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kengkengsee: ½ð±Ò+5, ¡ïÓаïÖú 2013-12-07 09:13:48
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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£º¹²²éµ½100¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . critonilide ÏàËÆ¶È:66.6% Phytochemistry 1994 37 1317-1321 Rearranged ent-eudesmane- and ent-eremophilane-type sesquiterpenoids from the liverwort Frullania dilatata Fumihiro Nagashima, Shigeru Takaoka, Siegfried Huneck, Yoshinori Asakawa Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . prespatane ÏàËÆ¶È:66.6% Journal of the Chemical Society, Perkin Transactions 1 2000 2703-2708 Biosynthesis of kelsoene and prespatane in cultured cells of the liverwort Ptychanthus striatus Kensuke Nabeta, Masateru Yamamoto, Kanako Fukushima and Kenji Katoh Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . prespatane C15H24 ÏàËÆ¶È:66.6% The Journal of Organic Chemistry 1997 62 3837-3840 New and Unusual Sesquiterpenes: Kelsoene, Prespatane, Epi-¦Ã-gurjunene, and T-Cadinthiol, from the Tropical Marine Sponge Cymbastela hooperi Gabriele M. König and Anthony D. Wright Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 4¦Â-hydroxy-3-oxo-1,2,5¦Á,6¦Â,11¦Â-H-eudesman-6,12-olide C15H22O4 ÏàËÆ¶È:60% Natural Product Research 2008 22 499-506 Biotransformation of tetrahydro-¦Á-santonins by Absidia coerulea Lin Yang; Jungui Dai Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 1¦Â,3¦Â-dihydroxy-4¦Â,5¦Á,11-H-eudesman-6¦Á,12-olide C15H24O4 ÏàËÆ¶È:60% Journal of Natural Products 1995 Vol 58 1498-1507 Microbial Transformations of 6¦Á- and 6 ¦Â-Eudesmanolides by Rhizopus nigricans Cultures Yolanda Garc¨ªa, Andr¨¦s Garc¨ªa-Granados, Antonio Mart¨ªnez, Andr¨¦s Parra, Francisco Rivas, Jos¨¦ Mar¨ªa Arias Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 5¦Á-Hydroxycostic acid ÏàËÆ¶È:60% Chemistry of Natural Compounds 2011 Vol. 47, No. 2 309-310 SESQUITERPENOIDS FROM Aster himalaicus Wei-Dong Xie,Cheng-Wu Weng,Tong Shen, and Xue Gao Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 5¦Á-Hydroxy-4¦Á,15-dihydrocostic acid ÏàËÆ¶È:60% Chemistry of Natural Compounds 2011 Vol. 47, No. 2 309-310 SESQUITERPENOIDS FROM Aster himalaicus Wei-Dong Xie,Cheng-Wu Weng,Tong Shen, and Xue Gao Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . racemosalactone E C15H22O3 ÏàËÆ¶È:60% Journal of Natural Products 2013 76 564-570 Structural Investigation and Biological Activity of Sesquiterpene Lactones from the Traditional Chinese Herb Inula racemosa Yan-Yan Ma, Deng-Gao Zhao, and Kun Gao Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . sibiriolide D C15H22O3 ÏàËÆ¶È:60% Phytochemistry Letters 2012 5 685-689 Sesquiterpene lactones from the aerial parts of Xanthium sibiricum and their cytotoxic effects on human cancer cell lines Van-Binh Bui, Shu-Ting Liu, Jing-Jing Zhu, Juan Xiong, Yun Zhao, Guo-Xun Yang, Gang Xia, Jin-Feng Hu Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . (+)-13-carbaartemisinin C16H24O4 ÏàËÆ¶È:56.2% Journal of Medicinal Chemistry 1996 39 1885-1897 Structure−Activity Relationships of the Antimalarial Agent Artemisinin. 3. Total Synthesis of (+)-13-Carbaartemisinin and Related Tetra- and Tricyclic Structures Mitchell A. Avery, Pingchen Fan, Jean M. Karle, Jason D. Bonk, Robert Miller, and D. Keith Goins Structure 13C NMR ̼Æ×Ä£Äâͼ |

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