24457-06-5

Upstream product

• 2668-47-5 2,6-di(t-butyl)-4-phenylphenol 
• 2525-38-4 2,6-di-tert-butyl-4-phenylphenoxyl 

Downstream Products

• 2668-47-5 2,6-di(t-butyl)-4-phenylphenol 
• 83638-55-5 5-acetylthio-3-t-butyl-1,1'-biphenyl-4-yl acetate 
• 83638-64-6 4-acetylthio-4-phenyl-2,6-di-t-butylcyclohexa-2,5-dienone 
• 20058-37-1 1,4-Diphenyl-2,6-di-t-butyl-cyclohexa-2,5-dien-1,4-diol 
• 6863-53-2 5'-(tert-butyl)-[1,1':3',1''-terphenyl]-4'-ol 
• 83638-66-8 4-(2-methylprop-2-enyl)-4-phenyl-2,6-di-t-butylcyclohexa-2,5-dienone 
• 83638-56-6 2-methyl-6-phenyl-4-t-butylbenzo-1,3-dioxole 
• 68757-65-3 5-t-butyl-1,1'-biphenyl-3,4-diyl diacetate 
• 83638-53-3 4-(2-acetoxy-2-methylpropyl)-4-phenyl-2,6-di-t-butylcyclohexa-2,5-dienone 
• 83638-52-2 3-(3-acetoxy-5-t-butyl-1,1'-biphenyl-4-oxy)-5-t-butyl-1,1'-biphenyl-4-ol 
• 83638-65-7 3-(3'-acetoxy-5-t-butyl-1,1'-biphenyl-4-oxy)-5-t-butyl-1,1'-biphenyl-4-yl acetate 
• 68757-64-2 4-acetoxy-4-phenyl-2,6-di-t-butylcyclohexa-2,5-dienone 
• 24456-99-3 5-phenyl-3-t-butyl-1,2-benzoquinone 
• 68757-66-4 4-hydroxy-5-t-butyl-1,1'-biphenyl-3-yl acetate 

Relevant academic research and scientific papers

Field control of regioselectivity in CoIII(salpr)(OH) promoted oxygenation of 4-aryl-2,6-di-terf-butylphenols

In the CoIII(salpr)(OH) catalyzed oxygenation of 4-aryl-2,6-di-tert-butylphenols, the position of dioxygen incorporation is completely controlled by the nature of solvent; dioxygen incorporation occurs only at ortho position in an uncoordinativ

SYNTHESES VIA ANODICALLY PRODUCED PHENOXENIUM IONS. APPLICATIONS IN THE FIELD OF PEPTIDES AND CARBOHYDRATES

Sterically hindered phenols are anodically oxidized to the corresponding phenoxenium ions which react with O- and N-nucleophiles to give cyclohexadienyl-protected nucleophiles. 4-Acyloxy substituted phenoxenium ions can transfer the acyl group to nucleoph