4.8 Article

Photochemical Synthesis of Indolocarbazoles through Tandem Indolization/Dimerization/Mannich Cyclization from Allenes

期刊

ORGANIC LETTERS
卷 24, 期 19, 页码 3582-3587

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.2c01371

关键词

-

资金

  1. National Natural Science Foundation of China [22061044, 21871228]
  2. Natural Science Foundation of Yunnan Province [202001BB050038, 2018FY001015]
  3. Program of Changjiang Scholars and Innovation Research Team in University [IRT17R94]

向作者/读者索取更多资源

The indolocarbazole ring system was synthesized through a photochemical method, demonstrating exceptional functional group tolerance and successfully applied in the concise synthesis of natural products tjipanazoles B and D.
Indolocarbazole alkaloids and their derivatives were discovered to have potent protein kinase and topoisomerase I inhibitory activities. Disclosed herein is the photochemical synthesis of the indolocarbazole ring system from N-allenyl-2-iodoanilines. The tandem protocol included visible-light-mediated 5-exo-trig radical cyclization and subsequent radical dimerization, followed by acid-promoted deprotection and intramolecular Mannich cyclization. This strategy showed exceptional functional group tolerance and was successfully applied in the concise synthesis of natural products tjipanazoles B and D.

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