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»¯ºÏÎï̼Æ×13.7,14.7, 19.7,27.2, 30.9, 31.6, 35.2, 36.5, 36.9,41.3,43.1, 45.4, 48.1, 51.2, 52.3, 66.7, 69.3,125.4, 145.1,164.7, 170.6, 198.9 [ Last edited by ׿Խ_ÏÈ·æ on 2015-4-28 at 12:11 ] |
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̼Æ×¿â£º Nat Syn ²éѯ½á¹û£º¹²²éµ½10¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . compound 17 ÏàËÆ¶È:68.1% Magnetic Resonance in Chemistry 1994 32 565-567 Carbon-13 NMR data for methylated steroids E. Mesk¨®, Gy. Schneider, Gy. Dombi and D. Zeigan Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 19-hydroxykovalic acid C22H36O5 ÏàËÆ¶È:63.6% Phytochemistry 1992 31 1703-1711 Clerodane and labdane derivatives from Olearia teretifolia C. Zdero, F. Bohlmann, R.M. King Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . oblongolide L C22H34O5 ÏàËÆ¶È:63.6% European Journal of Organic Chemistry 2005 2005 4009-4016 New Oblongolides Isolated from the Endophytic Fungus Phomopsis sp. from Melilotus dentata from the Shores of the Baltic Sea Jingqiu Dai, Karsten Krohn, Dietmar Gehle, Ines Kock, Ulrich Flörke, Hans-J¨¹rgen Aust, Siegfried Draeger, Barbara Schulz and Joachim Rheinheimer Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 5¦Á-androstan-3¦Â,5-diol-6,17-dione 3-acetate ÏàËÆ¶È:63.6% Canadian Journal of Chemistry 1979 57 3069-3072 13C nuclear magnetic resonance spectra of some halosteroids, 6-ketosteroids, and related compounds Herbert L. Holland, Everton M. Thomas Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . (Z)-dimethyl 7-oxocass-13(15)-ene-16,18-dioate ÏàËÆ¶È:63.6% Magnetic Resonance in Chemistry 1990 28 529-532 13C nuclear magnetic resonance spectra of several podocarpane and cassane diterpenoids A. Abad, C. Agull¨®, M. Arn¨®, L. R. Domingo and R. J. Zaragoz¨¢ Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 19-Norandrost-4-ene-3,17-dione C18H24O2 ÏàËÆ¶È:63.6% 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 7 . 2¦Â-(4-(Acetoxy-methyl)-1,2,3-triazol-1-yl)-3-hydroxy-5-androstan-17-one C24H35N3O4 ÏàËÆ¶È:62.5% Steroids 2012 77 738-744 Synthesis of ferrocene-labeled steroids via copper-catalyzed azide¨Calkyne cycloaddition. Reactivity difference between 2¦Â-, 6¦Â- and 16¦Â-azido-androstanes Klaudia Feh¨¦r, J¨¢nos Balogh, Zsolt Cs¨®k, Tam¨¢s K¨¦gl, L¨¢szl¨® Koll¨¢r, Rita Skoda-Földes Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . cordobic acid 18-acetate methyl ester ÏàËÆ¶È:60.8% Phytochemistry 1986 25 1389-1392 Labdane diterpenoids from Grindelia discoidea (asteraceae) Barbara N. Timmermann, Joseph J. Hoffmann, Shivanand D. Jolad, Robert B. Bates, Teruna J. Siahaan Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . 3-Hydroxy-2¦Â-(4-methoxycarbonyl-1,2,3-triazol-1-yl)-5-androstan-17-one C23H33N3O4 ÏàËÆ¶È:60.8% Steroids 2012 77 738-744 Synthesis of ferrocene-labeled steroids via copper-catalyzed azide¨Calkyne cycloaddition. Reactivity difference between 2¦Â-, 6¦Â- and 16¦Â-azido-androstanes Klaudia Feh¨¦r, J¨¢nos Balogh, Zsolt Cs¨®k, Tam¨¢s K¨¦gl, L¨¢szl¨® Koll¨¢r, Rita Skoda-Földes Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . Turranin C C23H34O3 ÏàËÆ¶È:60.8% Fitoterapia 2013 90 119-125 New steroids and sesquiterpene from Turraea pubescens Chun-Mao Yuan, Gui-Hua Tang, Xiao-Ying Wang, Yu Zhang, Ming-Ming Cao, Xiao-Hui Li, Yan Li, Shun-Lin Li, Ying-Tong Di, Hong-Ping He, Xiao-Jiang Hao, Hui-Ming Hua Structure 13C NMR ̼Æ×Ä£Äâͼ Copyright © 2009-2011 ÉϺ£Î¢Æ×ÐÅÏ¢¼¼ÊõÓÐÏÞ¹«Ë¾ Shanghai Micronmr Infor Technology Co., Ltd., All Rights Reserved |
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