The organophotocatalytic trifluoromethylation of 6-azauracils

An efficient, cost-effective, and metal-free photocatalytic trifluoromethylation of 6-azauracils has been developed using Langlois reagent (CF<sub>3</sub>SO<sub>2</sub>Na) under ambient air. The present protocol, which utilizes an inexpensive CF<sub>3</sub> reagent and an organophotocatalyst, provides a convenient way to prepare trifluoromethylated azauracil derivatives with a variety of functional groups. The experimental results suggest a radical mechanistic pathway for this methodology.

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Publication Details

Journal
RSC Advances
Published
2025-01-01
DOI
https://doi.org/10.1039/d5ra00743g
Citations
3
Primary Topic
Fluorine in Organic Chemistry
Type
article
Field-Weighted Citation Impact
2.37

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article

The organophotocatalytic trifluoromethylation of 6-azauracils

Krishna Kanta Das, Alakananda Hajra
3 citations
RSC Advances
Fluorine in Organic Chemistry
2.37
article

The organophotocatalytic trifluoromethylation of 6-azauracils

Krishna Kanta Das, Alakananda Hajra
article en
3 citations

Abstract

An efficient, cost-effective, and metal-free photocatalytic trifluoromethylation of 6-azauracils has been developed using Langlois reagent (CF<sub>3</sub>SO<sub>2</sub>Na) under ambient air. The present protocol, which utilizes an inexpensive CF<sub>3</sub> reagent and an organophotocatalyst, provides a convenient way to prepare trifluoromethylated azauracil derivatives with a variety of functional groups. The experimental results suggest a radical mechanistic pathway for this methodology.

RSC AdvancesVol. 15(15)
Visva-Bharati University (IN)
Council of Scientific and Industrial Research, India
Openalex Percentile: Top 12%
Fluorine in Organic Chemistry
2.37
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