128573-12-6

Upstream product

• 151908-49-5 (3(2S,3R),4R)-3-<2-Azido-3-(4-methoxyphenyl)butyroyl>-4-phenyl-2-oxazolidinone 
• 151800-31-6 (3(3S),4R)-3-<3-(4'-Methoxyphenyl)butanoyl>-4-phenyl-2-oxazolidinone 
• 151800-34-9 (2S,3R)-2-Azido-3-(4-methoxyphenyl)butyric acid 
• 104-92-7 1-bromo-4-methoxy-benzene 
• 758685-22-2 (2S,3R)-2-Amino-3-(4-methoxy-phenyl)-butyric acid 
• 600-18-0 2-Oxobutyric acid 
• 108-95-2 phenol 

Relevant academic research and scientific papers

Synthesis of (2S,3R)-β-Methyltyrosine Catalyzed by Tyrosine Phenol-Lyase

A one-step enzymatic synthesis of the conformationally restrained tyrosine analog (2S,3R)-β-methyltyrosine is reported. This synthesis extends the preparative chemistry associated with tyrosine phenol-lyase. This β-methyltyrosine derivative was shown to be an efficient protein tyrosine kinase substrate, suggesting that conformational restraint may ultimately be used to enhance tyrosine kinase recognition of substrates.

Efficient Method for the Total Asymmetric Synthesis of the Isomers of β-Methyltyrosine

α-Amino acids modified at the β-carbon atom can provide topographical constraints when incorporated into a peptide.Such modifications can modulate the physical, chemical, and biological properties of the compound.In order to properly evaluate the effect o