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²éѯģʽ£ºÄ£ºý²éѯ ̼Æ×Êý¾ÝÊäÈ룺 °´´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺 21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2 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 ÈܼÁÑ¡Ï È«²¿ CDCl3 CD3CD2OD CD2Cl2 C5D5N C3D7NO CD3SOCD3 C4D8O (CH3)4Si C4D8O2 CD3COOD C4D8O2 H2O D2O CF3COOD CD3OD ND3 CD3COCD3 C6D6 CD3CN ²éѯ¿ÕÖµ Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½336¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 intermediateHideo Tanino, Kazuhisa Fukuishi, Mina Ushiyama, Kunisuke Okada Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 intermediateHideo Tanino, Kazuhisa Fukuishi, Mina Ushiyama, Kunisuke Okada Structure 13C NMR ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×Ä£Äâͼ |
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-vallesamidine and related Aspidosperma and Hunteria type indole alkaloids from the common intermediate