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ÍõºìÄÝ: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2015-03-29 19:08:38
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ÍõºìÄÝ: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2015-03-29 19:08:38
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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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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-FarneseneChristian Chapuis Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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* |
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