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A revised structure for pterocarpin

โœ Scribed by J. B-son Bredenberg; James N. Shoolery


Publisher
Elsevier Science
Year
1961
Tongue
French
Weight
152 KB
Volume
2
Category
Article
ISSN
0040-4039

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โœฆ Synopsis


THE recent isolation of the antifungal glucoside trifolirhizin and its aglycone from Trifolium uratense L. 132 and the methylation of the aglycone to pterocarpin has drawn our attention to the structure of the latter compound. Tine subfamily Papilionatae is known as a rich source of isoflavanoid substances. A literature scrutiny of 2 '-oxygenated isoflavanoids that have a dimethoxy or a methylenedioxy group in the B-ring revealed an interesting observation.

All the investigated substances (rotenoid type compounds, 394 pachyrrhizin, jamaicin,6 '5 erosnin, 7 sophorol') except pterocarpin have the


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