| Literature DB >> 30614163 |
Zhonglin Liu1, Haiwen Xiao1, Benxiang Zhang1, Haigen Shen1, Lin Zhu1, Chaozhong Li1,2.
Abstract
Reported herein is an unprecedented protocol for trifluoromethylation of unactivated aliphatic C(sp3 )-H bonds. With Cu(OTf)2 as the catalyst, the reaction of N-fluoro-substituted carboxamides (or sulfonamides) with Zn(CF3 )2 complexes provides the corresponding δ-trifluoromethylated carboxamides (or sulfonamides) in satisfactory yields under mild reaction conditions. A radical mechanism involving 1,5-hydrogen atom transfer of N-radicals followed by CF3 -transfer from CuII -CF3 complexes to the thus formed alkyl radicals is proposed.Entities:
Keywords: copper; radicals; reaction mechanisms; synthetic methods; trifluoromethylation
Year: 2019 PMID: 30614163 DOI: 10.1002/anie.201813425
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336