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²éѯ½á¹û£º¹²²éµ½263¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . Ajmalicine ÏàËÆ¶È:100% Chromatographia 2010 73 841-847 Screening and Identification of Many of the Compounds Present in Rauvolfia verticillata by Use of High-Pressure LC and Quadrupole TOF MS Bo Hong, Weiming Cheng, Jian Wu, Chunjie Zhao Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . ajmalicine ÏàËÆ¶È:85.7% 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 3 . ajmalicine ÏàËÆ¶È:85.7% 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 4 . 3-isoajamalicina C21H22N2O4 ÏàËÆ¶È:76.1% Qu¨ªmica Nova 2004 27 878-881 Determination of relative configurations and conformations of oxindole alkaloids from Uncaria guianensis by NMR Carbonezi, Carlos Alberto; Hamerski, Lidilhone; Flausino Jr., Otavio Aparecido; Furlan, Maysa; Bolzani, Vanderlan da Silva; Young, Maria Claudia Marx Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . cabucine C22H26N2O4 ÏàËÆ¶È:72.7% Phytochemistry 1989 28 3221-3225 Alkaloids of Petchia ceylanica Atta-Ur-Rahman,Azra Pervin,Anjum Muzaffar,K.T.D. De Silva,W.S.J. Silva Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . ajmalicinine ÏàËÆ¶È:71.4% 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 7 . 3-isoajmalicine 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 8 . 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 9 . C/D-trans-akuammigine 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 10 . rauniticine ÏàËÆ¶È:71.4% 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 11 . ¦Â-yohimbine ÏàËÆ¶È:71.4% 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 12 . (-)-tetrahydroalstonine ÏàËÆ¶È:71.4% 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 13 . ¦Â-yohimbine ÏàËÆ¶È:71.4% 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 14 . Rauniticine ÏàËÆ¶È:71.4% 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 15 . tetrahydroalstonine 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 16 . compound 9a ÏàËÆ¶È:71.4% Journal of the American Chemical Society 1979 101 5370-5376 Total synthesis of the yohimbines Ernest Wenkert, Timothy D. J. Halls, Gerhard Kunesch, Kazuhiko Orito, Richard L. Stephens, Wayne A. Temple, Jhillu S. Yadav Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . 17-epi-ajmalicinine ÏàËÆ¶È:66.6% 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 18 . 19-epiajmalicine ÏàËÆ¶È:66.6% 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 19 . 3-isorauniticine ÏàËÆ¶È:66.6% 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 20 . alloyohimbine 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 21 . ¦Â-yohimbine ÏàËÆ¶È:66.6% 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 22 . 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 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 . tetrahydro ¦Â-carboline ÏàËÆ¶È:66.6% Journal of Natural Medicines 2007 61 208-212 Total synthesis and full NMR assignment of ourouparine, a yohimbane-type indole alkaloid isolated from Gelsemiumsempervirens Noriyuki Kogure, Ayumi Someya, Akiko Urano, Mariko Kitajima and Hiromitsu Takayama Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . 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 26 . methyl (1S,2R,12br)-2-propyl-1,2,3,4,6,7,12,12b-octahydroind-olo[2,3-a]quinolizine-1-carboxylate C20H26N2O2 ÏàËÆ¶È:66.6% European Journal of Organic Chemistry 2011 6755-6763 Organocatalyzed Cascade Reactions of Cyclic ¦Â-Enamino Esters and ,¦Â-Unsaturated Aldehydes Leading to Indoloquinolizidines and Benzoquinolizidines Xiaoyu Wu, Linlin Nie, Huihui Fang, Jie Chen, Weiguo Cao and Gang Zhao Structure 13C NMR ̼Æ×Ä£Äâͼ 27 . yohimbane ÏàËÆ¶È:66.6% Magnetic Resonance in Chemistry 1991 29 985-992 NMR spectroscopy of hexa- and octahydropyrazino [1¡ä, 2¡ä : 1,2]pyrido [3,4-b]indoles and 15-azayohimbanes Nativitat Valls, Victor M. Segarra and Josep Bonjoch Structure 13C NMR ̼Æ×Ä£Äâͼ 28 . compound 9c ÏàËÆ¶È:66.6% Journal of the American Chemical Society 1979 101 5370-5376 Total synthesis of the yohimbines Ernest Wenkert, Timothy D. J. Halls, Gerhard Kunesch, Kazuhiko Orito, Richard L. Stephens, Wayne A. Temple, Jhillu S. Yadav Structure 13C NMR ̼Æ×Ä£Äâͼ 29 . compound 10c ÏàËÆ¶È:66.6% Journal of the American Chemical Society 1979 101 5370-5376 Total synthesis of the yohimbines Ernest Wenkert, Timothy D. J. Halls, Gerhard Kunesch, Kazuhiko Orito, Richard L. Stephens, Wayne A. Temple, Jhillu S. Yadav Structure 13C NMR ̼Æ×Ä£Äâͼ |

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