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.

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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
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article

Site-Selective C(sp3)–H Bromination via Radical Relay

Jing Qin, Qian Wan, Jianghao Wu, Xiaotong Song et al.
The Journal of Organic Chemistry
Vanadium and Halogenation Chemistry
article

Site-Selective C(sp3)–H Bromination via Radical Relay

Jing Qin, Qian Wan, Jianghao Wu, Xiaotong Song, Ziheng Xu, Di Song, Haojie Gao, Gang Wang
article en

Abstract

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.

The Journal of Organic Chemistry
Shandong First Medical University (CN)
Openalex Percentile: Top 25%
Vanadium and Halogenation Chemistry
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Site-Selective C(sp3)–H Bromination via Radical Relay — Jing Qin, Qian Wan, et al. · The Journal of Organic Chemistry (2026) | TGRS Research Map | TGRS