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11.8,13.3,17.2,20.6,21.2,26.9,27.2,29.2,29.3,37.3,38.2,40.0,41.9,55.8,68.2,71.1,103.9,122.2,122.4,129.0,129.1,132.7,134.6,173.6,190.9,193.8
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yulin07002(Ëõ++Ó°´ú·¢): ½ð±Ò+30, Â¥Ö÷·´À¡£¬´úÂ¥Ö÷·¢·Å£¬Ð»Ð»Ó¦Öú 2013-10-09 18:13:03
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1 .     (3¦Â,20S)-pregn-5-ene-22S-benzyl-25,26-dehydropiperidincarboxylate
    ÏàËÆ¶È:59.2%
Bioorganic & Medicinal Chemistry Letters          2011          21          3608-3612
Synthesis and biological evaluation of desmethylveramiline, a micromolar Hedgehog inhibitor
Guillaume Guerlet, Thomas Spangenberg, Andr¨¦ Mann, H¨¦l¨¨ne Faure, Martial Ruat
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     compound
    ÏàËÆ¶È:57.6%
Journal of the American Chemical Society          2004          126          3704-3705
Total Synthesis and Structural Revision of (+)-Amphidinolide W
Arun K. Ghosh and Gangli Gong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     compound 1
C24H38O4     ÏàËÆ¶È:57.6%
Journal of the American Chemical Society          2004          126          3704-3705
Total Synthesis and Structural Revision of (+)-Amphidinolide W
Arun K. Ghosh and Gangli Gong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     compound 22
    ÏàËÆ¶È:57.6%
Journal of the American Chemical Society          2004          126          3704-3705
Total Synthesis and Structural Revision of (+)-Amphidinolide W
Arun K. Ghosh and Gangli Gong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     compound 26
    ÏàËÆ¶È:57.6%
Journal of the American Chemical Society          2004          126          3704-3705
Total Synthesis and Structural Revision of (+)-Amphidinolide W
Arun K. Ghosh and Gangli Gong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     24-methyl-5,14,26-ergostatrien-3¦Â-ol
C28H44O     ÏàËÆ¶È:57.1%
Chinese Traditional and Herbal Drugs          1998          29          433-435
Studies on the Triterpenes from Xiaolangdu (Euphorbia prolifera)
Zhang Jun; Yang Chengjin; Wu Dagang (The First Affiliated Hospital of Kuming Medical College; Kunming );
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     (2S,3R)-3-methyl-5-phenylsulfonyl-1-[(1S,4aS,8aS)-1,4,-4a,5,6,7,8,8a-octahydro-2,5,5,8a-tetramethyl-1-naphthalenyl]pentan-2-(tert-butyldimethylsilyl oxy)
C32H54O3SSi     ÏàËÆ¶È:57.1%
The Journal of Organic Chemistry          2001          66          7263-7269
Total Synthesis and Determination of the Absolute Configuration of Coscinosulfate. A New Selective Inhibitor of Cdc25 Protein Phosphatase
St¨¦phane Poigny, Samia Nouri, Ang¨¨le Chiaroni, Mich¨¨le Guyot, and Mohammad Samadi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     (22E,24R)-3¦Â-hydroxyergosta-7,22-dien-6-one
C28H44O2     ÏàËÆ¶È:57.1%
Phytochemistry          2013          92          137-145
Fomentarols A¨CD, sterols from the polypore macrofungus Fomes fomentarius
Yi Zang, Juan Xiong, Wen-Zhu Zhai, Lei Cao, Sheng-Ping Zhang, Yu Tang, Ji Wang, Jing-Jing Su, Guo-Xun Yang, Yun Zhao, Hui Fan, Gang Xia, Chuan-Gui Wang, Jin-Feng Hu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     pseudopterosin P
C27H38O7     ÏàËÆ¶È:55.5%
Helvetica Chimica Acta          2004          Vol. 87          1090
New Antibacterial Diterpenes from Pseudopterogorgia elisabethae
Athar Ata, Hla Y. Win, David Holt, Paul Holloway, Edward P. Segstro, and Gamini S. Jayatilake
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     ergosta-7,22-dien-3-one
    ÏàËÆ¶È:55.5%
Mycosystema          2011          30          459-463
Chemical constituents of Fomitiporia ellipsoidea fruiting bodies
LIU Han-Bin BAO Hai-Ying CUI Bao-Kai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     pseudopterosin C
C27H38O7     ÏàËÆ¶È:55.5%
The Journal of Organic Chemistry          1986          51          5140-5145
The pseudopterosins: a new class of antiinflammatory and analgesic diterpene pentosides from the marine sea whip Pseudopterogorgia elisabethae (Octocorallia)
Sally A. Look, William Fenical, Gayle K. Matsumoto, Jon Clardy
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     3,6,17-Trihydroxy-stigmasta-4,7,24(28)-triene
C29H46O3     ÏàËÆ¶È:55.1%
Natural Product Research          2010          24          1481-1487
New antifungal steroids from Turbinaria conoides (J. Agardh) Kutzing
S. Sadish Kumar; Y. Kumar; M. S. Y. Khan; V. Gupta
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     compound 8
C23H36O6     ÏàËÆ¶È:53.8%
Journal of Natural Products          2004          67          1580-1583
New Decalin Derivatives, Eujavanoic Acids A and B, from Eupenicillium javanicum
Shigeru Okamoto, Tomoo Hosoe, Takeshi Itabashi, Koohei Nozawa, Kaoru Okada, Galba Maria de Campos Takaki, Minoru Chikamori, Takashi Yaguchi, Kazutaka Fukushima, Makoto Miyaji, and Ken-ichi Kawai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
Tobeastriver
2Â¥2013-10-09 14:43:23
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yulin07002

½ð³æ (СÓÐÃûÆø)

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