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Issue 17, 2011
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Modular synthesis of 1-α- and 1-β-(indol-2-yl)-2′-deoxyribose C-nucleosides

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Abstract

A simple two-step method for the selective preparation of anomerically pure 1α- and 1β-(indol-2-yl)deoxyribose derivatives was developed. The synthesis was based on the Sonogashira reaction of 1α- and 1β-ethynyldeoxyribose and 2-haloanilines followed by a Pd-complex catalyzed cyclization to the corresponding indolyldeoxyribosides.

Graphical abstract: Modular synthesis of 1-α- and 1-β-(indol-2-yl)-2′-deoxyribose C-nucleosides

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Publication details

The article was received on 27 May 2011, accepted on 28 Jun 2011 and first published on 29 Jun 2011


Article type: Communication
DOI: 10.1039/C1OB05844D
Citation: Org. Biomol. Chem., 2011,9, 5934-5937
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    Modular synthesis of 1-α- and 1-β-(indol-2-yl)-2′-deoxyribose C-nucleosides

    D. Nečas, D. Hidasová, M. Hocek and M. Kotora, Org. Biomol. Chem., 2011, 9, 5934
    DOI: 10.1039/C1OB05844D

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