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ÕÒÕÒÎÒľ³æ (³õÈëÎÄ̳)
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[ÇóÖú]
69 ÒÑÓÐ1È˲ÎÓë
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| 13C NMR (100 MHz, CDCl3) ¦Ä12.3, 20.1, 20.4, 20.5, 21.022.4, 29.8, 34.0, 38.8, 42.8, 43.7, 45.4, 51.2, 62.1, 64.3, 64.4, 64.7, 69.2, 69.7, 70.6, 71.8, 73.0, 75.9, 76.7, 77.0, 77.2, 77.4, 94.7,95.9, 101.9, 112.4, 113.5, 119.4, 123.5,123.7, 145.6, 149.0, 151.8, 167.0, 168.3, 169.1, 170.0, 170.6,170.6 |
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ÕÒÕÒÎÒ: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2015-06-04 18:33:37
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ÕÒÕÒÎÒ: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2015-06-04 18:33:37
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1 . Incaside C32H38O17 ÏàËÆ¶È:63.6% Chemical & Pharmaceutical Bulletin 2009 57 765-796 Naturally Occurring Iridoids, Secoiridoids and Their Bioactivity. An Updated Review, Part 3 Biswanath DINDA,* Debashis ROY CHOWDHURY, and Bikas Chandra MOHANTA Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . (E)-Heptacetyl-10-(3,4-dihydroxycinnamoyloxy)loganoside ÏàËÆ¶È:61.3% Journal of Natural Products 1991 Vol 54 532 Plantes de Nouvelle-Caledonie, 137. Iridoïdes de Coelospermum billardieri Rabah Benkrief, Alexios-Leandros Skaltsounis, François Tillequin, Michel Koch, Jacques Preset Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2015-06-04 18:24:37
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3Â¥2015-06-04 18:33:32













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