A novel Fmoc protected duocarmycin subunit and utilization as a reagent in solid phase protein synthesis methodology. Also provided is a novel method of solid phase peptide synthesis, and in particular a method for the production of novel intermediates and novel monomeric and extended duocarmycin analogues having amino acid substituents
N,N’-diisopropylcarbodiimide (DIC) and OxymaPure are the reagents of choice for the formation of pep...
A solid-phaseFmoc-basedsynthesis strategy is described for oligourea peptidomimetics as well as a co...
In this communication, a new site specific synthesis of highly functionalized and multiple sulfated ...
The duocarmycins are potent antitumor agents with potential for use in the development of antibody–d...
The duocarmycins are potent antitumor agents with potential for use in the development of antibody–d...
The family is characterised by a common spirocyclopropylcyclohexadienone pharmacophore. This unusual...
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...
A rapid protocol based on Fmoc-chemistry for the solid phase peptide synthesis of vancomycin- and te...
<p>Synthetic protocol of Fmoc-His-OH derivatives and tripeptide HDAMP-1 using solid-phase peptide sy...
Peptide dimers and trimers linked through the epsilon-amino group of an N-terminal lysine residue ca...
The duocarmycins are a family of natural products first described in 1978 with the discovery of CC-1...
We report the synthesis of Fmoc protected single amino acid chelates (SAAC) and their metal complexe...
Solid-phase synthesis of oligomeric peptoids can be conveniently achieved by a repetitive cycle cons...
The glycopeptide antibiotics are an important class of complex, medically relevant peptide natural p...
N,N’-diisopropylcarbodiimide (DIC) and OxymaPure are the reagents of choice for the formation of pep...
A solid-phaseFmoc-basedsynthesis strategy is described for oligourea peptidomimetics as well as a co...
In this communication, a new site specific synthesis of highly functionalized and multiple sulfated ...
The duocarmycins are potent antitumor agents with potential for use in the development of antibody–d...
The duocarmycins are potent antitumor agents with potential for use in the development of antibody–d...
The family is characterised by a common spirocyclopropylcyclohexadienone pharmacophore. This unusual...
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...
A rapid protocol based on Fmoc-chemistry for the solid phase peptide synthesis of vancomycin- and te...
<p>Synthetic protocol of Fmoc-His-OH derivatives and tripeptide HDAMP-1 using solid-phase peptide sy...
Peptide dimers and trimers linked through the epsilon-amino group of an N-terminal lysine residue ca...
The duocarmycins are a family of natural products first described in 1978 with the discovery of CC-1...
We report the synthesis of Fmoc protected single amino acid chelates (SAAC) and their metal complexe...
Solid-phase synthesis of oligomeric peptoids can be conveniently achieved by a repetitive cycle cons...
The glycopeptide antibiotics are an important class of complex, medically relevant peptide natural p...
N,N’-diisopropylcarbodiimide (DIC) and OxymaPure are the reagents of choice for the formation of pep...
A solid-phaseFmoc-basedsynthesis strategy is described for oligourea peptidomimetics as well as a co...
In this communication, a new site specific synthesis of highly functionalized and multiple sulfated ...