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• W2152912997 abstract "Naturally occurring glucosides of benzyl alcohol, (+/-)-menthol, (+)-borneol, thymol, carvacrol and eugenol were synthesized by the Koenigs-Knorr-Zemplen method (yields 19.5-52.2%). Their beta-D-glucopyranosidic structures were determined by one- and two-dimensional homo- and heteronuclear H-1 and C-13 NMR spectroscopy. The beta-configuration was additionally confirmed by the hydrolysis with P-glucosidase. Tetraacetyl-beta-D-glucopyranosides, as intermediates, were GC-MS analyzed. Diastereomeric beta-glucoside tetraacetates of (+/-)-menthol were well separated on the HP-101 column. The mass spectra of glucopyranoside tetraacetates were mutually compared, as well as with the spectra of their aglycones." @default.
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• W2152912997 date "2004-10-25" @default.
• W2152912997 modified "2023-10-18" @default.
• W2152912997 title "Synthesis of Selected Naturally Occurring Glucosides of Volatile Compounds. Their Chromatographic and Spectroscopic Properties" @default.
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