Abstract
Abstract Oxidation of thymine and 1,3-dimethylthymine with hydrogen peroxide in hydrochloric acid (pH 1.0–2.2) at 35–38 °C gave the corresponding trans-5-chloro-6-hydroperoxy-5,6-dihydrothymines. The formation of the hydroperoxythymines was dependent on pH of the aqueous solutions. Reaction of the hydroperoxythymine with amino acids and nucleic acids related compounds in deuterium oxide was investigated by NMR spectroscopy.
Full Text 
Sign-in/Register to access full text options
Sign-in/Register to access full text options 
Published version (
Free)
Free) 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a call
