## Abstract Four new cholest‐type steroidal glycosides, junceellosides A–D, isolated from the EtOH/CH~2~Cl~2~ extracts of the South China Sea gorgonian coral __Junceella juncea__, were identified. Complete assignments of the ^1^H and ^13^C NMR chemical shifts for these compounds were achieved by me
Complete 1H and 13C NMR assignments of three new polyhydroxylated sterols from the South China Sea gorgonian Subergorgia suberosa
✍ Scribed by Shu-Hua Qi; Si Zhang; Yi-Fei Wang; Ming-Yi Li
- Publisher
- John Wiley and Sons
- Year
- 2007
- Tongue
- English
- Weight
- 145 KB
- Volume
- 45
- Category
- Article
- ISSN
- 0749-1581
- DOI
- 10.1002/mrc.2102
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✦ Synopsis
Abstract
Three new polyhydroxylated sterols, 3β,6α,11,20β,24‐pentahydroxy‐ 9,11‐seco‐5α‐24‐ethylcholest‐7,28‐diene‐9‐one (1), 3‐(1′,2′‐ethandiol)‐24‐ methylcholest‐8(9),22__E__‐diene‐3β,5α,6α,7α,11α‐pentaol (2), 24‐methylcholest‐7,22 E‐diene‐3β,5α,6β,25‐tetraol (3) together with five known sterols, were isolated from the EtOH/CH~2~Cl~2~ extract of the South China Sea gorgonian Subergorgia suberosa. The complete assignments of the ^1^H and ^13^C NMR chemical shifts for these new compounds were achieved by means of 1D and 2D NMR techniques, including HSQC, HMBC, ^1^H^1^H COSY, and NOESY spectra. Copyright © 2007 John Wiley & Sons, Ltd.
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