4.8 Article

Bioinspired Total Synthesis of Sespenine

期刊

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
卷 53, 期 34, 页码 9012-9016

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.201404191

关键词

biomimetic synthesis; cyclization; heterocycles; natural products; total synthesis

资金

  1. Ministry of Science Technology [2013CB836900]
  2. National Natural Science Foundation of China [21290180, 21172235, 21222202]

向作者/读者索取更多资源

The first total synthesis of sespenine, a rare indole sesquiterpenoid from a mangrove endophyte, has been accomplished. A bioinspired aza-Prins/Friedel-Crafts/retro Friedel-Crafts cascade reaction assembles the bridged tetrahydroquinoline core. Further investigations on the aza-Prins cyclization imply that the C3 configuration of the hydroxyindolenine intermediate is crucial to the biosynthesis of sespenine and its congener xiamycin A.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据