A new approach to the synthesis of 2-aminopurine-2'-deoxyriboside via tri- n-butyltin hydride reduction

Article abstract of DOI:10.1080/15257779508010704

A simple conversion of guanosine to 2-aminopurine-2'-deoxyriboside is described. Following the synthesis of the 2'-phenoxythiocarbonyl derivative of 6-chloroguanosine, 2-aminopurine-2'-deoxyriboside can be prepared by simultaneous reduction of both the 6-

Full text of DOI:10.1080/15257779508010704

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A New Approach to the Synthesis of 2-
Aminopurine-2′-deoxyriboside via Tri-
n-butyltin Hydride Reduction
Sabine Schmidt a & Dieter Cech a
a Institut für Chemie, Humboldt-Universität zu Berlin , Hessische
Str. 1–2, 10099, Berlin, Germany
Published online: 24 Sep 2006.
To cite this article: Sabine Schmidt & Dieter Cech (1995) A New Approach to the Synthesis of 2-
Aminopurine-2′-deoxyriboside via Tri-n-butyltin Hydride Reduction, Nucleosides and Nucleotides,
14:6, 1445-1452, DOI: 10.1080/15257779508010704
To link to this article: http://dx.doi.org/10.1080/15257779508010704
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