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1H and 13C NMR of acetyl derivatives of shamimin, a flavonol-C-glycoside

✍ Scribed by Shaheen Faizi; Muhammad Ali

Publisher: John Wiley and Sons
Year: 2000
Tongue: English
Weight: 60 KB
Volume: 38
Category: Article
ISSN: 0749-1581
DOI: 10.1002/1097-458x(200008)38:8<701::aid-mrc661>3.0.co;2-1

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✦ Synopsis

On acetylation, shamimin (1) a new flavonol-C-glycoside, furnished the penta-, hepta-and octaacetates, 5, 4 and 2, 3 respectively. Compound 2 hydrolysed into the tetraacetate 6 whereas 3 and 4 converted into 5 at room temperature. 1 H and 13 C NMR assignments are described.

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