1443675-87-3Relevant articles and documents
In-peptide synthesis of di-oxazolidinone and dehydroamino acid-oxazolidinone motifs as β-turn inducers
De Marco, Rossella,Greco, Arianna,Rupiani, Sebastiano,Tolomelli, Alessandra,Tomasini, Claudia,Pieraccini, Silvia,Gentilucci, Luca
, p. 4316 - 4326 (2013)
Small and easy-to-do mimetics of β-turns are of great interest to interfere with protein-protein recognition events mediated by β-turn recognition motifs. We propose a straightforward procedure for constraining the conformation of tetrapeptides lacking a pre-formed scaffold. According to the stereochemistry array, N-Ts tetrapeptides including Thr or PhSer (phenylserine) at the positions 2 or 3 gave rise in a single step to the sequences Oxd 2-Oxd3 or ΔAbu2-Oxd3 (Oxd, oxazolidin-2-one; ΔAbu, 2,3-dehydro-2-aminobutyric). These pseudo-Pro residues displayed highly constrained, and χ dihedral angles, and induced clear β-turns or inverse turns of type I or II, as determined by extensive spectroscopic and computational analyses. The Royal Society of Chemistry 2013.
