Synthesis of Diones via Visible Light‐Induced Oxidation of α‐Hydroxy Ketone Derivatives

Abstract A visible light‐induced oxidation of α‐hydroxy ketone derivatives is reported, which is carried out in the presence of CBrCl 3 and ruthenium photocatalyst, and the corresponding diketones are obtained in 49‐95% yields. This reaction has the advantages of moderate to excellent yields, good functional group tolerance, and mild reaction condition. The free radical reaction process was confirmed by the addition of radical scavenger 2,2,6,6‐tetramethylpiperidi‐1‐oxy (TEMPO). The fluorescence quenching experiment indicated that CBrCl 3 was participated in the oxidation quenching cycle.

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Journal
ChemistrySelect
Published
2024-11-28
DOI
https://doi.org/10.1002/slct.202404657
Primary Topic
Oxidative Organic Chemistry Reactions
Type
article
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Synthesis of Diones via Visible Light‐Induced Oxidation of α‐Hydroxy Ketone Derivatives

Dongping Cheng, Shuo Hu, Yaqian Liu, Xiaoliang Xu et al.
ChemistrySelect
Oxidative Organic Chemistry Reactions
article

Synthesis of Diones via Visible Light‐Induced Oxidation of α‐Hydroxy Ketone Derivatives

Dongping Cheng, Shuo Hu, Yaqian Liu, Xiaoliang Xu, Heran Yang, Chenyue Zhao
article en

Abstract

Abstract A visible light‐induced oxidation of α‐hydroxy ketone derivatives is reported, which is carried out in the presence of CBrCl 3 and ruthenium photocatalyst, and the corresponding diketones are obtained in 49‐95% yields. This reaction has the advantages of moderate to excellent yields, good functional group tolerance, and mild reaction condition. The free radical reaction process was confirmed by the addition of radical scavenger 2,2,6,6‐tetramethylpiperidi‐1‐oxy (TEMPO). The fluorescence quenching experiment indicated that CBrCl 3 was participated in the oxidation quenching cycle.

ChemistrySelectVol. 9(45)
Zhejiang University of Technology (CN)
Clean water and sanitation
Openalex Percentile: Top 84%
Oxidative Organic Chemistry Reactions
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