630110-72-4

Upstream product

• 87020-14-2 1-ethoxymethyl-2,4,5-tri-iodoimidazole 
• 630110-71-3 6-benzyloxy-1H-1-tert-butoxycarbonylindole-3-carbaldehyde 
• 24424-99-5 di-tert-butyl dicarbonate 
• 15903-94-3 6-benzyloxy-1H-indole 
• 92855-64-6 6-benzyloxy-1H-indole-3-carboxaldehyde 

Downstream Products

• 630110-73-5 tert-butyl 3-(1-ethoxymethyl-4,5-diiodo-1H-imidazole-2-carbonyl)-6-benzyloxy-1H-indole-1-carboxylate 
• 630110-77-9 [5-(1H-indole-3-carbonyl)-1H-imidazol-2-yl](6-benzyloxy-1H-indol-3-yl)methanone 
• 630110-76-8 [1-ethoxymethyl-5-(1H-indole-3-carbonyl)-1H-imidazol-2-yl](6-benzyloxy-1H-indol-3-yl)methanone 
• 630110-75-7 tert-butyl 3-[5-(1-tert-butoxycarbonyl-1H-indole-3-carbonyl)-1-ethoxymethyl-1H-imidazole-2-carbonyl]-6-benzyloxy-1H-indole-1-carboxylate 
• 630110-70-2 tert-butyl 3-[5-(1-tert-butoxycarbonyl-1H-indole-3-carbonyl)-1-ethoxymethyl-4-iodo-1H-imidazole-2-carbonyl]-6-benzyloxy-1H-indole-1-carboxylate 
• 630110-74-6 tert-butyl 3-{5-[(1-tert-butoxycarbonyl-1H-indol-3-yl)hydroxymethyl]-1-ethoxymethyl-4-iodo-1H-imidazole-2-carbonyl}-6-benzyloxy-1H-indole-1-carboxylate 

Relevant academic research and scientific papers

An efficient synthetic route to homocarbonyltopsentine

Efficient synthesis of homocarbonyltopsentine Ia, starting from readily available triiodoimidazole 9 and 3-formylindoles 2 and 18 is described. The key steps of the synthesis are selective halogen-metal exchanges at the imidazole nucleus and subsequent ad

Synthesis of homocarbonyltopsentine derivatives

Homocarbonyltopsentines I are known to exhibit interesting anti-inflammatory activity in vivo. In order to study the role of the heterocycles in the modulation of their activity, several analogues in which indoles were replaced either by substituted indol