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Our work on using aromatic oligoesters as helix mimetics has been published in Bioorganic and Medicinal Chemistry.

on helix mimetic scaffolds has been published in Biorganic and Medicinal Chemistry. This paper forms part of a special issue focused on .

The design, synthesis, and conformational analysis of a novel aromatic oligoester helix mimetic scaffold is reported. A range of amino acid-type side-chain functionality can be readily incorporated into monomer building blocks over three facile synthetic steps. Analysis of representative dimers revealed a stable conformer capable of effective mimicry of a canonical α-helix and the scaffold was found to be surprisingly stable to degradation in aqueous solutions at acidic and neutral pH.