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»¯ºÏÎï̼Æ×£º 13.71, 14.68, 19.70, 27.22, 30.85, 31.64, 35.18, 36.53, 36.92, 41.31, 43.10, 45.41, 48.07, 51.19, 52.34, 66.68, 69.33, 125.41, 145.12, 164.71, 170.61,198.94 [ Last edited by ׿Խ_ÏÈ·æ on 2015-5-13 at 13:14 ] |
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1 . 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . (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 Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . 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 Structure & 13C NMR ̼Æ×Ä£Äâͼ |
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