A quantitative reactivity scale for electrophilic fluorinating reagents
Electrophilic N-F fluorination agents underpin the introduction of fluorine in aliphatic systems across drug and academic research. The choice of N-F reagent is currently determined through empirical experimentation in the absence of quantitative values for electrophilicities. Here we report an expe...
Gespeichert in:
Veröffentlicht in: | Chemical science (Cambridge) 2018-12, Vol.9 (46), p.8692-8702 |
---|---|
Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | Electrophilic N-F fluorination agents underpin the introduction of fluorine in aliphatic systems across drug and academic research. The choice of N-F reagent is currently determined through empirical experimentation in the absence of quantitative values for electrophilicities. Here we report an experimentally-determined kinetic reactivity scale for ten N-F fluorinating reagents, including Selectfluor™, NFSI, Synfluor™ and several
-fluoropyridinium salts, in CH
CN. The reactivity scale, which covers eight orders of magnitude, employs
-substituted 1,3-diaryl-1,3-dicarbonyl derivatives to measure relative and absolute rate constants. The
-substituted 1,3-diaryl-1,3-dicarbonyl scaffold delivers a convenient, sensitive spectrophotometric reporter of reactivity that also led to the discovery of a unique form of tautomeric polymorphism. |
---|---|
ISSN: | 2041-6520 2041-6539 |
DOI: | 10.1039/c8sc03596b |