A hydrogen-bonding interface between helical aromatic oligoamide foldamers has been designed to promote the folding of a helix-turn-helix motif with a head-to-tail arrangement of two helices of opposite handedness. This design complements an earlier helix-turn-helix motif with a head-to-head arrangement of two helices of identical handedness interface. The two motifs were shown to have comparable stability and were combined in a unimolecular tetra-helix fold constituting the largest abiotic tertiary structure to date
The purpose of this work is to expand foldamer diversity by developing a novel class of abiotic β-sh...
Pour mimer le repliement des structures tridimensionnelles des biomolécules, les chimistes ont dével...
International audienceThe development of large synthetic ligands could be useful to target the sizea...
A hydrogen‐bonding interface between helical aromatic oligoamide foldamers has been designed to prom...
A hydrogen‐bonding interface between helical aromatic oligoamide foldamers has been designed to prom...
A hydrogen‐bonding interface between helical aromatic oligoamide foldamers has been designed to prom...
A hydrogen‐bonding interface between helical aromatic oligoamide foldamers has been designed to prom...
International audienceAbiotic foldamers, i.e. foldamers that have backbones chemically remote from p...
Abiotic foldamers, that is foldamers that have backbones chemically remote from peptidic and nucleot...
International audienceThe de novo design and synthesis of large and well-organized, tertiary-like, α...
To mimic the particular folding of the biomolecules’ three-dimensional structures, chemists have dev...
To mimic the particular folding of the biomolecules’ three-dimensional structures, chemists have dev...
Disulfide bridge formation was investigated in helical aromatic oligoamide foldamers. Depending on t...
To mimic the particular folding of the biomolecules’ three-dimensional structures, chemists have dev...
The purpose of this work is to expand foldamer diversity by developing a novel class of abiotic β-sh...
The purpose of this work is to expand foldamer diversity by developing a novel class of abiotic β-sh...
Pour mimer le repliement des structures tridimensionnelles des biomolécules, les chimistes ont dével...
International audienceThe development of large synthetic ligands could be useful to target the sizea...
A hydrogen‐bonding interface between helical aromatic oligoamide foldamers has been designed to prom...
A hydrogen‐bonding interface between helical aromatic oligoamide foldamers has been designed to prom...
A hydrogen‐bonding interface between helical aromatic oligoamide foldamers has been designed to prom...
A hydrogen‐bonding interface between helical aromatic oligoamide foldamers has been designed to prom...
International audienceAbiotic foldamers, i.e. foldamers that have backbones chemically remote from p...
Abiotic foldamers, that is foldamers that have backbones chemically remote from peptidic and nucleot...
International audienceThe de novo design and synthesis of large and well-organized, tertiary-like, α...
To mimic the particular folding of the biomolecules’ three-dimensional structures, chemists have dev...
To mimic the particular folding of the biomolecules’ three-dimensional structures, chemists have dev...
Disulfide bridge formation was investigated in helical aromatic oligoamide foldamers. Depending on t...
To mimic the particular folding of the biomolecules’ three-dimensional structures, chemists have dev...
The purpose of this work is to expand foldamer diversity by developing a novel class of abiotic β-sh...
The purpose of this work is to expand foldamer diversity by developing a novel class of abiotic β-sh...
Pour mimer le repliement des structures tridimensionnelles des biomolécules, les chimistes ont dével...
International audienceThe development of large synthetic ligands could be useful to target the sizea...