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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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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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 deliciosa
Asma Nasib, Syed Ghulam Musharraf, Sajjad Hussain, Saifullah Khan,Shazia Anjum, Shamsher Ali, Atta-ur-Rahman, and M. Iqbal Choudhary
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ
2Â¥2013-08-29 11:34:49
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