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- W2157573760 endingPage "13404" @default.
- W2157573760 startingPage "13390" @default.
- W2157573760 abstract "Constrained peptidomimetic scaffolds are of considerable interest for the design of therapeutically useful analogues of bioactive peptides. We present the single-step cyclization of (S)- or (R)-α-hydroxy-β(2)- or α-substituted-α-hydroxy-β(2, 2)-amino acids already incorporated within oligopeptides to 5-aminomethyl-oxazolidine-2,4-dione (Amo) rings. These scaffolds can be regarded as unprecedented β(2)- or β(2, 2)-homo-Freidinger lactam analogues, and can be equipped with a proteinogenic side chain at each residue. In a biomimetic environment, Amo rings act as inducers of extended, semi-bent or folded geometries, depending on the relative stereochemistry and the presence of α-substituents." @default.
- W2157573760 created "2016-06-24" @default.
- W2157573760 creator A5021039691 @default.
- W2157573760 creator A5025575773 @default.
- W2157573760 creator A5037011770 @default.
- W2157573760 creator A5065834714 @default.
- W2157573760 date "2014-09-02" @default.
- W2157573760 modified "2023-10-18" @default.
- W2157573760 title "Synthesis and Analysis of the Conformational Preferences of 5-Aminomethyloxazolidine-2,4-dione Scaffolds: First Examples of β<sup>2</sup>- and β<sup>2, 2</sup>-Homo-Freidinger Lactam Analogues" @default.
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