118630-99-2

Upstream product

• 118630-96-9 1-<(tert-Butyldimethylsilyl)oxy>-2,6-dimethyl-4-(2-propenyl)benzene 
• 18162-48-6 tert-butyldimethylsilyl chloride 
• 118631-05-3 3-<4-<(tert-Butyldimethylsilyl)oxy>-3,5-dimethylphenyl>-1-propanol 
• 13037-83-7 4-allyl-2,6-dimethylphenol 

Downstream Products

• 125437-44-7 2,6-Dimethyl-4-<3-(pyrrol-1-yl)propyl>phenol 
• 158555-85-2 7-[4-(tert-Butyl-dimethyl-silanyloxy)-3,5-dimethyl-phenyl]-3-oxo-heptanoic acid methyl ester 
• 125437-45-8 2,6-Dimethyl-4-<3-(pyrrol-1-yl)propylidene>-2,5-cyclohexadien-1-one 
• 125404-82-2 (+/-)-2,6-Dimethyl-4-(1,2-dihydropyrrolizin-3-yl)phenol 
• 125404-80-0 2,6-Dimethyl-4-<4-(furan-3-yl)butyl>phenol 
• 125404-83-3 2,6-Dimethyl-4-<4-(furan-3-yl)butylidene>-2,5-cyclohexadien-1-one 
• 125404-84-4 (+/-)-2,6-Dimethyl-4-(4,5,6,7-tetrahydrobenzofuran-7-yl)phenol 
• 118630-78-7 2,6-Dimethyl-4-(3-methylidenecyclopentyl)phenol 
• 118630-76-5 2,6-Dimethyl-4-<4-<(trimethylsilyl)methyl>-4-pentenyl>phenol 
• 118630-77-6 2,6-Dimethyl-4-<4-<(trimethylsilyl)methyl>-4-pentenylidene>-2,5-cyclohexadien-1-one 
• 118630-84-5 3-(3,5-Dimethyl-4-hydroxyphenyl)-2-(methoxycarbonyl)-2-cyclohexen-1-one 
• 118630-83-4 2,6-Dimethyl-4-<6-(methoxycarbonyl)-5-oxo-1-hexylidene>-2,5-cyclohexadien-1-one 
• 118630-82-3 Methyl 7-(3,5-dimethyl-4-hydroxyphenyl)-3-oxoheptanoate 
• 118630-81-2 (+/-)-3,3-Bis(ethoxycarbonyl)-6-(3,5-dimethyl-4-hydroxyphenyl)-1-methylenecycloheptane 

Relevant academic research and scientific papers

Formation of Carbon-Carbon Bonds via Quinone Methide-Initiated Cyclization Reactions

p-Quinone methides were found to be excellent electrophilic cyclization initiators for the formation of six-membered rings.Cyclizations to form five- and seven-membered rings were also studied.Oxidation of 2,6-disubstituted phenols with Ag2O afforded the

PARA-QUINONE METHIDE INITIATED INTRAMOLECULAR ELECTROPHILIC SUBSTITUTION REACTIONS

A study on the reactivity of para-quinone methides in intramolecular cyclization reactions is presented.The para-quinone methides were isolated and completely characterized prior to cyclization.A furan, a pyrrole and a mono-alkyl substituted benzene were