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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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 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 ̼Æ×Ä£Äâͼ |
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