Photocatalytic Synthesis of α-Fluoro-β-sulfonyl Carbonyl Compounds Using Nucleophilic Fluorine Sources
Abstract
Herein, we report a photocatalytic synthesis of α-fluoro-β-sulfonyl carbonyl compounds using nucleophilic fluorine sources under photo redox-neutral conditions. The key to this transformation is the generation of α-carbonyl carbocations via single-electron oxidation of β-sulfonyl-α-carbonyl radicals, which are formed through regioselective sulfonyl radical addition to α,β-unsaturated carbonyl compounds. This method offers efficient and general access to structurally diverse α-fluorinated carbonyl building blocks, expanding the synthetic toolbox for fluorinated molecule construction.
Fields of Study & Subjects
Fluorine in Organic Chemistry
Radical Photochemical Reactions
Sulfur-Based Synthesis Techniques
Publication details
- Journal / source
- Organic Letters
- Publisher
- American Chemical Society (ACS)
- Volume
- 28
- Issue
- 7
- Pages
- 2529–2533
- Publication date
- 9 February 2026
- Language
- EN