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2Â¥2012-11-04 12:43:22
lifeliuyan
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hanglin11: ½ð±Ò+20, ¡ïÓаïÖú 2012-11-04 13:29:33
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hanglin11: ½ð±Ò+20, ¡ïÓаïÖú 2012-11-04 13:29:33
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²éѯ½á¹û£º¹²²éµ½21¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . linderachalcone C25H28O4 ÏàËÆ¶È:57.6% Phytochemistry 1989 28 955-956 Two flavonoids from two Lindera umbellata varieties Kazuhiko Ichino Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . linderachalcone ÏàËÆ¶È:57.6% Chemistry Letters 1989 18 363-366 Isolation and Structures of Two New Flavonoids from Lindera umbellata Kazuhiko Ichino, Hitoshi Tanaka and Kazuo Ito Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . Lehualide E C24H32O4 ÏàËÆ¶È:57.6% Journal of Natural Products 2011 74 809-815 Lehualides E−K, Cytotoxic Metabolites from the Tongan Marine Sponge Plakortis sp. Jacqueline M. Barber, Natelle C. H. Quek, Dora C. Leahy, John H. Miller, David S. Bellows, and Peter T. Northcote Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . Pyrazine-2-carboxylic acid (1-benzylcarbamoyl-pentyl)-cyclohexyl-amide C24H32N4O2 ÏàËÆ¶È:53.8% Bioorganic & Medicinal Chemistry Letters 2007 17 5483-5486 Novel anti-tuberculosis agents from MCR libraries Alexander Dömling, Sepp Achatz, Barbara Beck Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . N-(3S-N-L-prolinyl-1,2,3,4-tetrahydroisoquinoline-3-carbonyl)-L-proline C20H25N3O4 ÏàËÆ¶È:53.8% Bioorganic & Medicinal Chemistry 2010 18 1536-1554 2, 3-Diamino acid modifying 3S-tetrahydroisoquinoline-3-carboxylic acids: Leading to a class of novel agents with highly unfolded conformation, selective in vitro anti-platelet aggregation and potent in vivo anti-thrombotic activity Xiaoyi Zhang, Wei Wang, Shenling Cheng, Ming Zhao, Meiqing Zheng, Heng Wei Chang, Jianhui Wu, Shiqi Peng Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . Lehualide G C25H34O4 ÏàËÆ¶È:53.8% Journal of Natural Products 2011 74 809-815 Lehualides E−K, Cytotoxic Metabolites from the Tongan Marine Sponge Plakortis sp. Jacqueline M. Barber, Natelle C. H. Quek, Dora C. Leahy, John H. Miller, David S. Bellows, and Peter T. Northcote Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . Myristinin D ÏàËÆ¶È:53.3% Archives of Pharmacal Research 2009 32 685-692 A new acyclic diterpene acid and bioactive compounds from Knema glauca Noppadon Rangkaew, Rutt Suttisri, Masataka Moriyasu and Kazuko Kawanishi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . ramosine C C30H38N4O5 ÏàËÆ¶È:51.8% Helvetica Chimica Acta 2003 Vol. 86 127 14-Membered Cyclopeptides from Paliurus ramosissimus and P. hemsleyanus Hui-yi Lin, Chung-Hsiung Chen, Karin C. S. Chen Liu, and Shoei-Sheng Lee Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . 1R,2S,3S,4S)-2-{1-[4-(tert-butyldiphenylsilyloxy)butyl]vinyl}-1,5,5-trimethyl-6-methylene-3-(phenylmethoxy)bicyclo[2.2.2]octan-2-ol C41H54O3Si ÏàËÆ¶È:51.7% Australian Journal of Chemistry 2004 57 53-66 Taxane Diterpene Synthesis Studies. Part 2: Towards Taxinine¡ªEnantiospecific Construction of an AB-ring Substructure Incorporating both Quaternary Carbon Centres and Attempts to Annulate the C-ring Martin G. Banwell , Malcolm D. McLeod and Andrew G. Riches Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . notoamide K C26H31N3O5 ÏàËÆ¶È:50% Journal of Natural Products 2008 71(12) 2064-2067 Notoamides F-K, Prenylated Indole Alkaloids Isolated from a Marine-Derived Aspergillus sp. Sachiko Tsukamoto, Hikaru Kato, Masayuki Samizo, Yuka Nojiri, Hiroyuki Onuki, Hiroshi Hirota, and Tomihisa Ohta Structure 13C NMR ̼Æ×Ä£Äâͼ |
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