## Abstract The hydrothermolysis of cardenolide and flavonoid glycosides is described. On heating with water or water/dioxane, cardenolide (1, 5, 11) and flavonoid glycosides (16, 20, 23, 27) are converted into their genuine aglycones and partially hydrolyzed products, together with saccharide comp
Thermal Degradation of Glycosides, IV. Degradation of flavonoid glycosides
β Scribed by Kim, Youn Chul ;Higuchi, Ryuichi ;Kitamura, Yoichi ;Komori, Tetsuya
- Publisher
- John Wiley and Sons
- Year
- 1991
- Tongue
- English
- Weight
- 487 KB
- Volume
- 1991
- Category
- Article
- ISSN
- 0947-3440
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β¦ Synopsis
Abstract
By mere heating, the flavone (1, 7), flavanone (4, 10), and flavonol glycosides (13, 14) are converted into their aglycones and monoglycosides. The products of pyrolysis have been isolated by chromatography and their structures elucidated by chemical and spectroscopic methods. The compound derived from the sugar moiety in the pyrolysis of glucosides has been identified as levoglucosan (17). From the structures of some minor products (16, 18, 19), generated by the thermal degradation, a mechanism of their generation and the elucidation of the structures of rearranged ions (for example [M + 146 + H]^+^), often generated in the FDβmass spectra of glycosides, are presented.
π SIMILAR VOLUMES
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I he tennal emcct on scctates of tritcrpcnoid and slcraid glycosides was examined. Contrary to thc casc or free glycosides, on heating ihc acciatcs of typical tritcrpcnoid and steroid glycosidcs (including cardi;ic glycosides) on a melting point apparatus the cleavage reactions c d sugar-aglycone an
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