95210-02-9

Upstream product

• 89991-08-2 5,8-Dimethoxy-1,2,3,4-tetrahydro-naphthalene-2,3-diol 
• 87035-70-9 2,3-bis-(2-mesyloxyethyl)-1,4-dimethoxybenzene 
• 58851-64-2 6,7-epoxy-5,6,7,8-tetrahydro-1,4-dimethoxynaphthalene 
• 55077-79-7 5,8-dimethoxy-1,4-dihydronaphthalene 
• 87035-71-0 2,3-bis(2-cyanoethyl)-1,4-dimethoxybenzene 

Downstream Products

• 33628-85-2 (+/-)-2-acetyl-2-hydroxy-1,2,3,4-tetrahydro-5,8-dimethoxynaphthalene 
• 87035-72-1 2,3-bis(2-ethoxycarbonylethyl)-1,4-dimethoxybenzene 

Relevant academic research and scientific papers

A novel racemization mechanism for the α-hydroxy ketone moiety(C9-position) of optically active anthracyclinone derivatives

The facile acid-catalyzed racemization of optically active anthracyclinone derivatives((S)(+)-1a,b) was found to proceed through the ring-expanded seven-membered α-hydroxyketones(2 and/or 3 for (S)(+)-1a) by subjecting various plausible intermediates to t