873326-10-4

Upstream product

• 626-15-3 1,3-bis-(bromomethyl)benzene 
• 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 
• 873326-09-1 (2S)-3-{3-[(2S)-2-carboxypropyl]phenyl}-2-methylpropanoic acid 
• 67-56-1 methanol 

Downstream Products

• 873326-25-1 N-[(2S)-3-(3-{(2R)-2-[(tert-butoxycarbonyl)amino]propyl}phenyl)-2-methylpropanoyl]-L-alanyl-N-[(1R)-3-tert-butoxy-1-(4-methoxyphenyl)-3-oxopropyl]-D-tryptophanamide 
• 873326-29-5 N-[(2S)-3-(3-{(2R)-2-[(tert-butoxycarbonyl)amino]propyl}phenyl)-2-methylpropanoyl]-L-alanyl-N-[(1R)-3-tert-butoxy-1-(4-methoxyphenyl)-3-oxopropyl]-N-methyl-D-tryptophanamide 
• 873326-17-1 methyl N-[(2S)-3-(3-{(2S)-2-[(tert-butoxycarbonyl)amino]propyl}phenyl)-2-methylpropanoyl]-L-alanyl-N-methyl-D-alanyl-L-phenylalaninate 
• 873326-13-7 methyl N-[(2S)-3-(3-{(2S)-2-[(tert-butoxycarbonyl)amino]propyl}phenyl)-2-methylpropanoyl]-L-alanyl-D-alanyl-L-phenylalaninate 
• 873326-05-7 (2S)-3-(3-{(2S)-2-[(tert-butoxycarbonyl)amino]propyl}phenyl)-2-methylpropanoic acid 
• 873326-12-6 methyl (2S)-3-(3-{(2S)-2-[(tert-butoxycarbonyl)amino]propyl}phenyl)-2-methylpropanoate 
• 873326-11-5 (2S)-3-{3-[(2S)-3-methoxy-2-methyl-3-oxopropyl]phenyl}-2-methylpropanoic acid 

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