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(R)-邻氯扁桃酸的制备技术进展
引用本文:钱晶,徐赛珍,薛亚平,郑裕国,沈寅初.(R)-邻氯扁桃酸的制备技术进展[J].化工进展,2011,30(2):396-401,406.
作者姓名:钱晶  徐赛珍  薛亚平  郑裕国  沈寅初
作者单位:浙江工业大学生物工程研究所,浙江 杭州 310014
摘    要:(R)-邻氯扁桃酸是一种具有广泛用途的药物中间体和精细化工产品,主要用于抗血小板聚集药物氯吡格雷的合成,其制备方法主要包括不对称合成法和光学异构体拆分法。本文主要对(R)-邻氯扁桃酸的各种制备方法进行了介绍,并比较了不同制备技术的优缺点,最后对手性邻氯扁桃酸的催化合成前景进行了展望。

关 键 词:邻氯扁桃酸  (R)-邻氯扁桃酸  不对称合成  拆分

Progress of synthesis of (R)-2-chloromandelic acid
QIAN Jing,XU Saizheng,XUE Yaping,ZHENG Yuguo,SHEN Yinchu.Progress of synthesis of (R)-2-chloromandelic acid[J].Chemical Industry and Engineering Progress,2011,30(2):396-401,406.
Authors:QIAN Jing  XU Saizheng  XUE Yaping  ZHENG Yuguo  SHEN Yinchu
Affiliation:Institute of Bioengineering,Zhejiang University of Technology,Hangzhou 310014,Zhejiang,China
Abstract:(R)-2-chloromandelic acid is one of the most important intermediates and fine chemicals with broad use. It can be used for the synthesis of clopidogrel,an anti-platelet drug that inhibits the ability of platelets to clump together as part of a blood clot. Presently,(R)-2-chloromandelic acid can be prepared by asymmetric synthesis and resolution of racemate. This review introduces various preparation methods of (R)-2-chloromandelic acid,and compares the advantages and disadvantages of these methods. The prospect of (R)-2-chloromandelic acid synthesis methods is also discussed.
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