59869-79-3

Upstream product

• 527-60-6 Mesitol 
• 25347-59-5 3,5,3',5'-tetramethyl-stilbene-4,4'-diol 
• 45952-56-5 3,5-dimethyl-4-hydroxybenzyl bromide 
• 67-66-3 chloroform 
• 94-36-0 dibenzoyl peroxide 
• 4906-82-5 6-acetoxy-2,4,6-trimethyl-cyclohexa-2,4-dienone 
• 75-91-2 tert.-butylhydroperoxide 
• 71-43-2 benzene 
• 4397-14-2 4-(hydroxymethyl)-2,6-dimethylphenol 
• 73324-22-8 1,1,1-trichloro-2,2-bis-(4-hydroxy-3,5-dimethyl-phenyl)-ethane 
• 88-05-1 2,4,6-trimethylaniline 

Downstream Products

• 25347-59-5 3,5,3',5'-tetramethyl-stilbene-4,4'-diol 
• 6476-26-2 4,4’-(ethane-1,2-diyl)bis(2,6-dimethylphenol) 
• 99949-66-3 α,α'-dibromo-3,5,3',5'-tetramethyl-bibenzyl-4,4'-diol 

Relevant academic research and scientific papers

Selective benzylic C-C coupling catalyzed by a bioinspired dicopper complex

A highly preorganized bioinspired dicopper complex with imidazole ligation catalyzes the selective benzylic para-C-H activation of 2,4,6-trimethylphenol under aerobic conditions, yielding either the stilbenequinone or 4-methoxymethyl-2,6-dimethylphenol depending on the solvent used. The Royal Society of Chemistry.

Copper-catalyzed oxidative coupling of 2,4,6-Trimethylphenol with oxygen

2,4,6-Trimethylphenol was oxidized with oxygen in the presence of (1,4,7-tribenzyl-1,4,7-triazacyclononane)copper(II) chloride as a catalyst to produce exclusively a coupled product stilbenequinone, without the formation of oxygenated products.