Reaction between 2,2′-anhydro-1-β-D-arabinofuranosyluracil and thiolate ions

@article{Divakar1982ReactionB2,
  title={Reaction between 2,2′-anhydro-1-$\beta$-D-arabinofuranosyluracil and thiolate ions},
  author={K. Divakar and C. Reese},
  journal={Journal of The Chemical Society-perkin Transactions 1},
  year={1982},
  volume={13},
  pages={1625-1628}
}
  • K. Divakar, C. Reese
  • Published 1982
  • Chemistry
  • Journal of The Chemical Society-perkin Transactions 1
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). 
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