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A quantitative reactivity scale for electrophilic fluorinating reagents.


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.

SUBMITTER: Rozatian N 

PROVIDER: S-EPMC6263395 | biostudies-literature | 2018 Dec

REPOSITORIES: biostudies-literature

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A quantitative reactivity scale for electrophilic fluorinating reagents.

Rozatian Neshat N   Ashworth Ian W IW   Sandford Graham G   Hodgson David R W DRW  

Chemical science 20180914 46


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 <i>N</i>-fluoropyridinium salts, in CH<sub>3</sub>CN. The reactivi  ...[more]

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