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lcyscau: ½ð±Ò+20, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-11-02 13:29:11
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²éѯģʽ£ºÄ£ºý²éѯ ̼Æ×Êý¾ÝÊäÈ룺 °´´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺 21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2 ÈܼÁÑ¡Ï Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½151¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . heptelidic acid chlorohydrin C15H21O5Cl ÏàËÆ¶È:100% The Journal of Antibiotics 1994 47 1562-1563 ANTITUMOR ACTIVITY OF HEPTELIDIC ACID CHLOROHYDRIN JUN KAWASHIMA, FUMI ITO, TAKASHI KATO, MITSURU NIWANO, HIROYUKI KOSHINO, MASAKAZU URAMOTO Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . trichoderonic acid A C16H24O6 ÏàËÆ¶È:81.2% Bioscience, Biotechnology, and Biochemistry 2010 74 793-801 Novel Terpenoids, Trichoderonic Acids A and B Isolated from Trichoderma virens, Are Selective Inhibitors of Family X DNA Polymerases Yasuhiro YAMAGUCHI, Daisuke MANITA, Toshifumi TAKEUCHI, Kouji KURAMOCHI, Isoko KURIYAMA, Fumio SUGAWARA, Hiromi YOSHIDA and Yoshiyuki MIZUSHINA Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . (4S)-10¦Á,15-epoxy-12-hydroxycadinan-3-one C15H24O3 ÏàËÆ¶È:60% Phytochemistry 2002 59 479-488 Microbial transformation of cadina-4,10(15)-dien-3-one,aromadendr-1(10)-en-9-one and methyl ursolate by Mucor plumbeus ATCC 4740 Dwight O. Collins, Peter L.D. Ruddock, Jessica Chiverton de Grasse,William F. Reynolds, Paul B. Reese Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . compound 53 C15H22O ÏàËÆ¶È:60% Canadian Journal of Chemistry 2006 84 1456-1469 Intramolecular [4 + 3] cycloadditions -Stereochemical issues in the cycloaddition reactions of cyclopentenyl cations - A synthesis of (+)-dactylol1 Michael Harmata, Paitoon Rashatasakhon, and Charles L. Barnes Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . laricinolic acid C15H24O3 ÏàËÆ¶È:60% Journal of the Chemical Society, Perkin Transactions 1 2000 2307-2309 The structure of laricinolic acid and its biomimetic transformation into officinalic acid Bernhard Erb, Hans-J¨¹rg Borschberg and Duilio Arigoni Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . (+)-Heptelidic acid C15H20O5 ÏàËÆ¶È:60% Bioscience, Biotechnology, and Biochemistry 2010 74 793-801 Novel Terpenoids, Trichoderonic Acids A and B Isolated from Trichoderma virens, Are Selective Inhibitors of Family X DNA Polymerases Yasuhiro YAMAGUCHI, Daisuke MANITA, Toshifumi TAKEUCHI, Kouji KURAMOCHI, Isoko KURIYAMA, Fumio SUGAWARA, Hiromi YOSHIDA and Yoshiyuki MIZUSHINA Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . laricinolicacid C15H24O3 ÏàËÆ¶È:60% Natural Product Research and Development 2011 23 267-269 Chemical Constituents of Loropetalum chinense Chemical Constituents of Loropetalum chinense Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 4¦Î-chloro-cadin-11-ene C15H25Cl ÏàËÆ¶È:60% Tetrahedron 1999 55 15099-15108 Synthesis of amorphane and cadinane sesquiterpenes from fabiana imbricata Koon-Sin Ngo, Geoffrey D. Brown Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . methyl (1R*,5R*,6R*,9R*)-5,9-dimethyl-2-oxo-3-oxabicyclo[4.3.0]nona-7-ene-1-carboxylate C12H16O4 ÏàËÆ¶È:60% Tetrahedron 2011 67 9909-9921 Scope and applications of second generation palladium-catalyzed cycloalkenylation. Stereoselective total syntheses of isoiridomyrmecin, isodihydronepetalactone, and ¦Á-skytanthine Kazutaka Takeda, Masahiro Toyota Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . (+)-vittatalactone C16H30O2 ÏàËÆ¶È:60% European Journal of Organic Chemistry 2011 4603-4608 Enantioselective Total Synthesis of (+)-Vittatalactone Jhillu S. Yadav, Nagendra Nath Yadav, T. Srinivasa Rao, B. V. Subba Reddy and Ahmad Al Khazim Al Ghamdi Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . cyclo(-Aho(t-Bu)-Ser(t-Bu)-Aho(t-Bu)-Ser(t-Bu)-Aho(t-Bu)-Ser(t-Bu)-) C54H99N9O15 ÏàËÆ¶È:60% Bioorganic & Medicinal Chemistry 2013 21 4296-4300 Synthesis and functional analysis of deferriferrichrysin derivatives: Application to colorimetric pH indicators Yuka Kobayashi, Shinya Oishi, Kazuya Kobayashi, Hiroaki Ohno, Hiroko Tsutsumi, Yoji Hata, Nobutaka Fujii Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . vittatalactone C16H30O2 ÏàËÆ¶È:56.2% Journal of Natural Products 2005 68 26-30 Vittatalactone, a ¦Â-Lactone from the Striped Cucumber Beetle, Acalymma vittatum Bruce D. Morris, Rebecca R. Smyth, Stephen P. Foster, Michael P.Hoffmann, Wendell L. Roelofs, Stephan Franke, and Wittko Francke Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . 10-Dehydroxydihydrobotridialone C17H26O5 ÏàËÆ¶È:56.2% Phytochemistry 1996 41 513-517 Biologically active sesquiterpenoid metabolites from the fungus Botrytis cinerea Isidro G. Collado, Rosario Hern¨¢ndez-Gal¨¢n, Victoria Prieto, James R. Hanson, Laureana G. Rebordinos Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . xylaric acid B C16H26O7 ÏàËÆ¶È:56.2% Chemistry & Biodiversity 2011 Vol. 8 1689-1700 Terpenoid and Phenolic Metabolites from the Fungus Xylaria sp. Associated with Termite Nests Sha Yan, Saifei Li, Wen Wu, Feng Zhao, Li Bao, Rong Ding, Hao Gao, Hua-An Wen, Fuhang Song, and Hong-Wei Liu Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . compound 10 C18H29NO8 ÏàËÆ¶È:56.2% Tetrahedron Letters 2004 45 5007-5009 Stereoselective routes to 3-hydroxy and 3,4-dihydroxy derivatives of 2-aminocyclohexanecarboxylic acid Ishmael B. Masesane, Patrick G. Steel Structure 13C NMR ̼Æ×Ä£Äâͼ |

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