Please use this identifier to cite or link to this item: http://hdl.handle.net/11189/6442
Title: Bromination products of 2-subsituted 5,7-dimethoxy-4-naphthols.
Authors: Green, Ivan R 
Hugo, VI 
Mei, MN 
Keywords: 2‐Acetoxymethyl‐5,7‐dimethoxy‐4‐naphthol;Brominations;5,7‐dimethoxy‐2‐methyl‐4‐napthol;Methyl 5,7‐dimethoxy‐4‐hydroxy‐2‐naphthoate
Issue Date: 2006
Publisher: Taylor & Francis
Source: Green, I.R., Hugo, V.I. and Mei, M.N.2006. Bromination Products of 2‐Substituted 5, 7‐Dimethoxy‐4‐Naphthols. Synthetic communications, 36(3): 331-346
Journal: Synthetic Communications 
Abstract: Bromination in acetic acid is favored at C‐8 in 5,7‐dimethoxy‐4‐naphthol when the C‐2 substituent is methyl carboxylate, whereas C‐1 is favored when the C‐2 substituent is either acetoxymethylene or methyl.
URI: http://hdl.handle.net/11189/6442
ISSN: 0039-7911
DOI: https://doi.org/10.1080/00397910500377370
Appears in Collections:Appsc - Journal Articles (DHET subsidised)

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