269085-45-2

Upstream product

• 50-00-0 formaldehyd 
• 268747-20-2 ((S)-1-Benzyl-2,3-dioxo-propyl)-carbamic acid benzyl ester 
• 15196-02-8 (S)-3-[(benzyloxycarbonyl)amino]-1-diazo-4-phenyl-2-butanone 
• 463-52-5 formamidine 
• 109453-49-8 (C₈H₇O₂)(NHCHCOO)(CH₂C₆H₅)(CO₂C₂H₅) 
• 1161-13-3 N-Cbz-L-Phe 
• 19317-12-5 (3S)-3-(N-benzyloxycarbonylamino)-3-benzyl-2-oxo-1-bromopropane 
• 3473-63-0 formamidine acetic acid 

Downstream Products

• 1135467-31-0 (S)-benzyl 1-[1-(ethoxymethyl)-1H-imidazol-5-yl]-2-phenylethylcarbamate 
• 1135467-15-0 (S)-benzyl 1-[1-(ethoxymethyl)-1H-imidazol-4-yl]-2-phenylethylcarbamate 
• 1258781-87-1 2-{[4-(1-(1S)-benzyloxycarbonylamino-2-phenylethyl)-1H-imidazol-1-yl]methyl}-6-{[5-(1-(1S)-benzyloxycarbonylamino-2-phenylethyl)-1H-imidazol-1-yl]methyl}pyridine 
• 1258781-81-5 2,6-bis{[4-(1-(1S)-benzyloxycarbonylamino-2-phenylethyl)-1H-imidazol-1-yl]methyl}pyridine 

Relevant academic research and scientific papers

Design and efficient synthesis of amino acid derived 2-substituted imidazoles by palladium-catalyzed cross-coupling reactions

Optically active imidazole derivatives featuring an α-amino acid motif substituted at the 2-position can be prepared in moderate to good yields by Negishi as well as Suzuki-Miyaura cross-couplings as the key synthetic steps. The reaction sequence involves

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

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.