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yjl2007: ½ð±Ò+20 2014-05-21 17:03:58
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yjl2007: ½ð±Ò+20 2014-05-21 17:03:58
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ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½23¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . isocalamendiol C15H26O2 ÏàËÆ¶È:73.3% Phytochemistry 1996 43 1175-1182 Sesquiterpenoids from Acorus calamus as germination inhibitors Kazue Nawamaki, Masanori Kuroyanagi Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . Isolongifolene Epoxide ÏàËÆ¶È:66.6% Journal of Agricultural and Food Chemistry 1994 42 138-142 Structure elucidation of oxidation-reduction products of isolongifolene Isabelle Bombarda, Jacqueline Smadja, Emile M. Gaydou, Jacques Yves Conan, Robert Faure Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . gajutsulactone A C15H22O2 ÏàËÆ¶È:60% Chemical & Pharmaceutical Bulletin 2001 49(12) 1558-1566 Medicinal Foodstuffs. XXVIII.1) Inhibitors of Nitric Oxide Production and New Sesquiterpenes, Zedoarofuran, 4-Epicurcumenol,Neocurcumenol, Gajutsulactones A and B, and Zedoarolides A and B, from Zedoariae Rhizoma Hisashi MATSUDA, Toshio MORIKAWA, Iwao TOGUCHIDA, Kiyofumi NINOMIYA, and Masayuki YOSHIKAWA Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . eudesma-11-en-2¦Á,4¦Á-diol ÏàËÆ¶È:60% Phytochemistry 2003 63 835-839 Eudesmane and megastigmane glucosides from Laggera alata Qunxiong Zheng, Zhaojun Xu, Xianfeng Sun, Wei Yao, Handong Sun,Christopher H. K. Cheng, Yu Zhao Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . canusesnol D C15H26O3 ÏàËÆ¶È:60% Journal of Natural Products 2004 67 1893-1896 New Sesquiterpenes from Capsicum annuum Yousuke Kawaguchi, Toshimasa Ochi, Yoshihisa Takaishi, Kazuyoshi Kawazoe, and Kuo-Hsiung Lee Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . Eudesm-11-en-2,4¦Ádiol C15H24O ÏàËÆ¶È:60% Phytochemistry 1993 34 567-568 Eudesm-11-en-2,4¦Á-diol from Nardostachys Chinensis Koichi Masuyama, Hiroshi Morita, Koichi Takeya, Hideji Itokawa Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . (1S,2S,3S,4R,6S,7R,8R,11R)-3-hydroxymethyl-3,7,11-tri-methyltricyclo[6.3.0.0(2,4)]undecan-6,7-diol(6,14-exo-dihydroxyglobulol) C15H24O2 ÏàËÆ¶È:60% 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 8 . (-)-eudesma-4(15)-en-2¦Â,11-diol ÏàËÆ¶È:60% 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 9 . gajutsulactone A 15H22O2 ÏàËÆ¶È:60% Heterocycles 2001 55 841-846 Inhibitors of Nitric Oxide Production and New Sesquiterpenes, 4-epi-Curcumenol, Neocurcumenol, Gajutsulactones A and B, and Zedoarolides A and B from Zedoariae Rhizoma Hisashi Matsuda, Toshio Morikawa, Iwao Toguchida, Kiyofumi Ninomiya, and Masayuki Yoshikawa Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 15-nor-amorph-11-en-4¦Â-ol C14H24O 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 11 . amorph-11-en-4¦Â-ol C15H26O 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 12 . 6¦Â,7¦Á,14-trihydroxyaromadendrane ÏàËÆ¶È:60% Journal of Chemical Research 1997 21 28-29 Hydroxylation of Aromadendrane Derivatives by Mucor plumbeus† Ricardo Guillermo, James R. Hanson and Almaz Truneh Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . 5(11)-epoxycadinane-4¦Â,5¦Â,10¦Â,11-tetraol C15H26O3 ÏàËÆ¶È:60% Planta Medica 2012 78 1010-1014 Sesquiterpenoids from the Rhizomes of Homalomena occulta Xie, Xiao-Yu; Wang, Rui; Shi, Yan-Ping: Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . compound 5b ÏàËÆ¶È:60% Indian Journal of Chemistry Section B 1995 34B 992-993 13C NMR assignments of ¦Á- and ¦Â-dihydroartemisinin Ashish Kumar Pathak, Dharam C Jain & Ram P Sharma Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . lupanine ÏàËÆ¶È:60% Magnetic Resonance in Chemistry 1998 36 779-796 13C NMR spectroscopy of tri- and tetracyclic quinolizidine alkaloids. Compilation and discussion B. Mikhova and H. Duddeck Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . serratidine ÏàËÆ¶È:56.2% Chemical & Pharmaceutical Bulletin 2003 51(10) 1163-1169 Ten New Lycopodium Alkaloids Having the Lycopodane Skeleton Isolated from Lycopodium serratum THUNB. Hiromitsu TAKAYAMA,Kazuaki KATAKAWA,Mariko KITAJIMA, Kentaro YAMAGUCHI,and Norio AIMI Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . serratidine ÏàËÆ¶È:56.2% Natural Product Research 2002 16 149-153 Three New Hydroxylated Serratidine Alkaloids from Huperzia Serrata Chang-Heng Tan; Xiao-Qiang; Shan-Hao Jiang; Da-Yuan Zhu Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . 1-dimethoxymethyl-7,7-dimethyl-2-phenylbicyclo[2.2.1]heptan-2-ol ÏàËÆ¶È:56.2% Russian Journal of Organic Chemistry 2003 39 1240-1243 New 2,10-Functionalized Camphor Derivatives N. S. Vostrikov, A. V. Abutkov, V. Z. Vasikov and M. S. Miftakhov Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . omaholidenol C20H30O3 ÏàËÆ¶È:56.2% European Journal of Organic Chemistry 2012 5208-5216 Diterpenoids from Marine Ciliates: Chemical Polymorphism of Euplotes rariseta Graziano Guella, Emanuela Callone, Ines Mancini, Fernando Dini and Graziano Di Giuseppe Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . 1-(trans-4-hydroxycyclohexyl)-1-phenyl-3-(1-piperidinyl)-1-propanol ÏàËÆ¶È:56.2% Bulletin des Soci¨¦t¨¦s Chimiques Belges 1983 92 995-998 Carbon-13 Chemical Shifts of Three Oxo-, Six Monohydroxy-, and Four Dihydroxycyclohexyl Derivatives of Trihexyphenidyl G. Paeme, R. Grim¨¦e and A. Vercruysse Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . ent-3¦Â,6¦Â,12¦Á-trihydroxy-13-epi-manoyl oxide ÏàËÆ¶È:55% Phytochemistry 1994 37 741-747 Chemical-microbiological synthesis of ent-13-epi-manoyl oxides with biological activities Andr¨¦s Garc¨ªa-Granados, M Belinda Jim¨¦nez, Antonio Mart¨ªnez, Andr¨¦s Parra, Francisco Rivas, Jos¨¦ Mar¨ªa Arias Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . varodiol (ent-3¦Â,12¦Á-dihydroxy-13-epi-manoyl oxide ) C19H31O3 ÏàËÆ¶È:55% Phytochemistry 1989 28 1851-1854 The microbiological transformation of some ent-13-epi-manoyl oxide diterpenes by Gibberella fujikuroi Braulio M. Fraga,pedro Gonz¨¢lez,Ricardo Guillermo,Melchor G. Hern¨¢ndez,Juana Rovirosa Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . varodiol ÏàËÆ¶È:55% Phytochemistry 1985 24 1789-1792 Diterpenoids from Sideritis varoi subspecies cuatrecasasii: 13C NMR of ent-13-epi-manoyl oxides functionalized at C-12 A. Garc¨ªa-Granados, A. Mart¨ªnez, A. Molina, M.E. Onorato, M. Rico, A.Saenz de Buruaga, J.M.Saenz de Buruaga Structure 13C NMR ̼Æ×Ä£Äâͼ |

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