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- W2092014632 abstract "Stereoselective synthesis of novel 2′,3′-didehydro-2′,3′-dideoxy-4′-selenonucleosides (4′-seleno-d4Ns) 4a−c was accomplished via 4′-selenoribofuranosyl pyrimidines 11a−c, as key intermediates. 4′-Selenoribofuranosyl pyrimidines 11a−c were efficiently synthesized from d-ribose or d-gulonic γ-lactone using a Pummerer-type condensation as a key step. Introduction of 2′,3′-double bond was achieved by treating cyclic 2′,3′-thiocarbonate with 1,3-dimethyl-2-phenyl-1,3,2-diazaphospholidine." @default.
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- W2092014632 date "2008-05-03" @default.
- W2092014632 modified "2023-10-07" @default.
- W2092014632 title "Stereoselective Synthesis and Conformational Study of Novel 2′,3′-Didehydro-2′,3′-dideoxy-4′-selenonucleosides" @default.
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- W2092014632 doi "https://doi.org/10.1021/jo8003277" @default.
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