A newly devised method for the debenzylation of N6-benzyladenosines. A convenient synthesis of [6-15N]-labeled adenosines

Article abstract of DOI:10.1080/15257779408012148

[6-¹⁵N]-Labeled adenosine was conveniently prepared from inosine (1a) by the silylation-benzylamination of 1a and subsequent oxidative debenzylation with ammonium peroxydisulfate in a pH 7.2 buffer solution.

Full text of DOI:10.1080/15257779408012148

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Nucleosides and Nucleotides
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A Newly Devised Method for the
Debenzylation of N 6-Benzyladenosines.
A Convenient Synthesis of [6-15 N]-
Labeled Adenosines
Magoichi Sako a , Hiroaki Ishikura a , Kosaku Hirota a & Yoshifumi
Maki a
a Laboratory of Medicinal Chemistry, Gifu Pharmaceutical University,
6-1, Mitahora-higashi 5 Chome, Gifu, 502, JAPAN
Version of record first published: 24 Sep 2006.
To cite this article: Magoichi Sako, Hiroaki Ishikura, Kosaku Hirota & Yoshifumi Maki (1994): A Newly
Devised Method for the Debenzylation of N 6-Benzyladenosines. A Convenient Synthesis of [6-15 N]-
Labeled Adenosines, Nucleosides and Nucleotides, 13:6-7, 1239-1246
To link to this article: http://dx.doi.org/10.1080/15257779408012148
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