Synthesis of polynucleotide analogs containing a polyvinyl alcohol backbone

Molecules. 2008 Mar 26;13(3):701-15. doi: 10.3390/molecules13030701.

Abstract

Water soluble homo-base polynucleotide analogues were synthesized in which polyvinyl alcohol and partially phosphonated polyvinyl alcohol constituted the backbones,onto which were grafted uracil or adenine via 1,3-dioxane spacers formed by acetal formation with the 1,3-diol moieties in PVA. The resulting adenine-PVA polynucleotide analogs exhibited hyperchromic effects, which was not the case for the corresponding uracil compounds. Mixtures of the adenine- and aracil PVA-phosphate polynucleotide analogs in solutions exhibited characteristic S-shaped UV-absorbance vs temperature and melting curves with melting points at approximately 40 degrees C.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenine / chemistry
  • Phosphates / chemistry
  • Polynucleotides / chemical synthesis*
  • Polynucleotides / chemistry
  • Polyvinyl Alcohol / chemistry*
  • Solubility
  • Spectrophotometry, Ultraviolet
  • Temperature
  • Uracil / chemistry

Substances

  • Phosphates
  • Polynucleotides
  • Uracil
  • Polyvinyl Alcohol
  • Adenine