Like other aromatic compounds, benzofurano-, indolo-, and benzothieno-3-sulfolenes can undergo electrophilic aromatic substitution reactions. These reactions involve the addition of electrophilic species to the aromatic ring. Common examples include nitration, halogenation, and sulfonation reactions.
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2-(1,1-Dioxo-2,3-dihydro-1H-1λ6-thiophen-3-yl)-phenol
(-)-2-(p-nitrophenyl)-2-nitrobutane
2-iodo-3-Methoxythiophene
1H-Indole, 1-acetyl-4,6-bis(trimethylsilyl)-
2-(2,2,2-Trifluoro-1-hydroxy-1-trifluoromethyl-ethyl)-benzene-1,3,5-triol
2,2,3,3,5,6-hexamethyl-1-oxo-2,3-dihydropyrazin-1-ium-4(1H)-olate
1,1-dichloro-2-methyl-2-(4-nitrophenyl)cyclopropane
N-<5-(4-Chlorophenyl)-1,3,4-thiadiazol-2-yl>acrylamide
2-bromo-1,3,4,5-tetramethoxybenzene
2-Dodecyne, 1,1-diethoxy-4-[(triphenylmethyl)thio]-
Benzoic acid, 3-formyl-4,6-dimethoxy-2,5-dimethyl-, methyl ester
(E,Z)-2-benzoyl-3-phenylbut-2-enenitrile
4-Iodo-1-methyl-1H-pyrazole
3-(2,2-Dimethyl-propionylamino)-2-(4-methoxy-phenyl)-propionic acid
