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- W1600732740 abstract "The following three new analogs of naringin (I) were synthesized. Naringein-7-[6′-O-methyl-O-α-l-mannopyranosyl-(1→2)-β-d-glucopyranoside] (II), naringenin-7-[6′-O-methyl-O-α-d-mannopyranosyl-(1→2)-β-d-glucopyranoside] (III) and naringenin-7-[O-α-l-rhamno-pyranosyl-(1→6)-β-d-galactopyranoside] (XVI).Compounds II, III, narirutin (naringenin-7-[O-α-l-rhamnopyranosyl-(1→6)-β-d-glucopyranoside] (XV) and XVI are 0.10, 0.13, 0.05 and 0.08 times as bitter as I, respectively. From the above organoleptic result it was concluded that the methyl group of l-rhamnose in I is one of the essential factors for intense bitterness. Attachment of α-l-rhamnose to the 6′′′-position of d-glucoside or d-galactoside of naringenin does not abolish the taste of the resulting glycosides but elicits a moderate bitter taste." @default.
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- W1600732740 date "1979-01-01" @default.
- W1600732740 modified "2023-09-23" @default.
- W1600732740 title "Synthesis of flavonoid glycosides. IX. Relationship between the structure and taste of some naringin analogs." @default.
- W1600732740 doi "https://doi.org/10.1271/bbb1961.43.231" @default.
- W1600732740 hasPublicationYear "1979" @default.
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