4.8 Article

Catalytic Friedel-Crafts Reaction of Aminocyclopropanes

期刊

ORGANIC LETTERS
卷 15, 期 14, 页码 3738-3741

出版社

AMER CHEMICAL SOC
DOI: 10.1021/ol401616a

关键词

-

资金

  1. EPFL
  2. SNF [200021_129874]
  3. F. Hoffmann-La Roche, Ltd.
  4. Swiss National Science Foundation (SNF) [200021_129874] Funding Source: Swiss National Science Foundation (SNF)

向作者/读者索取更多资源

A Lewis acid catalyzed Friedel-Crafts reaction between donor-acceptor aminocyclopropanes and indoles and other electron-rich aromatic compounds is reported. Indole alkylation at the C3 position was generally obtained for a broad range of functional groups and substitution patterns. In the case of C3-substituted indoles, C2 alkylation was observed. The reaction gives a rapid access to gamma amino acid derivatives present in numerous bioactive molecules.

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