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1 .     muurolane-4¦Â,5¦Â,10¦Â-triol
C15H28O3     ÏàËÆ¶È:61.1%
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
2 .     10¦Â,11-oxy-4¦Á,5¦Á,7¦Â-eremophil-1-ene
C15H24O     ÏàËÆ¶È:61.1%
Phytochemistry          1999          52          1063-1067
The hydroxylation of the sesquiterpenoid valerianol by Mucor plumbeus
Simone Fontes Arantes, James R. Hanson, Peter B. Hitchcock
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     cyclokessyl acetate
    ÏàËÆ¶È:61.1%
Phytochemistry          1992          31          3511-3514
Sesquiterpenoids and iridoid glycosides from Valeriana fauriei
Koichi Nishiya, Takefumi Kimura, Koichi Takeya, Hideji Itokawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     kessyl glycol 8-acetate
    ÏàËÆ¶È:61.1%
Phytochemistry          1992          31          3511-3514
Sesquiterpenoids and iridoid glycosides from Valeriana fauriei
Koichi Nishiya, Takefumi Kimura, Koichi Takeya, Hideji Itokawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     (-)-eudesma-4(15)-en-3¦Â,11-diol
    ÏàËÆ¶È:61.1%
Pharmazie          2002          57          59-61
Microbiological conversion of a - and -eudesmol mixture by Rhizopus
G.T. Maatooq - J.J. Hoffmann
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     (5S)-4-Bromo-3-methyl-5-[(1R,3R,5R)-1,3,5-trimethyloctyl]furan-2(5H)-one
C16H28BrO2     ÏàËÆ¶È:61.1%
Zeitschrift f¨¹r Naturforschung B          2009          64          639-645
Ex Chiral Pool Synthesis from a Highly Methyl-branched Wax Ester and Biological Properties of (+)-Capensifuranone
Y. Galeyeva, M. Morr, F. Sasse, R. Diestel, S. Laschat, A. Baro, and W. Frey
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     (-)-5,11-epoxy-4¦Á,5¦Â,10¦Á-eudesm-1-ene
    ÏàËÆ¶È:61.1%
Flavour and Fragrance Journal          2004          19          565-570
Terpenoids of the volatile oil of Bursera graveolens
Chiyoki Yukawa, Hisakatsu Iwabuchi, Tadao Kamikawa, Sadao Komemushi and Akiyoshi Sawabe
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     pacificin N
C22H36O3     ÏàËÆ¶È:59.0%
Chemical & Pharmaceutical Bulletin          2007          55(6)          890-893
Prenylbicyclogermacrane Diterpenoids from the Formosan Soft Coral Nephthea elongata
Ali Ali Hassan EL-GAMAL,Shang-Kwei WANG,and Chang-Yih DUH
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     compound 8
    ÏàËÆ¶È:59.0%
Phytochemistry          1986          25          1393-1395
Neo-clerodane diterpenoids from Baccharis rhomboidalis
Aurelio San-Mart¨ªn, Juana Rovirosa, Cecilia Labb¨¦, Arturo Givovich, Manuel Mah¨², Mariano Castillo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     vitedoin B
C19H30O4     ÏàËÆ¶È:57.8%
Journal of Natural Products          2004          67          2073-2075
Lignan Derivatives and a Norditerpene from the Seeds of Vitex negundo
Masateru Ono, Yoichiro Nishida, Chikako Masuoka, Jian-Chen Li, Masafumi Okawa, Tsuyoshi Ikeda, and Toshihiro Nohara
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     (4,10a-dimethyl-7b-iso-propyl-decaline-5ene)1a,4a-maleic acid anhydride
    ÏàËÆ¶È:57.8%
Canadian Journal of Chemistry          2007          85          996-1005
On the origin of some cubebene derivatives ¡ªDiels¨CAlder adducts and the diene structures of solidago compounds
Christopher K. Jankowski, Andr¨¦ Pelletier, Eduardo Diaz T.,Jacqueline M.R. Belanger, Jocelyn J.R. Par¨¦, Andre Aumelas,Thierry Besson, Maria de Fatima Pereira, and Laurent Mauclaire
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     loesenerine
C19H35N3O2     ÏàËÆ¶È:57.8%
Phytochemistry          1987          26          1847-1848
Loesenerine,an alkaloid from Maytenus loeseneri
Mar¨ªa D¨ªaz,Alfred Preiss,Helmut Ripperger
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     6¦Â,8¦Â-diacetoxyeremophil-7(11)-en-12,8¦Á-olide
C19H26O6     ÏàËÆ¶È:57.8%
Phytochemistry          1985          24          1531-1535
Eremophilenolides from petasites japonicus
Ko Sugama, Koji Hayashi, Hiroshi Mitsuhashi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     4¦Á,5¦Á-Epoxy-17¦Á-hydroxy-A-homo-4-oxapregnan-3,20-dione
C22H32O5     ÏàËÆ¶È:57.1%
Steroids          2006          71          116-119
Steroidal seven-membered A-ring epoxy lactones by oxidation of the corresponding ¦¤4-3-ketosteroids
Maria L. Di Gioia, Antonella Leggio, Adolfo Le Pera, Francesca Perri, Andrea F. Pitrelli, Angelo Liguori
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     5,16¦Á,17¦Á-Trihydroxy-2¦Á,3¦Á-isopropylidenedioxy-5¦Á-pregna-6,20-dione
C24H36O7     ÏàËÆ¶È:57.1%
Canadian Journal of Chemistry          2005          83          1084-1092
Synthesis and preliminary bioactivity evaluation of new pregnane brassinosteroid-like compounds
Daniel G. Rivera and Francisco Coll
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     16¦Á-Azido-5,17¦Á-dihydroxy-2¦Á,3¦Á-isopropylidenedioxy-5¦Á-pregna-6,20-dione
C24H35O6N3     ÏàËÆ¶È:57.1%
Canadian Journal of Chemistry          2005          83          1084-1092
Synthesis and preliminary bioactivity evaluation of new pregnane brassinosteroid-like compounds
Daniel G. Rivera and Francisco Coll
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     5¦Á-Androstan-3¦Â-yl acetate
C21H34O2     ÏàËÆ¶È:57.1%
Organic Magnetic Resonance          1977          9          439-464
13C n.m.r. spectra of steroids ¡ªa survey and commentary
J. W. Blunt and J. B. Stothers
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     rel-(3'R)-3',8'-dihydrotokinolide B
C24H30O4     ÏàËÆ¶È:56.5%
Natural Product Research          2011          Vol. 25, No. 13          1234-1242
Phthalides and other constituents from Ligusticum porteri; sedative and spasmolytic activities of some natural products and derivatives
Alejandra Le¨®n, Rub¨¦n A. Toscano, Jaime Tortoriello and Guillermo Delgado
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     9¦Á-hydroxy-1¦Â-methoxycaryolanol
C16H28O2     ÏàËÆ¶È:55.5%
Helvetica Chimica Acta          2008          Vol. 91          1894
Four New Compounds from Sinacalia tangutica
Ying Zhu, Yan Zhao, Guo-Du Huang, and Wang-Suo Wu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     rumphellolide A
C15H24O3     ÏàËÆ¶È:55.5%
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   Ì¼Æ×Ä£Äâͼ
21 .     rumphellolide B
3Â¥2013-08-18 12:21:49
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