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13C NMR (126 MHz, cd3od) ¦Ä

13.05, 22.31, 23.49, 25.59, 29.01, 29.31, 31.62, 32.61, 47.09, 47.26, 47.43, 47.60, 47.77,47.94, 48.11,  62.44, 65.08, 69.68, 72.06, 72.35, 74.54, 78.23, 115.05, 136.84,
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--ľľ: ½ð±Ò+15, ¡ïÓаïÖú 2015-06-10 10:21:47
7¦Á-Hydroxyrubijervine
C27H43NO3     ÏàËÆ¶È:59.2%
Helvetica Chimica Acta          2008          91          819−824
Biotransformation of Vermitaline by Cunninghamella echinulata
Yi-Feng L, Ke-Yu Chen, Hui-Liang Li, Yue-Hu Pei, Run-Hui Liu, Wei-Dong Zhang
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




2 .     16¦Â-Hydroxycardiopetaline
C21H33NO4     ÏàËÆ¶È:58.3%
Phytochemistry          2005          66          837-846
Norditerpene and diterpene alkaloids from Aconitum variegatum
Jes¨²s G. D¨ªaz, Juan Garc¨ªa Ruiza, Werner Herz
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




3 .     16¦Â-acetoxycardiopetaline
C23H35NO5     ÏàËÆ¶È:58.3%
Natural Product Research          1994          5          147-151
A New Norditerpenoid Alkaloid From Seeds of Aconitum Napellus SSP. Vulgare
Hongmei Liu; Alfred Katz
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




4 .     Sapranthin C
C21H28O3     ÏàËÆ¶È:58.3%
Phytochemistry Letters          2012          5          29-32
Enyne- and enediyne-¦Ã-lactones from the bark of Meiogyne cylindrocarpa
Hadjira Bousserouel,Khalijah Awang,Françoise Gu¨¦ritte,Marc Litaudon
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




5 .     16¦Â-hydroxycardiopetaline
    ÏàËÆ¶È:58.3%
Chinese Journal of Organic Chemistry          2014          34          909-915
A New C19-Diterpenoid Alkaloid from Aconitum vilmorinianum
Tang, Tianxing Chen, Donglin Wang, Fengpeng
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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6 .     Methyl 3¦Á,6¦Á,7¦Á,12¦Á-trahydroxy-5¦Â-cholanoate
C25H42O6     ÏàËÆ¶È:56%
Steroids          1990          55          530-539
Potential bile acid metabolites. 16. Synthesis of stereoisomeric 3¦Á,6,7,12¦Á-tetrahydroxy-5¦Â-cholanoic acids
Takashi Iida, Ichiro Komatsubara, Sciichiro Yoda, Junichi Goto, Toshio Nambara, Frederic C. Chang
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




7 .     compound 13
    ÏàËÆ¶È:56%
Magnetic Resonance in Chemistry          1993          31          421-424
Carbon-13 NMR spectra of bile acid derivatives. Part III. Unsaturated 5¦Â-cholanoic acids
Takashi Iida, Junichi Goto and Toshio Nambara
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------




8 .     methyl 3¦Á,6¦Á,7¦Á,12¦Á-tetrahydroxy-5¦Â-cholanoate
    ÏàËÆ¶È:56%
Magnetic Resonance in Chemistry          1993          31          645-651
Complete 1H and 13C resonance assignments of stereoisomeric 3¦Á,6,7,12¦Á-tetrahydroxycholanoic acids by two-dimensional shift-correlated NMR
Takashi Iida, Frederic C. Chang, Kumiko Mushiake, Junichi Goto and Toshio Nambara
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2Â¥2015-06-10 08:42:58
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