123975-76-8Relevant academic research and scientific papers
Macrocyclization of Peptide Side Chains by the Ugi Reaction: Achieving Peptide Folding and Exocyclic N-Functionalization in One Shot
Vasco, Aldrin V.,Pérez, Carlos S.,Morales, Fidel E.,Garay, Hilda E.,Vasilev, Dimitar,Gavín, José A.,Wessjohann, Ludger A.,Rivera, Daniel G.
, p. 6697 - 6707 (2015/10/06)
The cyclization of peptide side chains has been traditionally used to either induce or stabilize secondary structures (β-strands, helices, reverse turns) in short peptide sequences. So far, classic peptide coupling, nucleophilic substitution, olefin metat
Correlation between the Configurational Structure and the Asymmetric Hydrogenation of Δ1-, Δ2-, and Δ3-Dehydrotripeptides
Shin, Chung-gi,Ogawa, Kazumichi,Morooka, Katsuhiro,Yonezawa, Yasuchika
, p. 459 - 462 (2007/10/02)
The heterogeneous catalytic hydrogenation of Δ1-dehydrotripeptides (Δ1-DHP), which have a β-turn structure, was carried out to give the corresponding tripeptides indicative of the very large diastereomeric excess, comparing with thos
