630110-75-7

Upstream product

• 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 
• 24424-99-5 di-tert-butyl dicarbonate 
• 92855-64-6 6-benzyloxy-1H-indole-3-carboxaldehyde 
• 630110-71-3 6-benzyloxy-1H-1-tert-butoxycarbonylindole-3-carbaldehyde 
• 630110-73-5 tert-butyl 3-(1-ethoxymethyl-4,5-diiodo-1H-imidazole-2-carbonyl)-6-benzyloxy-1H-indole-1-carboxylate 
• 630110-72-4 tert-butyl 3-[(1-ethoxymethyl-4,5-diiodo-1H-imidazol-2-yl)hydroxymethyl]-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 
• 15903-94-3 6-benzyloxy-1H-indole 

Downstream Products

• 630110-76-8 [1-ethoxymethyl-5-(1H-indole-3-carbonyl)-1H-imidazol-2-yl](6-benzyloxy-1H-indol-3-yl)methanone 
• 630110-77-9 [5-(1H-indole-3-carbonyl)-1H-imidazol-2-yl](6-benzyloxy-1H-indol-3-yl)methanone 

Relevant academic research and scientific papers

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

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