949162-01-0

Upstream product

• 24424-99-5 di-tert-butyl dicarbonate 
• 555-16-8 4-nitrobenzaldehdye 
• 15164-44-0 p-(iodophenyl)carboxaldehyde 
• 107708-70-3 4-(4,4-dimethyl-2,6-dioxacyclohexyl)aniline 
• 101420-88-6 4-iodo-3-nitrobenzaldehyde 
• 99-99-0 1-methyl-4-nitrobenzene 
• 556-18-3 4-aminobenzaldehyde 
• 838-42-6 5,5-dimethyl-2-(4-nitro-phenyl)-[1,3]dioxane 
• 949161-98-2 methyl (E)-3'-tert-butoxycarbonylamino-4'-iodocinnamate 
• 949161-94-8 methyl (E)-3'-nitro-4'-iodocinnamate 
• 949161-95-9 methyl (E)-3'-amino-4'-iodocinnamate 
• 949161-93-7 2-(4-iodo-phenyl)-5,5-dimethyl-[1,3]dioxane 
• 949162-00-9 (E)-3'-tert-butoxycarbonylamino-4'-iodocinnamic acid 
• 99395-88-7 (S)-4-phenyl-2-oxazolidinone 

Downstream Products

• 949161-92-6 (S)-3-[3'-amino-4'-iodo-(E)-cinnamoyl]-4-phenyloxazolidin-2-one 

Relevant academic research and scientific papers

Preparation of the central tryptophan moiety of the celogentin/moroidin family of anti-mitotic cyclic peptides

The central functionalized tryptophan core of the celogentin/moroidin family of cyclic peptides has been prepared. The strategy incorporates a novel preparation of 4-iodobenzaldehyde and employs a Larock annulation as the key step. CSIRO 2006.