Exhaust gas control device for internal combustion engines
    1.
    发明授权
    Exhaust gas control device for internal combustion engines 失效
    内燃机排气控制装置

    公开(公告)号:US07007459B2

    公开(公告)日:2006-03-07

    申请号:US10433289

    申请日:2001-10-31

    申请人: Ju-Cheol Lee

    发明人: Ju-Cheol Lee

    IPC分类号: F01N5/00

    摘要: Disclosed herein is an exhaust gas control device for internal combustion engines. The exhaust gas control device has a main exhaust pipe (3) communicating with an exhaust manifold (2) used for guiding exhaust gas discharged from a combustion chamber (1) of an engine, a catalytic converter (6) arranged on a predetermined position of the main exhaust pipe (3) for purifying unburnt fuel discharged with the exhaust has and having a plurality of sequentially arranged catalyst units (6a, 6b, 6c), and an unburnt fuel collection tank (8) provided with a plurality of cooling fins (9) and connected to the catalytic converter (6) through a branch pipe (7). The collection tank (8) collects purified unburnt fuel after the unburnt fuel is treated by the catalytic converter (6) so as to remove noxious materials therefrom.

    摘要翻译: 这里公开了一种用于内燃机的排气控制装置。 排气控制装置具有与用于引导从发动机的燃烧室(1)排出的排气的排气歧管(2)连通的主排气管(3),设置在发动机的燃烧室(1)的预定位置的催化转化器 用于净化排气排出的未燃燃料的主排气管(3)具有多个顺序排列的催化剂单元(6a,6b,6c)和未燃燃料收集箱(8) 冷却翅片(9),并通过支管(7)连接到催化转化器(6)。 收集罐(8)在未燃燃料被催化转化器(6)处理之后收集纯化的未燃燃料,以便从中除去有害物质。

    Process for preparing cephalosporin antibiotics using new thiazole compound
    2.
    发明授权
    Process for preparing cephalosporin antibiotics using new thiazole compound 失效
    使用新的噻唑化合物制备头孢菌素抗生素的方法

    公开(公告)号:US06384212B1

    公开(公告)日:2002-05-07

    申请号:US09564980

    申请日:2000-05-04

    IPC分类号: C07D50124

    CPC分类号: C07D501/00

    摘要: The present invention relates to a new, simple, and easy process for preparing cephalosporin antibiotics of the following formula (I), such as ceftazidime and cefixime. The process comprises acylating a 7-amino cephalosporanic acid derivative of the following formula (III) with a crystalline aminothiazole compound of the following formula (II): wherein R1 and R2 are the same or different and independently represent H, a C1-4 alkyl or C3-5 cycloalkyl group, R4 represents acetoxymethyl, methylpyridine, or vinyl, X represents chlorine or bromine, and the acid in the acid addition salt represents an inorganic acid, such as hydrochloric acid, or an organic acid, such as formic acid or acetic acid.

    摘要翻译: 本发明涉及用于制备下列通式(I)的头孢菌素抗生素的新的,简单的和容易的方法,例如头孢他啶和头孢克肟。 该方法包括用下式(II)的结晶氨基噻唑化合物酰化下式(III)的7-氨基头孢菌酸衍生物:其中R 1和R 2相同或不同并且独立地代表H,C 1-4烷基 或C3-5环烷基,R4表示乙酰氧基甲基,甲基吡啶或乙烯基,X表示氯或溴,酸加成盐中的酸表示无机酸,如盐酸或有机酸,如甲酸或 醋酸。

    Preparation of glycerol derivatives and intermediates therefor
    4.
    发明授权
    Preparation of glycerol derivatives and intermediates therefor 有权
    甘油衍生物及其中间体的制备

    公开(公告)号:US07868196B2

    公开(公告)日:2011-01-11

    申请号:US11989074

    申请日:2006-07-18

    IPC分类号: C07F9/02

    CPC分类号: C11C3/04

    摘要: Disclosed is a process for the regioselective preparation of glycerol derivative in a high efficiency and yield. The process for the regioselective preparation of 1-R1-2-R2-3-acetyl-glycerol derivative comprises the steps of: obtaining 1-R1-3-protecting group-glycerol by introducing a protecting group to 3-position of 1-R1-glycerol; obtaining 1-R1-2-R2-3-protecting group-glycerol by introducing R2 group into 2-position of 1-R1-3-protecting group-glycerol; and carrying out the deprotection reaction and the acetylation reaction of 1-R1-2-R2-3-protecting group-glycerol at the same time. Wherein, R1 and R2 are fatty acid groups having 16 to 22 carbon atoms, and are different from each other; and the protecting group is trityl group or trialkylsilyl group.

    摘要翻译: 公开了以高效率和高产率区域选择性制备甘油衍生物的方法。 1-R1-2-R2-3-乙酰基 - 甘油衍生物的区域选择性制备方法包括以下步骤:通过将保护基引入1-R1的3-位获得1-R1-3保护基 - 甘油 甘油 通过将R2基团引入1-R1-3保护基 - 甘油的2-位获得1-R1-2-R2-3-保护基 - 甘油; 并同时进行1-R1-2-R2-3-保护基 - 甘油的去保护反应和乙酰化反应。 其中R1和R2是具有16-22个碳原子的脂肪酸基团,并且彼此不同; 保护基为三苯甲基或三烷基甲硅烷基。

    Preparation of glycerol derivatives ad intermediates therefor
    5.
    发明申请
    Preparation of glycerol derivatives ad intermediates therefor 有权
    甘油衍生物的制备及其中间体

    公开(公告)号:US20090253923A1

    公开(公告)日:2009-10-08

    申请号:US11989074

    申请日:2006-07-18

    IPC分类号: C07F9/02

    CPC分类号: C11C3/04

    摘要: Disclosed is a process for the regioselective preparation of glycerol derivative in a high efficiency and yield. The process for the regioselective preparation of 1-R1-2-R2-3-acetyl-glycerol derivative comprises the steps of: obtaining 1-R1-3-protecting group-glycerol by introducing a protecting group to 3-position of 1-R1-glycerol; obtaining 1-R1-2-R2-3-protecting group-glycerol by introducing R2 group into 2-position of 1-R1-3-protecting group-glycerol; and carrying out the deprotection reaction and the acetylation reaction of 1-R1-2-R2-3-protecting group-glycerol at the same time. Wherein, R1 and R2 are fatty acid groups having 16 to 22 carbon atoms, and are different from each other; and the protecting group is trityl group or trialkylsilyl group.

    摘要翻译: 公开了以高效率和高产率区域选择性制备甘油衍生物的方法。 1-R1-2-R2-3-乙酰基 - 甘油衍生物的区域选择性制备方法包括以下步骤:通过将保护基引入1-R1的3-位获得1-R1-3-保护基 - 甘油 甘油 通过将R2基团引入1-R1-3保护基 - 甘油的2-位获得1-R1-2-R2-3-保护基 - 甘油; 并同时进行1-R1-2-R2-3-保护基 - 甘油的去保护反应和乙酰化反应。 其中R1和R2是具有16-22个碳原子的脂肪酸基团,并且彼此不同; 保护基为三苯甲基或三烷基甲硅烷基。