4.8 Article

Selective Monoarylation of Primary Amines Using the Pd-PEPPSI-IPentCl Precatalyst

期刊

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
卷 54, 期 33, 页码 9507-9511

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.201502822

关键词

amination; cross-coupling; palladium; PEPPSI; selectivity

资金

  1. NSERC Canada
  2. Eli Lilly Research Award Program (LRAP)

向作者/读者索取更多资源

A single set of reaction conditions for the palladium-catalyzed amination of a wide variety of (hetero)aryl halides using primary alkyl amines has been developed. By combining the exceptionally high reactivity of the Pd-PEPPSI-IPent(Cl) catalyst (PEPPSI=pyridine enhanced precatalyst preparation, stabilization, and initiation) with the soluble and nonaggressive sodium salt of BHT (BHT=2,6-di-tert-butyl-hydroxytoluene), both six- and five-membered (hetero)aryl halides undergo efficient and selective amination.

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