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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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×Ä£Äâͼ
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