N-Bromosuccinimide as a Regioselective Nuclear Monobrominating Reagent for Phenols and Naphthols
- 1 November 1997
- journal article
- letter
- Published by Georg Thieme Verlag KG in Synlett
- Vol. 1997 (11) , 1241-1242
- https://doi.org/10.1055/s-1997-1553
Abstract
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.Keywords
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