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Abstract:
In this study, a visible-light-mediated two-component β-fluoro-fluorosulfonamidation reaction of styrenes is demonstrated. The bench-stable reagent, N-fluorosulfamoyl-pyridinium tetrafluoroborate can be used as a photoredox-active nitrogen-centered radical precursor and also as the fluoride source. This transformation can convert a series of styrenes to functional group-enriched products, including substrates with electron-donating or withdrawing groups, as well as di- and tri-substituents on the CC double bond. © 2025 Wiley-VCH GmbH.
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European Journal of Organic Chemistry
ISSN: 1434-193X
Year: 2025
Issue: 22
Volume: 28
2 . 5 0 0
JCR@2023
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ESI Highly Cited Papers on the List: 0 Unfold All
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30 Days PV: 2
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