4.8 Article

Asymmetric One-Pot Sequential Mannich/Hydroamination Reaction by Organo- and Gold Catalysts: Synthesis of Spiro[pyrrolidin-3,2 '-oxindole] Derivatives

期刊

ORGANIC LETTERS
卷 15, 期 8, 页码 1846-1849

出版社

AMER CHEMICAL SOC
DOI: 10.1021/ol4004542

关键词

-

资金

  1. National Basic Research Program of China [2009CB940903, 2009CB918502, 2012CB518005]
  2. NSFC [21021063, 91229204, 81025017]
  3. National S&T Major Projects [2012ZX09103-101-072]
  4. China-EU Science and Technology Cooperation Project [1109]
  5. Silver Project [260644]

向作者/读者索取更多资源

An asymmetric organo- and gold-catalyzed one-pot sequential Mannich/hydroamination reaction has been developed. Using this protocol, spiro[pyrrolidin-3,2'-oxindole] derivatives were synthesized in good yields (up to 91%) and excellent enantioselectivities (up to 97% ee).

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