1384461-36-2

Upstream product

• 188662-05-7 <2-<3,5-bis(benzyloxy)phenyl>ethyl>amine 
• 1384461-35-1 6,8-bis(benzyloxy)-3,4-dihydroisoquinoline 
• 18925-10-5 allylzinc bromide 

Downstream Products

• 1384461-37-3 (R)-1-(1-allyl-6,8-bis(benzyloxy)-3,4-dihydroisoquinolin-2(1H)-yl)-2-azidoethanone 
• 1384461-42-0 (S,E)-5-amino-9,11-bis(benzyloxy)-2,3,5,6-tetrahydrobenzo[d]azecin-4(1H)-one 
• 1384461-34-0 2-amino-1-(6,8-bis(benzyloxy)-1-vinyl-3,4-dihydroisoquinolin-2(1H)-yl)ethanone 
• 1384461-39-5 (R)-2-azido-1-(6,8-bis(benzyloxy)-1-vinyl-3,4-dihydroisoquinolin-2(1H)-yl)ethanone 
• 1384461-44-2 (R)-2-azido-1-(6,8-bis(benzyloxy)-1-(2-(2-nitrophenylselanyl)ethyl)-3,4-dihydroisoquinolin-2(1H)-yl)ethanone 
• 1384461-38-4 (R)-2-azido-1-(6,8-bis(benzyloxy)-1-(2-hydroxyethyl)-3,4-dihydroisoquinolin-2(1H)-yl)ethanone 
• 1384461-43-1 C₂₇H₂₆N₄O₄ 
• 1384461-41-9 C₄₂H₃₈N₂O₅ 
• 1384461-40-8 C₃₂H₃₆N₂O₅ 
• 949463-54-1 (3S,11bR)-3-amino-9,11-bis(benzyloxy)-2,3,6,7-tetrahydro-1H-pyrido[2,1-a]isoquinolin-4(11bH)-one 

Relevant academic research and scientific papers

Asymmetric formal synthesis of schulzeines A and C

The asymmetric formal synthesis of schulzeines A and C is described. Key features of the synthesis include the efficient and stereoselective construction of the benzoquinolizidine skeleton via the aza-Claisen rearrangement-induced ring expansion of the 1-