74272-43-8

Upstream product

• 917-64-6 methyl magnesium iodide 
• 60-29-7 diethyl ether 
• 14182-01-5 (2E)-2-methyl-1,3-diphenylprop-2-en-1-one 
• 4258-37-1 1,3-diphenyl-2-methylpropene-3-one 
• 7647-01-0 hydrogenchloride 
• 67-56-1 methanol 
• 41231-80-5 (+/-)-3-hydroxy-2-methyl-1.3-diphenyl-butene-⁽¹⁾ 
• 73377-59-0 2-methyl-1,3-diphenyl-2-cyclopropene-2-ethanol 
• 7664-93-9 sulfuric acid 
• 33815-42-8 1,2-Dimethyl-3-phenyl-indan-1-ol 
• 64-19-7 acetic acid 
• 75-16-1 methylmagnesium bromide 
• 26465-83-8 1,1-dimethyl-3-phenyl-1H-indene 
• 82482-64-2 3-(2-hydroxyethyl)-2-methyl-1-phenylindene 

Downstream Products

• 76773-26-7 C₃₀H₂₄O₂ 
• 76773-25-6 C₃₀H₂₄OS 
• 42842-58-0 1,2-dimethyl-3-phenyl-1H-indene 
• 58310-20-6 1,3-dimethyl-2-phenyl-1H-indene 
• 85-52-9 2-Benzoylbenzoic acid 
• 18019-57-3 2'-benzoylacetophenone 
• 26465-83-8 1,1-dimethyl-3-phenyl-1H-indene 

Relevant academic research and scientific papers

Mechanistic Aspects of the Silver(I)-Promoted Rearrangement of Cyclopropene Derivatives

The silver ion promoted isomerizations of several substituted cyclopropenes have been studied.The results of these studies have been compared to the rearrangements encountered on thermolysis and photolysis.Treatment of 1,3-diphenyl-2-methyl-3-benzylcyclop

Sigmatropic Indenyl Rearrangements Induced by Electronic Excitation

The photochemical rearrangement of several arylalkyl substituted indenes has been studied.The rearrangements were shown to be derived from the ?,?* singlet state since triplet sensitization led to no reaction or else resulted in a Paterno-Buchi