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ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½18¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 17¦Â-cyano-17¦Á-hydroxyandrosta-4,9(11)-dien-3-one ÏàËÆ¶È:60% Steroids 1990 55 109-113 The chemistry of 9¦Á-hydroxysteroids. 3. Methods for selective formation and dehydrations of 17¦Â-cyano-9¦Á,17¦Á-dihydroxyandrost-4-en-3-one Jacobus N. M. Batist, Nicolaas C. M. E. Barendse, Arthur F. Marx Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . oleanic acid ÏàËÆ¶È:56% Chinese Traditional and Herbal Drugs 2012 43 1285-1288 Study on chemical constituents from Potentilla supina ZHENG Guang-hai; PIAO Hui-shun Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . ent-13,17-dihydroxy-kauran-15-en-19-oic acid C20H30O4 ÏàËÆ¶È:55% Journal of Guangdong Phamaceutical University 2007 23 489-491 Identification of the chemical constituents of Rubus suavissimus S.Lee LU Hua-chong, WANG Jian-xia Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . compound 3 ÏàËÆ¶È:54.5% Steroids 1989 54 1-10 Carbon-13 nuclear magnetic resonance spectra of D-homoannulated 17-hydroxypregnan-20-ones Richard W. Draper, Mohindar S. Puar Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 11¦Â,17¦Á-Dihydroxy-17¦Â-hydroxymethyl-Dhomoandrosta-4-ene-3,17a-dione C21H30O5 ÏàËÆ¶È:52.3% Steroids 2006 71 1091-1096 D-homoannulation of 17¦Á,21-dihydroxy-20-keto steroids (corticosteroids) Angelo Liguori, Francesca Perri, Carlo Siciliano Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . Pregn-17(20)-ene-3¦Â,21-diol C21H34O2 ÏàËÆ¶È:52.3% Steroids 2011 76 497-501 A convenient synthesis of the side chain of loteprednol etabonate-An ocular soft corticosteroid from 20-oxopregnanes using metal-mediated halogenation as a key reaction Pritish Chowdhury∗, Juri Moni Borah, Papori Goswami, Archana Moni Das Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . haterumaimide F C20H30ClNO4 ÏàËÆ¶È:50% Journal of Natural Products 2001 64 1169-1173 Haterumaimides F-I, Four New Cytotoxic Diterpene Alkaloids from an Ascidian Lissoclinum Species M. Jasim Uddin, Susumu Kokubo, Katsuhiro Ueda, Kiyotake Suenaga, and Daisuke Uemura Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . haterumaimide G C20H28ClNO4 ÏàËÆ¶È:50% Journal of Natural Products 2001 64 1169-1173 Haterumaimides F-I, Four New Cytotoxic Diterpene Alkaloids from an Ascidian Lissoclinum Species M. Jasim Uddin, Susumu Kokubo, Katsuhiro Ueda, Kiyotake Suenaga, and Daisuke Uemura Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . compound 2 ÏàËÆ¶È:50% Steroids 1989 54 1-10 Carbon-13 nuclear magnetic resonance spectra of D-homoannulated 17-hydroxypregnan-20-ones Richard W. Draper, Mohindar S. Puar Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . compound 2C ÏàËÆ¶È:50% Steroids 1989 54 1-10 Carbon-13 nuclear magnetic resonance spectra of D-homoannulated 17-hydroxypregnan-20-ones Richard W. Draper, Mohindar S. Puar Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . compound 4A ÏàËÆ¶È:50% Steroids 1989 54 1-10 Carbon-13 nuclear magnetic resonance spectra of D-homoannulated 17-hydroxypregnan-20-ones Richard W. Draper, Mohindar S. Puar Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . nodosin ÏàËÆ¶È:50% Modern Chinese Medicine 2007 9(8) 10-11 Studies on the chemical Con stitun ts from Isodon Se rra (Maxim.) Kudo Liu Jinxiu, Gao Huimin, Wang Zhimin, Wang Weihao, Fu Xuetao Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . haterumaimide E C20H30NO4Cl2 ÏàËÆ¶È:50% Heterocycles 2001 54 1039-1047 Haterumaimides A-E, Five New Dichlorolissoclimide-Type Diterpenoids from an Ascidian, Lissoclinum Sp. Md. Jasim Uddin, Susumu Kokubo, Kiyotake Suenaga, Katsuhiro Ueda, and Daisuke Uemura Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . nodosin C20H26O6 ÏàËÆ¶È:50% Food Chemistry 2012 131 1009-1014 Isolation and identification of ent-kaurane-type diterpenoids from Rabdosia serra (MAXIM.) HARA leaf and their inhibitory activities against HepG-2, MCF-7, and HL-60 cell lines Lianzhu Lin, Qing Gao, Chun Cui, Haifeng Zhao, Liwu Fu, Liming Chen, Bao Yang, Wei Luo, Mouming Zhao Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . 3¦Á,5-cyclo-5¦Á-androstan-1¦Â,7¦Â,17¦Â-triol C19H30O3 ÏàËÆ¶È:50% Canadian Journal of Chemistry 1990 68 696-700 Enzymic hydroxylation and sulfoxidation of cyclopropyl compounds by fungal biotransformation Herbert L. Holland, Michael J. Chernishenko, Morgan Conn, Anthony Munoz, T. Samuel Manoharan, Michael A. Zawadski Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . (+)-2-[(1S,2R,4aS,8aS)-decahydro-2,5,5,8a-tetramethylnaphthalen-1-yl]-2-hydroxyacetonitrile(major isomer) ÏàËÆ¶È:50% Helvetica Chimica Acta 2014 97 197-214 Enantioselective Access to (− -Ambrox® Starting from ¦Â-FarneseneChristian Chapuis Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . haterumaimide Q C22H31NO4 ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 2006 14 6954-6961 Cytotoxic labdane alkaloids from an ascidian Lissoclinum sp.: Isolation, structure elucidation, and structure¨Cactivity relationship Jasim Uddin, Katsuhiro Ueda, Eric R.O. Siwu, Masaki Kita, Daisuke Uemura Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . compound 5 ÏàËÆ¶È:50% The Journal of Organic Chemistry 1979 44 2999-3003 Tetracyclic analogs of the rosane lactones from Eupatorium album Werner Herz, Serengolam V. Govindan, John F. Blount Structure 13C NMR ̼Æ×Ä£Äâͼ |

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