Synthetic route to 5-substituted uridines via a new type of desulfurizative stannylation

This publication has 20 references indexed in Scilit:

• Introduction of an Azido Group to the C-6 Position of Uridine by the Use of a 6-Iodouridine Derivative
  Nucleosides, Nucleotides and Nucleic Acids, 1985
• Lithiation of 3',5'--(tetraisopropyldisiloxane-1,3-diyl)-2'-deoxyuridine: synthesis of 6-substituted 2'-deoxyuridines
  Tetrahedron, 1985
• Lithiation of 5,6-dihydrouridine: a new route to 5-substituted uridines
  Tetrahedron, 1985
• Synthesis and reaction of 6-trialkylsilyl substituted uracils and uridines
  Tetrahedron Letters, 1984
• The reaction of 6-phenylthiouridine with sulfur nucleophiles: A simple and regiospecific preparation of 6-alkylthiouridines and 6-alkylthiouridylic acids.
  CHEMICAL & PHARMACEUTICAL BULLETIN, 1983
• Synthesis and biological activities of 5-substituted 6-phenylthio and 6-iodouridines, a new class of antileukemic nucleosides.
  CHEMICAL & PHARMACEUTICAL BULLETIN, 1983
• Lithium dialkylamides. 13C parameters and slow proton transfer
  Tetrahedron Letters, 1982
• First exceptions to the "Imbach rule" for .BETA.-D-ribofuranosyl nucleosides.
  CHEMICAL & PHARMACEUTICAL BULLETIN, 1982
• “Umpulong” of reactivity at the C-6 position of uridine: a simple and general method for 6-substituted uridines
  Tetrahedron, 1982
• Nucleosides. LXXIX. Facile base-catalyzed hydrogen isotope labeling at position 6 of pyrimidine nucleosides
  Journal of the American Chemical Society, 1973