Expeditious Synthesis of Highly Functional 4-Trifluoromethyl-Substituted Oxazoles Enabled by Cobalt(II) Metalloradical Catalysis

A synthetic strategy for the catalytic cycloaddition of α-trifluoromethyl-α-diazoketones with nitriles has been achieved based on cobalt(II) metalloradical catalysis. The easily accessible starting materials, cost-effective catalyst, and experimental simplicity rendered this protocol a robust and practical approach to construct diverse functionalized 4-CF3-substituted oxazoles with high efficiency. A wide substrate scope of both α-trifluoromethylated diazoketones and nitriles is amenable to this catalytic system. The high level of functional group tolerance of this protocol provides several opportunities for precise late-stage modifications of bioactive and drug-like molecules. Mechanistic experiments and spectroscopic investigations confirm the radical nature of the reaction and reveal the involvement of both monocarbene and biscarbene radical intermediates during the catalytic process.

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Publication Details

Journal
ACS Catalysis
Published
2024-12-25
DOI
https://doi.org/10.1021/acscatal.4c07209
Citations
8
Primary Topic
Fluorine in Organic Chemistry
Type
article
Field-Weighted Citation Impact
1.66

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article

Expeditious Synthesis of Highly Functional 4-Trifluoromethyl-Substituted Oxazoles Enabled by Cobalt(II) Metalloradical Catalysis

Qingyun Duan, Baiquan Wang, Bin Li, Hang Wang
8 citations
ACS Catalysis
Fluorine in Organic Chemistry
1.66
article

Expeditious Synthesis of Highly Functional 4-Trifluoromethyl-Substituted Oxazoles Enabled by Cobalt(II) Metalloradical Catalysis

Qingyun Duan, Baiquan Wang, Bin Li, Hang Wang
article en
8 citations

Abstract

A synthetic strategy for the catalytic cycloaddition of α-trifluoromethyl-α-diazoketones with nitriles has been achieved based on cobalt(II) metalloradical catalysis. The easily accessible starting materials, cost-effective catalyst, and experimental simplicity rendered this protocol a robust and practical approach to construct diverse functionalized 4-CF3-substituted oxazoles with high efficiency. A wide substrate scope of both α-trifluoromethylated diazoketones and nitriles is amenable to this catalytic system. The high level of functional group tolerance of this protocol provides several opportunities for precise late-stage modifications of bioactive and drug-like molecules. Mechanistic experiments and spectroscopic investigations confirm the radical nature of the reaction and reveal the involvement of both monocarbene and biscarbene radical intermediates during the catalytic process.

ACS CatalysisVol. 15(2)
Chinese Academy of Sciences (CN), Nankai University (CN), Shanghai Institute of Organic Chemistry (CN), State Key Laboratory of Organometallic Chemistry
National Natural Science Foundation of China
Openalex Percentile: Top 17%
Fluorine in Organic Chemistry
1.66
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