Nonafluorobutanesulfonyl Fluoride

Nonafluorobutanesulfonyl fluoride has diverse applications in organic synthesis:

• Diazotransfer Reagent: It serves as an efficient diazotransfer reagent due to its broad substrate range and stability, offering advantages over traditional reagents.
• Glycosylation Protocols: The compound has been utilized in innovative dehydrative glycosylation protocols that operate under mild alkaline conditions, facilitating the formation of disaccharides from glycosyl hemiacetals.
• Cross-Coupling Reactions: Nonafluorobutanesulfonyl fluoride is employed to generate aryl nonaflates via reactions with aryloxysilanes, which are crucial for various cross-coupling methodologies.

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