Design, synthesis, and structural analysis of D,L-mixed polypyrrolinones. 1. From nonpeptide peptidomimetics to nanotubes

Org Lett. 2010 Jul 2;12(13):2990-3. doi: 10.1021/ol101007n.

Abstract

To expand the potential conformational space available to the polypyrroline structural motif, an open chain, D,L-alternating hexapyrrolinone was designed and synthesized. Structural studies, including solution NMR and X-ray crystallographic analysis, revealed that the hexapyrrolinone adopts a turn conformation both in solution and in the solid state, with aggregation in solution and a nanotube-like quaternary structure in the crystal.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Crystallography, X-Ray
  • Magnetic Resonance Spectroscopy
  • Models, Molecular
  • Molecular Conformation
  • Nanotubes / chemistry*
  • Polymers / chemical synthesis*
  • Polymers / chemistry
  • Pyrrolidinones / chemical synthesis*
  • Pyrrolidinones / chemistry
  • Stereoisomerism

Substances

  • Polymers
  • Pyrrolidinones