Ring-closing metathesis (RCM) with α,α-diallylglycyl peptides is shown to furnish α,α-cyclopentenylglycyl peptides as conformationally restrained analogues in the form of post-translational type peptide modification suitable for both peptidomimetic and combinatorial chemistry applications.© Elsevie
Conformationally constrained amino acid derivatives are useful in the synthesis of peptidomimetics. ...
In this letter, we describe the ring-rearrangement metathesis (RRM) of bicyclic amino acid derivativ...
Bicyclic peptides are promising scaffolds for the development of inhibitors of biological targets th...
Ring-closing metathesis (RCM) with α,α-diallylglycyl peptides is shown to furnish α,α-cyclopentenylg...
This review surveys developments in the field of ring-closing metathesis and cross-metathesis reacti...
Peptidomimetics have found wide application as biostable, bioavailable, and often potent mimics of n...
Applications of ring-closing alkene metathesis (RCM) in acyclic α- and β-peptides and closely relate...
The demand for peptide drugs is increasing and in this context, "post-assembly (or post-translationa...
The synthesis of a series of “amide to amide” cyclized peptides by ring-closing metathesis (RCM) as ...
A γ-turn induced cyclisation of tripeptides 4 can be performed in a ring-closing metathesis rea...
Copyright © 2006 Elsevier B.V. All rights reserved.Three new classes of conformationally constrained...
Understanding protein structure and function is central for the development of therapeutics for the ...
This thesis aims at developing methods for introducing conformational restriction in Beta-turns, the...
Bis-alkene substrates, containing one fluoroalkene and linked by an amide moiety, have been designed...
Contains fulltext : 58942.pdf (publisher's version ) (Closed access)The applicatio...
Conformationally constrained amino acid derivatives are useful in the synthesis of peptidomimetics. ...
In this letter, we describe the ring-rearrangement metathesis (RRM) of bicyclic amino acid derivativ...
Bicyclic peptides are promising scaffolds for the development of inhibitors of biological targets th...
Ring-closing metathesis (RCM) with α,α-diallylglycyl peptides is shown to furnish α,α-cyclopentenylg...
This review surveys developments in the field of ring-closing metathesis and cross-metathesis reacti...
Peptidomimetics have found wide application as biostable, bioavailable, and often potent mimics of n...
Applications of ring-closing alkene metathesis (RCM) in acyclic α- and β-peptides and closely relate...
The demand for peptide drugs is increasing and in this context, "post-assembly (or post-translationa...
The synthesis of a series of “amide to amide” cyclized peptides by ring-closing metathesis (RCM) as ...
A γ-turn induced cyclisation of tripeptides 4 can be performed in a ring-closing metathesis rea...
Copyright © 2006 Elsevier B.V. All rights reserved.Three new classes of conformationally constrained...
Understanding protein structure and function is central for the development of therapeutics for the ...
This thesis aims at developing methods for introducing conformational restriction in Beta-turns, the...
Bis-alkene substrates, containing one fluoroalkene and linked by an amide moiety, have been designed...
Contains fulltext : 58942.pdf (publisher's version ) (Closed access)The applicatio...
Conformationally constrained amino acid derivatives are useful in the synthesis of peptidomimetics. ...
In this letter, we describe the ring-rearrangement metathesis (RRM) of bicyclic amino acid derivativ...
Bicyclic peptides are promising scaffolds for the development of inhibitors of biological targets th...