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| 15.43, 18.53, 20.96, 22.24, 24.63, 26.54, 35.20, 37.46, 44.77, 46.07, 48.14, 49.29, 64.31, 117.50, 146.56, 194.15. |
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²éѯ½á¹û£º¹²²éµ½455¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . compound 7b ÏàËÆ¶È:68.7% Indian Journal of Chemistry 1985 24B 1208-1214 Proton & Carbon-13 NMR Studies of trans-Clerodane Diterpenoids & Congeners:Stereochemical Implications & Certain Correlations with cis-Clerodanes A S SARMA & A K GAYEN Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . scortechterpene B C16H26O2 ÏàËÆ¶È:62.5% Journal of Natural Products 2005 68 1010-1017 Xanthone and Sesquiterpene Derivatives from the Fruits of Garcinia scortechinii Yaowapa Sukpondma,Vatcharin Rukachaisirikul, and Souwalak Phongpaichit Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . drechslerine A C14H24O2 ÏàËÆ¶È:62.5% Journal of Natural Products 2002 65 306-313 Rare Sesquiterpenes from the Algicolous Fungus Drechslera dematioidea Claudia Osterhage, Gabriele M. König, Ulrich Höller, and Anthony D. Wright Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . 6¦Á-hydroxyserratidine C16H23NO3 ÏàËÆ¶È:62.5% Natural Product Research 2002 16 149-153 Three New Hydroxylated Serratidine Alkaloids from Huperzia Serrata Chang-Heng Tan; Xiao-Qiang; Shan-Hao Jiang; Da-Yuan Zhu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . 2¦Á-(5-oxopentyl)-2¦Â-methyl-5¦Â-isopropenylcyclohexanone C15H24O2 ÏàËÆ¶È:62.5% Phytochemistry 1998 47 1577-1581 Sesquiterpenoids from Cyperus rotundus Susumu Ohira, Taisuke Hasegawa, Ken-Ichiro Hayashi, Takuji Hoshino, Daisuke Takaoka, Hiroshi Nozaki Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . neohuperzinine C16H23NO3 ÏàËÆ¶È:62.5% Acta Pharmaceutica Sinica 2002 Vol 37 946-949 STRUCTURAL IDENTIFICATION OF NEOHUPERZININE YUAN Shan-qin; ZHAO Yi-min; FENG Rui Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . Cadina-4,11-dien-14-al ÏàËÆ¶È:62.5% Phytochemistry 1995 39 91-97 Sesquiterpenoids and cyclic bisbibenzyls from the liverwort Reboulia hemisphaerica Han-Chao Wei, Shih-Jen Ma, Chia-Li Wu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . torreyol ÏàËÆ¶È:62.5% Phytochemistry 1988 27 1121-1123 Sesquiterpenoids from Pilgerodendron uv¨ªfera M.Luisa Oyarz¨²n,Juan A. Garbarino Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . Solanascone C15H22O ÏàËÆ¶È:62.5% Chemical Communications 1978 563-564 Solanascone: a novel sesquiterpene ketone from Nicotiana tabacum. X-Ray structure determination of the corresponding oxime Takane Fujimori, Reiko Kasuga, Hajime Kaneko, Sadao Sakamura, Masao Noguchi, Akio Furusaki, Nobuhiro Hashiba and Takeshi Matsumoto Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . 10¦Á-Methoxycadinan-4-en-3-one C16H26O2 ÏàËÆ¶È:62.5% Bioorganic & Medicinal Chemistry 2005 13 5915-5920 Two new sesquiterpenoids and anti-HIV principles from the root bark of Zanthoxylum ailanthoides Ming-Jen Cheng, Kuo-Hsiung Lee, Ian-Lih Tsai, Ih-Sheng Chen Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . 7¦Â-Acetoxy-19-hydroxy-ent-trachilobane C22H34O3 ÏàËÆ¶È:60% Phytochemistry 2012 81 60-70 Biotransformation of ent-kaur-16-ene and ent-trachylobane 7¦Â-acetoxy derivatives by the fungus Gibberella fujikuroi (Fusarium fujikuroi) Braulio M. Fraga, Carlo Bressa, Victoria Gonz¨¢lez-Vallejo, Pedro Gonz¨¢lez, Ricardo Guillermo Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . 3¦Á,5-cycloandrost-6-en-17-one ÏàËÆ¶È:57.8% Phytochemistry 1999 52 1279-1282 The microbiological hydroxylation of 3¦Á,5-cycloandrostanes by Cephalosporium aphidicola Caroline S. Bensasson, James R. Hanson, Yvan Le Huerou Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . 3¦Á,5¦Á-cycloandrost-6-en-17-one ÏàËÆ¶È:57.8% 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 -------------------------------------------------------------------------------- 14 . anisotomene-1,12-diol C20H32O ÏàËÆ¶È:57.8% Australian Journal of Chemistry 2000 53 939-944 Chemistry of New Zealand Apiaceae: New irregular diterpenes from Anisotome flexuosa and A. haastii showing conformational exchange John W. van Klink, Anna J. Barlow, Michael H. Benn, Nigel B. Perry and Rex T. Weavers Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . 3-O-Cellobiosyl-4-epihederagenin C42H68O14 ÏàËÆ¶È:57.1% Journal of Agricultural and Food Chemistry 2010 58 5509-5514 New Resistance-Correlated Saponins from the Insect-Resistant Crucifer Barbarea vulgaris Nikoline J. Nielsen, John Nielsen and Dan Staerk Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . (-)-¦Á-Chamipinene, (1S,6S,7S)-2,2,6,8-tetramethyltricyclo[5.3.1.01,6]undec-8-ene C15H24 ÏàËÆ¶È:56.2% Phytochemistry 2005 66 249-260 Sesquiterpenes from Cupressus macrocarpa foliage Laurence G. Cool Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . 1¦Á,6¦Â-dihydroxyambrox C16H28O3 ÏàËÆ¶È:56.2% Journal of Natural Products 2006 69(6) 957-959 Biotransformation of (− -Ambrox by Cell Suspension Cultures of Actinidia deliciosaAsma Nasib, Syed Ghulam Musharraf, Sajjad Hussain, Saifullah Khan,Shazia Anjum, Shamsher Ali, Atta-ur-Rahman, and M. Iqbal Choudhary Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . vittatalactone C16H30O2 ÏàËÆ¶È:56.2% Journal of Natural Products 2005 68 26-30 Vittatalactone, a ¦Â-Lactone from the Striped Cucumber Beetle, Acalymma vittatum Bruce D. Morris, Rebecca R. Smyth, Stephen P. Foster, Michael P.Hoffmann, Wendell L. Roelofs, Stephan Franke, and Wittko Francke Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . 9-thiocyanatopupukeanane C16H25SN ÏàËÆ¶È:56.2% Journal of Natural Products 2003 66 1512-1514 New 9-Thiocyanatopupukeanane Sesquiterpenes from the Nudibranch Phyllidia varicosa and Its Sponge-Prey Axinyssa aculeata Yasman, Ru Angelie Edrada,Victor Wray, and Peter Proksch Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . 4'a¦Á,8'aS)-5',8'a-dimethyl-3',4',4'a,8'a-tetrahydro-1'Hspiro([1,3]dioxolane-2,2'-naphthalene C14H20O2 ÏàËÆ¶È:56.2% Journal of Natural Products 2000 63 1292-1294 Efficient, Highly Enantioselective Synthesis of Selina-1,3,7(11)-trien-8-one, a Major Component of the Essential Oil of Eugenia uniflora Alice Kanazawa, Amaury Patin, and Andrew E. Greene Structure 13C NMR ̼Æ×Ä£Äâͼ |
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-Ambrox by Cell Suspension Cultures of Actinidia deliciosa