4.8 Article

Total Synthesis of Kopsinitarine E

期刊

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
卷 59, 期 49, 页码 22039-22042

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.202011093

关键词

cyclization; indole alkaloids; Mannich reaction; semi-pinacol rearrangement; total synthesis

资金

  1. Chinese Academy of Sciences
  2. Strategic Priority Research Program [XDB20020200, QYZDJ-SSW-SLH029]
  3. National Natural Science Foundation of China [21621002, 21831009]

向作者/读者索取更多资源

Kopsinitarines A-E are complex octacyclic cagedKopsiaalkaloids with strained cage skeletons and a unique cyclic hemiaminal bridge that makes total synthesis challenging. Herein, we disclose the first total synthesis of kopsinitarine E. The key synthetic features include a SmI2-mediated radical cascade cyclization and a subsequent semi-pinacol rearrangement to install the key carbocyclic skeleton, a chemoselective hydrosilyl amide reduction to construct the hemiaminal ether bridge, and an intramolecular Mannich reaction to establish the highly strained cage system.

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