4.8 Article

Cationic Ir/Me-BIPAM-Catalyzed Asymmetric Intramolecular Direct Hydroarylation of α-Ketoamides

期刊

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
卷 53, 期 10, 页码 2658-2661

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.201400147

关键词

asymmetric catalysis; C-H functionalization; iridium; oxindoles; phosphoramidites

资金

  1. MEXT (Japan) program Strategic Molecular and Materials Chemistry through Innovative Coupling Reactions of Hokkaido University
  2. Grants-in-Aid for Scientific Research [14J01208] Funding Source: KAKEN

向作者/读者索取更多资源

Asymmetric intramolecular direct hydroarylation of -ketoamides gives various types of optically active 3-substituted 3-hydroxy-2-oxindoles in high yields with complete regioselectivity and high enantioselectivities (84-98% ee). This is realized by the use of the cationic iridium complex [Ir(cod)(2)](BAr4F) and the chiral O-linked bidentate phosphoramidite (R,R)-Me-BIPAM.

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