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Structure and stereochemistry of novel ecdysteroids from the roots of Serratula wolffii
✍ Scribed by Mária Takács; András Simon; Erika Liktor-Busa; Mária Báthori; Ferenc Zsila; Zsolt Bikádi; Péter Horváth; Gábor Veress; András Gergely; Gábor Tóth
- Publisher
- John Wiley and Sons
- Year
- 2010
- Tongue
- English
- Weight
- 158 KB
- Volume
- 48
- Category
- Article
- ISSN
- 0749-1581
- DOI
- 10.1002/mrc.2581
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✦ Synopsis
Abstract
Three new natural ecdysteroids viz. 22‐dehydro‐20‐deoxy‐ajugasterone C (1), 1‐hydroxy‐22‐deoxy‐20,21‐didehydro‐ecdysone (2) and 22‐deoxy‐20,21‐didehydro‐ecdysone (3) were isolated from the methanol extract of the roots of Serratula wolffii. The structures of compounds 1–3 were established by various spectroscopic techniques, including one‐ and two‐dimensional NMR, circular dichroism and mass spectroscopic methods. Copyright © 2010 John Wiley & Sons, Ltd.
📜 SIMILAR VOLUMES
Baeckeins C (compound 1) and D (compound 2), a pair of new diastereomeric biflavonoids, were isolated from the roots of __Baeckea frutescens__. Their structures were elucidated on the basis of spectroscopic analysis, including HR‐ESI‐MS and one‐ and two‐dimensional NMR spectra (^1^H and ^13^C NMR, H