PulseExploreJournal ClubDebatesTrendingResearchersJournals
Instagram
HomeExploreJournal ClubTrending
Synapse
⌘+K
Synapse
April 12, 2026Chemical Communications1 citations

Copper-mediated photoinduced perfluoroalkylation of arylsulfonium salts

View Full Paper
YYYun YangLZLili ZhaoSLShengsheng Luo

Key Points

  • The research aims to develop a new method for site-selective perfluoroalkylation of arenes using copper and visible light.
  • Utilized copper-mediated cross-coupling
  • Incorporated aryl thianthrenium salts with [(DMPU)2Zn(Rf)2] reagents
  • Demonstrated through various substrates and functional groups
  • Applied visible light to promote the reaction
  • Successfully achieved a broad substrate scope for perfluoroalkylation
  • Showed outstanding tolerance for various functional groups
  • Created chain-length-tunable perfluoroalkylated compounds with diverse applications

Abstract

We herein report a copper-mediated, visible-light-promoted cross-coupling of aryl thianthrenium salts with (DMPU)2Zn(Rf)2 reagents for site-selective late-stage perfluoroalkylation of arenes. The protocol displays a broad substrate scope and outstanding functional-group tolerance, accommodating diverse functional moieties, heterocyclic motifs, and complex drug-derived scaffolds. This approach markedly enriches the repertoire of late-stage perfluoroalkylation methods, providing a unified, modular, and chain-length-tunable platform for the construction of perfluoroalkylated compounds with potential applications in materials science, medicinal chemistry, and agrochemical development.

Ask AI
Helpful
Bookmark
Share
View Full Paper

Cite This Study

Yang et al. (2026) studied this question.

synapsesocial.com/papers/69db36e64fe01fead37c4dc7https://doi.org/10.1039/d6cc01493c
Ask AI
Helpful
Bookmark
Share
View Full Paper