Prospect of Thiazole‐based γ‐Peptide Foldamers in Enamine Catalysis: Exploration of the Nitro‐Michael Addition Auteur(s): Aguesseau‐kondrotas Julie, Simon Matthieu, Legrand Baptiste, Bantignies J.-L., Kang Young Kee, Dumitrescu Dan, Van der lee Arie, Campagne Jean‐marc, de Figueiredo Renata Marcia, Maillard Ludovic (Article) Publié: Chemistry - A European Journal, vol. 25 p.7396-7401 (2019) Ref HAL: hal-02167326_v1 DOI: 10.1002/chem.201901221 WoS: 000469274700022 Exporter : BibTex | endNote 6 Citations Résumé: As three‐dimensional folding is prerequisite to biopolymer activity, complex functions may also be achieved through foldamer science. Because of the diversity of sizes, shapes and folding available with synthetic monomers, foldamer frameworks enable a numerous opportunities for designing new generations of catalysts. We herein demonstrate that heterocyclic γ‐peptide scaffolds represent a versatile platform for enamine catalysis. One central feature was to determine how the catalytic activity and the transfer of chiral information might be under the control of the conformational behaviours of the oligomer. |