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²éѯģʽ£ºÄ£ºý²éѯ ̼Æ×Êý¾ÝÊäÈ룺 °´´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺 21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2 ÈܼÁÑ¡Ï Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½87¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 6E,8E-¦¤8-siphonarienfuranone C20H32O3 ÏàËÆ¶È:65% Journal of Natural Products 2012 75 497−501 Polypropionates from the South African Marine Mollusk Siphonaria oculus Candice L. Bromley, Wendy L. Popplewell, Shirley C. Pinchuck, Alan N. Hodgson,and Michael T. Davies-Coleman Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . siphonarienfuranone C20H34O3 ÏàËÆ¶È:59.0% Tetrahedron 1990 46 1669-1678 New metabolites from the marine mollusc siphonaria grisea Manuel Norte, Fernando Cataldo, Antonio G. Gonz¨¢lez, Matias L. Rodr¨ªguez, Catalina . Ruiz-Perez Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 3¦Â-hydroxy-4-pregnen-20-one ÏàËÆ¶È:57.1% Steroids 1985 45 39-51 Synthesis of the allylic gonadal steroids, 3¦Á-hydroxy-4-pregnen-20-one and 3¦Á-hydroxy-4-androsten-17-one, and of 3¦Á-hydroxy-5¦Á-pregnan-20-one J. P. Wiebe, C. Deline, K. D. Buckingham, Vinod Dave, J. B. Stothers Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . cervicol C15H24O ÏàËÆ¶È:55.5% Journal of Natural Products 2004 67 1650-1653 Steroids and Sesquiterpenoids from the Soft Corals Dendronephthya gigantea and Lemnalia cervicorni Chang-Yih Duh, Ali A. H. El-Gamal, Pei-Ying Song, Shang-Kwei Wang, and Chang-Feng Dai Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . compound 4b C22H48O2Si ÏàËÆ¶È:55.5% Heterocycles 2007 72 529-540 Alkyl-and Arylation of Oxacyclic Ethers with Triethylsilyl Triflate¡ª2, 4, 6-Collidine¡ªGilman Reagent Combination: Remarkable Discrimination of Two Ether Oxygens Hiromichi Fujioka, Takuya Ohnaka, Takashi Okitsu, Ozora Kubo, Kazuhisa Okamoto, Yoshinari Sawama, and Yasuyuki Kita Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . (1R*,3S*)-3-[4-(1,1-dimethylheptyl)phenyl]cyclohexanol C21H34O ÏàËÆ¶È:55.5% Bioorganic & Medicinal Chemistry 2008 16 322-335 Synthesis and pharmacology of 1-deoxy analogs of CP-47,497 and CP-55,940 John W. Huffman, Alicia L.S. Thompson, Jenny L. Wiley, Billy R. Martin Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . (1R*,3R*)-3-[4-(1,1-dimethylheptyl)phenyl]cyclohexanol C21H34O ÏàËÆ¶È:55.5% Bioorganic & Medicinal Chemistry 2008 16 322-335 Synthesis and pharmacology of 1-deoxy analogs of CP-47,497 and CP-55,940 John W. Huffman, Alicia L.S. Thompson, Jenny L. Wiley, Billy R. Martin Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . compound 8 ÏàËÆ¶È:55.5% Australian Journal of Chemistry 1984 37 785-793 The chemistry of Eremophila spp. XXI. Structural study of a new eremane diterpene KD Croft, EL Ghisalberti, PR Jefferies, TA Mori, BW Skelton and AH White Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . compound 4d C25H56O2Si2 ÏàËÆ¶È:52.6% Heterocycles 2007 72 529-540 Alkyl-and Arylation of Oxacyclic Ethers with Triethylsilyl Triflate¡ª2, 4, 6-Collidine¡ªGilman Reagent Combination: Remarkable Discrimination of Two Ether Oxygens Hiromichi Fujioka, Takuya Ohnaka, Takashi Okitsu, Ozora Kubo, Kazuhisa Okamoto, Yoshinari Sawama, and Yasuyuki Kita Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 10¦Â-( 1'-Azirinyl)-3¦Â-hydroxyestr-5-en-17-one C20H27O2N ÏàËÆ¶È:52.6% Steroids 1996 61 138-143 Synthesis of 10¦Â-(1'-azirinyl)estr-4-en-3,17-dione as an aromatase inhibitor Vincent C. O. Njar, Jörg D¨¹erkop, Rolf W. Hartmann Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 5¦Â,6¦Á-Dibromoandrostan-I 7-one C19C28OBr2 ÏàËÆ¶È:52.6% Steroids 1995 60 499-505 Competing pathway involved in allylic acetoxylation of androst-5-en-17-one, and oxidation of allylic alcohols with chromium oxides Mitsuteru Numazawa, Mii Tachibana, Miyako Kamiza Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . 4¦Â,5¦Â-Epoxyandrostane-6,17-dione ÏàËÆ¶È:52.6% Steroids 1995 60 499-505 Competing pathway involved in allylic acetoxylation of androst-5-en-17-one, and oxidation of allylic alcohols with chromium oxides Mitsuteru Numazawa, Mii Tachibana, Miyako Kamiza Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . (1R*,3S*)-3-[4-(1,1-dimethyloctyl)phenyl]cyclohexanol C22H36O ÏàËÆ¶È:52.6% Bioorganic & Medicinal Chemistry 2008 16 322-335 Synthesis and pharmacology of 1-deoxy analogs of CP-47,497 and CP-55,940 John W. Huffman, Alicia L.S. Thompson, Jenny L. Wiley, Billy R. Martin Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . (1R*,3R*)-3-[4-(1,1-dimethyloctyl)phenyl]cyclohexanol C22H36O ÏàËÆ¶È:52.6% Bioorganic & Medicinal Chemistry 2008 16 322-335 Synthesis and pharmacology of 1-deoxy analogs of CP-47,497 and CP-55,940 John W. Huffman, Alicia L.S. Thompson, Jenny L. Wiley, Billy R. Martin Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . androsta-3,5-dien-17-one ÏàËÆ¶È:52.6% Helvetica Chimica Acta 2014 97 39-46 Insights into the Synthesis of Steroidal A-Ring Olefins Carla L. Varela, Fernanda M. F. Roleira, Saul C. P. Costa, Alexandra S. C. T. Pinto, Ana I. O. S. Martins, Rui A. Carvalho, Nat¨¦rcia A. Teixeira, Georgina Correia-da-Silva and Elisi¨¢rio Tavares-da-Silva Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . 3¦Â-acetoxyandrost-4-ene-6,17-dione ÏàËÆ¶È:52.3% Steroids 1998 63 650-664 The scope and limitations of the reaction of ¦Ä5-steroids with mercury(II) trifluoroacetate Peter L. D. Ruddock, David J. Williams, Paul B. Reese Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . 19-sulfamoyloxypregn-2-en-20-one C21H33NO4S ÏàËÆ¶È:52.3% Bioorganic & Medicinal Chemistry 2009 17 6526-6533 Synthesis and GABAA receptor activity of 2,19-sulfamoyl analogues of allopregnanolone Fernando J. Dur¨¢n, Valeria C. Edelsztein, Alberto A. Ghini, Mariana Rey, H¨¦ctor Coirini, Philippe Dauban, Robert H. Dodd, Gerardo Burton Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . compound 10 ÏàËÆ¶È:52.3% Magnetic Resonance in Chemistry 1987 25 1087-1090 13C NMR spectra of eudesmanolides. II. Eudesman-12,8-olides J. A. Marco and M. Carda Structure 13C NMR ̼Æ×Ä£Äâͼ |

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