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5015425 
Journal Article 
Peptoid residues and beta-turn formation 
Rainaldi, M; Moretto, V; Crisma, M; Peggion, E; Mammi, S; Toniolo, C; Cavicchioni, G 
2002 
Yes 
Journal of Peptide Science
ISSN: 1075-2617 
8 
6 
241-252 
English 
12093001 
A set of terminally protected tripeptoids containing a residue of either N-methylglycine or N-isobutylglycine in position i + 1/i + 2 were synthesized and tested for intramolecularly H-bonded beta-turn formation. By exploiting FT-IR absorption and 1H NMR techniques, their folding tendencies were compared with those of a variety of reference peptides. The amount of beta-turn induction and the relative extent of the various types of intramolecularly H-bonded beta-turn conformers were determined in chloroform solution. 
• Chloroform Combined (current)
     Chloroform (original)
          References: 2000-2018
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