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²éѯ½á¹û£º¹²²éµ½512¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . muurolane-4¦Â,5¦Â,10¦Â-triol C15H28O3 ÏàËÆ¶È:61.1% Chemical & Pharmaceutical Bulletin 2003 51(8) 986-989 Cadinane-Type Sesquiterpenes from the Roots of Taiwania cryptomerioides HAYATA Yueh-Hsiung KUO, Chiou-Fung CHYU, and Hsiu-Chuan LIN Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 10¦Â,11-oxy-4¦Á,5¦Á,7¦Â-eremophil-1-ene C15H24O ÏàËÆ¶È:61.1% Phytochemistry 1999 52 1063-1067 The hydroxylation of the sesquiterpenoid valerianol by Mucor plumbeus Simone Fontes Arantes, James R. Hanson, Peter B. Hitchcock Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . cyclokessyl acetate ÏàËÆ¶È:61.1% Phytochemistry 1992 31 3511-3514 Sesquiterpenoids and iridoid glycosides from Valeriana fauriei Koichi Nishiya, Takefumi Kimura, Koichi Takeya, Hideji Itokawa Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . kessyl glycol 8-acetate ÏàËÆ¶È:61.1% Phytochemistry 1992 31 3511-3514 Sesquiterpenoids and iridoid glycosides from Valeriana fauriei Koichi Nishiya, Takefumi Kimura, Koichi Takeya, Hideji Itokawa Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . (-)-eudesma-4(15)-en-3¦Â,11-diol ÏàËÆ¶È:61.1% Pharmazie 2002 57 59-61 Microbiological conversion of a - and -eudesmol mixture by Rhizopus G.T. Maatooq - J.J. Hoffmann Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . (5S)-4-Bromo-3-methyl-5-[(1R,3R,5R)-1,3,5-trimethyloctyl]furan-2(5H)-one C16H28BrO2 ÏàËÆ¶È:61.1% Zeitschrift f¨¹r Naturforschung B 2009 64 639-645 Ex Chiral Pool Synthesis from a Highly Methyl-branched Wax Ester and Biological Properties of (+)-Capensifuranone Y. Galeyeva, M. Morr, F. Sasse, R. Diestel, S. Laschat, A. Baro, and W. Frey Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . (-)-5,11-epoxy-4¦Á,5¦Â,10¦Á-eudesm-1-ene ÏàËÆ¶È:61.1% Flavour and Fragrance Journal 2004 19 565-570 Terpenoids of the volatile oil of Bursera graveolens Chiyoki Yukawa, Hisakatsu Iwabuchi, Tadao Kamikawa, Sadao Komemushi and Akiyoshi Sawabe Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . pacificin N C22H36O3 ÏàËÆ¶È:59.0% Chemical & Pharmaceutical Bulletin 2007 55(6) 890-893 Prenylbicyclogermacrane Diterpenoids from the Formosan Soft Coral Nephthea elongata Ali Ali Hassan EL-GAMAL,Shang-Kwei WANG,and Chang-Yih DUH Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . compound 8 ÏàËÆ¶È:59.0% Phytochemistry 1986 25 1393-1395 Neo-clerodane diterpenoids from Baccharis rhomboidalis Aurelio San-Mart¨ªn, Juana Rovirosa, Cecilia Labb¨¦, Arturo Givovich, Manuel Mah¨², Mariano Castillo Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . vitedoin B C19H30O4 ÏàËÆ¶È:57.8% Journal of Natural Products 2004 67 2073-2075 Lignan Derivatives and a Norditerpene from the Seeds of Vitex negundo Masateru Ono, Yoichiro Nishida, Chikako Masuoka, Jian-Chen Li, Masafumi Okawa, Tsuyoshi Ikeda, and Toshihiro Nohara Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . (4,10a-dimethyl-7b-iso-propyl-decaline-5ene)1a,4a-maleic acid anhydride ÏàËÆ¶È:57.8% Canadian Journal of Chemistry 2007 85 996-1005 On the origin of some cubebene derivatives ¡ªDiels¨CAlder adducts and the diene structures of solidago compounds Christopher K. Jankowski, Andr¨¦ Pelletier, Eduardo Diaz T.,Jacqueline M.R. Belanger, Jocelyn J.R. Par¨¦, Andre Aumelas,Thierry Besson, Maria de Fatima Pereira, and Laurent Mauclaire Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . loesenerine C19H35N3O2 ÏàËÆ¶È:57.8% Phytochemistry 1987 26 1847-1848 Loesenerine,an alkaloid from Maytenus loeseneri Mar¨ªa D¨ªaz,Alfred Preiss,Helmut Ripperger Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . 6¦Â,8¦Â-diacetoxyeremophil-7(11)-en-12,8¦Á-olide C19H26O6 ÏàËÆ¶È:57.8% Phytochemistry 1985 24 1531-1535 Eremophilenolides from petasites japonicus Ko Sugama, Koji Hayashi, Hiroshi Mitsuhashi Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . 4¦Á,5¦Á-Epoxy-17¦Á-hydroxy-A-homo-4-oxapregnan-3,20-dione C22H32O5 ÏàËÆ¶È:57.1% Steroids 2006 71 116-119 Steroidal seven-membered A-ring epoxy lactones by oxidation of the corresponding ¦¤4-3-ketosteroids Maria L. Di Gioia, Antonella Leggio, Adolfo Le Pera, Francesca Perri, Andrea F. Pitrelli, Angelo Liguori Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . 5,16¦Á,17¦Á-Trihydroxy-2¦Á,3¦Á-isopropylidenedioxy-5¦Á-pregna-6,20-dione C24H36O7 ÏàËÆ¶È:57.1% Canadian Journal of Chemistry 2005 83 1084-1092 Synthesis and preliminary bioactivity evaluation of new pregnane brassinosteroid-like compounds Daniel G. Rivera and Francisco Coll Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . 16¦Á-Azido-5,17¦Á-dihydroxy-2¦Á,3¦Á-isopropylidenedioxy-5¦Á-pregna-6,20-dione C24H35O6N3 ÏàËÆ¶È:57.1% Canadian Journal of Chemistry 2005 83 1084-1092 Synthesis and preliminary bioactivity evaluation of new pregnane brassinosteroid-like compounds Daniel G. Rivera and Francisco Coll Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . 5¦Á-Androstan-3¦Â-yl acetate C21H34O2 ÏàËÆ¶È:57.1% Organic Magnetic Resonance 1977 9 439-464 13C n.m.r. spectra of steroids ¡ªa survey and commentary J. W. Blunt and J. B. Stothers Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . rel-(3'R)-3',8'-dihydrotokinolide B C24H30O4 ÏàËÆ¶È:56.5% Natural Product Research 2011 Vol. 25, No. 13 1234-1242 Phthalides and other constituents from Ligusticum porteri; sedative and spasmolytic activities of some natural products and derivatives Alejandra Le¨®n, Rub¨¦n A. Toscano, Jaime Tortoriello and Guillermo Delgado Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . 9¦Á-hydroxy-1¦Â-methoxycaryolanol C16H28O2 ÏàËÆ¶È:55.5% Helvetica Chimica Acta 2008 Vol. 91 1894 Four New Compounds from Sinacalia tangutica Ying Zhu, Yan Zhao, Guo-Du Huang, and Wang-Suo Wu Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . rumphellolide A C15H24O3 ÏàËÆ¶È:55.5% Chemical & Pharmaceutical Bulletin 2007 55(9) 1296-1301 Rumphellolides A¡ªF, Six New Caryophyllane-Related Derivatives from the Formosan Gorgonian Coral Rumphella antipathies Ping-Jyun SUNG,Li-Fan CHUANG,Jimmy KUO,Jih-Jung CHEN,Tung-Yung FAN,Jan-Jung LI,Lee-Shing FANG,and Wei-Hsien WANG Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . rumphellolide B |
3Â¥2013-08-18 12:21:49
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