Synthesis of D-fructofuranosylpurine nucleosides

Article abstract of DOI:10.1080/15257779408013257

The Mitsunobu reaction has been applied to the formation of purine nucleosides of D-fructofuranose. The use of O-benzyl protection results in a predominance of the β-configuration in these novel compounds and both α- and β-D-fructofuranosyladenine are obtained in stereochemically pure form.

Full text of DOI:10.1080/15257779408013257

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Nucleosides and Nucleotides
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Synthesis of D-Fructofuranosylpurine
Nucleosides
Abderrahime Bouali a , David F. Ewing a & Grahame Mackenzie a
a School of Chemistry, University of Hull , Hull, HU6 7RX, UK
Published online: 23 Sep 2006.
To cite this article: Abderrahime Bouali , David F. Ewing & Grahame Mackenzie (1994) Synthesis
of D-Fructofuranosylpurine Nucleosides, Nucleosides and Nucleotides, 13:1-3, 491-499, DOI:
10.1080/15257779408013257
To link to this article: http://dx.doi.org/10.1080/15257779408013257
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