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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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ÎÒÈÏΪл¯¿ÉÄÜÐԺܴó£¬ÄãÔÚÇö¨Ï ²éѯ½á¹û£º¹²²éµ½299¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×Ä£Äâͼ |

2Â¥2013-10-09 14:43:23
yulin07002
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3Â¥2013-10-09 18:37:49









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