Nucleobase modified peptide nucleic acid

Nucleosides Nucleotides Nucleic Acids. 2003 May-Aug;22(5-8):1029-33. doi: 10.1081/NCN-120022728.

Abstract

The Pd0/Cu1 catalyzed cross-coupling of terminal alkynes onto peptide nucleic acid monomers or submonomers bearing iodinated nucleobases has been utilized as a route to base-modified oligomers. Both 5-iodouracil and 5-iodocytosine derivatives undergo the cross-coupling to give the expected products in moderate to good yields. However, depending on the particular substrates and reaction conditions, the cross-coupling may be followed by a ring closing reaction to give the fluorescent furano- and pyrrolo-fused uracil and cytosine derivatives, respectively.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Binding Sites
  • Cross-Linking Reagents
  • Cytosine / analogs & derivatives*
  • Cytosine / chemistry
  • Indicators and Reagents
  • Kinetics
  • Molecular Structure
  • Peptide Nucleic Acids / chemistry*
  • Uracil / analogs & derivatives*
  • Uracil / chemistry

Substances

  • Cross-Linking Reagents
  • Indicators and Reagents
  • Peptide Nucleic Acids
  • iodouracil
  • 5-iodocytosine
  • Uracil
  • Cytosine