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丹参素及其衍生物的合成
引用本文:张彦文,冯淑华. 丹参素及其衍生物的合成[J]. 天津医科大学学报, 2005, 11(4): 522-524
作者姓名:张彦文  冯淑华
作者单位:1. 天津医科大学药学院,天津,300070
2. 北京联合大学生物医药系
基金项目:天津市教委基金资助(编号:20010701)
摘    要:目的:探讨丹参素的合成方法,并以苯基乳酸为先导化合物,通过设计、合成衍生物,对其进行结构修饰。方法:使用硼氢化钾代替锌汞齐还原羰基,通过乙酰化反应对丹参素及其衍生物进行结构修饰。结果:使用硼氢化钾将羰基还原成羟基,合成了丹参素及其衍生物的乙酰化产物,经^1H—NMR证实其结构。结论:使用硼氢化钾还原羰基,产物单一,条件温和,易于控制。

关 键 词:丹参素 合成 还原反应 硼氢化钾
文章编号:1006-8147(2005)04-0522-03
修稿时间:2005-05-27

Synthesis of danshensu and derivatives
ZHANG Yan-wen,FENG Shu-hua. Synthesis of danshensu and derivatives[J]. Journal of Tianjin Medical University, 2005, 11(4): 522-524
Authors:ZHANG Yan-wen  FENG Shu-hua
Affiliation:1.Pharmacy College of Tianjing Medical University,Tianjin 300070, China ; 2.Biochemical Engineering College of Beijing Union University
Abstract:Objective: To study the method of synthesising danshensu and derivatives of phenyllactic acid as the lead compound was designed and synthesized;modify on its structure. Methods: Carbonyl group was reducted with potassium borohydride in stead of zinc amalgam; the danshensu and its derivatives were acetylated. Results: Carbonyl group was reducted with potassium borohydride to hydroxyl group aeetylated danshensu and its derivatives were synthesized ; the structures of danshensu and its derivatives were confirmed by 1H-NMR. Conclusion: The condition of reduction with potassium borohydrid is mildness and in control.
Keywords:Danshengsu    Synthesising   Reduction reaction   Potassium borohydride
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