研究简报

化学与生物转化法合成帕立骨化醇

  • 万阳 ,
  • 文鹏 ,
  • 张攀 ,
  • 陆群
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  • 西南交通大学生命科学与工程学院 成都 610031

收稿日期: 2012-04-12

  修回日期: 2012-06-06

  网络出版日期: 2012-06-19

基金资助

四川省科技支撑基金(No. 2010SZ124)资助项目.

Novel Synthesis of Paricalcitol by Chem-biotransformation

  • Wan Yang ,
  • Wen Peng ,
  • Zhang Pan ,
  • Lu Qun
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  • School of Life Science and Engineering, Southwest Jiaotong University, Chengdu 610031

Received date: 2012-04-12

  Revised date: 2012-06-06

  Online published: 2012-06-19

Supported by

Project supported by the Science and Technology Support Fundation of Sichuan Province (No. 2010SZ124).

摘要

以维生素D2 (1)为原料, 通过七步有机合成反应和一次生物转化, 成功获得了帕立骨化醇9, 并得到了一条新的合成帕立骨化醇的路线, 收率为3.24%. 该合成方法路线短, 操作简便, 收率较文献中的方法有较大提高. 所有产物结构经1H NMR, 13C NMR和MS表征.

本文引用格式

万阳 , 文鹏 , 张攀 , 陆群 . 化学与生物转化法合成帕立骨化醇[J]. 有机化学, 2012 , 32(10) : 1988 -1992 . DOI: 10.6023/cjoc201204015

Abstract

Paricalcitol (9) was obtained from Vitamin D2 via a route of the combination of seven-step organic reaction and biotransformation. The overall yield was 3.24%, which was higher than those of the reported methods. The structures of all intermediates and product were confirmed by 1H NMR, 13C NMR and MS techniques.

参考文献

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