its inversion frequency must bc so high as to prevent retention of its configuration over the short life it has before being captured by the waiting diethylthallic ions. This example will illustrate the kind of work currently in progress. We have not yet seriously begun to use the powerful new metho
✦ LIBER ✦
Desoxypodophyllinsäure-1 β-D-glucopyranosyl-ester, ein neues. Lignanderivat aus Podophyllum peltatum L. und P. emodi WALL. 13. Mitteilung über mitosehemmende Naturstoffe
✍ Scribed by Max Kuhn; A. von Wartburg
- Publisher
- John Wiley and Sons
- Year
- 1963
- Tongue
- German
- Weight
- 845 KB
- Volume
- 46
- Category
- Article
- ISSN
- 0018-019X
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✦ Synopsis
Abstract
The isolation of lignan J, C~28~H~34~O~13~, a new compound from the roots and rhizomes of American Podophyllum peltatum L. and Indian P. emodi Wall. is described. Lignan J is easily cleaved to desoxypodphyllotoxin and D‐glucose. By degradation of its penta‐phenylurethane, the structure of lignan J has been deduced as the 1β‐D‐glucopyranosylester of desoxypodophyllinic acid. It is suggested that glucose esters of this type may act as intermediates in the biogenesis of lignans.
📜 SIMILAR VOLUMES
Podophyllum-Lignane 4′-Demethyl-desoxypo
✍
A. von wartburg; M. Kuhn; H. Lichti
📂
Article
📅
1964
🏛
John Wiley and Sons
🌐
German
⚖ 449 KB