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. Author manuscript; available in PMC: 2017 Jul 25.
Published in final edited form as: Angew Chem Int Ed Engl. 2016 Jun 20;55(31):8923–8927. doi: 10.1002/anie.201603149

Table 1.

Optimization of cyclooctane fluorination

graphic file with name nihms805967u2.jpg
Entry NFSI [equiv.] Catalyst [mol%] Light Source[a] Yield [%][b]
1 1.5 UO2(OAc)2•4H2O (1) A 8
2 1.5 UO2(NO3)2•6H2O (1) A 52
3 1.5 UO2(NO3)2•6H2O (1) B >95
4 1.5 UO2(NO3)2•6H2O (1) none not observed
5 1.5 none B not observed
6 1.2 UO2(NO3)2•6H2O (1) B 73
7 1.5 UO2(NO3)2•6H2O (0.5) B 52
8[c] 1.5 UO2(NO3)2•6H2O (1) B >95
[a]

Light source A: High Density blue LED strip; Light source B: high intensity blue LED lamp

[b]

Yield determined by NMR through integration relative to a methyl acetate internal standard

[c]

Acetone-d6 used as solvent