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1 .     14-acetyl-12-methoxypodocarpa-8,11,13-triene-7-one
C20H26O3     ÏàËÆ¶È:57.1%
Australian Journal of Chemistry          1993          46          1825-1843
Investigation of the Structures of Some Natural Products From the Neem Tree
JG Bendall, RC Cambie, PS Rutledge and PD Woodgate
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     isodonhenrin B
C23H32O7     ÏàËÆ¶È:56.5%
Chemical & Pharmaceutical Bulletin          2011          59          1562-1566
Cytotoxic ent-Kaurane Diterpenoids from Isodon henryi
Zhuo Hu, Rui Zhan, Xue Du, Jia Su, Xiao-Nian Li, Jian-Hong Yang, Hai-Bo Zhang, Yan Li, Han-Dong Sun, Gan-Peng Li and Jian-Xin Pu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     18-hydroxy-3-deoxyhugorosenone
C20H30O2     ÏàËÆ¶È:52.3%
Phytochemistry          2008          69          200-205
Antifungal rosane diterpenes and other constituents of Hugonia castaneifolia
Lilechi D. Baraza, Cosam C. Joseph, Joan J.E. Munissi, Mayunga H.H. Nkunya,Norbert Arnold, Andrea Porzel, Ludger Wessjohann
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     cinnamadin
C17H24O5     ÏàËÆ¶È:52.3%
Journal of Natural Products          2008          71(1)          123-126
Secondary Metabolites of Cinnamosma madagascariensis and Their #-Glucosidase Inhibitory Properties
Liva Harinantenaina, Katsuyoshi Matsunami, Hideaki Otsuka,Masatoshi Kawahata, Kentaro Yamaguchi, and Yoshinori Asakawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     cinnamodial 11¦Á,12¦Â-dimethyl¦Âacetal
C19H30O6     ÏàËÆ¶È:52.3%
Journal of Natural Products          2008          71(1)          123-126
Secondary Metabolites of Cinnamosma madagascariensis and Their #-Glucosidase Inhibitory Properties
Liva Harinantenaina, Katsuyoshi Matsunami, Hideaki Otsuka,Masatoshi Kawahata, Kentaro Yamaguchi, and Yoshinori Asakawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     deoxycorticosterone
    ÏàËÆ¶È:52.3%
Phytochemistry          1998          49          2359-2362
The microbiological hydroxylation of some steroids with a cortical side chain by Cephalosporium aphidicola
James R. Hanson, A. Christy Hunter
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     compound 10
    ÏàËÆ¶È:52.3%
Phytochemistry          1989          28          3377-3381
Drimane-type sesquiterpenoids from the liverwort Makinoa crispata
Toshihiro Hashimoto,Motoo Tori,Yoshinori Asakawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     1-adamantyl-3-chloro-4-(2-(2,4-dihydroxyphenyl)-5-methoxy-1H-indol-3-yl)azetidin-2-one
C28H29ClN2O4     ÏàËÆ¶È:52.3%
Indian Journal of Chemistry          2010          49B          1398-1405
Synthesis and antiparkinsonian activity of some new adamantyl thiazolidinonyl/azeti-dinonyl in-dole derivatives
Sunil Kumar,Hemlata Kaur,K K Saxena,Monica Sharma,Pinki Vishwakarma & Ashok Kumar*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     (R)-N-benzyloxycarbonyl-S-4-methoxybenzyl-2-methylcysteine-L-threonine methyl ester
C25H32N2O7S     ÏàËÆ¶È:52.3%
Heterocycles          2002          58          601-634
Thiazoline Ring Formation from 2-Methylcysteines and 2-Halomethylalanines
Brant L. Kedrowski and Clayton H. Heathcock*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     cochliodone A
C34H38O12     ÏàËÆ¶È:52.3%
Tetrahedron          2008          64          9636-9645
Bis-spiro-azaphilones and azaphilones from the fungi Chaetomium cochliodes VTh01 and C. cochliodes CTh05
Nutchanat Phonkerd, Somdej Kanokmedhakul, Kwanjai Kanokmedhakul, Kasem Soytong, Samran Prabpai, Palangpon Kongsearee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     (5aR,6aS,10aS,10cR)-7,7,10a,10c-tetra-methyl-2,5a,6,6a,7,8,9,10,10a,10c-decahydro-4H-5-oxa-acephenanthrylene-3-carboxylic acid methyl ester
C21H30O3     ÏàËÆ¶È:52.3%
Tetrahedron          2003          59          9523-9536
Synthetic studies on the preparation of oxygenated spongiane diterpenes from carvone
Antonio Abad, Consuelo Agull¨®, Ana C Cuñat, Ana Bel¨¦n Garcı́a, Carlos Gim¨¦nez-Saiz
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     7¦Á-hydroxy-11-oxo-spongia-13-en-16-one
C20H28O4     ÏàËÆ¶È:52.3%
Tetrahedron          2005          61          1961-1970
Syntheses of oxygenated spongiane diterpenes from carvone. Synthesis of dorisenone C
Antonio Abad, Consuelo Agull¨®, Ana C. Cuñat, Ana Bel¨¦n Garc¨ªa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     11¦Â,17¦Á-dihydroxypregna-4-ene-3,20-dione
    ÏàËÆ¶È:52.3%
Organic Magnetic Resonance          1984          22          586-591
A carbon-13 nuclear magnetic resonance study of the 1,4-diene analogues of steroid hormones and related steroids
Mario D. Gonzalez and Gerardo Burton
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     21-Hydroxypregn-4-ene-3,20-dione deoxycorticosterone
C21H30O3     ÏàËÆ¶È:52.3%
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   Ì¼Æ×Ä£Äâͼ
Domyallbesttohaveahappylife.
4Â¥2013-07-24 10:35:29
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2Â¥2013-07-24 08:45:01
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2Â¥: Originally posted by wangkaibo123 at 2013-07-24 08:45:01
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3Â¥2013-07-24 09:19:14
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