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13C NMR (101 MHz, CDCl3) ¦Ä              


14.65,15.15,16.19,17.21,17.54,18.48,28.73,29.69,30.17,35.91,35.96,45.96,48.91,208.38,212.92
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mrdone.0907: ½ð±Ò+20, ¡ïÓаïÖú 2013-10-25 13:20:35
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1 .     compound 15
    ÏàËÆ¶È:60%
Phytochemistry          1998          47          1577-1581
Sesquiterpenoids from Cyperus rotundus
Susumu Ohira, Taisuke Hasegawa, Ken-Ichiro Hayashi, Takuji Hoshino, Daisuke Takaoka, Hiroshi Nozaki
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     compound(part ref 98)
    ÏàËÆ¶È:60%
Phytochemistry          1994          37          597-623(605)
The daucane (carotane) class of sesquiterpenes
Emilio L. Ghisalberti
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     compound 10
    ÏàËÆ¶È:60%
Tetrahedron Letters          2002          43          221-224
Synthesis of the napalilactone and pathylactone A spirocyclic skeleton
James R. Vyvyan, Courtney A. Rubens, Jason A. Halfen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     (5R,6S,7S,10S)-7-isopropyl-10-methyl-6-trimethylsilyloxyspiro[4.5]decan-2-one
C17H32O2Si     ÏàËÆ¶È:60%
Tetrahedron          2005          61          10853-10860
Silicon guided rearrangement of epoxydecalines to spirocyclic compounds. Synthesis of gleenol and axenol from carvone
Gonzalo Blay, Ana M. Collado, Begoña Garc¨ªa, Jos¨¦ R. Pedro
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     Gibberosin A
C19H28O3     ÏàËÆ¶È:57.8%
Bulletin of the Chemical Society of Japan          2006          79          1547-1551
New ¦Â-Caryophyllene-Derived Terpenoids from the Formosan Soft Coral Sinularia gibberosa
Shin-Pin Chen, Chih-Hua Chao, Ho-Cheng Huang, Yang-Chang Wu, Chung-Kuang Lu, Chang-Feng Dai, Jyh-Horng Sheu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     (R)-di-tert-butyl 1-(2-methyl-1-oxopentan-2-yl)hydrazine-1,2-dicarboxylate
    ÏàËÆ¶È:56.2%
Tetrahedron          2013          69          5438-5443
¦Â-tert-Butyl aspartate as an organocatalyst for the asymmetric ¦Á-amination of ¦Á,¦Á-disubstituted aldehydes
Alexis Theodorou, Giorgos N. Papadopoulos, Christoforos G. Kokotos
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     14,15-dinorclerod-3-ene-2,13-dione
C18H28O2     ÏàËÆ¶È:55.5%
Helvetica Chimica Acta          2003          Vol. 86          3187
Dinorditerpene, Diterpenes, Alkaloids, and Coumarins from Clausena dunniana
Hong-Ping He, Yue-Mao Shen, Guo-Ying Zuo, Xiao-Sheng Yang, and Xiao-Jiang Hao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     (4aR,7R,8S,8aR)-4,4a,7,8-tetramethyl-8-(3-oxobutyl)-4a,5,6,7,8,8a-hexahydronaphthalen-2(1H)-one
C18H28O2     ÏàËÆ¶È:55.5%
Zeitschrift f¨¹r Naturforschung B          2007          62b          577-579
A Novel Norditerpene from Eupatorium adenophorum
Ming-ZhongWang, Xiang-Hai Cai, Guo-Shun Du, and Xiao-Dong Luo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     (1R,3aR,5S,7aR)-5-Azido-1-((R)-1,5-dimethylhexyl)-3a,7a-dimethyloctahydroinden-4-one
    ÏàËÆ¶È:55.5%
Bioorganic & Medicinal Chemistry          2013          21          1925-1943
Stereoselective synthesis of a new class of potent and selective inhibitors of human ¦¤8,7-sterol isomerase
Mathias König, Christoph M¨¹ller, Franz Bracher
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     Gibberosin E
C20H30O2     ÏàËÆ¶È:55%
Bulletin of the Chemical Society of Japan          2006          79          1547-1551
New ¦Â-Caryophyllene-Derived Terpenoids from the Formosan Soft Coral Sinularia gibberosa
Shin-Pin Chen, Chih-Hua Chao, Ho-Cheng Huang, Yang-Chang Wu, Chung-Kuang Lu, Chang-Feng Dai, Jyh-Horng Sheu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     (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   Ì¼Æ×Ä£Äâͼ
12 .     elongatol B
C15H22O3     ÏàËÆ¶È:53.3%
Chemical & Pharmaceutical Bulletin          2007          55(5)          762-765
Nardosinane Sesquiterpenoids from the Formosan Soft Coral Nephthea elongata
Shang-Kwei WANGa and Chang-Yih DUH
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     3-deoxypseudoanisatin
C15H22O5     ÏàËÆ¶È:53.3%
Chemical & Pharmaceutical Bulletin          2004          52(1)          104-107
Seven Novel seco-Prezizaane-Type Sesquiterpenes from the Pericarps of Illicium merrillianum
Jian-Mei HUANG,Chun-Shu YANG,Ren ZHAO,Hironobu TAKAHASHI,and Yoshiyasu FUKUYAMA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     (1S,4S,5S,6R,7S,10S)-dihydroxymaaliane
C15H26O2     ÏàËÆ¶È:53.3%
Chemical & Pharmaceutical Bulletin          2000          48(11)          77-80
Three New Sesquiterpenoid Glucosides of Ficus pumila Fruit
Junichi KITAJIMA,Kaoru KIMIZUKA,and Yasuko TANAKA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     (1S,10S)-9¦Â-Hydroxy-allo-aromadendrane
C15H26O     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
16 .     compound 9
    ÏàËÆ¶È:53.3%
Journal of Natural Products          2005          68          1208-1212
Oxygenated Terpenoids from a Formosan Soft Coral Sinularia gibberosa
Atallah F. Ahmed, Yao-Haur Kuo, Chang-Feng Dai, and Jyh-Horng Sheu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     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   Ì¼Æ×Ä£Äâͼ
18 .     4¦Á,7¦Â-Dihydroxyeudesmane
C15H28O2     ÏàËÆ¶È:53.3%
Journal of Asian Natural Products Research          2006          8          723-731
Eudesmane-type sesquiterpenoids from the liverwort Lepidozia fauriana
H.-S. SHY and C.-L. WU
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     japodic acid
C13H22O3     ÏàËÆ¶È:53.3%
Records of Natural Products          2008          2          100-106
Japodic acid, A Novel Aliphatic Acid from Jatropha podagrica Hook
Olapeju O. Aiyelaagbe and James B. Gloer
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2Â¥2013-10-25 12:18:07
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