103143-22-2

Upstream product

• 3382-18-1 6,7-dimethoxy-3,4-dihydro-isoquinoline 
• 99-73-0 para-bromophenacyl bromide 

Downstream Products

• 103143-19-7 1-(4-Bromo-phenyl)-2-(6,7-dimethoxy-3,4-dihydro-1H-isoquinolin-2-yl)-ethanone 
• 103143-20-0 1-(4-Bromo-phenyl)-2-(6,7-dimethoxy-3,4-dihydro-1H-isoquinolin-2-yl)-ethanol 

Relevant academic research and scientific papers

Novel oxidation of substituted pyrrolidines by n-bromosuccinimide; Rapid synthesis of pyrrolo[2,1-α]isoquinolines

A new method for converting 1,2,3,5,6,10b-hexahydropyrrolo[2,1-α] isoquinolines into 5,6-dihydropyrrolo[2,1-a]isoquinolines by the use of N-bromosuccinimide as an oxidant is presented. Georg Thieme Verlag Stuttgart - New York.

Novel oxidation of substituted pyrrolidines by N-bromosuccinimide - Rapid synthesis of pyrrolo[2,1-a]isoquinolines

A new method for converting 1,2,3,5,6,10b-hexahydropyrrolo[2,1-a] isoquinolines into 5,6-dihydropyrrolo[2,1-a]isoquinolines using N-bromosuccinimide as an oxidant is presented. Georg Thieme Verlag Stuttgart.

A Mild and Chemoselective Reduction of Cyclic Iminium Salts

N-Substituted cyclic iminium salts are conveniently reduced to the corresponding tertiary amines in good yields by reaction with tributylstannane in methanol at room temperature.A variety of functional groups (such as ketonic groups) present in the molecule are not affected under these conditions.