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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:85%
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   Ì¼Æ×Ä£Äâͼ
2 .     crotohalimaneic acid
C20H28O3     ÏàËÆ¶È:80%
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   Ì¼Æ×Ä£Äâͼ
3 .     (-)-5R,6R-microcionin-2
    ÏàËÆ¶È:70.5%
Tetrahedron          2005          61          11032-11037
Pelseneeriol-1 and -2: new furanosesquiterpene alcohols from porostome nudibranch Doriopsilla pelseneeri
Helena Gaspar, Margherita Gavagnin, Gonçalo Calado, Francesco Castelluccio, Ernesto Mollo, Guido Cimino
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     (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   Ì¼Æ×Ä£Äâͼ
5 .     Compound 4
    ÏàËÆ¶È:65%
Phytochemistry          1990          29          316-318
Diterpenes from Eremophila species
Emilio L. Ghisailberti, Phillip R. Jefferies, Thi Ngoc Vu Hieu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     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   Ì¼Æ×Ä£Äâͼ
7 .     compound 11
C21H28O4     ÏàËÆ¶È:64.7%
Journal of Natural Products          2003          66          1263-1265
Determination of the Absolute Stereochemistry of Cyclosmenospongine
Natalia K.Utkina,Vladimir A. Denisenko, Olga V. Scholokova, and Aleksandra E. Makarchenko
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     (-)-Lepidozenal
C15H24O     ÏàËÆ¶È:64.7%
Journal of the Chemical Society, Perkin Transactions 1          1984                   203-214
Structures and conformations of (¨C)-isobicyclogermacrenal and (¨C)-lepidozenal, two key sesquiterpenoids of the cis- and trans-10,3-bicyclic ring systems, from the liverwort Lepidozia vitrea : X-ray crystal structure analysis of the hydroxy derivative of (
Akihiko Matsuo, Hir¨­shi Nozaki, Naoji Kubota, Seiryo Uto and Mitsuru Nakayama
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     Dendrolasin
C15H22O     ÏàËÆ¶È:64.7%
Journal of Chemical Ecology          1993          19          339-356
Defensive allomones in three species ofHypselodoris (gastropoda: Nudibranchia) from the Cantabrian sea
A. Fontana, C. Avila, E. Martinez, J. Ortea, E. Trivellone, G. Cimino
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     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   Ì¼Æ×Ä£Äâͼ
11 .     (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   Ì¼Æ×Ä£Äâͼ
12 .     13,19-dihydroxy-halima-5(10),14-diene
C20H34O2     ÏàËÆ¶È:61.1%
Biochemical Systematics and Ecology          2004          32          45-53
Diterpenes from Stevia gilliesii
Tamara L. Meragelman, Diego S. Pedrosa, Roberto R. Gil
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     vitetrifolin G
C20H32O2     ÏàËÆ¶È:60%
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   Ì¼Æ×Ä£Äâͼ
14 .     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   Ì¼Æ×Ä£Äâͼ
15 .     Tessmannic acid
C20H30O3     ÏàËÆ¶È:60%
Phytochemistry          2009          70          1233-1238
Anti-mosquito and antimicrobial nor-halimanoids, isocoumarins and an anilinoid from Tessmannia densiflora
Charles Kihampa, Mayunga H.H. Nkunya, Cosam C. Joseph, Stephen M. Magesa, Ahmed Hassanali, Matthias Heydenreich , Erich Kleinpeter
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     infuscatrienol
C20H34O     ÏàËÆ¶È:60%
Chemical & Pharmaceutical Bulletin          1996          44          1628-1630
A NEW MONOCYCLIC DITERPENE FROM THE LIVERWORT JUNGERMANNIA INFUSCA (MITT.) STEPH.
Fumihiro NAGASHIMA,Akiko TAMADA and Yoshinori ASAKAWA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     jasonin-a
C20H26O2     ÏàËÆ¶È:60%
Natural Product Research          2005          19          253-265
Three new diterpenes and the biological activity of different extracts of Jasonia montana
Tawfeq A. Al-Howiriny; Adnan J. Al-Rehaily; Joanna R. Pols; John R. Porter; Jaber S. Mossa; Bahar Ahmed
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     infuscatrienol
C20H34O     ÏàËÆ¶È:60%
Phytochemistry          1997          46          1203-1208
Terpenoids from the Japanese liverworts Jackiella javanica and Jungermannia infusca
Fumihiro Nagashima, Akiko Tamada, Noriko Fujii, Yoshinori Asakawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     Epoxy cyclic hemiacetal
C20H30O3     ÏàËÆ¶È:60%
Organic & Biomolecular Chemistry          2004          2          466-473
Total synthesis of (¡À)-phomactin G, a platelet activating factor antagonist from the marine fungus Phoma sp.
William P. D. Goldring and Gerald Pattenden
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     (1S,2E,4R,6E,8S,11S,12S)-2,6-cembradiene-4,8,11,12-tetrol
    ÏàËÆ¶È:60%
Acta Chemica Scandinavica          1986          40B          123-134
Tobacco Chemistry. 63. Syntheses and Stereostructures of Six Tobacco Seco-Cembranoids.
Wahlberg, Inger; Arndt, Rolf; Nishida, Toshiaki; Enzell, Curt R.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     compound 8
    ÏàËÆ¶È:60%
Journal of the Chemical Society, Perkin Transactions 1          1977                   497-499
The structure of ballotenol, a new diterpenoid from Ballota nigra
Giuseppe Savona, Franco Piozzi, James R. Hanson and Michael Siverns
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     compound 11
    ÏàËÆ¶È:60%
Tetrahedron          1986          42          1305-1313
New diterpenes from chiliotrichium rosmarinifolium and nardophyllum lanatum
J. Jakupovic, S. Banerjee, F. Bohlmann, R.M. King, H. Robinson
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     (1R*,3E,7Z,12R*)-20-hydroxycembra-3,7,15-trien-19-oic acid
    ÏàËÆ¶È:60%
Australian Journal of Chemistry          1985          38          1365-1370
Unsaturated Cembrane Acids From Cleome viscosa L. (Capparidaceae)
S Kosela, E Ghisalberti, P Jefferies, B Skelton and A White
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
24 .     Dehydroambliol-A
C20H30O     ÏàËÆ¶È:60%
The Journal of Organic Chemistry          1981          46          1098-1102
Diterpenes from the sponge Dysidea amblia
Roger P. Walker, D. John Faulkner
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
25 .     compound 5
    ÏàËÆ¶È:60%
The Journal of Organic Chemistry          1981          46          4279-4284
Decaryiol, a new cembrane diterpene from the marine soft coral Sarcophyton decaryi
Shmuel Carmely, Amiram Groweiss, Yoel Kashman
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2Â¥2015-07-01 11:30:10
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