Olefin metathesis has been successfully applied to the synthesis of macrocyclic helical peptides [Eq. (a)]. Carbon–carbon bond tethers between amino acid side chains were introduced by ring‐closing metathesis. This macrocyclization protocol is a novel and mild procedure for introducing nonnative covalent cross‐links into peptide helices
Molecular processes depending on protein-protein interactions can use consensus recognition sequence...
The synthesis of a series of “amide to amide” cyclized peptides by ring-closing metathesis (RCM) as ...
Understanding protein structure and function is central for the development of therapeutics for the ...
In our ongoing efforts to build a bridge between peptide chemistry and organic chemistry, we are cur...
This review surveys developments in the field of ring-closing metathesis and cross-metathesis reacti...
Peptide macrocycles form an outstanding class of natural and synthetic bioactive compounds. This cha...
The ring-closing metathesis reaction can be used to cross-link allylated serine residues situated at...
This thesis investigates the application of cross metathesis and ring-closing metathesis to amino ac...
Olefin tethers of variable length, introduced into a natural amino acid (side-chain of Ser, Cys; N-t...
Bicyclic peptides are promising scaffolds for the development of inhibitors of biological targets th...
In Nature, multicyclic peptides constitute a versatile molecule class with various biological functi...
Suitably functionalized glycine derivatives undergo a cross-enyne and ring-closing metathesis cascad...
Macrocyclization can be used to constrain peptides in their bioactive conformations, thereby support...
We designed and synthesized helical short oligopeptides with an L-proline on the N-terminus and hydr...
Suitably functionalized glycine derivatives undergo a cross-enyne and ring-closing metathesis cascad...
Molecular processes depending on protein-protein interactions can use consensus recognition sequence...
The synthesis of a series of “amide to amide” cyclized peptides by ring-closing metathesis (RCM) as ...
Understanding protein structure and function is central for the development of therapeutics for the ...
In our ongoing efforts to build a bridge between peptide chemistry and organic chemistry, we are cur...
This review surveys developments in the field of ring-closing metathesis and cross-metathesis reacti...
Peptide macrocycles form an outstanding class of natural and synthetic bioactive compounds. This cha...
The ring-closing metathesis reaction can be used to cross-link allylated serine residues situated at...
This thesis investigates the application of cross metathesis and ring-closing metathesis to amino ac...
Olefin tethers of variable length, introduced into a natural amino acid (side-chain of Ser, Cys; N-t...
Bicyclic peptides are promising scaffolds for the development of inhibitors of biological targets th...
In Nature, multicyclic peptides constitute a versatile molecule class with various biological functi...
Suitably functionalized glycine derivatives undergo a cross-enyne and ring-closing metathesis cascad...
Macrocyclization can be used to constrain peptides in their bioactive conformations, thereby support...
We designed and synthesized helical short oligopeptides with an L-proline on the N-terminus and hydr...
Suitably functionalized glycine derivatives undergo a cross-enyne and ring-closing metathesis cascad...
Molecular processes depending on protein-protein interactions can use consensus recognition sequence...
The synthesis of a series of “amide to amide” cyclized peptides by ring-closing metathesis (RCM) as ...
Understanding protein structure and function is central for the development of therapeutics for the ...