The Journal of Organic Chemistry· 2026Q2
Visible-Light-Induced Synthesis for Sulfonyl (Thio)chromones and 4-Quinolones from 2-Alknyl Benzaldehydes and Sodium Sulfinates via a Cascade Sulfonylation/Cyclization/Isomerization Processes
- 0citations
- Q2SCImago
- 2026year
Short summary
A new visible-light photoredox reaction enables a one-pot synthesis of sulfonyl 4-(thio)chromones and 4-quinolones from 2-alkynyl benzaldehydes and sodium sulfinates.
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Key points
- Visible-light photoredox reaction for synthesizing sulfonyl 4-(thio)chromones and 4-quinolones.
- Employs 2-alkynyl benzaldehydes and sodium sulfinates as starting materials.
- One-pot cascade process involves radical sulfonylation, cyclization, and isomerization.
- Enables straightforward assembly of protecting-group-free sulfonyl 4-quinolones.
- Protocol offers broad substrate scope and excellent functional group compatibility.
AI-generated from the title and abstract; the full text is not read.
Abstract
Abstract Herein, we report a visible-light-mediated photoredox reaction for the synthesis of sulfonyl 4-(thio)chromones and 4-quinolone derivatives. This transformation employs easily accessible 2-alkynyl benzaldehydes and sodium sulfinates as starting materials, enabling a one-pot cascade process involving radical sulfonylation, cyclization, and isomerization under mild conditions. Notably, this strategy allows the straightforward assembly of protecting-group-free sulfonyl 4-quinolones. Benefiting from its operational simplicity, broad substrate scope, and excellent functional group compatibility, this protocol provides a practical approach for the construction of valuable 4-(thio)chromones and 4-quinolone derivatives with potential biological and synthetic applications
The authors' abstract, as published at the source. The Journal of Organic Chemistry, 2026 · DOI ↗
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Field: Organic Chemistry
Organic ChemistryChemistry