Oxidation of sialic acid using hydrogen peroxide as a new method to tune the reducing activity

摘要

Functionalized sialic acids are useful intermediates to prepare a wide range of biological products. As they often occur at a non-reducing terminal of oligosaccharides, the most used technique to activate them is by periodate-mediated oxidation of their glycerol side chain. Here, we describe an alternative, non toxic, and environmentally-friendly method to activate the sialic acid residues by hydrogen peroxide oxidation. Four oxidative systems involving H_2O_2, EDTA, iron chloride, and UV light were studied and the products obtained were analyzed by LC–MS and NMR, before and after a derivatization reaction. At first, we observed, for each system, an irreversible decarbonylation reaction at the reducing end. Then, the decarbonylated sialic acid (DSA) was oxidized and fragmented into a mix of carbonyls and carboxyl acids, more or less fast according to the experimental conditions. Analysis of the reaction indicated an apparent radical mechanism and heterolytic alpha-hydroxy-hydroperoxide cleavages. The modest reducing activity was mainly explained as a consequence of over-oxidation reactions.