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Asymmetric Diaryliodonium Tosylates Useful for Metal-free Arylations

Asymmetric diaryliodonium salts bearing 1,3,5-trimethoxyphenyl (TMP) and an aryl group, are applicable to multiple arylation reactions without using a transition metal complex.1) For example, the 4-biphenylyl derivative (1) can smoothly react with phenol, sodium benzenesulfinate, and sodium azide as O-, N- and S- nucleophiles to give the corresponding O-, N- and S-aryl products.2) Furthermore, reactions with 18fluorinating agents have been reported. This 18F labeling procedure can be applied to the synthesis of molecular probe contrast agents for PET (Positron Emission Tomography) scan diagnostics.3)

P2412,T3622,D5145,B5269,T1110,F1111, B5573,B5269

Related Products

P2412
Phenyl(2,4,6-trimethoxyphenyl)iodonium p-Toluenesulfonate
T3622
[(4-Trifluoromethyl)phenyl](2,4,6-trimethoxyphenyl)iodonium p-Toluenesulfonate
D5145
(3,5-Dichlorophenyl)(2,4,6-trimethoxyphenyl)iodonium p-Toluenesulfonate
F1110
(5-Fluoro-2-nitrophenyl)(2,4,6-trimethoxyphenyl)iodonium p-Toluenesulfonate
F1111
[4-Fluoro-3-(trifluoromethyl)phenyl](2,4,6-trimethoxyphenyl)iodonium p-Toluenesulfonate
B5573
4-Biphenylyl(2,4,6-trimethoxyphenyl)iodonium Trifluoromethanesulfonate
B5269
[4-(Bromomethyl)phenyl](2,4,6-trimethoxyphenyl)iodonium p-Toluenesulfonate

References

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