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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 2.

Fluorination of hydrocarbons

graphic file with name nihms805967u3.jpg
Entry substrate product Yield [%][a]
1 graphic file with name nihms805967t1.jpg graphic file with name nihms805967t2.jpg > 95
2 graphic file with name nihms805967t3.jpg graphic file with name nihms805967t4.jpg 42
3 graphic file with name nihms805967t5.jpg graphic file with name nihms805967t6.jpg 32
4 graphic file with name nihms805967t7.jpg graphic file with name nihms805967t8.jpg 55
5 graphic file with name nihms805967t9.jpg graphic file with name nihms805967t10.jpg 60
6 graphic file with name nihms805967t11.jpg graphic file with name nihms805967t12.jpg trace
7 graphic file with name nihms805967t13.jpg graphic file with name nihms805967t14.jpg trace
[a]

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