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1 .     coronaridine
    ÏàËÆ¶È:85.7%
Acta Pharmaceutica Sinica          2010          45          471-474
Monomeric indole alkaloids from the aerial parts of Catharanthus roseus
ZHONG Xiang-zhang, WANG Guo-cai, WANG Ying, ZHANG Xiao-qi, YE Wen-cai*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     coronaridine
    ÏàËÆ¶È:76.1%
China Journal of Chinese Materia Medica          2007          32          1296-1299
Study on chemical constituents in rhigome of Ervatamia hainanensis
LIANG Shuang, CHENG Haisheng, JIN Yongsheng, JIN Li, LU Jia, DU Jingling
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     Coronaridine
    ÏàËÆ¶È:76.1%
Phytochemistry          1980          19          1213-1218
Anticancer indole alkaloids of Ervatamia heyneana
Sarath P. Gunasekera, Geoffrey Cordell, Norman R. Farnsworth
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     compound 1
C21H26N2O2     ÏàËÆ¶È:71.4%
Chemical & Pharmaceutical Bulletin          1992          40          2041-2043
Indonesian Medicinal Plants. II. Chemical Structures of Pongapinones A and B, Two New Phenylpropanoids from the Bark of Pongamia pinnata (Papilionaceae)
Isao KITAGAWA,Ru-song ZHANG,Kazuyuki HORI,Katsutoshi TSUCHIYA and Hirotaka SHIBUYA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     coronaridine
    ÏàËÆ¶È:71.4%
Phytochemistry          1990          29          3007-3011
Alkaloids from leaves and stem bark of Ervatamia polyneura
Pascale Clivio,Bernard Richard,Hamid A. Hadi,Bruno David,Thierry Sevenet,Monique Zeches,Louisette Le Men-Olivier
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     N1-methyl-isovoacangine
    ÏàËÆ¶È:69.5%
Journal of Natural Products          1981          Vol 44          459-465
Contribution A L'¨¦tude des Tabernaemontan¨¦es Am¨¦ricaines. III. Alcaloides de Anartia cf. meyeri
F. Ladhar, M. Damak, A. Ahond, C. Poupat, P. Potier, C. Moretti
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     voacangine
    ÏàËÆ¶È:68.1%
Helvetica Chimica Acta          1999          Vol. 82          170
A New Rearrangement in Iboga Alkaloids
Alberto Madinaveitia, Gabriel de la Fuente, and Antonio Gonz¨¢lez
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     voacangine
    ÏàËÆ¶È:68.1%
Chemical & Pharmaceutical Bulletin          1992          40          2041-2043
Indonesian Medicinal Plants. II. Chemical Structures of Pongapinones A and B, Two New Phenylpropanoids from the Bark of Pongamia pinnata (Papilionaceae)
Isao KITAGAWA,Ru-song ZHANG,Kazuyuki HORI,Katsutoshi TSUCHIYA and Hirotaka SHIBUYA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     voacangine
    ÏàËÆ¶È:68.1%
China Journal of Chinese Materia Medica          2007          32          1296-1299
Study on chemical constituents in rhigome of Ervatamia hainanensis
LIANG Shuang, CHENG Haisheng, JIN Yongsheng, JIN Li, LU Jia, DU Jingling
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     Voacangine
    ÏàËÆ¶È:68.1%
Phytochemistry          1980          19          1213-1218
Anticancer indole alkaloids of Ervatamia heyneana
Sarath P. Gunasekera, Geoffrey Cordell, Norman R. Farnsworth
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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11 .     voacangine
    ÏàËÆ¶È:68.1%
Phytochemistry          1984          23          175-178
13C NMR analysis of alkaloids from peschiera fuchsiaefolia
Raquel M. Braga, Hermogenes F. Leit¨¢o Filho, Francisco De A.M. Reist
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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12 .     voacangine
    ÏàËÆ¶È:68.1%
Journal of the Chemical Society, Perkin Transactions 1          1976                   1432-1438
Structures of tabernaelegantines A¨CD and tabernaelegantinines A and B, new indole alkaloids from Tabernaemontana elegans
Ezio Bombardelli, Attilio Bonati, Bruno Gabetta, Ernesto M. Martinelli, Giuseppe Mustich and Bruno Danieli
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     coronaridine
    ÏàËÆ¶È:66.6%
Journal of Natural Products          1988          Vol 51          528
Heyneanine Hydroxyindolenine, A New Indole Alkaloid from Ervatamia coronaria var. plena
Perveen Sharma, Geoffrey A. Cordell
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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14 .     coronaridine
    ÏàËÆ¶È:66.6%
Helvetica Chimica Acta          1976          59          2437-2442
13C-NMR. Spectroscopy of Naturally Occurring Substances. XLV. Iboga Alkaloids
Ernest Wenkert, David W. Cochran, Hugo E. Gottlieb, Edward W. Hagaman, Raimundo Braz Filho, Francisco Jos¨¦ de Abreu Matos and Maria Iracema Lacerda Machado Madruga
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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15 .     19S-Heyneanine
    ÏàËÆ¶È:66.6%
Phytochemistry          1980          19          1213-1218
Anticancer indole alkaloids of Ervatamia heyneana
Sarath P. Gunasekera, Geoffrey Cordell, Norman R. Farnsworth
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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16 .     (-)-3R-Methoxycoronaridine
    ÏàËÆ¶È:63.6%
Phytochemistry          1994          37          1729-1735
Indole alkaloids and terpenoids fromTabernaemontana markgrafiana
Helene B. Nielsen, Alan Hazell, Rita Hazell, Felipe Ghia, Kurt B.G. Torssell
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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17 .     voacangine
    ÏàËÆ¶È:63.6%
Helvetica Chimica Acta          1976          59          2437-2442
13C-NMR. Spectroscopy of Naturally Occurring Substances. XLV. Iboga Alkaloids
Ernest Wenkert, David W. Cochran, Hugo E. Gottlieb, Edward W. Hagaman, Raimundo Braz Filho, Francisco Jos¨¦ de Abreu Matos and Maria Iracema Lacerda Machado Madruga
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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18 .     alstoyunine A
C20H24N2O3     ÏàËÆ¶È:61.9%
Journal of Natural Products          2009          72          1836-1841
Monoterpenoid Indole Alkaloids from Alstonia yunnanensis
Tao Feng, Yan Li,Xiang-Hai Cai, Xun Gong, Ya-Ping Liu, Rong-Ting Zhang, Xiang-Yun Zhang, Qin-Gang Tan, and Xiao-Dong Luo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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19 .     19-Heyneanine
C21H26N2O3     ÏàËÆ¶È:61.9%
Chemistry of Natural Compounds          2008          44          675-678
INDOLE ALKALOIDS FROM Ervatamia flabellformia
Shuang Liang, Haisheng Chen, Li Jin,Weidong Xuan, and Wei-Dong Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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20 .     compound 18
    ÏàËÆ¶È:61.9%
Natural Product Research          1996          8          75-82
Studies on the Synthesis of Strychnos Alkaloids
Daniele Passarella; Swargam Sathyanarayana; Mercedes Amat; Joan Bosch
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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21 .     19-heyneanine
    ÏàËÆ¶È:61.9%
China Journal of Chinese Materia Medica          2007          32          1296-1299
Study on chemical constituents in rhigome of Ervatamia hainanensis
LIANG Shuang, CHENG Haisheng, JIN Yongsheng, JIN Li, LU Jia, DU Jingling
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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22 .     5,6-Dehydrocoronaridine
    ÏàËÆ¶È:61.9%
Phytochemistry          1994          37          1729-1735
Indole alkaloids and terpenoids fromTabernaemontana markgrafiana
Helene B. Nielsen, Alan Hazell, Rita Hazell, Felipe Ghia, Kurt B.G. Torssell
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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23 .     leepacine
C21H22N2O3     ÏàËÆ¶È:61.9%
Phytochemistry          1991          30          1285-1293
Alkaloids from Rhazya stricta
Atta-ur-Rahman, Khurshid Zaman, Shahnaz Perveen, Habib-ur-Rehman, Anium Muzaffar, M.Iqbal Choudhary, Azra Pervin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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24 .     stapfinine
    ÏàËÆ¶È:61.9%
Phytochemistry          1986          25          1781-1782
Stapfinine, an indole alkaloid from Ervatamia coronaria
Atta-ur-Rahman, Anjum Muzaffar, Nader Daulatabadi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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25 .     conopharyngine
    ÏàËÆ¶È:60.8%
Journal of Natural Products          1985          Vol 48          400-423
Antimicrobially Active Alkaloids from Tabernaemontana chippii
Teris A. Van Beek, Robert Verpoorte, Anders Baerheim Svendsen, Roel Fokkens
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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26 .     Conopharyngine
    ÏàËÆ¶È:60.8%
Phytochemistry          1984          23          1771-1778
Antimicrobially active alkaloids from Tabernaemontana pachysiphon
T. A. van Beek, F. L. C. Kuijlaars, P. H. A. M. Thomassen, R. Verpoorte, A. Baerheim Svendsen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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27 .     pseudoakuammigine
    ÏàËÆ¶È:59.0%
Planta Medica          1989          55          463-466
Indole Alkaloids from Aistonia angustjfolia
Wen-lan Hi, Ji-ping Zhu, and Manfred Hesse
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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28 .     (-)-akuammicin
    ÏàËÆ¶È:59.0%
Planta Medica          1989          55          463-466
Indole Alkaloids from Aistonia angustjfolia
Wen-lan Hi, Ji-ping Zhu, and Manfred Hesse
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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29 .     voacristine
    ÏàËÆ¶È:59.0%
Planta Medica          1983          49          148-150
Tertiary Indole Alkaloids from Leaves of Tabernaemontana dichotoma
Premila Perera, Gunnar Samuelsson, Tens A. van Beek and Robert Verpoorte
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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30 .     10-deoxyakuammine
    ÏàËÆ¶È:59.0%
Journal of Natural Products          1992          Vol 55          380
Akuammine and Dihydroakuammine, Two Indolomonoterpene Alkaloids Displaying Affinity for Opioid Receptors
Guy Lewin, Patrick Le M¨¦nez, Yves Rolland, Anne Renouard, Eva Giesen-Crouse
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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31 .     Voacangarine
    ÏàËÆ¶È:59.0%
Phytochemistry          1980          19          1213-1218
Anticancer indole alkaloids of Ervatamia heyneana
Sarath P. Gunasekera, Geoffrey Cordell, Norman R. Farnsworth
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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32 .     3-(2-oxopropyl)coronaridine
    ÏàËÆ¶È:58.3%
China Journal of Chinese Materia Medica          2007          32          1296-1299
Study on chemical constituents in rhigome of Ervatamia hainanensis
LIANG Shuang, CHENG Haisheng, JIN Yongsheng, JIN Li, LU Jia, DU Jingling
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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33 .     17-O-aaztyl-19,20-dihydrovoachalotine
C24H30N2O4     ÏàËÆ¶È:58.3%
Phytochemistry          1976          15          2021-2022
17-O-acetyl-19,20-dihydrovoachalotine, a new alkaloid from Voacanga chalotiana
Ezio Bombardelli, Attilio Bonati, Bruno Gabetta, Ernesto Martinelli, Giuseppe Mustich, Bruno Danieli
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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34 .     flabelliformine
C21H26N2O3     ÏàËÆ¶È:57.1%
Helvetica Chimica Acta          2008          Vol. 91          239
Three New Monoterpenoid Indole Alkaloids from Ervatamia flabelliformis
Shuang Liang, Hai-Sheng Chen, Yun-Heng Shen, Wei-Dong Zhang, Yong-Sheng Jin, and Run-Hui Liu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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35 .     yohimbine
    ÏàËÆ¶È:57.1%
Journal of Natural Products          2001          64          193-195
Hydroxylation of Yohimbine in Superacidic Media: One-Step Access to Human Metabolites 10 and 11-Hydroxyyohimbine
Alain Duflos,Florence Redoules,Jacques Fahy, Jean-Claude Jacquesy, and Marie-Paule Jouannetaud
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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36 .     compound 19
    ÏàËÆ¶È:57.1%
Chemistry of Natural Compounds          1986          22          1-13
APPLICATIONS OF 1H AND 13C NMR SPECTROSCOPY IN STRUCTURAL INVESTIGATIONS OF Vinca INDOLE ALKALOIDS
M. R. Yagudaev
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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37 .     10,11-demethoxychippiine
    ÏàËÆ¶È:57.1%
Natural Product Research          1999          13          143-146
Dippinine A, A New Alkaloid of the Chippiinetype From A Malayan Tabernaemontana
Toh-Seok Kam; Kooi-Mow Sim
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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38 .     Vinblastine
    ÏàËÆ¶È:57.1%
Journal of Natural Products          1992          Vol 55          269
Metabolism of the Catharanthus Alkaloids: from Streptomyces griseus to Monoamine Oxidase B
John P. N. Rosazza, Michael W. Duffel, Sayed El-Marakby, Sung Ho Ahn
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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39 .     undulifoline
C20H24N2O3     ÏàËÆ¶È:57.1%
Phytochemistry          1992          31          1078-1079
Alkaloids from alstonia undulifolia
Georges Massiot, Ahcene Boumendjel, Jean-Marc Nuzillard, Bernard Richard, Louisette Le Men-Olivier, Bruno David, Hamid A. Hadi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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40 .     heyneanine
    ÏàËÆ¶È:57.1%
Helvetica Chimica Acta          1976          59          2437-2442
13C-NMR. Spectroscopy of Naturally Occurring Substances. XLV. Iboga Alkaloids
Ernest Wenkert, David W. Cochran, Hugo E. Gottlieb, Edward W. Hagaman, Raimundo Braz Filho, Francisco Jos¨¦ de Abreu Matos and Maria Iracema Lacerda Machado Madruga
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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41 .     cleavamine
    ÏàËÆ¶È:57.1%
Helvetica Chimica Acta          1976          59          2711-2723
13C-NMR. Spectroscopy of Naturally Occuring Substances. XLII. Conformational analysis of quebrachamine-like indole alkaloids and related substances
Ernest Wenkert, Edward W. Hagaman, Nicole Kunesch, Nai-yi Wang and B¨¦la Zsadon
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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42 .     16¦Á-carbomethoxy-15,20¦Â-dihydrocleavamine
    ÏàËÆ¶È:57.1%
Helvetica Chimica Acta          1976          59          2711-2723
13C-NMR. Spectroscopy of Naturally Occuring Substances. XLII. Conformational analysis of quebrachamine-like indole alkaloids and related substances
Ernest Wenkert, Edward W. Hagaman, Nicole Kunesch, Nai-yi Wang and B¨¦la Zsadon
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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43 .     16-epivoacarpine
    ÏàËÆ¶È:57.1%
Chemical & Pharmaceutical Bulletin          1987          35          4668-4671
INDOLE ALKALOIDS ISOLATED FROM GELSEMIUM ELEGANS (THAILAND) : 19- (Z) -AKUAMMIDINE, 16-EPI-VOACARPINE, 19-HYDROXYDIHYDRO-GELSEVIRINE, AND THE REVISED STRUCTURE OF KOUMIDINE
Shin-ichiro Sakai,Sumphan Wongseripipatana,Dhavadee Ponglux,Masaki Yokota,Koreharu Ogata,Hiromitsu Takayama and Norio Aimi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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44 .     3-hydroxy-3,4-secocoronaridine
C21H28O3N2     ÏàËÆ¶È:57.1%
Phytochemistry          1990          29          3007-3011
Alkaloids from leaves and stem bark of Ervatamia polyneura
Pascale Clivio,Bernard Richard,Hamid A. Hadi,Bruno David,Thierry Sevenet,Monique Zeches,Louisette Le Men-Olivier
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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45 .     compound 33
    ÏàËÆ¶È:57.1%
Journal of Heterocyclic Chemistry          2000          37          245-251
Synthesis of vinca alkaloids and related compounds part 94. Epimerization of compounds with aspidospermane and D-secoaspidospermane skeleton
György Kalaus, Lajos Szab¨®, J¨¢nos Éles, Csaba Sz¨¢ntay, Imre Juh¨¢sz, IstvÁn Greiner, J¨¢nos Brlik and M¨¢ria Kajt¨¢r-Peredy
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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46 .     19Z-16-epi-Voacarpine
C21H25N2O4     ÏàËÆ¶È:57.1%
Tetrahedron Letters          2005          46          5857-5861
Six new indole alkaloids from Gelsemium sempervirens Ait. f.
Noriyuki Kogure, Chika Nishiya, Mariko Kitajima, Hiromitsu Takayama
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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47 .     16-epi-voacarpine
    ÏàËÆ¶È:57.1%
Tetrahedron Letters          2005          46          5857-5861
Six new indole alkaloids from Gelsemium sempervirens Ait. f.
Noriyuki Kogure, Chika Nishiya, Mariko Kitajima, Hiromitsu Takayama
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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48 .     compound 7a
    ÏàËÆ¶È:57.1%
Bulletin of the Chemical Society of Japan          1989          62          880-887
Isolation of Four 2,3,5,6,11,11b-Hexahydro-3-oxo-1H-indolizino[8,7-b]indole-5-carboxylic Acids from Clerodendron Trichotomum Thunb and Properties of Their Derivatives
Hajime Irikawa, Yasuhiro Toyoda, Hiroaki Kumagai, Yasuaki Okumura
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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49 .     (16R,17S)-14¦Á-hydroxy-3-isorauniticine methyl acetal
C22H28N2O5     ÏàËÆ¶È:54.5%
Chemical & Pharmaceutical Bulletin          1986          34          3713-3721
A New Indole Alkaloid, 14¦Á-Hydroxyrauniticine : Structure Revision and Partial Synthesis
ETSUJI YAMANAKA,ETSUKO MARUTA,SATOE KASAMATSU,NORIO AIMI,SHIN-ICHIRO SAKAI,DHAVADEE PONGLUX,SUMPHAN WONGSERIPIPATANA,TANOMJIT SUPAVITA and J. DAVID PHILLIPSON
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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50 .     (¡À)-(8¦Â,9¦Á,14¦Á)-2-Methoxy-11¦Â-methoxymethyl-17-acetylgona-1,3,5(10),13(17)-tetraene
C22H28O3     ÏàËÆ¶È:54.5%
Steroids          2006          71          459-468
Efficient synthesis of C-11 functionalized steroids
Patrick Bazzini, Malika Ibrahim-Ouali, H¨¦l¨¨ne Pellissier, Maurice Santelli
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ  

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1 .     coronaridine hydroxyindolenine
C21H26N2O3     ÏàËÆ¶È:66.6%
Chemistry of Natural Compounds          2008          44          675-678
INDOLE ALKALOIDS FROM Ervatamia flabellformia
Shuang Liang, Haisheng Chen, Li Jin,Weidong Xuan, and Wei-Dong Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     coronaridine hydroxyindolenine
    ÏàËÆ¶È:66.6%
China Journal of Chinese Materia Medica          2007          32          1296-1299
Study on chemical constituents in rhigome of Ervatamia hainanensis
LIANG Shuang, CHENG Haisheng, JIN Yongsheng, JIN Li, LU Jia, DU Jingling
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     Coronaridine hydroxyindolenine
    ÏàËÆ¶È:65%
Phytochemistry          1994          37          1729-1735
Indole alkaloids and terpenoids fromTabernaemontana markgrafiana
Helene B. Nielsen, Alan Hazell, Rita Hazell, Felipe Ghia, Kurt B.G. Torssell
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     vocangine-7-hydroxyindolenine
    ÏàËÆ¶È:61.9%
Planta Medica          1988          54          364
Alkaloids from Trachelospermum jasmino ides
Atta-ur-Rahman , T. Fatima, George Crank, and Shaheen Wasti
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     (2RS,7SR)-7,9,10,11-Tetrahydro-10,10-dimethyl-3-phenyl-2,7-methano-1-benzoxonin-8(2H)-one
C21H22O2     ÏàËÆ¶È:57.8%
Helvetica Chimica Acta          2011          Vol. 94          1431-1439
Manganese(III) Acetate Catalyzed Oxidative Radical Additions of ¦Á-Dicarbonyl Compounds to 1- and 2-Phenylcyclohepta-1, 3, 5-triene
Esra Findik and Mustafa Ceylan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     ketotriester
    ÏàËÆ¶È:55.5%
Journal of Natural Products          1984          Vol 47          592-599
Cmr Spectroscopy of Labdanic Diterpenes and Related Substances
Josette Bastard, Do Khac Duc, Marcel Fetizon, Malcolm J. Francis, Peter K. Grant, Rex T. Weavers, Chikara Kaneko, G. Vernon Baddeley, Jean-Marie Bernassau, Ivor R. Burfitt, Peter M. Wovkulich, Ernest Wenkert
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     N-((N-Boc-amino)hexanoyl)-para-hydroxyphenyl-L-para-tyrosinamide
C26H35N3O6     ÏàËÆ¶È:55.5%
Steroids          2012          77          403-412
Design of novel tyrosine-nitrogen mustard hybrid molecules active against uterine, ovarian and breast cancer cell lines
Caroline Descôteaux, Kevin Brasseur, Val¨¦rie Leblanc, Sophie Parent, Éric Asselin, Gervais B¨¦rub¨¦
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     Compound 2g
    ÏàËÆ¶È:55.5%
Magnetic Resonance in Chmesitry          2001          39          105-108
1H and 13C spectral assignment of 1, 4, 5, 6, 7, 8-hexahydroquinolines and their oxa-analogues 5, 6, 7, 8-tetrahydro-4H-chromenes
Margarita Su¨¢rez, Dolores Molero, Esperanza Salfran, Nazario Mart¨ªn, Yamila Verdecia, Roberto Martinez, Estael Ochoa, Livan Alba, Margarita Quinteiro and Carlos Seoane
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     circinatin
C20H31O7N3     ÏàËÆ¶È:55%
Experientia          1990          46          1206-1209
The structure of circinatin, a non-toxic metabolite from the plant pathogenic fungusPericonia circinata
V. Macko, M. B. Stimmel, H. Peeters, T. J. Wolpert and L. D. Dunkle, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     methyl 4-[(3,4-dihydro-2H-[1,3]oxazino[3,2-a]indole-10-carbonyl)amino]-1-methylpiperidinylpentanoate
C24H33N3O4     ÏàËÆ¶È:54.5%
Bioorganic & Medicinal Chemistry          2010          18          8600-8613
Synthesis and pharmacological properties of novel hydrophilic 5-HT4 receptor antagonists
Bjarne Brudeli, Lise Rom¨¢n Moltzau, Kjetil Wessel Andressen, Kurt A. Krobert, Jo Klaveness, Finn Olav Levy
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

11 .     rauflorine
    ÏàËÆ¶È:52.6%
Planta Medica          1996          62          577-579
A1H- and 13C-NMR Study of Seven Ajma line-Type Alkaloids
Reija Jokela and Mauri Lounasmaa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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12 .     (3aS,8aR)-3a-Ethyl-1,2,3,3a,8,8a-hexahydro-1,8-dimethyl-5-[4-(pyrrolidin-1-ylmethyl)-1H-1,2,3-triazol-1-yl]pyrrolo[2,3-b]indole
C21H30N6     ÏàËÆ¶È:52.6%
Helvetica Chimica Acta          2011          Vol. 94          1496-1505
An Efficient Synthesis of a (-)-Physostigmine s Library for Identifying Potential Anti-Alzheimer s Agents
Yi Wu, Fusheng Wang, Hao Song, and Yong Qin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

13 .     compound 2c
    ÏàËÆ¶È:52.6%
Phytochemistry          1987          26          745-747
Oxygenated fatty acids from Lemna trisulca
Pietro Monaco,Lucio Previtera
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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14 .     compound 44
C21H25NO4     ÏàËÆ¶È:52.6%
Heterocycles          2006          70          423-459
Aza-[3+3] Annulations. Part 6. Total Synthesis of Putative (-)-Lepadiformine and (-)-Cylindricine C
Jiashi Wang, Jacob J. Swidorski, Nadiya Sydorenko, Richard P. Hsung,* Heather A. Coverdale, Jennifer M. Kuyava, and Jia Liu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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15 .     2-(Benzhydrylsulfinyl)acetic acid-1-{(3-cyclohexyl-propyl)-1H-[1,2,3]triazol-4-yl}methyl ester
C27H33N3O3S     ÏàËÆ¶È:52.6%
Molecules          2011          16          10409-10419
Convenient Synthesis and Biological Evaluation of Modafinil Derivatives: Benzhydrylsulfanyl and Benzhydrylsulfinyl [1,2,3]triazol-4-yl-methyl Esters
Jae-Chul Jung, Yeonju Lee, Jee-Young Son, Eunyoung Lim, Mankil Jung and Seikwan Oh
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

16 .     5-methoxystrictamine
C21H24N2O3     ÏàËÆ¶È:52.3%
Helvetica Chimica Acta          2005          Vol. 88          2508
Three New Indole Alkaloids from the Leaves of Alstonia scholaris
Hua Zhou, Hong-Ping He, Xiao-Dong Luo, Yue-Hu Wang, Xian-Wen Yang, Ying-Tong Di,and Xiao-Jiang Hao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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17 .     16¦Á-carbomethoxy-15,20¦Á-dihydrocleavamine
    ÏàËÆ¶È:52.3%
Helvetica Chimica Acta          1976          59          2711-2723
13C-NMR. Spectroscopy of Naturally Occuring Substances. XLII. Conformational analysis of quebrachamine-like indole alkaloids and related substances
Ernest Wenkert, Edward W. Hagaman, Nicole Kunesch, Nai-yi Wang and B¨¦la Zsadon
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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18 .     (¡À)-iboxyphylline
C21H26N2O3     ÏàËÆ¶È:52.3%
Heterocycles          2008          75          65-76
Synthesis of Vinca Alkaloids and Related Compounds. Part 109. An Intramolecular [4+2] Cycloaddition Mediated Biomimetic Synthesis of (¡À)-Iboxyphylline
Fl¨®ri¨¢n T¨®th, György Kalaus, Gergely Pipa, Istv¨¢n Greiner, Áron Szollosy, Attila Rill, Ágnes Gömöry, L¨¢szl¨® Hazai, and Csaba Sz¨¢ntay
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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19 .     tacamine
    ÏàËÆ¶È:52.3%
Tetrahedron letters          1982          23          4827-4830
Tacamine, the first example of a new class of indole alkaloids
T.A. Van Beek, P.P. Lankhorst, R. Verpoorte, A.Baerheim Svendsen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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20 .     methyl 4-[(3,4-dihydro-2H-[1,3]oxazino[3,2-a]indole-10-carbonyl)amino]-1-methylpiperidinylhexanoate
C25H35N3O4     ÏàËÆ¶È:52.1%
Bioorganic & Medicinal Chemistry          2010          18          8600-8613
Synthesis and pharmacological properties of novel hydrophilic 5-HT4 receptor antagonists
Bjarne Brudeli, Lise Rom¨¢n Moltzau, Kjetil Wessel Andressen, Kurt A. Krobert, Jo Klaveness, Finn Olav Levy
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

21 .     4-[(3,4-dihydro-2H-[1,3]oxazino[3,2-a]indole-10-car-bonyl)amino]-1-methylpiperidinylpropanoic acid
C21H27N3O4     ÏàËÆ¶È:52.1%
Bioorganic & Medicinal Chemistry          2010          18          8600-8613
Synthesis and pharmacological properties of novel hydrophilic 5-HT4 receptor antagonists
Bjarne Brudeli, Lise Rom¨¢n Moltzau, Kjetil Wessel Andressen, Kurt A. Krobert, Jo Klaveness, Finn Olav Levy
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

22 .     panduratin H
C20H26O2     ÏàËÆ¶È:50%
Chemical & Pharmaceutical Bulletin          2008          56(4)          491-496
Panduratins D¡ªI, Novel Secondary Metabolites from Rhizomes of Boesenbergia pandurata
Nwet Nwet WIN,Suresh AWALE,Hiroyasu ESUMI,Yasuhiro TEZUKA,and Shigetoshi KADOTA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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23 .     demethoxypurpeline
C20H22N2O     ÏàËÆ¶È:50%
Phytochemistry          2002          60          315-320
Indole alkaloids from Rauvolfia bahiensis A.DC. (Apocynaceae)
Lucilia Kato, Raquel Marques Braga, Ingrid Koch, Luiza Sumiko Kinoshita
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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24 .     phlogacantholide B
C20H28O4     ÏàËÆ¶È:50%
Journal of Natural Products          2005          68          86-89
Two Diterpenes and Three Diterpene Glucosides from Phlogacanthus curviflorus
Xiao-Hong Yuan, Bo-Gang Li, Xiu-Yun Zhang, Hua-Yi Qi, Min Zhou, and Guo-Lin Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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25 .     9¦Â-hydroxy-2¦Â-methoxyclovan-10-one
C16H26O3     ÏàËÆ¶È:50%
Journal of Natural Products          2004          67          793-798
Structure−Activity Relationships in the Fungistatic Activity against Botrytis cinerea of Clovanes Modified on Ring C
Athina Deligeorgopoulou, Antonio J. Macas-Snchez, Daniel J.Mobbs, Peter B. Hitchcock, James R. Hanson, and Isidro G. Collado
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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26 .     5(6)-dihydro-6-methoxyterreyclic acid A
C16H24O4     ÏàËÆ¶È:50%
Journal of Natural Products          2003          66          1567-1573
Cytotoxic Constituents of Aspergillus terreus from the Rhizosphere of Opuntia versicolor of the Sonoran Desert
E. M. Kithsiri Wijeratne,Thomas J. Turbyville,Zhongge Zhang, Donna Bigelow,Leland S. Pierson, III,Hans D. VanEtten, Luke Whitesell,Louise M. Canfield, and A. A. Leslie Gunatilaka
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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27 .     8¦Á,14-dihydro-7-oxohelioscopinolide A
C20H28O4     ÏàËÆ¶È:50%
Journal of Natural Products          1998          61          749-756
Macrocyclic Diterpenoids from Euphorbia semiperfoliata
Giovanni Appendino, Sven Jakupovic, Gian Cesare Tron, Jasmin Jakupovic, Veronique Milon, and Mauro Ballero
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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28 .     ent-1¦Á-hydroxykauran-12-one
C20H32O2     ÏàËÆ¶È:50%
Journal of Natural Products          1997          60          421-424
1-Hydroxyditerpenes from Two New Zealand Liverworts, Paraschistochila pinnatifolia and Trichocolea mollissima
Stephen D. Lorimer, Nigel B. Perry, Elaine J. Burgess, and Lysa M. Foster
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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29 .     Voacangine hydroxyindolenine
C22H28N2O4     ÏàËÆ¶È:50%
Chemistry of Natural Compounds          2008          44          675-678
INDOLE ALKALOIDS FROM Ervatamia flabellformia
Shuang Liang, Haisheng Chen, Li Jin,Weidong Xuan, and Wei-Dong Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

30 .     4-epiabietic acid
C20H30O2     ÏàËÆ¶È:50%
Acta Bot. Boreal. -Occident. Sin.          2009          29          2326-2330
Isolation and identification of Antifungal Components from Juniperus chinensis cv. Kaizuca
NIU Xin-wei, LUO Lan, SUN Jia-long, LU Shi-wei, YUAN Zhong-lin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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31 .     parvineostemonine
C17H25NO2     ÏàËÆ¶È:50%
Chinese Chemical Letters          2003          14          173-175
A Novel Alkaloid from Stemona parviflora
Chang Qiang KE, Zhi Sheng HE, Yi Ping YANG, Yang YE
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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32 .     compound 5g
    ÏàËÆ¶È:50%
Chinese Chemical Letters          2006          17          150-152
Multicomponent Reaction in Ionic Liquid: A Novel and Green Synthesis of 1, 4-Dihydropyridine Derivatives
Xin Ying ZHANG, Yan Zhen LI, Xue Sen FAN, Gui Rong QU,Xue Yuan HU, Jian Ji WANG
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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33 .     Methyl 2-(1-naphthyl)tetrahydro-1H-thieno[3,4-b]pyrrole-6a(6H)-carboxylate
C18H19NO2S     ÏàËÆ¶È:50%
Molecules          1998          3          60-63
Intramolecular Cycloaddition of Imines of Cysteine Derivatives
Ana M. T. D. P. V. Cabral, Antonio M. d'A Rocha Gonsalves and Teresa M. V. D. Pinho e Melo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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34 .     (20R,23S,25S)-De-A,B-25-Trimethylsilylhydroxy-cholestane-8-one-26,23-N-methyl lactam
    ÏàËÆ¶È:50%
Molecules          2003          8          488-499
Novel Heteroatom-containing Vitamin D3 Analogs: Efficient Synthesis of 1¦Á, 25-Dihydroxyvitamin D3-26, 23-lactam
Yuko Kato, Yuichi Hashimoto and Kazuo Nagasawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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35 .     (2S,3'S)-2-(2-oxo-2,3,4,5-tetrahydro-1H-benzoazepin-3-ylamino)-4-phenylbutyricacid ethyl ester
C22H26N2O3     ÏàËÆ¶È:50%
Molecules          2006          11          641-648
Formal Synthesis of the ACE Inhibitor Benazepril¡¤HCl via an Asymmetric Aza-Michael Reaction
Luo-Ting Yu, Ji-Ling Huang, Ching-Yao Chang and Teng-Kuei Yang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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36 .     3¦Á,8¦Á,9¦Á-trihydroxycedrane
    ÏàËÆ¶È:50%
Phytochemistry          1996          42          1583-1586
Biotransformation of cedrol and related compounds by Mucor plumbeus
Braulio M. Fraga, Ricardo Guillermo, James R. Hanson, Almaz Truneh
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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37 .     heteroscyphic acid A
C20H32O2     ÏàËÆ¶È:50%
Phytochemistry          1994          37          1263-1268
Diterpenes of the clerodane-type from cultured cells of Heteroscyphus planus
Kensuke Nabeta, Tadashi Oohata, Noriko Izumi, Kenji Katoh
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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38 .     13¦Á-(4'hydroxytigloyloxy)lupanine
C20H30N2O4     ÏàËÆ¶È:50%
Phytochemistry          1993          32          1603-1605
(+)-13¦Á-(4'-Hydroxytigloyloxy) lupanine from Ormosia krugii
Martua P. Nasution, A.Douglas Kinghorn
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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39 .     pearsonine
    ÏàËÆ¶È:50%
Phytochemistry          1991          30          3631-3634
Co-occurrence of hydroxylated lupanines and their corresponding angelate esters inPearsonia species
Gerhard H. Verdoorn, Ben-Erik van Wyk
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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40 .     Dimethyl 2,2-dimethoxy-4-(3-nitrobenzyl)glutarate
C16H21NO8     ÏàËÆ¶È:50%
Chemical Research in Chinese Universities          2007          23          284-288
Syntheses and Bioactivities of 4-Ar-2-oxo-glutaric Acids
CHEN Qiu-yun,ZHANG Rong-xian, LIU Qing-shan and Scho field Christopher
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

41 .     2-{1-[(3aS,8aR)-3a-Ethyl-1,2,3,3a,8,8a-hexahydro-1,8-dimethylpyrrolo[2,3-b]indol-5-yl]-1H-1,2,3-triazol-4-yl}ethanol
C18H25N5O     ÏàËÆ¶È:50%
Helvetica Chimica Acta          2011          Vol. 94          1496-1505
An Efficient Synthesis of a (-)-Physostigmine s Library for Identifying Potential Anti-Alzheimer s Agents
Yi Wu, Fusheng Wang, Hao Song, and Yong Qin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

42 .     15S-Hydroxy-7S-methoxy-2-methyl-2E,4E,10E-hexadecatrienoic Acid
C18H30O4     ÏàËÆ¶È:50%
Journal of Natural Products          2001          64          472-479
Synthesis of (7S,15S)- and (7R,15S)-Dolatrienoic Acid
Jonathan J. Duffield and George R. Pettit
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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43 .     15S-Hydroxy-7R-methoxy-2-methyl-2E,4E,10E-hexadecatrienoic acid
C18H30O4     ÏàËÆ¶È:50%
Journal of Natural Products          2001          64          472-479
Synthesis of (7S,15S)- and (7R,15S)-Dolatrienoic Acid
Jonathan J. Duffield and George R. Pettit
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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44 .     compound [2H3]-9
    ÏàËÆ¶È:50%
Chemical & Pharmaceutical Bulletin          2009          57          1421-1424
A Facile Method for Preparation of [2H3]-Sufentanil and Its Metabolites
Sankareswaran Srimurugan, Kaliyappan Murugan and Chinpiao Chen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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45 .     compound 3
    ÏàËÆ¶È:50%
Tetrahedron Letters          2000          41          603-607
Documentation of a rare example of an intramolecular 1,2-addition of a trialkylborane to a carbonyl group
Robert K. BoeckmanJr., Lorna H. Mitchell, Pengcheng Shao, Rene J. Lachicotte
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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46 .     pearsonine
    ÏàËÆ¶È:50%
Phytochemistry          1990          29          1297-1302
Esters of quinolizidine alkaloids from the genus Pearsonia
Gerhard H. Verdoorn,Ben-Erik van Wyk
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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47 .     3-hydroxy-3,4-secocoronaridine
C21H28O3N2     ÏàËÆ¶È:50%
Phytochemistry          1990          29          3007-3011
Alkaloids from leaves and stem bark of Ervatamia polyneura
Pascale Clivio,Bernard Richard,Hamid A. Hadi,Bruno David,Thierry Sevenet,Monique Zeches,Louisette Le Men-Olivier
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

48 .     1,9,17,25-tetraazapentacyclo[23.7.1.19,17.010,15.027,32]tetra-triaconta-10(15),11,13,27(32),28,30-hexaene-16,26,33,34-tetrone
C30H36N4O4     ÏàËÆ¶È:50%
Journal of Heterocyclic Chemistry          2007          44          1501-1504
Synthesis of quinazolinophanes containing bridgehead nitrogen atoms from quinazoline-2,4(1H,3H)-dione
R. L. Sharam,Jasbir Singh,Surinder Kumar,Daljeet Kour,Anand Sachar,Shallu,Poonam and Bhawana
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

49 .     methyl 2-tert-butoxycarbonylamino-5-[(3-iodo-1H-indole-2-yl)carbonylamino]pent-2-enoate
    ÏàËÆ¶È:50%
Journal of Heterocyclic Chemistry          2005          42          1433-1441
Preparation and reactivity of 5-substituted azepino[3,4-b]indoles
C. Montagne,N. Laurent,B. Joseph and J.-Y. M¨¦rour
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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50 .     compound 9b
C20H24IN3O5     ÏàËÆ¶È:50%
Journal of Heterocyclic Chemistry          2005          42          1433-1441
Preparation and reactivity of 5-substituted azepino[3,4-b]indoles
C. Montagne,N. Laurent,B. Joseph and J.-Y. M¨¦rour
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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