Synlett p. 1241 - 1242 (1997)
Update date:2022-08-11
Topics:
Carre?o, M. Carmen
García Ruano, José L.
Sanz, Gema
Toledo, Miguel A.
Urbano, Antonio
A wide range of substituted phenols and naphthols were regioselectively monobrominated with N-bromosuccinimide, at para position in acetonitrile and at ortho position in carbon disulfide, under mild conditions in good yields. Methylphenols afforded only nuclear bromination products.
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