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13C NMR (100MHz,CDCl3):
11.04,11.15,11.46,12.24,14.00,14.13,14.21,19.26,19.63,22.74,23.06,23.81,24.04,26.15,26.36,26.83,27.53,28.61,28.99,29.34,29.53,29.78,30.43,30.61,31.93,32.56,33.14,34.42,36.16,36.55,36.65,38.79,38.96,66.24,66.33,66.58,66.64,68.60,128.90,130.15,132.07,132.77,165.15,166.62,167.28

[ Last edited by ׿Խ_ÏÈ·æ on 2015-5-25 at 10:39 ]
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lxjsun(׿Խ_ÏÈ·æ´ú·¢): ½ð±Ò+15 2015-06-07 13:45:44
1 .     5,6¦Â-Epoxysitosteryl oleate
C47H82O3     ÏàËÆ¶È:68.8%
Steroids          2008          73          1098-1109
Synthesis of highly pure oxyphytosterols and (oxy)phytosterol esters: Part II. (Oxy)-sitosterol esters derived from oleic acid and from 9,10-dihydroxystearic acid [1]
Diane Julien-David, Philippe Geoffroy, Eric Marchioni, Françis Raul, Dalal Aoud¨¦-Werner, Michel Miesch
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2 .     ¦Â-stitosterol linoleate
    ÏàËÆ¶È:65.9%
Chinese Joumal of Experimental Traditional Medical Fomulae          2013          19          86-89
Chemical Constituents from Ampelopsis japonica
MI Jun-ling, WU Chun-jie, SUN Ling-gen, LI Chun-tong, XI Feng-min, CHEN Wan-sheng
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
3 .     ¦Â-sitosteryl linoleate
    ÏàËÆ¶È:65.9%
Asian Journal of Chemistry          2013          25          1875-1878
Antioxidative Coumarins from the Roots of Ferulago subvelutina
M. NASERI, H.R. MONSEF-ESFEHANI, S. SAEIDNIA, D. DASTAN and A.R. GOHARI
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
4 .     ¦Â-Sitosteryl linoleate
    ÏàËÆ¶È:65.2%
Zeitschrift f¨¹r Naturforschung C          2012          67          172-180
Anti-Helicobacter pylori Activity of the Methanolic Extract of Geum iranicum and its Main Compounds
Somayeh Shahani, Hamid R. Monsef-Esfahani, Soodabeh Saeidnia, Parastoo Saniee, Farideh Siavoshi, Alireza Foroumadi, Nasrin Samadi, and Ahmad R. Gohari
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
5 .     ¦Â-sistosterol linoleate
C47H80O2     ÏàËÆ¶È:65.2%
Chinese Joumal of Experimental Traditional Medical Fomulae          2012          18          123-126
Chemical Constituents of Lindera aggregata
ZHU Yue-zhen, LIU Ming-chuan, HU De-yu, JIN Lin-hong, XUE Wei, YANG Song
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
6 .     cholestery 9,12-octadecadienoate
    ÏàËÆ¶È:64.4%
Chinese Pharmaceutical Journal          2011          46          17-20
Studies on Chemical Constituents of Sarcopyramis nepdensis
ZHANG Jin-wen, CHEN Hua-dong, LIAO Mei, ZHANG Yong-hui
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
7 .     ¦Â-sitosterol linoleate
    ÏàËÆ¶È:63.8%
Chinese Pharmaceutical Journal          2007          42          661-663
Studies on Chemical Constituents of Paeonia veitchii L.
WANG Rui, CHOU Gui-xin, ZHU En-yuan, WANG Zheng-tao, BI Kai-shun
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
8 .     ¦Â-sitosteryl linoleate
    ÏàËÆ¶È:63.8%
Natural Product Research and Development          2012          24          1738-1742
Chemical Constituents of Ceratocarpus arenarius L£®
LIU Shan-shan, SUN Wen, YANG Hong-bing*, SUN Wan-fu
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
9 .     5,6¦Â-Epoxysitosteryl-9,10-dihydroxystearate
C47H84O5     ÏàËÆ¶È:63.0%
Steroids          2008          73          1098-1109
Synthesis of highly pure oxyphytosterols and (oxy)phytosterol esters: Part II. (Oxy)-sitosterol esters derived from oleic acid and from 9,10-dihydroxystearic acid [1]
Diane Julien-David, Philippe Geoffroy, Eric Marchioni, Françis Raul, Dalal Aoud¨¦-Werner, Michel Miesch
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
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