A versatile solid-phase approach to sequence-defined polyamidoamines was developed. Four different Fmoc-polyamino acid building blocks were synthesized by selective protection of symmetrical oligoethylenimine precursors followed by introduction of a carboxylic acid handle using cyclic anhydrides and subsequent Fmoc-protection. The novel Fmoc-polyamino acids were used to construct polyamidoamines demonstrating complete compatibility to standard Fmoc reaction conditions. The straightforward synthesis of the building blocks and the high efficiency of the solid-phase coupling reactions allow the versatile synthesis of defined polycations
This article reports on a simple and straightforward preparation method of poly(amidoamine)s (PAAs) ...
The family is characterised by a common spirocyclopropylcyclohexadienone pharmacophore. This unusual...
Cyclic eight-ring pyrrole−imidazole polyamides are sequence-specific DNA-binding small molecules tha...
A versatile solid-phase approach to sequence-defined polyamidoamines was developed. Four different F...
Polyamides containing N-methylimidazole (Im) and N-methylpyrrole (Py) amino acids are synthetic liga...
We present for the first time the synthesis of asymmetrically branched sequence-defined poly/oligo(...
The solid phase synthesis of sequence specific DNA binding polyamides containing N-methylimidazole (...
Pyrrole−imidazole polyamides are DNA-binding molecules that are programmable for a large repertoire ...
Muramic acid is found in many peptide natural products containing oligo(poly)saccharide moieties. Ta...
The versatile polymerization of bisacrylamides with mono- and difunctional amines, first investigate...
The versatile polymerization of bisacrylamides with mono- and difunctional amines, first investigate...
In this work, iterative methods have been studied to prepare sequence-defined oligomers on solid and...
We report a novel solid phase method for the sequential coupling of heterobifunctional macromonomers...
We report the one-pot synthesis of hyperbranched polyethers possessing amino functionality by using ...
Cyclic Py-Im polyamides containing two GABA turn units exhibit enhanced DNA binding affinity, but ex...
This article reports on a simple and straightforward preparation method of poly(amidoamine)s (PAAs) ...
The family is characterised by a common spirocyclopropylcyclohexadienone pharmacophore. This unusual...
Cyclic eight-ring pyrrole−imidazole polyamides are sequence-specific DNA-binding small molecules tha...
A versatile solid-phase approach to sequence-defined polyamidoamines was developed. Four different F...
Polyamides containing N-methylimidazole (Im) and N-methylpyrrole (Py) amino acids are synthetic liga...
We present for the first time the synthesis of asymmetrically branched sequence-defined poly/oligo(...
The solid phase synthesis of sequence specific DNA binding polyamides containing N-methylimidazole (...
Pyrrole−imidazole polyamides are DNA-binding molecules that are programmable for a large repertoire ...
Muramic acid is found in many peptide natural products containing oligo(poly)saccharide moieties. Ta...
The versatile polymerization of bisacrylamides with mono- and difunctional amines, first investigate...
The versatile polymerization of bisacrylamides with mono- and difunctional amines, first investigate...
In this work, iterative methods have been studied to prepare sequence-defined oligomers on solid and...
We report a novel solid phase method for the sequential coupling of heterobifunctional macromonomers...
We report the one-pot synthesis of hyperbranched polyethers possessing amino functionality by using ...
Cyclic Py-Im polyamides containing two GABA turn units exhibit enhanced DNA binding affinity, but ex...
This article reports on a simple and straightforward preparation method of poly(amidoamine)s (PAAs) ...
The family is characterised by a common spirocyclopropylcyclohexadienone pharmacophore. This unusual...
Cyclic eight-ring pyrrole−imidazole polyamides are sequence-specific DNA-binding small molecules tha...