27845-48-3

Upstream product

• 107-10-8 propylamine 
• 100-52-7 benzaldehyde 
• 618-31-5 benzylidene dibromide 

Downstream Products

• 74069-25-3 3,5-diphenyl-4-propyl-1,2,4-oxadiazoline 
• 74069-21-9 3-methyl-5-phenyl-4-propyl-1,2,4-oxadiazoline 
• 135665-15-5 4,5-Dibutyl-1,3-diaza-bicyclo[3.1.0]hex-3-ene 
• 135665-11-1 4-Butyl-5-phenyl-1-propyl-1H-imidazole 
• 97351-01-4 (2-Methyl-1-phenyl-but-3-enyl)-propyl-amine 
• 124857-23-4 C₂₂H₂₆N₂O₄ 
• 97351-01-4 threo N-propyl-2-methyl-1-phenyl-3-butenylamine 
• 97351-01-4 erythro N-propyl-2-methyl-1-phenyl-3-butenylamine 
• 97351-10-5 erythro N-propyl-2-methyl-1-phenyl-3-pentenylamine 
• 59169-19-6 2,4,5,6-Tetraphenyl-1,3-diaza-bicyclo[3.1.0]hex-3-ene 
• 55041-11-7 2,4,5-triphenyl-1-propyl-1H-imidazole 
• 94956-91-9 Acetic acid 2-methylene-4-phenyl-4-propylamino-butyl ester 
• 77597-03-6 3-ethyl-5-phenyl-4-propyl-1,2,4-oxadiazoline 
• 1837-56-5 2,4-Diphenyl-1-propylimidazole 

Relevant academic research and scientific papers

Direct synthesis of imines from gem-dibromomethylaryl derivatives: Application to unsymmetrically substituted bipyridine frameworks

An efficient methodology for the one-pot synthesis of imines is described starting from gem-dibromomethylaryl compounds and primary amines. The synthesis was applied to various aliphatic mono- and polyamines as well as to electron-rich anilines. The proto

Synthesis of 1,5-dihydro-2H-pyrrol-2-ones from an alkyne, an imine and carbon dioxide via an organotitanium intermediate

Azatitanacyclopentene complexes 2 react with carbon dioxide under atmospheric pressure to afford 1,5-dihydro-2H pyrrol-2-ones, thus providing a one-pot procedure for synthesizing a variety of 1,5-dihydro-2H-pyrrol-2-ones from an alkyne, an imine and carbo