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A quantitative reactivity scale for electrophilic fluorinating reagents.
Rozatian, Neshat; Ashworth, Ian W; Sandford, Graham; Hodgson, David R W.
Afiliação
  • Rozatian N; Chemistry Department , Durham University , South Road , Durham , DH1 3LE , UK . Email: d.r.w.hodgson@durham.ac.uk.
  • Ashworth IW; AstraZeneca , Pharmaceutical Technology & Development , Macclesfield , SK10 2NA , UK.
  • Sandford G; Chemistry Department , Durham University , South Road , Durham , DH1 3LE , UK . Email: d.r.w.hodgson@durham.ac.uk.
  • Hodgson DRW; Chemistry Department , Durham University , South Road , Durham , DH1 3LE , UK . Email: d.r.w.hodgson@durham.ac.uk.
Chem Sci ; 9(46): 8692-8702, 2018 Dec 14.
Article em En | MEDLINE | ID: mdl-30595834
ABSTRACT
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 N-fluoropyridinium salts, in CH3CN. The reactivity scale, which covers eight orders of magnitude, employs para-substituted 1,3-diaryl-1,3-dicarbonyl derivatives to measure relative and absolute rate constants. The para-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.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2018 Tipo de documento: Article