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²éѯ½á¹û£º¹²²éµ½18¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . 3-Ethylcarbamoyl-16,17[d]-pyrimidino-5-androsten-3¦Â-ol C24H33N3O2 ÏàËÆ¶È:62.5% Steroids 2002 67 749-756 Syntheses and advanced NMR structure determination of androsteno-[17,16-d]-pyrimidine derivatives Peter Forgo, Ir¨¦n Vincze Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . compound 7C ÏàËÆ¶È:60.8% 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 -------------------------------------------------------------------------------- 3 . 3¦Â-Acetoxy-17-hydroxy-17-methyl-16-nitrile-16,17-seco-5-androstene C22H33NO3 ÏàËÆ¶È:56.5% Steroids 2001 66 645-653 New D-modified androstane derivatives as aromatase inhibitors Katarina M. Penov Gai, Slobodanka M. Stankovi, J¨¢nos J. Csan¨¢di, Evgenija A. Djurendi, Marija N. Saka, Ljubica Medi Mijaevi, Otto N. Arcson, Srdjan Z. Stojanovi, Silvana Andri, Dora Molnar Gabor, Radmila Kovaĕević Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . compound 2b ÏàËÆ¶È:55.5% Australian Journal of Chemistry 1977 30 917-921 Carbon-13 nuclear magnetic resonance spectroscopy of naturally occurring substances. LI. Solanum glycoalkaloids RJ Weston, HE Gottlieb, EW Hagaman and E Wenkert Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . 16,17[d]-Pyrimidino-androst-5-en-3¦Â-ol C21H28N2O ÏàËÆ¶È:52.1% Steroids 2002 67 749-756 Syntheses and advanced NMR structure determination of androsteno-[17,16-d]-pyrimidine derivatives Peter Forgo, Ir¨¦n Vincze Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . compound 3D ÏàËÆ¶È:52.1% 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 -------------------------------------------------------------------------------- 7 . compound 6D ÏàËÆ¶È:52.1% 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 -------------------------------------------------------------------------------- 8 . compound 7D ÏàËÆ¶È:52.1% 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 -------------------------------------------------------------------------------- 9 . abiesadine C C20H32O5 ÏàËÆ¶È:52.1% Bioorganic & Medicinal Chemistry 2010 18 744-754 Isolation, structure, and bioactivities of abiesadines A¨CY, 25 new diterpenes from Abies georgei Orr Xian-Wen Yang, Lin Feng, Su-Mei Li, Xiao-Hua Liu, Yong-Li Li, Liang Wu, Yun-Heng Shen, Jun-Mian Tian, Xi Zhang, Xin-Ru Liu, Ning Wang, Yonghong Liu, Wei-Dong Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . (4R)-4-ethenyl-2-[(2R,3S,5S)-2,3,5-trimethyl-7-((2R)-N-methyl-2-methylbutyramido)-heptyl]oxazoline C21H38N2O2 ÏàËÆ¶È:52.1% Tetrahedron 2004 60 6859-6880 An expeditious total synthesis of kalkitoxins: determination of the absolute stereostructure of natural kalkitoxin Fumiaki Yokokawa, Toshinobu Asano, Tatsufumi Okino, William H. Gerwick, Takayuki Shioiri Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . (4S)-4-ethenyl-2-[(2S,3R,5R)-2,3,5-trimethyl-7-((2S)-N-methyl-2-methylbutyramido-heptyl)]oxazoline C21H38N2O2 ÏàËÆ¶È:52.1% Tetrahedron 2004 60 6859-6880 An expeditious total synthesis of kalkitoxins: determination of the absolute stereostructure of natural kalkitoxin Fumiaki Yokokawa, Toshinobu Asano, Tatsufumi Okino, William H. Gerwick, Takayuki Shioiri Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . Cyclospongiaquinone-2 C22H30O4 ÏàËÆ¶È:52.1% Australian Journal of Chemistry 1978 31 2685-2697 New quinones from a dictyoceratid sponge R Kazlauskas, PT Murphy, RG Warren, RJ Wells and JF Blount Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . triptocalline B C28H42O3 ÏàËÆ¶È:50% Helvetica Chimica Acta 2007 Vol. 90 277 Novel Triterpenoids from Microtropis triflora with Antitumor Activities Kui-Wu Wang, Hong Zhang and Yuan-Jiang Pan Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . ursodeoxycholic acid ÏàËÆ¶È:50% China Journal of Chinese Materia Medica 2010 35 2416-2419 Chemical constituents of bear bile LUO Qiang; CHEN Quancheng; WU Yao; JIANG Miaomiao; CHEN Zhihong; ZHANG Xiaokun; CHEN Haifeng Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . chenodeoxychloic acid ÏàËÆ¶È:50% China Journal of Chinese Materia Medica 2010 35 2416-2419 Chemical constituents of bear bile LUO Qiang; CHEN Quancheng; WU Yao; JIANG Miaomiao; CHEN Zhihong; ZHANG Xiaokun; CHEN Haifeng Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . 3-[2-(3-tert-Butyl-ureido)-3,3-dimethyl-butyryl]-6,6-dichloro-3-aza-bicyclo[3.1.0]hexane-2-carboxylic acid(2-carbamoyl-1-cyclobutylmethyl-2-oxo-ethyl)-amide C25H39N5O5Cl2 ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 2008 16 1874-1883 Potent and selective small molecule NS3 serine protease inhibitors of Hepatitis C virus with dichlorocyclopropylproline as P2 residue Kevin X. Chen, Bancha Vibulbhan, Weiying Yang, Kuo-Chi Cheng, Rong Liu, John Pichardo, Nancy Butkiewicz, F. George Njoroge Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . (4R)-4-phenyl-3-[(3R,4S,6R)-3,4,6-trimethyl-8-((2S)-N-methyl-2-methylbutyramido)-octanoyl]-2-oxa-zolidinone C26H40N2O4 ÏàËÆ¶È:50% Tetrahedron 2004 60 6859-6880 An expeditious total synthesis of kalkitoxins: determination of the absolute stereostructure of natural kalkitoxin Fumiaki Yokokawa, Toshinobu Asano, Tatsufumi Okino, William H. Gerwick, Takayuki Shioiri Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . 24(S)-ergostan-3¦Â,5¦Á,6¦Â,25-tetraol C28H50O4 ÏàËÆ¶È:50% Acta Scientiarum Naturalium Universitatis Sunyatseni 2005 44(4) 59-62 Studies on the Chemical Constituents of Soft Coral Sarcophyton tortuosum LAN Wen-jian, SU Jing-yu, ZENG Long-mei Structure 13C NMR ̼Æ×Ä£Äâͼ |
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4Â¥2012-11-25 23:50:24
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