Design of Helical Peptide Foldamers through α,β → β,γ Double-Bond Migration

Org Lett. 2019 Jun 21;21(12):4500-4504. doi: 10.1021/acs.orglett.9b01365. Epub 2019 Jun 3.

Abstract

The direct transformation of nonhelical α,γ-hybrid peptides composed of alternating α- and E-vinylogous amino acids into 12-helical structures through a base-mediated α,β → β,γ double-bond migration is reported. The conformations of double-bond-migrated new 12-helices were studied in single crystals and in solution. Instructively, the 12-helices reported here were found to be acid labile, and they completely break down into the corresponding amino acid derivatives upon treatment with acids.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acids / chemistry
  • Crystallography, X-Ray
  • Models, Molecular
  • Peptides / chemical synthesis*
  • Peptides / chemistry
  • Protein Conformation

Substances

  • Amino Acids
  • Peptides