616888-52-9

Upstream product

• 100-39-0 benzyl bromide 
• 146335-32-2 2-benzyloxy-5-iodobenzoic acid 
• 119-30-2 2-hydroxy-5-iodobenzoic acid 
• 636594-69-9 (2-benzyloxy-5-iodophenyl)methanol 

Downstream Products

• 636594-70-2 diethyl 2-(2-benzyloxy-5-iodobenzyl)-2-tert-butoxycarbonylaminomalonate 
• 616888-54-1 (S)-2-Amino-3-(2-benzyloxy-5-iodo-phenyl)-1-((1S,5R,7R)-10,10-dimethyl-3,3-dioxo-3λ⁶-thia-4-aza-tricyclo[5.2.1.0^1,5]dec-4-yl)-propan-1-one 
• 616888-51-8 benzyl 3-(2-benzyloxy-5-iodophenyl)-2(S)-tert-butoxycarbonylaminopropionate 
• 616888-56-3 (-)-3-(2-benzyloxy-5-iodophenyl)-2(S)-tert-butoxycarbonylaminopropionic acid 
• 616888-55-2 (S)-2-benzyloxy-5-iodophenylalanine 

Relevant academic research and scientific papers

Antibacterial amide macrocycles

The invention relates to antibacterial amide macrocycles, to methods for the production thereof, and to the use of the same for producing pharmaceuticals for the treatment and/or prophylaxis of illness, especially bacterial infections.

A new convergent approach to biphenomycin antibiotics

A new, convergent approach to the biaryl key intermediate of Schmidt's biphenomycin B total synthesis has been accomplished via a palladacycle complex catalyzed Stille cross-coupling of two o-tyrosine building blocks.