76304-20-6

Upstream product

• 852358-46-4 methyl 2-[N-(2-bromobenzyl)amino]acetate 
• 6630-33-7 ortho-bromobenzaldehyde 
• 864738-29-4 N-(2-bromobenzyl)-N-[(4-methylphenyl)sulfonyl]glycyl chloride 
• 864738-30-7 8-bromo-2-[(4-methylphenyl)sulfonyl]-2,3-dihydro-1H-isoquinolin-4-one 
• 864738-33-0 8-bromo-2-[(4-methylphenyl)sulfonyl]-1,2,3,4-tetrahydroisoquinoline 
• 864738-37-4 8-(3,4-dimethoxyphenyl)-2-[(4-methylphenyl)sulfonyl]-1,2,3,4-tetrahydroisoquinoline 
• 76304-21-7 8-(3,4-dimethoxyphenyl)isoquinoline 
• 864738-28-3 N-(2-bromobenzyl)-N-[(4-methylphenyl)sulfonyl]glycine 
• 864738-27-2 methyl N-(2-bromobenzyl)-N-[(4-methylphenyl)sulfonyl]glycinate 

Relevant academic research and scientific papers

Synthesis of new 8-arylisoquinoline derivatives by application of palladium-catalyzed Suzuki cross-coupling reactions

New 8-(het)aryltetrahydroisoquinolines (10-14), 8- aryltetrahydroisoquinolin-4-ols (15,16), and 8-phenylisoquinolin-4-ol (17), flexible analogues of aporphine, were synthesized in good yields using palladium-catalyzed Suzuki cross-coupling reactions from

Versatile and Efficient Synthesis of Aryl-1,2,3,4-tetrahydroisoquinolines: Nickel(II) Phosphine Ligand Catalyzed Coupling of Arylmagnesium Halides to Haloisoquinolines

Dichloronickel(II) (dppp) was used as catalyst to prepare some previously unreported arylisoquinolines 3, which were in turn hydrogenated to aryl-1,2,3,4-tetrahydroisoquinolines 2.This procedure is the most direct and ef