95377-53-0

Upstream product

• 36547-83-8 2-benzoyl-8-benzyloxy-1,2-dihydro-7-methoxy-isoquinoline-1-carbonitrile 
• 112378-14-0 8-benzyloxy-1-(2'-bromo-3',4'-dimethoxybenzyl)-7-methoxy-N-methylisoquinolinium iodide 
• 112378-11-7 8-benzyloxy-N-benzoyl-1-(2'-bromo-3',4'-dimethoxybenzyl)-1,2-dihydro-7-methoxyisoquinoline-1-carbonitrile 
• 112378-16-2 8-benzyloxy-1-(2'-bromo-3',4'-dimethoxybenzyl)-1,2,3,4-tetrahydro-7-methoxy-N-methylisoquinoline 
• 112378-12-8 8-benzyloxy-1-(2'-bromo-3',4'-dimethoxybenzyl)-7-methoxyisoquinoline 
• 7477-50-1 2-bromo-1-chloromethyl-3,4-dimethoxy-benzene 
• 112456-21-0 1,2,3,4-tetrahydro-1-(2'-bromo-3',4'-dimethoxybenzyl)-7-methoxy-N-methylisoquinolin-8-ol 
• 546-67-8 lead(IV) tetraacetate 

Relevant academic research and scientific papers

Synthetic Approaches To Cularines. II . Ullmann Condensation.

The first total syntheses of O-methylcularicine 9b and sarcocapnine 9c are described together with a new synthesis of cularine 9a using the Ullmann condensation reaction of the appropriate 2'-bromo-8-hydroxytetrahydrobenzylisoquinoline formed by phase-tra

(+)-4-HYDROXYSARCOCAPNINE: STRUCTURE AND STEREOCHEMICAL CONSIDERATIONS

(+)-4-Hydroxysarcocapnine obtained from Sarcocapnos enneaphylla(L.)DC.has been shown by spectral studies and synthesis to posses the new 4-hydroxyisocularine structure(1a).Straightforward assignment of the configuration of a 4-hydroxycularine by NMR is also discussed.