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ÍõºìÄÝ: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2015-03-29 19:08:38
1 .     7¦Á-H-9(10)-ene-11,12-epoxy-8-oxoeremophilane
C15H22O2     ÏàËÆ¶È:86.6%
Phytochemistry Letters          2014          8          121-125
Fragrant agarofuran and eremophilane sesquiterpenes in agarwood ¡®Qi-Nan¡¯ from Aquilaria sinensis
De-Lan Yang, Hao Wang, Zhi-Kai Guo, Wei Li, Wen-Li Mei, Hao-Fu Dai
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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2 .     7¦Â-H-9(10)-ene-11,12-epoxy-8-oxoeremophilane
C15H22O2     ÏàËÆ¶È:66.6%
Phytochemistry Letters          2014          8          121-125
Fragrant agarofuran and eremophilane sesquiterpenes in agarwood ¡®Qi-Nan¡¯ from Aquilaria sinensis
De-Lan Yang, Hao Wang, Zhi-Kai Guo, Wei Li, Wen-Li Mei, Hao-Fu Dai
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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3 .     (+)-2-[(1S,2S,4aS,8aR)-decahydro-2,5,5,8a-tetramethylnaphthalen-1-yl]ethanol
    ÏàËÆ¶È:62.5%
Helvetica Chimica Acta          2014          97          197-214
Enantioselective Access to (−-Ambrox® Starting from ¦Â-Farnesene
Christian Chapuis
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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4 .     compound 4
    ÏàËÆ¶È:60%
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    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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5 .     15¦Â-hydroxyandrost-4-en-3,17-dione
    ÏàËÆ¶È:57.8%
Journal of Industrial Microbiology & Biotechnology          2006          33          725-733
Studies on the microbial transformation of androst-1, 4-dien-3, 17-dione with Acremonium strictum
Mohammad Ali Faramarzi, Mojtaba Tabatabaei Yazdi, Hoda Jahandar, Mohsen Amini, Hamid Reza Monsef-Esfahani
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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6 .     rumphellolide C
C14H22O3     ÏàËÆ¶È:57.1%
Chemical & Pharmaceutical Bulletin          2007          55(9)          1296-1301
Rumphellolides A¡ªF, Six New Caryophyllane-Related Derivatives from the Formosan Gorgonian Coral Rumphella antipathies
Ping-Jyun SUNG,Li-Fan CHUANG,Jimmy KUO,Jih-Jung CHEN,Tung-Yung FAN,Jan-Jung LI,Lee-Shing FANG,and Wei-Hsien WANG
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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7 .     drimane-11,12-diol
C15H28O2     ÏàËÆ¶È:57.1%
Journal of Natural Products          1999          62          1488-1491
Synthesis of 11, 12-Epoxydrim-8, 12-en-11-ol, 11, 12-Diacetoxydrimane, and Warburganal from (-)-Sclareol
A. F. Barrero, M. Cort¨¦s, E. A. Manzaneda, E. Cabrera, R. Chahboun, M. Lara, and A. R. Rivas
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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8 .     (+)-drimane-8¦Â,11-diol
C15H26O     ÏàËÆ¶È:57.1%
Journal of Natural Products          1996          59          900-901
Absolute Stereochemistry of Puupehenone and Related Metabolites
Sylvia Urban and Robert J. Capon
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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9 .     epi-oxyphyllenone
    ÏàËÆ¶È:57.1%
Molecules          2015          20          1551−1559
New Sesquiterpenoids and a Diterpenoid from Alpinia oxyphylla
Lei Hou, Gang Ding, Baolin Guo, Wenhua Huang, Xiaojian Zhang, Zhiyong Sun and Xiangfen Shi
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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10 .     4,5,7,8-tetrahydro-3,8,8-trimethyl-3a,7-methanoazulene-2,6-dione
C14H18O2     ÏàËÆ¶È:57.1%
Heterocycles          2004          63          1359-1374
Intramolecular Pauson-Khand Reaction of 3-Alkynyl-1-alkylidenecycles: A Convenient Synthesis of [5.n.1.01,5] Tricyclic Compounds
Miyuki Ishizaki,* Mina Masamoto, Osamu Hoshino, Kiyoshi Nishitani, and Hiroshi Hara*
2Â¥2015-03-29 10:56:44
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