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1 .     withacoagin
C28H38O5     ÏàËÆ¶È:67.8%
Bulletin of the Chemical Society of Japan          1988          61          4479-4481
Withacoagin, a New Withanolide from Withania coagulans Roots
Partha Neogi, Masao Kawai, Yasuo Butsugan, Yuji Mori, Makoto Suzuki
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     steroid Lactone
    ÏàËÆ¶È:64.2%
Chemistry of Natural Compounds          1986          22          300-305
WITHASTEROIDS OF PHISALIS VI. 1H AND 13C NMR SPECTRA OF WITHASTEROIDS IXOCARPALACTONE A AND IXOCARPANOLIDE
N. D . Abdullaev, O. E. Vasina,V. A. Maslennikova, and N. K. Abubakirov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     withaphysalin I
C29H38O6     ÏàËÆ¶È:62.0%
Journal of Natural Products          2000          63          1329-1332
Withanolides from Vassobia lorentzii
Rosana I. Misico, Roberto R. Gil, Juan C. Oberti, Adriana S. Veleiro, and Gerardo Burton
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     jaborosalactone 37
    ÏàËÆ¶È:60.7%
Journal of Natural Products          2006          69          783-789
Phytotoxic Withanolides from Jaborosa rotacea
Viviana E. Nicotra, Natalia S. Ramacciotti, Roberto R. Gil, Juan C. Oberti, Gabriela E.Feresin, Cecilia A. Guerrero, Ricardo F. Baggio, M. Teresa Garland, and Gerardo Burton
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     ixocarpanolide
C28H40O6     ÏàËÆ¶È:60.7%
Chemistry of Natural Compounds          1986          22          300-305
WITHASTEROIDS OF PHISALIS VI. 1H AND 13C NMR SPECTRA OF WITHASTEROIDS IXOCARPALACTONE A AND IXOCARPANOLIDE
N. D . Abdullaev, O. E. Vasina,V. A. Maslennikova, and N. K. Abubakirov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     ixocarpanolide
    ÏàËÆ¶È:60.7%
Chemistry of Natural Compounds          1986          22          560-565
WITHASTEROIDS OF Physalis.VII.14¦Á-HYDROXYIXOCARPANOLIDE AND 24,25-EPOXYWITHANOLIDE D
O. E. Vasina, V. A. Maslennikova, N. D. Abdullaev, and N. K. Abubakirov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     6¦Â-Methoxy-22-toluenesulfonyloxy-3¦Á,5-cyclo-5¦Á-23,24-bisnorcholane
    ÏàËÆ¶È:60.7%
Steroids          2005          70          551-562
Preparation of (25R)- and (25S)-26-functionalized steroids as tools for biosynthetic studies of cholic acids
Vladimir A. Khripach, Vladimir N. Zhabinskii, Olga V. Konstantinova, Natalya B. Khripach, Alexey V. Antonchick, Andrey P. Antonchick, Bernd Schneider
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     18-acetoxy-5,6-deoxy-5-withenolide D
    ÏàËÆ¶È:60%
Journal of Natural Products          2001          64          720-725
Trypanocidal Withanolides and Withanolide Glycosides from Dunalia brachyacantha
Jos¨¦ A. Bravo B.,Michel Sauvain, Alberto Gimenez T.,Elfride Balanza, Laurent Serani,Olivier Lapr¨¦vote, Georges Massiot, and Catherine Lavaud
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     1¦Á-Acetoxy-2¦Â,3¦Â-isopropylidendioxy-4¦Á-methyl-5¦Á-androstan-l7-on
C25H38O5     ÏàËÆ¶È:60%
Helvetica Chimica Acta          1980          63          1562-1581
Steroide und Sexualhormone. 261. Mitteilung. Quassinoide Bitterstoffe II. Partialsynthetischer Zugang zu Quassin: Überf¨¹hrung von Testosteron in eine Schl¨¹sselverbindung mit angulärer 8¦Â-Methylgruppe
Johannes Pfenninger, Walter Graf
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     compound 2a
    ÏàËÆ¶È:60%
Phytochemistry          1999          52          1547-1550
Diterpenes from Haplopappus chrysanthemifolius
Francesca Faini, Cecilia Labbe, Rene Torres, Franco Delle Monache, Giuliano Delle Monache
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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11 .     18-acetoxy-5,6-deoxy-5-withenolide D
C30H40O7     ÏàËÆ¶È:60%
Journal of Natural Products          1991          Vol 54          1601
The Withanolides of Iochroma fuchsioides
Robert F. Raffauf, Melvin J. Shemluck, Philip W. Le Quesne
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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12 .     compound 7
C22H34O3     ÏàËÆ¶È:60%
Journal of Natural Products          1992          Vol 55          1421
Diterpene Metabolites from Two Chemotypes of the Marine Sponge Myrmekioderma styx
Susan H. Sennett, Shirley A. Pompeni, Amy E. Wright
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     3¦Â-chlorocholest-5-ene
    ÏàËÆ¶È:59.2%
Chemistry of Natural Compounds          2000          36          595-598
13C NMR SPECTRA OF FUNCTIONALLY SUBSTITUTED 3 ¦Â-CHLORODERIVATIVES OF CHOLESTEROL AND ¦Â -SITOSTEROL
N. V. Kovganko, Zh. N. Kashkan, and E. V. Borisov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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14 .     4¦Â-Chloro-5¦Á-cholestane-3¦Â,5¦Á,6¦Â-triol
    ÏàËÆ¶È:59.2%
Steroids          2007          72          95-104
4,5-Epoxycholestane-3,6-diols: Templates for generating the full set of eight cholestane-3,5,6-triol stereoisomers in multigram scales, but not for a cholestane-3,4,6-triol
Kejun Zhao, Yongfeng Wang, Li Han
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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15 .     2¦Á-Bromo-5¦Á-choiestan-3¦Â-ol
C27H47BrO     ÏàËÆ¶È:59.2%
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

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16 .     3¦Â-Chlorocholest-5-ene
C27H45Cl     ÏàËÆ¶È:59.2%
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

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17 .     labda-7,14-dien-13(R)-ol-¦Á-L-rhamnopyranoside
    ÏàËÆ¶È:57.6%
Journal of Natural Products          2002          65          1102-1106
Five New Labdane Diterpenes from Aster oharai
Sang Zin Choi,Hak Cheol Kwon, Sang Un Choi, and Kang Ro Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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18 .     dicholesteryl ether
    ÏàËÆ¶È:57.6%
Steroids          2008          73          543-548
Unusual electrochemical oxidation of cholesterol
Jan Kowalski, Zenon Łotowski, Jacek W. Morzycki, Jolanta Płoszy¨½ska, Andrzej Sobkowiak, Agnieszka Z. Wilczewska
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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19 .     (20R,22R)-20,22-Dihydroxycholest-5-ene
C27H46O3     ÏàËÆ¶È:57.6%
Steroids          2008          73          1452-1464
Synthesis of ponasterone A derivatives with various steroid skeleton moieties and evaluation of their binding to the ecdysone receptor of Kc cells
Hirokazu Arai, Bunta Watanabe, Yoshiaki Nakagawa, Hisashi Miyagawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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20 .     (24R)-24-methyl-5¦Á-cholest-7-ene-3¦Â,5,6¦Â-triol
C28H46O2     ÏàËÆ¶È:57.6%
Journal of Natural Products          1989          Vol 52          952
New Polyhydrozysterols fron the Di tyoceratid Sponges Hippospongia Communis, Spongia officinalis, Ircinia Variabilis, and Spongionella gracilis
Anna Madaio, Vincenzo Piccialli, Donato Sica, Giuseppe Corriero
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2Â¥2012-10-26 10:49:06
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