A solid-phaseFmoc-basedsynthesis strategy is described for oligourea peptidomimetics as well as a convenient general synthesis approach for the preparation of the required building blocks 5a−j and 5k. These are suitable for use in peptide or robot synthesizers, which is illustrated by the synthesis of oligourea peptidomimetics of part of Leu-enkephalin (10) and a neurotensin derivative (17)
The active part or receptor-binding sequence of peptide hormones can usually be defined by a span of...
The great versatility and the inherent high affinities of peptides for their respective targets have...
Structurally well-defined liquid crystalline oligopeptides based upon a side-chain mesogenically sub...
A solid-phaseFmoc-basedsynthesis strategy is described for oligourea peptidomimetics as well as a co...
Solid-phase synthesis of oligomeric peptoids can be conveniently achieved by a repetitive cycle cons...
Following the discovery of naturally occurring biopolymers with potent and/or specific biological ac...
Octapeptins are naturally derived cyclic lipopeptide antibiotics with activity against a range of Gr...
A rapid protocol based on Fmoc-chemistry for the solid phase peptide synthesis of vancomycin- and te...
International audienceA rapid and efficient Fmoc/t-Bu solid-phase peptide synthesis (SPPS) of cyclic...
A rapid protocol based on Fmoc-chemistry for the solid phase peptide synthesis of vancomycin- and te...
Fmoc-amino acid chlorides were employed in the solid phase synthesis of the opioid peptides Leuenkep...
The solid-phase synthesis of Gly-Ψ[CH(CF3)NH]-peptides is presented. In order to achieve this goal, ...
Novel methodology, involving the Hofmann rearrangement of L-amino amides, has been developed for inc...
Fmoc-N-Protected β-amino acids of (S)-configuration bearing the side chains of Ala, Val, Leu, and Ph...
In this work, iterative methods have been studied to prepare sequence-defined oligomers on solid and...
The active part or receptor-binding sequence of peptide hormones can usually be defined by a span of...
The great versatility and the inherent high affinities of peptides for their respective targets have...
Structurally well-defined liquid crystalline oligopeptides based upon a side-chain mesogenically sub...
A solid-phaseFmoc-basedsynthesis strategy is described for oligourea peptidomimetics as well as a co...
Solid-phase synthesis of oligomeric peptoids can be conveniently achieved by a repetitive cycle cons...
Following the discovery of naturally occurring biopolymers with potent and/or specific biological ac...
Octapeptins are naturally derived cyclic lipopeptide antibiotics with activity against a range of Gr...
A rapid protocol based on Fmoc-chemistry for the solid phase peptide synthesis of vancomycin- and te...
International audienceA rapid and efficient Fmoc/t-Bu solid-phase peptide synthesis (SPPS) of cyclic...
A rapid protocol based on Fmoc-chemistry for the solid phase peptide synthesis of vancomycin- and te...
Fmoc-amino acid chlorides were employed in the solid phase synthesis of the opioid peptides Leuenkep...
The solid-phase synthesis of Gly-Ψ[CH(CF3)NH]-peptides is presented. In order to achieve this goal, ...
Novel methodology, involving the Hofmann rearrangement of L-amino amides, has been developed for inc...
Fmoc-N-Protected β-amino acids of (S)-configuration bearing the side chains of Ala, Val, Leu, and Ph...
In this work, iterative methods have been studied to prepare sequence-defined oligomers on solid and...
The active part or receptor-binding sequence of peptide hormones can usually be defined by a span of...
The great versatility and the inherent high affinities of peptides for their respective targets have...
Structurally well-defined liquid crystalline oligopeptides based upon a side-chain mesogenically sub...