BX <sub>3</sub> -Mediated Directed Electrophilic Borylation: Advances, Applications, and Mechanistic Insights

) under mild conditions. We highlight the chelation-assisted activation of both C-H and C-C bonds facilitated by tailored directing groups, encompassing substrates based on indoles, pyrroles, amides, phosphines, enamides, and cyclopropanes.The Account is structured to guide readers through the conceptual development, substrate scope, limitations, and mechanistic foundations of these directed electrophilic transformations. Mechanistic insights, derived from integrated experimental and computational studies, are presented to clarify key intermediates and reaction pathways that govern the selectivity and reactivity. In the concluding section, we acknowledge significant contributions from other research groups, outline persisting challenges, and suggest future directions essential for advancing the field─with the aim of inspiring further research and innovation.

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Publication Details

Journal
Accounts of Chemical Research
Published
2026-04-27
DOI
https://doi.org/10.1021/acs.accounts.6c00094
Primary Topic
Organoboron and organosilicon chemistry
Type
article
Field-Weighted Citation Impact
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article

BX 3 -Mediated Directed Electrophilic Borylation: Advances, Applications, and Mechanistic Insights

Zhuangzhi Shi, Jiahang Lv
Accounts of Chemical Research
Organoboron and organosilicon chemistry
article

BX 3 -Mediated Directed Electrophilic Borylation: Advances, Applications, and Mechanistic Insights

Zhuangzhi Shi, Jiahang Lv
article en

Abstract

) under mild conditions. We highlight the chelation-assisted activation of both C-H and C-C bonds facilitated by tailored directing groups, encompassing substrates based on indoles, pyrroles, amides, phosphines, enamides, and cyclopropanes.The Account is structured to guide readers through the conceptual development, substrate scope, limitations, and mechanistic foundations of these directed electrophilic transformations. Mechanistic insights, derived from integrated experimental and computational studies, are presented to clarify key intermediates and reaction pathways that govern the selectivity and reactivity. In the concluding section, we acknowledge significant contributions from other research groups, outline persisting challenges, and suggest future directions essential for advancing the field─with the aim of inspiring further research and innovation.

Accounts of Chemical Research
Yangzhou University (CN), Nanjing University (CN)
Openalex Percentile: Top 8%
Organoboron and organosilicon chemistry
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