1095089-35-2

Upstream product

• 1095089-26-1 (S)-2-(tert-butyloxycarbonyl)amino-3-(2-methoxy-5-iodphenyl)propionic acid methyl ester 
• 73183-34-3 bis(pinacol)diborane 
• 1095089-24-9 (S)-2-(tert-butyloxycarbonylamino)-3-(5-iodo-2-methoxyphenyl)-propionic acid 
• 1095089-33-0 (S)-2-amino-3-(5'-iodo-2'-methoxyphenyl)propanoic acid hydrochloride 
• 24424-99-5 di-tert-butyl dicarbonate 

Downstream Products

• 1095089-39-6 (2S,2’’’S)-2-(benzyloxcarbonylamino)-3-(4’,4’’-bis-methoxy-3’’-[tert-butyloxycarbonylamino-2’’’-methoxycarbonylethyl]-biphenyl-3’-yl)-propionic acid 
• 1095089-47-6 C₄₉H₇₀N₆O₁₂Si 
• 1095089-51-2 (4S,7S,10S,2’R)-10-benzyoxycarbonylamino-1¹,2¹-bis-methoxy-7-[3’-azido-2’-(tert-butyldimethyl-silyloxy)propyl]-5,8-diaza-6,9-dioxo-1,2(4,2)-dibenzenacycloundecaphane-4-methyl carboxylate 
• 1095089-49-8 C₄₀H₅₄N₆O₁₀Si 
• 1313436-86-0 C₃₉H₅₂N₄O₉Si 
• 1313436-87-1 C₃₃H₃₈N₄O₉ 

Relevant academic research and scientific papers

Biphenomycin B and derivatives: Total synthesis and translation inhibition

A full account on the synthesis of the antibiotic natural product biphenomycin B and several derivatives is reported, which employs a Suzuki coupling reaction of a free carboxylic acid and macrolactam formation as key transformations. Liberal exchange of

Flexible total synthesis of biphenomycin B

A total synthesis of the biaryl antibiotic biphenomycin B is reported which makes use of three independent building blocks (key steps were a clean Suzuki-Miyaura coupling of a free acid iodide, a novel 4-hydroxyornithine synthesis, and a high-yielding macrolactamization); a practical deprotection protocol allowed isolation of the target compound with excellent recovery and purity. The Royal Society of Chemistry.