1337550-58-9

Upstream product

• 767330-04-1 (-)-(3S)-1-[4-(benzyloxy)phenyl]hex-5-en-3-ol 
• 68486-77-1 3-(4-(benzyloxy)phenyl)propanal 
• 186895-45-4 ethyl 3-(4-(benzyloxy)phenyl)propanoate 
• 87030-11-3 ethyl 3-(4-(benzyloxy)phenyl)acrylate 
• 1187819-84-6 (S)-5-(4-(benzyloxy)phenyl)-3-(tert-butyldimethylsilyloxy)pentan-1-ol 
• 1187819-79-9 (3S)-5-[4-(benzyloxy)phenyl]-3-{[tert-butyl(dimethyl)silyl]oxy}pentanal 
• 1638640-04-6 ({(3S)-1-[4-(benzyloxy)phenyl]hex-5-en-3-yl}oxy)(tert-butyl)(dimethyl)silane 

Downstream Products

• 1335038-28-2 C₃₉H₃₆F₆O₇ 
• 1335038-26-0 C₃₉H₃₆F₆O₇ 

Relevant academic research and scientific papers

Stereoselective total synthesis of (3S,5S)-1,7-bis(4-hydroxyphenyl)heptane-3,5-diol, (3S,5S)-alpinikatin, and its diastereoisomers

Stereoselective synthesis of the diarylheptanoids, (3S,5S)-1,7-bis(4-hydroxyphenyl)heptane-3,5-diol (1), (3S,5S)-alpinikatin (3), and their diastereoisomers (2 and 4, resp.), was achieved from readily available 4-hydroxybenzaldehyde. The synthetic sequenc

Lewis acid catalyzed synthesis of cyclic carbonates, precursors of 1,2- and 1,3-diols

An eco-friendly synthesis of cyclic carbonates through a Lewis acid catalyzed cyclization of tert-butyl carbonates is described. These cyclic carbonates are precursors of 1,2- and 1,3-diols, and the developed method was applied to a short synthesis of a diarylheptanoid, (3S,5S)-alpinikatin.