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Issue 1, 1994
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New and efficient synthesis of protected 2-azido-2-deoxy-glycopyranoses from the corresponding glycal

Abstract

Diversely protected 2-azido-2-deoxy-D-glycopyranoses are prepared by azido phenylselenylation of the corresponding glycal followed by hydrolysis of the resulting selenoglycosides: from protected D-galactal, protected 2-azido-2-deoxy-D-galactopyranose is obtained, as the sole product in 72% overall yield.

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Article information


J. Chem. Soc., Chem. Commun., 1994, 35-36
Article type
Paper

New and efficient synthesis of protected 2-azido-2-deoxy-glycopyranoses from the corresponding glycal

S. Czernecki, E. Ayadi and D. Randriamandimby, J. Chem. Soc., Chem. Commun., 1994, 35
DOI: 10.1039/C39940000035

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