4.8 Article

Internal residue loss: Rearrangements occurring during the fragmentation of carbohydrates derivatized at the reducing terminus

Journal

ANALYTICAL CHEMISTRY
Volume 74, Issue 4, Pages 734-740

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ac0109321

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Rearrangement reactions involving migration of fucose and, occasionally, other residues have been found in the CID spectra of [M + H](+) and [M + 2H](2+) ions, but not [M + Na](+) ions, generated from several O-linked carbohydrates and milk sugars derivatized at their reducing termini with aromatic amines such as 2-aminobenzamide. Such rearrangements, which are similar to those reported by other investigators from several underivatized carbohydrates and glycosides, cause an apparent loss of sugar residues from within a carbohydrate chain and can produce ambiguous results during spectral interpretation. A mechanism, involving initial protonation of the amine nitrogen atom of the derivative, is proposed to account for the formation of the observed ions.

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