Progress in Radical Fluorosulfonyl Reagents

Abstract Sulfur(VI) fluoride exchange (SuFEx) chemistry that relies on the unique reactivity–stability balance of high valent organosulfur has emerged as a promising topic for the next-generation click reaction. Sulfonyl fluorides are the most widely used connective hubs of the SuFEx click reaction with widespread applications in the fields of chemical biology, drug discovery, and materials science. Compared with current methods, direct fluorosulfonylation with fluorosulfonyl radicals has emerged as a concise and efficient approach for the production of sulfonyl fluorides. The highly active SO2F radical was an unstable and inaccessible precursor until it was observed in the decomposition of fluorosulfonyl azide, which inspired efforts towards the production of fluorosulfonyl radical precursors for direct radical fluorosulfonylation processes. This review presents and discusses current breakthroughs in the generation of fluorosulfonyl radicals from various radical precursors, as well as their application in the synthesis of diverse functionalized sulfonyl fluorides. 1 Introduction 2 FSO2Cl as a Radical Precursor 3 Benzimidazolium Fluorosulfonates as Radical Precursors 4 Alk-1-ynylsulfonyl Fluorides as Radical Precursors 5 (Diarylmethylene)sulfamoyl Fluorides as Radical Precursors 6 Vinyl Fluorosulfates as Radical Precursors 7 Conclusion and Outlook

Authors

Publication Details

Journal
Synthesis
Published
2024-11-11
DOI
https://doi.org/10.1055/s-0043-1775417
Citations
6
Primary Topic
Fluorine in Organic Chemistry
Type
article
Field-Weighted Citation Impact
1.25

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article

Progress in Radical Fluorosulfonyl Reagents

Heyin Li, Yi Wang
6 citations
Synthesis
Fluorine in Organic Chemistry
1.25
article

Progress in Radical Fluorosulfonyl Reagents

Heyin Li, Yi Wang
article en
6 citations

Abstract

Abstract Sulfur(VI) fluoride exchange (SuFEx) chemistry that relies on the unique reactivity–stability balance of high valent organosulfur has emerged as a promising topic for the next-generation click reaction. Sulfonyl fluorides are the most widely used connective hubs of the SuFEx click reaction with widespread applications in the fields of chemical biology, drug discovery, and materials science. Compared with current methods, direct fluorosulfonylation with fluorosulfonyl radicals has emerged as a concise and efficient approach for the production of sulfonyl fluorides. The highly active SO2F radical was an unstable and inaccessible precursor until it was observed in the decomposition of fluorosulfonyl azide, which inspired efforts towards the production of fluorosulfonyl radical precursors for direct radical fluorosulfonylation processes. This review presents and discusses current breakthroughs in the generation of fluorosulfonyl radicals from various radical precursors, as well as their application in the synthesis of diverse functionalized sulfonyl fluorides. 1 Introduction 2 FSO2Cl as a Radical Precursor 3 Benzimidazolium Fluorosulfonates as Radical Precursors 4 Alk-1-ynylsulfonyl Fluorides as Radical Precursors 5 (Diarylmethylene)sulfamoyl Fluorides as Radical Precursors 6 Vinyl Fluorosulfates as Radical Precursors 7 Conclusion and Outlook

SynthesisVol. 57(10)
National Natural Science Foundation of China, China Postdoctoral Science Foundation
Clean water and sanitation
Openalex Percentile: Top 23%
Fluorine in Organic Chemistry
1.25
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Progress in Radical Fluorosulfonyl Reagents — Heyin Li, Yi Wang · Synthesis (2024) | TGRS Research Map | TGRS