21394-84-3

Upstream product

• 1268388-07-3 acetic acid 2-methyl-3-phenyl-2-phenylazopropyl ester 
• 46438-07-7 α-methyl-α-carbethoxy-β-phenethylamine 
• 16024-41-2 2-acetylamino-2-methyl-3-phenyl-propionic acid methyl ester 

Downstream Products

• 88084-21-3 N-(4-phenylbutyryl)-L-proline DL-3-hydroxy-2-methyl-1-phenylpropylamide 
• 88084-15-5 N-carbobenzoxy-L-proline DL-3-hydroxy-2-methyl-1-phenylpropylamide 
• 902146-40-1 C₁₂H₂₀N₂O₃S 
• 902146-42-3 2-benzyl-2-methyl-aziridine-1-sulfonic acid dimethylamide 
• 902146-41-2 C₁₃H₂₂N₂O₅S₂ 
• 88084-22-4 (S)-1-(4-Phenyl-butyryl)-pyrrolidine-2-carboxylic acid (1-formyl-1-methyl-2-phenyl-ethyl)-amide 
• 88105-70-8 N-carbobenzoxy-L-prolyl-L-2-amino-2-methyl-1-phenylpropanal 
• 88084-38-2 N^α-[N-(4-phenylbutyryl)-L-propyl-DL-2-amino-2-methyl-3-phenylpropyl]-L-arginine 
• 88105-72-0 N^α--N^ω-nitro-L-arginine 
• 88105-71-9 N^α--N^ω-nitro-L-arginine methyl ester 
• 853303-79-4 tert-butyl 1-hydroxy-2-methyl-3-phenylpropan-2-ylcarbamate 
• 154631-81-9 benzyl N-(1-benzyl-2-hydroxy-1-methyl)ethylcarbamate 

Relevant academic research and scientific papers

Chiral azo compounds: Enantioselective synthesis and transformations into β-amino alcohols and α-amino acids with a quaternary stereocenter

Taking advantage of radical carboaminations producing azo compounds, a new chemo-enzymatic approach to enantiomerically enriched azo alcohols, β-amino alcohols and non-natural (aromatic) amino acids with a quaternary stereocenter is reported.