4.7 Article

Triethylborane-Initiated Radical Chain Fluorination: A Synthetic Method Derived from Mechanistic Insight

期刊

JOURNAL OF ORGANIC CHEMISTRY
卷 79, 期 18, 页码 8895-8899

出版社

AMER CHEMICAL SOC
DOI: 10.1021/jo501520e

关键词

-

资金

  1. NSF [CHE 1152996]
  2. Johns Hopkins
  3. Division Of Chemistry
  4. Direct For Mathematical & Physical Scien [1152996] Funding Source: National Science Foundation

向作者/读者索取更多资源

We offer a mild, metal-free sp(3) C-H fluorination alternative using Selectfluor and a substoichiometric amount of triethylborane-an established radical initiator in the presence of O-2. This radical-chain-based synthetic method is particularly noteworthy as an offspring of the insight gained from a mechanistic study of copper-promoted aliphatic fluorination, constructively turning O-2 from an enemy to an ally. Furthermore, BEt3/O-2 is a preferred initiator in industrial processes, as it is economical, is low in toxicity, and lends way to easier workup.

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