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cuitianzeng(¶¹¸ç´ú·¢): ½ð±Ò+10, лл 2013-12-02 14:17:06
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cuitianzeng(¶¹¸ç´ú·¢): ½ð±Ò+10, лл 2013-12-02 14:17:06
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²éѯģʽ£ºÄ£ºý²éѯ ̼Æ×Êý¾ÝÊäÈ룺 °´´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺 21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2 ÈܼÁÑ¡Ï Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½32¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . jacquilenin ÏàËÆ¶È:93.3% Helvetica Chimica Acta 2004 Vol. 87 976 Five New Sesquiterpenoids from Parasenecio petasitoides Hua Zhang, Zhi-Xin Liao, and Jian-Min Yue Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . jacquilenin ÏàËÆ¶È:80% Chinese Traditional and Herbal Drugs 2001 32 970-972 Chemical constituents of Notoseris gracilipes YE Xiao xia; WANG Ming kui; HUANG Ke xin; GUAN Jia fa; DING Li sheng Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . leucodin ÏàËÆ¶È:66.6% Phytochemistry 1997 46 1045-1049 A guaianolide and a germacranolide from Achillea santolina Basma A. A. A. Balboul, Ahmed A. Ahmed, Hideaki Otsuka, Masahiko Bando, Masaru Kido, Yoshio Takeda Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . leukodin ÏàËÆ¶È:66.6% Journal of Natural Products 1988 Vol 51 221 Conformational Analysis of Achillin and Leukodin Mariano Martinez V., Alejandra Muñoz-Zamora, Pedro Joseph-Nathan Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . leucodin C15H18O3 ÏàËÆ¶È:66.6% Journal of Natural Products 1994 Vol 57 433 Oxodesoxyligustrin, Arborescin, 1,10-Epiarborescin, 11¦Â,13-Dihydroludartin, 8-Deoxy-11¦Â,13-dihydrorupicolin B, 8-Deoxyrupicolin B, 3,4-Epiludartin, Ludartin, Kauniolide, Dehydroleucodin, and Leucodin Masayoshi Ando, Kunihiko Ibayashi, Naoki Minami, Tomomasa Nakamura, Koji Isogai, Hideki Yoshimura Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . notoserolide D C15H16O5 ÏàËÆ¶È:66.6% Acta Pharmaceutica Sinica 2002 Vol 37 37-40 CHEMICAL CONSTITUENTS OF NOTOSERIS RHOMBIFORMIS LIAO Zhi xin; WANG Ming kui; PENG Shu lin; CHEN Yao zu; DING Li sheng Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . compound 12 C15H18O4 ÏàËÆ¶È:60% Journal of Asian Natural Products Research 2006 8 317-331 Biotransformation of a- and 11b-santonin by fungus and plant cell cultures L. YANG, J. DAI, J.-I. SAKAI and M. ANDO Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 8-Desoxylactucin C15H16O4 ÏàËÆ¶È:60% Phytochemistry 1995 40 1659-1665 Biosynthetic studies of lactucin derivatives in hairy root cultures of Lactuca floridana Qi Song, Marco L. Gomez-Barrios, Elise L. Hopper, Martin A. Hjortso, Nikolaus H. Fischer Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . compound 20 C14H18O4 ÏàËÆ¶È:57.1% Tetrahedron 2000 56 6331-6338 Synthesis of 3-Oxa-guaianolides from Santonin Gonzalo Blay, Luz Cardona, Begoña Garcı́a, Luisa Lahoz, Bel¨¦n Monje, Jos¨¦ R Pedro Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . compound 6 ÏàËÆ¶È:53.3% Journal of Asian Natural Products Research 2009 11 991-996 Stereoselective hydrogenation on the exocyclic and conjugated double bond of sesquiterpene lactones by Aspergillus versicolor D-1 Dan Wang, Li Yang, Hong Guan, Yi-Nan Chen, Wei-Zhuo Xu and Song You Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 8-desoxyartelin C15H18O4 ÏàËÆ¶È:53.3% Phytochemistry 1998 48 201-203 Sesquiterpene lactones from Ixeris sonchifolia Ji-Yuan Ma, Zheng-Tao Wang, Luo-Shan Xu, Guo-Jun Xu, Shigetoshi Kadota, Tsuneo Namba Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . compound 2 ÏàËÆ¶È:53.3% Journal of Natural Products 1995 Vol 58 1358-1364 Eight New Eremophilane Derivatives from the Roots of Ligularia przewalskii Yu Zhao, Zhongjian Jia, Hairuo Peng Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . 8-desoxyartelin ÏàËÆ¶È:53.3% Chinese Pharmaceutical Journal 2005 40 1613-1615 Study on chemical constituents from Ixeris sonchifolia YE Guan, FAN Ming-song, HUANG Cheng-gang, QU Xuan-yan Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . compound 3 C15H22O3 ÏàËÆ¶È:53.3% Tetrahedron 1989 45 6297-6308 A new stereochemical class of bicyclic sesquiterpenes from eremophila virgata W.V. Fitzg. (Myoporaceae) E.L. Ghisalberti, P.R. Jefferies, B.W. Skelton, A.H. White, R.S.F. Williams Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . 2-chlorohuperzine E C16H19NO2 ÏàËÆ¶È:50% Helvetica Chimica Acta 2007 Vol. 90 153 Lycopodium Alkaloids from Huperzia serrata Heng-Bin Wang, Chang-Heng Tan, Jun-Jie Tan, Ming-Yao Gao, Yi-Ming Li, Shan-Hao Jiang, and Da-Yuan Zhu Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . (-)-11¦ÂH,13-dihydromicheliolide C15H22O3 ÏàËÆ¶È:50% Journal of Natural Products 2002 65 1703-1706 Stereoselective Synthesis of (+)-11aH,13-Dihydroestafiatin,(+)-11¦ÂH,13-Dihydroludartin, (-)-Compressanolide, and (-)-11¦ÂH,13-Dihydromicheliolide from Santonin Victoria Bargues, Gonzalo Blay, Luz Cardona, Begoña Garc¨ªa, and Jos¨¦ R. Pedro Structure 13C NMR ̼Æ×Ä£Äâͼ |

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