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| 13C NMR (101 MHz, MeOD) ¦Ä £º12.7,18.1,25.4,26.8,27.4,34.0,38.2,58.6,68.9,72.9,77.9,78.0,105.7,117.4,128.2,128.6,129.8,131.0,132.6,136.5,145.7,153.5,166.6,167.8 |
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M201175065: ½ð±Ò+8, ¡ï¡ï¡ïºÜÓаïÖú 2014-11-24 15:43:22
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M201175065: ½ð±Ò+8, ¡ï¡ï¡ïºÜÓаïÖú 2014-11-24 15:43:22
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1 . oxepinamide G C22H23N3O4 ÏàËÆ¶È:66.6% European Journal of Organic Chemistry 2011 802-807 Oxepinamides: Novel Liver X Receptor Agonists from Aspergillus puniceus Xin-Hua Lu, Qing-Wen Shi, Zhi-Hui Zheng, Ai-Bing Ke, Hua Zhang, Chang-Hong Huo, Ying Ma, Xiao Ren, Ye-Ying Li, Jie Lin, Qin Jiang, Yu-Cheng Gu and Hiromasa Kiyota Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . compound 2b ÏàËÆ¶È:60% Tetrahedron Letters 2003 44 2199-2202 A short and highly stereoselective synthesis of ¦Á-(2-aminothiazolyl)-C-nucleosides Jean-Michel Navarre, Dominique Guianvarc'h, Audrey Farese-Di Giorgio, Roger Condom, Rachid Benhida Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . (3aS*,4S*,5R*,6S*,7R*,7aS*)-6-{[(tert-butyldiphenylsilyl)oxy]methyl}-2,2,2',2'-tetramethyl-7-nitrotetrahydro-3aH-spiro[1,3-benzodioxole-4,4-[1,3]dioxolan]-5-ol 30H41NO8Si ÏàËÆ¶È:58.3% European Journal of Organic Chemistry 2010 6741-6747 A Cascade Annulation Based Convergent Approach to Racemic Tetrodotoxin Fernando Cagide-Fag¨ªn and Ricardo Alonso Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . (R)-2-((4S,5R)-5-(5-(benzyloxy)pentyl)-2,2-dimethyl-1,3-dioxolan-4-yl)-2-(methylsulfonyloxy)ethyl benzoate C27H36O8S ÏàËÆ¶È:58.3% Tetrahedron 2013 69 1881-1896 Metal-mediated alkynediol cycloisomerization: first and second generation formal total syntheses of didemniserinolipid B Shyamsundar Das, Boddeti Induvadana, C.V. Ramana Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . Pseudopterosin P C26H38O6 ÏàËÆ¶È:57.6% Tetrahedron 2004 60 10627-10635 Pseudopterosins P¨CV, new compounds from the gorgonian octocoral Pseudopterogorgia elisabethae from Providencia island, Colombian Caribbean Carmenza Duque, M¨®nica Puyana, Ginna Narv¨¢ez, Oscar Osorno, Noriyuki Hara, Yoshinori Fujimoto Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . taxicin II ÏàËÆ¶È:57.1% Journal of Chinese Medicinal Materials 2014 37 243-252 Chemical Constituents of B ark of T axus chinensis var. m airei SU Jian, SHI Hong-xing, WANG Li-jun, GUO Rui-xia, REN Tian-kun, WU Yi-bing Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . 4,7,8,10,13-pentadeacetylabeobaccatin VI C27H36O9 ÏàËÆ¶È:56% Phytochemistry 1994 36 407-411 Rearranged taxanes from Taxus baccata Giovanni Appendino, Giancarlo Cravotto, Renata Enri¨´, Jasmin Jakupovic, Pierluigi Gariboldi, B. Gabetta, E. Bombardell Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . (3aS,4S,5R,6R,7R,7aS)-2,2-Dimethyl-7-(4-methylphenylsulfonamido)-4-(tert-butyldimethylsilyloxy)-5-phenylcarbonyloxy-6-(1-ethynyl)perhydro-1,3-benzodioxole C31H41NO7SSi ÏàËÆ¶È:56% Canadian Journal of Chemistry 2006 84 1313-1337 Cyclotrimerization approach to unnatural structural modifications of pancratistatin and other amaryllidaceae constituents - Synthesis and biological evaluation1 Tomas Hudlicky, Michael Moser, Scott C. Banfield, Uwe Rinner, Jean-Charles Chapuis, and George R. Pettit Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . compound 7 ÏàËÆ¶È:56% Tetrahedron Letters 2004 45 8507-8510 A fused GalNAc-thiazole from a singular and unanticipated fragmentation Spencer Knapp, Benjamin Amorelli, George A. Doss Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . O-cinnamoyltaxicin-II C29H36O6 ÏàËÆ¶È:55.5% Journal of Natural Products 1996 59 117-123 Identification of Six Taxine Alkaloids from Taxus baccata Needles Louis H. D. Jenniskens, Erik L. M. van Rozendaal, and Teris A. van Beek Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . 3-O-benzoate C36H42O10 ÏàËÆ¶È:55.5% Chemical & Pharmaceutical Bulletin 1997 45 152-160 Studies on the Constituents of Scutellaria Species. XVIII. Structures of Neoclerodane-Type Diterpenoids from the Whole Herb of Scutellaria rivularis WALL. Haruhisa KIZU,Yoshitaka IMOTO,Tsuyoshi TOMIMORI,Tohru KIKUCHI,Shigetoshi KADOTA and Koji TSUBONO Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . Compound 3 C27H34O7 ÏàËÆ¶È:55.5% Bioorganic & Medicinal Chemistry Letters 2010 20 2847-2850 New diterpenoids from Caesalpinia species and their cytotoxic activity Biswanath Das, Yallamalla Srinivas, Chithaluri Sudhakar, Ibram Mahender, Keetha Laxminarayana, Parigi Raghavendar Reddy, Tuniki Venugopal Raju, Naga Mahesh Jakka, Janapala Venkateswara Rao Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . 9¦Á,10¦Â-Dihydroxy-2¦Á-acetoxy-5¦Á-cinnamoyloxy-taxa-4(20),11-diene-13-one C31H38O7 ÏàËÆ¶È:55.1% Bioorganic & Medicinal Chemistry 2003 11 293-303 New minor taxanes analogues from the needles of Taxus canadensis Qing Wen Shi, Françoise Sauriol, Orval Mamer, Lolita O Zamir Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . 2¦Á-acetoxy-5¦Á-cinnamoyloxy-9¦Á,10¦Â-dihydroxy-taxa-4 (20),11-diene-13-one ÏàËÆ¶È:55.1% Chinese Traditional and Herbal Drugs 2013 44 1380-1385 Chemical constituents from seeds of Taxus yunnanensis LIU Li-hua, WANG Li-jun, REN Tian-kun, SHI Qing-wen, ZHANG Man-li Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . cytochalasin Z12 C28H35NO5 ÏàËÆ¶È:54.1% Journal of Natural Products 2008 71(7) 1127-1132 Novel Open-Chain Cytochalsins from the Marine-Derived Fungus Spicaria elegans Rui Liu, Zhenjian Lin, Tianjiao Zhu, Yuchun Fang, Qianqun Gu, and Weiming Zhu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . 1¦Â-O-E-cinnamoyl-5¦Á-hydroxypolygodial C24H28O5 ÏàËÆ¶È:54.1% Phytochemistry 2009 70 546-553 Cytotoxic sesquiterpenoids from Winteraceae of Caledonian rainforest Noureddine Allouche, C¨¦cile Apel, Marie-Th¨¦r¨¨se Martin, Vincent Dumontet, Françoise Gu¨¦ritte, Marc Litaudon Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . all-E-3,7-dimethyl-7-(phenylsulfonyl)-9-(2,6,6-trimethyl-1-cyclohexen-1-yl)-2,4,8-nonatroenyl-ol C26H36O3S ÏàËÆ¶È:54.1% Helvetica Chimica Acta 1976 59 397-405 Eine Synthese von Vitamin A nach der Sulfonmethode Albert Fischli, Hans Mayer, Werner Simon und Hans-Jorg Stoller Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |

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