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1 .     17¦Â-cyano-17¦Á-hydroxyandrosta-4,9(11)-dien-3-one
    ÏàËÆ¶È:60%
Steroids          1990          55          109-113
The chemistry of 9¦Á-hydroxysteroids. 3. Methods for selective formation and dehydrations of 17¦Â-cyano-9¦Á,17¦Á-dihydroxyandrost-4-en-3-one
Jacobus N. M. Batist, Nicolaas C. M. E. Barendse, Arthur F. Marx
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     oleanic acid
    ÏàËÆ¶È:56%
Chinese Traditional and Herbal Drugs          2012          43          1285-1288
Study on chemical constituents from Potentilla supina
ZHENG Guang-hai; PIAO Hui-shun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     ent-13,17-dihydroxy-kauran-15-en-19-oic acid
C20H30O4     ÏàËÆ¶È:55%
Journal of Guangdong Phamaceutical University          2007          23          489-491
Identification of the chemical constituents of Rubus suavissimus S.Lee
LU Hua-chong, WANG Jian-xia
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     compound 3
    ÏàËÆ¶È:54.5%
Steroids          1989          54          1-10
Carbon-13 nuclear magnetic resonance spectra of D-homoannulated 17-hydroxypregnan-20-ones
Richard W. Draper, Mohindar S. Puar
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     11¦Â,17¦Á-Dihydroxy-17¦Â-hydroxymethyl-Dhomoandrosta-4-ene-3,17a-dione
C21H30O5     ÏàËÆ¶È:52.3%
Steroids          2006          71          1091-1096
D-homoannulation of 17¦Á,21-dihydroxy-20-keto steroids (corticosteroids)
Angelo Liguori, Francesca Perri, Carlo Siciliano
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     Pregn-17(20)-ene-3¦Â,21-diol
C21H34O2     ÏàËÆ¶È:52.3%
Steroids          2011          76          497-501
A convenient synthesis of the side chain of loteprednol etabonate-An ocular soft corticosteroid from 20-oxopregnanes using metal-mediated halogenation as a key reaction
Pritish Chowdhury∗, Juri Moni Borah, Papori Goswami, Archana Moni Das
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     haterumaimide F
C20H30ClNO4     ÏàËÆ¶È:50%
Journal of Natural Products          2001          64          1169-1173
Haterumaimides F-I, Four New Cytotoxic Diterpene Alkaloids from an Ascidian Lissoclinum Species
M. Jasim Uddin, Susumu Kokubo, Katsuhiro Ueda, Kiyotake Suenaga, and Daisuke Uemura
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     haterumaimide G
C20H28ClNO4     ÏàËÆ¶È:50%
Journal of Natural Products          2001          64          1169-1173
Haterumaimides F-I, Four New Cytotoxic Diterpene Alkaloids from an Ascidian Lissoclinum Species
M. Jasim Uddin, Susumu Kokubo, Katsuhiro Ueda, Kiyotake Suenaga, and Daisuke Uemura
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     compound 2
    ÏàËÆ¶È:50%
Steroids          1989          54          1-10
Carbon-13 nuclear magnetic resonance spectra of D-homoannulated 17-hydroxypregnan-20-ones
Richard W. Draper, Mohindar S. Puar
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     compound 2C
    ÏàËÆ¶È:50%
Steroids          1989          54          1-10
Carbon-13 nuclear magnetic resonance spectra of D-homoannulated 17-hydroxypregnan-20-ones
Richard W. Draper, Mohindar S. Puar
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     compound 4A
    ÏàËÆ¶È:50%
Steroids          1989          54          1-10
Carbon-13 nuclear magnetic resonance spectra of D-homoannulated 17-hydroxypregnan-20-ones
Richard W. Draper, Mohindar S. Puar
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     nodosin
    ÏàËÆ¶È:50%
Modern Chinese Medicine          2007          9(8)          10-11
Studies on the chemical Con stitun ts from Isodon Se rra (Maxim.) Kudo
Liu Jinxiu, Gao Huimin, Wang Zhimin, Wang Weihao, Fu Xuetao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     haterumaimide E
C20H30NO4Cl2     ÏàËÆ¶È:50%
Heterocycles          2001          54          1039-1047
Haterumaimides A-E, Five New Dichlorolissoclimide-Type Diterpenoids from an Ascidian, Lissoclinum Sp.
Md. Jasim Uddin, Susumu Kokubo, Kiyotake Suenaga, Katsuhiro Ueda, and Daisuke Uemura
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     nodosin
C20H26O6     ÏàËÆ¶È:50%
Food Chemistry          2012          131          1009-1014
Isolation and identification of ent-kaurane-type diterpenoids from Rabdosia serra (MAXIM.) HARA leaf and their inhibitory activities against HepG-2, MCF-7, and HL-60 cell lines
Lianzhu Lin, Qing Gao, Chun Cui, Haifeng Zhao, Liwu Fu, Liming Chen, Bao Yang, Wei Luo, Mouming Zhao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     3¦Á,5-cyclo-5¦Á-androstan-1¦Â,7¦Â,17¦Â-triol
C19H30O3     ÏàËÆ¶È:50%
Canadian Journal of Chemistry          1990          68          696-700
Enzymic hydroxylation and sulfoxidation of cyclopropyl compounds by fungal biotransformation
Herbert L. Holland, Michael J. Chernishenko, Morgan Conn, Anthony Munoz, T. Samuel Manoharan, Michael A. Zawadski
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     (+)-2-[(1S,2R,4aS,8aS)-decahydro-2,5,5,8a-tetramethylnaphthalen-1-yl]-2-hydroxyacetonitrile(major isomer)
    ÏàËÆ¶È:50%
Helvetica Chimica Acta          2014          97          197-214
Enantioselective Access to (−-Ambrox® Starting from ¦Â-Farnesene
Christian Chapuis
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     haterumaimide Q
C22H31NO4     ÏàËÆ¶È:50%
Bioorganic & Medicinal Chemistry          2006          14          6954-6961
Cytotoxic labdane alkaloids from an ascidian Lissoclinum sp.: Isolation, structure elucidation, and structure¨Cactivity relationship
Jasim Uddin, Katsuhiro Ueda, Eric R.O. Siwu, Masaki Kita, Daisuke Uemura
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     compound 5
    ÏàËÆ¶È:50%
The Journal of Organic Chemistry          1979          44          2999-3003
Tetracyclic analogs of the rosane lactones from Eupatorium album
Werner Herz, Serengolam V. Govindan, John F. Blount
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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