N-Heterocyclic Selone-Generated Selenium-Centered Radical for Covalent Radical Catalysis

Abstract Covalent radical catalysis represents an emerging synthetic paradigm that exploits open-shell radical species as catalysts to drive chemical transformations. By enabling selective manipulation of highly reactive radical intermediates via controlled addition–elimination sequences, this approach offers a mild and versatile route for constructing complex cyclic frameworks with high efficiency and precision. This highlight article briefly summarizes recent advances in this area, with emphasis on our development of redox-active N-heterocyclic selones (NHSs) as catalysts. These catalysts facilitate a radical-catalyzed [2σ + 2π] cycloaddition platform, providing direct access to 1,3-bicyclohexanes—geometrically congruent bioisosteres of meta-substituted benzene.

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Publication Details

Journal
Synlett
Published
2026-01-30
DOI
https://doi.org/10.1055/a-2785-2464
Primary Topic
Radical Photochemical Reactions
Type
article
Field-Weighted Citation Impact
0.00
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article

N-Heterocyclic Selone-Generated Selenium-Centered Radical for Covalent Radical Catalysis

Tingshun Zhu, Kejun Lin
Synlett
Radical Photochemical Reactions
article

N-Heterocyclic Selone-Generated Selenium-Centered Radical for Covalent Radical Catalysis

Tingshun Zhu, Kejun Lin
article en

Abstract

Abstract Covalent radical catalysis represents an emerging synthetic paradigm that exploits open-shell radical species as catalysts to drive chemical transformations. By enabling selective manipulation of highly reactive radical intermediates via controlled addition–elimination sequences, this approach offers a mild and versatile route for constructing complex cyclic frameworks with high efficiency and precision. This highlight article briefly summarizes recent advances in this area, with emphasis on our development of redox-active N-heterocyclic selones (NHSs) as catalysts. These catalysts facilitate a radical-catalyzed [2σ + 2π] cycloaddition platform, providing direct access to 1,3-bicyclohexanes—geometrically congruent bioisosteres of meta-substituted benzene.

Synlett
Sun Yat-sen University (CN)
Life in Land
Openalex Percentile: Top 72%
Radical Photochemical Reactions
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