Addition of carbon radicals to 4′,5′-unsaturated uracilnucleosides by the use of organoselenium reagents: A new stereoselective entry to CC bond formation at the 5′-position

[1]  D. Boger,et al.  Phenyl selenoesters as effective precursors of acyl radicals for use in intermolecular alkene addition reactions , 1989 .

[2]  T. Miyasaka,et al.  Cleavage of a nucleosidic oxetane with carbanions: synthesis of a highly promising candidate for anti-HIV agents — a phosphonate isostere of AZT 5′-phosphate , 1989 .

[3]  H. Hayakawa,et al.  Reaction of organometallic reagents with 2'- and 3'-ketouridine derivatives: Synthesis of uracil nucleosides branched at the 2'- and 3'-positions. , 1987 .

[4]  R. T. Walker,et al.  The synthesis of some branched-chain-sugar nucleoside analogues. , 1987, Nucleic acids research.

[5]  H. Hayakawa,et al.  Direct C-8 lithiation of naturally-occurring purine nucleosides. A simple method for the synthesis of 8-carbon-substituted purine nucleosides , 1987 .

[6]  H. Hayakawa,et al.  A simple and general entry to 5-substituted uridines based on the regioselective lithiation controlled by a protecting group in the sugar moiety , 1987 .

[7]  A. Matsuda,et al.  A lithiation route to C-5 substitution of an imidazole nucleoside and its application to the synthesis of 3-deazaguanosine , 1986 .

[8]  D. Neckers,et al.  Low temperature free-radical reactions initiated with tert-butyl p-benzoylperbenzoate. Selective acyl radical additions to substituted olefins , 1985 .

[9]  D. Scopes,et al.  Novel nucleoside analogues via direct attack of carbon : Nucleophiles on nucleosides containing epoxy-sugars , 1985 .

[10]  A. Matsuda,et al.  A SIMPLIFIED SYNTHESIS OF 8-SUBSTITUTED PURINE NUCLEOSIDES VIA LITHIATION OF 6-CHLORO-9-(2, 3-O-ISOPROPYLIDENE-β-D-RIBOFURANOSYL) PURINE , 1983 .

[11]  H. Hayakawa,et al.  “Umpulong” of reactivity at the C-6 position of uridine: a simple and general method for 6-substituted uridines , 1982 .

[12]  D. Santi,et al.  Model studies of thymidylate synthetase. Neighboring-group facilitation of electrophilic substitution reactions of uracil furanosides. , 1968, Journal of the American Chemical Society.