38464-75-4

Upstream product

• 138952-00-8 3-acetyl-2,2-diphenylpropionaldehyde 
• 86-29-3 Diphenylacetonitrile 
• 21599-40-6 2,2-diphenyl-4-pentynenitrile 
• 53750-13-3 5,5-diphenyl-2-cyclopenten-1-one 
• 35115-45-8 2,2-diphenylcyclopentanol 
• 138951-99-2 2,2-diphenylpent-4-ynal 
• 947-91-1 Diphenylacetaldehyde 
• 224319-39-5 2-amino-1-cyano-5,5-diphenyl-1,3-cyclopentadiene 
• 22351-60-6 3.3-Diphenyl-cyclopenten 

Downstream Products

• 15324-42-2 2,2-diphenylcyclopentanone 
• 81245-77-4 5,5-dideuterio-4,4-diphenylcyclopent-2-en-1-one 
• 81245-75-2 1,4,4-triphenylcyclopent-2-en-1-ol 
• 138951-50-5 (R,S)-N-tert-butyl-4,4-diphenyl-2-cyclopentenylamine 
• 4982-35-8 1,2,3-triphenylcyclopentadiene 
• 5074-28-2 1,2,4-triphenyl-1,3-cyclopentadiene 
• 81245-60-5 1,4,5-triphenylcyclopentadiene 
• 81245-55-8 2,5,5-triphenylcyclopentadiene 
• 81245-47-8 3-phenyl-3-(2,2-diphenylvinyl)cyclopropene 
• 81245-48-9 3-phenyl-3-(1-deuterio-2,2-diphenylvinyl)cyclopropene 
• 81245-62-7 5-deuterio-1,4,5-triphenylcyclopentadiene 
• 81245-56-9 1-deuterio-2,5,5-triphenylcyclopentadiene 
• 81255-41-6 5,5-dideuterio-1,4,4-triphenylcyclopent-2-en-1-ol 
• 81245-82-1 1,4,7,10-tetraphenyl-2,4,6-triazatricyclo<5.2.1.0^2,6>dec-8-ene-3,5-dione 

Relevant academic research and scientific papers

Reaction of 1-chlorovinyl p-tolyl sulfoxides with carbanion of acetonitrile: A novel synthesis of cyclopentanone derivatives with three consecutive carbon-carbon bond-formations via the enaminonitriles

Treatment of 1-chlorovinyl p-tolyl sulfoxides derived from ketones with cyanomethyllithium gave cyclopentadienyl enaminonitriles in high yields with three consecutive carbon- carbon bond-formations. However, the 1-chlorovinyl p-tolyl sulfoxides derived from aldehydes did not give good results. The mechanism of this reaction and the reaction of the enaminonitriles to convert cyclopentanone derivatives were investigated. Several α-carbanion of nitriles other than acetonitrile added to the 1-chlorovinyl p-tolyl sulfoxides at low temperature in good yield; however, they did not cyclize upon warming to room temperature. (C) 2000 Elsevier Science Ltd.

Agents for the treatment of overactive detrusor. V. Synthesis and inhibitory activity on detrusor contraction of N-tert-butyl-4,4-diphenyl-2- cyclopentenylamine

N-tert-Butyl-4,4-diphenyl-2-cyclopentenylamine ((±)-3) was designed to restrict the conformation of terodiline I and was synthesized in a 6-step approach starting with diphenylacetaldehyde (10) or in a 4-step approach starting with 2,2-diphenyl-4-pentenoi

Substituted-amine compound and a process for the preparation thereof

The compound (-)-N-t-butyl-4,4-diphenyl-2-cyclopentenylamine, or its hydrochloride salt has anticholinergic activity, and thus has a variety of pharmaceutical utilities.