Glycal Scavenging in the Synthesis of Disaccharides Using Mannosyl Iodide Donors1

Publisher Website
Google Scholar
Abstract
[reaction: see text] High mannose glycans composed of alpha (1-->2) and alpha (1-->6) branched sugars are important components of the HIV-associated envelope glycoprotein, gp120. These substructures can be efficiently prepared in solution from glycosyl iodide precursors requiring only a slight excess of the iodide donor, which offers advantages over solid-phase methods that require more than 5 equiv of donor. During the reaction, excess iodide is converted to a glycal that is not easily separated from the desired disaccharide. To overcome this difficulty, a phase-trafficking methodology that relies upon nucleophilic interception of the 1,2 anhydrosugar resulting from oxidation of the glycal has been developed.