196872-52-3

Upstream product

• 196872-48-7 (R,S)-2-(4-ethoxycarbonylphenyl)-1,4,9,10-tetrahydro-5,8-dimethoxy-9,10-(o-benzeno)anthracene-1,4-dione 
• 402582-31-4 (R,S)-2-(4-ethoxycarbonylphenyl)-9,10-dihydro-5,8-dimethoxy-9,10-(o-benzeno)anthracene-1,4-diol 
• 402582-34-7 (R,S)-1,4,9,10-tetrahydro-2-(4-hydroxymethylphenyl)-5,8-dimethoxy-9,10-(o-benzeno)anthracene-1,4-dione 

Downstream Products

• 402582-39-2 (R,S)-2-(4-formylphenyl)-9,10-dihydro-5,8-dimethoxy-9,10-(o-benzeno)anthracene-1,4-diol 

Relevant academic research and scientific papers

Electron donor-acceptor compounds: Exploiting the triptycene geometry for the synthesis of porphyrin quinone diads, triads, and a tetrad

Rigidly and covalently linked porphyrin quinones are well established as model compounds for studying photo-induced electron transfer (PET) reactions like those occurring during the primary processes of photosynthesis. In this context, the synthesis of a