Synthesis of 6-substituted purine N7-(2-deoxy-β-D-ribonucleosides) via anion glycosylation and anomerization during the N7/N9-glycosyl transfer

Article abstract of DOI:10.1080/15257779508014658

The synthesis of the 7-(2-deoxy-β-D-erythro-pentofuranosyl)adenine (1b) as well as the corresponding hypoxanthine- and purine nucleosides 3 and 4 is described employing the stereoselective nucleobase anion glycosylation. The N⁷/N⁹-is

Full text of DOI:10.1080/15257779508014658

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Synthesis of 6-Substituted Purine
N7-(2-Deoxy-β-D-Ribonucleosides)
via Anion Glycosylation and
Anomerization During the N7/N9-
Glycosyl Transfer
Frank Seela a & Holger Winter a
a Laboratorium für Organische und Bioorganische Chemie ,
Institut für Chemie, Universität Osnabrück , Barbarastr. 7,
D-49069, Osnabrück, Germany
Published online: 24 Sep 2006.
To cite this article: Frank Seela & Holger Winter (1995) Synthesis of 6-Substituted Purine N7-(2-
Deoxy-β-D-Ribonucleosides) via Anion Glycosylation and Anomerization During the N7/N9-Glycosyl
Transfer, Nucleosides and Nucleotides, 14:1-2, 129-142, DOI: 10.1080/15257779508014658
To link to this article: http://dx.doi.org/10.1080/15257779508014658
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