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M201175065

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M201175065: ½ð±Ò+8, ¡ï¡ï¡ïºÜÓаïÖú 2014-11-24 15:43:22
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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×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     Ì¼Æ×Ä£Äâͼ
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