75010-96-7

Upstream product

• 186581-53-3 diazomethane 
• 13128-74-0 4,4-diphenylcyclohexane-1,3-dione 
• 67-56-1 methanol 
• 119-61-9 benzophenone 
• 781-35-1 1,1-diphenylacetone 

Downstream Products

• 4528-64-7 4,4-diphenyl-2-cyclohexen-1-one 
• 103367-61-9 4-methyl-5,5-diphenylcyclohex-2-en-1-one 
• 103367-60-8 3-methyl-4,4-diphenylcyclohex-1-ene 
• 103367-63-1 C₂₇H₂₉NO₂S 
• 103367-59-5 3-methyl-4,4-diphenylcyclohex-2-ene-1-one tosylhydrazone 
• 103367-65-3 (+)-4-methyl-5,5-diphenylcyclohex-2-en-1-one 
• 103367-64-2 (-)-4-methyl-5,5-diphenylcyclohex-2-en-1-one 
• 103367-68-6 (-)-2-trans-propenyl-3,3-diphenylcyclobutanone 
• 103367-47-1 3,4,4-triphenylcyclohex-2-en-1-one 
• 17429-38-8 3-methyl-4,4-diphenylcyclohex-2-ene-1-one 

Relevant academic research and scientific papers

Synthesis of 1,3-Cycloalkadienes from Cycloalkenes: Unprecedented Reactivity of Oxoammonium Salts

Few methods allow for the direct conversion of cycloalkenes into cycloalkadienes with high chemo- and regioselectivity. Herein, we report a convenient one-pot process for this transformation that involves the unprecedented N-preferential group transfer of N-oxoammonium salts to cycloalkenes, followed by Cope elimination, to afford cycloalkadienes at room temperature and pressure.

Type A Zwitterions and Cyclohexadienone Photochemical Rearrangements. Mechanistic and Exploratory Organic Photochemistry

The photochemistry of 3-methoxy-4,4-diphenyl-2,5-cyclohexadienone was studied.The type A rearrangement proved to be regioselective with a preference for formation of 4-methoxy-6,6-diphenylbicyclohex-3-en-2-one relative to 5-methoxy-6,6-diphenylbicy