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.
Sign-in/Register to access full text options 
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 callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
