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chenbangjiao: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2014-10-10 16:50:35
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1 .     (1R,10R)-9¦Â-hydroxyaromadendrane
C15H26O     ÏàËÆ¶È:66.6%
Phytochemistry          2002          60          475-481
Aromadendrane transformations by Curvularia lunata ATCC 12017
Dwight O. Collins, William F. Reynolds, Paul B. Reese
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2 .     (1S,10S)-9¦Á-hydroxy-allo-aromadendrane
C15H26O     ÏàËÆ¶È:60%
Phytochemistry          2002          60          475-481
Aromadendrane transformations by Curvularia lunata ATCC 12017
Dwight O. Collins, William F. Reynolds, Paul B. Reese
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
3 .     [1RS,2RS,5E,9SR,10RS]-1,5,8,8-tetramethylbicyclo[8.1.0]undec-5-ene-2,9-diol
C15H26O2     ÏàËÆ¶È:60%
Journal of Natural Products          2005          68          1441-1442
A Stable Rearrangement Product of Humulene-4,5-epoxide
Raymond M. Carman
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
4 .     11-Hydroxy-4,5-secoeudesmane-4,5-dione
    ÏàËÆ¶È:60%
Phytochemistry          1995          39          603-607
Sesquiterpenes from leaves of Cryptomeria japonica
Wen-Chiung Su, Jim-Min Fang, Yu-Shia Cheng
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
5 .     (1R,4R,9S)-5-hydroxy-caryophyll-3Z-en-14-al
C15H24O2     ÏàËÆ¶È:60%
Phytochemistry          1990          29          757-763
Rearranged caryophyllenes by biotransformation with Chaetomium cochliodes
Wolf-Rainer Abraham,Ludger Ernst,Hans-Adolf Arfmann
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
6 .     [(1R,2R,5R)-1-allyl-2-isopropyl-5-methylcyclopentyl]methanol
C13H24O     ÏàËÆ¶È:60%
European Journal of Organic Chemistry          2011                   5167-5175
Enantioselective Synthesis of the Unnatural Enantiomers of the Fungal Sesquiterpenoids Acorenone and Trichoacorenol
Nelson L. Brock and Jeroen S. Dickschat
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
7 .     N,N,N-Trimethyl-3-(2-(2-octanoyloxazol-5-yl)ethylsulfonyl)propan-1-ammonium iodide
C19H35N2O4S     ÏàËÆ¶È:56.2%
Bioorganic & Medicinal Chemistry          2012          20          1100-1112
Design, synthesis and evaluation of polar head group containing 2-keto-oxazole inhibitors of FAAH
Marion Rusch,Stefan Zahov,Ingrid R. Vetter, Matthias Lehr, Christian Hedberg
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
8 .     (+)-2-[(1S,2S,4aS,8aR)-decahydro-2,5,5,8a-tetramethylnaphthalen-1-yl]ethanol
    ÏàËÆ¶È:56.2%
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
9 .     compound 2
C20H30O     ÏàËÆ¶È:55%
Journal of Natural Products          2006          69          1411-1416
Cytotoxic Constituents from the Formosan Soft Coral Clavularia inflata var. luzoniana
Shang-Kwei Wang, Min-Jay Huang, and Chang-Yih Duh
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
10 .     (10¦Â)-10-Hydroxyaristolan-9-one
C15H24O2     ÏàËÆ¶È:53.3%
Helvetica Chimica Acta          2007          Vol. 90          385
Aristolane Sesquiterpenes and Highly Brominated Indoles from the Marine Red Alga Laurencia similis (Rhodomelaceae)
Nai-Yun Ji, Xiao-Ming Li, Lan-Ping Ding, and Bin-Gui Wang
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
11 .     4-Epicurcumenol
C15H22O2     ÏàËÆ¶È:53.3%
Chemical & Pharmaceutical Bulletin          2001          49(12)          1558-1566
Medicinal Foodstuffs. XXVIII.1) Inhibitors of Nitric Oxide Production and New Sesquiterpenes, Zedoarofuran, 4-Epicurcumenol,Neocurcumenol, Gajutsulactones A and B, and Zedoarolides A and B, from Zedoariae Rhizoma
Hisashi MATSUDA, Toshio MORIKAWA, Iwao TOGUCHIDA, Kiyofumi NINOMIYA, and Masayuki YOSHIKAWA
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
12 .     1a ,10a -dihydro-derivative
    ÏàËÆ¶È:53.3%
Chemical & Pharmaceutical Bulletin          2001          49(12)          1558-1566
Medicinal Foodstuffs. XXVIII.1) Inhibitors of Nitric Oxide Production and New Sesquiterpenes, Zedoarofuran, 4-Epicurcumenol,Neocurcumenol, Gajutsulactones A and B, and Zedoarolides A and B, from Zedoariae Rhizoma
Hisashi MATSUDA, Toshio MORIKAWA, Iwao TOGUCHIDA, Kiyofumi NINOMIYA, and Masayuki YOSHIKAWA
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
13 .     drimenal
C15H24O     ÏàËÆ¶È:53.3%
Phytochemistry          2004          65          2583-2588
Bioactivity guided isolation of antifungal compounds from the liverwort Bazzania trilobata (L.) S.F. Gray
Jochen M. Scher, John-Bryan Speakman, Josef Zapp, Hans Becker
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
14 .     (1R,10R)-aromadendran-9-one
C15H24O     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    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
15 .     (1R,10R)-13-hydroxyaromadendr-9-one
C15H24O2     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    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
16 .     (-)-(1S,6S,9R)-4-acetyl-1-hydroxy-6-isopropyl-9-methylbicyclo[4.3.0]non-4-en-3-one
C15H22O3     ÏàËÆ¶È:53.3%
Journal of Natural Products          2006          69          1261-1266
Minor Sesquiterpenes with New Carbon Skeletons from the Brown Alga Dictyopteris divaricata
Fuhang Song, Xiuli Xu, Shuai Li, Sujuan Wang, Jielu Zhao,Yongchun Yang, Xiao Fan, Jiangong Shi, and Lan He
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
17 .     compound 2a
C15H22O3     ÏàËÆ¶È:53.3%
Journal of Natural Products          2004          67          31-36
Africane-Type Sesquiterpenoids from the Argentine Liverwort Porella swartziana and Their Antibacterial Activity
Graciela Bovi Mitre, Norma Kamiya, Alicia Bardn, and Yoshinori Asakawa
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
18 .     (-)-(1R,6S,7S,10R)-1-hydroxycadinan-3-en-5-one
C15H24O2     ÏàËÆ¶È:53.3%
Journal of Natural Products          2004          67          1644-1649
Cadinane Sesquiterpenes from the Brown Alga Dictyopteris divaricata
Fuhang Song, Xiao Fan, Xiuli Xu, Jielu Zhao, Yongchun Yang, and Jiangong Shi
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
19 .     silphinen-3,5-dione
C15H20O2     ÏàËÆ¶È:53.3%
Journal of Natural Products          2002          65          448-453
C-5-Substituted Antifeedant Silphinene Sesquiterpenes from Senecio palmensis
Mat¨ªas Reina, Matthias Nold, Omar Santana,Juan Carlos Orihuela, and Azucena Gonz¨¢lez-Coloma
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
20 .     mirabilin B
C15H23N3     ÏàËÆ¶È:53.3%
Journal of Natural Products          1997          60          704-707
Three New Tricyclic Guanidine Alkaloids from the Sponge Batzella sp.
Ashok D. Patil, Alan J. Freyer, Priscilla Offen, Mark F. Bean, and Randall K. Johnson
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
21 .     compound 16
    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    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
22 .     compound 1
    ÏàËÆ¶È:53.3%
Phytochemistry          2000          55          749-753
The stereochemistry of ledol from Renealmia chrysotrycha: an NMR study
Maria Auxiliadora C. Kaplan, Helena R.L. Pugialli, Daise Lopes, Hugo E. Gottlieb
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
23 .     tricyclo[5,3,1,0(2,4)]-3-aldehyde-3,11-dimethyl-8-methanoic acid
C15H22O3     ÏàËÆ¶È:53.3%
Chemistry of Natural Compounds          2008          44          308-310
A NOVEL SESQUITERPENOID FROM Ecdysanthera rosea
Fu-Quan Xu, Hai-Yang Liu,Chang-Xiang Chen, and Hui-Min Zhong
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
24 .     aristolan-10-ol-9-one
C15H24O2     ÏàËÆ¶È:53.3%
Chinese Chemical Letters          2007          18          178-180
Two new aristolane sesquiterpenes from Laurencia similis
Nai Yun Ji, Xiao Ming Li, Lan Ping Ding, Bin Gui Wang
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
25 .     3-(1',2',2'-Trimethyl-6'-oxo-1'-cyclohexyl)propionsaure-methylester
C13H22O3     ÏàËÆ¶È:53.3%
Helvetica Chimica Acta          1980          63          1833-1855
Photochemische Reaktionen 111. Mitteilung [1] Zur Photochemie , -ungesättigter , -Epoxyester I: Singulett- versus Triplettreaktivität
Alex Peter Alder, Hans Richard Wolf, Oskar Jeger
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
26 .     10-Hydroxyaristolan-9-one
C15H24O2     ÏàËÆ¶È:53.3%
Molecules          2009          14          1889-1897
Sesquiterpenes from Laurencia similis
Hua Su, Da-Yong Shi, Jing Li, Shu-Ju Guo, Li-Li Li, Zhao-Hui Yuan and Xiao-Bin Zhu
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
27 .     Aristolan-9-en-1-one
C15H22O     ÏàËÆ¶È:53.3%
Molecules          2009          14          1889-1897
Sesquiterpenes from Laurencia similis
Hua Su, Da-Yong Shi, Jing Li, Shu-Ju Guo, Li-Li Li, Zhao-Hui Yuan and Xiao-Bin Zhu
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2Â¥2014-10-08 11:52:13
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