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΢Æ×ÇóÖú£¬Ð»Ð» ÒÑÓÐ1È˲ÎÓë
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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
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--ľľ: ½ð±Ò+15, ¡ïÓаïÖú 2015-06-10 10:21:47
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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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×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 ̼Æ×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 ̼Æ×Ä£Äâͼ |
2Â¥2015-06-10 08:42:58














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