132802-71-2

Upstream product

• 132802-62-1 1-(tert-Butyldimethylsiloxy)-3-(allyloxy)benzene 
• 106-95-6 allyl bromide 
• 108-46-3 recorcinol 
• 132802-63-2 6-allyl-3-(tert-butyldimethylsilyloxy)phenol 
• 1616-51-9 3-allyloxyphenol 

Downstream Products

• 132802-72-3 (+/-)-trans-2-(3,4-dimethoxyphenyl)-2,3-dihydro-5-allyl-6-(allyloxy)-3-methylbenzofuran 
• 104265-73-8 rac-(2S,3S)-5-allyl-6-hydroxy-2-(3,4-dimethoxyphenyl)-3-methyl-2,3-dihydrobenzofuran 

Relevant academic research and scientific papers

Mechanistic Aspects and Synthetic Applications of the Electrochemical and Iodobenzene Bis(trifluoroacetate) Oxidative 1,3-Cycloadditions of Phenols and Electron-Rich Styrene Derivatives

Anodic oxidation of p-methoxy-substituted phenols and electron-rich styrene or propenylbenzene derivatives affords in good yield trans-dihydrobenzofurans derived from a formal 1,3-oxidative cycloaddition of the phenol to the styrene derivative.The yield o

A Convergent Route to Dihydrobenzofuran Neolignans via a Formal 1,3-Cycloaddition to Oxidized Phenols

Oxidation of p-methoxy-substituted phenols with iodobenzene bis-trifluoroacetate in the presence of electron-rich styrene derivatives affords trans-dihydrobenzofurans stereoselectively.