Photocatalytic Boron Insertion into Thiaarenes via Boryl Radicals

Abstract Skeletal editing of aromatic heterocycles represents a straightforward approach to rapidly expand the accessible chemical space. While notable progress has been made on the direct modification of various nitrogen‐ and oxygen‐heterocycles, editing of prevalent sulfur‐containing heteroarenes, especially for single‐atom insertion, remains exceedingly rare. This disparity is primarily attributed to the sulfur atom's inherent nucleophilicity and high susceptibility to oxidation. Here we present a conceptually distinct photocatalytic strategy that enables the insertion of a boron atom into a diverse range of thiaarenes, furnishing previously inaccessible cyclic thioborane scaffolds and synthetically valuable alkyl boronates in an efficient manner. Furthermore, mechanistic studies have revealed that the boron insertion step proceeds through an unprecedented mechanism.

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Publication Details

Journal
Angewandte Chemie
Published
2025-05-19
DOI
https://doi.org/10.1002/ange.202508379
Citations
2
Primary Topic
Sulfur-Based Synthesis Techniques
Type
article
Field-Weighted Citation Impact
1.87

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article

Photocatalytic Boron Insertion into Thiaarenes via Boryl Radicals

Ermeng Wang, Yubing Pang, Juntao Ye
2 citations
Angewandte Chemie
Sulfur-Based Synthesis Techniques
1.87
article

Photocatalytic Boron Insertion into Thiaarenes via Boryl Radicals

Ermeng Wang, Yubing Pang, Juntao Ye
article en
2 citations

Abstract

Abstract Skeletal editing of aromatic heterocycles represents a straightforward approach to rapidly expand the accessible chemical space. While notable progress has been made on the direct modification of various nitrogen‐ and oxygen‐heterocycles, editing of prevalent sulfur‐containing heteroarenes, especially for single‐atom insertion, remains exceedingly rare. This disparity is primarily attributed to the sulfur atom's inherent nucleophilicity and high susceptibility to oxidation. Here we present a conceptually distinct photocatalytic strategy that enables the insertion of a boron atom into a diverse range of thiaarenes, furnishing previously inaccessible cyclic thioborane scaffolds and synthetically valuable alkyl boronates in an efficient manner. Furthermore, mechanistic studies have revealed that the boron insertion step proceeds through an unprecedented mechanism.

Angewandte ChemieVol. 137(29)
Shanghai Jiao Tong University (CN), Shanghai Institute of Organic Chemistry (CN)
National Natural Science Foundation of China, National Key Research and Development Program of China
Openalex Percentile: Top 16%
Sulfur-Based Synthesis Techniques
1.87
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