53449-11-9

Upstream product

• 1607-57-4 Triphenylvinyl bromide 
• 15480-89-4 potassium enolate of acetophenone 
• 10266-31-6 trans-3-Benzoyl-1,2,2-triphenylcyclopropane 
• 614-47-1 1,3-diphenyl-propen-3-one 
• 98-86-2 acetophenone 
• 859999-13-6 2,2,3,5-Tetraphenyl-5-hydroxy-tetrahydrofuran 

Downstream Products

• 2639-26-1 1,1,2,4,4-Pentaphenyl-butadien-(1,3) 
• 2491-44-3 1.1.3.4.4-Pentaphenyl-buten-⁽³⁾-ol-⁽¹⁾ 

Relevant academic research and scientific papers

Copper-catalyzed electrosynthesis of 1-acyl-2,2-diphenylcyclopropanes and their behaviour in acidic medium

The formation of 1-acyl-2,2-diphenylcyclopropanes is performed under mild electrochemical conditions. These cyclopropane derivatives, through acid-catalyzed ring-opening, lead to γ,γ-diphenyl-β,γ-unsaturated carbonyl compounds which evolve into either substituted naphthalenes, or β-benzhydryl-α,β-cycloalkenones depending on the acyclic or cyclic nature of the intermediate allyl ketone.