915281-92-4

Upstream product

• 563-79-1 2,3-Dimethyl-2-butene 
• 22125-54-8 1,1-dibromo-2,2-bis(4-fluorophenyl)cyclopropane 
• 6175-14-0 1,1-bis-(4-fluorophenyl)ethene 

Downstream Products

• 1016232-03-3 C₂₅H₂₆F₂O₃ 
• 1016232-12-4 C₂₈H₃₀F₂O₅ 
• 1028333-68-7 4-(2,2-bis(4-fluorophenyl)vinylidene)-2,2,3,3,5-pentamethyl-3,4-dihydro-2H-pyrrole 
• 1047997-78-3 4-bromo-5,5-bis(4-fluorophenyl)-2-methyl-3-(propan-2-ylidene)pent-4-en-2-ol 
• 1064087-34-8 C₂₁H₂₀F₂ 
• 1093645-94-3 1-(4-(bis(4-fluorophenyl)methylene)-2,2-dimethyl-3-(propan-2-ylidene)cyclopentyl)ethanone 
• 1133246-77-1 2,2-bis(4-fluorophenyl)-3-(2,2,3,3-tetramethylcyclopropylidene)-2,3-dihydrobenzofuran 
• 1133247-00-3 2,2-bis(4-fluorophenyl)-5-methyl-3-(2,2,3,3-tetramethylcyclopropylidene)-2,3-dihydrobenzofuran 
• 1133247-02-5 5-chloro-2,2-bis(4-fluorophenyl)-3-(2,2,3,3-tetramethylcyclopropylidene)-2,3-dihydrobenzofuran 
• 1133247-06-9 2,2-bis(4-fluorophenyl)-3-(2,2,3,3-tetramethylcyclopropylidene)-1-tosylindoline 
• 1134157-13-3 C₂₉H₂₇F₂NO₂ 
• 1134157-07-5 C₂₉H₂₇F₂NO₂ 
• 1092071-91-4 C₄₄H₃₈F₂O₂ 
• 1092071-79-8 C₄₂H₃₄F₂ 

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

A catalytic method for the preparation of polysubstituted cyclopentanes: [3+2] cycloaddition of vinylidenecyclopropanes with activated olefins catalyzed by triflic imide

[3+2] Cycloadditions of vinylidenecyclopropanes (VDCPs) with electron-deficient olefins, such as methyl vinyl ketone (MVK) and acrylaldehyde, proceed smoothly in the presence of a catalytic amount of triflic imide (Tf2NH) to give the corresponding functio

Palladium-catalyzed coupling reactions of diarylvinylidenecyclopropanes with 2-iodophenol and N-(2-iodophenyl)-4-methylbenzenesulfonamide

A palladium-catalyzed cross-coupling reaction of diarylvinylidenecyclopropanes with 2-iodophenol and N-(2-iodophenyl)-4- methylbenzenesulfonamide provided a variety of cyclopropane-containing 2,2-diaryl-3-tetramethylcyclopropylidene-2,3-dihydrobenzofuran

Bronsted acid TfOH-mediated [3 + 2] cycloaddition reactions of diarylvinylidenecyclopropanes with nitriles

(Chemical Equation Presented) Diarylvinylidenecyclopropanes undergo a [3 + 2] cycloaddition reaction with MeCN in the presence of Bronsted acid TfOH to give the corresponding 3,4-dihydro-2H-pyrrole derivatives 2 in moderate to excellent yields under reflu