Fe(III)-Promoted <i>ortho</i> -Selective C–H Borylation of Aryl Selenoesters

Herein, a novel protocol for the Fe(OTf)<sub>3</sub>-promoted <i>ortho</i>-selective C-H borylation of aryl selenoesters is described. The corresponding borylated selenoesters are obtained with excellent site selectivity in moderate to good yields under mild conditions. The borylated products can be converted to various useful intermediates. Additionally, the differential reactivity of some substrates is illustrated by a detailed density functional theory calculation.

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Publication Details

Journal
Organic Letters
Published
2025-12-22
DOI
https://doi.org/10.1021/acs.orglett.5c04837
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
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article

Fe(III)-Promoted ortho -Selective C–H Borylation of Aryl Selenoesters

Y M Zhang, Ping Li, Kai Yang, zezhao Liu et al.
Organic Letters
Catalytic C–H Functionalization Methods
article

Fe(III)-Promoted ortho -Selective C–H Borylation of Aryl Selenoesters

Y M Zhang, Ping Li, Kai Yang, zezhao Liu, Zijuan Li, Shen Shan, Gaorong Wu
article en

Abstract

Herein, a novel protocol for the Fe(OTf)<sub>3</sub>-promoted <i>ortho</i>-selective C-H borylation of aryl selenoesters is described. The corresponding borylated selenoesters are obtained with excellent site selectivity in moderate to good yields under mild conditions. The borylated products can be converted to various useful intermediates. Additionally, the differential reactivity of some substrates is illustrated by a detailed density functional theory calculation.

Organic LettersVol. 28(1)
Jiangxi University of Traditional Chinese Medicine (CN), Nankai University (CN), Gannan Medical University (CN)
Openalex Percentile: Top 33%
Catalytic C–H Functionalization Methods
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