ArticleScience advances2025
Photoredox-controlled chemo-divergent, regio-, and stereoselective difunctionalization of olefins via switchable SO
Article in Science advances, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
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Who cites it
3 citing papers in PubMed.
- Beyond Supportive Care: Mitochondria as a Strategic Therapeutic Avenue in Acute Pancreatitis.Digestive diseases and sciences · 2026Review
- Catalytic Enantioselective Construction of Carbon-Sulfur Bonds: Recent Advances and Future Perspectives.Molecules (Basel, Switzerland) · 2026Review
- Ultrasound-guided closed-loop control of magnetic hydrogel microrobots with adaptive gait switching.Microsystems & nanoengineering · 2026Article
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Authors and funding
8 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
While radical difunctionalization offers substantial potential for molecular diversification, existing methodologies predominantly focus on styrenes and activated alkenes, leaving fundamental light olefins (e.g., ethylene and propylene) largely unexplored. Moreover, achieving stereoselective transformations of light olefins remains a formidable challenge. Here, we present a visible-light-mediated photoredox-catalyzed chemo-divergent and regioselective radical difluoromethylation/polyfluoroarylsulfonylation and difluoromethylation/polyfluoroarylation of structurally diverse alkenes through switchable sulfur dioxide reintegration. The method demonstrates broad applicability across styrenes, unactivated alkenes, and gaseous ethylene/propylene substrates. The photocatalyst functions as a switch, and Sodium difluoromethanesulfinate (CF
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Registered trials
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