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| 13C NMR (CDCl3) ¦Ä 14.2, 22.7, 24.9, 25.8, 27.5, 29.2, 29.3, 29.5, 29.7, 29.9, 31.7, 35.5, 36.9, 71.7, 125.2, 133.7, 179.3 |
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hotony: ½ð±Ò+10 2015-04-21 00:32:17
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1 . R-octadec-9Z-en-7-ol ÏàËÆ¶È:88.2% Chemistry of Natural Compounds 2005 41 643-649 Ozonolysis of Ricinolic Acid Derivatives and Transformations of the Ozonolysis Products under Barton Reaction Conditions G. Yu. Ishmuratov, R. Ya. Kharisov, A. Kh. Shayakhmetova, L. P. Botsman, O. V. Shitikova, G. A. Tolstikov Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . compound 10 C19H36O3 ÏàËÆ¶È:84.2% Tetrahedron 2012 68 5583-5589 Enantio-selective reduction of the flowering related compound KODA and its analogues in Pharbitis nil cv. Violet Ariaki Murata, Kenji Kai, Ken Tsutsui, Jun Takeuchi, Yasushi Todoroki, Kazuo Furihata, Mineyuki Yokoyama, Susanne Baldermann, Naoharu Watanabe Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . n-octadec-8,11-dien-7a-ol-1-oic acid C18 H32O3 ÏàËÆ¶È:83.3% Natural Product Research 2013 27 1848-1855 Five new secondary metabolites from Monascus purpureus-fermented Hordeum vulgare and Sorghum bicolor Md. Pravej Ansari, Alka Puri, M. Ali & Bibhu Prasad Panda Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . (E)-11-hydroxy-octadeca-12-enoic acid C18H34O3 ÏàËÆ¶È:77.7% Zeitschrift f¨¹r Naturforschung B 2009 64b 1199-1207 Three New Unsaturated Fatty Acids from the Marine Green Alga Ulva fasciata Delile Ghada S. E. Abou-ElWafa, Mohamed Shaaban, Khaled A. Shaaban,Mohamed E. E. El-Naggar, and Hartmut Laatsch Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . acido 5-hidroxi-octadeca-6(E)-8(Z)-dienoico C18H32O3 ÏàËÆ¶È:77.7% Qu¨ªmica Nova 2013 36 519-523 PREGNANOS E OUTROS CONSTITUINTES DAS RA¨ªZES DE Macrosiphonia petraea (A. St.-Hil.) Kuntze (Apocynaceae) Luiz Roberto de Assis Junior, Fernanda Rodrigues Garcez e Walmir Silva Garcez, Zaira da Rosa Guterres Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . ¦Å-palmitolactone C16H30O2 ÏàËÆ¶È:76.4% Phytochemistry 1990 29 305-306 ¦Å-palmitolactone from Ageratina viscosa Rub¨¦n Torrenegra,Julio A. Pedrozo,Jorge Robles,Omar Fuentes Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . (3R,5Z)-and (3S,5Z)-5-tetradecene-1,3-diol C14H28O2 ÏàËÆ¶È:76.4% The Journal of Organic Chemistry 1998 63 3925-3932 Absolute Structure and Total Synthesis of Lipogrammistin-A, a Lipophilic Ichthyotoxin of the Soapfish Hiroyuki Onuki, Kei Ito, Yoshimasa Kobayashi, Nobuaki Matsumori, and Kazuo Tachibana, Nobuhiro Fusetani Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . (9E,11Z) 14-Hydroxyoctadecan-9,11-dienoic acid C18H32O3 ÏàËÆ¶È:76.4% Natural Product Communications 2006 1 101-107 Constituents of Erythrina lysistemon: Their Brine ShrimpLethality, Antimicrobial and Radical Scavenging Activities Benard F. Juma and Runner R. T. Majinda Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . decyl 8-hydroxyheptadecanoate ÏàËÆ¶È:72.2% Indian Journal of Chemistry Section B 2010 49B 1648-1652 Total synthesis of three natural products: Decyl 8-hydroxyheptadecanoate,undecyl hexadecanoate and 2,3-dihydroxypropyl hexadecanoate Ashima Singh,M L Sharma & Jasvinder Singh* Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . (9Z,11E)-13-hydroxy-9,11-octadecadienoic acid C18H32O3 ÏàËÆ¶È:72.2% Bioscience, Biotechnology, and Biochemistry 2000 64 882-886 (10E,12Z,15Z)-9-Hydroxy-10,12,15-octadecatrienoic Acid Methyl Ester as an Anti-inflammatory Compound from Ehretia dicksonii Mei DONG, Yukiko ODA, Mitsuru HIROTA Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . piliferolide A C18H32O3 ÏàËÆ¶È:72.2% Heterocycles 1994 39 561-569 Unsaturated Fatty Acid Lactones from the Fungus Ophiostoma piliferum William A. Ayerand Abdul Q. Khan Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . (9S,10E,12Z)-9-Hydroxy-10,12-octadecadienoic Acid C18H32O3 ÏàËÆ¶È:72.2% Journal of Agricultural and Food Chemistry 2008 56 5062-5068 Isolation and Identification of Antifungal Fatty Acids from the Basidiomycete Gomphus floccosus Charles L. Cantrell, Bethany P. Case, E. Edward Mena, Toby M. Kniffin, Stephen O. Duke and David E. Wedge Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |

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