915281-93-5

Upstream product

• 18218-20-7 1-(4-chlorophenyl)-1-phenylethene 

Downstream Products

• 1016232-04-4 C₂₅H₂₇ClO₃ 
• 1016232-13-5 C₂₈H₃₁ClO₅ 
• 1047997-82-9 4-bromo-5-(4-chlorophenyl)-2-methyl-5-phenyl-3-(propan-2-ylidene)-5-p-tolylpent-4-en-2-ol 
• 1093646-04-8 1-(4-((4-chlorophenyl)(phenyl)methylene)-2,2-dimethyl-3-(propan-2-ylidene)cyclopentyl)ethanone 
• 1093645-95-4 1-(4-((4-chlorophenyl)(phenyl)methylene)-2,2-dimethyl-3-(propan-2-ylidene)cyclopentyl)ethanone 
• 1187948-00-0 1-(2-(4-chlorophenyl)-2-phenylvinyl)-2,2,3,3-tetramethylcyclopropyl diphenylphosphinodithioate 
• 1240017-69-9 C₃₄H₂₉ClO 
• 1332583-77-3 C₂₇H₂₇ClO₂ 
• 1332583-90-0 C₂₉H₃₁ClO₂ 
• 1403484-28-5 C₂₁H₂₁ClO 
• 1403484-29-6 C₂₁H₂₁ClO 
• 1160169-86-7 ethyl 2-(8-(4-chlorophenyl)-2,2-dimethyl-1,3-di(propan-2-ylidene)-1,2,3,3a-tetrahydrocyclopenta[a]inden-3a-yl)acetate 
• 1189751-97-0 C₄₄H₃₇Cl 
• 1160126-91-9 C₅₁H₅₁NO₆S 

Relevant academic research and scientific papers

An efficient method for the synthesis of alkylidenecyclobutanones by gold-catalyzed oxidative ring enlargement of vinylidenecyclopropanes

Rings of gold: Vinylidenecyclopropanes can undergo efficient oxidative ring enlargements under mild conditions to give the corresponding alkylidenecyclobutanone derivatives in good yields (see scheme). A plausible mechanism for this transformation has bee