868670-42-2

Upstream product

• 15196-02-8 (S)-3-[(benzyloxycarbonyl)amino]-1-diazo-4-phenyl-2-butanone 
• 97206-05-8 methyl N-(benzyloxycarbonyl)-(3S)-3-amino-4-phenylbutanoate 
• 26250-86-2 (S)-3-benzyloxycarbonylamino-4-phenylbutyric acid 

Downstream Products

• 610772-74-2 (2R,4E,7R)-2-(tert-butyloxycarbonylamino)-7-(benzyloxycarbonylamino)-1-(3-indolyl)-8-phenyloct-4-en-3-one 
• 868670-09-1 2-[(benzyloxycarbonyl)amino]-5-(methoxycarbonyl)-8,8-dimethyl-1-phenyl-4,7-nonanedione 
• 875918-19-7 2-[(benzyloxycarbonyl)amino]-5-(methoxycarbonyl)-1-phenyl-4,7-octanedione 
• 875918-41-5 1-benzyl-2-[2-(benzyloxycarbonylamino)-3-phenylpropyl]-3-(methoxycarbonyl)-5-methylpyrrole 
• 875918-71-1 (S)-2-{[1-Benzyl-2-((S)-2-benzyloxycarbonylamino-3-phenyl-propyl)-5-methyl-1H-pyrrole-3-carbonyl]-amino}-propionic acid methyl ester 

Relevant academic research and scientific papers

Synthesis of 2,6-disubstituted piperidine-bearing α-amino acid side-chains

A straightforward synthesis of 2,6-disubstituted piperidines bearing α-amino acid side-chains was developed. Synthesis was based on a Horner-Wadsworth-Emmons condensation of a β-ketophosphonate derived from an α-amino acid residue with a β-homologated ald

Peptidyl β-homo-aspartals: Specific inhibitors of interleukin-1β converting enzyme and its homologues (caspases)

Inhibition of interleukin-1β convening enzyme (ICE), apopain, papain, thrombin and trypsin with substrate like peptidyl L- and D-α-aldehydes and their L-β-homo-aldehyde analogues was investigated. The L-β-homo-aspartals appear to be specific inhibitors fo