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19.3,21.8,32.7,36.2,39.6,47.2,53.4,56.9,59.9,67.9,75.7,108.2,110.7,118.2,119.5,121.4,127.4,134.6,136.0  
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1 .     3-isorauniticine
    ÏàËÆ¶È:71.4%
Planta Medica          1981          41          406-418
13C NMR Data of 3-Isoajmalicine and 19-Epiajmalicine
Raimo Uusvuori and Mauri Lounasmaa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     (3S)-14,15-dihydroeburnamenine
C19H24N2     ÏàËÆ¶È:68.4%
Tetrahedron          2004          60          3273-3282
Total syntheses of (−-vallesamidine and related Aspidosperma and Hunteria type indole alkaloids from the common intermediate
Hideo Tanino, Kazuhisa Fukuishi, Mina Ushiyama, Kunisuke Okada
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     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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4 .     (-)-tetrahydroalstonine
    ÏàËÆ¶È:66.6%
Journal of Natural Products          1985          Vol 48          273-278
Partial Synthesis via Indole Alkaloids: A New Hexacyclic Derivative of (-)-Tetrahydroalstonine
Bernhard Mompon, Thierry Vassal, Philippe Poirier
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     sitsirikine
    ÏàËÆ¶È:66.6%
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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6 .     yohimbine
    ÏàËÆ¶È:66.6%
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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7 .     19,20-dehydro-¦Â-yohimbine
    ÏàËÆ¶È:65%
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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8 .     elaeocarpidine
    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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9 .     elaeocarpidine
    ÏàËÆ¶È:63.1%
Planta Medica          1992          58          289-291
Elaeocarpidine, a Naturally Occurring Racemate, from Tarenna vanprukii
Iliromitsu Takayama,Makiko Katsura, Norio Seki,Mariko Kitajima,Norio flirni,Shin-ichiro Sakai,Damrnrong Scintiarworn , and Boonsoin Liawruangrath
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     compound 5
    ÏàËÆ¶È:63.1%
Planta Medica          1987          53          386-388
Elaboration of the Ethylidene Side Chain in the Synthesis of Indole Alkaloids: Preparation of (¡À)-Deplancheine and its Analogues
Reij a Jokela, Anne Juntunen, and Mauri Lounasmaa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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11 .     elaeocarpidine
C17H21N3     ÏàËÆ¶È:63.1%
Natural Product Research          1996          8          105-112
Elaeocarpidine Alkaloids from Pelargonium Species (Geraniaceae)
Maria Lis Balchin; Peter J. Houghton; Tibebe Z. Woldemariam
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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12 .     epielaeocarpidine
C17H21N3     ÏàËÆ¶È:63.1%
Natural Product Research          1996          8          105-112
Elaeocarpidine Alkaloids from Pelargonium Species (Geraniaceae)
Maria Lis Balchin; Peter J. Houghton; Tibebe Z. Woldemariam
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     dihydrocorynantheol
    ÏàËÆ¶È:63.1%
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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14 .     borrerine
    ÏàËÆ¶È:63.1%
Journal of Natural Products          1985          Vol 48          120-123
RMN du Carbone 13 des Alcaloïdes du Type Borr¨¦rine-Borr¨¦v¨¦rine-Isoborr¨¦v¨¦rine
F. Tillequin, M. Koch, A. Rabaron
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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15 .     yohimbol
    ÏàËÆ¶È:63.1%
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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16 .     decarbomethoxytetrahydrosecodine
    ÏàËÆ¶È:63.1%
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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17 .     borrerine
    ÏàËÆ¶È:63.1%
Phytochemistry          1991          30          997-1000
Spermacoceine, a bis-indole alkaloid from Borreria verticillata
A.M. Bald¨¦, L.A. Pieters, A. Gergely, V. Wray, M. Claeys, A.J. Vlietinck
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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18 .     corynantheol
    ÏàËÆ¶È:63.1%
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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19 .     ajmalicine
    ÏàËÆ¶È:63.1%
Helvetica Chimica Acta          1976          59          2254-2260
13C-NMR. Analysis of the Roxburghines
Lucio Merlini, Rosanna Mondelli, Gianluca Nasini, Felix W. Wehrli, Edward W. Hagaman and Ernest Wenkert
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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20 .     akuammigine
    ÏàËÆ¶È:63.1%
Helvetica Chimica Acta          1976          59          2254-2260
13C-NMR. Analysis of the Roxburghines
Lucio Merlini, Rosanna Mondelli, Gianluca Nasini, Felix W. Wehrli, Edward W. Hagaman and Ernest Wenkert
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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21 .     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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22 .     corynantheol
    ÏàËÆ¶È:63.1%
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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23 .     corynantheol
    ÏàËÆ¶È:63.1%
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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24 .     corynantheol
    ÏàËÆ¶È:63.1%
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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25 .     compound 30
    ÏàËÆ¶È:63.1%
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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26 .     [2R-(2¦Á,4a¦Á,14a¦Â)]-1,2,3,4,4a,5,7,8,13,14a-decahydroindolo[2',3':3,4]pyrido[1,2-b]isoquinolin-2-ol
C19H22N2O     ÏàËÆ¶È:63.1%
Journal of Heterocyclic Chemistry          2000          37          1081-1087
Addition reactions of allyl stannanes to an indolo[2',3':3,4]pyrido[1,2-b]isoquinoline imminium salt
Paul C. Unangst, Larry D. Bratton, David T. Connor, Bruce D. Roth, J. Ronald Rubin and Bharat K. Trivedi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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27 .     1-methyl-1-phenylsulfanyl-1,2,3,4-tetrahydro-¦Â-carboline
    ÏàËÆ¶È:63.1%
Heterocycles          2003          59          691-705
A Facile Synthesis of 1,1-Disubstituted 1,2,3,4-Tetrahydro-¦Â-carbolines via Trifluoroacetic Acid Catalyzed Pictet-Spengler Reaction Using Titanium (IV) Isopropoxide as an Imination Reagent
Yoshie Horiguchi,* Masayoshi Nakamura, Akiko Kida, Hirokazu Komada, Toshiaki Saitoh, and Takehiro Sano
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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28 .     compound 7b
    ÏàËÆ¶È:63.1%
Tetrahedron Letters          2001          42          8297-8299
6',7'-Dihydrokeramamine C and analogues: synthesis and biological evaluation
Annie Pouilh¨¨s, Monica Duval-Lungulescu, St¨¦phanie Lambel, St¨¦phane L¨¦once, Yves Langlois
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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29 .     Rac-cis-1-[amino]-1,2,4,5,7,8,13b-heptahydro-[1,4]-thiazepino[4',5':1,2]pyrido[3,4-b]indole
C15H19N3S1     ÏàËÆ¶È:63.1%
Bioorganic & Medicinal Chemistry          1997          5          955-970
Antiviral and tumor cell antiproliferative SAR studies on tetracyclic eudistomins¡ªII
Jan H. van Maarseveen, Hans W. Scheeren, Erik De Clercq, Jan Balzarini, Chris G. Kruse
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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30 .     (-)-nitraraine
C20H24N2O     ÏàËÆ¶È:63.1%
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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31 .     [3-(diethoxyphosphoryl)propyl]-1,2,3,4-tetrahydro-2-(2,2,2-trichloroethoxycarbonyl)-¦Â-carboline
C21H28N2O5Cl3P     ÏàËÆ¶È:63.1%
Heterocycles          2001          55          1165-1171
A Concise Formal Synthesis of (¡À)-Deplancheine
Takashi Itoh, Yûji Matsuya, Yasuko Enomoto, and Akio Ohsawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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32 .     (-)-alloyohimbane
C19H24N2     ÏàËÆ¶È:63.1%
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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33 .     3-methyl-3-(3'-nitropropyl)-1,2,3,4-tetrahydrocarbazole
C16H21O2N     ÏàËÆ¶È:63.1%
Tetrahedron          1999          55          11095-11108
Synthesis of aspidospermidine alkaloids from 1,2,3,4-tetrahydrocarbazole: Total stereoselective synthesis of (¡À)-18-noraspidospermidine
Anah¨ª Urrutia, J.Gonzalo Rodr¨ªguez
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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34 .     ajmalicine
    ÏàËÆ¶È:63.1%
Helvetica Chimica Acta          1976          59          2254-2260
13C-NMR. Analysis of the Roxburghines
Lucio Merlini, Rosanna Mondelli and Gianluca Nasini
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

35 .     akuammigine
    ÏàËÆ¶È:63.1%
Helvetica Chimica Acta          1976          59          2254-2260
13C-NMR. Analysis of the Roxburghines
Lucio Merlini, Rosanna Mondelli and Gianluca Nasini
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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36 .     17-epi-ajmalicinine
    ÏàËÆ¶È:61.9%
Journal of Natural Products          1996          59          185-189
Obovamine, a New Indole Alkaloid from Stemmadenia obovata
Alberto Madinaveitia, Matias Reina, Gabriel de la Fuente, and Antonio G. Gonzalez
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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37 .     ¦Á-yohimbine
C21H27N2O3     ÏàËÆ¶È:61.9%
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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38 .     rauniticine
    ÏàËÆ¶È:61.9%
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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39 .     ¦Á-yohimbine
C21H26N203     ÏàËÆ¶È:61.9%
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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40 .     ¦Á-yohimbine
    ÏàËÆ¶È:61.9%
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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41 .     17-epi-alloyohimbine
    ÏàËÆ¶È:61.9%
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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42 .     ¦Â-yohimbine
    ÏàËÆ¶È:61.9%
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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43 .     ¦Â-yohimbine
    ÏàËÆ¶È:61.9%
Phytochemistry          1992          31          2031-2034
Alkaloid distribution in Malaysian Uncaria
Toh-Seok Kam, Kee-Huat Lee, Swee-Hock Goh
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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44 .     dihydrositsirikine
    ÏàËÆ¶È:61.9%
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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45 .     ¦Â-yohimbine
    ÏàËÆ¶È:61.9%
Phytochemistry          1991          30          1352-1353
3-epi-¦Â-yohimbine from roots of Rauwolfia linearifolia
Jorge A.Martinez P¨¨rez, Carlos G¨°mez Gonz¨¢lez, Mar¨ªa E.Sosa Rodr¨ªguez, Leticia T.Noda Llerena
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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46 .     19,20-dihydroisositsirikine
    ÏàËÆ¶È:61.9%
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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47 .     yohimbine
    ÏàËÆ¶È:61.9%
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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48 .     Rauniticine
    ÏàËÆ¶È:61.9%
Phytochemistry          1980          19          2013-2016
Alkaloids of Uncaria attenuata from Thailand
Dhavadee Ponglux, Tanomjit Supavita, Robert Verpoorte, David Phillipson
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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49 .     tetrahydroalstonine
    ÏàËÆ¶È:61.9%
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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50 .     ¦Á-yohimbine
    ÏàËÆ¶È:61.9%
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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51 .     nitrarine
    ÏàËÆ¶È:60%
Natural Product Research          1995          6          119-125
Alkaloids from Nitraria billardieri
May Ying Shen; Jos¨¦ Angelo Zuanazzi; Christiane Kan; Jean-Charles Quirion; Henri-Philippe Husson; I. R. C. Bick
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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52 .     3,14-dihydrodecussine
    ÏàËÆ¶È:60%
Journal of Natural Products          1981          Vol 44          415-421
Some New Decussine-Type Alkaloids From Strychnos decussata, Strychnos dale and Strychnos elaecocarpa
Wenche N. A. Rolfsen, Ajibola A. Olaniyi, Robert Verpoorte, Lars Bohlin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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53 .     16¦Â-hydroxymethyl-(+)-quebrachamine
    ÏàËÆ¶È:60%
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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54 .     Crassarine F
C20H32O2     ÏàËÆ¶È:60%
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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55 .     3-hydroxy-3,4-secocoronaridine
C21H28O3N2     ÏàËÆ¶È:60%
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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56 .     (3R,12bS)-methyl (3-ethyl-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizin-2-yl)acetate
C20H26O2N2     ÏàËÆ¶È:60%
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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57 .     amsonic acid
C20H24N2O4     ÏàËÆ¶È:60%
Chinese Traditional and Herbal Drugs          2003          34          390-392
Studies on chemical constituents of Amsonia sinensis
WANG Ai-guo; FENG Xiao-zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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58 .     naucleofficine D
    ÏàËÆ¶È:60%
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

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

59 .     corynantheine
C22H27N2O3     ÏàËÆ¶È:59.0%
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

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

60 .     17¦Á-O-methylyohimbine
    ÏàËÆ¶È:59.0%
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

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

61 .     dihydrocorynantheine
C22H28N2O3     ÏàËÆ¶È:59.0%
Phytochemistry          1985          24          880-881
Alkaloids of Uncaria callophylla
S. H. Goh, Siti Asiah, Ahmad Junan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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62 .     indolo[2,3-a]quinolizidine
    ÏàËÆ¶È:57.8%
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

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

63 .     1-[2-(2,3,4,9-tetrahydro-1H-¦Â-carbolin-1-yl)ethyl]-pyrrolidin-2-one
    ÏàËÆ¶È:57.8%
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

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

64 .     1,2,3,4,6,7,12,12b-octahydroindolo[2,3-¦Á]quinolizine
    ÏàËÆ¶È:57.8%
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

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

65 .     trans-(H-1/H-12b)-1-hydroxy-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-¦Á]quinolizine
C15H18N2O     ÏàËÆ¶È:57.8%
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

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

66 .     compound 4c
    ÏàËÆ¶È:57.8%
Chemistry of Natural Compounds          2004          40          585-590
DIASTEREOTOPIC SYNTHESIS OF 1- AND 1,1-SUBSTITUTED 4-PHENYL-2,3,4,9-TETRAHYDRO-1H-b-CARBOLINES
B. B. Semenov, K. A. Novikov, A. N. Spitsin,V. N. Azev, and V. V. Kachala
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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67 .     compound 6a
C22H22N2O2     ÏàËÆ¶È:57.8%
Natural Product Research          1993          2          49-56
Construction of Tetracyclic Indole Bases Via Aza-Diels-Alder Reaction of Indolylethylimines with Brassard's Diere
Ralf Lock; Herbert Waldmann
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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68 .     demethoxy carbonyltetrahy drosecodine
    ÏàËÆ¶È:57.8%
Natural Product Research          1994          5          197-200
Total Synthesis of Crooksidine
P. Aclinou; G. Massiot; B. Menhour
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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69 .     compound 7
    ÏàËÆ¶È:57.8%
Natural Product Research          1994          5          197-200
Total Synthesis of Crooksidine
P. Aclinou; G. Massiot; B. Menhour
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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70 .     ibogamin-3-one
    ÏàËÆ¶È:57.8%
China Journal of Chinese Materia Medica          2006          31          1166-1168
Studies on constituents from root and stem of Ervatamia hainanensis
HUANG Jianpeng, MA Yangmin, JIANG Jianshuang, ZHANG Peicheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

71 .     epi-yohimbol
    ÏàËÆ¶È:57.8%
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

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

72 .     19(S)-hydroxydihydrocorynantheol
C19H26N2O2     ÏàËÆ¶È:57.8%
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

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

73 .     2-ethyl-3-[2-(3-ethylpiperdine)ethyl]-indole
C19H28N2     ÏàËÆ¶È:57.8%
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

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

74 .     16¦Â-hydroxymethylcleavamine
C20H26N2O     ÏàËÆ¶È:57.8%
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

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

75 .     16¦Â-methoxycleavamine
    ÏàËÆ¶È:57.8%
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

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

76 .     N12-Propyl-N12-isopentyltryptamine
C18H28N2     ÏàËÆ¶È:57.8%
Bioorganic & Medicinal Chemistry          2011          19          3120-3127
Tryptamine derivatives as novel non-nucleosidic inhibitors against hepatitis B virus
Shi-Jin Qu , Gui-Feng Wang ,Wen-Hu Duan,Shan-Yan Yao, Jian-Ping Zuo , Chang-Heng Tan ,Da-Yuan Zhu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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77 .     Kororamide A
C18H21Br3N3O     ÏàËÆ¶È:57.8%
Tetrahedron Letters          2012          53          2873-2875
Kororamide A, a new tribrominated indole alkaloid from the Australian bryozoan Amathia tortuosa
Anthony R. Carroll, Seanan J. Wild, Sandra Duffy, Vicky M. Avery
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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78 .     (¡À)-demethoxycarbonyldihydrogambirtannine
C19H18N2     ÏàËÆ¶È:57.8%
Tetrahedron Letters          2000          41          5035-5038
Transition metal complexes in organic synthesis. Part 62: Total synthesis of (¡À)-demethoxycarbonyldihydrogambirtannine and norketoyobyrine by an iron-mediated [2+2+1] cycloaddition
Hans-Joachim Knölker, Simon Cämmerer
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

79 .     (¡À)1,2,3,4,6,7,12,12b-octahydro-indole[2,3-a]-quinolizine
    ÏàËÆ¶È:57.8%
Journal of Heterocyclic Chemistry          2007          44          1459-1463
A novel synthesis of (¡À)-harmacine and (¡À)1,2,3,4,6,7,12,12b-octahydroindole[2,3-a]quinolizine
Frank D. King
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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80 .     compound 8d
C17H25N3O3S     ÏàËÆ¶È:57.8%
Indian Journal of Chemistry          2009          48B          134-136
Tungstate-catalyzed oxidation of triptans with hydrogen peroxide: A novel method for the synthesis of N,N- dimethyltryptamine N-oxides
Ray,Purna Chandra; Mittapelli,Vasantha; Chauhan,Yogendra Kumar; Konudula,Babu Rao; Tyagi,Om Dutt
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

81 .     6,7,12,12b-tetrahydro-1H-indolo[2,3-a]quinolizin-4-one
    ÏàËÆ¶È:57.8%
Heterocycles          2004          63          655-661
Syntheses of 1,2,3,4,6,7,12,12b-Octahydroindolo[2,3-a]quinolizine and Harmicine Using a Chiral 1-Allyl-1,2,3,4-tetrahydro-¦Â-carboline as the Starting Material
Takashi Itoh, Michiko Miyazaki, Kazuhiro Nagata, Shigeru Nakamura, and Akio Ohsawa*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

82 .     1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizine
    ÏàËÆ¶È:57.8%
Heterocycles          2004          63          655-661
Syntheses of 1,2,3,4,6,7,12,12b-Octahydroindolo[2,3-a]quinolizine and Harmicine Using a Chiral 1-Allyl-1,2,3,4-tetrahydro-¦Â-carboline as the Starting Material
Takashi Itoh, Michiko Miyazaki, Kazuhiro Nagata, Shigeru Nakamura, and Akio Ohsawa*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

83 .     1,2,3,4-tetrahydro-1-(3-hydroxypropyl)-2-(2,2,2-trichloroethoxycarbonyl)-¦Â-carboline
C17H19N2O3Cl3     ÏàËÆ¶È:57.8%
Heterocycles          2004          63          655-661
Syntheses of 1,2,3,4,6,7,12,12b-Octahydroindolo[2,3-a]quinolizine and Harmicine Using a Chiral 1-Allyl-1,2,3,4-tetrahydro-¦Â-carboline as the Starting Material
Takashi Itoh, Michiko Miyazaki, Kazuhiro Nagata, Shigeru Nakamura, and Akio Ohsawa*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

84 .     2-formyl-1-methyl-1-phenylsulfanyl-1,2,3,4-tetrahydro-¦Â-carboline
C20H20N2OS     ÏàËÆ¶È:57.8%
Heterocycles          2003          59          691-705
A Facile Synthesis of 1,1-Disubstituted 1,2,3,4-Tetrahydro-¦Â-carbolines via Trifluoroacetic Acid Catalyzed Pictet-Spengler Reaction Using Titanium (IV) Isopropoxide as an Imination Reagent
Yoshie Horiguchi,* Masayoshi Nakamura, Akiko Kida, Hirokazu Komada, Toshiaki Saitoh, and Takehiro Sano
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

85 .     2-formyl-1,2,3,4-tetrahydro-¦Â-carboline-1-spirocyclopentane
C16H18N2O     ÏàËÆ¶È:57.8%
Heterocycles          2003          59          691-705
A Facile Synthesis of 1,1-Disubstituted 1,2,3,4-Tetrahydro-¦Â-carbolines via Trifluoroacetic Acid Catalyzed Pictet-Spengler Reaction Using Titanium (IV) Isopropoxide as an Imination Reagent
Yoshie Horiguchi,* Masayoshi Nakamura, Akiko Kida, Hirokazu Komada, Toshiaki Saitoh, and Takehiro Sano
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

86 .     compound 6
    ÏàËÆ¶È:57.8%
Bioorganic & Medicinal Chemistry          1997          5          955-970
Antiviral and tumor cell antiproliferative SAR studies on tetracyclic eudistomins¡ªII
Jan H. van Maarseveen, Hans W. Scheeren, Erik De Clercq, Jan Balzarini, Chris G. Kruse
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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87 .     Methyl cis-1,3,3a,4,5,10c-hexahydrofuro[3,4-c]carbazole-3a-carboxylate
C16H17NO3     ÏàËÆ¶È:57.8%
Zeitschrift f¨¹r Naturforschung B          2011          66          1209-1218
Investigations into the Regioselectivity of Fischer Indole and Friedländer Quinoline Syntheses with Octahydroisobenzofuran and Octahydroisoindole Derivatives
M. Bender and J. Christoffers
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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88 .     1,2,3,4-tetrahydro-2-(2,2,2-trichloroethoxycarbonyl)-¦Â-carboline
C17H17N2O2Cl3     ÏàËÆ¶È:57.8%
Heterocycles          2001          55          1165-1171
A Concise Formal Synthesis of (¡À)-Deplancheine
Takashi Itoh, Yûji Matsuya, Yasuko Enomoto, and Akio Ohsawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

89 .     1,2,3,4-tetrahydro-2-(2,2,2-trichloroethoxycarbonyl)-¦Â-carboline(minor)
C17H17N2O2Cl3     ÏàËÆ¶È:57.8%
Heterocycles          2001          55          1165-1171
A Concise Formal Synthesis of (¡À)-Deplancheine
Takashi Itoh, Yûji Matsuya, Yasuko Enomoto, and Akio Ohsawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

90 .     1,2,3,4-tetrahtdrohydro-1-(3-hydroxypropyl)-2-(2,2,2-trichloroethoxycarbonyl)-¦Â-carboline
C17H219N2O3Cl3     ÏàËÆ¶È:57.8%
Heterocycles          2001          55          1165-1171
A Concise Formal Synthesis of (¡À)-Deplancheine
Takashi Itoh, Yûji Matsuya, Yasuko Enomoto, and Akio Ohsawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

91 .     1,2,3,4-tetrahydro-1-(3-iodopropyl)-2-(2,2,2-trichloroethoxy-carbonyl)-¦Â-carboline
C17H18N2O2Cl3I     ÏàËÆ¶È:57.8%
Heterocycles          2001          55          1165-1171
A Concise Formal Synthesis of (¡À)-Deplancheine
Takashi Itoh, Yûji Matsuya, Yasuko Enomoto, and Akio Ohsawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

92 .     (3R,16R)-14,15-dihydroeburnamenin-19-one
C19H22N2O     ÏàËÆ¶È:57.8%
Tetrahedron          2004          60          3273-3282
Total syntheses of (−-vallesamidine and related Aspidosperma and Hunteria type indole alkaloids from the common intermediate
Hideo Tanino, Kazuhisa Fukuishi, Mina Ushiyama, Kunisuke Okada
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

93 .     cyclo(4-hydroxy-S-Pro-S-Trp)
    ÏàËÆ¶È:57.8%
Journal of Asian Natural Products Research          2011          13          1146-1150
A bisamide and four diketopiperazines from a marine-derived Streptomyces sp.
Bin Li, Gang Chen, Jiao Bai, Yong-Kui Jing & Yue-Hu Pei
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

94 .     kopsiyunnanine D
C21H30N2O     ÏàËÆ¶È:57.1%
Journal of Natural Products          2009          72          204-209
Rhazinilam and Quebrachamine Derivatives from Yunnan Kopsia arborea
Yuqiu Wu,Mayu Suehiro, Mariko Kitajima, Takeshi Matsuzaki, Shusuke Hashimoto,Masato Nagaoka,Rongping Zhang,and Hiromitsu Takayama
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

95 .     deserpidic Acid Lactone
C21H24N2O3     ÏàËÆ¶È:57.1%
Journal of Natural Products          2005          68          1629-1631
Synthesis of Deserpidine from Reserpine
Greta Varchi, Arturo Battaglia, Cristian Samor, Eleonora Baldelli, Bruno Danieli, Gabriele Fontana, Andrea Guerrini, and Ezio Bombardelli
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

96 .     ajmalicinine
    ÏàËÆ¶È:57.1%
Journal of Natural Products          1996          59          185-189
Obovamine, a New Indole Alkaloid from Stemmadenia obovata
Alberto Madinaveitia, Matias Reina, Gabriel de la Fuente, and Antonio G. Gonzalez
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

97 .     dihydrocorynantheine
C22H29N2O3     ÏàËÆ¶È:57.1%
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

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

98 .     amsosinine
C21H26N2O4     ÏàËÆ¶È:57.1%
Planta Medica          1991          57          566-568
New Indole Alkaloids from Amsonia sinensis
Hong-MeiLiu, Bin Wu,Qi-TaiZheng,and Xiao-ZhangFeng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

99 .     16-epi-isositsirikin
    ÏàËÆ¶È:57.1%
Planta Medica          1982          46          88-90
Alkaloide in Tabernaemontana-Arten, XVI [1] 1 2-Methoxy-17,18-dehydro-vincamine and 1 6-epi-Isositsirikine, Alkaloids from Tabernaemontana psorocarpa
H. Achenbach, C. Renner und I. AddaeMensah
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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

100 .     19-epiajmalicine
    ÏàËÆ¶È:57.1%
Planta Medica          1981          41          406-418
13C NMR Data of 3-Isoajmalicine and 19-Epiajmalicine
Raimo Uusvuori and Mauri Lounasmaa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2Â¥2012-05-28 10:04:37
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