FAST-ATOM-BOMBARDMENT MASS AND TANDEM MASS-SPECTRA OF PROTONATED AND ALKALI CATIONIZED ALDOBIOURONIC AND PSEUDOALDOBIOURONIC ACID PER-O-METHYL DERIVATIVES

Citation
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
Citations number
18
Categorie Soggetti
Chemistry Inorganic & Nuclear",Spectroscopy,"Chemistry Inorganic & Nuclear",Spectroscopy,"Chemistry Inorganic & Nuclear",Spectroscopy
Journal title
ISSN journal
0030493X
Volume
29
Issue
12
Year of publication
1994
Pages
707 - 712
Database
ISI
SICI code
0030-493X(1994)29:12<707:FMATMO>2.0.ZU;2-4
Abstract
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.