Specific interactions of deprotonated carboxylic group with uracil and thymine provoke diketo-->keto-enol tautomeric transition in bases

Ukr Biokhim Zh (1999). 2001 Jul-Aug;73(4):128-31.

Abstract

The 1H NMR and MNDO/H calculation data combined indicate the uracil and thymine tautomeric transitions from the ground diketo tautomeric state to the high-energy keto-enol one stimulated by specific interaction with carboxylate ion in anhydrous DMSO, which is blocked by base methylation at the 1 or 3 positions.

MeSH terms

  • Carboxylic Acids / chemistry*
  • Magnetic Resonance Spectroscopy
  • Thermodynamics
  • Thymine / chemistry*
  • Uracil / chemistry*

Substances

  • Carboxylic Acids
  • Uracil
  • Thymine