16020-97-6

Upstream product

• 1210-39-5 3,3-diphenyl-2-propenal 
• 24104-20-9 2,2-diphenylcyclobutanone 
• 18107-18-1 diazomethyl-trimethyl-silane 
• 16020-95-4 2,2-Diphenyl-5-nitro-cyclopentanon 
• 119-61-9 benzophenone 
• 3917-26-8 1,1-diphenyl-3-vinyloxyprop-1-ene 
• 93878-29-6 3,3-diphenylhexanedioic acid 
• 157311-36-9 3,3-Diphenyl-hexanedioic acid diethyl ester 
• 16020-96-5 1-Nitro-3.3-diphenyl-cyclopenten 

Downstream Products

• 99647-87-7 (+/-)-4-methyl-4-phenyl-3,4-dihydronaphthalen-1(2H)-one 
• 39617-51-1 1-dimethylamino-3,3-diphenylcyclopentane 
• 24771-20-8 3,3-Diphenyl-cyclopentanol 

Relevant academic research and scientific papers

Catalytic and regioselective ring expansion of arylcyclobutanones with trimethylsilyldiazomethane. Ligand-dependent entry to β-ketosilane or enolsilane adducts

Divergent reactivity is uncovered in the homologation of arylcyclobutanones with trimethylsilyldiazomethane. With Sc(OTf)3 as catalyst, enolsilanes are obtained with a high preference for methylene migration. By contrast, Sc(hfac)3 g

Metal mediated one-pot synthesis of cyclopentanones from allyl vinyl esters or diallyl ethers via tandem Claisen rearrangement and hydroacylation

Cyclopentanones 3 and 7 are generated in a one-pot procedure from allyl vinyl ethers 1 and diallyl ethers 4, respectively. The conversion is carried out in the presence of RhCl(cod)(dppe) or RuCl2(PPh3)3 at elevated temper