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ÏÄÌìµÄÑ©2359: ½ð±Ò+50, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, 3Q! 2013-05-01 15:01:17
1 .     eujavanicol A
C19H32O4     ÏàËÆ¶È:73.6%
Journal of Natural Products          2007          70          1510-1512
Eujavanicols A¨CC, Decalin Derivatives from Eupenicillium jaWanicum
Shou Nakadate,Koohei Nozawa,Hitoshi Horie, Yuichi Fujii, Masahiro Nagai, Tomoo Hosoe,Ken-ichi Kawai,Takashi Yaguchi, and Kazutaka Fukushima
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     eujavanicol A
C19H32O4     ÏàËÆ¶È:73.6%
Chemistry of Natural Compounds          2009          45          753-755
DEHYDRODECALIN DERIVATIVE FROM MARINEISOLATE OF THE FUNGUS Wardomyces inflatus
O. F. Smetanina, A. I. Kalinovskii, A. A. Kicha,A. N. Yurchenko M. V. Pivkin,and T. A. Kuznetsova
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     6¦Â-Hydroxy-15,16-epoxy-labda-8,13(16),14-trien-7-one
C20H28O3     ÏàËÆ¶È:65%
Phytochemistry          1995          40          875-879
Persianone, a dimeric diterpene from Ballota aucheri
A. Rustaiyan, M. H. Mosslemin-Kupaii, F. Papastergiou, J. Jakupovic
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     8¦Á,13-dihydroxy-labda-6,14-diene
C20H32O     ÏàËÆ¶È:65%
Phytochemistry          1991          30          3683-3691
Seco-, nor-, normal and rearranged labdanes fromHaplopappus parvifolius
C. Zdero, F. Bohlmann, H.M. Niemeyer
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     6-oxo-14,15-nor-labda-7-ene
C18H28O2     ÏàËÆ¶È:65%
Phytochemistry          1991          30          3683-3691
Seco-, nor-, normal and rearranged labdanes fromHaplopappus parvifolius
C. Zdero, F. Bohlmann, H.M. Niemeyer
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     3-hydroxy-19-oxo-ent-labda-8(17),13-dien-16,15-olide
C20H28O4     ÏàËÆ¶È:65%
Fitoterapia          2012          83          1506-1513
Quinone reductase (QR) inducers from Andrographis paniculata and identification of molecular target of andrographolide
Yonglei Yuan, Long Ji, Liping Luo, Juan Lu, Xiaoqiong Ma, Zhongjun Ma, Zhe Chen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     3,7-dimethyl-1-[2-O-(2-methylbutyroyl)-3-O-acetyl-¦Â-D-xylopyranosyloxy]-6-octene
C22H38O7     ÏàËÆ¶È:63.6%
Phytochemistry          1988          27          517-522
Terpenoid and flavone constituents of Polemonium viscosum
Donald B. Stierle,Andrea A. Stierle,R.D. Larsen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     eujavanicol B
C19H32O4     ÏàËÆ¶È:63.1%
Journal of Natural Products          2007          70          1510-1512
Eujavanicols A¨CC, Decalin Derivatives from Eupenicillium jaWanicum
Shou Nakadate,Koohei Nozawa,Hitoshi Horie, Yuichi Fujii, Masahiro Nagai, Tomoo Hosoe,Ken-ichi Kawai,Takashi Yaguchi, and Kazutaka Fukushima
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     (3R,4S,5R,7S,9R)-3-hydroxy-9-isobutanoyloxysolavetivone
C19H28O4     ÏàËÆ¶È:63.1%
Journal of Natural Products          1998          61          1516-1519
Phytoalexins from Hairy Roots of Hyoscyamus albus Treated with Methyl Jasmonate
Masanori Kuroyanagi, Takeshi Arakawa, Yoji Mikami, Kenichi Yoshida, Nobuo Kawahar, Tatsuo Hayashi, and Hidehiko Ishimaru
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     (10R)-12-acetoxy-1-oxo-13,14,15,16-tetranor-ent-haliman-18-oate
C19H30O5     ÏàËÆ¶È:63.1%
Molecules          2006          11          792-807
Synthetic Studies Towards the ent-Labdane Diterpenoids: Rearrangement of ent-Halimanes
Isidro S. Marcos, Mar¨ªa J. Sexmero, Felix A. Hern¨¢ndez, Marta Corrales, Pilar Basabe, David D¨ªez and Julio G. Urones
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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11 .     1¦Á-acetoxyeudesm-4-en-6¦Â,11¦ÂH-12,6-olide
    ÏàËÆ¶È:63.1%
Phytochemistry          1994          37          477-485
Sesquiterpene lactones from North African Artemisia species
J.Alberto Marco, Juan F. Sanz-Cervera, Jose M. Pareja, Felix Sancenon, Joan Valles-Xirau
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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12 .     torrentin acetate
    ÏàËÆ¶È:63.1%
Phytochemistry          1989          28          2505-2506
Revision of the structure of torrentin
J.Alberto Marco,Juan F. Sanz,M. Carda
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     14,15-dinor-7-labden-13-one
    ÏàËÆ¶È:63.1%
Phytochemistry          1990          29          2223-2228
Terpenoid compounds from Parentucellia latifolia
J.G. Urones,I.S. Marcos,I. Cubillo,N.Martin Garrido,P. Basabe
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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14 .     (20S)-16-Ene-22-thia-24-nor-26,27-dimethyl-8-ol tert-butyldimethylsilyl ether
C24H46O2SSi     ÏàËÆ¶È:63.1%
Bioorganic & Medicinal Chemistry          2008          16          1796-1815
Synthesis and structure¨Cactivity relationships of 16-ene-22-thia-1¦Á,25-dihydroxy-26,27-dimethyl-19-norvitamin D3 analogs having side chains of different sizes
Hajime Takaku, Yukiko Miyamoto, Shiori Asami, Mika Shimazaki, Sachiko Yamada, Keiko Yamamoto, Nobuyuki Udagawa, Hector F. DeLuca, Masato Shimizu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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15 .     16¦Â,17-dihydroxy-7-oxo-ent-atisan-19-al
C19H26O4     ÏàËÆ¶È:63.1%
Phytochemistry          2010          71          1313-1321
Biotransformation of 7¦Á-hydroxy- and 7-oxo-ent-atis-16-ene derivatives by the fungus Gibberella fujikuroi
Braulio M. Fraga, Pedro Gonzalez, Victoria Gonzalez-Vallejo, Ricardo Guillermo, Luz N. Diaz
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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16 .     ethyl (-)-(3R,4aS,4bS,8R,8aR,10aR)-3-methyl-9-oxo-1,4a,4b,7,8,8a,9,10a-octahydro-2,4,10-trioxaphenanthrene-8-carboxylate
C15H20O6     ÏàËÆ¶È:63.1%
European Journal of Organic Chemistry          2011                   2789-2800
Synthesis of Naturally Occurring Cyclohexene Rings Using Stereodirected Intramolecular Diels¨CAlder Reactions Through Asymmetric 1,3-Dioxane Tethering
Hajer Abdelkafi, Laurent Evanno, Alexandre Deville, Lionel Dubost, Ang¨¨le Chiaroni and Bastien Nay
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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17 .     9¦Á,11-epoxy-androst-4-ene-3,12,17-trione
C19H22O4     ÏàËÆ¶È:63.1%
Tetrahedron          2012          68          9249-9255
Oxidation of unsaturated steroid ketones with hydrogen peroxide catalyzed by Fe(bpmen)(OTf)2. New methodology to access biologically active steroids by chemo-, and stereoselective processes
David Clemente-Tejeda, Alejandro L¨®pez-Moreno, Francisco A. Bermejo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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18 .     18-oxoferruginol
C20H28O2     ÏàËÆ¶È:63.1%
Tetrahedron          2012          68          9612-9615
Short syntheses of (+)-ferruginol from (+)-dehydroabietylamine
Miguel A. Gonz¨¢lez, David P¨¦rez-Guaita
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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19 .     N-pivaloyl-(S)-3-methyl-(S)-2-pentylindoline
C19H29NO     ÏàËÆ¶È:63.1%
Tetrahedron          2013          69          2542-2549
Mitsunobu cyclodehydration of N-pivaloyl-2-aminophenethyl alcohol for asymmetric synthesis of trans-2,3-disubstituted indolines
Kyoung Hee Kang, Yelim Kim, Chan Im, Yong Sun Park
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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20 .     1¦Á-acetoxyeudesm-4-en-6¦ÂH,11¦ÂH-12,6-olide
    ÏàËÆ¶È:63.1%
Natural Medicines          2003          57          114-116
Sesquiterpenoids from Artemisia tenuisecta
Kawazoe Kazuyoshi,Morishita Nao,et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2Â¥2013-04-30 19:38:07
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