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1 .     mustakone
    ÏàËÆ¶È:100%
Phytochemistry          1988          27          3319-3321
Mandassidione and other sesquiterpenic ketones from Cyperus articulatus
B. Nyasse,R. Ghogomu,Tih B.L. Sondengam,M. T. Martin,B. Bodo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     4-oxo-¦Á-ylangene
C15H22O     ÏàËÆ¶È:86.6%
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   Ì¼Æ×Ä£Äâͼ

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3 .     ¦Á-ylangene ketone
    ÏàËÆ¶È:80%
Tetrahedron letters          1977          18          1191-1194
Vulgarone B, a novel sesquiterpene ketone from Chrysanthemum vulgare and its photochemical transformation to vulgarone A
Y. Uchio, A. Matsuo, S. Eguchi, M. Nakayama, S. Hayashi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     tinocordifolin
    ÏàËÆ¶È:66.6%
Phytochemistry          1998          49          1343-1345
Tinocordifolin, a sesquiterpene from Tinospora cordifolia
Rakesh Maury¦Á, Sukhdev S Handa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     isolemnalol
C15H24O     ÏàËÆ¶È:60%
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   Ì¼Æ×Ä£Äâͼ

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6 .     14¦Á-hydroxymatrine
    ÏàËÆ¶È:60%
Chemical & Pharmaceutical Bulletin          1996          44          1951-1953
(-)-14¦Â-Hydroxymatrine, a New Lupine Alkaloid from the Roots of Sophora tonkinensis
Ping XIAO,Jiashi LI,Hajime KUBO,Kazuki SAITO,Isamu MURAKOSHI and Shigeru OHMIYA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     copa-3-en-2¦Á-ol
C15H24O     ÏàËÆ¶È:60%
Phytochemistry          1996          43          811-814
Sesquiterpenoid constituents of Entandrophragma cylindricum
Wlodzimierz M. Daniewski, Waldemar Anczewski, Maria Gumulka, Witold Danikiewicz, Ulla Jacobsson, Torbjorn Norin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     (1S,2S)-1,3,3-trimethyl-2-(3-oxobutyl)cyclohexyl acetate
C15H26O3     ÏàËÆ¶È:60%
Chemistry & Biodiversity          2010          7          421-439
Bioactive Compounds with Added Value Prepared from Terpenes Contained in Solid Wastes from the Olive Oil Industry
Andres Parra, Pilar E. Lopez and Andres Garcia-Granados
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     ¦Á-copaene
    ÏàËÆ¶È:60%
European Journal of Organic Chemistry          1993          1993          1117-1123
Terpenes and Terpene Derivatives, XXXII. New Cadinene and Bisabolene Derivatives from the Essential Oil of Pulicaria gnaphalodes
Peter Weyerstahl, Hans-Christian Wahlburg, Helga Marschall and Abdolhossein Rustaiyan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     4¦Â,8¦Á,10,10-tetramethyl-11-acetyloxytricyclo[6.2.1.0(4.11)]undecane
    ÏàËÆ¶È:58.8%
Journal of Natural Products          1994          Vol 57          738
Inhibition of Botrytis cinerea by New Sesquiterpenoid Compounds Obtained from the Rearrangement of Isocaryophyllene
Isidro G. Collado, Josefina Aleu, Antonio J. Mac¨ªas-S¨¢nchez, Rosario Hern¨¢ndez-Gal¨¢n
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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11 .     chrysothol monoacetyl derivative
C17H28O3     ÏàËÆ¶È:53.3%
Phytochemistry          2006          67          1547-1553
Constituents of Chrysothamnus viscidiflorus
Ahmed A. Ahmed , Mohamed-Elamir F. Hegazy, Nahed M. Hassan,Malgorzata Wojcinska, Joe Karchesy, Paul W. Pare, Tom J. Mabry
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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12 .     juniper camphor
C15H26O     ÏàËÆ¶È:53.3%
Phytochemistry          1998          47          1085-1088
Eudesmane sesquiterpenes from laggera alata
Phila Raharivelomanana, Jean-Pierre Bianchini, Armand R. P. Ramanoelina, Jean R. E. Rasoarahona, Robert Faure, Aime Cambon
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     compound 6
    ÏàËÆ¶È:53.3%
Journal of Natural Products          1994          Vol 57          369
Conformational Analysis of Moreliene Derivatives
Carlos M. Cerda-Garc¨ªa-Rojas, Rosa E. del R¨ªo, Pedro Joseph-Nathan, Luisa U. Rom¨¢n, Juan D. Hern¨¢ndez
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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14 .     indipone
    ÏàËÆ¶È:53.3%
Phytochemistry          1995          40          177-181
Thujopsene- and cis-Muurolane-related sesquiterpenoids from Cupressus bakeri
Laurence G. Cool, Keni Jiang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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15 .     1(10)-Aristolen-13-al
C15H22O     ÏàËÆ¶È:53.3%
Phytochemistry          1995          38          905-907
Revision of the structure of an aristolane sesquiterpene aldehyde isolated from the root of Plectranthus hereroensis and Aristolochia debilis
Benjam¨ªn Rodr¨ªguez, Maria C. de la Torre, Fatima Simoes, Olga Batista, Jos¨¦ Nascimento, Aida Duarte, Ralf Mayer
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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16 .     cyclomyltaylan-3-ol monoketone
    ÏàËÆ¶È:53.3%
Phytochemistry          1991          30          3037-3040
Sesquiterpenoids from the liverwort Bazzania japonica
Yoshinori Asakawa, Masao Toyota, Akiko Ueda, Motoo Tori, Yoshimasa Fukazawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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17 .     10¦Á-ôÇ»ù´Ì²Î-4-ͪ£¨10¦Á-hydroxyoplopan-4-one]
C15H24O2     ÏàËÆ¶È:53.3%
Chinese Traditional and Herbal Drugs          2011          42(4)          664-667
Chemical constituents of Dracocephalum heterophyllum and antibacterial activity
REN Ai-mei
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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18 .     (1S,4R,5R)-1-Isopropyl-4-methylbicyclo[3.1.0]hex-2-en-3-yl trifluoromethanesulfonate
C11H15F3O3S     ÏàËÆ¶È:53.3%
Bioorganic & Medicinal Chemistry          2011          19          2939-2949
Replacement of the hydrophobic part of 9-cis-retinoic acid with cyclic terpenoid moiety results in RXR-selective agonistic activity
Takashi Okitsu ,Kana Sato ,Kinya Iwatsuka, Natsumi Sawada, Kimie Nakagawa , Toshio Okano,Shoya Yamada, Hiroki Kakuta, Akimori Wada
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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19 .     cyclo(L-Pro-D-Leu),(3R,8aS)-3-isobutyl-hexahydropyrrolo[1,2-a]pyrazine-1,4-dione
C11H18N2O2     ÏàËÆ¶È:53.3%
Chinese Journal of Marine Drugs          2011          30(1)          40-43
Preliminary study on antimicrobial activity and bioactive metabolites produced by marine bacteria from Zhejiang coast
HUANG Bei, LIU Xiao-yu, TANG Jing-liang, WANG Jie-yu, HU Hao-yan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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20 .     9-Epi-myrionine
C15H26N2O     ÏàËÆ¶È:53.3%
Organic Letters          2007          Vol. 9, No. 18          3531-3534
Solution and Crystal Conformations of Myrionine, a New 8¦Â-Alkyl-cis-decahydroquinoline of Myrioneuron nutans
Van Cuong Pham, Akino Jossang, Ang¨¨le Chiaroni, Thierry S¨¦venet,Van Hung Nguyen, and Bernard Bodo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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21 .     4,4,4,4',4',4'-Hexafluorovalyl-N-methyl-L-leucyl-L-alanine Benzyl Ester
    ÏàËÆ¶È:53.3%
Helvetica Chimica Acta          2010          93          1583-1601
Stereoselective Synthesis of [5-[4,4,4,4¡ä,4¡ä,4¡ä-Hexafluoro-N-(2-hydroxyethoxy)-D-valine]]- and [5-[4,4,4,4¡ä,4¡ä,4¡ä-Hexafluoro-N-(2-hydroxyethoxy)-L-valine]cyclosporin A
Marcel K. Eberle and Reinhart Keese
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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22 .     ¦Á-Copaene
    ÏàËÆ¶È:53.3%
Magnetic Resonance in Chmesitry          2001          39          621-624
Enantiomeric differentiation of terpenic olefins by carbon-13 NMR using chiral binuclear shift reagents
Nicolas Baldovini, F¨¦lix Tomi and Joseph Casanova
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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23 .     compound 9
C15H22O     ÏàËÆ¶È:53.3%
Phytochemistry          1984          23          1647-1649
Oxidized aristolane sesquiterpenes from Aristolochia debilis
Gerhard R¨¹cker, Ralf Mayer, Eberhard Breitmaier, Georg Will, Armin Kirfel, Mohamed El Kordy
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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24 .     Curcumanolide B
C15H22O2     ÏàËÆ¶È:53.3%
Phytochemistry          1985          24          2629-2633
Curcumenone, curcumanolide A and curcumanolide B, three sesquiterpenoids from curcuma zedoaria
Yoshinori Shiobara, Yoshinori Asakawa, Mitsuaki Kodama, Koji Yasuda, Tsunematsu Takemoto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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25 .     oplopanone
C15H24O2     ÏàËÆ¶È:53.3%
Chinese Traditional and Herbal Drugs          2010          41          1608-1612
Chemical constituents in Senecio vulgaris
LIU Yong-heng; ZHANG Zi-ping; WANG Yong-li
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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26 .     (1R,6R,7R,10S)-6-Hydroxy-7-(1-methylethyl)-10-methylbicyclo[4.4.0]decan-4-one
C14H24O2     ÏàËÆ¶È:53.3%
Journal of the Chemical Society, Perkin Transactions 1          2000                   189-194
Synthesis of sesquiterpene allylic alcohols and sesquiterpene dienes from Cupressus bakeri and Chamaecyparis obtusa
Koon-Sin Ngo and Geoffrey D. Brown
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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27 .     junipercamphor
    ÏàËÆ¶È:53.3%
Natural Product Research and Development          2010          22          1012-1014
Chemical Constituents of Salicornia bigelovii Torr.
XIA Guo-ping; FENG Xu; CHEN Yu; WANG Ming; DONG Yun-fa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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28 .     sophoranol
    ÏàËÆ¶È:53.3%
Natural Product Research and Development          1994          6(1)          10-13
STUDIES ON THE ALKALOIDS OF SOPHORA FLAVESCENS
Zhao Yuying; Pang Qingyun; Liu Jingbo; Chen Yayan; Lou Zhicen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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29 .     (-)-9-epi-myrionine
C15H26N2O     ÏàËÆ¶È:53.3%
The Journal of Organic Chemistry          2008          73          7565-7573
Structure and Total Synthesis of (−-Myrionidine and (−-Schoberine, Antimalarial Alkaloids from Myrioneuron nutans
Van Cuong Pham, Akino Jossang, Philippe Grellier, Thierry Sevenet, Van Hung Nguyen and Bernard Bodo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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30 .     compound 3
    ÏàËÆ¶È:53.3%
Indian Journal of Chemistry          2011          50B          611-614
An efficient microwave technique for exo- to endo-double bond migration in natural products
Kaur, Damandeep; Setia, R R; Chahal, K K; Chhabra, B R
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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31 .     (2-endo-acetoxy-7,7-dimethylbicyclo[2.2.1]hept-1-yl)methylacetate
C14H22O4     ÏàËÆ¶È:53.3%
Russian Journal of Organic Chemistry          2003          39          1076-1082
Reactions of Epoxides Prepared from Some Monoterpenes with Acetic Anhydride on Aluminosilicate Catalysts
L. E. Tatarova, D. V. Korchagina, K. P. Volcho, N. F. Salakhutdinov and V. A. Barkhash
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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32 .     Anthogorgiene A
C15H18O2     ÏàËÆ¶È:53.3%
Journal of Agricultural and Food Chemistry          2012          60          112-123
Anthogorgienes A¨CO, New Guaiazulene-Derived Terpenoids from a Chinese Gorgonian Anthogorgia Species, and Their Antifouling and Antibiotic Activities
Dawei Chen, Shanjiang Yu, Leen van Ofwegen, Peter Proksch, and Wenhan Lin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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33 .     ¦Á-ylangene
    ÏàËÆ¶È:53.3%
European Journal of Organic Chemistry          1993          1993          1117-1123
Terpenes and Terpene Derivatives, XXXII. New Cadinene and Bisabolene Derivatives from the Essential Oil of Pulicaria gnaphalodes
Peter Weyerstahl, Hans-Christian Wahlburg, Helga Marschall and Abdolhossein Rustaiyan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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34 .     moxartenone
C17H24O3     ÏàËÆ¶È:52.9%
Chemical & Pharmaceutical Bulletin          1996          44          1656-1662
Bioactive Constituents of Chinese Natural Medicines. I. New Sesquiterpene Ketones with Vasorelaxant Effect from Chinese Moxa, the Processed Leaves of Artemisia argyi LEVL. et VANT. : Moxartenone and Moxartenolide
Masayuki YOSHIKAWA,Hiromi SHIMADA,Hisashi MATSUDA,Johji YAMAHARA and Nobutoshi MURAKAMI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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35 .     15-copaenyl acetate
    ÏàËÆ¶È:52.9%
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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36 .     6¦Â-acetoxy-(1¦Á,10¦Â),(4¦Â,5R)-diepoxi-2¦Â-hydroxygermacrane
C17H28O5     ÏàËÆ¶È:52.9%
The Journal of Organic Chemistry          2005          70          338-341
Enzyme-Catalyzed Rearrangement of a Diepoxy-germacrane Compound into New 7-epi-Eudesmane Derivatives
Andr¨¦s Garc¨ªa-Granados, Mar¨ªa C. Guti¨¦rrez, Antonio Mart¨ªnez, and Francisco Rivas
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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37 .     compound 29
    ÏàËÆ¶È:52.6%
Journal of Natural Products          1989          Vol 52          481
Preparation and Characterization of Naturally Occurring Longipinene Esters
Pedro Joseph-Nathan, Carlos M. Cerda, Luisa U. Rom¨¢n, Juan D. Hern¨¢ndez
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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38 .     methyl 13-hydroxy-7¦Á,8¦Á-epoxy-14,15-dinor-labdan-17-oate
    ÏàËÆ¶È:50%
Molecules          2004          9          300-322
From Labdanes to Drimanes. Degradation of the Side Chain of Dihydrozamoranic Acid.
Jes¨²s M. Rodilla, D. D¨ªez, J. G. Urones and Pedro M. Rocha
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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39 .     lactapiperanol D
C18H28O5     ÏàËÆ¶È:50%
Chemical & Pharmaceutical Bulletin          1999          47          894-896
Structures of New Marasmane Sesquiterpenoids from Lactarius piperatus(SCOP. : FR.)S. F. GRAY
Yasunori YAOITA,Kaori MACHIDA and Masao KIKUCHI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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40 .     5¦Á,10¦Á-epoxy-pinguisane-11,6-olide-15-carboxylic acid methyl ester
C16H22O5     ÏàËÆ¶È:50%
Phytochemistry          1998          49          1079-1083
Pinguisane sesquiterpenes from the liverwort porella Navicularis,
Michael Bungert, Jens Gabler, Klaus-Peter Adam, Josef Zapp, Hans Becker
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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41 .     (S)-6-((1R,3aR,7aR,E)-4-(bromomethylene)-7a-methyloctahydro-1H-inden-1-yl)-2-methylheptane-2-ol
C19H33BrO     ÏàËÆ¶È:50%
Heterocycles          2010          81          381-394
Synthesis of 20-Epi-eldecalcitol [20-Epi-1¦Á,25-dihydroxy-2¦Â-(3-hydroxypropoxy)vitamin D3: 20-Epi-ED-71]
Madoka Yoshino, Kohei Eto, Keisuke Takahashi, Jun Ishihara, Susumi Hatakeyama, Yoshiyuki Ono, Hitoshi Saito, and Noboru Kubodera
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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42 .     norbotryal acetate
C16H24O3     ÏàËÆ¶È:50%
Phytochemistry          1977          16          1061-1062
Norbotryal acetate, a nor-sesquiterpenoid aldehyde from Botrytis cinerea
Olga Cuevas, James R. Hanson
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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43 .     3¦Â-methoxy-21-hydroxy-5-pregnen-20-one
C22H34O3     ÏàËÆ¶È:50%
Steroids          1982          39          181-190
Acyl migration in the Reformatsky reaction of 21-acyloxy-5-pregnen-20-one derivatives with ethyl bromoacetate
Alicia M. Seldes, Eduardo G. Gros
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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44 .     compound 8
C19H31NO3     ÏàËÆ¶È:50%
The Journal of Organic Chemistry          2005          70          658-663
Structure Elucidation and Synthesis of Lycoposerramine-B, a Novel Oxime-Containing Lycopodium Alkaloid from Lycopodium serratum Thunb.
Kazuaki Katakawa, Mariko Kitajima, Norio Aimi, Hiroko Seki, Kentaro Yamaguchi, Kazuo Furihata, Takashi Harayama, and Hiromitsu Takayama
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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45 .     grandisine B
C16H22N2O     ÏàËÆ¶È:50%
The Journal of Organic Chemistry          2005          70          1889-1892
Grandisine A and B, Novel Indolizidine Alkaloids with Human ¦Ä-Opioid Receptor Binding Affinity from the Leaves of the Australian Rainforest Tree Elaeocarpus grandis
Anthony R. Carroll, Garrie Arumugan, Ronald J. Quinn, Joanne Redburn, Gordon Guymer, and Paul Grimshaw
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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46 .     N-[1,4-diacetyl-7-cyano-6,7,9,10,13,14,14a,15-octahydro-2,11-dimethoxy-3,12,16-trimethyl-10,13-dioxo-6¦Á,7¦Á,9¦Á,14a¦Á,15¦Á-6,15-imino-5H-isoquino[3,2-b][3]benza-zocin-9-yl]-methyl]-2-oxopropanamide
C33H36N4O10     ÏàËÆ¶È:50%
Tetrahedron          2000          56          9937-9944
Structure of Saframycin R
Naoki Saito, Noriko Kameyama, Akinori Kubo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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