Issue 17, 1975

First syntheses of disaccharides by use of cycloaddition in a key step

Abstract

O-α-D-altrosyl-(1 → 3)-1,2;5,6-di-O-isopropyli-dene-α-D-glucofuranose, and its O-α-L-altrosyl and O-β-L-altrosyl analogues have been prepared in 35, 42, and ca. 38% yields from the products of the cycloaddition of butyl glyoxylate to 3-O-(buta-1,3-dienyl)-1,2;5,6-di-O- iso-propylidene-β-glucofuranose.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1975, 701-702

First syntheses of disaccharides by use of cycloaddition in a key step

S. David, A. Lubineau and J. Vatèle, J. Chem. Soc., Chem. Commun., 1975, 701 DOI: 10.1039/C39750000701

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