共 49 条
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
相关论文