Reaction between 2,2′-anhydro-1-β-D-arabinofuranosyluracil and thiolate ions
- 1 January 1982
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Journal of the Chemical Society, Perkin Transactions 1
- No. 7,p. 1625-1628
- https://doi.org/10.1039/p19820001625
Abstract
2,2′-Anhydro-1-β-D-arabinofuranosyluracil [2,2′-anhydrouridine](1a) reacts with the conjugate bases of thiophenol, toluene-4-thiol, ethanethiol, propane-1-thiol, 2-methylpropane-2-thiol and 4-methoxyphenylmethanethiol to give good to high yields of the corresponding 2′-deoxy-2′-mercaptouridine derivatives (2a; R2= Ph, 4-MeC6H4, Et, Pr, But, and 4-MeOC6H4CH2, respectively).This publication has 2 references indexed in Scilit:
- Interconversion of 8,2′-O-cycloadenosine and 2′,3′-anhydro-8-oxyadenosineJournal of the Chemical Society, Chemical Communications, 1976
- Ein neuer Weg zu 3′‐Desoxy‐uridin aus UridinEuropean Journal of Inorganic Chemistry, 1968