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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£º¹²²éµ½667¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . Rosenonolactone ÏàËÆ¶È:70.8% 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:70.8% 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:66.6% 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 . 17-(N,N-pentan-1,5-diylcarboxamido)-androst-5,16-diene-3-ethylene ketal C27H39O3N ÏàËÆ¶È:65.3% Steroids 2011 76 280-290 Systematic investigation on the synthesis of androstane-based 3-, 11-and 17-carboxamides via palladium-catalyzed aminocarbonylation P¨¦ter ¨¢cs, Attila Tak¨¢cs, Merc¨¦desz Kiss, No¨¦mi P¨¢link¨¢s, S¨¢ndor Mah¨®, L¨¢szl¨® Koll¨¢r Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 17¦Á-(6'-Hydroxyhex-1'-ynyl)-3,3'-ethylenedioxy-5¦Á-androstan-17¦Â-ol ÏàËÆ¶È:62.9% Steroids 1992 57 122-134 Synthesis and characterization by 1H and 13C nuclear magnetic resonance spectroscopy of 17¦Á-hexanoic derivatives of 5¦Á-dihydrotestosterone and testosterone Elisabeth Mappus, M¨¦lanie Renaud, Marc Rolland de Ravel, Catherine Grenot, Claude Y. Cuilleron Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 17-(N,N-3-oxapentan-1,5-diyl-carboxamido)-androst-5,16-diene-3-ethylene ketal C26H37O4N ÏàËÆ¶È:62.5% Steroids 2011 76 280-290 Systematic investigation on the synthesis of androstane-based 3-, 11-and 17-carboxamides via palladium-catalyzed aminocarbonylation P¨¦ter ¨¢cs, Attila Tak¨¢cs, Merc¨¦desz Kiss, No¨¦mi P¨¢link¨¢s, S¨¢ndor Mah¨®, L¨¢szl¨® Koll¨¢r Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . Compound 6a C24H38O6 ÏàËÆ¶È:62.5% 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 8 . Compound 6m ÏàËÆ¶È:62.5% 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 9 . 1 7¦Á-(Acetamidomethyl)-3,3'-(ethylenedioxy)-5¦Á-androstan-17¦Â-ol C24H39O4N ÏàËÆ¶È:62.5% Steroids 1997 62 603-620 Synthesis and characterization by 1H and 13C nuclear magnetic resonance spectroscopy of 17¦Á-cyano, 17¦Á-aminomethyl, and 17¦Á-alkylamidomethyl derivatives of 5¦Á-dihydrotestosterone and testosterone Elisabeth Mappus, Christophe Chambon, Marc Rolland de Ravel, Catherine Grenot, Claude Y. Cuilleron Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 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 11 . compound 18 ÏàËÆ¶È:60% Organic Magnetic Resonance 1983 21 305-309 Carbon-13 NMR spectra of hydroxylated bile acid stereoisomers Takashi Iida, Toshitake Tamura, Taro Matsumoto and Frederic C. Chang Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . compound 12b C28H48O4Si ÏàËÆ¶È:60% Journal of Natural Products 2012 75 1944-1950 Regio- and Diastereoselective Synthesis and X-ray Structure Determination of (+)-2-Deoxyoryzalexin S from (+)-Podocarpic Acid. Structural Nonidentity with Its Nominal Natural Isolated Enantiomer Francesca Leonelli, Valentina Latini, Andrea Trombetta, Gabriele Bartoli, Francesca Ceccacci, Angela La Bella, Alessio Sferrazza, Doriano Lamba, Luisa M. Migneco, and Rinaldo Marini Bettolo Structure 13C NMR ̼Æ×Ä£Äâͼ |

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