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qinpei8901: ½ð±Ò+20, ¡ï¡ï¡ïºÜÓаïÖú 2012-10-28 16:32:49
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²éѯ½á¹û£º¹²²éµ½642¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ |
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