879885-56-0Relevant academic research and scientific papers
Bromination products of 2-substituted 5,7-dimethoxy-4-naphthols
Green, Ivan R.,Hugo, Victor I.,Mei, Mawonga N.
, p. 331 - 346 (2006)
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. Copyright Taylor & Francis LLC.
