A quantitative reactivity scale for electrophilic fluorinating reagents

被引:54
作者
Rozatian, Neshat [1 ]
Ashworth, Ian W. [2 ]
Sandford, Graham [1 ]
Hodgson, David R. W. [1 ]
机构
[1] Univ Durham, Chem Dept, South Rd, Durham DH1 3LE, England
[2] AstraZeneca, Pharmaceut Technol & Dev, Macclesfield SK10 2NA, Cheshire, England
关键词
CATALYTIC ENANTIOSELECTIVE FLUORINATION; PHENYL-SUBSTITUTED ALKENES; ALPHA-FLUORINATION; CARBONYL-COMPOUNDS; ORGANIC-COMPOUNDS; SALTS; POWER; 1,3-DIKETONES; CHEMISTRY; TAUTOMERS;
D O I
10.1039/c8sc03596b
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
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 (TM), NFSI, Synflour (TM) 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.
引用
收藏
页码:8692 / 8702
页数:11
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