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Synthesis 1985; 1985(6/7): 605-609
DOI: 10.1055/s-1985-34138
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Stereospecific Synthesis of ß-D-Xylofuranosides of Adenine and Guanine

N. E. Poopeiko* , E. I. Kvasyuk, I. A. Mikhailopulo, M. J. Lidaks
  • *Institute of Bioorganic Chemistry, Byelorussian SSR Academy of Sciences, 220600 Minsk, U.S.S.R.
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Publication Date:
18 September 2002 (online)

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A convenient preparation of the 9-ß-D-xylofuranosides of adenine (xylo-A) and guanine (xylo-G) is described. 1,2-Di-O-acetyl-3,5-Di-O-(p-nitrobenzoyl)-D-xylofuranose is used as the glycosylating agent and a modified procedure for its preparation is given. The method is stereospecific for the ß-anomers.

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