415726-46-4Relevant academic research and scientific papers
α-aminoxy peptoids: A unique peptoid backbone with a preference for cis-amide bonds
Krieger, Viktoria,Ciglia, Emanuele,Thoma, Roland,Vasylyeva, Vera,Frieg, Benedikt,de Sousa Amadeu, Nader,Kurz, Thomas,Jania, Christoph,Gohlke, Holger,Hansen, Finn K.
supporting information, p. 3699 - 3707 (2017/03/21)
α-Peptoids, or N-substituted glycine oligomers, are an important class of peptidomimetic foldamers with proteolytic stability. Nevertheless, the presence of cis/transamide bond conformers, which contribute to the high flexibility of α-peptoids, is conside
Solution-phase synthesis of aminooxy peptoids in the C to N and N to C directions.
Shin, Injae,Park, Kisoo
, p. 869 - 872 (2007/10/03)
[structure: see text] Aminooxy peptoids, which are potential peptidomimetics, were synthesized by a stepwise monomer assembly. Ns-protected N-substituted aminooxyacetate tert-butyl esters were used as a monomer in both the C to N and the N to C directions
