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• W2082904334 startingPage "1275" @default.
• W2082904334 abstract "The 1 : 1 adduct ion formation between a series of per-O-acetylated aldopyranoses (family 1) or N-butylated glycosylamines (family 2) and an organic/metallic cation (n-C8H17NH3+/K+ or Li+) has been examined using quantitative FAB mass Spectrometry. The per-O-acetyl modifications dramatically lead to negated selectivity of the carbohydrates toward the cation which has been clearly observed in per-O-methyl modifications. On the other hand, the mono-N-butyl modifications provide a similar selectivity pattern to mono-O-methyl ones. These results are understood on the basis of electronic and structural considerations." @default.
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• W2082904334 date "1992-05-01" @default.
• W2082904334 modified "2023-10-14" @default.
• W2082904334 title "1 : 1 Adduct Ion Formation of Simple Carbohydrate Derivatives with Cations Using FAB Mass Spectrometry. Comparison of<i>O</i>-Acetyl,<i>N</i>-Butyl, and<i>O</i>-Methyl Modifications" @default.
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• W2082904334 doi "https://doi.org/10.1246/bcsj.65.1275" @default.
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