89474-91-9

Upstream product

• 106-48-9 4-chloro-phenol 
• 52431-59-1 5-chloro-8-hydroxynaphthalene-1,4-dione 
• 89474-89-5 5-Benzyloxy-8-chlor-1,4-naphthochinon 
• 77-78-1 dimethyl sulfate 

Downstream Products

• 89474-89-5 5-Benzyloxy-8-chlor-1,4-naphthochinon 
• 31039-64-2 5,6-dihydroxy-1,4-naphthoquinone 
• 99316-65-1 6,,6'-Dibenzyloxy-4,4',5,5'-tetramethoxy-2,2'-binaphthyliden-1,1'-dion 
• 99316-64-0 7,7'-Dibenzyloxy-4,4',8,8'-tetramethoxy-2,2'-binaphthyliden-1,1'-dion 
• 99316-57-1 6-Benzyloxy-5-hydroxy-1,4-naphthochinon 
• 99316-59-3 6-Benzyloxy-5-methoxy-1,4-naphthochinon 
• 99316-60-6 6-Benzyloxy-5-methoxy-naphthalene-1,4-diol 
• 99316-63-9 6-Benzyloxy-4,5-dimethoxy-1-naphthol 
• 99316-61-7 7-Benzyloxy-4,8-dimethoxy-1-naphthol 
• 99316-62-8 6-Benzyloxy-1,4,5-trimethoxynaphthalin 
• 99316-58-2 5,6-Dibenzyloxy-1,4-naphthochinon 
• 99316-66-2 7,7'-Dibenzyloxy-8,8'-dimethoxy-2,2'-binaphthyl-1,4:1',4'-dichinon 

Relevant academic research and scientific papers

Dimeric Naphthoquinones, IX. - Isodiospyrin and Elliptinone. - Synthesis of 6,6'-Dimeric Bijuglones by Phenol Oxidation

Oxidative coupling of the naphthol 37a gave the potential natural product 7,7'-dimethyl-6,6'-bijuglone (5) and, in lower yield, isodiospyrin (21).Regiospecific syntheses of 5, elliptinone (10), and 6,6'-bijuglone (45a) were achieved by phenol oxidation of suitable substituted p-chloronaphthols.