115237-88-2

Upstream product

• 67-56-1 methanol 
• 115237-86-0 4-hydroxy-1,1':2',1”-terphenyl 
• 148517-58-2 3'-methyl-2'-vinyl-4-biphenylol 
• 148517-74-2 Acetic acid 2'-(1-methoxy-ethyl)-3'-methyl-biphenyl-4-yl ester 
• 148517-73-1 4-Hydroxy-4-[2-(1-methoxy-ethyl)-3-methyl-phenyl]-cyclohexa-2,5-dienone 
• 148517-57-1 2'-(1-methoxyethyl)-3'-methyl-4-biphenylol 
• 535961-79-6 2-bromo-6-methylbenzoyl chloride 
• 148517-56-0 methyl ether of 2-bromo-6-methyl-α-methylbenzyl alcohol 
• 148517-71-9 1-(2-bromo-6-methylphenyl)ethanone 
• 148517-72-0 2-bromo-6-methyl-α-methylbenzyl alcohol 
• 4389-50-8 2-amino-6-methylbenzoic acid 
• 90259-31-7 2-bromo-6-methylbenzoic acid 
• 935-50-2 4,4-dimethoxycyclohexa-2,5-dienone 
• 2052-07-5 2-Bromobiphenyl 

Relevant academic research and scientific papers

SPIRO-ANNULATED CYCLOHEXA-2,5-DIENONES VIA ELECTROOXIDATION OF P-ARYL PHENOLS A NOVEL MODE OF ANODIC CARBON-CARBON BOND FORMATION

Intramolecular trapping of the reactive intermediate from anodic oxidation of 2'-alkenyl substituted p-aryl phenols, followed by solvent capture, affords 4-aryl-4-alkyl-cyclohexa-2,5-dienones.

Intramolecular Anodic Carbon-Carbon Bond-Forming Reactions of Oxidized Phenol Intermediates Leading to Spirodienones. Structural Effects on Reactivity and Evidence for a Phenoxonium Ion Intermediate

Anodic oxidation of 4-phenylphenol in methanol leads to 4-methoxy-4-phenylcyclohexa-2,5-dienones whereas anodic oxidation of 4-(2-alkenylphenyl)-phenols leads to spirocyclic 2,5-cyclohexadienones in competition with methanol addition to the 4-position.Usi