331676-35-8Relevant academic research and scientific papers
An efficient method for the synthesis of alkylidenecyclobutanones by gold-catalyzed oxidative ring enlargement of vinylidenecyclopropanes
Yuan, Wei,Dong, Xiang,Wei, Yin,Shi, Min
, p. 10501 - 10505 (2012/11/13)
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
Li, Wei,Shi, Min
supporting information; experimental part, p. 856 - 860 (2009/06/20)
[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
Li, Wei,Shi, Min
supporting information; scheme or table, p. 270 - 274 (2009/06/21)
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
Li, Wei,Shi, Min
, p. 4151 - 4154 (2008/09/21)
(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
