1089672-00-3

Upstream product

• 637-69-4 4-Methoxystyrene 
• 65100-24-5 dibenzyl 2-bromomalonate 

Downstream Products

• 1089671-90-8 dibenzyl 2-[2-(4-methoxyphenyl)-4-oxo-4-phenylbutyl]malonate 
• 1089671-91-9 dibenzyl 2-[2-(4-methoxyphenyl)-3-methyl-4-oxo-4-phenylbutyl]malonate 
• 1089671-92-0 dibenzyl 2-[2-(4-methoxyphenyl)-3-methyl-4-oxopentyl]malonate 
• 1089671-99-7 dibenzyl 2-hydroxy-4-(4-methoxyphenyl)-2-phenylcyclopentane-1,1-dicarboxylate 
• 1089671-97-5 dibenzyl 2-[2-(4-methoxyphenyl)-2-(2-oxocyclohexyl)ethyl]malonate 
• 1089671-95-3 4,4-dibenzyl 1-ethyl 2-(4-methoxyphenyl)butane-1,4,4-tricarboxylate 
• 1089671-94-2 dibenzyl 2-[2-(4-methoxyphenyl)-6-methyl-4-oxoheptyl]malonate 
• 1089671-96-4 dibenzyl 2-[(E)-2-(4-methoxyphenyl)-4-oxo-6-phenylhex-5-enyl]malonate 
• 1089671-98-6 dibenzyl 2-[2-(4-methoxyphenyl)-2-(2-oxocyclopentyl)ethyl]malonate 
• 1235889-89-0 (2R,5R)-dibenzyl 1-(2-methoxybenzyl)-5-(4-methoxyphenyl)-2-phenylpyrrolidine-3,3-dicarboxylate 

Relevant academic research and scientific papers

A facile formal [2+1] cycloaddition of styrenes with alpha-bromocarbonyls catalyzed by copper: Efficient synthesis of donor-acceptor cyclopropanes

Reactions of 2-bromoesters and styrenes underwent a [2+1] cycloaddition reaction, i.e., cyclopropanation, to produce donor-acceptor (D-A) cyclopropanes through a radical addition-ring closure process. In this reaction, the combination of copper(ii) comple