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karl2100: ½ð±Ò+1, 3Q 2013-11-03 08:33:43
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karl2100: ½ð±Ò+1, 3Q 2013-11-03 08:33:43
kengkengsee: ½ð±Ò+5, ¡ïÓаïÖú 2013-11-04 09:48:46
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²éѯ½á¹û£º¹²²éµ½396¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . 6¦Á-hydroxyambreinolide C17H28O3 ÏàËÆ¶È:64.7% Journal of Natural Products 1996 59 113-116 Norditerpenes and Norsesterterpenes from Salvia yosgadensis G¨¹lac¨¹ti Topç, and Ayhan Ulubelen Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . compound 8 ÏàËÆ¶È:62.5% Planta Medica 1999 65 153-156 Sesquiterpene Lactone Glycosides from Arnica longifolia Claus M.Passreiter,Massimo De Carlo,and A.Steigel Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . atractylenolid III C15H20O3 ÏàËÆ¶È:62.5% Planta Medica 1989 55 59-61 Constituents of Atractylis koreana Peter Pachaly , AstridLansing, and Kwan Seog Sin Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . 9¦Á-hydroxy-calarene C15H24O ÏàËÆ¶È:62.5% Phytochemistry 1992 31 3749-3755 Microbial oxidation of tricyclic sesquiterpenoids containing a dimethylcyclopropane ring Wolf-Rainer Abraham, Klaus Kieslich, Burkhard Stumpf, Ludger Ernst Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . 5¦Á-hydroxy-4¦Á,15-dihydrocositic acid methyl ester C16H26O3 ÏàËÆ¶È:62.5% Phytochemistry 1990 29 3201-3206 Eudesmane derivatives other constituents from Apalochlamys spectabilis Cassinia species C. Zdero,F. Bohlmann,R.M. King Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . 2¦Á-methyldiplopterol ÏàËÆ¶È:62.5% Magnetic Resonance in Chemistry 2010 48 951-954 NMR spectral assignment of 2- and 3¦Â-methylhopanes and evidence for boat conformation in D ring of 17(H), 21(H)-hopanes (pages 951¨C954) Geir Kildahl-Andersen, Hans Peter Nytoft and Jon Eigill Johansen Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . ²ÔÊõÄÚõ¥ III C15H21O3 ÏàËÆ¶È:62.5% Chinese Traditional and Herbal Drugs 2008 39 1149-1151 µØïþµÄ»¯Ñ§³É·ÖÑо¿ ÌÆÂõ;Áα¦Õä;ÁÖËç;µË˼ɺ Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . atractylenolid III C15H20O3 ÏàËÆ¶È:62.5% Chinese Journal of Natural Medicines 2008 6 404-407 A New Sesquiterpenoid from the Roots of Chloranthus fortunei WANG Xia-Chang; WU Wei-Qun; MA Shi-Ping; LIU Jing-Han; HU Li-Hong Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . (3a¦Â,4a¦Á,8a¦Â,9a¦Â)-3a,4,4a,5,6,7,8,8a,9,9a-Decahydro-8a-methyl-5-methylenenaphtho[2,3-b]furan-2(3H)-one C14H20O2 ÏàËÆ¶È:62.5% Journal of the Chemical Society, Perkin Transactions 1 1993 239-247 Total synthesis of three eudesman-12,8-olides, (¡À)-isoalantolactone, (¡À)-dihydrocallitrisin and (¡À)-septuplinolide; structure revision of septuplinolide Masahiro Tada, Hirokazu Yamada, Akira Kanamori and Kazuhiro Chiba Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . (-)-juneol ÏàËÆ¶È:62.5% Journal of Oleo Science 2004 53 343-348 Eudesmane-Type Sesquiterpenoids in the Volatile Oil from Bursera graveolens Chiyoki YUKAWA, Hisakatsu IWABUCHI, Sadao KOMEMUSHI, Akiyoshi SAWABE Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . 1¦Â-Hydroxy-6,7¦Á-dihydroxyeudesm-4(15)-ene C15H26O3 ÏàËÆ¶È:62.5% Journal of Natural Products 2011 74 937-942 Estrogenic Activity of Chemical Constituents from Tephrosia candida Mohamed-Elamir F. Hegazy, Abou El-Hamd H. Mohamed, Ali M. El-Halawany, Pierre C. Djemgou, Abdelaaty A. Shahat, and Paul W. Par¨¦ Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . 1,10¦Â-Epoxy-3,4¦Á-dichloromethano-13-trichloromethyl-5,7¦Á(H),6,11¦Â(H)-guai-12,6-olide C17H19Cl5O3 ÏàËÆ¶È:58.8% Chemistry of Natural Compounds 2007 43 548-551 PREPARATION AND STRUCTURE ELUCIDATION OF TWO MINOR PRODUCTS FROM REACTION OF ARGLABIN WITH CHLOROFORM IN THE PRESENCE OF A CROWN ETHER R. I. Jalmakhanbetova, G. A. Atazhanova, V. A. Raldugin,I. Yu. Bagryanskaya, Yu. V. Gatilov, M. M. Shakirov,and S. M. Adekenov Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . methyl-13-epi-manoyloxide-18-oate C20H30O3 ÏàËÆ¶È:57.1% Phytochemistry 1991 30 211-213 Diterpenes from Leyssera gnaphaloides F. Tsichritzis, J. Jakupovic Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . 5¦Á,6¦Á,7¦Á,8¦Á-diepoxy-eudesmane ÏàËÆ¶È:56.2% Phytochemistry 2002 60 333-338 Terpenoids from Guarea guidonia João Henrique G. Lago, Cl¨¢udia B. Brochini, N¨ªdia F. Roque Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . compound 6a C16H26O2 ÏàËÆ¶È:56.2% Journal of Natural Products 2003 66 1623-1627 Facile Access to Optically Active Labdane-Type Diterpenes from (+)-Manool. Synthesis of (+)-Coronarin E, (+)-15,16-Epoxy-8(17),13(16),14-labdatriene, and (+)-Labda-8(17),13(Z)-diene-15,16-diol Jos¨¦ Villamizar, Juan Fuentes, Franklin Salazar, Eleonora Tropper, and Randolph Alonso Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . compound 7 C16H28O ÏàËÆ¶È:56.2% Journal of Natural Products 2003 66 1623-1627 Facile Access to Optically Active Labdane-Type Diterpenes from (+)-Manool. Synthesis of (+)-Coronarin E, (+)-15,16-Epoxy-8(17),13(16),14-labdatriene, and (+)-Labda-8(17),13(Z)-diene-15,16-diol Jos¨¦ Villamizar, Juan Fuentes, Franklin Salazar, Eleonora Tropper, and Randolph Alonso Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . (11S)-4¦Â,6¦Â,11,12-tetrahydroxyeudesman-1-one C15H26O5 ÏàËÆ¶È:56.2% Journal of Natural Products 2002 65 1011-1015 Chemical-Microbiological Synthesis of Cryptomeridiol Derivatives by Gliocladium roseum: Semisynthesis of 11-Hydroxyeudesmanolides Andr¨¦s Garc¨ªa-Granados, Mar¨ªa C. Guti¨¦rrez, Andr¨¦s Parra, and Francisco Rivas Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . compound 7 C17H32O6S2 ÏàËÆ¶È:56.2% Journal of Natural Products 2001 64 348-349 Synthesis of (+)-Cyclozonarone and the Absolute Configuration of Naturally Occurring (-)-Cyclozonarone Manuel Cort¨¦s, Jaime A. Valderrama, Mauricio Cuellar, Ver¨®nica Armstrong, and Marcelo Preite Structure 13C NMR ̼Æ×Ä£Äâͼ |
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