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9.7, 15.3, 20.0, 30.9, 34.5, 38.2, 41.4, 43.3, 49.6, 56.3, 61.4, 65.1, 65.9, 108.0, 116.1, 130.6, 143.7, 158.5, 170.9, 206.4
  
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1 .     3-Methoxy-17,17-ethylenedioxy-1,3,5 (10)-estratrien-4-ol
C21H28O4     ÏàËÆ¶È:57.1%
Steroids          2001          66          615-621
Selective synthesis of 4-methoxyestrogen from 4-hydroxyestrogen
Masanori Teranishi, Mayumi Kashihara, Youichi Fujii
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     compound 9a
C20H30O2     ÏàËÆ¶È:55%
Journal of Natural Products          2003          66          1623-1627
Facile Access to Optically Active Labdane-Type Diterpenes from (+)-Manool. Synthesis of (+)-Coronarin E, (+)-15,16-Epoxy-8(17),13(16),14-labdatriene, and (+)-Labda-8(17),13(Z)-diene-15,16-diol
Jos¨¦ Villamizar, Juan Fuentes, Franklin Salazar, Eleonora Tropper, and Randolph Alonso
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     14-acetoxymodhephene
C17H26O2     ÏàËÆ¶È:55%
Phytochemistry          1999          51          75-78
Modhephene derivatives from Pluchea sericea
Benito Reyes-Trejoa, Pedro Joseph-Nathan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     curcucomosin C
C20H30O3     ÏàËÆ¶È:55%
Journal of Natural Products          2010          73          724-728
Labdane Diterpenes from the Aerial Parts of Curcuma comosa Enhance Fetal Hemoglobin Production in an Erythroid Cell Line
Ratchanaporn Chokchaisiri, Nattawara Chaneiam, Saovaros Svasti, Suthat Fucharoen, Jim Vadolas and Apichart Suksamrarn
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     Zerumin B
C20H30O4     ÏàËÆ¶È:55%
Phytochemistry          1996          42          149-151
Labdane diterpenes from Alpinia zerumbet
Hong-Xi Xu, Hui Dong, Keng-Yeow Sim
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     13Z-6¦Á-Hydroxylabda-8(17),13-dien-15-oic Acid
C20H32O3     ÏàËÆ¶È:55%
Chemistry of Natural Compounds          2011          Vol. 47, No. 3          397-403
SYNTHESIS OF ent-CROTONADIOL AND COMPOUNDS RELATED TO IT FROM (+)-LARIXOL
P. F. Vlad, A. Chokyrlan, M. D'Ambrosio, M. N. Koltsa, A. N. Barba, K. Edu, A. Byryyak, A. Nikolescu, A. Mari, and K. Deleanu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     11¦Â-hydroxy-20-nor-8(9),15-isopimaradien-7-one
C19H28O2     ÏàËÆ¶È:55%
Phytochemistry          1988          27          3913-3915
Norditerpenoids from Vellozia pusilla
Angelo C. Pinto,Ligia Maria M. Valente,Rosaly S. Da Silva
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     15¦Á,16¦Á-Epoxy-17-hydroxy-ent-kauran-19-oic acid
    ÏàËÆ¶È:55%
Archives of Pharmacal Research          2009          32          1399-1408
Cholinesterase and BACE1 inhibitory diterpenoids from Aralia cordata
Hyun Ah Jung, Eun Ju Lee, Ju Sun Kim, Sam Sik Kang and Je-Hyun Lee, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     (+)-zerumin B
    ÏàËÆ¶È:55%
The Journal of Organic Chemistry          2006          71          6670-6673
Synthesis and Stereochemistry of the Antitumor Diterpenoid (+)-Zerumin B
John Boukouvalas, Jian-Xin Wang, Olivier Marion, and Bruno Ndzi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     zerumin B
    ÏàËÆ¶È:55%
Food Chemistry          2011          124          527-532
Labdane diterpenes in Curcuma mangga rhizomes inhibit lipid peroxidation, cyclooxygenase enzymes and human tumour cell proliferation
Yunbao Liu, Muraleedharan G. Nair
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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11 .     5-[4-[2-(Benzoxazol-2-yl-butyl-amino)-ethoxy]-benzyl]-thiazolidine-2,4-dione
    ÏàËÆ¶È:54.5%
Archives of Pharmacal Research          2004          27          1099-1105
Synthesis and biological activity of Benzoxazole containing thiazolidinedione derivatives
Raok Jeon and SoYeon Park
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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12 .     compound 3
C20H30O4     ÏàËÆ¶È:52.3%
Journal of Natural Products          1999          62          1173-1174
A New Labdane Diterpenoid from Renealmia alpinia Collected in the Suriname Rainforest
Shu-Wei Yang, Bing-Nan Zhou, Stan Malone, Marga C. M. Werkhoven, Frits van Troon, Jan H. Wisse, and David G. I. Kingston
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     2¦Á,3¦Á,4¦Â-trihydroxypregnan-16-one
    ÏàËÆ¶È:52.3%
Phytochemistry          1997          45          1495-1500
Androstane and pregnane 2¦Â, 19-hemiketal steroids from Trichilia claussenii
Mônica T. Pupo, Paulo C. Vieira, João B. Fernandes, M. F¨¢tima das G.F. da Silva, Edson Rodrigues Fo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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14 .     Kamebacetal B
    ÏàËÆ¶È:52.3%
Pharmazie          2005          60          458-460
Cytotoxic ent-kaurane diterpenoids from Isodon weisiensis C. Y. Wu
Lan Ding, Guo-Ah Liu, Dong-Juan Yang, Han Wang, Lai Wang and Kun Sun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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15 .     (+)-zerumin B
    ÏàËÆ¶È:52.3%
The Journal of Organic Chemistry          2006          71          6670-6673
Synthesis and Stereochemistry of the Antitumor Diterpenoid (+)-Zerumin B
John Boukouvalas, Jian-Xin Wang, Olivier Marion, and Bruno Ndzi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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16 .     [(1S,2Z,3aS,5aS,6R,8aR)-1,3a,4,5,5a,6,7,8-octahydro-1,3a,6-trimethylcyclopenta[c]pentalen-2- yl]methyl acetate
C17H26O2     ÏàËÆ¶È:50%
Helvetica Chimica Acta          2003          Vol. 86          733
New Lignan, Benzofuran, and Sesquiterpene Derivatives from the Roots of Leontopodium alpinum and L. leontopodioides
Michael J. Dobner, Ernst P. Ellmerer, Stefan Schwaiger, Odonchimeg Batsugkh,Samdan Narantuya, Michaela St¸tz, and Hermann Stuppner
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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17 .     teulamifin B
    ÏàËÆ¶È:50%
Helvetica Chimica Acta          2002          Vol. 85          2547
Clerodane Diterpenoids from Kinostemon alborubrum
Deng Yea), Peng Shu-Lin a), Zhang Qiangb), Liao Xuna), and Ding Li-Sheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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18 .     fruticolone
    ÏàËÆ¶È:50%
Phytochemistry          2004          65          387-392
Neo-clerodane diterpenes from Teucrium fruticans
Josep Coll, Yudelsy Tandr¨®n
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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19 .     xerophilusin G
C22H30O8     ÏàËÆ¶È:50%
Phytochemistry          2001          58          179-183
Cytotoxic 7,20-epoxy ent-kauranoids from Isodon xerophilus
Ai-Jun Hou, Qin-Shi Zhao, Ma-Lin Li, Bei Jiang, Zhong-Wen Lin,Han-Dong Sun, Yi-Ping Zhou, Yang Lu, Qi-Tai Zheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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20 .     akaol B
C22H31O6SNa     ÏàËÆ¶È:50%
Journal of Natural Products          2003          66          686-689
New Sesquiterpene Quinols from a Micronesian Sponge, Aka sp.
Venugopal J. R. V. Mukku, Ru A. Edrada, Francis J. Schmitz,Michelle Kelly Shanks, Babathosh Chaudhuri, and Doriano Fabbro
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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21 .     siphonodictyol I
C21H29O7SNa     ÏàËÆ¶È:50%
Journal of Natural Products          2003          66          686-689
New Sesquiterpene Quinols from a Micronesian Sponge, Aka sp.
Venugopal J. R. V. Mukku, Ru A. Edrada, Francis J. Schmitz,Michelle Kelly Shanks, Babathosh Chaudhuri, and Doriano Fabbro
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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22 .     15,16-epoxy-12-hydroxy-labda-8(17),13(16),14-triene(a)
    ÏàËÆ¶È:50%
Journal of Natural Products          1998          61          1394-1396
A Concise Conversion of (-)-Sclareol into (+)-Coronarin E and (-)-7-epi-Coronarin A
Mankil Jung, Imju Ko, and Seokjoon Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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23 .     teumassin
    ÏàËÆ¶È:50%
Journal of Natural Products          1998          61          1242-1247
Neoclerodane Diterpenoids from Teucrium massiliense
Gianfranco Fontana, Maria Pia Paternostro, Giuseppe Savona, Benjam¨ªn Rodr¨ªguez, and Mar¨ªa C. de la Torre
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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24 .     acasiane D
C20H30O4     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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25 .     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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26 .     xerophilusin G
C22H30O8     ÏàËÆ¶È:50%
Acta Botanica Yunnanica          2000          22(2)          197-200
Three New ent - Kaurane Diterpenoides from Isodon xerophilus
HOU Ai-Jun,J IANGBei,YANG Hui,ZHAO Qin-Shi,LIN Zhong-Wen,SUN Han-Dong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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27 .     delatisine
C20H25NO3     ÏàËÆ¶È:50%
Chemistry of Natural Compounds          2000          36          419-477
HETISANE-TYPE DITERPENOID ALKALOIDS
I. A. Bessonova and Sh. A. Saidkhodzhaeva
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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28 .     delfissinol
C20H27NO3     ÏàËÆ¶È:50%
Chemistry of Natural Compounds          2000          36          419-477
HETISANE-TYPE DITERPENOID ALKALOIDS
I. A. Bessonova and Sh. A. Saidkhodzhaeva
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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29 .     luteinine
C19H25NO3     ÏàËÆ¶È:50%
Chemistry of Natural Compounds          1996          32          596-675
ALKALOIDS. PLANTS, STRUCTURES, PROPERTIES" Chapter 2, continued
R. Shakirov, M. V. Telezhenetskaya, I. A. Bessonova,S. F. Aripova, I. A. Israilov, M. N. Sultankhodzhaev,V. I. Vinogradova, V. I.Akhmedzhanova, T. S. Tulyaganov,B. T. Salimov, and V. A. Tel'nov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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30 .     6a¦Á,11¦Á-dihydroxy-4,4,8,11b¦Â-tetramethyl-2,3,4a¦Á,5,6,7,10a¦Â-octahydro-1H-phenanthro-[3,2-b]furan-9-one
C20H30O4     ÏàËÆ¶È:50%
Chemistry of Natural Compounds          1985          21          315-321
NEW DITERPENE LACTONES FROM Euphorbia pallasii
A. I. Sirchina, M. F. Larin, and A. A. Semenov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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31 .     enanderianin C
C22H30O7     ÏàËÆ¶È:50%
Chinese Chemical Letters          1998          9          733-734
A New 1¦Â-hydroxy-ent-kaurenoid From Isodon Enanderianus
Yan Hong Wang,Yao Zu CHEN,Zhong Wen LIN,Han Dong SUN
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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32 .     15¦Á,16¦Á-epoxy-17-hydroxy-ent-kaurane-19-oic acid
C20H28O4     ÏàËÆ¶È:50%
Chinese Chemical Letters          2006          17          45-48
Two New Diterpenes from Helianthus annuus L.
Mao Rong SUO, Jun Shan YANG, Yang LU, Li WU, Qi Tai ZHENG
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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33 .     teumarin B
C22H28O8     ÏàËÆ¶È:50%
Natural Product Research          2004          18          557-564
Phytochemical characters of teucrium marum from Sardinia: an endemic plant
Armandodoriano Bianco; Alessia Ramunno; Anna Maria Serrilli; Michelangelo Lo Castro; Ballero Mauro; Mauro Serafini
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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34 .     (¡À)-lyoniresinol
    ÏàËÆ¶È:50%
China Journal of Chinese Materia Medica          2005          30          42-43
Studies on the chemical constituents I nvine stem of Bauhinia championii (I)
BAI Haiyun, ZHANG Qingfeng, XIA Zenghua, LAO Aina
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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35 .     13-acetoxymodhephene
    ÏàËÆ¶È:50%
Phytochemistry          1999          51          75-78
Modhephene derivatives from Pluchea sericea
Benito Reyes-Trejoa, Pedro Joseph-Nathan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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36 .     compound 2
    ÏàËÆ¶È:50%
Phytochemistry          1998          49          1741-1744
Determination of the absolute stereochemistry of the epoxide group in alpinia epoxide by NMR
Lai-King Sy, Geoffrey D. Brown
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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37 .     enanderianin B
C22H30O9     ÏàËÆ¶È:50%
Phytochemistry          1998          48          1267-1269
7,20-Epoxy-ent-kaurenoids from Isodon enanderianus
Yan-Hong Wang, Yao-Zu Chen, Zhong-Wen Lin, Han-Dong Sun, Jin-Song Fan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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38 .     ent-kaurane-15¦Á,16¦Á-epoxy-17-al-19-oic acid
C20H28O4     ÏàËÆ¶È:50%
Acta Pharmaceutica Sinica          2007          Vol 42          166-170
Diterpenes from Helianthus annuus and their cytotoxicity in vitro
SUO Mao-rong; TIAN Ze; YANG Jun-shan; L¨¹ Yang; WU Li
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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39 .     compound 10
C20H32O2     ÏàËÆ¶È:50%
Phytochemistry          1995          40          797-800
Biotransformation of ent-16¦Â, 19-dihydroxykaurane by Cephalosporium aphidicola
James R. Hanson, Peter B. Hitchcock, Jacqueline A. Takahashi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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40 .     spicatolide B
C19H26O8     ÏàËÆ¶È:50%
Phytochemistry          1993          33          627-629
Germacranolides from Pseudoelephantopus spicatus
Consolacion Y. Ragasa, William G. Padolina, Tatsuo Yamauchi, Hideaki Otsuka, Kazuo Yamasaki, Tomohiro Satoh
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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41 .     11-oxomanoyloxide
    ÏàËÆ¶È:50%
Phytochemistry          1993          34          865-867
Hydroxymanoyloxides from Kyllinga erecta
Yaya Mahmout, Jean-Marie Bessiere, Ren¨¦ Dolmazon
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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42 .     delfissinol diacetyl derivative
C20H27NO3     ÏàËÆ¶È:50%
Phytochemistry          1993          34          1165-1167
Diterpene alkaloids from Delphinium fissum subsp. Anatolicum
A. Ulubelen, A.H. Mericli, F. Mericli, R. Ilarslan, W. Voelter
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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43 .     compound 13
C20H24O6     ÏàËÆ¶È:50%
Phytochemistry          1991          30          613-617
The absolute stereochemistry of some clerodane diterpenoids isolated from Teucrium species
Ana Lourenço, Mar¨ªa C. de la Torre, Benjam¨ªn Rodr¨ªguez, Maurizio Bruno, Franco Piozzi, Giuseppe Savona
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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44 .     Crassarine H
C20H30O2     ÏàËÆ¶È:50%
Marine drugs          2011          9          1955-1968
Bioactive Cembranoids from the Soft Coral Sinularia crassa
Chih-Hua Chao,Kuei-Ju Chou,Chiung-Yao Huang,Zhi-Hong Wen,Chi-Hsin Hsu,Yang-Chang Wu,Chang-Feng Dai and Jyh-Horng Sheu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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45 .     8,13-epoxy-labd-14-en-11-one
    ÏàËÆ¶È:50%
Phytochemistry          1989          28          859-862
Minor diterpenoids of Coleus forskohlii
Bruno Gabetta,Gianfranco Zini,Bruno Danieli
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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46 .     ent-15¦Â,16¦Â-epoxykauran-17-ol acetate
    ÏàËÆ¶È:50%
Phytochemistry          1990          29          662-664
Diterpenes from Euphorbia neriifolia
A.S. Ng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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47 .     15-acetoxy-13E-labden-8¦Â-ol
    ÏàËÆ¶È:50%
Phytochemistry          1990          29          2223-2228
Terpenoid compounds from Parentucellia latifolia
J.G. Urones,I.S. Marcos,I. Cubillo,N.Martin Garrido,P. Basabe
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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48 .     13-Acetoxy-modhephen
C17H26O2     ÏàËÆ¶È:50%
Phytochemistry          1980          19          579-582
Neue sesquiterpene aus Liabum-arten
Ferdinand Bohlmann, Christa Zdero, Rolf Bohlmann, Robert M. King, Harold Robinson
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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49 .     12(S)-15,16-epoxy-13(16),14-labdaiene-8,12-diol
C20H30O2     ÏàËÆ¶È:50%
Acta Chemica Scandinavica          1978          32          203-215
Tobacco Chemistry. 50. (3S,5R,8S,9xi)-5,8-Epoxy-6-megastigmene-3,9-diol and (3S*,5R*,6R*,7E,9xi)-3,6-Epoxy-7-megastigmene-5,9-diol. Two New Nor-carotenoids of Greek Tobacco.
Behr, Dan; Wahlberg, Inger; Nishida, Toshiaki; Enzell, Curt R.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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50 .     fruticolone
C22H30O6     ÏàËÆ¶È:50%
Journal of the Chemical Society, Perkin Transactions 1          1978                   356-359
Two new diterpenoids from Teucrium fruticans
Giuseppe Savona, Salvatore Passannanti, M. Pia Paternostro, Franco Piozzi, James R. Hanson, Peter B. Hitchcock and Michael Siverns
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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51 .     (+)-(1S,4S,4aR,8aR)-4-(3-hydroxypropyl)-4a,8,8-trimethyl-3-methylenedecahydro-1-naphthalenol
C17H30O2     ÏàËÆ¶È:50%
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   Ì¼Æ×Ä£Äâͼ

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52 .     (+)-(4S,4aR,8aS)-4-(3-{tert-butyl(dimethyl)sily]oxy]-propyl)-4a,8,8-trimethyl-3-methylene-octahydro-1(2H)-naphthalenone
C22H38O2Si     ÏàËÆ¶È:50%
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   Ì¼Æ×Ä£Äâͼ

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53 .     cespihypotin F
C20H26O4     ÏàËÆ¶È:50%
Tetrahedron          2007          63          10914-10920
Eight new diterpenoids from soft coral Cespitularia hypotentaculata
Ya-Ching Shen, Ying-Ru Wu, Jyun-Jhou Lin, Kuang-Liang Lo, Yuh-Chi Kuo, Ashraf Taha Khalil
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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54 .     larixol
C20H34O2     ÏàËÆ¶È:50%
Tetrahedron          2001          57          5663-5679
The synthesis of Ambrox®-like compounds starting from (+)-larixol
Marjon G Bolster, Ben J.M Jansen, Aede de Groot
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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55 .     (+)-4-((1S,4S,4aS,8aR)-4-hydroxy-5,5,8a-trimethyl-2-methylenedecahydro-1-naphthalenyl)-2-butanone
C18H30O2     ÏàËÆ¶È:50%
Tetrahedron          2001          57          5663-5679
The synthesis of Ambrox®-like compounds starting from (+)-larixol
Marjon G Bolster, Ben J.M Jansen, Aede de Groot
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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56 .     (+)-4-((1S,4S,4aS,8aR)-4-hydroxy-5,5,8a-trimethyl-2-methylenedecahydro-1-naphthalenyl)-2-butanone
C18H28O     ÏàËÆ¶È:50%
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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57 .     18-methyl-3-methoxy-17¦Â-ethoxy-8-isoestra-1,3,5(10)-triene
C22H32O2     ÏàËÆ¶È:50%
Russian Journal of Organic Chemistry          2003          39          194-200
Synthesis and Investigation of Estradiol Receptors Modulators
M. S. Egorov, S. I. Selivanov and A. G. Shavva
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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58 .     6,11-epoxy-15-nor-4-oxo-5,10-pinguisadien-12-acetate
C16H20O4     ÏàËÆ¶È:50%
Zeitschrift f¨¹r Naturforschung C          2002          57          413-417
Pinguisane-Type Sesquiterpenes from the South American Liverwort Porella recurva (Taylor) Kuhnemann
Key words: Bryophyte, Jungermanniales, Norsesquiterpenes
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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59 .     marrubenol
    ÏàËÆ¶È:50%
Natural Product Communications          2006          1          585-592
The Diterpenoids of the Genus Marrubium (Lamiaceae)
Franco Piozzi, Maurizio Bruno, Sergio Rosselli and Antonella Maggio
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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60 .     (11S)-3,3-(Ethylenedioxy)eudesmano-13-ol-6¦Â-acetate
    ÏàËÆ¶È:50%
Archives of Pharmacal Research          2011          34          191-198
Synthesis of C6-epimer derivatives of diacetoxy acetal derivative of santonin and their inducing effects on HL-60 leukemia cell differentiation
Sin Ho Kweon, Keun Tae Kim, Joon Hee Hong, Tae Sung Kim and Bo Gil Choi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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61 .     (11S)-3,3-(Ethylenedioxy)eudesmano-6¦Â-ol-13-acetate
    ÏàËÆ¶È:50%
Archives of Pharmacal Research          2011          34          191-198
Synthesis of C6-epimer derivatives of diacetoxy acetal derivative of santonin and their inducing effects on HL-60 leukemia cell differentiation
Sin Ho Kweon, Keun Tae Kim, Joon Hee Hong, Tae Sung Kim and Bo Gil Choi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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62 .     Jolkinolide B
    ÏàËÆ¶È:50%
Molecules          2011          16          466-476
Feeding Deterrents against Two Grain Storage Insects from Euphorbia fischeriana
Zhu Feng Geng, Zhi Long Liu, Cheng Fang Wang, Qi Zhi Liu, Sheng Min Shen, Zi Mu Liu, Shu Shan Du, and Zhi Wei Deng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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63 .     Schrenkianaone
C20H22O2     ÏàËÆ¶È:50%
Chinese Journal of Analytical Chemistry          2009          37          888-892
Elementary Identification of PotentialAutotoxins from Picea Schrenkiana L itters
LI Zhao-H u i, WANG Qiang, LIAO Jun-Jun, RUAN X iao, PAN Cun-De, JIANG De-An, LUO Chen-Ca i
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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64 .     ent-12¦Á-chloro-8¦Â-cyanomethyl-podocarp-13(17)-en-19-oic acid
C20H28ClNO2     ÏàËÆ¶È:50%
Journal of Natural Products          2011          74          1379-1385
Transformation of Isosteviol Lactam by Fungi and the Suppressive Effects of Its Transformed Products on LPS-Induced iNOS Expression in Macrophages
Bo-Hon Chou, Li-Ming Yang, Shwu-Fen Chang, Feng-Lin Hsu, Li-Hsuan Wang, Wen-Kuang Lin, Pan-Chun Liu, and Shwu-Jiuan Lin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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65 .     longikaurin D
C22H30O7     ÏàËÆ¶È:50%
Acta Scientiarum Naturalium Universitatis Sunyatseni          2000          39(2)          125-127
Two 7, 20-Epoxy-ent-Kauren Diterpenes
WANG Yan-hong, CHEN Yao-zu, SUN Han-dong, LIN Zhong-wen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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66 .     kamebacetal A
C22H30O7     ÏàËÆ¶È:50%
Chinese Journal of Natural Medicines          2012          10          43-47
Chemical constituents of flowers and fruits of Rabdosia excisa
Yue-Xia WU, Wei ZHANG, Ji-Cheng LI, Na LIU
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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