81585-22-0

Upstream product

• 81585-22-0 threo-diethyl 2,3-bis(4-benzoyloxy-3-methoxybenzoyl)butane-1,4-dioate 
• 1486-52-8 3-methoxy-4-benzyloxybenzoyl chloride 
• 81581-25-1 ethyl 2-(4-benzyloxy-3-methoxybenzoyl)acetoacetate 
• 60525-32-8 ethyl 3-[4-(benzyloxy)-3-methoxyphenyl]-3-oxopropanoate 
• 1486-53-9 4-(benzyloxy)-3-methoxybenzoic acid 
• 7572-90-9 ethyl 2-bromo-3-(4-benzyloxy-3-methoxyphenyl)-3-oxopropionate 

Downstream Products

• 38209-42-6 threo-2,3-bis-(α-hydroxy-4-hydroxy-3-methoxybenzyl)butane-1,4-diol 
• 67560-64-9 2,4-bis-(4-benzyloxy-3-methoxyphenyl)-3,7-dioxabicyclo<3.3.0>octane 
• 500214-33-5 erythro-2,3-bis-(α-hydroxy-4-benzyloxy-3-methoxybenzyl)butane-1,4-diol 

Relevant academic research and scientific papers

Synthesis and N.m.r. Spectra of 2,6- and 2,4-Diaryl-3,7-dioxabicyclooctanes

A series of isomeric 2,6- and 2,4-diaryl-3,7-dioxabicyclooctanes have been prepared via the corresponding threo, and erythro-dioxo-diesters.Comparison of their 1H and 13C n.m.r. spectra reveals small differences in chemical shifts and coupling constants which could be diagnostic in assigning structures to such compounds.The structure of 4-hydroxysesamin has been confirmed by direct correlation with sesamin.