157034-61-2

Upstream product

• 64482-27-5 2-bromo-5,6-dimethoxybenzoyl chloride 
• 185245-80-1 methyl 6,7-methylenedioxy-1,2,3,4-tetrahydroisoquinoline-1-acetate 
• 185245-78-7 7,8-methylenedioxy-1,4,5,9b-tetrahydro-2H-azeto<2,1-a>isoquinoline 
• 185245-88-9 8,9-methylenedioxy-1,2,5,6-tetrahydro-4H-3,6-epoxy-3-benzazocine 
• 185245-89-0 6-hydroxy-8,9-methylenedioxy-1,2,3,4,5,6-hexahydro-3-benzazocine 
• 185245-86-7 1-(2-hydroxyethyl)-6,7-methylenedioxy-1,2,3,4-tetrahydroisoquinoline 
• 185245-87-8 1-(chloroethyl)-6,7-methylenedioxy-1,2,3,4-tetrahydroisoquinoline 
• 112342-26-4 6,7-methylenedioxy-1-(Z)-(methoxycarbonyl)-methylidene-1,2,3,4-tetrahydroisoquinoline 
• 60555-93-3 6-bromo-2,3-dimethoxybenzoic acid 
• 185245-95-8 N-(6-bromo-2,3-dimethoxybenzoyl)-6-hydroxy-8,9-methylenedioxy-1,2,3,4,5,6-hexahydro-3-benzazocine 

Downstream Products

• 157034-62-3 7-(6-Bromo-2,3-dimethoxy-benzoyl)-9-phenylsulfanyl-6,7,8,9-tetrahydro-5H-1,3-dioxa-7-aza-cycloocta[f]inden-10-one 

Relevant academic research and scientific papers

An efficient synthesis of magallanesine using [1,2]-Meisenheimer rearrangement and Heck cyclization

A straightforward total synthesis of magallanesine 1 was accomplished from readily available isoquinolineacetate 14. This synthesis is emphasized by the following two points; i. the [1,2]-Meisenheimer rearrangement of the azetidine N-oxide 22 for the prep

A Total Synthesis of Magallanesine via -Meisenheimer Rearrangement

A straightforward synthesis of magallanesine 1 from azetoisoquinoline 4 has been accomplished via -Meisenheimer rearrangement and an intramolecular Heck cyclization as the key reactions.