N-Fluoropyridinium triflate
N-Fluoropyridinium triflate can be used as electrophilic fluorinating agent or one-electron oxidant.
See also: N-Fluoro-2,4,6-trimethylpyridinium triflate
Recent Literature
Organoselenium catalysis enables an efficient synthesis of oxygen and nitrogen
heterocycles via exo-cyclization under mild conditions in the presence of
1-fluoropyridinium triflate. The reaction offers good functional group tolerance
and excellent regioselectivity.
R. Guo, J. Huang, H. Huang, X. Zhao, Org. Lett., 2016, 18,
504-507.
Organoselenium catalysis enables an efficient synthesis of oxygen and nitrogen
heterocycles via exo-cyclization under mild conditions in the presence of
1-fluoropyridinium triflate. The reaction offers good functional group tolerance
and excellent regioselectivity.
R. Guo, J. Huang, H. Huang, X. Zhao, Org. Lett., 2016, 18,
504-507.
