1374005-02-3

Upstream product

• 1374004-96-2 1-(5-benzyloxy-1H-indol-4-yl)-2-(4-benzyloxy-3-methoxy-phenyl)-ethanone 
• 1374004-91-7 2-(4-benzyloxy-3-methoxy-phenyl)-1-[5-benzyloxy-1-(toluene-4-sulfonyl)-1H-indol-4-yl]-ethanol 
• 1374004-99-5 1-[5-benzyloxy-3-(2-hydroxy-acetyl)-1H-indol-4-yl]-2-(4-benzyloxy-3-methoxy-phenyl)-ethanone 
• 1374004-85-9 4-[2-(4-benzyloxy-3-methoxy-phenyl)-1-hydroxy-ethyl]-1-(toluene-4-sulfonyl)-1H-indol-5-ol 
• 1374004-95-1 2-(4-benzyloxy-3-methoxy-phenyl)-1-[5-benzyloxy-1-(toluene-4-sulfonyl)-1H-indol-4-yl]-ethanone 
• 2426-87-1 3-methoxy-4-(phenylmethoxy)benzaldehyde 
• 16209-52-2 <4-(benzyloxy)-3-methoxyphenyl>acetaldehyde 
• 210173-72-1 1-benzyloxy-2-methoxy-4-(2-methoxyethenyl)benzene 

Downstream Products

• 1374004-86-0 1-benzyl-6-benzyloxy-5-(4-benzyloxy-3-methoxy-benzyl)-4-hydroxy-1H-benzo[cd]indol-3-one 

Relevant academic research and scientific papers

Synthetic studies of decursivine derivatives: Preparation of key indole alkaloids via α-hydroxyalkylation

2-Hydroxyacetyl indole modified at C-3 position was prepared with an eye to developing a total synthesis of decursivine derivatives (decursivine, serotobenine, moschaminindolol, and flavumindole). The indole was prepared through a sequence of oxalyl chlor