128573-11-5

Upstream product

• 104-92-7 1-bromo-4-methoxy-benzene 
• 151800-33-8 (3(2R,3S),4S)-3-<2-Azido-3-(4-methoxyphenyl)butyroyl>-4-phenyl-2-oxazolidinone 
• 128707-85-7 (S)-3-[(2R,3S)-2-Azido-3-(4-methoxy-phenyl)-butyryl]-4-benzyl-oxazolidin-2-one 
• 128693-82-3 (3(3R),4S)-4-benzyl-3-<3-(4'-methoxyphenyl)butanoyl>-2-oxazolidinone 
• 128677-81-6 C₁₆H₂₂O₄ 
• 4974-05-4 (R)-(-)-4'-methoxy-3-phenylbutyric acid 
• 148706-34-7 (S)-3-[(2S,3S)-2-Bromo-3-(4-methoxy-phenyl)-butyryl]-4-phenyl-oxazolidin-2-one 
• 146137-35-1 (3(3R),4S)-4-phenyl-3-<3-(4'-methoxyphenyl)butanoyl>-2-oxazolidinone 
• 754977-47-4 (2R,3S)-2-Amino-3-(4-methoxy-phenyl)-butyric acid 
• 128677-84-9 (2R,3S)-2-Azido-3-(4-methoxyphenyl)butyric acid 

Relevant academic research and scientific papers

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

ASYMMETRIC SYNTHESIS OF UNUSUAL AMINO ACIDS: SYNTHESIS OF OPTICALLY PURE ISOMERS OF β-METHYLTYROSINE

Synthesis of optically pure isomers of β-methyltyrosine has been accomplished.