19078-76-3

Upstream product

• 100-42-5 styrene 
• 96-32-2 bromoacetic acid methyl ester 
• 1821-12-1 4-Phenylbutyric acid 
• 2046-17-5 methyl 3-(benzyl)propanoate 

Downstream Products

• 143593-10-6 5-Phenyl-1-(2,4,6-trimethoxy-phenyl)-pyrrolidine-2,2-diol 
• 143593-09-3 N-(2,4,6-Trimethoxyphenyl)-4-phenyl-4-butanelactam 
• 461383-66-4 S-(2-iodophenethyl) 4-azido-4-phenylbutanethioate 
• 461383-59-5 4-azido-4-phenylbutanoyl chloride 
• 22050-10-8 (+/-)-5-phenyl-2-pyrrolidinone 
• 461383-58-4 4-azido-4-phenylbutanoic acid 
• 461383-57-3 methyl 4-azido-4-phenylbutanoate 

Relevant academic research and scientific papers

Light-mediated dual phosphine-/copper-catalyzed atom transfer radical addition reaction

The atom transfer radical addition reaction catalyzed by triphenylphosphine and copper(I) halide is described. The reaction proceeds under irradiation with 365 nm light using a light-emitting diode and was performed in regular glassware. The proposed mech

Intramolecular Cyclization of Acyl Radicals onto the Azido Group: A New Radical Approach to Cyclized Lactams

(Equation Presented) Reagents: i, Bu3SnH/AlBN; ii, (TMS)3SiH/AlBN. Aryl- and alkyl-derived azidoacyl radicals, generated from thiolesters by intramolecular homolytic substitution at the sulfur, can undergo five- and six-membered cyclization onto the azido moiety to give cyclized lactams.