Chiral furan amino acids were synthesized as novel peptide building blocks. Cyclooligomerization of these monomers by a single-step process led to the selective formation of chiral C3-symmetric cyclic trimers, which were studied for their structures and properties, like anion binding and antimicrobial activities
Chiral induction was utilized for the synthesis of diastereopure cyclic peptoids containing an N-ben...
By analogy to the structural diversity of covalent bond networks between atoms within organic molecu...
The synthesis of tetrahydrofuran C(alpha)-tetrasubstituted amino acids (TAAs) and their effect on th...
Chiral furan amino acids were synthesized as novel peptide building blocks. Cyclooligomerization of ...
To produce a novel class of structurally ordered poly-β-prolines, an emergent method for synthesizin...
Peptide-based drug research has received high attention in the field of medicinal chemistry over the...
A rational strategy for the facile and efficient cyclization of amino acid-based linear precursors f...
Using a combined chemical/chiral chromatographic approach we synthesized an N-protected derivative o...
Fluorine-containing organic molecules have generated increasing impact in drug research over the pas...
Using a combined chemical/chiral chromatographic approach we synthesized an N-protected derivative o...
The synthesis of two new diastereomeric 6-amino-3-azabicyclo[3.2.1]octane-6-carboxylic acids exo- an...
Modification of the ring nucleus of tetramic acids derived from serine gives chiral heterocyclic lib...
Asymmetric synthetic organic chemistry of amino acids is of fundamental importance for the study of ...
To produce a novel class of structurally ordered poly-beta-prolines, an emergent method for synthesi...
Complementary to hydrophobic five membered ring β-amino acids (e.g. ACPC), β-sugar amino acids (β-SA...
Chiral induction was utilized for the synthesis of diastereopure cyclic peptoids containing an N-ben...
By analogy to the structural diversity of covalent bond networks between atoms within organic molecu...
The synthesis of tetrahydrofuran C(alpha)-tetrasubstituted amino acids (TAAs) and their effect on th...
Chiral furan amino acids were synthesized as novel peptide building blocks. Cyclooligomerization of ...
To produce a novel class of structurally ordered poly-β-prolines, an emergent method for synthesizin...
Peptide-based drug research has received high attention in the field of medicinal chemistry over the...
A rational strategy for the facile and efficient cyclization of amino acid-based linear precursors f...
Using a combined chemical/chiral chromatographic approach we synthesized an N-protected derivative o...
Fluorine-containing organic molecules have generated increasing impact in drug research over the pas...
Using a combined chemical/chiral chromatographic approach we synthesized an N-protected derivative o...
The synthesis of two new diastereomeric 6-amino-3-azabicyclo[3.2.1]octane-6-carboxylic acids exo- an...
Modification of the ring nucleus of tetramic acids derived from serine gives chiral heterocyclic lib...
Asymmetric synthetic organic chemistry of amino acids is of fundamental importance for the study of ...
To produce a novel class of structurally ordered poly-beta-prolines, an emergent method for synthesi...
Complementary to hydrophobic five membered ring β-amino acids (e.g. ACPC), β-sugar amino acids (β-SA...
Chiral induction was utilized for the synthesis of diastereopure cyclic peptoids containing an N-ben...
By analogy to the structural diversity of covalent bond networks between atoms within organic molecu...
The synthesis of tetrahydrofuran C(alpha)-tetrasubstituted amino acids (TAAs) and their effect on th...
DOI
Add to ORKG