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lxjsunÒø³æ (СÓÐÃûÆø)
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΢Æ×ÇóÖú£¬Ð»Ð»Å¶ ÒÑÓÐ1È˲ÎÓë
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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
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lxjsun(׿Խ_ÏÈ·æ´ú·¢): ½ð±Ò+15 2015-06-07 13:45:44
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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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×Ä£Äâͼ |

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