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| 13C NMR (101 MHz, MeOD) ¦Ä 6.65, 18.32, 19.18, 21.09, 21.11, 35.24, 40.52, 42.11, 54.16, 56.76, 71.48, 104.19, 120.47, 162.68, 173.29 |
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²éѯ½á¹û£º¹²²éµ½1160¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 4¦Á,8¦Â-Dihydroxy-5¦Á(H)-eudesm-7(11)-en-8,12-olide C15H22O4 ÏàËÆ¶È:100% Helvetica Chimica Acta 2010 93 803-810 Terpenoids from Roots of Chloranthus spicatus Zhi-Yong Xiao, Xia-Chang Wang, Gui-Ping Zhang, Zhong-Liang Huang and Li-Hong Hu Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 4¦Â,8¦Â-dihydroxy-5¦Á(H)-eudesm-7(11)-en-8,12-olide C15H22O4 ÏàËÆ¶È:86.6% Journal of Natural Products 2012 75 694-698 Terpenoids from Chloranthus serratus and Their Anti-inflammatory Activities Mi Zhang, Munekazu Iinuma, Jun-Song Wang, Masayoshi Oyama, Tetsuro Ito, and Ling-Yi Kong Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 4¦Á-Hydroxy-5¦Á,8¦Â(H)-eudesm-7(11)-en-8,12-olide C15H22O3 ÏàËÆ¶È:86.6% Helvetica Chimica Acta 2010 93 803-810 Terpenoids from Roots of Chloranthus spicatus Zhi-Yong Xiao, Xia-Chang Wang, Gui-Ping Zhang, Zhong-Liang Huang and Li-Hong Hu Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 4¦Á,8¦Â,9¦Á-Trihydroxy-5¦ÁH-7(11)-eudesmen-12,8¦Á-olide C15H22O5 ÏàËÆ¶È:80% Phytochemistry 2008 69 2231-2236 Cytotoxic sesquiterpenes from Ligularia platyglossa Jian-Qun Liu,Mian Zhang,Chao-Feng Zhang, Huan-Yang Qi, Alan Bashall, S.W. Annie Bligh, Zheng-Tao Wang Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . Chloraeudolide C15H22O5 ÏàËÆ¶È:80% Journal of Natural Products 2011 74 16-20 Sesquiterpenes from Chloranthus japonicus Qiu-Hong Wang, Hai-Xue Kuang, Bing-You Yang, Yong-Gang Xia, Jun-Song Wang, and Ling-Yi Kong Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . Multistalactone C C15H20O4 ÏàËÆ¶È:80% Phytochemistry 2013 88 112-118 Sesquiterpenoids from Chloranthus multistachys Hai-Yang Liu, Xin-Hui Ran, Ning-Bo Gong, Wei Ni, Xu-Jie Qin, Yan-Yan Hou, Yang L¨¹, Chang-Xiang Chen Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 4¦Â-hydroxy-5¦Á,8¦Â(H)-eudesm-7(11)-en-8,12-olide C15H22O3 ÏàËÆ¶È:73.3% Journal of Natural Products 2012 75 694-698 Terpenoids from Chloranthus serratus and Their Anti-inflammatory Activities Mi Zhang, Munekazu Iinuma, Jun-Song Wang, Masayoshi Oyama, Tetsuro Ito, and Ling-Yi Kong Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . Curcolide C15H22O5 ÏàËÆ¶È:73.3% Chemistry & Biodiversity 2010 7 1245-1253 Four New Sesquiterpenes from Curcuma wenyujin and Their Inhibitory Effects on Nitric-Oxide Production Yan Lou, Feng Zhao, Hao He, Kai-Feng Peng, Li-Xia Chen and Feng Qiu Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . compound 6 ÏàËÆ¶È:73.3% Acta Chemica Scandinavica 1981 35 573-576 Tobacco Chemistry. 54. (1S,2E,4S,6E,8S,11R,12S)-8,11-Epoxy-2,6-cembradiene-4,12-diol, a New Constituent of Greek Tobacco. Wahlberg, Inger; Behr, Dan; Eklund, Ann-Marie; Nishida, Toshiaki; Enzell, Curt R.; Berg, Jan-Eric Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . compound 1 C15H26O ÏàËÆ¶È:73.3% Agricultural and Biological Chemistry 1983 47 1075-1078 Structures of TwoNewSesquiterpenes from Aspergillus oryzae Kojiro Wada, Seiichi Tanaka, Shingo Marumo Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . Multistalactone B C15H20O4 ÏàËÆ¶È:73.3% Phytochemistry 2013 88 112-118 Sesquiterpenoids from Chloranthus multistachys Hai-Yang Liu, Xin-Hui Ran, Ning-Bo Gong, Wei Ni, Xu-Jie Qin, Yan-Yan Hou, Yang L¨¹, Chang-Xiang Chen Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . Chlorajapolide I C17H26O4 ÏàËÆ¶È:70.5% Fitoterapia 2012 83 1604-1609 Sesquiterpenes from the aerial part of Chloranthus japonicus and their cytotoxicities Mi Zhang, Jun-Song Wang, Peng-Ran Wang, Masayoshi Oyama, Jun Luo, Tetsuro Ito, Munekazu Iinuma, Ling-Yi Kong Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . 4¦Á-Hydroxy-5¦Á(H)-8¦Â-methoxyeudesm-7(11)-en-8,12-olide C16H24O4 ÏàËÆ¶È:68.7% Helvetica Chimica Acta 2010 93 803-810 Terpenoids from Roots of Chloranthus spicatus Zhi-Yong Xiao, Xia-Chang Wang, Gui-Ping Zhang, Zhong-Liang Huang and Li-Hong Hu Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . compound 2 ÏàËÆ¶È:66.6% Journal of Natural Products 2001 64 348-349 Synthesis of (+)-Cyclozonarone and the Absolute Configuration of Naturally Occurring (-)-Cyclozonarone Manuel Cort¨¦s, Jaime A. Valderrama, Mauricio Cuellar, Ver¨®nica Armstrong, and Marcelo Preite Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . 5¦ÁH,7¦ÁH-eudesman-4¦Á,6¦Á,11,12-tetraol C15H28O4 ÏàËÆ¶È:66.6% Planta Medica 2005 71 706-710 New Sesquiterpene Lactones from Laurus nobilis Leaves as Inhibitors of Nitric Oxide Production Simona De Marino,Nicola Borbone,Franco Zollo,Angela Ianaro,Paola Di Meglio, Maria Iorizzi Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . Serralactone C C15H22O5 ÏàËÆ¶È:66.6% Helvetica Chimica Acta 2009 92 1298-1303 Four New Eudesmane Sesquiterpenoid Lactones from Chloranthus serratus Fei Teng, Hui-Min Zhong, Chang-Xiang Chen, Hai-Yang Liu Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . Enantio-7(11).eudesmen-4-ol C15H26O ÏàËÆ¶È:66.6% Chinese Chemical Letters 1996 7 1093-1094 EUDESMANES AND EUDESMANOIC GLUCOSIDES FROM LAGGERA PETERODONTA YU ZHAO,JIAN MIN YUE,JING KAI DING,ZHONG WEN LIN AND HAN DONG SUN Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . (1R,6R)-1,7,7-Trimethy1-2,3-dimethylidenbicyclo[4.4.0]decan C15H24 ÏàËÆ¶È:66.6% Helvetica Chimica Acta 1980 63 154-190 Photochemische Reaktionen. 106. Mitteilung. Zur Photochemie tetraalkylsubstituierter ¦Ã-Keto-olefine Jacob Berger, Michikazu Yoshioka, Markus P. Zink, Hans R. Wolf, Oskar Jeger Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . pterodolide [3¦Á-(2-methyl-2,3-epoxy)-butyric-4¦Á-acetoxy-8¦Â-ethoxy eudesma-7(11)-en-8¦Á,12-olide C24H34O8 ÏàËÆ¶È:66.6% Journal of Asian Natural Products Research 2007 9 233-237 Two eudesmane sesquiterpenes from Laggera pterodonta Y.-B. LIU†, W. JIA, Z. YAO, Q. PAN, Y. TAKAISHIk and H.-Q. DUAN Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . 7(11)-eremophilen-12,8¦Á-olide ÏàËÆ¶È:66.6% China Journal of Chinese Materia Medica 2008 33 1697-1699 Study On Sesquiterpene Components of Ligularia altaica DC ZHANG Chaofeng, WANG Qiong, ZHANG Mian Structure 13C NMR ̼Æ×Ä£Äâͼ |
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