4.7 Article

Ni-Catalyzed α-arylation of esters and amides with phenol derivatives

期刊

CHEMICAL COMMUNICATIONS
卷 51, 期 5, 页码 855-857

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/c4cc08426h

关键词

-

资金

  1. JSPS [220GR049]
  2. MEXT [25105720, 25708005]
  3. International Research Training Group Munster/Nagoya
  4. World Premier International Research Center (WPI) Initiative, Japan
  5. Grants-in-Aid for Scientific Research [25105720, 25708005] Funding Source: KAKEN

向作者/读者索取更多资源

A nickel-catalyzed alpha-arylation of esters and amides with phenol derivatives has been accomplished. In the presence of our unique nickel catalyst, prepared in situ from Ni(cod)(2), 3,4-bis(dicyclohexyl-phosphino) thiophene (dcypt), and K3PO4, various esters and amides undergo alpha-arylation with O-arylpivalates or O-arylcarbamates to afford the corresponding coupling products. The thus obtained alpha-aryl esters and amides are useful precursors of privileged motifs such as alpha-arylcarboxylic acids and beta-arylamines.

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

4.7
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