Ugi multicomponent reaction to prepare peptide–peptoid hybrid structures with diverse chemical functionalities

Literature Information

Publication Date 2017-12-21
DOI 10.1039/C7PY01953J
Impact Factor 5.582
Authors

Manuel Hartweg, Elham Radvar, Dominic Collis, Mehedi Reza, Janne Ruokolainen, Robert Rambo, Ian W. Hamley, Helena S. Azevedo, C. Remzi Becer


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Abstract

Monodisperse sequenced peptides and peptoids present unique nano-structures based on their self-assembled secondary and tertiary structures. However, the generation of peptide and peptoid hybrid oligomers in a sequence-defined manner via Ugi multicomponent reaction has not yet been studied. Herein, we report a synthetic strategy that enables both the modification of peptides as well as the generation of sequence-defined peptide–peptoid hybrid structures. Our synthetic methodology rests on the fusion of solid phase peptide synthesis with Ugi multicomponent reactions. We evidence that a diversity of chemical functionalities can be inserted into peptides or used in the design of peptide–peptoid hybrids exploiting a wide functional array including amines, carboxylic acids, hydrocarbons, carbohydrates as well as polymers, introducing a sequence-defined synthetic platform technology for precision peptoid hybrids.

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