Uranyl-Enabled Photocatalytic C(sp <sup>3</sup> )–H Functionalization with Azoles

Under mild conditions, uranyl nitrate catalyzed C(sp<sup>3</sup>)-center/azole coupling without external additives, offering a broad substrate scope and high yields (up to 95%). The method was further validated under sunlight and in scale-up experiments, highlighting its industrial potential. Experimental and theoretical studies show that uranyl nitrate acts via both hydrogen-atom transfer (HAT) and non-HAT concerted proton-electron transfer mechanisms. This approach provides a green, efficient protocol for C(sp<sup>3</sup>)-azole bond formation.

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Publication Details

Journal
Organic Letters
Published
2026-01-30
DOI
https://doi.org/10.1021/acs.orglett.5c05026
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
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article

Uranyl-Enabled Photocatalytic C(sp 3 )–H Functionalization with Azoles

Y Z Luo, Yan-Xin Jiang, Jing Su, Songbai Tang et al.
Organic Letters
Catalytic C–H Functionalization Methods
article

Uranyl-Enabled Photocatalytic C(sp 3 )–H Functionalization with Azoles

Y Z Luo, Yan-Xin Jiang, Jing Su, Songbai Tang, Shu-Yun Zhang, Jia-Hao Ruan
article en

Abstract

Under mild conditions, uranyl nitrate catalyzed C(sp<sup>3</sup>)-center/azole coupling without external additives, offering a broad substrate scope and high yields (up to 95%). The method was further validated under sunlight and in scale-up experiments, highlighting its industrial potential. Experimental and theoretical studies show that uranyl nitrate acts via both hydrogen-atom transfer (HAT) and non-HAT concerted proton-electron transfer mechanisms. This approach provides a green, efficient protocol for C(sp<sup>3</sup>)-azole bond formation.

Organic LettersVol. 28(6)
Sichuan University (CN)
Industry, innovation and infrastructure
Openalex Percentile: Top 72%
Catalytic C–H Functionalization Methods
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