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1 .     isocalamendiol
C15H26O2     ÏàËÆ¶È:73.3%
Phytochemistry          1996          43          1175-1182
Sesquiterpenoids from Acorus calamus as germination inhibitors
Kazue Nawamaki, Masanori Kuroyanagi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     Isolongifolene Epoxide
    ÏàËÆ¶È:66.6%
Journal of Agricultural and Food Chemistry          1994          42          138-142
Structure elucidation of oxidation-reduction products of isolongifolene
Isabelle Bombarda, Jacqueline Smadja, Emile M. Gaydou, Jacques Yves Conan, Robert Faure
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     gajutsulactone A
C15H22O2     ÏàËÆ¶È:60%
Chemical & Pharmaceutical Bulletin          2001          49(12)          1558-1566
Medicinal Foodstuffs. XXVIII.1) Inhibitors of Nitric Oxide Production and New Sesquiterpenes, Zedoarofuran, 4-Epicurcumenol,Neocurcumenol, Gajutsulactones A and B, and Zedoarolides A and B, from Zedoariae Rhizoma
Hisashi MATSUDA, Toshio MORIKAWA, Iwao TOGUCHIDA, Kiyofumi NINOMIYA, and Masayuki YOSHIKAWA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     eudesma-11-en-2¦Á,4¦Á-diol
    ÏàËÆ¶È:60%
Phytochemistry          2003          63          835-839
Eudesmane and megastigmane glucosides from Laggera alata
Qunxiong Zheng, Zhaojun Xu, Xianfeng Sun, Wei Yao, Handong Sun,Christopher H. K. Cheng, Yu Zhao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     canusesnol D
C15H26O3     ÏàËÆ¶È:60%
Journal of Natural Products          2004          67          1893-1896
New Sesquiterpenes from Capsicum annuum
Yousuke Kawaguchi, Toshimasa Ochi, Yoshihisa Takaishi, Kazuyoshi Kawazoe, and Kuo-Hsiung Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     Eudesm-11-en-2,4¦Ádiol
C15H24O     ÏàËÆ¶È:60%
Phytochemistry          1993          34          567-568
Eudesm-11-en-2,4¦Á-diol from Nardostachys Chinensis
Koichi Masuyama, Hiroshi Morita, Koichi Takeya, Hideji Itokawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     (1S,2S,3S,4R,6S,7R,8R,11R)-3-hydroxymethyl-3,7,11-tri-methyltricyclo[6.3.0.0(2,4)]undecan-6,7-diol(6,14-exo-dihydroxyglobulol)
C15H24O2     ÏàËÆ¶È:60%
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
8 .     (-)-eudesma-4(15)-en-2¦Â,11-diol
    ÏàËÆ¶È:60%
Pharmazie          2002          57          59-61
Microbiological conversion of a - and -eudesmol mixture by Rhizopus
G.T. Maatooq - J.J. Hoffmann
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     gajutsulactone A
15H22O2     ÏàËÆ¶È:60%
Heterocycles          2001          55          841-846
Inhibitors of Nitric Oxide Production and New Sesquiterpenes, 4-epi-Curcumenol, Neocurcumenol, Gajutsulactones A and B, and Zedoarolides A and B from Zedoariae Rhizoma
Hisashi Matsuda, Toshio Morikawa, Iwao Toguchida, Kiyofumi Ninomiya, and Masayuki Yoshikawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     15-nor-amorph-11-en-4¦Â-ol
C14H24O     ÏàËÆ¶È:60%
Tetrahedron          1999          55          15099-15108
Synthesis of amorphane and cadinane sesquiterpenes from fabiana imbricata
Koon-Sin Ngo, Geoffrey D. Brown
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     amorph-11-en-4¦Â-ol
C15H26O     ÏàËÆ¶È:60%
Tetrahedron          1999          55          15099-15108
Synthesis of amorphane and cadinane sesquiterpenes from fabiana imbricata
Koon-Sin Ngo, Geoffrey D. Brown
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     6¦Â,7¦Á,14-trihydroxyaromadendrane
    ÏàËÆ¶È:60%
Journal of Chemical Research          1997          21          28-29
Hydroxylation of Aromadendrane Derivatives by Mucor plumbeus†
Ricardo Guillermo, James R. Hanson and Almaz Truneh
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     5(11)-epoxycadinane-4¦Â,5¦Â,10¦Â,11-tetraol
C15H26O3     ÏàËÆ¶È:60%
Planta Medica          2012          78          1010-1014
Sesquiterpenoids from the Rhizomes of Homalomena occulta
Xie, Xiao-Yu; Wang, Rui; Shi, Yan-Ping:
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     compound 5b
    ÏàËÆ¶È:60%
Indian Journal of Chemistry Section B          1995          34B          992-993
13C NMR assignments of ¦Á- and ¦Â-dihydroartemisinin
Ashish Kumar Pathak, Dharam C Jain & Ram P Sharma
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     lupanine
    ÏàËÆ¶È:60%
Magnetic Resonance in Chemistry          1998          36          779-796
13C NMR spectroscopy of tri- and tetracyclic quinolizidine alkaloids. Compilation and discussion
B. Mikhova and H. Duddeck
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     serratidine
    ÏàËÆ¶È:56.2%
Chemical & Pharmaceutical Bulletin          2003          51(10)          1163-1169
Ten New Lycopodium Alkaloids Having the Lycopodane Skeleton Isolated from Lycopodium serratum THUNB.
Hiromitsu TAKAYAMA,Kazuaki KATAKAWA,Mariko KITAJIMA, Kentaro YAMAGUCHI,and Norio AIMI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     serratidine
    ÏàËÆ¶È:56.2%
Natural Product Research          2002          16          149-153
Three New Hydroxylated Serratidine Alkaloids from Huperzia Serrata
Chang-Heng Tan; Xiao-Qiang; Shan-Hao Jiang; Da-Yuan Zhu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     1-dimethoxymethyl-7,7-dimethyl-2-phenylbicyclo[2.2.1]heptan-2-ol
    ÏàËÆ¶È:56.2%
Russian Journal of Organic Chemistry          2003          39          1240-1243
New 2,10-Functionalized Camphor Derivatives
N. S. Vostrikov, A. V. Abutkov, V. Z. Vasikov and M. S. Miftakhov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     omaholidenol
C20H30O3     ÏàËÆ¶È:56.2%
European Journal of Organic Chemistry          2012                   5208-5216
Diterpenoids from Marine Ciliates: Chemical Polymorphism of Euplotes rariseta
Graziano Guella, Emanuela Callone, Ines Mancini, Fernando Dini and Graziano Di Giuseppe
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     1-(trans-4-hydroxycyclohexyl)-1-phenyl-3-(1-piperidinyl)-1-propanol
    ÏàËÆ¶È:56.2%
Bulletin des Soci¨¦t¨¦s Chimiques Belges          1983          92          995-998
Carbon-13 Chemical Shifts of Three Oxo-, Six Monohydroxy-, and Four Dihydroxycyclohexyl Derivatives of Trihexyphenidyl
G. Paeme, R. Grim¨¦e and A. Vercruysse
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     ent-3¦Â,6¦Â,12¦Á-trihydroxy-13-epi-manoyl oxide
    ÏàËÆ¶È:55%
Phytochemistry          1994          37          741-747
Chemical-microbiological synthesis of ent-13-epi-manoyl oxides with biological activities
Andr¨¦s Garc¨ªa-Granados, M Belinda Jim¨¦nez, Antonio Mart¨ªnez, Andr¨¦s Parra, Francisco Rivas, Jos¨¦ Mar¨ªa Arias
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     varodiol (ent-3¦Â,12¦Á-dihydroxy-13-epi-manoyl oxide )
C19H31O3     ÏàËÆ¶È:55%
Phytochemistry          1989          28          1851-1854
The microbiological transformation of some ent-13-epi-manoyl oxide diterpenes by Gibberella fujikuroi
Braulio M. Fraga,pedro Gonz¨¢lez,Ricardo Guillermo,Melchor G. Hern¨¢ndez,Juana Rovirosa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     varodiol
    ÏàËÆ¶È:55%
Phytochemistry          1985          24          1789-1792
Diterpenoids from Sideritis varoi subspecies cuatrecasasii: 13C NMR of ent-13-epi-manoyl oxides functionalized at C-12
A. Garc¨ªa-Granados, A. Mart¨ªnez, A. Molina, M.E. Onorato, M. Rico, A.Saenz de Buruaga, J.M.Saenz de Buruaga
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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