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GF-5 CDCL3 153.9,140.4,129.9,129.6,111.4,110.9,110.8,100.3,67.9,59.9,56,50.5,45.4,43.8,40.6,30.6,29.6,27.6,26,11.6 GF-8 MEOD 141.2,138.3,138.2,127.5,122.1,119.8,118.7,114.7,111.9,106.2,61.1,57,53.6,51.2,43.7,27.9,27.5,23.5,12.9 GF-9 MEOD 139.4,138.2,136.4,128.8,122,119.8,118.6,118,111.9,104.4,65.2,56.7,56.1,51.7 ,45.5,34.5,28.7,27.8,13 GF-11 MEOD 166,164.4,157.1,151.8,131.7,129.5,113.3,113.3,104.8,103.6,95.2,78.9,78.5,74.5,71.3,62.5,58.6,56.1,40.9,38.9,32.6,29.4,28.6,27.2,11.7 |
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Ò¹ò¶ù: »ØÌûÖö¥ 2013-11-06 21:19:09
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GF-5 CDCL3 11.6,26,27.6,29.6,30.6,40.6,43.8,45.4,50.5,56,59.9,67.9,100.3,110.8,110.9,111.4,129.6,129.9,140.4,153.9 GF-8 MEOD 12.9,23.5,27.5,27.9,43.7,51.2,53.6,57,61.1,106.2,111.9,114.7,118.7,119.8,122.1,127.5,138.2,138.3,141.2 GF-9 MEOD 13,27.8,28.7,34.5,45.5,51.7,56.1,56.7,65.2,104.4,111.9,118,118.6,119.8,122,128.8 ,136.4,138.2,139.4 GF-11 MEOD 11.7,27.2,28.6,29.4,32.6,38.9,40.9,56.1,58.6,62.5,71.3,74.5,78.5,78.9,95.2,103.6,104.8,113.3,113.3,129.5,131.7,151.8,157.1,164.4,166 |
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²éѯ½á¹û£º¹²²éµ½108¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . ibogaine ÏàËÆ¶È:60% 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 -------------------------------------------------------------------------------- 2 . ibogaine ÏàËÆ¶È:60% Helvetica Chimica Acta 1976 59 2437-2442 13C-NMR. Spectroscopy of Naturally Occurring Substances. XLV. Iboga Alkaloids Ernest Wenkert, David W. Cochran, Hugo E. Gottlieb, Edward W. Hagaman, Raimundo Braz Filho, Francisco Jos¨¦ de Abreu Matos and Maria Iracema Lacerda Machado Madruga Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . ibogaine ÏàËÆ¶È:60% Phytochemistry 1984 23 175-178 13C NMR analysis of alkaloids from peschiera fuchsiaefolia Raquel M. Braga, Hermogenes F. Leit¨¢o Filho, Francisco De A.M. Reist Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . 2-Methoxy-3,17¦Â-O,O-bis(sulfamoyl)estradiol C19H28N2O7S2 ÏàËÆ¶È:60% Steroids 2012 77 864-870 Synthesis of 2-[11C]methoxy-3,17¦Â-O,O-bis(sulfamoyl)estradiol as a new potential PET agent for imaging of steroid sulfatase (STS) in cancers Min Wang, Lu Xu, Mingzhang Gao, Kathy D. Miller, George W. Sledge, Qi-Huang Zheng Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . 2-methoxy-5-methyl-5,6,7,8,9,10-hexahydrocyclohept-indole-10-carboxamide C16H20N2O2 ÏàËÆ¶È:60% Journal of Medicinal Chemistry 1998 41 451-467 Mapping the Melatonin Receptor. 5. Melatonin Agonists and Antagonists Derived from Tetrahydrocyclopentindoles, Tetrahydrocarbazoles and Hexahydrocycloheptindoles David J. Davies, Peter J. Garratt, Derek A. Tocher, and Stefan Vonhoff, John Davies, Muy-Teck Teh and David Sugden Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . N-cyclobutanoyl-10-(aminomethyl)-2-methoxy-5-meth-yl-5,6,7,8,9,10-hexahydrocycloheptindole C20H26N2O2 ÏàËÆ¶È:60% Journal of Medicinal Chemistry 1998 41 451-467 Mapping the Melatonin Receptor. 5. Melatonin Agonists and Antagonists Derived from Tetrahydrocyclopentindoles, Tetrahydrocarbazoles and Hexahydrocycloheptindoles David J. Davies, Peter J. Garratt, Derek A. Tocher, and Stefan Vonhoff, John Davies, Muy-Teck Teh and David Sugden Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . epiibogaine C20H26N2O ÏàËÆ¶È:60% Tetrahedron 2012 68 7155-7165 Total synthesis of ibogaine, epiibogaine and their analogues Goutam Kumar Jana, Surajit Sinha Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . (¡À)-(8¦Â,9¦Á,14¦Á)-2-Methoxy-11¦Â-methoxymethyl-17-acetylgona-1,3,5(10),13(17)-tetraene C22H28O3 ÏàËÆ¶È:59.0% Steroids 2006 71 459-468 Efficient synthesis of C-11 functionalized steroids Patrick Bazzini, Malika Ibrahim-Ouali, H¨¦l¨¨ne Pellissier, Maurice Santelli Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . (¡À)-(8¦Â,9¦Á,14¦Á)-2-Methoxy-11¦Â-hydroxymethyl-17-acetylgona-1,3,5(10),13(17)-tetraene C21H26O3 ÏàËÆ¶È:57.1% Steroids 2006 71 459-468 Efficient synthesis of C-11 functionalized steroids Patrick Bazzini, Malika Ibrahim-Ouali, H¨¦l¨¨ne Pellissier, Maurice Santelli Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . (¡À)-(8¦Â,9¦Á,14¦Á)-2-Methoxy-11¦Â-aminomethyl-17-acetylgona-1,3,5(10),13(17)-tetraene C21H27NO2 ÏàËÆ¶È:57.1% Steroids 2006 71 459-468 Efficient synthesis of C-11 functionalized steroids Patrick Bazzini, Malika Ibrahim-Ouali, H¨¦l¨¨ne Pellissier, Maurice Santelli Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . (¡À)-(8¦Â,9¦Á,14¦Á)-2-Methoxy-11¦Â-aminomethyl-17-acetylgona-1,3,5(10),13(17)-tetraene ethylene ketal C23H31NO3 ÏàËÆ¶È:56.5% Steroids 2006 71 459-468 Efficient synthesis of C-11 functionalized steroids Patrick Bazzini, Malika Ibrahim-Ouali, H¨¦l¨¨ne Pellissier, Maurice Santelli Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . ibogaine ÏàËÆ¶È:55% Helvetica Chimica Acta 1999 Vol. 82 170 A New Rearrangement in Iboga Alkaloids Alberto Madinaveitia, Gabriel de la Fuente, and Antonio Gonz¨¢lez Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . Ibogaine C20H26N2O ÏàËÆ¶È:55% Chemistry of Natural Compounds 2008 44 675-678 INDOLE ALKALOIDS FROM Ervatamia flabellformia Shuang Liang, Haisheng Chen, Li Jin,Weidong Xuan, and Wei-Dong Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . (¡À)-(8¦Â,9¦Á,14¦Á)-2-Methoxy-11¦Â-carboethoxy-17acetylgona-1,3,5(10),13(17)-tetraene C23H28O4 ÏàËÆ¶È:55% Steroids 2006 71 459-468 Efficient synthesis of C-11 functionalized steroids Patrick Bazzini, Malika Ibrahim-Ouali, H¨¦l¨¨ne Pellissier, Maurice Santelli Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . (¡À)-(8¦Â,9¦Á,14¦Á)-2-Methoxy-11¦Â-amino-17-acetylgona-1,3,5(10),13(17)-tetraene C20H25NO2 ÏàËÆ¶È:55% Steroids 2006 71 459-468 Efficient synthesis of C-11 functionalized steroids Patrick Bazzini, Malika Ibrahim-Ouali, H¨¦l¨¨ne Pellissier, Maurice Santelli Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . ibogaine ÏàËÆ¶È:55% China Journal of Chinese Materia Medica 2007 32 1296-1299 Study on chemical constituents in rhigome of Ervatamia hainanensis LIANG Shuang, CHENG Haisheng, JIN Yongsheng, JIN Li, LU Jia, DU Jingling Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . 7-methoxy-1,3,3-trimethyl-1-(phenylsulfanylmethyl)-1H-3,4-dihydro-2-benzopyran C20H24O2S ÏàËÆ¶È:55% Heterocycles 2010 81 2361-2368 Synthesis of Isochromans by Hydriodic Acid or Iodine Mediated Cyclization Reactions of 1-(2-Vinylphenyl)propan-2-ols Kazuhiro Kobayashi, Kazuaki Shikata, Hiroki Maegawa, Shuhei Fukamachi, Miyuki Tanmatsu, and Hisatoshi Konishi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . Chrysoeriol-3'-O-¦Â-D-apifuranosidyl(1¡ú2)-glucopyranoside ÏàËÆ¶È:55% Chemistry of Natural Compounds 2010 46 459-461 Chemical investigation of Ervatamia yunnanensis Jing-Ling Du, Yong-Sheng Jin, Li-Ming Qiao, Li Jin and Hai-Sheng Chen Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . compound 1 ÏàËÆ¶È:55% Tetrahedron Letters 2003 44 583-586 Asymmetric synthesis and conformational analysis of the two enantiomers of the saturated analog of the potent thrombin inhibitor MOL-376 Jessy Mathew, Ken Farber, Hiroshi Nakanishi, Maher Qabar Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . compound 2 ÏàËÆ¶È:55% Tetrahedron Letters 2003 44 583-586 Asymmetric synthesis and conformational analysis of the two enantiomers of the saturated analog of the potent thrombin inhibitor MOL-376 Jessy Mathew, Ken Farber, Hiroshi Nakanishi, Maher Qabar Structure 13C NMR ̼Æ×Ä£Äâͼ |
4Â¥2013-11-06 21:43:58
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²éѯ½á¹û£º¹²²éµ½167¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . compound 1 C19H22N2O ÏàËÆ¶È:78.9% Tetrahedron Letters 2003 44 8013-8017 The first enantiospecific synthesis of (− -koumidine via the intramolecular palladium-catalyzed enolate driven cross coupling reaction. The stereospecific introduction of the 19-(Z) ethylidene side chainHui Cao, Jianming Yu, Xiangyu Z. Wearing, Chunchun Zhang, Xiaoxiang Liu, Jeffery Deschamps, James M. Cook Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . Gardnerine ÏàËÆ¶È:75% Tetrahedron Letters 2005 46 4219-4224 First regiospecific, enantiospecific total synthesis of gardnerine and gardnutine Hao Zhou, Dongmei Han, Xuebin Liao, James M. Cook Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . gardnerine ÏàËÆ¶È:73.6% Chemical & Pharmaceutical Bulletin 1978 26 3444-3449 Gardneria Alkaloids. XII. Carbon Magnetic Resonance Spectra of Gardneria Alkaloids. A Study on the Configuration of the Side Chain Double Bonds of Indole Alkaloids NORIO AIMI,KEIICHI YAMAGUCHI,SHINICHIRO SAKAI,JOJU HAGINIWA and AKINORI KUBO Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . compound 18 ÏàËÆ¶È:73.6% Chemistry of Natural Compounds 1986 22 1-13 APPLICATIONS OF 1H AND 13C NMR SPECTROSCOPY IN STRUCTURAL INVESTIGATIONS OF Vinca INDOLE ALKALOIDS M. R. Yagudaev Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . Gardnerine ÏàËÆ¶È:70% Tetrahedron Letters 2005 46 4219-4224 First regiospecific, enantiospecific total synthesis of gardnerine and gardnutine Hao Zhou, Dongmei Han, Xuebin Liao, James M. Cook Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . N(4)-demethyltaberpsychine C19H22N2O ÏàËÆ¶È:68.4% Phytochemistry 2009 70 1182-1186 Four tetracyclic oxindole alkaloids and a taberpsychine derivative from a Malayan Tabernaemontana Kuan-Hon Lim, Kooi-Mow Sim, Guan-Huat Tan, Toh-Seok Kam Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . 18-hydroxygardnerine ÏàËÆ¶È:68.4% Chemical & Pharmaceutical Bulletin 1978 26 3444-3449 Gardneria Alkaloids. XII. Carbon Magnetic Resonance Spectra of Gardneria Alkaloids. A Study on the Configuration of the Side Chain Double Bonds of Indole Alkaloids NORIO AIMI,KEIICHI YAMAGUCHI,SHINICHIRO SAKAI,JOJU HAGINIWA and AKINORI KUBO Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . compound 11 C19H20N2 ÏàËÆ¶È:68.4% Tetrahedron Letters 2003 44 8013-8017 The first enantiospecific synthesis of (− -koumidine via the intramolecular palladium-catalyzed enolate driven cross coupling reaction. The stereospecific introduction of the 19-(Z) ethylidene side chainHui Cao, Jianming Yu, Xiangyu Z. Wearing, Chunchun Zhang, Xiaoxiang Liu, Jeffery Deschamps, James M. Cook Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . 3-Hydroxykoumidine C19H22N2O2 ÏàËÆ¶È:68.4% Tetrahedron 2010 66 5987-5992 New oxindole and indole alkaloids from Gelsemium rankinii Mariko Kitajima, Hiromi Kobayashi, Noriyuki Kogure, Hiromitsu Takayama Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . 10-methoxypericyclivine C21H24N2O3 ÏàËÆ¶È:66.6% Phytochemistry 1990 29 3341-3344 Alkaloids from Alstonia undulata The´rs`e-Marie Pinchon,Jean-Marc Nuzillard,Bernard Richard,Georges Massiot,Louisette Le Men-Olivier,Thierry Sevenet Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . amsosinine ÏàËÆ¶È:66.6% 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 -------------------------------------------------------------------------------- 12 . pericyclivine ÏàËÆ¶È:65% Journal of Natural Products 1981 Vol 44 335-339 Catharanthus Alkaloids. XXXVI. Isolation of Vincaleukoblastine (VLB) and Periformyline From Catharanthus trichophyllus and Pericyclivine From Catharanthus roseus Sibabrata Mukhopadhyay, Geoffrey A. Cordell Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . isoretulinal ÏàËÆ¶È:65% Phytochemistry 1988 27 3293-3304 Alkaloids from roots of Strychnos matopensis Georges Massiot,Bernard Massoussa,Marie-Jos¨¦ Jacquier,Philippe Th¨¦p¨¦nier,Louisette Le Men-Olivier,Cl¨¦ment Delaude,Robert Verpoorte Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . 19(S),20(R)-dihydroperaksine C18H22N2O ÏàËÆ¶È:63.1% Journal of Natural Products 2002 65 1006-1010 New Alkaloids of the Sarpagine Group from Rauvolfia serpentina Hairy Root Culture Yuri Sheludko,Irina Gerasimenko, Heinz Kolshorn, and Joachim Stöckigt Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . compound 19 ÏàËÆ¶È:63.1% Chemistry of Natural Compounds 1986 22 1-13 APPLICATIONS OF 1H AND 13C NMR SPECTROSCOPY IN STRUCTURAL INVESTIGATIONS OF Vinca INDOLE ALKALOIDS M. R. Yagudaev Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . 20-epiuleine ÏàËÆ¶È:63.1% Journal of Natural Products 1983 Vol 46 200-205 Studies on the Uleine Alkaloids I. Carbon-13 Nmr Studies on Uleine, 20-Epiuleine and (4S)-Uleine-Nb-Oxide Robert P. Borris, David C. Lankin, Geoffrey A. Cordell Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . 18-hydroxygardnerine ÏàËÆ¶È:63.1% Journal of Natural Products 1986 Vol 49 829 Alcaloïdes Indoliques de Rauvolfia biauriculata J. Abaul, E. Philog¨¨ne, P. Bourgeois, G. M¨¦rault, C. Poupat, A. Ahond, P. Potier Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . 18,19-dihydro-(20R)-antirhine ÏàËÆ¶È:63.1% Phytochemistry 1992 31 2873-2876 Alkaloids from roots of Strychnos potatorum Georges Massiot, Philippe Thepenier, Marie-Jos¨¦ Jacquier, Louisette Le Men-Olivier, Cl¨¦ment Delaude Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . normacusine B ÏàËÆ¶È:63.1% 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 -------------------------------------------------------------------------------- 20 . koumidine ÏàËÆ¶È:63.1% Phytochemistry 1987 26 2875-2876 Revision of the stereochemistry of koumidine Yeh Schun,Geoffrey A. Cordell Structure 13C NMR ̼Æ×Ä£Äâͼ |
5Â¥2013-11-06 21:44:15
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ÖÁ×ðľ³æ (Ö°Òµ×÷¼Ò)
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²éѯ½á¹û£º¹²²éµ½172¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . vellosiminol C19H22N2O ÏàËÆ¶È:89.4% Journal of Ethnopharmacology 2012 139 471-477 In vitro antiplasmodial activity of indole alkaloids from the stem bark of Geissospermum vellosii Flaubert Mbeunkui, Mary H. Grace, Carmen Lategan, Peter J. Smith, Ilya Raskin, Mary Ann Lila Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . compound 19 ÏàËÆ¶È:84.2% Chemistry of Natural Compounds 1986 22 1-13 APPLICATIONS OF 1H AND 13C NMR SPECTROSCOPY IN STRUCTURAL INVESTIGATIONS OF Vinca INDOLE ALKALOIDS M. R. Yagudaev Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . affnisina ÏàËÆ¶È:75% Qu¨ªmica Nova 2009 32 1834-1838 Iboga alkaloids from Peschiera affinis (Apocynaceae) - unequivocal 1H and 13C chemical shift assignments: antioxidant activity Santos, Allana Kellen L.; Magalhães, Ticiane S.; Monte, Francisco Jose Q.; Mattos, Marcos Carlos de; Oliveira, Maria Conceição F. de; Almeida, Maria Mozarina B.; Lemos, Telma L. G.; Braz-Filho, Raimundo Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . 16-epigardnerine ÏàËÆ¶È:70% Chemical & Pharmaceutical Bulletin 1978 26 3444-3449 Gardneria Alkaloids. XII. Carbon Magnetic Resonance Spectra of Gardneria Alkaloids. A Study on the Configuration of the Side Chain Double Bonds of Indole Alkaloids NORIO AIMI,KEIICHI YAMAGUCHI,SHINICHIRO SAKAI,JOJU HAGINIWA and AKINORI KUBO Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . gardnerine ÏàËÆ¶È:70% Journal of Natural Products 1986 Vol 49 829 Alcaloïdes Indoliques de Rauvolfia biauriculata J. Abaul, E. Philog¨¨ne, P. Bourgeois, G. M¨¦rault, C. Poupat, A. Ahond, P. Potier Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . (16R)-16-hydroxy-16,17-dihydrouleine ÏàËÆ¶È:68.4% Journal of Natural Products 1983 Vol 46 206-210 Studies on the Uleine Alkaloids. II. Some Chemical Transformations of Uleine Robert P. Borris, David C. Lankin, Geoffrey A. Cordell Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . 19-(Z)-koumidine C19H22N2O ÏàËÆ¶È:68.4% Chinese Traditional and Herbal Drugs 2011 42 222-225 Chemical constituents from Gelsemium elegans ZHANG Zhen, LIU Guang-ming, XIAO Huai, ZHANG Zhen, HE Hong-ping, HAO Xiao-jiang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . alstoyunine A C20H24N2O3 ÏàËÆ¶È:65% Journal of Natural Products 2009 72 1836-1841 Monoterpenoid Indole Alkaloids from Alstonia yunnanensis Tao Feng, Yan Li,Xiang-Hai Cai, Xun Gong, Ya-Ping Liu, Rong-Ting Zhang, Xiang-Yun Zhang, Qin-Gang Tan, and Xiao-Dong Luo Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . 19(S),20(R)-dihydroperaksine-17-al C18H22N2O ÏàËÆ¶È:63.1% Journal of Natural Products 2002 65 1006-1010 New Alkaloids of the Sarpagine Group from Rauvolfia serpentina Hairy Root Culture Yuri Sheludko,Irina Gerasimenko, Heinz Kolshorn, and Joachim Stöckigt Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . (16R)-17- hydroxy-16,17-dihydrouleine ÏàËÆ¶È:63.1% Journal of Natural Products 1983 Vol 46 206-210 Studies on the Uleine Alkaloids. II. Some Chemical Transformations of Uleine Robert P. Borris, David C. Lankin, Geoffrey A. Cordell Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . voachalotinal C22H24N2O3 ÏàËÆ¶È:61.9% Phytochemistry 1990 29 3341-3344 Alkaloids from Alstonia undulata The´rs`e-Marie Pinchon,Jean-Marc Nuzillard,Bernard Richard,Georges Massiot,Louisette Le Men-Olivier,Thierry Sevenet Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . pleiocarpamine C20H22N2O2 ÏàËÆ¶È:60% 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 -------------------------------------------------------------------------------- 13 . vincamedine C22H24NO ÏàËÆ¶È:59.0% Planta Medica 1986 52 66-67 A New Alkaloid Difforine and Normacusine B from Vinca difformis J. Gamier and J. Mahuteau Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . 19(S),20(R)-dihydroperaksine C18H22N2O ÏàËÆ¶È:57.8% Journal of Natural Products 2002 65 1006-1010 New Alkaloids of the Sarpagine Group from Rauvolfia serpentina Hairy Root Culture Yuri Sheludko,Irina Gerasimenko, Heinz Kolshorn, and Joachim Stöckigt Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . N(4)-demethyltaberpsychine C19H22N2O ÏàËÆ¶È:57.8% Phytochemistry 2009 70 1182-1186 Four tetracyclic oxindole alkaloids and a taberpsychine derivative from a Malayan Tabernaemontana Kuan-Hon Lim, Kooi-Mow Sim, Guan-Huat Tan, Toh-Seok Kam Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . 2,3,10,11-tetrasubstituted-5,6-dihydro-protoberberine C19H17NO4 ÏàËÆ¶È:57.8% Natural Product Research 2003 17 397-402 Two new alkaloids from Miliusa cuneata Bin Chen; Chung Feng; Bio-Gang Li; Guo-Lin Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . (16R)-16,17-dihydrouleine ÏàËÆ¶È:57.8% Journal of Natural Products 1983 Vol 46 206-210 Studies on the Uleine Alkaloids. II. Some Chemical Transformations of Uleine Robert P. Borris, David C. Lankin, Geoffrey A. Cordell Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . normacusine B ÏàËÆ¶È:57.8% 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 -------------------------------------------------------------------------------- 19 . cleavamine 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 -------------------------------------------------------------------------------- 20 . dehydrokoumidine C19H20N2O ÏàËÆ¶È:57.8% Chemistry ¨C An Asian Journal 2011 6 166-173 Seven New Monoterpenoid Indole Alkaloids from Gelsemium elegans Yousuke Yamada, Mariko Kitajima, Noriyuki Kogure, Sumphan Wongseripipatana, and Hiromitsu Takayama Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 21 . koumidine ÏàËÆ¶È:57.8% Phytochemistry 1987 26 2875-2876 Revision of the stereochemistry of koumidine Yeh Schun,Geoffrey A. Cordell Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 22 . 2-[3-(1-methylpiperidin-4-yl)-1H-indol-5-yl]ethanesulfonic acid benzylmethylamide C24H31N3O2S ÏàËÆ¶È:57.8% Heterocycles 2003 60 2441-2455 Synthesis of 5-Substituted Indole Derivatives. Part 4: Naratriptan from ¦Á-Anilinoacetaldehyde Dimethylacetal by TiCl4-Mediated Cyclisation B¨¦la Pete,* Gyula Simig, L¨¢szl¨® Posz¨¢v¨¢cz, and L¨¢szl¨® Toke Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 23 . normacusine B C19H22N2O ÏàËÆ¶È:57.8% Phytochemical Analysis 1997 8 115-119 Tertiary Alkaloid Fraction of Strychnos atlantica: Confirmation of the Identity and Structures of Indole Alkaloids by High Field Nuclear Magnetic Resonance Spectroscopy Rabindranath Mukherjee, Tania M. S. da Silva, João B. L. Guimarães, Eduardo de J. Oliveira, Paul A. Keifer and James N. Shoolery Structure 13C NMR ̼Æ×Ä£Äâͼ |
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²éѯ½á¹û£º¹²²éµ½50¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . 6-O-(p-methoxybenzoyl)-ajugol ÏàËÆ¶È:56% Phytochemistry 1993 32 371-373 Iridoids from Tabebuia avellanedae Kimiko Nakano, Kazuki Maruyama, Ktar Murakami, Yoshihisa Takaishi, Toshiaki Tomimatsu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . ligupurpuroside I ÏàËÆ¶È:56% Chemistry & Biodiversity 2013 10 96-128 Chemical Constituents and Biological Activities of Plants from the Genus Ligustrum Bei-Bei Gao, Gai-Mei She and Dong-Mei She Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . 5'-¦Â-D-glucopyranosyloxyjasmonic butyl ester C22H36O9 ÏàËÆ¶È:56% Acta Chimica Sinica 2007 65 1649-1653 Chemical Constituents of Lavandula augustifolia WU, Xia LIU, Jing YU, Zhi-Bing YE, Yun-Hua ZHOU, Ya-Wei* Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . l0-hydroxystrictosam C26H30N2O9 ÏàËÆ¶È:53.8% Planta Medica 1991 57 149-152 New Indole Alkaloid Glycosides from Nauclea orientalis C. A. J. Erdelmeier, A. D. Wright, .1. Orjala, B. Baumgartner, T. Rali, and O. Stiche Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . (8'R)(-)-¦Á-(E-3,4-Methylenedioxy-2-glucosyloxybenzylidene)-¦Â-(3',4'-dimethoxybenzyl)-¦Ã-butyrolactone C27H30O12 ÏàËÆ¶È:53.8% Phytochemistry 1994 37 1693-1698 Lignans and lignan glycosides fromHaplophyllum cappadocicum Belkis Go¡§zler, Mustafa A. O¡§nu¡§r, Tekant Go¡§zler, Gu¡§lden Kadan, Manfred Hesse Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . 3-methoxy-D-dihomo-estra-17b¦Â-(¦Â-D-glucopyranosyloxy)-1,3,5(10),16-tetraene C27H38O7 ÏàËÆ¶È:53.8% European Journal of Organic Chemistry 2011 1064-1077 Synthesis of a Small Library of Estradiol-Based Glycosteroid Mimics Containing a Modified D-Ring Filip S. Ekholm, Gyula Schneider, J¨¢nos Wölfling and Reko Leino Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . cauferoside ÏàËÆ¶È:53.3% Journal of Natural Products 2010 73 1958-1962 Sesquiterpene Coumarins from Ferula gumosa Mehrdad Iranshahi, Milena Masullo, Ali Asili, Ali Hamedzadeh, Bentolhoda Jahanbin, Michela Festa, Anna Capasso, and Sonia Piacente Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . 2'-O-(4-methoxycinnamoyl)mussaenosidic acid C26H32O12 ÏàËÆ¶È:52% Chemistry & Biodiversity 2006 Vol. 3 799 Iridoid Glucosides and Flavones from the Aerial Parts of Avicennia marina Yan Feng, Xiao-Ming Li, Xiao-Juan Duan, and Bin-Gui Wang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . medicine C25H22O12 ÏàËÆ¶È:52% Helvetica Chimica Acta 2001 Vol. 84 656 Novel Coumarin Glycosides from Daphne oleoides Muhammad Riaz and Abdul Malik Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . spinonin dimethyl ether derivative C25H28O10 ÏàËÆ¶È:52% Journal of Natural Products 1997 60 378-381 Spinonin, a Novel Glycoside from Ononis spinosa subsp. Leiosperma S¨¹heyla Kırmızıg¨¹l, Nezhun Gören, Shu-Wei Yang, Geoffrey A. Cordell, and Candan Bozok-Johansson Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . alangiside ÏàËÆ¶È:52% Chemical & Pharmaceutical Bulletin 1994 42 2208-2210 THREE TETRAHYDROISOQUINOLINE-MONOTERPENE GLUCOSIDES FROM ALANGIUM LAMARCKII : THE FIRST OCCURRENCE OF GLUCOSIDES WITH THE SAME ABSOLUTE CONFIGURATIONS AS DEACETYLISOIPECOSIDE, A KEY INTERMEDIATE IN THE BIOSYNTHESIS OF IPECAC ALKALOIDS Atsuko ITOH,Takao TANAHASHI and Naotaka NAGAKURA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . curculigoside C22H26O11 ÏàËÆ¶È:52% Acta Botanica Sinica 2004 46 621-624 Curculigoside C, a New Phenolic Glucoside from Rhizomes of Curculigo orchioides FU Da-Xu, LEI Guang-Qing, CHENG Xiao-Wei, CHEN Jia-Kuan, ZHOU Tong-Shui Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . compound 2 ÏàËÆ¶È:52% Natural Product Research 1998 11 119-126 Novel 11¦Á-O-¦Â-d-Glucopyranosylrotenoid Isolated from Clitoria fairchildiana Leda Mathias; Ivo J. C. Vieira; Raimundo Braz-filho; Edson Rodrigues-filho Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . scuterivulactone D C27H34O7 ÏàËÆ¶È:52% Chemical & Pharmaceutical Bulletin 1997 45 152-160 Studies on the Constituents of Scutellaria Species. XVIII. Structures of Neoclerodane-Type Diterpenoids from the Whole Herb of Scutellaria rivularis WALL. Haruhisa KIZU,Yoshitaka IMOTO,Tsuyoshi TOMIMORI,Tohru KIKUCHI,Shigetoshi KADOTA and Koji TSUBONO Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . alangiside ÏàËÆ¶È:52% Phytochemistry 1997 46 1225-1229 Five tetrahydroisoquinoline-monoterpene glycosides with a disaccharide moiety from Alangium lamarckii Atsuko Itoh, Takao Tanahashi, Naotaka Nagakura Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . macrophylloside D ÏàËÆ¶È:52% Phytochemistry 1996 42 1305-1313 Acyl secoiridoids and antifungal constituents from Gentiana macrophylla R. X. Tan, J. -L. Wolfender, L. X. Zhang, W. G. Ma, N. Fuzzati, A. Marston, K. Hostettmann Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . alangiside ÏàËÆ¶È:52% Phytochemistry 1996 41 651-656 Acylated tetrahydroisoquinoline-monoterpene glucosides from Alangium lamarckii Atsuko Itoh, Takao Tanahashi, Naotaka Nagakura Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . (R)-peucedanol 7-O-¦Â-D-glucopyranoside C20H26O10 ÏàËÆ¶È:52% Phytochemistry 1994 35 1339-1341 Coumarin glycosides from Peucedanum japonicum Yasumasa Ikeshiro, Izumi Mase, Yutaka Tomita Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . Alanyiside ÏàËÆ¶È:52% Phytochemistry 1994 36 383-387 Tetrahydroisoquinoline-monoterpene glucosides from Alangium lamarckii and Cephaelis ipecacuanha Atsuko Itoh, Takao Tanahashi, Naotaka Nagakura, Hidekazu Nayeshiro Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . 10-ôÇ»ùÒ쳤´º»¨ÜÕÄÚõ£°·(10-hydroxy strictosamide) ÏàËÆ¶È:52% China Journal of Chinese Materia Medica 2011 Vol 36,Issue 8 1037-1039 Study on chemical constituents from leaves of Naudea officinalis XIE Dawen,LI Yonghui,ZHAO LI,DING Gang,YUAN Shao weI,XU Jia, ZHU Hua rong,XIAO Wei Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 21 . Macrophylloside D C25H34O14 ÏàËÆ¶È:52% Journal of Natural Medicines 2007 61 269-279 The chemical constituents of fresh Gentian Root Hidehiro Ando, Yasuaki Hirai, Mikio Fujii, Yumiko Hori and Motonori Fukumura, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 22 . 2'-m-hydroxybenzoylsweroside ÏàËÆ¶È:52% Chinese Traditional and Herbal Drugs 1995 26 7-10 Studies on the Glucoside Constituents of Shengengzhangyacai (Swertia elongata) Kong Deyun; Jiang Yi; Yao Ying; et al(Address:Kong Deyun; shanghai Institute of Pharmaceutical Industry; Shanghai); Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 23 . 8-O-¦Â-D-glucopyranosyl-1,5-dihydroxy-3-methoxyxanthone ÏàËÆ¶È:52% Chinese Traditional and Herbal Drugs 1995 26 7-10 Studies on the Glucoside Constituents of Shengengzhangyacai (Swertia elongata) Kong Deyun; Jiang Yi; Yao Ying; et al(Address:Kong Deyun; shanghai Institute of Pharmaceutical Industry; Shanghai); Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 24 . deacetylcentapicrin ÏàËÆ¶È:52% Chinese Journal of Medicinal Chemistry 2010 20 125-128 Isolation and identification of the Chemical constituents from Swertia yunnanensis Burk. YU Ying, WANG Shi-sheng*, DING Feng-uan, ZHU Jing-bo, ZHAO Wei-jie Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 25 . drymariatin C C27H30O13 ÏàËÆ¶È:52% Journal of Integrative Plant Biology 2005 47 1140-1144 Three New Flavone Glycosides from Drymaria diandra Bl. Zhong-Tao DING*, Xue-Qiong YANG, Qiu-E CAO and Fei LI Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 26 . sclerochitonoside C ÏàËÆ¶È:52% Journal of Chemical Ecology 2011 37 301-310 Leaf Chemistry and Foliage Avoidance by the Thrips Frankliniella occidentalis and Heliothrips haemorrhoidalis in Glasshouse Collections Alison S. Scott Brown, Nigel C. Veitch, Monique S. J. Simmonds Structure 13C NMR ̼Æ×Ä£Äâͼ |
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-koumidine via the intramolecular palladium-catalyzed enolate driven cross coupling reaction. The stereospecific introduction of the 19-(Z) ethylidene side chain
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