Site-Selective C(sp3)–H Bromination via Radical Relay
Abstract A cobalt-catalyzed site-selective C(sp3)–H bromination via radical relay is reported. The mild and practical protocol uses NBS as the brominating reagent with only 1 mol % CoBr2 as the catalyst and achieves excellent benzylic selectivity (>20:1) over aliphatic C–H bonds, overcoming limitations of conventional bromination methods. It also features a broad substrate scope, good functional group tolerance, and scalability and enables late-stage bromination of complex bioactive natural products and pharmaceutical molecules.
Authors
- Jing Qin (ORCID: https://orcid.org/0009-0002-0022-5771)
- Qian Wan (ORCID: https://orcid.org/0000-0001-9243-8939)
- Jianghao Wu
- Xiaotong Song
- Ziheng Xu
- Di Song
- Haojie Gao
- Gang Wang (ORCID: https://orcid.org/0009-0001-3907-6841)
Institutions
- Shandong First Medical University (CN)
Publication Details
- Journal
- The Journal of Organic Chemistry
- Published
- 2026-09-22
- DOI
- https://doi.org/10.1021/acs.joc.6c01295
- Primary Topic
- Vanadium and Halogenation Chemistry
- Type
- article
- Field-Weighted Citation Impact
- 0.00