## Abstract A pair of novel isomeric 6‐methylflavonoids, named baeckeins A (**1**) and B (**2**), were isolated from the roots of __Baeckea frutescens.__ The two compounds possess a unique C~23~ skeleton, resulting from the 6‐methylation and 8‐arylation of a flavonol (=3‐hydroxy‐2‐phenyl‐4__H__‐1‐b
Structure determination of baeckeins C and D from the roots of Baeckea frutescens
✍ Scribed by Bei-Xi Jia; Yu-Xin Zhou; Xiao-Qing Chen; Xiao-Bing Wang; Jie Yang; Mao-Xiang Lai; Qiang Wang
- Publisher
- John Wiley and Sons
- Year
- 2011
- Tongue
- English
- Weight
- 281 KB
- Volume
- 49
- Category
- Article
- ISSN
- 0749-1581
- DOI
- 10.1002/mrc.2803
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✦ Synopsis
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, HSQC, HMBC, and ROESY). The absolute configurations of the 2,3‐epoxide moiety for compounds 1 and 2 were determined by circular dichroism spectrometry combined with quantum chemical calculations. Copyright © 2011 John Wiley & Sons, Ltd.
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