Synthesis and Structural Characterization of Macrocyclic α-ABpeptoids and Their DNA-Encoded Library

Org Lett. 2024 Feb 9;26(5):1100-1104. doi: 10.1021/acs.orglett.3c04387. Epub 2024 Jan 31.

Abstract

The first synthesis of macrocyclic α-ABpeptoids with varying lengths is described. X-ray crystal structures reveal that cyclic trimer displays a chair-like conformation with a cct amide sequence and cyclic tetramer has a saddle-like structure with an uncommon cccc amide arrangement. The creation of a DNA-encoded combinatorial library of macrocyclic α-ABpeptoids is described.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amides / chemistry
  • Crystallography, X-Ray
  • DNA* / chemistry
  • Gene Library
  • Macrocyclic Compounds / chemistry
  • Molecular Conformation
  • Peptoids* / chemistry

Substances

  • Amides
  • DNA
  • Macrocyclic Compounds
  • Peptoids