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1 .     15-hydroxyspathulenol
C15H24O2     ÏàËÆ¶È:60%
Journal of Natural Products          2004          67          614-621
Further Labdane and Kaurane Diterpenoids and Other Constituents from Plectranthus fruticosus
Cristina Gaspar-Marques, M. Ftima Simes, and Benjamn Rodrguez
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     ent-3¦Â-Hydroxyspathulenol
    ÏàËÆ¶È:60%
Phytochemistry          2000          53          845-849
Sesquiterpenoids and diterpenoids from the Chilean liverwort Lepicolea ochroleuca
Huei-Ju Liu, Chia-Li Wu, Hans Becker, Josef Zapp
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     Pogostol
C15H28O3     ÏàËÆ¶È:60%
Journal of Natural Products          2012          75          798-801
Guaiane Sesquiterpenes from Biscogniauxia nummularia Featuring Potent Antigerminative Activity
Séverine Amand, Aude Langenfeld, Alain Blond, Joëlle Dupont, Bastien Nay, and Soizic Prado
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     stemaphylline
C17H29NO2     ÏàËÆ¶È:58.8%
Journal of Natural Products          2009          72          848-851
Alkaloids from the Roots of Stemona aphylla
Pitchaya Mungkornasawakul, Sukanda Chaiyong, Thanapat Sastraruji, Araya Jatisatienr, Chaiwat Jatisatienr,Stephen G. Pyne, Alison T. Ung, John Korth,and Wilford Lie
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     pogostol O-methyl ether
C16H28O     ÏàËÆ¶È:56.2%
Journal of Natural Products          1997          60          1054-1056
Pogostol O-Methyl Ether and Artabotrol: Two Novel Sesquiterpenes from the Stem Bark of Artabotrys stenopetalus
Theophilus C. Fleischer, Roger D. Waigh, and Peter G. Waterman
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     8,19-dimethyl-1-oxa-9,10,17,18-tetraaza-8,18-cyclopentacosadien-2,11,16-trione
    ÏàËÆ¶È:56.2%
Chemistry of Natural Compounds          2009          45          465-469
SYNTHESIS OF MACROLIDES WITH N-CONTAINING(AZINE OR HYDRAZIDE) GROUPS
G. Yu. Ishmuratov, M. P. Yakovleva, G. R. Mingaleeva, R. R. Muslukhov, E. M. Vyrypaev, E. G. Galkin,S. P. Ivanov, and A. G. Tolstikov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     (1S,4R,4aR,8aS)-4-isopropyl-6-methyl-1,2,3,4,4a,7,8,8a-octahydronaphthalene-1-carbonitrile
C15H23N     ÏàËÆ¶È:56.2%
The Journal of Organic Chemistry          2011          76          6558-6573
Total Synthesis of 10-Isocyano-4-cadinene and Its Stereoisomers and Evaluations of Antifouling Activities
Keisuke Nishikawa, Hiroshi Nakahara, Yousuke Shirokura, Yasuyuki Nogata, Erina Yoshimura,Taiki Umezawa, Tatsufumi Okino, and Fuyuhiko Matsuda
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     cladioxazole
C16H27NO     ÏàËÆ¶È:56.2%
Tetrahedron Letters          2003          44          6951-6953
Cladioxazole: a novel sesquiterpene from a marine soft coral of genus Cladiella
Athar Ata, Joe Ackerman, Parvataneni Radhika
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     8,19-dimethyl-1-oxa-9,10,17,18-tetraazacyclopentacosa-8,18-diene-2,11,16-trione
C22H38N4O4     ÏàËÆ¶È:56.2%
Russian Journal of Organic Chemistry          2011          47          1410-1415
Synthesis of macrolides containing an azine or hydrazide fragment via successive tishchenko disproportionation and [1 + 1]-condensation
G. Yu. Ishmuratov, G. R. Mingaleeva, M. P. Yakovleva, R. R. Muslukhov and O. O. Shakhanova, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     (¡À)-PM-toxin B
    ÏàËÆ¶È:56.2%
Agricultural and Biological Chemistry          1985          49          149-158
Synthesis of a Stereoisomeric Mixture of (¡À)-PM-Toxin B, a Host-specific Corn Pathotoxin Produced by Phyllosticta maydis
Yoshikatsu SUZUKI, S. J. DANKO, Yoshiki KONO, J. M. DALY, Setsuo TAKEUCHI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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11 .     ¦Á-hydroxy ester
    ÏàËÆ¶È:56.2%
European Journal of Organic Chemistry          1985          1985          378-382
¦Ø-Cycloheptyl-¦Á-hydroxyundecanoic Acid, a New Fatty Acid from a Thermo-acidophilic Bacillus Species
Karl Poralla, G¨¹nther Jung and Hermann Allgaier
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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12 .     3¦Á,7¦Á-dihydroxy-15-oxo-ent-(16S)-kaurane
C20H32O3     ÏàËÆ¶È:55%
Journal of Natural Products          1996          59          952-957
The Biotransformation of Two 3, 15-Oxygenate ent-Kaurane Derivatives by Gibberella fujikuroi
Braulio M. Fraga, Melchor G. Hern¨¢ndez, and Ricardo Guillermo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     eremophil-6-en-11-ol
C15H26O     ÏàËÆ¶È:53.3%
Helvetica Chimica Acta          2008          Vol. 91          1712
Two New Eremophilane-Type Sesquiterpenoids from the Rhizomes of Ligularia veitchiana (Hemsl.) Greenm
Cai-FangWang, Yu Zhao, Yan-Ze Liu, and Zhen-Zhong Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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14 .     eudesm-4(15),7-diene-9¦Á,11-diol
C15H24O2     ÏàËÆ¶È:53.3%
Phytochemistry          2008          69          2088-2094
Three types of sesquiterpenes from rhizomes of Atractylodes lancea
He-Xiang Wang, Chun-Mei Liu, Quan Liu, Kun Gao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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15 .     compound 1a
    ÏàËÆ¶È:53.3%
Phytochemistry          2002          61          885-890
Immunomodulatory sesquiterpene glycosides from Dendrobium nobile
Qinghua Ye, Guowei Qin, Weimin Zhao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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16 .     maaliane-5¦Á,8¦Á,9¦Á-triol
    ÏàËÆ¶È:53.3%
Phytochemistry          2002          59          39-44
Microbial metabolism of partheniol by Mucor circinelloides
Galal T. Maatooq
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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17 .     aromadendra-1,9-diene
C15H26     ÏàËÆ¶È:53.3%
Phytochemistry          2002          60          475-481
Aromadendrane transformations by Curvularia lunata ATCC 12017
Dwight O. Collins, William F. Reynolds, Paul B. Reese
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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18 .     (4S,9S,10R)-4,10,11-tribromo-10,11-seco-lippifoli-1(6)-en-5-one
    ÏàËÆ¶È:53.3%
Journal of Natural Products          2005          68          659-665
Absolute Configuration of Lippifoliane and Africanane Derivatives
Carlos M. Cerda-Garca-Rojas, Angelina del C. Coronel, Marina E.P. de Lampasona, Csar A. N. Cataln, and Pedro Joseph-Nathan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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19 .     (1S,6R,7S,10R)-10-Hydroxy-4(5)-muurolen-3-one
C15H24O2     ÏàËÆ¶È:53.3%
Journal of Natural Products          2004          67          799-805
Isolation of a Library of Aromadendranes from Landolphia dulcis and Its Characterization Using the VolSurf Approach
Brian Skole, Flemming S. Jrgensen, Bogdan A. Budnik, Patrick Ekpe, and Jerzy W. Jaroszewski
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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20 .     (4R,5R,8R)-4,5-epoxycaryophyllan-8-ol
C14H23O2     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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21 .     clovan-2¦Á,9¦Â-diol
C16H28O2     ÏàËÆ¶È:53.3%
Journal of Natural Products          1998          61          1348-1351
The Biotransformation of Some Clovanes by Botrytis cinerea
Isidro G. Collado, James R. Hanson, Antonio J. Mac¨ªas-S¨¢nchez, and D. Mobbs
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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22 .     compound 11
    ÏàËÆ¶È:53.3%
Journal of Natural Products          1997          60          1026-1030
Sesquiterpene Glycosides and Phenylpropanoid Esters from Phonus arborescens (Carthamus arborescens)
Alejandro F. Barrero, Pilar Arteaga, Jos¨¦F. Qu¨ªlez, Ignacio Rodr¨ªguez, and M. Mar Herrador
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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23 .     3¦Â-hydroxy-Pterodontic acid
C15H22O3     ÏàËÆ¶È:53.3%
Acta Botanica Yunnanica          1996          18£¨3£©          349-352
FOUR NEW SESQUITERPENOIDS FROM LAGGERA PTERODONTA
LI Shun-Lin, DING Jing-Kai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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24 .     ¦Â-elemol
    ÏàËÆ¶È:53.3%
Acta Botanica Yunnanica          1995          17(2)          201-203
SESQUITERPENOIDS FROM HEDYCHIUM YUNNANENSE
ZHAO Qing,HAO Xiao-Jiang,CHEN Yao-Zu,ZOU-Cheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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25 .     ¨S9(10)-eremophilen-11-ol
C15H24     ÏàËÆ¶È:53.3%
Chemical & Pharmaceutical Bulletin          1985          33          1148-1153
Agarofuran-, Eudesmane-and Eremophilane-Type Sesquiterpenoids from Alpinia japonica (THUNB.) MIQ.
HIDEJI ITOKAWA,HIROSHI MORITA,KINZO WATANABE,SUSUMU MIHASHI and YOICHI IITAKA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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26 .     8,16-dimethyl-1-oxa-9,10,14,15-tetraaza-8,15-cyclodocosadien-2,11,13-trione
    ÏàËÆ¶È:53.3%
Chemistry of Natural Compounds          2009          45          465-469
SYNTHESIS OF MACROLIDES WITH N-CONTAINING(AZINE OR HYDRAZIDE) GROUPS
G. Yu. Ishmuratov, M. P. Yakovleva, G. R. Mingaleeva, R. R. Muslukhov, E. M. Vyrypaev, E. G. Galkin,S. P. Ivanov, and A. G. Tolstikov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

27 .     (-)-10¦Á-hydroxy-4-muurolen-3-one B
C15H24O2     ÏàËÆ¶È:53.3%
Chinese Chemical Letters          2008          19          1265-1267
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