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13-C NMR(126Hz,Pyr)73.25,71.67,70.37,43.46,43.08,41.90,38.55,34.27,30.26,29.90,29.59,26.21,22.21,21.86,19.87,16.07

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13-C NMR(126Hz,Pyr)
16.07£¬19.87,21.86,22.21,26.21,29.59,29.90,30.26,34.27,38.55,41.90,43.08,43.46,70.37,71.67,73.25
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ÌýÓêÆ·Üø: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú, ¶àл 2013-01-22 14:17:24
1 .     muurolane-4¦Â,5¦Â,10¦Â-triol
C15H28O3     ÏàËÆ¶È:68.7%
Chemical & Pharmaceutical Bulletin          2003          51(8)          986-989
Cadinane-Type Sesquiterpenes from the Roots of Taiwania cryptomerioides HAYATA
Yueh-Hsiung KUO, Chiou-Fung CHYU, and Hsiu-Chuan LIN
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     (()-3,7,11-trimethyl-1,7,11-dodecanetriol
C15H32LiO3     ÏàËÆ¶È:68.7%
Journal of Natural Products          2002          65          1319-1322
African Elephant Sesquiterpenes. II. Identification and Synthesis of New Derivatives of 2,3-Dihydrofarnesol
Thomas E. Goodwin,Felisia D. Brown, Richard W. Counts, Nichole C. Dowdy, Patrick L. Fraley,Randall A. Hughes, Daniel Z. Liu, Courtney D. Mashburn, Josh D. Rankin, Russell S. Roberson, Katie D. Wooley, Elizabeth L. Rasmussen, Scott W. Riddle, Heidi S. Ridd
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     pterodondiol
C15H28O2     ÏàËÆ¶È:68.7%
Acta Botanica Yunnanica          1993          15(3)          303-305
THREE NEW SESPUITERPENOLS FROM LAGGERA PTERODONTA
LI Shun-Lin, DING Jing-Kai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     1R,3S,6S,7R,10S-7-Isopropyl-4,10-dimethylbicyclo[4.4.0]dec-4-en-3,10-diol
C15H26O2     ÏàËÆ¶È:68.7%
Chemistry of Natural Compounds          2002          38          154-160
SYNTHESIS OF THE ELEUTHESIDE CORE FROM (+)-d-CADINOL:CONSTRUCTION OF SIDE CHAINS ON THE MENTHANE RING
I. P. Tsypysheva, A. M. Kunakova, O. V. Shitikova,L. V. Spirikhin, F. A. Valeev, and G. A. Tolstikov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     Pterodondiol
    ÏàËÆ¶È:68.7%
Journal of Asian Natural Products Research          2007          9          277-283
Sesquiterpenoids from Hedychium yunnanense and Porana discifera, and the structural revision of two sesquiterpenoids from Laggera pterodonta
W.-M. ZHU, Q. ZHAO, S.-L. LI and X.-J. HAO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     1¦Â,4¦Â,5¦Á-trihydroxy-6¦Â-acetoxyeudesmane
C17H30O5     ÏàËÆ¶È:68.7%
Journal of Natural Products          1988          Vol 51          475
Epoxidation Reaction of 6¦Â-Acetoxyeudesmenes and Acid-catalyzed Transformations of the Epoxy Compounds
E. Cabrera, A. Garcia-Granados, M. A. Quecuty
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     pterodondiol
    ÏàËÆ¶È:68.7%
Chinese Pharmaceutical Journal          1995          30          264-265
Chemical study on Laggera pterodonta
Zhao Aihua, Zhu Yan, Wei Junxian
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




8 .     cadinane-4¦Â,5¦Á,10¦Á-triol
C15H28O3     ÏàËÆ¶È:68.7%
Planta Medica          2012          78          1010-1014
Sesquiterpenoids from the Rhizomes of Homalomena occulta
Xie, Xiao-Yu; Wang, Rui; Shi, Yan-Ping:
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     acetylation of cadinanetriol
C17H28O3     ÏàËÆ¶È:64.7%
Planta Medica          1997          63          250-254
Minor Components with Smooth Muscle Relaxing Properties from Scented Myrrh (Commiphora guidotti)
Maria Andersson, Ola Bergendorff, Rudong Shan, Peter Zygmunt, and OIov Sterner
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     12-epilycodoline N-oxide
C16H25NO3     ÏàËÆ¶È:62.5%
Helvetica Chimica Acta          2004          Vol. 87          1963
Lycopodine-Type Lycopodium Alkaloids from Huperzia serrata
Chang-Heng Tan and Da-Yuan Zhu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




11 .     cadinane-4¦Â,5¦Á,10¦Â-triol
C15H28O3     ÏàËÆ¶È:62.5%
Chemical & Pharmaceutical Bulletin          2003          51(8)          986-989
Cadinane-Type Sesquiterpenes from the Roots of Taiwania cryptomerioides HAYATA
Yueh-Hsiung KUO, Chiou-Fung CHYU, and Hsiu-Chuan LIN
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




12 .     (-)1¦Â,4¦Â,6¦Átrihydroxy-eudesmane
C15H28O3     ÏàËÆ¶È:62.5%
Phytochemistry          2008          69          2367-2373
Sesquiterpenoids from Homalomena occulta affect osteoblast proliferation,differentiation and mineralization in vitro
Yong-Mei Hu, Chuan Liu, Ka-Wing Cheng, Herman H.-Y. Sung, Lan D. Williams,Zhong-Lin Yang Wen-Cai Ye
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     (1S,10S)-9¦Á-hydroxy-allo-aromadendrane
C15H26O     ÏàËÆ¶È:62.5%
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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14 .     (1R,4R,5R,8S,9S,13S)-caryolane-5,8,13-triol
C15H26O3     ÏàËÆ¶È:62.5%
Journal of Natural Products          2006          69(10)          1429-1434
Microbial Transformation and Butyrylcholinesterase Inhibitory Activity of (−-Caryophyllene Oxide and Its Derivatives
Muhammad Iqbal Choudhary, Zafar A. Siddiqui, Sarfraz A. Nawaz, and Atta-ur-Rahman
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




15 .     compound 3
    ÏàËÆ¶È:62.5%
Journal of Natural Products          2002          65          1319-1322
African Elephant Sesquiterpenes. II. Identification and Synthesis of New Derivatives of 2,3-Dihydrofarnesol
Thomas E. Goodwin,Felisia D. Brown, Richard W. Counts, Nichole C. Dowdy, Patrick L. Fraley,Randall A. Hughes, Daniel Z. Liu, Courtney D. Mashburn, Josh D. Rankin, Russell S. Roberson, Katie D. Wooley, Elizabeth L. Rasmussen, Scott W. Riddle, Heidi S. Ridd
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




16 .     (4Z,8¦Á,11S)-caryophyll-4(5)-ene-8,14-diol
C15H26O2     ÏàËÆ¶È:62.5%
Journal of Natural Products          2000          63          44-47
Biotransformation of (4E,8R)-Caryophyll-4(5)-en-8-ol by Botrytis cinerea
Rosa Dur¨¢n-Patr¨®n, Josefina Aleu, Rosario Hern¨¢ndez-Gal¨¢n, and Isidro G. Collado
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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17 .     (4Z,3S,8R)-caryophyll-4(5)-ene-3,8-diol
C15H26O2     ÏàËÆ¶È:62.5%
Journal of Natural Products          2000          63          44-47
Biotransformation of (4E,8R)-Caryophyll-4(5)-en-8-ol by Botrytis cinerea
Rosa Dur¨¢n-Patr¨®n, Josefina Aleu, Rosario Hern¨¢ndez-Gal¨¢n, and Isidro G. Collado
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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18 .     7¦ÂH-eudesm-2-ene-4¦Á,11-diol
C15H26O2     ÏàËÆ¶È:62.5%
Journal of Natural Products          1998          61          22-28
Enantioselective Total Syntheses of (-)-7¦ÂH-Eudesmane-4¦Á, 11-diol and (+)-ent-7¦ÂH-Eudesmane-4¦Á, 11-diol
Fumito Shimoma, Hisao Kondo, Saori Yuuya, Toshio Suzuki, Hisahiro Hagiwara, and Masayoshi Ando
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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19 .     4¦Â,5¦Á, 10¦Â-trihydroxycadinane
C15H26O2     ÏàËÆ¶È:62.5%
Planta Medica          1997          63          250-254
Minor Components with Smooth Muscle Relaxing Properties from Scented Myrrh (Commiphora guidotti)
Maria Andersson, Ola Bergendorff, Rudong Shan, Peter Zygmunt, and OIov Sterner
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




20 .     pterodontriol B
    ÏàËÆ¶È:62.5%
Acta Botanica Yunnanica          1994          16(3)          313-314
THE STRUCTURE OF PTERODONTETRAOL FROM LAGGERA PTERODONTA
LI Shun-Lin, DING Jing-Kai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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21 .     pterodontetraol
C15H28O4     ÏàËÆ¶È:62.5%
Acta Botanica Yunnanica          1994          16(3)          313-314
THE STRUCTURE OF PTERODONTETRAOL FROM LAGGERA PTERODONTA
LI Shun-Lin, DING Jing-Kai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




22 .     pterodontriol A
C15H28O3     ÏàËÆ¶È:62.5%
Acta Botanica Yunnanica          1993          15(3)          303-305
THREE NEW SESPUITERPENOLS FROM LAGGERA PTERODONTA
LI Shun-Lin, DING Jing-Kai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




23 .     pterodontriol B
Cl5H28O3     ÏàËÆ¶È:62.5%
Acta Botanica Yunnanica          1993          15(3)          303-305
THREE NEW SESPUITERPENOLS FROM LAGGERA PTERODONTA
LI Shun-Lin, DING Jing-Kai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




24 .     ent-oplopanone
C15H26O2     ÏàËÆ¶È:62.5%
Chemical & Pharmaceutical Bulletin          1987          35          124-135
Marine Natural Products. XVII. Nephtheoxydiol, a New Cytotoxic Hydroperoxy-Germacrane Sesquiterpene, and Related Sesquiterpenoids from an Okinawan Soft Coral of Nephthea sp. (Nephtheidae)
ISAO KITAGAWA,ZHENG CUI,BYENG WHA SON,MOTOMASA KOBAYASHI and YOSHIMASA KYOGOKU
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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25 .     laggerone A
C15H26O3     ÏàËÆ¶È:62.5%
Chinese Chemical Letters          1996          7          1093-1094
EUDESMANES AND EUDESMANOIC GLUCOSIDES FROM LAGGERA PETERODONTA
YU ZHAO,JIAN MIN YUE,JING KAI DING,ZHONG WEN LIN AND HAN DONG SUN
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




26 .     Pterodontriol B
    ÏàËÆ¶È:62.5%
Journal of Asian Natural Products Research          2007          9          277-283
Sesquiterpenoids from Hedychium yunnanense and Porana discifera, and the structural revision of two sesquiterpenoids from Laggera pterodonta
W.-M. ZHU, Q. ZHAO, S.-L. LI and X.-J. HAO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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




27 .     oplopanone
C15H26O4     ÏàËÆ¶È:62.5%
Natural Product Research          2003          17          445-449
A new xanthone from Hedychium gardnerianum
Maria João Carvalho; Lu¨ªs M. Carvalho; Ana Margarida Ferreira; Artur M. S. Silva
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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