1628058-67-2

Upstream product

• 1628058-56-9 1-(2-((tert-butyldiphenylsilyloxy)methyl)phenyl)propane-1,3-diol 
• 1628058-57-0 3-(tert-butyldimethylsilyloxy)-1-(2-((tert-butyldiphenylsilyloxy)methyl)phenyl)propan-1-one 
• 149170-33-2 (2-((tert-butyldiphenylsilyloxy)methyl)phenyl)methanol 
• 1628058-60-5 C₃₃H₄₆O₂Si₂ 
• 1628058-59-2 3-(2-((tert-butyldiphenylsilyloxy)methyl)phenyl)but-3-en-1-ol 
• 84-66-2 Diethyl phthalate 
• 1628058-64-9 C₃₄H₃₈O₄SSi 
• 1628058-66-1 C₂₇H₃₁N₃OSi 
• 612-14-6 phthalyl alcohol 
• 1628058-55-8 1-(2-((tert-butyldiphenylsilyloxy)methyl)phenyl)but-3-en-1-ol 
• 175158-50-6 2-(tert-Butyl-diphenyl-silanyloxymethyl)-benzaldehyde 

Downstream Products

• 1628058-61-6 N-(3-(2-((tert-butyldiphenylsilyloxy)methyl)phenyl)but-3-enyl)-4-methylbenzenesulfonamide 
• 1628058-62-7 N-(3-(2-(hydroxymethyl)phenyl)but-3-enyl)-4-methylbenzenesulfonamide 

Relevant academic research and scientific papers

Prins spirocyclization for the synthesis of spiro[isobenzofuran-pyran] derivatives

A Prins cascade process was developed for the synthesis of tetrahydro-3H-spiro[isobenzofuran-pyran] derivatives in good yields and selectivity by the condensation of 3-[2-(hydroxymethyl)phenyl]but-3-en-1-ols with aldehydes or ketones. The reaction proceeds smoothly in the presence of indium(III) trifluoromethanesulfonate (30 mol-%) in dichloroethane at 80 C. This is the first report on the synthesis of tetrahydro-3H-spiro[isobenzofuran- pyran] scaffolds through a Prins cascade reaction. Copyright