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1 .     dihydrocorynantheol
    ÏàËÆ¶È:100%
Journal of Natural Products          1983          Vol 46          694-707
Aspidosperma de Guyane: Alcaloïdes de Aspidosperma marcgravianum
G. M. T. Robert, A. Ahond, C. Poupat, P. Potier, C. Joll¨¨s, A. Jousselin, H. Jacquemin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     (3R,12bS)-methyl (3-ethyl-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizin-2-yl)acetate
C20H26O2N2     ÏàËÆ¶È:85%
Heterocycles          2010          81          1791-1798
Formal Syntheses of Dihydrocorynantheine and Isorhynchophylline via Proline Catalyzed Mannich-Michael Reaction
Kazuhiro Nagata, Hitomi Ishikawa, Ayako Tanaka, Michiko Miyazaki, Takuya Kanemitsu, and Takashi Itoh
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     dihydrocorynantheol
    ÏàËÆ¶È:78.9%
Planta Medica          1986          52          73-74
The Isolation and 13C-NMR of Dihydrocorynantheol and Rhazimol (Deacetylakuammiline), Alkaloids from the Roots of Rhazya stricta
Atta-ur-Rahman and Khurshid Zaman
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     corynantheol
    ÏàËÆ¶È:78.9%
Phytochemistry          1991          30          1697-1700
Matadine, a cytotoxic alkaloid from Strychnos gossweileri
J. Quetin-Leclercq, P. Coucke, C. Delaude, R. Warin, R. Bassleer, L. Angenot
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     corynantheol
    ÏàËÆ¶È:78.9%
Phytochemistry          1987          26          2839-2846
Alkaloids of Strychnos johnsonii
Georges Massiot,Philippe Th¨¦penier,Marie-Jos¨¦ Jacquier,Louisette Le Men-Olivier,Robert Verpoorte,Cl¨¦ment Delaude
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     corynantheol
    ÏàËÆ¶È:78.9%
Phytochemistry          1988          27          1923-1926
10-Hydroxy-Nb-methyl-corynantheol,a new quaternary alkaloid from the stem bark of Strychnos usambarensis
J. Quetin-Leclercq,L. Angenot
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     10-methoxy-dihydrocorynantheol
    ÏàËÆ¶È:75%
Phytochemistry          1992          31          2507-2511
Indole alkaloids from Aspidosperma pruinosum
Jos¨¦ J. Taveira, Domingos S. Nunes, Luzia Koike, Francisco de A.M. Reis
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     10-hydroxydihydrocorynantheol
C19H26N2O2     ÏàËÆ¶È:73.6%
Journal of Natural Products          1981          Vol 44          193-199
Contribution À L'¨¦tude des Ochrosiin¨¦es: Alcaloïdes de Ochrosia moorei
A. Ahond, H. Fernandez, M. Julia-Moore, C. Poupat, V. S¨¢nchez, P. Potier, S. K. Kan, T. S¨¦venet
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     decarbomethoxytetrahydrosecodine
    ÏàËÆ¶È:73.6%
Phytochemistry          1993          33          217-219
Crooksidine, an indole alkaloid from Haplophyton crooksii
M.A. Mroue, M.A. Ghuman, M. Alam
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     dihydrositsirikine
    ÏàËÆ¶È:71.4%
Phytochemistry          1992          31          2507-2511
Indole alkaloids from Aspidosperma pruinosum
Jos¨¦ J. Taveira, Domingos S. Nunes, Luzia Koike, Francisco de A.M. Reis
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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11 .     19,20-dihydroisositsirikine
    ÏàËÆ¶È:71.4%
Phytochemistry          1991          30          3785-3792
Alkaloids from leaves and root bark ofErvatamia hirta
Pascale Clivio, Bernard Richard, Jean-Robert Deverre, Thierry Sevenet, Monique Zeches, Louisette Le Men-Oliver
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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12 .     ¦Á-yohimbine
    ÏàËÆ¶È:71.4%
Natural Product Research and Development          2007          19          235-239
Indole Alkaloids from Rauwolfia vomitoria
LI Lin;HE Hong-ping; ZHOU Hua; HAO Xiao-jiang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     0-methoxydihydrocorynantheol
C18H28N2O2     ÏàËÆ¶È:70%
Planta Medica          1996          62          42-45
Total Syntheses of 10-Methoxydihydrocorynantheol and 10-Methoxycorynantheidol
Miettinen, J.; Jokela, R.; Lounasmaa, M.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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14 .     epi-yohimbol
    ÏàËÆ¶È:68.4%
Journal of Natural Products          1994          Vol 57          287
Indole Alkaloids from Antirhea portoricensis
Bernard Weniger, Robert Anton, Teresa Varea, Jean-Charles Quirion, Jaume Bastida, Ricardo Garcia
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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15 .     corynantheol
    ÏàËÆ¶È:68.4%
Phytochemistry          1987          26          2839-2846
Alkaloids of Strychnos johnsonii
Georges Massiot,Philippe Th¨¦penier,Marie-Jos¨¦ Jacquier,Louisette Le Men-Olivier,Robert Verpoorte,Cl¨¦ment Delaude
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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16 .     (-)-nitraraine
C20H24N2O     ÏàËÆ¶È:68.4%
Heterocycles          2001          54          43-47
Cascading Single-step Stereoselective Construction of the ¦Á-Alloyohimbine Framework: A New Synthesis of (-)-Nitraraine
Hideki Sakagami and Kunio Ogasawara
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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17 .     (-)-alloyohimbane
C19H24N2     ÏàËÆ¶È:68.4%
Heterocycles          2000          52          261-272
Application of Oxidative Desymmetrization of meso-Tetrahydrofurans: Syntheses of Functionalized Chiral Building Blocks and of (-)-Alloyohimbane
Akio Miyafuji, Katsuji Ito, and Tsutomu Katsuki*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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18 .     dihydrocorynantheine
    ÏàËÆ¶È:68.1%
Journal of the Chemical Society, Perkin Transactions 1          1987                   571-575
Structure elucidation of the binary indole alkaloid uncaramine
Alberto Arnone, Gianluca Nasini and Lucio Merlini
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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19 .     corynanthine
C21H25N2O3     ÏàËÆ¶È:66.6%
Planta Medica          2000          66          531-536
Leishmanicidal,Antiplasmodial and Cytotoxic Activity of Indole Alkaloids from Corynanthe pachyceras
Dan Stærk,Else Lemmich,Jette Christensen, Arsalan Kharazmi,Carl Erik Olsen,Jerzy W.Jaroszewski
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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20 .     dihydrocorynantheine
C22H29N2O3     ÏàËÆ¶È:66.6%
Planta Medica          2000          66          531-536
Leishmanicidal,Antiplasmodial and Cytotoxic Activity of Indole Alkaloids from Corynanthe pachyceras
Dan Stærk,Else Lemmich,Jette Christensen, Arsalan Kharazmi,Carl Erik Olsen,Jerzy W.Jaroszewski
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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21 .     ¦Á-yohimbine
C21H26N203     ÏàËÆ¶È:66.6%
Chemistry of Natural Compounds          1996          32          386-512
ALKALOIDS. PLANTS, STRUCTURES, PROPERTIES CHAPTER , continued
R. Shakirov, M. V. Telezhenetskaya, I. A. Bessonova,S. F. Aripova, I. A. Israilov, M. N. Suitankhodzhaev,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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22 .     ¦Á-yohimbine
    ÏàËÆ¶È:66.6%
Journal of Natural Products          1983          Vol 46          708-722
Aspidosperma de Guyane: Alcaloïdes des Graines de Aspidosperma oblongum
G. M. T. Robert, A. Ahond, C. Poupat, P. Potier, H. Jacquemin, S. K. Kan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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23 .     yohimbine
    ÏàËÆ¶È:66.6%
Phytochemistry          1990          29          3377-3379
17¦Á-O-Methylyohimbine and vallesiachotamine from roots ofAmsonia elliptica
Martina Sauerwein,Koichiro Shimomura
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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24 .     1-(4,4-diethoxybutyl)-2,3,4,9-tetrahydro-1H-¦Â-carboline
C20H30N2O2     ÏàËÆ¶È:65%
Tetrahedron          1998          54          6135-6146
Synthesis of the brominated marine alkaloids (¡À)-arborescidine A, B and C
Brigitte E.A. Burm, Michaël M. Meijler, Jacco Korver, Martin J. Wanner, Gerrit-Jan Koomen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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25 .     naucleofficine D
    ÏàËÆ¶È:65%
Acta Pharmaceutica Sinica          2010          45          747-751
Alkaloids from the leaves of Nauclea officinalis
FAN Long, FAN Chun-lin, WANG Ying, ZHANG Xiao-qi, ZHANG Qing-wen, ZHANG Jun-qing, YE Wen-cai*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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26 .     indolo[2,3-a]quinolizidine
    ÏàËÆ¶È:63.1%
Journal of Natural Products          1997          60          791-793
Reductive Pictet-Spengler Cyclization of Nitriles in the Presence of Tryptamine: Synthesis of Indolo[2, 3-a]quinolizidine, Nazlinine, and Elaeocarpidine
Khalid Diker, Khalid El Biach, Mich¨¨le Dö¨¦de Maindreville, and Jean L¨¦vy
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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27 .     nazlinine
    ÏàËÆ¶È:63.1%
Journal of Natural Products          1997          60          791-793
Reductive Pictet-Spengler Cyclization of Nitriles in the Presence of Tryptamine: Synthesis of Indolo[2, 3-a]quinolizidine, Nazlinine, and Elaeocarpidine
Khalid Diker, Khalid El Biach, Mich¨¨le Dö¨¦de Maindreville, and Jean L¨¦vy
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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28 .     1,2,3,4,6,7,12,12b-octahydroindolo[2,3-¦Á]quinolizine
    ÏàËÆ¶È:63.1%
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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29 .     2-ethyl-3-[2-(3-ethylpiperdine)ethyl]-indole
C19H28N2     ÏàËÆ¶È:63.1%
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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30 .     2-(4-(2,3,4-Tetrahydro-1H-pyrido[3,4-b]indol-1-yl)butyl)isoindoline 1,3-dione
C23H23N3O2     ÏàËÆ¶È:63.1%
Journal of Natural Products          2011          74          1972-1979
Antimalarial ¦Â-Carbolines from the New Zealand Ascidian Pseudodistoma opacum
Susanna T. S. Chan, A. Norrie Pearce, Michael J. Page, Marcel Kaiser, and Brent R. Copp
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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