325709-68-0

Upstream product

• 325709-64-6 3-(2(S)-azido-3(S)-phenyl-4-ene-1-oxopentyl)-4(S)-(benzyl)-2-oxazolidinone 
• 325709-82-8 3-(3(S)-phenyl-4-ene-1-oxopentyl)-4(S)-(benzyl)-2-oxazolidinone 
• 5703-57-1 3-phenylpent-4-enoic acid 

Relevant academic research and scientific papers

Triproline analogues of Pro-Leu-Gly-NH2 with Pro/Leu and Pro/Phe chimeric amino acids in position 2

Synthesis of the cis- and trans-isomers of the proline-leucine (3-i-Pr-Pro) and proline-phenylalanine (3-Ph-Pro) chimeric amino acids was accomplished by intramolecular reductive-cycloalkylation of the appropriate azido-olefin. These chimeric amino acids were incorporated into the triprolyl analogues of Pro-Leu-Gly-NH2: Pro-cis-3-i-Pr-Pro-Pro-NH2 (3), Pro-trans-3-i-Pr-Pro-Pro-NH2 (4), Pro-cis-3-Ph-Pro-Pro-NH2 (5), Pro-trans-3-Ph-Pro-Pro-NH2 (6). (C) 2000 Elsevier Science Ltd.