S, X-acetals in nucleoside chemistry. III1. Synthesis of 2′- and 3′-O-azidomethyl derivatives of ribonucleosides

Article abstract of DOI:10.1080/15257770008045472

2′- and 3′-O-azidomethyl derivatives of ribonucleosides were obtained by splitting the corresponding methylthiomethyl derivatives of ribonucleosides with bromine or SO₂Cl₂ followed by lithium azide treatment.

Full text of DOI:10.1080/15257770008045472

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Nucleosides, Nucleotides and Nucleic
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S,X-Acetals in Nucleoside Chemistry. III1.
Synthesis of 2′-and 3′-O-Azidomethyl
Derivatives of Ribonucleosides
S. G. Zavgorodny a , A. E. Pechenov b , V. I. Shvets b & A. I.
Miroshnikov a
a Shemyakin-Ovchinnikov Institute of Bioorganic Chemistry, Russian
Academy of Sciences, ul. Miklukho-Maklaya, 16/10, Moscow, 117871,
Russia
b Lomonosov Academy of Fine Chemical Technology, Vernadsky pr.,
86, Moscow, 117571, Russia
Version of record first published: 17 Apr 2008
To cite this article: S. G. Zavgorodny, A. E. Pechenov, V. I. Shvets & A. I. Miroshnikov (2000):
S,X-Acetals in Nucleoside Chemistry. III1. Synthesis of 2′-and 3′-O-Azidomethyl Derivatives of
Ribonucleosides, Nucleosides, Nucleotides and Nucleic Acids, 19:10-12, 1977-1991
To link to this article: http://dx.doi.org/10.1080/15257770008045472
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