Synthesis of some fully 3' and 4'-C-branched-chain sugar nucleoside analogues

Article abstract of DOI:10.1080/15257779908041556

The synthesis of some new 3'-azido-3'-C-substituted pyrimidine nucleoside analogues is described. The key step is the geminal disubstitution of an appropriated ketone carbohydrate, via the regioselective ring opening of the corresponding tosyl-epoxide der

Full text of DOI:10.1080/15257779908041556

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Nucleosides and Nucleotides
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Synthesis of Some Fully 3′ and 4′-
C-Branched-Chain Sugar Nucleoside
Analogues
T. Ton-That a
a CNRS-UM II 5625, Laboratoire de Chimie Bioorganique , Université
Montpellier II , Place Eugène Bataillon, 34095, Montpellier Cedex 5,
France
Published online: 04 Oct 2006.
To cite this article: T. Ton-That (1999) Synthesis of Some Fully 3′ and 4′-C-Branched-
Chain Sugar Nucleoside Analogues, Nucleosides and Nucleotides, 18:4-5, 731-732, DOI:
10.1080/15257779908041556
To link to this article: http://dx.doi.org/10.1080/15257779908041556
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