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地尔硫卓手性中间体合成进展
引用本文:潘江,许建和,叶勤. 地尔硫卓手性中间体合成进展[J]. 生物加工过程, 2009, 7(3): 9-15
作者姓名:潘江  许建和  叶勤
作者单位:华东理工大学,生物反应器工程国家重点实验室,上海,200237
基金项目:国家高技术研究发展计划(863计划) 
摘    要:地尔硫卓是重要的心血管药物,在其分子结构中含有2个手性中心,可产生4个立体异构体,其中只有(2s,3s)-异构体具有药理活性,因此其立体选择性合成具有很大的挑战性。研究人员采用多种方法合成单一构型的地尔硫卓手性中间体,其中包括化学拆分、化学不对称合成以及化学-酶法合成等方法。对地尔硫卓手性中间体的制备方法进行了综述。

关 键 词:地尔硫卓  手性中间体  拆分  不对称合成  化学-酶法合成

Advance in synthesis of chiral intermediate for diltiazem
PAN Jiang,XU Jian-he,YE Qin. Advance in synthesis of chiral intermediate for diltiazem[J]. Chinese Journal of Bioprocess Engineering, 2009, 7(3): 9-15
Authors:PAN Jiang  XU Jian-he  YE Qin
Affiliation:(State Key Laboratory of Bioreactor Engineering, East China University of Science and Technology, Shanghai 200237, China)
Abstract:Diltiazem is an important coronary vasodilating drug and contains two chiral centers while only the (2S, 3S)-isomer has the desired activity. Many methods were investigated for the synthesis of the single enantiomer of the chiral intermediate, including chemical resolution, chemical asymmetric synthesis and chemo-enzymatie synthesis. In this paper, these methods for the preparation of diltiazem intermediate were reviewed.
Keywords:diltiazem  chiral intermediate  resolution  asymmetric synthesis  chemo-enzymatic synthesis
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