4.5 Article

Chiral Phosphoric Acid Catalyzed Asymmetric Friedel-Crafts Alkylation of Indole with 3-Hydroxyisoindolin-1-one: Enantioselective Synthesis of 3-Indolyl-Substituted Isoindolin-1-ones

期刊

EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
卷 2011, 期 5, 页码 892-897

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/ejoc.201001408

关键词

Enantioselectivity; Alkylation; Nitrogen heterocycles; Organocatalysis

资金

  1. National Natural Science Foundation of China [20772058, 20972070]
  2. National Basic Research Program of China (973 program) [2010CB833301]
  3. Key laboratory of Elemento-Organic Chemistry

向作者/读者索取更多资源

Chiral phosphoric acids have been proven to be effective organocatalysts for the asymmetric Friedel-Crafts alkylation of indoles with 3-hydroxyisoindolin-1-ones. The corresponding products were obtained in excellent chemical yields (up to 99%) with moderate to excellent enantioselectivities (up to >99% ee after a single recrystallization). This is the first example of the catalytic asymmetric synthesis of valuable 3-substituted isoindolin-1-ones in high yields and enantioselectivities.

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

4.5
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