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Issue 24, 1998
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Synthesis of 2-deoxy and 2,6-dideoxy glycosides under neutral conditions in LiClO4/Et2O mixtures

Abstract

Glycosides of 2-deoxy and 2,6-dideoxy carbohydrates were built up in high yields and with high stereoselectivity in 0.1 M LiClO4/Et2O mixtures; the glycosidations proceed under neutral conditions and without need for an additional promoter such as a strong Lewis acid, a heavy metal salt or an alkylating reagent.

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Article type: Paper
DOI: 10.1039/A807734G
Citation: Chem. Commun., 1998,0, 2759-2769

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    Synthesis of 2-deoxy and 2,6-dideoxy glycosides under neutral conditions in LiClO4/Et2O mixtures

    H. Schene and H. Waldmann, Chem. Commun., 1998, 0, 2759
    DOI: 10.1039/A807734G

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