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STEREOSELECTIVE TOTAL SYNTHESIS OF CHRYSANTHEMOL

机译:菊花醇的立体选择性全合成

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摘要

Chrysanthemol (1), a trans-eudesmane type sesquiterpene from Chrysanthemum indicum L.,possesses certain anti-inflammatory activity. Its total synthesis was approached from two alternative routes and finally accomplished in ten steps from R-(+)-carvone via α-eudesmol (10) as the key intermediate. The overall yield is 2.4% and the spectral data of the synthetic target compound were identical with that of natural chrysanthemol (1). Seven intermediary compounds were tested for inhibitory effects on the carragenan-induced swelling of mouse paw but demonstrated no obvious activities.
机译:菊花(1)是一种来自菊科植物的反欧德香型倍半萜烯,具有一定的抗炎活性。它的总合成是通过两种替代途径进行的,最终通过R-(+)-香芹酮以α-eudesmol(10)作为关键中间体,从十个步骤完成。总产率为2.4%,合成目标化合物的光谱数据与天然菊花(1)相同。测试了七个中间化合物对角叉菜胶诱导的小鼠爪肿胀的抑制作用,但没有明显的活性。

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  • 来源
    《亚洲天然物产研究(英文版)》 |2001年第2期|103-116|共14页
  • 作者单位

    Institute of Materia Medica, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100050, China;

    Institute of Materia Medica, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100050, China;

    Institute of Materia Medica, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100050, China;

    Institute of Materia Medica, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100050, China;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 chi
  • 中图分类 植物学;
  • 关键词

    Chrysanthemol (1); Total synthesis; Anti-inflammatory activity;

    机译:菊花(1);全合成;抗炎活性;
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