Formation of a hydrogen-bonded barbiturate [2]-rotaxane

Org Lett. 2014 Mar 7;16(5):1358-61. doi: 10.1021/ol500099u. Epub 2014 Feb 26.

Abstract

Interlocked structures containing the classic Hamilton barbiturate binding motif comprising two 2,6-diamidopyridine units are reported for the first time. Stable [2]-rotaxanes can be accessed either through hydrogen-bonded preorganization by a barbiturate thread followed by a Cu(+)-catalyzed "click" stoppering reaction or by a Cu(2+)-mediated Glaser homocoupling reaction.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amides / chemistry
  • Barbiturates / chemistry*
  • Barbiturates / metabolism
  • Copper / chemistry
  • Hydrogen Bonding
  • Models, Molecular
  • Molecular Structure
  • Nuclear Magnetic Resonance, Biomolecular
  • Pyridines / chemistry
  • Rotaxanes / chemical synthesis*
  • Rotaxanes / chemistry

Substances

  • Amides
  • Barbiturates
  • Pyridines
  • Rotaxanes
  • diamidopyridine
  • Copper
  • barbituric acid