73691-20-0

Upstream product

• 3963-62-0 2,2-Diphenylethylamine 
• 87519-56-0 1-(2,2-diphenylethyl)pyrrolidine-2,5-dione 
• 73691-13-1 1-(2,2-Diphenyl-ethyl)-5-ethoxy-pyrrolidin-2-one 
• 118474-86-5 1,5,6,10bα-tetrahydro-6α-phenylpyrrolo<2,1-a>isoquinolin-3(2H)-one 
• 118474-87-6 1,5,6,10bβ-tetrahydro-6α-phenylpyrrolo<2,1-a>isoquinolin-3(2H)-one 

Downstream Products

• 118474-87-6 1,5,6,10bβ-tetrahydro-6α-phenylpyrrolo<2,1-a>isoquinolin-3(2H)-one 
• 87519-83-3 (6R,10bR)-6-Phenyl-1,2,3,5,6,10b-hexahydro-pyrrolo[2,1-a]isoquinoline; hydrochloride 
• 118474-86-5 1,5,6,10bα-tetrahydro-6α-phenylpyrrolo<2,1-a>isoquinolin-3(2H)-one 
• 90390-52-6 6-phenyl-1,2,3,5,6,10b-hexahydropyrrolo[2,1-a]isoquinoline 
• 90390-51-5 rac-MCN-4612-E 
• 90457-60-6 1,2,3,5,6,10bβ-hexahydro-6α-phenylpyrrolo<2,1-a>isoquinoline 
• 90457-59-3 (6S,10bR)-6-Phenyl-1,2,3,5,6,10b-hexahydro-pyrrolo[2,1-a]isoquinoline 

Relevant academic research and scientific papers

Stereochemistry of Intramolecular Amidoalkylation Reactions in the Synthesis of Polycyclic Isoquinoline Derivatives

N-Acyliminium cyclizations onto benzenoid rings to give tetrahydroisoquinoline ring systems were studied.Particular attention was paid to the stereochemical effect of substituents present on the isoquinoline ring.High stereoselectivity (> 90 percent) was