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½ðͯҩѧ: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2014-12-18 18:46:30
1 .     5-[2-(furan-3-yl)ethyl]-1,5,6-trimethyl-1,2,3,4,5,6,7,8-octahydronaphthalene-1-carboxylic acid
C20H28O3     ÏàËÆ¶È:95%
Journal of Natural Products          2005          68          7-10
ent-Halimane Diterpenes and a Guaiane Sesquiterpene from Cladogynos orientalis
Mayuree Kanlayavattanakul, Nijsiri Ruangrungsi, Toshiko Watanabe, Masatoshi Kawahata, Bruno Therrien, Kentaro Yamaguchi, and Tsutomu Ishikawa
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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2 .     crotohalimaneic acid
C20H28O3     ÏàËÆ¶È:90%
Planta Medica          2004          70          87-89
New Halimane Diterpenoids from Croton oblongifolius
Sophon Roengsumran ,Surachai Pornpakaku, Nongnuj Muangsin ,Polkit Sangvanich , Thumnoon Nhujak , Pravit Singtothong,Narongsak Chaichit , Songchan Puthong , Amorn Petsom
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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3 .     (6¦Â)-5(R)-[2-(3-Furanyl)ethyl]-1,1,5,6-tetramethyl-1,2,3,4,5,6,7,8-octahydronaphthalene
C20H30O     ÏàËÆ¶È:70%
Journal of Natural Products          2000          63          1623-1625
Synthesis of 16,18-Dihydroxycleroda-3,13Z-dien-16,15-olide,(+)-16-Hydroxycleroda-3,13Z-dien-16,15-olide, and (-)-Hydroxyhalima-5(10),13-dien-16,15-olide from (+)-Hardwickiic Acid
Paulo M. Imamura, and Marta Costa
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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4 .     vitetrifolin G
C20H32O2     ÏàËÆ¶È:65%
Chemical & Pharmaceutical Bulletin          2001          49(9)          1220-1222
Four New Halimane-Type Diterpenes, Vitetrifolins D¡ªG, from the Fruit of Vitex trifolia
Masateru ONO,Yasuyuki ITO,and Toshihiro NOHARA
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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5 .     pacificin A
C20H34O2     ÏàËÆ¶È:65%
Journal of Natural Products          2005          68          74-77
Prenylbicyclogermacrane Diterpenoids from the Formosan Soft Coral Nephthea pacifica
Ali A. H. El-Gamal, Shang-Kwei Wang, Chang-Feng Dai, I-Gin Chen, and Chang-Yih Duh
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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6 .     crotohalimoneic acid
C20H26O4     ÏàËÆ¶È:65%
Planta Medica          2004          70          87-89
New Halimane Diterpenoids from Croton oblongifolius
Sophon Roengsumran ,Surachai Pornpakaku, Nongnuj Muangsin ,Polkit Sangvanich , Thumnoon Nhujak , Pravit Singtothong,Narongsak Chaichit , Songchan Puthong , Amorn Petsom
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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7 .     Cacospongin A
C20H30O     ÏàËÆ¶È:65%
Tetrahedron          2000          56          9025-9030
New Terpenoids from a Cacospongia sp. from the Philippines
Deniz Tasdemir, Gisela P. Concepci¨®n, Gina C. Mangalindan, Mary Kay Harper, Eduardo Hajdu, Chris M. Ireland
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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8 .     cacospongin A
    ÏàËÆ¶È:65%
Tetrahedron          2001          57          5681
Corrigendum to ¡°New Terpenoids from a Cacospongia sp. from the Philippines¡± [Tetrahedron 56 (2000) 9025¨C9030]
Deniz Tasdemir, Gisela P. Concepci¨®n, Gina C. Mangalindan, Mary Kay Harper, Eduardo Hajdu, Chris M. Ireland
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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9 .     5(10),14-ent-halimadien-3¦Â,13S-diol
C20H34O2     ÏàËÆ¶È:65%
Zeitschrift f¨¹r Naturforschung C          2010          65          39-42
Anticancer Activity of Diterpenoids from Amoora ouangliensis and Amoora stellato-squamosa
S.-M. Yang, D.-G. Wu, and X.-K. Liu
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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10 .     dehydroambliol-A
    ÏàËÆ¶È:65%
Natural Product Communications          2014          9          329-335
Use of (S)-trans-¦Ã-Monocyclofarnesol as a Useful Chiral Building Block for the Stereoselective Synthesis of Diterpenic Natural Products
Stefano Serra, Alessandra A. Cominetti and Veronica Lissoni
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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11 .     (1S,4aS,7R,8aR)-7-Hydroxy-1,4a,6-trimethyl-5-[2-(furan-3-yl)ethyl]-1,2,3,4,4a,7,8,8a-octahydronaphthalen-1-carboxylic Acid [7R-Hydroxy-15,16-epoxy-8(9),13(16),14-labdatrien-18-oic Acid]
C20H28O4     ÏàËÆ¶È:65%
Chemistry of Natural Compounds          2012          48          250-257
Synthetic transformations of higher terpenoids. XXVII.* Synthesis of 7-hydroxylabdanoids and their transformations
Yu. V. Kharitonov, E. E. Shul´ts, Yu. V. Gatilov, I. Yu. Bagryanskaya and M. M. Shakirov, et al.
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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12 .     compound 2
C20H28O4     ÏàËÆ¶È:65%
Journal of Natural Products          2012          75          2188-2192
Clerodane Diterpenoids from Croton crassifolius
Guo-Cai Wang, Jia-Gui Li, Guo-Qiang Li, Jiao-Jiao Xu, Xia Wu, Wen-Cai Ye, and Yao-Lan Li
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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13 .     Ambliol-A
C20H30O     ÏàËÆ¶È:63.1%
The Journal of Organic Chemistry          1981          46          1098-1102
Diterpenes from the sponge Dysidea amblia
Roger P. Walker, D. John Faulkner
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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14 .     (1S,4S)-18-norcembra-2Z,11E-trien-4-ol
    ÏàËÆ¶È:63.1%
Chemistry of Natural Compounds          1990          26          543-545
Dependence of the growth-regulating activity of macrocyclic allyl alcohols of the cembrane series on the stereochemistry of the disubstituted double bond
A. V. Vorob'ev, N. A. Larionova, V. A. Raldugin
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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15 .     15,16-epoxylabda-7,13(16),14-trien-18-oic acid
C21H30O3     ÏàËÆ¶È:61.9%
Phytochemistry          1992          31          1723-1726
Furolabdanes and linear diterpenes from Gutierrezia resinosa
C. Zdero, F. Bohlmann, H.M. Niemeyer
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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16 .     coleon U 12-methyl ether
    ÏàËÆ¶È:61.9%
Australian Journal of Chemistry          1998          51          175-176
Two New Abietanes from Lycopodium deuterodensum
Hiroyuki Fuchino, Hisanori Nakamura, Yuka Toyoshima, Takashi Hakamatsuka, Nobutoshi Tanaka, Richard C. Cambie and John E. Braggins
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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17 .     triptonoterpene methyl ether
C21H30O3     ÏàËÆ¶È:61.9%
Planta Medica          2013          79          797-805
Simultaneous Quantification of 18 Bioactive Constituents in Tripterygium wilfordii Using Liquid Chromatography-Electrospray Ionization-Mass Spectrometry
Zeng, Feng; Wang, Wei; Guan, Shuhong; Cheng, Chunru; Yang, Min; Avula, Bharathi; Khan, Ikhlas A.; Guo, De-an:
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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18 .     (-)-(1R,4S,4aR,8aS)-4((3S)-3-([tert-butyl(dimethyl)silyl]oxy-3-methyl-4-pentenyl)-3,4a,8,8-tetramethyl-1,4,4a,5,6,7,8,8a-octahydro-1-naphthalenol
C26H48O2Si     ÏàËÆ¶È:60.8%
Tetrahedron          2002          58          5275-5285
The synthesis of Ambra oxide related compounds starting from (+)-larixol. Part 3
Marjon G Bolster, Ben J.M Jansen, Aede de Groot
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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19 .     sarcotin K
C20H28O2     ÏàËÆ¶È:60%
Journal of Natural Products          2002          65          1307-1314
Cytotoxic Pyrrolo- and Furanoterpenoids from the Sponge Sarcotragus Species
Yonghong Liu, Jongki Hong, Chong-O. Lee, Kwang Sik Im, Nam Deuk Kim, Jae Sue Choi, and Jee H. Jung
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ

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20 .     (6¦Â)-5(R)-[2-(2,5-Dihydro-5-hydroxy-2-oxo-4-furanyl)-ethyl]-1,1,5,6-tetramethyl-1,2,3,4,5,6,7,8-octahydronaphthalene
C20H30O3     ÏàËÆ¶È:60%
Journal of Natural Products          2000          63          1623-1625
Synthesis of 16,18-Dihydroxycleroda-3,13Z-dien-16,15-olide,(+)-16-Hydroxycleroda-3,13Z-dien-16,15-olide, and (-)-Hydroxyhalima-5(10),13-dien-16,15-olide from (+)-Hardwickiic Acid
Paulo M. Imamura, and Marta Costa
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
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