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1 .     6¦Á-hydroxyambreinolide
C17H28O3     ÏàËÆ¶È:64.7%
Journal of Natural Products          1996          59          113-116
Norditerpenes and Norsesterterpenes from Salvia yosgadensis
G¨¹lac¨¹ti Topç, and Ayhan Ulubelen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     compound 8
     ÏàËÆ¶È:62.5%
Planta Medica          1999          65          153-156
Sesquiterpene Lactone Glycosides from Arnica longifolia
Claus M.Passreiter,Massimo De Carlo,and A.Steigel
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     atractylenolid III
C15H20O3     ÏàËÆ¶È:62.5%
Planta Medica          1989          55          59-61
Constituents of Atractylis koreana
Peter Pachaly , AstridLansing, and Kwan Seog Sin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     9¦Á-hydroxy-calarene
C15H24O     ÏàËÆ¶È:62.5%
Phytochemistry          1992          31          3749-3755
Microbial oxidation of tricyclic sesquiterpenoids containing a dimethylcyclopropane ring
Wolf-Rainer Abraham, Klaus Kieslich, Burkhard Stumpf, Ludger Ernst
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     5¦Á-hydroxy-4¦Á,15-dihydrocositic acid methyl ester
C16H26O3     ÏàËÆ¶È:62.5%
Phytochemistry          1990          29          3201-3206
Eudesmane derivatives other constituents from Apalochlamys spectabilis Cassinia species
C. Zdero,F. Bohlmann,R.M. King
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     2¦Á-methyldiplopterol
     ÏàËÆ¶È:62.5%
Magnetic Resonance in Chemistry          2010          48          951-954
NMR spectral assignment of 2- and 3¦Â-methylhopanes and evidence for boat conformation in D ring of 17(H), 21(H)-hopanes (pages 951¨C954)
Geir Kildahl-Andersen, Hans Peter Nytoft and Jon Eigill Johansen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     ²ÔÊõÄÚõ¥ III
C15H21O3     ÏàËÆ¶È:62.5%
Chinese Traditional and Herbal Drugs          2008          39          1149-1151
µØïþµÄ»¯Ñ§³É·ÖÑо¿
ÌÆÂõ;Áα¦Õä;ÁÖËç;µË˼ɺ
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     atractylenolid III
C15H20O3     ÏàËÆ¶È:62.5%
Chinese Journal of Natural Medicines          2008          6          404-407
A New Sesquiterpenoid from the Roots of Chloranthus fortunei
WANG Xia-Chang; WU Wei-Qun; MA Shi-Ping; LIU Jing-Han; HU Li-Hong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     (3a¦Â,4a¦Á,8a¦Â,9a¦Â)-3a,4,4a,5,6,7,8,8a,9,9a-Decahydro-8a-methyl-5-methylenenaphtho[2,3-b]furan-2(3H)-one
C14H20O2     ÏàËÆ¶È:62.5%
Journal of the Chemical Society, Perkin Transactions 1          1993                   239-247
Total synthesis of three eudesman-12,8-olides, (¡À)-isoalantolactone, (¡À)-dihydrocallitrisin and (¡À)-septuplinolide; structure revision of septuplinolide
Masahiro Tada, Hirokazu Yamada, Akira Kanamori and Kazuhiro Chiba
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     (-)-juneol
     ÏàËÆ¶È:62.5%
Journal of Oleo Science          2004          53          343-348
Eudesmane-Type Sesquiterpenoids in the Volatile Oil from Bursera graveolens
Chiyoki YUKAWA, Hisakatsu IWABUCHI, Sadao KOMEMUSHI, Akiyoshi SAWABE
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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11 .     1¦Â-Hydroxy-6,7¦Á-dihydroxyeudesm-4(15)-ene
C15H26O3     ÏàËÆ¶È:62.5%
Journal of Natural Products          2011          74          937-942
Estrogenic Activity of Chemical Constituents from Tephrosia candida
Mohamed-Elamir F. Hegazy, Abou El-Hamd H. Mohamed, Ali M. El-Halawany, Pierre C. Djemgou, Abdelaaty A. Shahat, and Paul W. Par¨¦
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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12 .     1,10¦Â-Epoxy-3,4¦Á-dichloromethano-13-trichloromethyl-5,7¦Á(H),6,11¦Â(H)-guai-12,6-olide
C17H19Cl5O3     ÏàËÆ¶È:58.8%
Chemistry of Natural Compounds          2007          43          548-551
PREPARATION AND STRUCTURE ELUCIDATION OF TWO MINOR PRODUCTS FROM REACTION OF ARGLABIN WITH CHLOROFORM IN THE PRESENCE OF A CROWN ETHER
R. I. Jalmakhanbetova, G. A. Atazhanova, V. A. Raldugin,I. Yu. Bagryanskaya, Yu. V. Gatilov, M. M. Shakirov,and S. M. Adekenov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     methyl-13-epi-manoyloxide-18-oate
C20H30O3     ÏàËÆ¶È:57.1%
Phytochemistry          1991          30          211-213
Diterpenes from Leyssera gnaphaloides
F. Tsichritzis, J. Jakupovic
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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14 .     5¦Á,6¦Á,7¦Á,8¦Á-diepoxy-eudesmane
     ÏàËÆ¶È:56.2%
Phytochemistry          2002          60          333-338
Terpenoids from Guarea guidonia
João Henrique G. Lago, Cl¨¢udia B. Brochini, N¨ªdia F. Roque
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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15 .     compound 6a
C16H26O2     ÏàËÆ¶È:56.2%
Journal of Natural Products          2003          66          1623-1627
Facile Access to Optically Active Labdane-Type Diterpenes from (+)-Manool. Synthesis of (+)-Coronarin E, (+)-15,16-Epoxy-8(17),13(16),14-labdatriene, and (+)-Labda-8(17),13(Z)-diene-15,16-diol
Jos¨¦ Villamizar, Juan Fuentes, Franklin Salazar, Eleonora Tropper, and Randolph Alonso
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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16 .     compound 7
C16H28O     ÏàËÆ¶È:56.2%
Journal of Natural Products          2003          66          1623-1627
Facile Access to Optically Active Labdane-Type Diterpenes from (+)-Manool. Synthesis of (+)-Coronarin E, (+)-15,16-Epoxy-8(17),13(16),14-labdatriene, and (+)-Labda-8(17),13(Z)-diene-15,16-diol
Jos¨¦ Villamizar, Juan Fuentes, Franklin Salazar, Eleonora Tropper, and Randolph Alonso
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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17 .     (11S)-4¦Â,6¦Â,11,12-tetrahydroxyeudesman-1-one
C15H26O5     ÏàËÆ¶È:56.2%
Journal of Natural Products          2002          65          1011-1015
Chemical-Microbiological Synthesis of Cryptomeridiol Derivatives by Gliocladium roseum: Semisynthesis of 11-Hydroxyeudesmanolides
Andr¨¦s Garc¨ªa-Granados, Mar¨ªa C. Guti¨¦rrez, Andr¨¦s Parra, and Francisco Rivas
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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18 .     compound 7
C17H32O6S2     ÏàËÆ¶È:56.2%
Journal of Natural Products          2001          64          348-349
Synthesis of (+)-Cyclozonarone and the Absolute Configuration of Naturally Occurring (-)-Cyclozonarone
Manuel Cort¨¦s, Jaime A. Valderrama, Mauricio Cuellar, Ver¨®nica Armstrong, and Marcelo Preite
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2Â¥2013-11-02 13:49:30
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