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̼Æ×¿â£º   Nat Syn


²éѯ½á¹û£º¹²²éµ½10¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼)
1 .     compound 17
    ÏàËÆ¶È:68.1%
Magnetic Resonance in Chemistry          1994          32          565-567
Carbon-13 NMR data for methylated steroids
E. Mesk¨®, Gy. Schneider, Gy. Dombi and D. Zeigan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     19-hydroxykovalic acid
C22H36O5     ÏàËÆ¶È:63.6%
Phytochemistry          1992          31          1703-1711
Clerodane and labdane derivatives from Olearia teretifolia
C. Zdero, F. Bohlmann, R.M. King
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     oblongolide L
C22H34O5     ÏàËÆ¶È:63.6%
European Journal of Organic Chemistry          2005          2005          4009-4016
New Oblongolides Isolated from the Endophytic Fungus Phomopsis sp. from Melilotus dentata from the Shores of the Baltic Sea
Jingqiu Dai, Karsten Krohn, Dietmar Gehle, Ines Kock, Ulrich Flörke, Hans-J¨¹rgen Aust, Siegfried Draeger, Barbara Schulz and Joachim Rheinheimer
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     5¦Á-androstan-3¦Â,5-diol-6,17-dione 3-acetate
    ÏàËÆ¶È:63.6%
Canadian Journal of Chemistry          1979          57          3069-3072
13C nuclear magnetic resonance spectra of some halosteroids, 6-ketosteroids, and related compounds
Herbert L. Holland, Everton M. Thomas
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     (Z)-dimethyl 7-oxocass-13(15)-ene-16,18-dioate
    ÏàËÆ¶È:63.6%
Magnetic Resonance in Chemistry          1990          28          529-532
13C nuclear magnetic resonance spectra of several podocarpane and cassane diterpenoids
A. Abad, C. Agull¨®, M. Arn¨®, L. R. Domingo and R. J. Zaragoz¨¢
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     19-Norandrost-4-ene-3,17-dione
C18H24O2     ÏàËÆ¶È:63.6%
Organic Magnetic Resonance          1977          9          439-464
13C n.m.r. spectra of steroids ¡ªa survey and commentary
J. W. Blunt and J. B. Stothers
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     2¦Â-(4-(Acetoxy-methyl)-1,2,3-triazol-1-yl)-3-hydroxy-5-androstan-17-one
C24H35N3O4     ÏàËÆ¶È:62.5%
Steroids          2012          77          738-744
Synthesis of ferrocene-labeled steroids via copper-catalyzed azide¨Calkyne cycloaddition. Reactivity difference between 2¦Â-, 6¦Â- and 16¦Â-azido-androstanes
Klaudia Feh¨¦r, J¨¢nos Balogh, Zsolt Cs¨®k, Tam¨¢s K¨¦gl, L¨¢szl¨® Koll¨¢r, Rita Skoda-Földes
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     cordobic acid 18-acetate methyl ester
    ÏàËÆ¶È:60.8%
Phytochemistry          1986          25          1389-1392
Labdane diterpenoids from Grindelia discoidea (asteraceae)
Barbara N. Timmermann, Joseph J. Hoffmann, Shivanand D. Jolad, Robert B. Bates, Teruna J. Siahaan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     3-Hydroxy-2¦Â-(4-methoxycarbonyl-1,2,3-triazol-1-yl)-5-androstan-17-one
C23H33N3O4     ÏàËÆ¶È:60.8%
Steroids          2012          77          738-744
Synthesis of ferrocene-labeled steroids via copper-catalyzed azide¨Calkyne cycloaddition. Reactivity difference between 2¦Â-, 6¦Â- and 16¦Â-azido-androstanes
Klaudia Feh¨¦r, J¨¢nos Balogh, Zsolt Cs¨®k, Tam¨¢s K¨¦gl, L¨¢szl¨® Koll¨¢r, Rita Skoda-Földes
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     Turranin C
C23H34O3     ÏàËÆ¶È:60.8%
Fitoterapia          2013          90          119-125
New steroids and sesquiterpene from Turraea pubescens
Chun-Mao Yuan, Gui-Hua Tang, Xiao-Ying Wang, Yu Zhang, Ming-Ming Cao, Xiao-Hui Li, Yan Li, Shun-Lin Li, Ying-Tong Di, Hong-Ping He, Xiao-Jiang Hao, Hui-Ming Hua
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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