有机化学 ›› 2016, Vol. 36 ›› Issue (2): 283-296.DOI: 10.6023/cjoc201507001 上一篇    下一篇

综述与进展

对映纯3,4-二氢嘧啶酮衍生物的合成研究进展

饶红红a, 权正军b, 白林a, 叶鹤琳a   

  1. a 兰州城市学院化学与环境科学院学院 兰州 730070;
    b 西北师范大学化学化工学院 兰州 730070
  • 收稿日期:2015-07-01 修回日期:2015-09-14 发布日期:2015-10-13
  • 通讯作者: 饶红红 E-mail:rhh@nwnu.edu.cn
  • 基金资助:

    国家自然科学基金(Nos. 21265009, 21362032)资助项目.

Progress on the Synthesis of Enantiomerically Pure 3,4-Dihydropyrimidin-2-one Derivatives

Rao Honghonga, Quan Zhengjunb, Bai Lina, Ye Helina   

  1. a School of Chemistry and Environmental Science, Lanzhou City University, Lanzhou 730070;
    b College of Chemistry and Chemical Engineering, Northwest Normal University, Lanzhou 730070
  • Received:2015-07-01 Revised:2015-09-14 Published:2015-10-13
  • Supported by:

    Project supported by the National Natural Science Foundation of China (Nos. 21265009, 21362032).

3,4-二氢嘧啶酮本身是不对称分子, 但绝大多数Biginelli反应得到的都是外消旋的3,4-二氢嘧啶酮类化合物. 大量研究表明3,4-二氢嘧啶酮的C(4)立体中心的绝对构型对其生物活性有重要影响. 主要归纳了获得对映纯3,4-二氢嘧啶酮类化合物的新发展, 特别是不对称催化Biginelli反应合成此类化合物的文献方法.

关键词: 对映纯3,4-二氢嘧啶酮, 不对称催化, Biginelli反应, 多组分反应

3,4-Dihydropyrimidinethiones are chiral molecules, however, only racemic products are isolated in the most reported Biginelli reactions. It has been proved that the absolute configuration of the C(4) stereogenic center has significant influence on the biological activity. The development in the accessing of optically active 3,4-dihydropyrimidinethiones focusing on the recent advances in the asymmetric catalytic Biginelli reactions is summarized.

Key words: enantiomerically pure 3,4-dihydropyrimidin-2-(1H)-ones, asymmetric catalysis, Biginelli reaction, multicomponent reactions