864381-75-9

Upstream product

• 254909-21-2 (3R,7S,7aS)-7-Cyanomethyl-5-oxo-3-phenyl-tetrahydro-pyrrolo[1,2-c]oxazole-6-carboxylic acid ethyl ester 
• 501-53-1 benzyl chloroformate 
• 254909-28-9 (1S,2S,6R)-2-(5-aza-7-oxa-4-oxo-6-phenylbicyclo[3.3.0]oct-2-yl)ethanenitrile 
• 166765-36-2 (2R,5S)-7-ethoxycarbonyl-8-oxo-2-phenyl-1-aza-3-oxa-bicyclo[3.3.0]oct-6-ene 
• 864381-91-9 (2R,5S,6S,7S)-7-ethyloxycarbonyl-6-cyanomethyl-8-oxo-2-phenyl-1-aza-3-oxa-bicyclo[3.3.0]octane 
• 864381-59-9 (2R,5S,6S)-6-(N-benzyloxycarbonyl-2-aminoethyl)-8-oxo-2-phenyl-1-aza-3-oxa-bicyclo[3.3.0]octane 

Relevant academic research and scientific papers

Stereoselective synthesis of conformationally constrained ω -amino acid analogues from pyroglutamic acid

Bicyclic lactams derived from pyroglutamic acid provide a useful scaffold for synthesis of conformationally restricted analogues of lysine, ornithine and glutamine, as well as an Ala-Ala dipeptide analogue. Amino alcohol and carboxylic acid derivatives ar

Novel peptidomimetic structures: Enantioselective synthesis of conformationally constrained lysine, ornithine and alanine analogues from pyroglutamic acid

Conformationally constrained lysine and ornithine analogues, and an L- Ala-L-Ala dipeptide analogue, are available from pyroglutamic acid.