The activated arenediazonium salt reacts with the arene through a C-H arylation process. This reaction results in the introduction of the aryl group onto the arene, replacing a hydrogen atom on the aromatic ring. The reaction can be selective for specific C-H bonds, depending on the conditions and the substrates used.
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4-bromo-2-(4-nitrophenyl)furan
N-((6-bromopyridin-2-yl)-methyl)benzamide
2-<4-(ethoxycarbonyl)phenyl>pyridine N-oxide
tryptamine
C15H11Cl3O
3-(4-methoxyphenyl)-2-phenylimidazo[1,2-a]pyridine
1-methyl-5-phenyl-1H-1,2,4-triazole
2-methoxy-5-nitro-3-phenylpyridine
