A precisely positioned sulfimide chiral center on-tether of a thio-ether tethered peptide determines the peptide secondary structure by chemoselective oxaziridine modification. This method provides a facile way to tune peptides’ secondary structures and biophysical properties
A chemoselective, convenient, and mild synthetic strategy to modify peptides on a cysteine sulfhydry...
Chemical methods that enable the synthesis and the site-selective modification of biomolecules offer...
Thioamides are an important, but a largely underexplored class of amide bioisostere in peptides. Rep...
A precisely positioned sulfilimine chiral center in the tether of a stabilized peptide would determi...
The facile chemical modification on the peptide cross-linking moiety is an important strategy for im...
Thanks to their large binding interfaces, peptides are attractive ligands targeting protein-protein ...
Inducing alpha-helicity through side-chain cross-linking is a strategy that has been pursued to impr...
The addition of a precisely positioned chiral center in the tether of a constrained peptide is repor...
A sulfilimine chiral center in the tether at i, i + 3 positions of short peptides was systematically...
Hybrid peptides whose N-terminal residues are activated in the form of α-methylisoserine-derived cyc...
Asp‐ecially useful : A synthetic β‐mercapto aspartate residue facilitates the rapid ligation to a ra...
A method for site- and stereoselective peptide modification using a cyclic sulfamidate scaffold cont...
Ligation reactions have emerged as an important tool for the chemoselective conjugation of large and...
Because almost all peptides and proteins have only one N- and one C-terminus, modification targeting...
The chemical synthesis of polypeptides can be accomplished with a technique called Native Chemical L...
A chemoselective, convenient, and mild synthetic strategy to modify peptides on a cysteine sulfhydry...
Chemical methods that enable the synthesis and the site-selective modification of biomolecules offer...
Thioamides are an important, but a largely underexplored class of amide bioisostere in peptides. Rep...
A precisely positioned sulfilimine chiral center in the tether of a stabilized peptide would determi...
The facile chemical modification on the peptide cross-linking moiety is an important strategy for im...
Thanks to their large binding interfaces, peptides are attractive ligands targeting protein-protein ...
Inducing alpha-helicity through side-chain cross-linking is a strategy that has been pursued to impr...
The addition of a precisely positioned chiral center in the tether of a constrained peptide is repor...
A sulfilimine chiral center in the tether at i, i + 3 positions of short peptides was systematically...
Hybrid peptides whose N-terminal residues are activated in the form of α-methylisoserine-derived cyc...
Asp‐ecially useful : A synthetic β‐mercapto aspartate residue facilitates the rapid ligation to a ra...
A method for site- and stereoselective peptide modification using a cyclic sulfamidate scaffold cont...
Ligation reactions have emerged as an important tool for the chemoselective conjugation of large and...
Because almost all peptides and proteins have only one N- and one C-terminus, modification targeting...
The chemical synthesis of polypeptides can be accomplished with a technique called Native Chemical L...
A chemoselective, convenient, and mild synthetic strategy to modify peptides on a cysteine sulfhydry...
Chemical methods that enable the synthesis and the site-selective modification of biomolecules offer...
Thioamides are an important, but a largely underexplored class of amide bioisostere in peptides. Rep...