Novel tetrazolinone derivatives | US10873357 | 2004-06-21 | US20040242895A1 | 2004-12-02 | Akihiko Yanagi; Shinichi Narabu; Toshio Goto; Seishi Ito; Chieko Ueno |
| The invention relates to novel tetrazolinone derivatives of general formula (I) wherein R1 represents halogen, C1-4 alkyl, C1-4 haloalkyl, C1-4 alkoxy, C1-4 alkylthio, C1-4 alkylsulfonyl, C1-4 alkylsulfonyloxy, C2-5 alkoxycarbonyl, C2-6 alkoxyalkyl, C2-6 alkylthioalkyl, nitro or cyano, R2 represents a hydrogen atom, C1-6 alkyl, C3-6 cycloalkyl which may be optionally substituted with halogen or C1-3 alkyl, C1-4 haloalkyl, or phenyl which may be optionally substituted with halogen, C1-3 alkyl, C1-3 haloalkyl or nitro, m represents 0, 1 or 2, n represents 0 or 1, Q represents one of the groups which are mentioned in the description. The invention further relates to their use as herbicides and a process together with the intermediates for their preparation. 1 | ||||||
| 23 | N-acyl-N-phenyltetrahydrophthalamic acid derivatives, methods of producing same, and herbicides containing same as effective components | US849063 | 1992-04-22 | US5292922A | 1994-03-08 | Tetsuo Takematsu; Takashi Kume; Takeo Komata; Kiyoshi Suzuki; Matsue Minezaki; Yumiko Shirakawa; Kaoru Mori |
| The invention provides N-acyl-N-phenyltetrahydrophthalamic acid derivatives represented by the general formula [I], methods of producing the same, and herbicides containing the same as the effective components, ##STR1## wherein X and Y each individually represent hydrogen atoms or halogen atoms, R.sup.1 represents a hydrogen atom, a halogen atom, a lower alkoxy group, a lower alkenyloxy group, a lower alkynyloxy group, a lower alkoxyalkoxy group or a lower alkoxycarbonylalkoxy group, R.sup.2 represents a lower alkyl group, a halogenated lower alkyl group, or a substituted or unsubstituted phenyl group, and R.sup.3 represents a lower alkoxy group, a lower alkenyloxy group, a lower alkynyloxy group, a lower alkoxyalkoxy group, a benzyloxy group or a lower alkoxycarbonylalkoxy group. The herbicides which are very useful can be widely applied to upland, paddy field, orchard, turf, forest, non-crop land, etc, and are not harmful to crops. | ||||||
| 24 | Novel immonium salts | US37217173 | 1973-06-21 | US3873530A | 1975-03-25 | VIEHE HEINZ GUNTER; VAN VYVE THERESE; JANOUSEK ZDENEK |
| WHEREIN R and R1 are individually selected from the group consisting of lower alkyl, phenyl optionally substituted with halogen and benzyl and taken together are selected from the group consisting of lower alkylene, -CH2-CH2-O-CH2-CH2- and
WHERE R4 is alkyl of 1 to 5 carbon atoms, R2 and R3 are individually selected from the group consisting of hydrogen, alkyl of 1 to 5 carbon atoms and phenyl and taken together are selected from the group consisting of alkylene of 3 to 5 carbon atoms and benzoalkylene of 7 to 10 carbon atoms, X is halogen and Y is selected from the group consisting of dilower alkylamino wherein the alkyl have 1 to 5 carbon atoms, morpholino, piperidino and 1-pyrrolidinyl. Novel intermediates useful for organic synthesis which are immonium salts of the formula |
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| 25 | 비에스티 전구체용 리간드의 합성 방법 및 이를 이용한유전막의 제조 방법 | KR1020070064594 | 2007-06-28 | KR1020090000491A | 2009-01-07 | 김윤수; 이익모; 조규호; 이동환; 박상언; 조민호; 김호섭 |
| A method of synthesizing ligands for a BST precursor is provided to improve the yield and selectivity of a ligand for a barium strontium titanate precursor while reducing the reaction time. A method of synthesizing ligands for a BST precursor comprises (S1) a step for manufacturing a mixture including beta - die ketone indicated as the chemical formula 1 and a primary amine indicated as R3NH2; and (S2) a step for irradiating the microwave to the mixture. In the chemical formula 1, R1, R2 and R3 are C1-8 linear or branched alkyl group, alkyl fluoride group or aryl group. | ||||||
| 26 | Insecticide containing hydrazone derivatives as the active ingredient and novel hydrazone derivates | US10500925 | 2003-01-10 | US20050203149A1 | 2005-09-15 | Shinji Kawata; Shuko Okui; Shigeru Suzuki; Toshiki Fukuchi; Akiyuki Suwa |
| A insecticide characterized by containing as active ingredient a hydrazone derivative of formula (I) wherein A and Q are an aryl or a heterocyclic group, W is oxygen atom, an aminylene, an alkylene group, an oxyalkylene group or an alkyleneoxy, X1 and X2 are hydrogen atom, an alkyl, an alkenyl, an alkynyl, an aryl, a heterocyclic group, formyl, an acyl, an alkoxycarbonyl, an aryloxycarbonyl, a heterocyclic oxycarbonyl, an alkylsulfinyl, an arylsulfinyl, a heterocyclic sulfinyl, an alkylsulfonyl, an arylsulfonyl or a heterocyclic sulfonyl, Y is oxygen atom or sulfur atom, Z is hydrogen atom, a halogen atom, cyano, an alkyl, an alkenyl, an alkynyl, an amino, an alkoxy or an alkylthio, the substituents may be substituted; and novel hydrazon derivatives. | ||||||
| 27 | N-unsubstituted amidinium salts | US10958870 | 2004-10-05 | US20050043403A1 | 2005-02-24 | Helmut Kraus; Rosemarie Wodarsch |
| The invention relates to N-unsubstituted imidic ester alkyl sulphates, N-unsubstituted amidinium alkyl sulphates and a process for their preparation, which is characterized in that carboxamides are converted with sulphuric diesters into the corresponding imidic ester alkyl sulphates, which are reacted further with ammonia to give the analogous amidinium alkyl sulphates. | ||||||
| 28 | Catalysts containing per-ortho aryl substituted aryl or heteroaryl substituted nitrogen donors | US10413150 | 2003-04-15 | US06844446B2 | 2005-01-18 | Leslie Shane Moody; Peter Borden Mackenzie; Christopher Moore Killian; Gino Georges Lavoie; James Allen Ponasik, Jr.; Thomas William Smith; Jason Clay Pearson; Anthony Gerard Martin Barrett |
| Catalyst compositions useful for the polymerization of olefins are disclosed. These compositions comprise a Group 8-10 metal complex comprising a bidentate or variable denticity ligand comprising one or two nitrogen donor atom or atoms independently substituted by an aromatic or heteroaromatic ring(s), wherein the ortho positions of said ring(s) are substituted by aryl or heteroaryl groups. Also disclosed are processes for the polymerization of olefins using the catalyst compositions. | ||||||
| 29 | Process for the preparation of 2-aryl-5-(perfluoroalkyl) pyrrole compounds from N-(perfluoroalkylmethyl) arylimidoyl chloride compounds | US247778 | 1999-02-09 | US5965773A | 1999-10-12 | Venkataraman Kameswaran |
| There is provided a process for the preparation of 2-aryl-5-(perfluoroalkyl)pyrrole compounds from N-(perfluoroalkylmethyl)arylimidoyl chloride compounds. The 2-aryl-5-(perfluoroalkyl)pyrrole compounds are useful for the control of insect and acarid pests, and may also be used to prepare other pesticidal arylpyrrole compounds.In addition, the present invention provides N-(perfluoroalkylmethyl)arylimidoyl chloride compounds which are useful as intermediates in the preparation of arylpyrrole compounds. | ||||||
| 30 | N-aryloxyacyl-n-phenyltetrahydrophthalamic acid derivatives, methods of producing same, and herbicides containing same as effective components | US256646 | 1994-07-19 | US5481022A | 1996-01-02 | Tetsuo Takematsu; Takashi Kume; Shoji Yamaoka; Takeo Komata; Kiyoshi Suzuki; Yukio Ikeda; Matsue Kawamura; Yumiko Koda; Kaoru Mori |
| The invention provides N-aryloxyacyl-N-phenyltetrahydrophthalamic acid derivatives represented by the general formula [I], a method of producing the same, and a herbicide containing the same as the effective components, ##STR1## wherein X and Y each individually represent hydrogen atoms or halogen atoms, Ar represents a substituted or unsubstituted phenyl group or naphthyl group, R.sup.1 represents a hydrogen atom, a halogen atom, a lower alkyl group, a lower alkoxy group, a lower alkenyloxy group, a lower alkynyloxy group, a lower alkoxyalkoxy group or a lower alkoxycarbonylalkoxy group, R.sup.2 represents a hydrogen atom or a lower alkyl group, R.sup.3 represents a hydroxyl, a lower alkoxy group, a lower alkenyloxy group, a lower alkynyloxy group, a lower alkoxyalkoxy group, a benzyloxy group or a lower alkoxycarbonylalkoxy group, and m is an integer ranging from 0 to 5. This herbicide which is very useful can be widely applied to upland, paddy field, orchard, turf, forest, non-crop land, etc., and is not harmful to crops. | ||||||
| 31 | 1,4-diamine-2,3-dihydroxy butanes | US167659 | 1993-12-17 | US5430155A | 1995-07-04 | Prabhakar K. Jadhav; Lawrence R. McGee; Ashok Shenvi; Carl N. Hodge |
| There are provided novel 1,4 Diamine 2,3 Dihydroxybutanes useful as antiviral agents, pharmaceutical compositions containing them and processes for preparing such compounds. | ||||||
| 32 | 1,4-diamino-2,3-dihydroxybutanes | US714042 | 1991-05-31 | US5294720A | 1994-03-15 | Prabhakar K. Jadhav; Lawrence R. McGee; Ashok Shenvi; Carl N. Hodge |
| There are provided novel 1,4 Diamine 2,3 Dihydroxybutanes useful as antiviral agents, pharmaceutical compositions containing them and processes for preparing such compounds. | ||||||
| 33 | Hydrazone compounds, processes for their production, intermediates useful for their production and pesticidal compositions containing them | US834835 | 1992-02-13 | US5288727A | 1994-02-22 | Tadaaki Toki; Toru Koyanagi; Kiyomitsu Yoshida; Hiroshi Sasaki; Masayuki Morita; Tetsuo Yoneda |
| The present invention relates to a hydrazone compound of the formula (I) or its salt, a process for its preparation, an intermediate of the formula (II-5), a pesticidal composition containing said hydrazone compound or its salt as the active ingredient, and a pesticidal method of applying an effective amount thereof: ##STR1## | ||||||
| 34 | Imino chloride derivative production method and phenylimidazole derivative production method | JP2012244056 | 2012-11-06 | JP2014091722A | 2014-05-19 | SUGITA SHUICHI; KATO EISAKU |
| PROBLEM TO BE SOLVED: To provide an imino chloride derivative production method and a phenylimidazole derivative production method which are highly safe and can achieve a high yield.SOLUTION: A compound represented by the general formula (1) and a chlorinating agent are reacted in the presence of a nitrogen-containing reaction aid, to produce an imino chloride derivative represented by the general formula (2). [In the formulas, Rand Rrepresent a branched alkyl group having three or more carbon atoms or a cycloalkyl group; Rrepresents a substituent; Rrepresents an aromatic hydrocarbon ring group or an aromatic heterocyclic group; and n represents an integer between 0 and 3.] | ||||||
| 35 | Method of manufacturing the aryl triazolopyrimidines class and its novel intermediate | JP2001530112 | 2000-10-12 | JP4954409B2 | 2012-06-13 | エス ゴーダー，ジャイデブ |
| 36 | Insecticide, compound contained in the insecticide, and method of using the compound | JP2008053697 | 2008-03-04 | JP2009209090A | 2009-09-17 | KATSUTA HIROYUKI; KAI AKIYOSHI; WAKITA TAKEO; YOSHIDA KEI; KOBAYASHI YUMI; TAKAHASHI YUSUKE; TAKAHASHI KIYOSHI; TSUKADA HIDETAKA; NOMURA MICHIKAZU; DAIDO HIDENORI; KAWAHARA NOBUYUKI; INOMATA SHINICHI; KAWAHARA ATSUKO; MAKI JUNJI |
| <P>PROBLEM TO BE SOLVED: To provide an insecticide which exhibits a high insecticidal effect even in a low dosage. <P>SOLUTION: There are provided a compound represented by general formula (1) and an insecticide containing the compound as an active ingredient. In the formula (1), L<SB>1</SB>is Q<SB>1</SB>or D<SB>1</SB>Q<SB>1</SB>; L<SB>2</SB>is Q<SB>2</SB>or D<SB>2</SB>Q<SB>2</SB>(wherein D<SB>1</SB>and D<SB>2</SB>represent various bonding manners; Q<SB>1</SB>is a 1-6C alkyl group, a 1-6C haloalkyl group, a substituted phenyl group, a substituted heterocyclic group, or the like; Q<SB>2</SB>is a substituted phenyl group, a substituted heterocyclic group, or the like); X is hydrogen atom or a halogen atom; n is an integer of 0-4; A is a carbon atom, a nitrogen atom, or the like which may be substituted with X; and K is a non-metallic atomic group necessary to form a 5- or 6-membered aromatic ring-derived cyclic bonding group together with A and the two carbon atoms to which A is bonded. <P>COPYRIGHT: (C)2009,JPO&INPIT | ||||||
| 37 | Insecticide containing hydrazone derivative as active component and new hydrazone derivative | JP2002262256 | 2002-09-09 | JP2004091451A | 2004-03-25 | KAWADA SHINJI; OKUI SHIYUUKO; SUZUKI SHIGERU; FUKUCHI TOSHIKI; SUWA AKIYUKI |
| <P>PROBLEM TO BE SOLVED: To obtain an insecticide having a broad insecticidal spectrum and excellent insecticidal activity and safety. <P>SOLUTION: The insecticide contains a hydrazone derivative of formula (I) as an active component. The hydrazone derivative is e.g. N-(4-chlorobenzyl)-2-(4-trifluoromethylhydrazono)propionic acid amide. <P>COPYRIGHT: (C)2004,JPO | ||||||
| 38 | Method of manufacturing the aryl triazolopyrimidines class and its novel intermediate | JP2001530112 | 2000-10-12 | JP2004500341A | 2004-01-08 | ゴーダー，ジャイデブ エス |
| 【課題】工業的に有用な除草性化合物を高収率且つ高純度に製造する。
【解決手段】ｉ）式（Ａ）のアミドラゾンをカルボニル化剤でカルボニル化するか又はｉｉ）式（Ａ）のヒドラゾノイル誘導体を環形成剤で縮合させて式（Ｉ）の１−アリールトリアゾリノンをつくる。 好ましいのはＷがハロゲン又は−ＮＨＲ（Ｒは水素又はハロアルキル）で、ＸとＹが水素、塩素又はフッ素で、Ｚが水素、臭素、ヨウ素、アミノ又はメチルスルホニルアミノで、Ｒ １がメチルの化合物である。 式（Ａ）の化合物には新規化合物もある。 【化１】 |
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| 39 | Fluoroazomethine compound, liquid crystal composition and liquid crystal display element | JP2002037727 | 2002-02-15 | JP2003238517A | 2003-08-27 | KATO TAKASHI |
| PROBLEM TO BE SOLVED: To obtain a compound having low viscosity, large dielectric anisotropy, moderate optical anisotropy and excellent compatibility with other liquid crystal compounds, a liquid crystal composition containing the compound, and to provide a liquid crystal display element containing the composition. SOLUTION: The compound is expressed by formula (1) (Y 1 is a 1-10C alkyl, or the like; A 1, A 2, A 3 and A 4 are each independently 1,4-cyclohexylene, 1,4- phenylene, or the like; Z 1, Z 2 and Z 3 are each independently a single bond, (CH 2) 2, or the like; and (p) and (q) are each independently 0 or 1). This invention further relates to the liquid crystal composition containing the compound and the liquid crystal display element containing the composition. COPYRIGHT: (C)2003,JPO | ||||||
| 40 | Chloroacetic acid ester derivative | JP6344387 | 1987-03-18 | JPH0637453B2 | 1994-05-18 | 功 一ノ瀬; 芳和 久保田; 隆文 志田 |
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