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ºù«ÍÞÍÞÍÞ: ½ð±Ò+8, ¡ïÓаïÖú 2014-10-15 15:30:55
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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£º¹²²éµ½688¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . Rosenonolactone ÏàËÆ¶È:73.9% Molecules 2008 13 2474-2481 Norcyperone, a Novel Skeleton Norsesquiterpene from Cyperus rotundus L. Yan Xu, Hong-Wu Zhang, Chang-Yuan Yu, Yang Lu, Ying Chang and Zhong-Mei Zou Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 6¦Â-hydroxyrosenonolactone ÏàËÆ¶È:73.9% The Journal of Microbiology 2010 48 784-790 Endophytic Fungus Trichothecium roseum LZ93 Antagonizing Pathogenic Fungi In Vitro and Its Secondary Metabolites XiaoMei Zhang, GuoHong Li, Juan Ma, Ying Zeng, WeiGuang Ma, and PeiJi Zhao Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . Rosenonolactone ÏàËÆ¶È:69.5% Phytochemistry 1978 17 572-573 The 13C NMR spectra of some rosane diterpenoids Brian Dockerill, James R. Hanson, Michael Siverns Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . effusenone A C23H36O5 ÏàËÆ¶È:65.2% Helvetica Chimica Acta 2007 Vol. 90 1289 Diterpenoid and Phenolic Compounds from Juncus effusus L. Guang Zhong Yang, Hong Xia Li, Fa Jun Song, and Yu Chen Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . Compound 6a C24H38O6 ÏàËÆ¶È:65.2% Molecules 2012 17 1744-1750 The Incubation of 13¦Á,17-Dihydroxystemodane with Cephalosporium aphidicola Braulio M. Fraga, Ricardo Guillermo,Melchor G. Hern¨¢ndez ,Mar¨ªa C. Chamy and Juan A. Garbarino Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . Compound 6m ÏàËÆ¶È:65.2% Molecules 2012 17 1744-1750 The Incubation of 13¦Á,17-Dihydroxystemodane with Cephalosporium aphidicola Braulio M. Fraga, Ricardo Guillermo,Melchor G. Hern¨¢ndez ,Mar¨ªa C. Chamy and Juan A. Garbarino Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . lupeol C30H50O ÏàËÆ¶È:62.5% Chinese Traditional and Herbal Drugs 2012 43 1071-1074 Chemical constituents from twigs and leaves of Fordia cauliflora LIU Jin-lei; PAN Zheng-hong; SU Tao; YAN Xiao-jie; LI Dian-peng Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 4¦Â-hydroxyclerodan-15-oic acid C20H36O3 ÏàËÆ¶È:60.8% Helvetica Chimica Acta 2003 Vol. 86 3187 Dinorditerpene, Diterpenes, Alkaloids, and Coumarins from Clausena dunniana Hong-Ping He, Yue-Mao Shen, Guo-Ying Zuo, Xiao-Sheng Yang, and Xiao-Jiang Hao Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . 3,18-O-isopropylidenelagochilin ÏàËÆ¶È:60.8% Chemistry of Natural Compounds 1979 15 33-35 13C NMR SPECTRUM OF LA GOCHILIN AND ITS DERIVATIVES Z. I. Ma vlyankulova , U. N. Zainutdinov, S. I. Mukhamedkhanova , V. B. Leont'ev, and Kh. A. Aslanov Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . populifolic acid ÏàËÆ¶È:60.8% Phytochemistry 1992 31 3277-3279 Epi-populifolic acid from Aristolochia cymbifera Gilda G. Leit¨¤o, Maria Auxiliadora C. Kaplan, Corrado Galeffi Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . (5R,8R,9S,10R)-ent-3-cleroden-15-oic acid methyl ester C21H36O2 ÏàËÆ¶È:60.8% Phytochemistry 1992 31 3277-3279 Epi-populifolic acid from Aristolochia cymbifera Gilda G. Leit¨¤o, Maria Auxiliadora C. Kaplan, Corrado Galeffi Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . 3¦Â-hydroxyetio-17¦Â-dammaranic acid C23H38O3 ÏàËÆ¶È:60.8% Chinese Chemical Letters 2011 22 1461-1464 Two new dammarane-type sapogenins from Gynostemma pentaphyllum Xia Li,Jia Qing Cao,Lin Shi,Yu Qing Zhao Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . Merhyl 4¦Á-carbomethoxygrindelate C22H34O5 ÏàËÆ¶È:60.8% Phytochemistry 1980 19 2689-2693 Grindelane diterpenoids from Chrysothamnus nauseosus Allan F. Rose Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . compound 6 ÏàËÆ¶È:60.8% Phytochemistry 1981 20 167-169 Carbon-13 nmr spectra of some ent-rosane diterpenoids Maria C. Garc¨ªa-Alvarez, Benjam¨ªn Rodr¨ªguez, Serafin Valverde, Braulio M. Fragat, Antonio G. Gonzal¨¦z Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . compound 6 C26H42O7 ÏàËÆ¶È:60.8% Tetrahedron Letters 2002 43 4605-4608 Covilanone: a new rearranged labdane type diterpene J.M.L. Rodilla, M.I. Ismael, L.A. Silva, J.P. Ces¨¢rio Serrano, J.G. Urones, F. Sanz Structure 13C NMR ̼Æ×Ä£Äâͼ |

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