23451-58-3

Upstream product

• 75-18-3 dimethylsulfide 
• 1794-48-5 1-bromo-3-phenylprop-2-yne 

Downstream Products

• 23451-59-4 (2-Phenyl-Δ^2,3-butadienyl)-methylsulfid 
• 27334-37-8 Methyl-2-phenyl-4-(1-hydroxycyclohexyl)-2,3-butadienyl sulfide 
• 27455-89-6 (Z)-1-(Dimethyl-λ⁴-sulfanylidene)-3,4-diphenyl-but-3-en-2-one 
• 30747-30-9 2-Methylsulfanylethynyl-1,2,3-triphenyl-propane-1,3-dione 
• 30725-14-5 Acetic acid (Z)-1-benzyl-3-oxo-3-phenyl-propenyl ester 
• 27364-29-0 Benzoic acid (E)-1-[1-methylsulfanyl-meth-(Z)-ylidene]-2,3-diphenyl-allyl ester 
• 30725-16-7 2-Methanesulfonylethynyl-1,2,3-triphenyl-propane-1,3-dione 
• 94897-34-4 3,4-diphenyl-2-butanone 
• 1308273-98-4 5-cyclohexyl-3-iodo-2-phenyl-1-(toluene-4-sulfonyl)-1H-pyrrole 
• 1308274-18-1 5-cyclohexyl-3-(4-methoxyphenyl)-2-phenyl-1-(toluene-4-sulfonyl)-1H-pyrrole 

Relevant academic research and scientific papers

Counterion effects in a gold-catalyzed synthesis of pyrroles from alkynyl aziridines

Aryl-substituted N-tosyl alkynyl aziridines undergo a gold-catalyzed ring expansion to afford 2,5-substituted pyrrole products. Under certain conditions, a ring-expansion and rearrangement leads to 2,4-substituted pyrroles. The reaction pathway is determi

A facile and regioselective synthesis of 2,5-disubstituted pyrroles via gold-catalyzed cycloisomerization of acetylenylaziridines

Gold-catalyzed cycloisomerization reaction of acetylenylaziridines provides 2,5-disubstituted pyrroles in high yields. The presence of protic species accelerates the reaction rate and improves the yields of pyrrole products.