| 序号 | 专利名 | 申请号 | 申请日 | 公开（公告）号 | 公开（公告）日 | 发明人 |
|---|---|---|---|---|---|---|
| 61 | 非水電解液、それを用いた電気化学素子、及びそれに用いられる1,2−ジオキシプロパン化合物 | JP2012508251 | 2011-03-24 | JP5692219B2 | 2015-04-01 | 三好 和弘; 古藤 雄一; 敷田 庄司 |
| 62 | 環状スルホン酸エステルの製造方法及びその中間体 | JP2011525889 | 2010-08-03 | JP5668684B2 | 2015-02-12 | 絢子 蔵本; 訓明 岡本; 勉 綿引; 元重 角野 |
| 63 | Actinic ray sensitive or radiation sensitive resin composition, and resist film, pattern forming method, method for manufacturing electronic device and electronic device using the same | JP2011207018 | 2011-09-22 | JP2013068778A | 2013-04-18 | IWATO KAORU; TAKAHASHI HIDETOMO; SHIRAKAWA MICHIHIRO |
| PROBLEM TO BE SOLVED: To provide an actinic ray sensitive or radiation sensitive resin composition capable of suppressing occurrence of pattern collapse or bridge defects after developing, and having a high residual film ratio, in a negative pattern formation by means of organic solvent developing, and to provide a resist film, a pattern forming method, a method for manufacturing an electronic device, and an electronic device using the same.SOLUTION: There is provided an actinic ray sensitive or radiation sensitive resin composition including: a resin (P) having a repeating unit (a) represented by the following general formula (I); a compound (B) represented by any one of specific general formulae (B-1) to (B-3); and a solvent. In the general formula (I), Rrepresents a hydrogen atom or a methyl group. R, Rand Reach independently represent a linear or branched alkyl group. | ||||||
| 64 | 環状スルホン酸エステルの製造方法及びその中間体 | JP2011525889 | 2010-08-03 | JPWO2011016440A1 | 2013-01-10 | 絢子 蔵本; 訓明 岡本; 勉 綿引; 元重 角野 |
| 環状スルホン酸エステル(スルトン)を、安価で収率良く得ることができるばかりでなく、工業スケールでも安定して当該環状スルホン酸エステル(スルトン)を得ることが可能な、効率の良い製造方法を提供することを目的とし、本発明は、特定構造のジオールとハロゲン化チオニルとを反応させて、特定構造の環状亜硫酸エステルを得る第1の工程と、当該環状亜硫酸エステルを水又は/及びアルコールと反応させる第2の工程と、を含んでなることを特徴とする、ヒドロキシスルトンの製造方法、特定構造のヒドロキシスルトンを酸ハロゲン化物又は酸無水物と反応させて中間体を得、次いで当該中間体を塩基で処理する第3の工程を含んでなることを特徴とする、特定構造の不飽和スルトンの製造方法、並びに特定構造の環状亜硫酸エステルに関する。 | ||||||
| 65 | Iminium salts in the cleaning composition | JP2004511269 | 2003-06-04 | JP4316497B2 | 2009-08-19 | グレゴリー、スコット、ミラクル; ジョージ、ダグラス、ヒラー、ザ、セカンド; レベッカ、マジー、グレイ; 田 将 村 |
| 66 | Its use in the preparation and asymmetric synthesis of P chiral phosphorane | JP2007505651 | 2005-03-23 | JP2007530657A | 2007-11-01 | スチュワート ホジ ガレット |
| Ｐキラル性モノホスホランおよびビスホスホランを調製するための材料および方法を開示する。 この方法は、立体選択的な環化を使用してホスホラン環を生成した後、ピラミッド反転によって様々なＰキラル性ホスホランに到達するものである。 開示されるＰキラル性ホスホランは、ロジウムなどの遷移金属に結合させると、プレガバリンを含む、医薬としての価値ある化学的存在の不斉合成で触媒として使用することができる。
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| 67 | Manufacturing method of the polysulfide compound and rubber composition containing the same | JP2004056647 | 2004-03-01 | JP3761552B2 | 2006-03-29 | 源文 崔 |
| 68 | Iminium salts in the cleaning composition | JP2004511269 | 2003-06-04 | JP2005538823A | 2005-12-22 | グレゴリー、スコット、ミラクル; ジョージ、ダグラス、ヒラー、ザ、セカンド; レベッカ、マジー、グレイ; 将 村田 |
| 本発明は、イミニウム又はオキサジリジニウム部分を含む有機触媒、このような触媒を含む洗浄組成物；並びにこのような触媒及び洗浄製品を製造及び使用するための方法に関する。 | ||||||
| 69 | Method of manufacturing a cyclo propane nitrile derivative | JP33186391 | 1991-12-16 | JP3092272B2 | 2000-09-25 | ハンセルマン パウル |
| 70 | The novel 1,3,2-dioxathiolane s oxide derivatives, their preparation and their use | JP23748891 | 1991-08-23 | JPH0826012B2 | 1996-03-13 | 智 熊沢; 正典 美濃口 |
| 71 | JPH06508848A - | JP50226492 | 1992-07-02 | JPH06508848A | 1994-10-06 | |
| 72 | JPH06507631A - | JP51076192 | 1992-05-21 | JPH06507631A | 1994-09-01 | |
| 73 | Production of cyclic sulfates | JP5306189 | 1989-03-07 | JPH0285276A | 1990-03-26 | PIEERU RU ROWA; BERUNADETSUTO MANDARUUKAZAN |
| PURPOSE: To economically obtain the subject compd. useful as an intermediate by oxidizing a cyclic sulfite by using an alkali or alkaline earth metal hypohalide at a specific temp. in the presence of a catalytic amt. of a ruthenium derivative in an aq. medium or a water-org. medium. CONSTITUTION: A cyclic sulfite represented by formula I (wherein R 1-R 6 are each H, halogen, alkyl, aryl, alkoxy or the like; and n is 0 or 1) is oxidized by using an alkali or alkaline earth metal hypohalide (e.g.; hypochlorite, etc.), pref., sodium hypochlorite in the presence of a catalytic amt. of a ruthenium derivative (e.g.; RuO 2, RuCl 3, etc.), in an aq. medium or a water-org. medium at a low temp. of 10°C or less to obtain a cyclic sulfate represented by formula II. This method is especially useful for producing a compd. represented by formula II (wherein n is 0 or 1 and R 1-R 6 are each H or 1-4C alkyl). COPYRIGHT: (C)1990,JPO | ||||||
| 74 | Production of cyclic sulfuric ester | JP11883389 | 1989-05-15 | JPH0217183A | 1990-01-22 | BIBIAN MASONO; MISHIERU MIYUROZE |
| PURPOSE: To produce the subject compd. useful as an intermediate product for executing hydroxyethylation reaction in an industrially advantageous manner by reacting specific glycol with conc. sulfuric ester under a specific temp. condition and recovering the formed product. CONSTITUTION: Glycol (e.g. ethylene glycol) represented by formula I (wherein R 1-R 6 are each H, halogen, alkyl, aryl, alkoxy, aryloxy or alkylcarbonyl and n is 0 or 1. Herein, an alkyl group is 1-4C and an aryl group is 6-10C) and conc. sulfuric acid are mixed and this mixture is added to a reactor 2 by using a syringe 1 to be heated to 150-250°C by a heating tape 3 to be reacted while an apparatus is reduced in pressure and the reaction product is gathered in a column 5 and, at a time of the completion of reaction, the column is washed with a solvent and a soln. is gathered in a receiver 4 and the solvent is distilled off to obtain a cyclic ester represented by formula II. COPYRIGHT: (C)1990,JPO | ||||||
| 75 | Aromatic compound | JP28786688 | 1988-11-16 | JPH02159A | 1990-01-05 | HAWAADO MASHIYUU KORUKUHAUN; KURISUTOFUAA KAATEISU DADOMAN; MAAKU TOOMASU |
| NEW MATERIAL: A macrocyclic compd. having at least one kind of a polyarylene unit containing two or more arylene rings and at least two kinds of other cyclic units bonded to a macro ring thereof and characterized by that the polyarylene unit and the other units are bonded to the adjacent units by a divalent single atom or 2-6C alkylene. USE: An aromatic compd., especially, a macrocyclic polymer containing an aromatic ring and an ether and/or thioether bond. PROCESS: A halogen compd. represented by formula X-Ar-J-Ar-X [wherein X is halogen other than F, Ar is arylene, J is a cyclic unit represented by formula -E-Ar'-D (wherein Ar' is an aromatic ring, D is O or S and E is an electron withdrawing group] is reacted with a metal (e.g.; zero valent Ni) effective for forming halide and a group Ar is bonded to form a polyarylene unit to obtain the macrocyclic compd. COPYRIGHT: (C)1990,JPO | ||||||
| 76 | Manufacture of furanone | JP16307085 | 1985-07-25 | JPS6137777A | 1986-02-22 | KURISUCHIYAN FUIZE |
| 77 | NON-AQUEOUS ELECTROLYTE FOR LITHIUM-ION BATTERY AND LITHIUM-ION BATTERY | US16316621 | 2016-12-30 | US20190237804A1 | 2019-08-01 | Qiao Shi; Muchong Lin; Shiguang Hu; Xionggui Lin; Jiaojiao Yun; Chang'an Zeng |
| A non-aqueous electrolyte for a lithium-ion battery and a lithium-ion battery. The non-aqueous electrolyte comprises unsaturated phosphate compounds and unsaturated cyclic carboxylic acid anhydride compounds. The unsaturated phosphate compounds have the structure illustrated in structural formula 4; structural formula 4: R13, R11, and R12 are independently selected from hydrocarbon groups having 1-5 carbon atoms respectively, and at least one of R13, R11, and R12 is an unsaturated hydrocarbon group containing double bonds or triple bonds; the unsaturated cyclic carboxylic acid anhydride compounds have the structure illustrated in structural formula 5; structural formula 5: R14 is independently selected from vinylidene having 2-4 carbon atoms or fluoro-substituted vinylidene. By means of the synergistic effect of two compounds, the non-aqueous electrolyte has excellent high-temperature cycling performance and storage performance, and also has lower impedance and good low-temperature performance. | ||||||
| 78 | 15-oxospiramilactone derivatives, preparation method and uses thereof | US14785075 | 2014-04-21 | US10112918B2 | 2018-10-30 | Xiaojiang Hao; Chen Yan; Haiyang Liu; Lin Li; Xiaoli He; Quan Chen |
| The invention relates to a derivative of 15-oxospiramilacton, particularly to a compound of Formula I or II, or an isomer, a solvate or a pharmaceutically acceptable salt thereof. The invention also relates to a pharmaceutical composition comprising the compound as pharmaceutically active ingredient, a method for preparing the same, and use thereof in manufacture of an anti-tumor agent. The derivative of 15-oxospiramilactone of the invention have an activity against multiple tumor cell lines, and the anti-tumor activity is positively correlated to an activity inhibiting the Wnt signaling pathway. | ||||||
| 79 | OXATHIAZINE DERIVATIVES AS ANTIBACTERIAL AND ANTICANCER AGENTS | US15472550 | 2017-03-29 | US20170196876A1 | 2017-07-13 | Rolf W. PFIRRMANN |
| New oxathiazin-like compounds and their derivatives are useful as antineoplastic and antimicrobial agents. Compositions and methods of using oxathiazin-like compounds and their derivatives are disclosed. | ||||||
| 80 | 15-Oxospiramilactone Derivatives, Preparation Method and Uses Thereof | US14785075 | 2014-04-21 | US20160185743A1 | 2016-06-30 | Xiaojiang Hao; Chen Yan; Haiyang Liu; Lin Li; Xiaoli He; Quan Chen |
| The invention relates to a derivative of 15-oxospiramilacton, particularly to a compound of Formula I or II, or an isomer, a solvate or a pharmaceutically acceptable salt thereof. The invention also relates to a pharmaceutical composition comprising the compound as pharmaceutically active ingredient, a method for preparing the same, and use thereof in manufacture of an anti-tumor agent. The derivative of 15-oxospiramilactone of the invention have an activity against multiple tumor cell lines, and the anti-tumor activity is positively correlated to an activity inhibiting the Wnt signaling pathway. | ||||||
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