Synthesis of Thymine Nucleosides Derived from 1-Deoxy-D-psicofuranose

@inproceedings{FaivreBuet1992SynthesisOT,
  title={Synthesis of Thymine Nucleosides Derived from 1-Deoxy-D-psicofuranose},
  author={V{\'e}ronique Faivre-Buet and Annie V. Grouiller and G{\'e}rard Descotes},
  year={1992}
}
Abstract The use of D-(+)-ribonic γ-lactone 1a,b as a chiral synthon leads to an efficient synthesis of the ketose 1-deoxy-D-psicofuranose 2a,b. Condensation of the corresponding acetyl derivative 3a,b with silylated thymine, followed by deprotection of 4a,b affords an anomeric mixture of ketosyl nucleoside 6 (predominately the β-anomer) in an improved overall yield of 49%.