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- W2025773275 abstract "Abstract The syntheses of 6-(4) and 7-p-chlorphenyl-1-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)-lumazine (6), was well as the debenzoylation to the corresponding free nucleosides 5 and 7, were improved. Thiation of 4 and 6 by P4S10 led in excellent yields to 4-thiolumazine nucleosides (8, 10) which could be deblocked to 9 and 11 and converted on treatment with ammonia into the isopterin-N-1- ribofuranosides 13 and 14. 2,2′-Anhydro-nucleoside formation worked well with 5 and 7 respectively to give 15 and 16, which formed on acid hydrolysis the 6- and 7-substituted 1-β-D-arabinofuranosyl-lumazines 18 and 19. The new nucleosides have been characterized by UV and 1H-NMR spectra." @default.
- W2025773275 created "2016-06-24" @default.
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- W2025773275 date "1989-01-01" @default.
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- W2025773275 title "Nucleosides, XLVI<sup>1</sup>Syntheses and Reactions of 6- and 7-p-Chlorophenyllumazine Nucleosides" @default.
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- W2025773275 doi "https://doi.org/10.1080/07328318908048856" @default.
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