108534-63-0

Upstream product

• 67-56-1 methanol 
• 62790-87-8 4-(tert-butyldimethylsilyloxy)anisole 
• 18162-48-6 tert-butyldimethylsilyl chloride 

Downstream Products

• 935-50-2 4,4-dimethoxycyclohexa-2,5-dienone 
• 108534-51-6 4-((tert-butyldimethylsilyl)oxy)-4-methoxycyclohexa-2,5-dienone 
• 114251-21-7 4-(tert-Butyl-dimethyl-silanyloxy)-4-methoxy-1-methyl-cyclohexa-2,5-dienol 
• 114251-37-5 1-tert-Butyl-4-(tert-butyl-dimethyl-silanyloxy)-4-methoxy-cyclohexa-2,5-dienol 
• 114251-25-1 1-Butyl-4-(tert-butyl-dimethyl-silanyloxy)-4-methoxy-cyclohexa-2,5-dienol 
• 114251-27-3 4-(tert-Butyl-dimethyl-silanyloxy)-1-(3,3-dimethyl-but-1-ynyl)-4-methoxy-cyclohexa-2,5-dienol 
• 114251-29-5 4-(tert-Butyl-dimethyl-silanyloxy)-1-(1-ethoxy-cyclopropyl)-4-methoxy-cyclohexa-2,5-dienol 
• 114251-23-9 4-(tert-Butyl-dimethyl-silanyloxy)-4-methoxy-1-phenyl-cyclohexa-2,5-dienol 
• 114251-30-8 4-(tert-Butyl-dimethyl-silanyloxy)-1-(4,5-dimethoxy-2-vinyl-phenyl)-4-methoxy-cyclohexa-2,5-dienol 

Relevant academic research and scientific papers

The Addition of Organolithium Reagents to Quinone Silyl Methyl Monoketals. A Useful Expedient in the Synthesis of p-Quinols Having Acid-Sensitive Groups

Acid hydrolyses of dimethyl ketals 4-alkyl- and 4-aryl-4-hydroxy-2,5-cyclohexadienones having an acid-sensitive functionality often afford low or no yields of the respective 4-substituted 4-hydroxy-2,5-cyclohexadienones (p-quinols).However, addition of me

Mixed Methyl Silyl Ketals of Quinones: Their Preparation via Anodic Oxidation and Their Chemistry

Anodic oxidation of tert-butyldimethylsilyl and tert-butyldiphenylsilyl derivatives of p-methoxyphenols affords quinone bisketals containing the uncommon alkyl silyl ketal unit.Acid hydrolysis of these quinone bisketals affords monoketals derived from hyd