Synlett
DOI: 10.1055/a-2791-8971
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Site-Selective Copper-Catalyzed Halogenation at an Unactivated C(sp3)–H Bond: Mechanistic Insights and Advances

Autor*innen

  • Jordan Diaz

    1   School of Chemistry, Monash University, Clayton, Australia
  • Philip Wai Hong Chan

    1   School of Chemistry, Monash University, Clayton, Australia

This work was supported by a Discovery Project Grant (DP250103974) from the Australian Research Council.


Graphical Abstract

Abstract

Copper-catalyzed methods for the halogenation of unactivated C(sp3)–H bonds has emerged as a powerful tool in modern chemical synthesis. Their rapid and elegant development has been driven by recent advances in radical and redox chemistry. This account provides an overview of these recent efforts in copper-mediated unactivated C(sp3)–H halogenation strategies that have focused and exploited mechanistic paradigms such as inter- and intra-hydrogen-atom transfer reactions and Cu(I)/Cu(II)/Cu(III) redox cycling.



Publikationsverlauf

Eingereicht: 02. Dezember 2025

Angenommen nach Revision: 19. Januar 2026

Artikel online veröffentlicht:
05. Februar 2026

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