213668-40-7

Upstream product

• 4397-53-9 p-benzyloxybenzaldehyde 
• 213668-31-6 (2S,5R)-2-(4-bromobenzyl)-5-isopropyl-3,6-dimethoxy-2,5-dihydropyrazine 
• 623-05-2 (4-hydroxyphenyl)methanol 
• 836-43-1 4-benzyloxybenzyl alcohol 
• 109838-85-9 (2R)-2,5-dihydro-2-isopropyl-3,6-dimethoxypyrazine 
• 100-39-0 benzyl bromide 
• 589-15-1 1-bromomethyl-4-bromobenzene 

Downstream Products

• 213668-33-8 (4-Benzyloxy-phenyl)-[4-((2S,5R)-5-isopropyl-3,6-dimethoxy-2,5-dihydro-pyrazin-2-ylmethyl)-phenyl]-methanone 
• 213668-35-0 (S)-2-Amino-3-[4-(4-benzyloxy-benzoyl)-phenyl]-propionic acid methyl ester 

Relevant academic research and scientific papers

Synthesis of (S)- and (R)-enantiomers of p-(4- hydroxybenzoyl)phenylalanine, useful photoaffinity labeling probes for peptide-protein binding sites

A high yield, multigram synthesis of both enantiomers of p-(4- hydroxybenzoyl)phenylalanine, cross-linking probes for peptide-protein binding interactions, is reported. The synthesis was accomplished using Schollkopf chiral auxiliary reagents.