873326-29-5

Upstream product

• 5292-43-3 bromoacetic acid tert-butyl ester 
• 626-15-3 1,3-bis-(bromomethyl)benzene 
• 143590-12-9 (R)-4-benzyl-3-(2-(4-methoxyphenyl)acetyl)oxazolidin-2-one 
• 131791-78-1 (R)-methyl-2-((S)-2-((tert-butoxycarbonyl)amino)-N-methylpropanamido)-3-(1H-indol-3-yl) propanoate 
• 131831-87-3 N-methyl-(R)-tryptophan methyl ester 
• 122747-97-1 methyl (R)-3-(1H-indol-3-yl)-2-(N-tert-butoxycarbonyl-N-methylamino)propanoate 
• 873326-28-4 N-(tert-butoxycarbonyl)-L-alanyl-N-[(1R)-3-tert-butoxy-1-(4-methoxyphenyl)-3-oxopropyl]-N-methyl-D-tryptophanamide 
• 873326-08-0 (4R)-4-benzyl-3-[(2S)-3-(3-{(2S)-3-[(4R)-4-benzyl-2-oxo-1,3-oxazolidin-3-yl]-2-methyl-3-oxopropyl}phenyl)-2-methylpropanoyl]-1,3-oxazolidin-2-one 
• 873326-21-7 tert-butyl (3R)-3-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}-3-(4-methoxyphenyl)propanoate 
• 873326-19-3 tert-butyl (3R)-4-[(4R)-4-benzyl-2-oxo-1,3-oxazolidin-3-yl]-3-(4-methoxyphenyl)-4-oxobutanoate 
• 873326-27-3 (R)-2-((S)-2-((tert-butoxycarbonyl)amino)-N-methyl propanamido)-3-(1H-indol-3-yl)propanoic acid 
• 873326-12-6 methyl (2S)-3-(3-{(2S)-2-[(tert-butoxycarbonyl)amino]propyl}phenyl)-2-methylpropanoate 
• 873326-09-1 (2S)-3-{3-[(2S)-2-carboxypropyl]phenyl}-2-methylpropanoic acid 
• 873326-10-4 methyl (2S)-3-{3-[(2S)-3-methoxy-2-methyl-3-oxopropyl]phenyl}-2-methylpropanoate 

Relevant academic research and scientific papers

Synthesis of jasplakinolide analogues containing a novel ω-amino acid

The synthesis of the ω-amino acid 4 is described utilizing a two-dimensional synthesis strategy combined with an enzymatic differentiation of homotopic ester groups. The amino acid 4 features two non-bonded interactions that result in conformational const