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Collect. Czech. Chem. Commun. 1984, 49, 2689-2697
https://doi.org/10.1135/cccc19842689

Reaction of 2,2'-anhydro-1-(β-D-arabinofuranosyl)-6-azauracil, 4-chloropyrimidine and 6-chloropurine nucleosides with amino acids

Hubert Hřebabecký and Jiří Beránek

Institute of Organic Chemistry and Biochemistry, Czechoslovak Academy of Sciences, 166 10 Prague 6

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  • Berzina Maria Ya., Eletskaya Barbara Z., Kayushin Alexei L., Dorofeeva Elena V., Lutonina Olga I., Fateev Ilya V., Paramonov Alexander S., Kostromina Maria A., Zayats Evgeniy A., Abramchik Yulia A., Maltsev Dmitriy V., Naumenko Ludmila V., Taran Alena S., Yakovlev Dmitry S., Spasov Alexander A., Miroshnikov Anatoly I., Esipov Roman S., Konstantinova Irina D.: Synthesis of 2-chloropurine ribosides with chiral amino acid amides at C6 and their evaluation as A1 adenosine receptor agonists. Bioorganic Chemistry 2022, 126, 105878. <https://doi.org/10.1016/j.bioorg.2022.105878>
  • Pal'chykovska L. H., Platonov M. O., Alexeeva I. V., Shved A. D.: Design of the potential transcription inhibitors based on the 6-azacytosine and 6-aza-iso-cytosine. Nonempirical quantum chemical analysis, synthesis and physico-chemical studies. Biopolym. Cell 2004, 20, 131. <https://doi.org/10.7124/bc.00069D>
  • Al-Masoudi Najim A., Issa Fadhel B., Pfleiderer Wolgang, Lazrek Hassan B.: Synthesis and Biological Activity of Some 5-Substituted-6-azauracil-N-1-Nucleosides of 2-Acetamido-2-Deoxy-D-glucose. Nucleosides and Nucleotides 1995, 14, 1693. <https://doi.org/10.1080/15257779508009750>
  • Al-Masoudi Najim A., Pfleiderer Wolfgang, Lazrek Hassan B.: Synthesis of Some Novel 1-(5-Thio-ß-D-glucopyranosyl)-6-azauracil Derivatives - Thiosugar Nucleosides. Nucleosides and Nucleotides 1993, 12, 687. <https://doi.org/10.1080/07328319308021503>
  • HREBABECKY H., BERANEK J.: ChemInform Abstract: ANALOGS OF NUCLEOSIDES. XLI. REACTION OF 2,2′-ANHYDRO-1-(β-D-ARABINOFURANOSYL)-6-AZAURACIL, 4-CHLOROPYRIMIDINE AND 6-CHLOROPURINE NUCLEOSIDES WITH AMINO ACIDS. Chemischer Informationsdienst 1985, 16. <https://doi.org/10.1002/chin.198516335>