4.8 Article

Synthesis of α-Trifluoromethylated Ketones from Vinyl Triflates in the Absence of External Trifluoromethyl Sources

期刊

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
卷 56, 期 5, 页码 1342-1345

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.201608591

关键词

boranes; radicals; reaction mechanisms; synthetic methods; trifluoromethylation

资金

  1. Asahi Glass Foundation
  2. JSPS [16K17869]
  3. Grants-in-Aid for Scientific Research [16K17869] Funding Source: KAKEN

向作者/读者索取更多资源

A novel method for the conversion of vinyl triflates into a-trifluoromethylated ketones in the absence of external trifluoromethyl sources is described. This process accomplishes an efficient migration of the trifluoromethyl group of the triflate to the a-position in the ketone through a radical process. The reaction proceeds by the addition of a trifluoromethyl radical to the vinyl triflate and subsequent fragmentation of the trifluoromethane sulfonyl radical. Based on this reaction, a one-pot two-step procedure for the trifluoromethylation of ketones was developed. The method presented herein also allows the transfer of perfluoroalkyl groups from vinyl perfluoroalkanesulfonates, which are readily accessible from alkynes and perfluoroalkanesulfonic acids.

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