Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5216067 | Tetrahedron | 2014 | 5 Pages |
Abstract
A straightforward semisynthesis of neohesperidose was performed in three-steps with 43% overall yield starting from naringin, the main flavonoid of grapefruit. In addition, the behaviour of two pairs of flavonoid 7-O-rhamnoglucosides (neohesperidosides naringin and rhoifolin; rutinosides hesperidin and diosmin) under same acetolysis conditions was compared. Results demonstrated the crucial influence of the oxidation state of the aglycone (flavanone or flavone), and of the nature of the disaccharidic moiety on the course of the reaction.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Guy Lewin,