有机化学 ›› 2015, Vol. 35 ›› Issue (4): 760-769.DOI: 10.6023/cjoc201501002 上一篇    下一篇

综述与进展

Indoxamycin家族分子的合成研究进展

何驰, 丁寒锋   

  1. 浙江大学化学系 杭州 310028
  • 收稿日期:2015-01-05 修回日期:2015-02-03 发布日期:2015-01-05
  • 通讯作者: 丁寒锋 E-mail:hfding@zju.edu.cn
  • 基金资助:

    国家自然科学基金(Nos. 21472167, 21202144)、新博士点教师基金(No. 20120101120087)资助项目.

Synthetic Progress of Indoxamycin Family

He Chi, Ding Hanfeng   

  1. Department of Chemistry, Zhejiang University, Hangzhou 310028
  • Received:2015-01-05 Revised:2015-02-03 Published:2015-01-05
  • Supported by:

    Project supported by the National Natural Science Foundation of China (Nos. 21472167, 21202144) and the Research Fund For the Doctoral Program of Higher Education of China (No. 20120101120087).

Indoxamycins A~F是从海洋放线菌中分离得到的一类聚酮化合物, 它们均含有空间拥挤的[5,5,6]三环类笼状结构和6个连续的手性中心. 前期活性研究表明, indoxamycins A和F对HT-29肿瘤细胞株具有显著的生长抑制活性. 该综述总结了Carreira和丁寒锋两个小组在此家族天然产物全合成中取得的进展情况.

关键词: indoxamycins, 烯炔, 重排, 串联反应, 全合成

Indoxamycins A~F represent a novel class of polyketides isolated from the salin cultures of actinomycetes, which contain a common sterically congested [5,5,6] tricyclic cage-like structure featuring six contiguous stereogenic centers. Indoxamycins A and F were reported to exhibit significant growth-inhibition activity against HT-29 tumor cell lines. This review summarizes the synthetic progress towards indoxamycin family members both by the Carreira and Ding groups.

Key words: indoxamycins, enynes, rearrangement, tandem reaction, total synthesis