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1 .     (7¦Á)-8-oxoeudesm-4(14)-en-12-oic acid
C15H22O3     ÏàËÆ¶È:60%
Helvetica Chimica Acta          2007          Vol. 90          1586
Cadinane and Eudesmane Sesquiterpenoids from Chloranthus henryi
Bin Wu, Shan He, Xiao-Dan Wu, De-Kang Wu, and Yuan-Jiang Pan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     Xylaranic acid
C15H24O5     ÏàËÆ¶È:60%
Helvetica Chimica Acta          2010          93          796-802
Four New Terpenoids from Xylaria sp. 101
Yao-Yao Li, Zhi-Yu Hu, Chun-Hua Lu and Yue-Mao Shen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     (2E,9E)-6,7-dibromo-2,9-humuradien-8-one
C15H22OBr2     ÏàËÆ¶È:60%
The Journal of Organic Chemistry          1999          64          2667-2672
Chemistry of Zerumbone. 1. Simplified Isolation, Conjugate Addition Reactions, and a Unique Ring Contracting Transannular Reaction of Its Dibromide
Takashi Kitayama and Tadashi Okamoto, Richard K. Hill, Yasushi Kawai and Sho Takahashi, Shigetomo Yonemori, Yukio Yamamoto, Kouichi Ohe and Sakae Uemura, Seiji Sawada
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     compound 13
     ÏàËÆ¶È:60%
Indian Journal of Chemistry Section B          2000          39B          42-56
Two new terpenoid derivatives from a new soft coral species of the Nephthea genus of the India ocean
A S R Anjaneyulu, M V R Krishna Murthy
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     (+)-(3aR,5S,5aS,9aS,9bR)-3a,6,6,9a-tetramethyldodecahydronaphtho[2,1-b]furan-5-yl methanesulfonate
C17H30O4S     ÏàËÆ¶È:58.8%
Tetrahedron          2001          57          5663-5679
The synthesis of Ambrox®-like compounds starting from (+)-larixol
Marjon G Bolster, Ben J.M Jansen, Aede de Groot
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     compound 14
C18H32O3     ÏàËÆ¶È:58.8%
European Journal of Organic Chemistry          2010                   1483-1493
Synthetic Studies Directed Towards Various Homologues of Natural Sesquiterpene-Coumarin Ethers: The Domino Approach
Andrei Corbu, Juan M. Castro, Maurizio Aquino, Zoila Gandara, Pascal Retailleau and Sim¨¦on Arseniyadis
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     compound 6
     ÏàËÆ¶È:56.2%
Phytochemistry          1996          42          771-774
A tetranorfriedolabdane diterpene from Vellozia stipitata
Ângelo C. Pinto, Octavio A. C. Antunes, Moacir G. Pizzolatti, Victor M. Rumjanek
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     compound 24a
C16H24O4     ÏàËÆ¶È:56.2%
Tetrahedron Letters          2004          45          383-386
Carbanion cyclisation of esters. Part 2: Enantiospecific construction of the tricyclic framework of the marine sesquiterpenes, spirodysins
A. Srikrishna, P. Ravi Kumar, S.S.V. Ramasastry
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     tetrahydroakagerine
     ÏàËÆ¶È:55.5%
Australian Journal of Chemistry          1993          46          969-976
The Alkaloids of Ophiorrhiza cf. ferruginea
D Arbain, NH Lajis, DP Putra, MV Sargent, BW Skelton and AH White
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     spiramilactone C
C20H28O4     ÏàËÆ¶È:55%
Phytochemistry          1998          48          1213-1215
Diterpenes from Spiraea japonica
Xiao-Jiang Hao, Jing-Lei Nie
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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11 .     compound 11
     ÏàËÆ¶È:55%
Phytochemistry          1991          30          2991-3000
Diterpenes and norditerpenes from the Aristeguetia group
C. Zdero, F. Bohlmann, R.M. King
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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12 .     (1S,3¦ÁR,4- S,8¦ÁS,9R)-Decahydro-4,8,8-trimethyl-1,4-methanoazulene-9-carboxylic Acid
     ÏàËÆ¶È:53.3%
Helvetica Chimica Acta          2003          Vol. 86          106
The Ozonolysis of Longifolene: A Tool for the Preparation of Useful Chiral Compounds. Configuration Determination of New StereogenicCenters by NMR Spectroscopy and X-Ray Crystallography
Vladimir Dimitrov, Gudrun Hopp Rentsch, Anthony Linden, and Manfred Hesse
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     alismol
     ÏàËÆ¶È:53.3%
Phytochemistry          2003          63          877-881
Guaiane-type sesquiterpenoids from Alisma orientalis
Guo-Ping Peng, Gang Tian, Xian-Feng Huang, Feng-Chang Lou
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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14 .     nardosinanol H
C14H23O4     ÏàËÆ¶È:53.3%
Journal of Natural Products          2008          71(3)          375-380
Nardosinanols A#I and Lemnafricanol, Sesquiterpenes from Several Soft Corals, Lemnalia sp., Paralemnalia clavata, Lemnalia africana, and Rhytisma fulvum fulvum
Ashgan Bishara, Dina Yeffet, Mor Sisso, Guy Shmul, Michael Schleyer, Yehuda Benayahu, Amira Rudi, and Yoel Kashman
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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15 .     cyperusol D
C15H24O3     ÏàËÆ¶È:53.3%
Journal of Natural Products          2004          67          569-576
Structures of New Sesquiterpenes and Hepatoprotective Constituents from the Egyptian Herbal Medicine Cyperus longus
Fengming Xu, Toshio Morikawa, Hisashi Matsuda, Kiyofumi Ninomiya, and Masayuki Yoshikawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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16 .     3¦Â-Hydroxyeudesma-1,11(13)-dieno-12,6¦Â-lactone
C15H20O3     ÏàËÆ¶È:53.3%
Journal of Natural Products          2003          66          810-817
Synthetic Method and Biological Activities of cis-Fused ¦Á-Methylene ¦Ã-Lactones
Yohsuke Higuchi, Fumito Shimoma, and Masayoshi Ando
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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17 .     subergorgiol
C15H24O     ÏàËÆ¶È:53.3%
Journal of Natural Products          2002          65          1033-1036
Two New Subergane-Based Sesquiterpenes from a Taiwanese Gorgonian Coral Subergorgia suberosa
Guey-Horng Wang, Atallah F. Ahmed, Yao-Haur Kuo, and Jyh-Horng Sheu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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18 .     2¦Â-hydroxysubergorgic acid
     ÏàËÆ¶È:53.3%
Journal of Natural Products          2002          65          1033-1036
Two New Subergane-Based Sesquiterpenes from a Taiwanese Gorgonian Coral Subergorgia suberosa
Guey-Horng Wang, Atallah F. Ahmed, Yao-Haur Kuo, and Jyh-Horng Sheu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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19 .     (4R,5R,8S)-4,5-epoxycaryophyllan-8-ol
C15H26O2     ÏàËÆ¶È:53.3%
Journal of Natural Products          1999          62          41-44
Biotransformation of Caryophyllene Oxide by Botrytis cinerea
Rosa Duran, Elena Corrales, Rosario Hern¨¢ndez-Gal¨¢n, and Isidro G. Collado
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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20 .     2-¦Â-hydroxysubergorgic acid
C15H22O3     ÏàËÆ¶È:53.3%
Journal of Natural Products          1998          61          832-834
Studies on the Secondary Metabolites from the Indian Gorgonian Subergorgia suberosa: Isolation and Characterization of Four Analogues of the Cardiotoxin Subergorgic Acid
P. S. Parameswaran, C. G. Naik, S. Y. Kamat, M. S. Puar, P. Das, and Vinod R. Hegde
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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21 .     compound 10
     ÏàËÆ¶È:53.3%
Chemical & Pharmaceutical Bulletin          1994          42          2430-2435
Crude Drugs from Aquatic Plants. V. On the Constituents of Alismatis Rhizoma. (3). Stereostructures of Water-Soluble Bioactive Sesquiterpenes, Sulfoorientalols a, b, c, and d, from Chinese Alismatis Rhizoma
Masayuki YOSHIKAWA,Shoko YAMAGUCHI,Hisashi MATSUDA,Nobumitsu TANAKA,Johji YAMAHARA and Nobutoshi MURAKAMI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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22 .     (1S,10S),(4S,5S)-germacrone-1(10),4-diepoxide
C15H22O3     ÏàËÆ¶È:53.3%
Chemical & Pharmaceutical Bulletin          1991          39          843-853
A Series of Sesquiterpenes with a 7¦Á-Isopropyl Side Chain and Related Compounds Isolated from Curcuma wenyujin
Kenzo HARIMAYA,Ji-Fu GAO,Tamiko OHKURA,Takeshi KAWAMATA,Yoichi IITAKA,Yong-Tian GUO and Seiichi INAYAMA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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23 .     wenjine
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