269085-41-8

Upstream product

• 1670-14-0 benzamidine monohydrochloride 
• 362610-31-9 (3-bromo-1-(S)-(1-methylethyl)-2-oxopropyl)carbamic acid benzyl ester 
• 1149-26-4 (S)-N-(benzyloxycarbonyl)valine 
• 90105-46-7 benzyl (S)-(1-diazo-4-methyl-2-oxopentan-3-yl)carbamate 

Downstream Products

• 852248-38-5 (S)-2-methyl-1-(2-phenyl-1H-imidazol-4-yl)propan-1-amine 

Relevant academic research and scientific papers

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

Synthesis of amino acid-derived imidazoles from enantiopure N-protected α-amino glyoxals

A range of novel imidazoles, including three histidine derivatives, with chiral side chains derived from amino acids and dipeptides have been synthesised from N-Cbz-protected α-amino glyoxals. (C) 2000 Elsevier Science Ltd.