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All articles of this category 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. regioselectivity - phenols - naphthols - bromination - NBS
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Carreño et al. (1997) studied this question.
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