## Abstract Four new furostanol saponins (1–4), two pairs of diastereoisomers, were isolated from methanolic extracts of __T__upistra chinensis rhizomes and their structures were assigned from ^1^H and ^13^C NMR spectra, DEPT, and by 2D COSY, NOESY, HMQC, and HMBC experiments. Copyright © 2008 John
Structure elucidation of two new unusual monoterpene glycosides from Euphorbia decipiens, by 1D and 2D NMR experiments
✍ Scribed by Ozlem Demirkiran; Gulacti Topcu; Javid Hussain; Viqar Uddin Ahmad; M. Iqbal Choudhary
- Publisher
- John Wiley and Sons
- Year
- 2011
- Tongue
- English
- Weight
- 137 KB
- Volume
- 49
- Category
- Article
- ISSN
- 0749-1581
- DOI
- 10.1002/mrc.2795
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✦ Synopsis
Abstract
Two new unusual monoterpene glycosides, (Z)‐3,6‐dimethyl‐3‐(β‐D‐O‐glucosylmethylene)cyclohept‐4‐ene‐1‐one (1) and 3,6‐dimethyl‐3‐(β‐D‐O‐glucosylmethylene)cycloheptanone (2) have been isolated along with five known compounds, 3‐hydroxy‐4‐methoxybenzoic acid, 6,7‐dihydroxycoumarin, luteolin, apigenin 5‐O‐αl‐L‐rhamnoside, and pinocembrin‐7‐O‐rutinoside from ethyl acetate extract of Euphorbia decipiens. The structures of the isolated compounds were elucidated by extensive 1D‐ and 2D‐NMR, and mass spectroscopic analyses. Copyright © 2011 John Wiley & Sons, Ltd.
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