3493-18-3

Upstream product

• 1889-78-7 2-bromo-1-(4-chlorophenyl)-2-phenylethanone 
• 1889-71-0 4'-chloro-2-phenylacetophenone 
• 23722-45-4 p-Chlorbenzil-monohydrazon 

Downstream Products

• 22711-23-5 4-chlorobenzil 
• 89849-98-9 (E)-1-(4-chlorophenyl)-1-phenylvinylene 1,2-bis(trifluoromethanesulfonate) 
• 89849-99-0 (Z)-1-(4-chlorophenyl)-1-phenylvinylene 1,2-bis(bisfluoromethanesulfonate) 
• 31464-86-5 1-(4-Chlorphenyl)-2-phenylethandion-2,2'-azin 
• 101315-44-0 (E)-1-(4-Chlorphenyl)-1-(nonafluorbutylsulfonyloxy)-2-(1,1,2,2,3,3,4,4-octafluorbutylsulfonyloxy)-2-phenylethen 
• 101315-46-2 (Z)-1-(4-Chlorphenyl)-1-(nonafluorbutylsulfonyloxy)-2-(1,1,2,2,3,3,4,4-octafluorbutylsulfonyloxy)-2-phenylethen 
• 101315-31-5 (E)-1-(4-Chlorphenyl)-2-phenylvinylen-bis(nonafluorbutansulfonat) 
• 33142-34-6 (4-chloro-phenyl)-phenyl-acetic acid anilide 
• 93-89-0 benzoic acid ethyl ester 
• 7335-27-5 ethyl 4-chlorobenzoate 
• 5359-54-6 ethyl 2-(4-chlorophenyl)-2-phenylacetate 
• 1126-46-1 Methyl 4-chlorobenzoate 
• 93-58-3 benzoic acid methyl ester 

Relevant academic research and scientific papers

Gold-Catalyzed [3+2]-Annulations of α-Aryl Diazoketones with the Tetrasubstituted Alkenes of Cyclopentadienes: High Stereoselectivity and Enantioselectivity

This work reports gold-catalyzed [3+2]-annulations of α-diazo ketones with highly substituted cyclopentadienes, affording bicyclic 2,3-dihydrofurans with high regio- and stereoselectivity. The reactions highlights the first success of tetrasubstituted alkenes to undergo [3+2]-annulations with α-diazo carbonyls. The enantioselective annulations are also achieved with high enantioselectivity using chiral forms of gold and phosphoric acid. Our mechanistic analysis supports that cyclopentadienes serve as nucleophiles to attack gold carbenes at the more substituted alkenes, yielding gold enolates that complex with chiral phosphoric acid to enhance the enantioselectivity.