α,γ-Cyclic peptide ensembles with a hydroxylated cavity - Organic & Biomolecular
Chemistry (RSC Publishing) DOI:10.1039/B911247M Royal Society of Chemistry View PDF …

The design and synthesis of β-sheet-based self-assembling cyclic peptides with tunable
cavities is described. The incorporation of a γ-amino acid with a hydroxyl group at C2 allows …

Three different tetraphenylalanine (FFFF) based peptides that differ at the N‐and C‐termini
have been synthesized by using standard procedures to study their ability to form different …

Folding and hierarchical structure formation have been shown to adjust and control the
dimensions, shapes and functionalities of macromolecules (eg, proteins, nucleic acids) …

The secondary structures of oligomeric organic molecules are known to reveal fascinating
architectures that can be responsible for their aesthetic beauty as well as their biological …

The hierarchical self‐assembly properties of a dimer‐forming cyclic peptide that bears a
nicotinic acid moiety to form molecular pom‐pom‐like structures are described. This dimeric …

The de novo design of new peptide assemblies that expands the repertoire of biomaterial
nanostructures has been of a tremendous challenge. Hence, it is evident that a successful …

Interest in unnatural oligomers (“foldamers”) with discrete conformational propensities akin
to those of proteins has led to numerous recent explorations of peptides constructed from-, γ …

Chirality correction, asymmetry, ring‐chain tautomerism and hierarchical assemblies are
fundamental phenomena in nature. They are geometrically related and may impact the …

According to their restricted conformational freedom, heterocyclic γ‐amino acids are usually
considered to be related to Z‐vinylogous γ‐amino acids. In this context, oligomers …