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1 .     Jatrophalactone
C20H26O5     ÏàËÆ¶È:90%
Tetrahedron          2012          68          972-976
Three new diterpenes from Jatropha curcas
Jie-Qing Liu, Yuan-Feng Yang, Cui-Fang Wang, Yan Li, Ming-Hua Qiu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     8,12-dienabieta-11,14-dione-19-acid
    ÏàËÆ¶È:65%
Chinese Traditional and Herbal Drugs          2006          37          1473-1474
µÆÓÍÌٵĻ¯Ñ§³É·ÖÑо¿
³ÑÇËÕ;ÑîÊÀÁÖ;ÐìÀöÕä;³ÂºÏ±ö
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     9-acetoxy-10-hydroxyaromadendrane
C17H28O3     ÏàËÆ¶È:61.1%
Phytochemistry          2003                   1335-1340
Secondary metabolites from the liverwort Tylimanthus renifolius
Hildegard Feld, Josef Zapp, Hans Becker
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     (+)-2-{(1S)-1-[(1R)-3,3-Dimethylcyclohexyl]ethoxy}-2-oxoethyl (3,3,3-2H3)Propanoate
    ÏàËÆ¶È:61.1%
Helvetica Chimica Acta          2009          92          1782-1799
Synthesis of Deuterium-Labeled Perfume Ingredients as Internal Standards for Their GC/MS Quantification
Christian Chapuis, Carole Cantatore, Peter Fankhauser, Ren¨¦ Challand, Jean-Jacques Riedhauser
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     3¦Â-acetoxycostic acid methyl ester
    ÏàËÆ¶È:61.1%
Natural Product Research          1997          11          1-4
Eudesmane Derivatives from Flourensia thurifera: Structure and Biological Activity
Francesca Faini; Cecilia Labbe; Rene Torres; Giuliano Delle Monache; Franco Delle Monache; Jose Coll
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     pernetyl malonate
C18H28O5     ÏàËÆ¶È:61.1%
Phytochemistry          1994          35          425-433
The sesquiterpenes of Fabiana imbricata
Geoffrey D. Brown
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     5-Acetoxy-aromadendrane-4¦Â,10¦Á-diol
    ÏàËÆ¶È:61.1%
Journal of the Brazilian Chemical Society          2003          14          828-813
Antifungal Aromadendrane Sesquiterpenoids from the Leaves of Xylopia brasiliensis
Isabel C. Moreira, João Henrique G. Lago, Maria Cl¨¢udia M. Young and N¨ªdia F. Roque
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     4¦Â-hydroxyclerodan-15-oic acid
C20H36O3     ÏàËÆ¶È:60%
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 .     (1S,4aR,5S,6R,8aR)-5-(5-hydroxy-3-methylpentyl)-1,5,6,8a-tetramethyl-decahydronaphthalen-1-ol
    ÏàËÆ¶È:60%
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
10 .     3,4-epoxyclerodan-13E-en-15-oic acid
C20H32O3     ÏàËÆ¶È:60%
Journal of Natural Products          2006          69          768-773
Bioactive Diterpenes from the Fruits of Detarium microcarpum
Anne-Laure Cavin, Anne-Emmanuelle Hay, Andrew Marston, Helen Stoeckli-Evans, Rosario Scopelliti, Drissa Diallo, and Kurt Hostettmann
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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