FAST-ATOM-BOMBARDMENT MASS AND TANDEM MASS-SPECTRA OF PROTONATED AND ALKALI CATIONIZED ALDOBIOURONIC AND PSEUDOALDOBIOURONIC ACID PER-O-METHYL DERIVATIVES
V. Kovacik et al., FAST-ATOM-BOMBARDMENT MASS AND TANDEM MASS-SPECTRA OF PROTONATED AND ALKALI CATIONIZED ALDOBIOURONIC AND PSEUDOALDOBIOURONIC ACID PER-O-METHYL DERIVATIVES, Organic mass spectrometry, 29(12), 1994, pp. 707-712
The positive-ion fast atom bombardment mass spectra of permethylated a
ldo- and pseudoaldobiouronic acids can be used to distinguish these cl
asses of compounds. The collisional-induced dissociation spectra of th
e [M + H](+) ions show fragment ions resulting from glycosidic bond cl
eavage and successive losses of methanol molecules. These spectra toge
ther with those of the [M + H - MeOH](+) oxonium ions allow the identi
fication of the type of interglycosidic linkage. Collisional activatio
n of the relatively stable [M + Na](+) ions show many fragmentations w
hich are common to alkali cationized permethylated saccharides. Moreov
er, fragment ions resulting from two-bond ring cleavage processes yiel
d additional information with respect to the linkage between the hexos
e and uronic acid units.