C-Glycosylflavonoids. II. The synthesis of 7,4'-Di-O-methylpuerarin (8-C-β-D-Glucopyranosyl-7,4'-dimethoxyisoflavone)
- 1 January 1978
- journal article
- research article
- Published by CSIRO Publishing in Australian Journal of Chemistry
- Vol. 31 (12) , 2699-2706
- https://doi.org/10.1071/ch9782699
Abstract
The product of reaction of 2'-acetoxy-4,4'-dimethoxy-3'-(tetraacetyl-β-D-glucopyranosyl)chalcone (4) with thallium(III) nitrate in methanol/trimethyl orthoformate solution gave, after acid hydrolysis, a high yield of 7,4'-di-O-methylpuerarin (2). The dimethyl acetal (6) and the enol ether (7) have been isolated from the reaction of the chalcone (4) with thallium(III) nitrate in methanol. Both the acetal (6) and ether (7) gave 7,4'-di-O-methylpuerarin on reaction with acid or base.Keywords
This publication has 2 references indexed in Scilit:
- New isoflavonoid glycosides from Dalbergia paniculataPhytochemistry, 1976
- The Constituents of Pueraria RootCHEMICAL & PHARMACEUTICAL BULLETIN, 1959