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1 .     pedunculatic acid B
C20H30O5     ÏàËÆ¶È:60%
Helvetica Chimica Acta          2006          Vol. 89          1017
Two New Diterpenoids from Callicarpa pedunculata
Hai-Yang Liu, Hong-Ping He, Suo Gao, Chang-Xiang Chen, Yue-Mao Shen, and Xiao-Jiang Hao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     drechslerine B
C15H22O3     ÏàËÆ¶È:55.5%
Journal of Natural Products          2002          65          306-313
Rare Sesquiterpenes from the Algicolous Fungus Drechslera dematioidea
Claudia Osterhage, Gabriele M. König, Ulrich Höller, and Anthony D. Wright
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     trichocarane A
C15H20O4     ÏàËÆ¶È:55.5%
Journal of Natural Products          2000          63          1197-1200
Bioactive Carotanes from Trichoderma virens
Francisco A. Mac¨ªas,Rosa M. Varela, Ana M. Simonet,Horace G. Cutler, Stephen J. Cutler,Michael A. Eden,and Robert A. Hill
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     (1R,3aR,4S,7aR)-1-((S)-6-hydroxy-6-methylheptan-2-yl)-7a-methyloctahydro-1H-inden-4(2H)-one
C18H32O2     ÏàËÆ¶È:55.5%
Heterocycles          2010          81          381-394
Synthesis of 20-Epi-eldecalcitol [20-Epi-1¦Á,25-dihydroxy-2¦Â-(3-hydroxypropoxy)vitamin D3: 20-Epi-ED-71]
Madoka Yoshino, Kohei Eto, Keisuke Takahashi, Jun Ishihara, Susumi Hatakeyama, Yoshiyuki Ono, Hitoshi Saito, and Noboru Kubodera
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     compound 5
C17H33O7NS     ÏàËÆ¶È:55.5%
The Journal of Organic Chemistry          1997          62          3831-3836
Taurospongin A, a Novel Acetylenic Fatty Acid Derivative Inhibiting DNA Polymerase ¦Â and HIV Reverse Transcriptase from Sponge Hippospongia sp.
Haruaki Ishiyama, Masami Ishibashi, Akio Ogawa, Shonen Yoshida, and Jun'ichi Kobayashi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     methyl 2-(((3S,7S,9R)-7,9-O-isopropylidene-3-methyl-3,7,9-trihydroxydecanoyl)amino)ethanesulfonate
C17H33O7NS     ÏàËÆ¶È:55.5%
The Journal of Organic Chemistry          1997          62          3831-3836
Taurospongin A, a Novel Acetylenic Fatty Acid Derivative Inhibiting DNA Polymerase ¦Â and HIV Reverse Transcriptase from Sponge Hippospongia sp.
Haruaki Ishiyama, Masami Ishibashi, Akio Ogawa, Shonen Yoshida, and Jun'ichi Kobayashi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     7¦Á-acetoxydeacetylbotryenedial
C17H24O5     ÏàËÆ¶È:55.5%
The Journal of Antibiotics          2008          61          556-562
Six New Induced Sesquiterpenes from the Cultures of Ascomycete Daldinia concentrica
Xiang-Dong Qin, Hong-Jun Shao, Ze-Jun Dong and Ji-Kai Liu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     de-A,B-25-hydroxycholestan-8-one
    ÏàËÆ¶È:55.5%
Journal of Medicinal Chemistry          1994          37          2387-2393
14-Epi Stereoisomers of 25-Hydroxy- and 1.alpha.,25-Dihydroxyvitamin D3: Synthesis, Isomerization to Previtamins, and Biological Studies
David F. Maynard, William G. Trankle, Anthony W. Norman, William H. Okamura
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     1¦Â,2¦Â;11R,-13-diepoxy-3¦Â-senecioyloxy-5¦ÂH,6RH,7RH,10RMe-eudesm-4(15)-en-6,12-olide
C20H24O6     ÏàËÆ¶È:55%
Journal of Natural Products          2006          69          1566-1571
Sesquiterpenes from Thapsia nitida var.meridionalis and Thapsia nitida var. nitida
Juan J. Rubal, Francisco M. Guerra, F. Javier Moreno-Dorado, Zacaras D. Jorge, Guillermo M. Massanet,Helmer Shoel, Ulla W. Smitt, Karla Frydenvang, S. Brgger Christensen, Charlotte Nielsen, and Margit Eriksson
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     (-)-(3S,4aS,8aS,2'R,3'R)-2-[3'-Azido-2'-hydroxy-4'-phenyl-butyl]-N-tert-butyldecahydro-isoquinoline-3-carboxamide
C24H37N5O2     ÏàËÆ¶È:55%
Bioorganic & Medicinal Chemistry          2008          16          902-908
Stereocontrolled synthesis and biological activity of two diastereoisomers of the potent HIV-1 protease inhibitor saquinavir
Giuliana Righi, Simona Ciambrone,Carlo Bonini and Pietro Campaner
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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11 .     Xeniolide J
C22H30O7     ÏàËÆ¶È:54.5%
Tetrahedron          2006          62          12092-12097
Novaxenicins A¨CD and xeniolides I¨CK, seven new diterpenes from the soft coral Xenia novaebrittanniae
Ashgan Bishara, Amira Rudi, Israel Goldberg, Yehuda Benayahu, Yoel Kashman
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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12 .     hatcherenone
C20H32O2     ÏàËÆ¶È:52.6%
Chemical & Pharmaceutical Bulletin          1999          47          138-139
A Novel Skeletal Diterpenoid from the German Liverwort Barbilophozia hatcheri (EVANS) LOESKE
Fumihiro NAGASHIMA,Yoko MURAKAMI and Yoshinori ASAKAWA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     8R-tert-Butyldimethylsilyloxy-20-methyl-18-(2-hydroxy-ethoxy)-de-A,B-pregnane
    ÏàËÆ¶È:52.6%
Bioorganic & Medicinal Chemistry          1998          6          2029-2039
New 1¦Á,25-dihydroxy vitamin D3 analogues with side chains attached to C-18: synthesis and biological activity
Gunnar Grue-Sørensen, Christina Mørk Hansen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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14 .     (+)-(1S,3R,4R,4aS,8aS)-4-(2-{[tert-butyl(dimethyl)silyl]oxy}ethyl)-3,4a,8,8-tetramethyldecahydro-1,3-naphthalenediol
C21H40O3Si     ÏàËÆ¶È:52.6%
Tetrahedron          2001          57          8369-8379
The synthesis of Ambrox®-like compounds starting from (+)-larixol. Part 2
Marjon G Bolster, B¨¦atrice M.F Lagnel, Ben J.M Jansen, Christophe Morin, Aede de Groot
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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15 .     actinonin
C19H35N3O5     ÏàËÆ¶È:52.6%
The Journal of Antibiotics          1985          38          1629-1630
PRODUCTION OF ACTINONIN, AN INHIBITOR OF AMINOPEPTIDASE M, BY ACTINOMYCETES
HAMAO UMEZAWA, TAKAAKI AOYAGI, TOSHIYUKI TANAKA, HIROYUKI SUDA, AKIRA OKUYAMA, HIROSHI NAGANAWA, MASA HAMADA, TOMIO TAKEUCHI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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16 .     compound 2
    ÏàËÆ¶È:52.3%
Tetrahedron Letters          2000          41          4743-4749
Design of an organic sequence suitable for the solid phase combinatorial synthesis of libraries of macro-heterocycles
Mahesh Ramaseshan, John W. Ellingboe, Yves L. Dory, Pierre Deslongchamps
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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17 .     compound 10c
    ÏàËÆ¶È:52.3%
Bioorganic & Medicinal Chemistry          1998          6          2029-2039
New 1¦Á,25-dihydroxy vitamin D3 analogues with side chains attached to C-18: synthesis and biological activity
Gunnar Grue-Sørensen, Christina Mørk Hansen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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18 .     Isoadenolin C
C21H30O7     ÏàËÆ¶È:52.3%
Journal of Natural Products          2011          74          1213-1220
Structure and Cytotoxicity of Diterpenoids from Isodon adenolomus
Wei Zhao, Jian-Xin Pu, Xue Du, Jia Su, Xiao-Nian Li, Jian-Hong Yang, Yong-Bo Xue, Yan Li, Wei-Lie Xiao, and Han-Dong Sun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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19 .     methyl ent-2,4-seco-4-oxo-3,19-dinorbeyer-15-en-2-oate
    ÏàËÆ¶È:50%
Phytochemistry          2007          68          546-553
ent-Beyerane diterpenoids from the heartwood of Excoecaria parvifolia
Mary H. Grace, Juan A. Faraldos, Mary Ann Lila, Robert M. Coates
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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20 .     helminthosporol
C15H24O2     ÏàËÆ¶È:50%
Journal of Natural Products          2002          65          306-313
Rare Sesquiterpenes from the Algicolous Fungus Drechslera dematioidea
Claudia Osterhage, Gabriele M. König, Ulrich Höller, and Anthony D. Wright
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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21 .     agallochin H
C20H30O3     ÏàËÆ¶È:50%
Journal of Natural Products          2002          65          382-385
ent-Kaurane and Beyerane Diterpenoids from Excoecaria agallocha1
Ammanamanchi S. R. Anjaneyulu, Vadali Lakshmana Rao, and Karanam Sreedhar
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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22 .     9-deoxy-7,8-epoxyxeniloide-e
C20H28O4     ÏàËÆ¶È:50%
Journal of Natural Products          2002          65          1882-1885
New Cytotoxic Xenia Diterpenoids from the Formosan Soft Coral Xenia umbellata
Chang-Yih Duh,Ali Ali H. El-Gamal, Chin-Ying Chiang, Chih-Ju Chu, Shang-Kwei Wang, and Chang-Feng Dai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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23 .     acasiane B
C20H34O2     ÏàËÆ¶È:50%
Planta Medica          2009          75          256-261
Acasiane A and B and Farnesirane A and B, Diterpene Derivatives From the Roots of Acacia farnesiana
An-Shen Lin, Chia-Rong Lin, Ying-Chi Du, Tilo L¨¹bken, Michael Y. Chiang, I-Hsiao Chen, Chin-ChungWu,Tsong-Long Hwang, Shu-Li Chen, Ming-Hong Yen, Fang-Rong Chang, Yang-ChangWu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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24 .     marrubenol
    ÏàËÆ¶È:50%
Planta Medica          2003          69          75-77
The Vasorelaxant Activity of Marrubenol and Marrubiin from Marrubium vulgare
Sanae El Bardai,Nicole Morel,Maurice Wibo,Nicolas Fabre,Gabriel Llabres, Badiaa Lyoussi,Joëlle Quetin-Leclercq
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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25 .     13,17-dioxo-18,19,24-trisnorcheilanth-6¦Á-ol
C22H36O3     ÏàËÆ¶È:50%
Chemical & Pharmaceutical Bulletin          1996          44          695-698
Fern Constituents : Sesterterpenoids Isolated from Fronds of Aleuritopteris agetae
Rumiko KAMAYA,Kazuo MASUDA,Hiroyuki AGETA and Hsien-Chang CHANG
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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26 .     rabdokaurin D
C22H30O7     ÏàËÆ¶È:50%
Chemical & Pharmaceutical Bulletin          1993          41          685-687
Rabdokaurins C and D, Two New Diterpenes from Rabdosia longituba
Yoshio TAKEDA,Yukako FUTATSUISHI,Teruyoshi ICHIHARA,Takashi MATSUMOTO,Hiromitsu TERAO,Hiroshi TERADA and Hideaki OTSUKA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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27 .     Ethyl Ester of 2-acetyl-7-acetoxy-2-(3-butenyl)-5-methylheptanoic acid
    ÏàËÆ¶È:50%
Chemistry of Natural Compounds          2005          41          715-718
SYNTHESIS OF (3S,6RS)- AND (3RS,6RS)-ANALOGS OF COMPONENT AI OF THE Aonidiella aurantii SEX PHEROMONE BY STEPWISE ALKYLATION OF ACETOACETIC ESTER
G. Yu. Ishmuratov, R. Ya. Kharisov, M. P. Yakovleva,A. V. Galyautdinova, R. R. Gazetdinov,R. R. Muslukhov and G. A. Tolstikov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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28 .     Ethyl 2-acetyl-7-acetoxy-5-methylheptanoate
    ÏàËÆ¶È:50%
Chemistry of Natural Compounds          2001          37          486-489
UNIVERSAL APPROACH TO THE SYNTHESIS OF JUVENOID HYDROPRENE AND METHOPRENE FROM 4-METHYLTETRAHYDROPYRAN
G. Yu. Ishmuratov, M. P. Yakovleva, A. V. Galyautdinova,L. V. Faifer, R. Ya. Kharisov,V. V. Zorin,and G. A. Tolstikov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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29 .     sessilistemonamine D
C22H33NO4     ÏàËÆ¶È:50%
Chinese Chemical Letters          2007          18          152-154
A new alkaloid from Stemona sessilifolia
Peng Wang, Hai Lin Qin , Zhi Hong Li, Ai Lin Liu, Guan Hua Du
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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30 .     (3S,6S,7aR)-6-[2-(2-Bromoethyl)-3-methylbut-2-en-1-yl]-3-isopropyl-6,7a-dimethyltetrahydropyrrolo[2,1-b][1,3]oxazol-5(6H)-one
C18H30BrNO2     ÏàËÆ¶È:50%
Molecules          2006          11          707-713
Asymmetric Synthesis of (7aS)-7a-Methyl-4, 5, 7, 7a-tetrahydro-1H-indene-2, 6-dione and Useful Derivatives Thereof
Samuël Demin, Dirk Van Haver and Pierre J. De Clercq
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2Â¥2013-05-20 20:17:33
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