Abstract
Tunable cis/trans prolyl amide bond configuration in substituted β-proline (β-Pro) and β-homoproline (β-Hpro) homodimers was explored, based on position and nature of the substituent. Tertiary amide bond in β-proline (β2,3-substituted) dimers show distinct trans configuration and β-homoproline (β3-substituted) dimers preferably exhibited cis configuration.
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