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Practical synthesis of 4′-selenopyrimidine nucleosides using hypervalent iodine
Authors:Hirotsugu TaniikeYusuke Inagaki  Akira MatsudaNoriaki Minakawa
Institution:a Graduate School of Pharmaceutical Sciences, The University of Tokushima, Shomachi 1-78-1, Tokushima 770-8505, Japan
b Faculty of Pharmaceutical Sciences, Hokkaido University, Kita-12, Nishi-6, Kita-ku, Sapporo 060-0812, Japan
Abstract:We report herein a synthesis of 4′-selenouridine 12 and 4′-selenocytidine 14, substrates for the synthesis of 4′-selenoRNA. The Pummerer-like reaction between the selenoxide 9 and a silylated uracil afforded the desired 4′-selenouridine derivative 10; however, the chemical yield of 10 was rather low. In addition, the reproducibility of this reaction was poor because of the instability of the selenoxide 9. Improvement of this Pummerer-like reaction to give 10 was achieved when the 4-selenosugar 8 was treated with TMSOTf, 2,6-lutidine and the silylated uracil in the presence of iodosylbenzene.
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