362610-31-9

Upstream product

• 191731-16-5 (S)-tert-butyl 4-(benzyloxycarbonyl)amino-5-methyl-3-oxohexanoate 
• 1149-26-4 (S)-N-(benzyloxycarbonyl)valine 
• 90105-46-7 benzyl (S)-(1-diazo-4-methyl-2-oxopentan-3-yl)carbamate 
• 119153-86-5 C₁₆H₂₁NO₆ 

Downstream Products

• 1237501-95-9 C₁₇H₂₀N₄O₅ 
• 1237501-77-7 Z-Val-CH₂N₃ 
• 852248-38-5 (S)-2-methyl-1-(2-phenyl-1H-imidazol-4-yl)propan-1-amine 
• 269085-41-8 2-phenyl-4-(1-(S)-benzyloxycarbonylamino-2-methylpropyl)-1H-imidazole 
• 362610-35-3 ((1S,2S)-3-Bromo-2-hydroxy-1-isopropyl-propyl)-carbamic acid benzyl ester 

Relevant academic research and scientific papers

Facile synthesis of optically active imidazole derivatives

Five optically active imidazole derivatives have been synthesized via a facile 4-step reaction sequence starting from commercially available and inexpensive N-Cbz amino acids. While microwave assisted condensation was unsuccessful, the condensation of the

Chiral imidazole derivatives synthesis from enantiopure N-protected α-amino acids

A route to the preparation of enantiopure ligands based on a 2-phenylimidazol ring is described. The stereogenic centre is placed into the chain bonded to the fourth carbon of the imidazole ring. The synthesis starts from inexpensive and readily available

Highly stereoselective synthesis of anti-N-protected-α-amino epoxides

A simple and efficient method for the synthesis of anti-N-protected amino epoxides from carbamate-protected amino acids is described. The two key steps are the monobromination of a β-ketoester and chelation-controlled reduction of a bromomethyl ketone intermediate. Good overall yields, high diastereoselectivity, and excellent functional group compatibility are characteristic.