GC-MS characterization of acetylated O-glucofuranosides: direct glucosylation of volatile alcohols from unprotected glucose
Autor: | Jerković, I., Mastelić, J., Ivica Blažević, Šindler-Kulyk, M., Vikić-Topić, D. |
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Jazyk: | angličtina |
Rok vydání: | 2005 |
Předmět: | |
Zdroj: | Croatica Chemica Acta ResearcherID Scopus-Elsevier |
Popis: | O-Glucosylation of 1-pentanol, 1-octanol, 2-phenylethanol, benzyl alcohol, (+/-)-2-pentanol and (+/-)-menthol in 1,4-dioxane, using anhydrous FeCl(3), afforded anomeric mixture of the corresponding glucofuranosides as major and glucopyranosides as minor products in overall yields 20-52 %. Practical advantages of GC-MS for characterizing the prepared acetylated glucofuranosides are in the focus of this paper. Glucofuranoside tetruacetate spectra contain characteristic signals of glucone (acetylated glucose) along with fragments of the aglucone moiety. The mass range was 50-600 mass units and acetyl ion was not present in the spectra, which is of interest for differentiating glucofuranoside and glucopyranoside tetraacetates. |
Databáze: | OpenAIRE |
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