Undirected Primary CH Functionalization of Alkanes via Hydrogen Atom Transfer
Hydrogen atom transfer (HAT) which can produce radical intermediates from alkanes provides a strategy to achieve undirected C(sp 3 )‐H functionalization. Typically, primary CH bonds are the least reactive in HAT processes, compared to tertiary CH or activated benzylic CH. It is noteworthy that HAT‐mediated primary CH functionalization has recently been realized through the adjustment of various factors such as the catalyst or reagent design. This review summarizes recent advances in undirected primary CH functionalization via the HAT process. These examples will be discussed according to the HAT reagent. Reaction conditions, primary selectivity of various substrates, mechanism, and origin of the primary selectivity will be highlighted.
Authors
- Jie Qin
- Yating Zhao (ORCID: https://orcid.org/0009-0004-3809-082X)
- Wujiong Xia
- Jingjing Xia
Institutions
- Harbin Institute of Technology (CN)
- Quzhou University (CN)
- Henan Normal University (CN)
Publication Details
- Journal
- European Journal of Organic Chemistry
- Published
- 2026-03-09
- DOI
- https://doi.org/10.1002/ejoc.202500887
- Primary Topic
- Radical Photochemical Reactions
- Type
- article
- Field-Weighted Citation Impact
- 0.00