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Indoxamycin家族分子的合成研究进展

Synthetic Progress of Indoxamycin Family
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摘要 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. 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. In- doxamycins 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.
作者 何驰 丁寒锋
机构地区 浙江大学化学系
出处 《有机化学》 SCIE CAS CSCD 北大核心 2015年第4期760-769,共10页 Chinese Journal of Organic Chemistry
基金 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~~
关键词 indoxamycins 烯炔 重排 串联反应 全合成 indoxamycins enynes rearrangement tandem reaction total synthesis
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参考文献52

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