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Conformational studies of C2 symmetric peptidomimetics with identical peptide strands attached on both sides of 2,5-anhydro sugar diacid and 2,5-anhydro sugar diamine scaffolds revealed the presence of nine-membered pseudo β-turns in the sugar diacid based molecules consisting of identical intramolecular hydrogen bonds at the two ends between the AA 2 NH and sugarOH.

Conformational studies of C2 symmetric peptidomimetics based on 2,5-anhydro sugar diacid and 2,5-anhydro sugar diamine scaffolds