Login / Signup

Catalytic Radical Trifluoromethylalkynylation of Unactivated Alkenes.

Shaofang ZhouTao SongHe ChenZhonglin LiuHaigen ShenChaozhong Li
Published in: Organic letters (2017)
The trifluoromethylalkynylation of unactivated alkenes with alkynyl sulfones and Togni's reagent was developed. The reaction was catalyzed by 2,4,6-trimethylpyridine, leading to various β-trifluoromethylated alkynes under metal-free conditions with a broad substrate scope and wide functional group compatibility. A mechanism involving catalytic nonchain radical processes is proposed.
Keyphrases
  • crystal structure
  • room temperature
  • amino acid