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1...... 21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2 12.3,22.9,28.0,28.8,33.2,37.1,40.0,53.0,54.0,54.7,56.4,58.1,110.8,111.6,118.9,119.7,122.3,129.8,137.6,138.5,176.4 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£º¹²²éµ½141¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . coronaridine ÏàËÆ¶È:85.7% Acta Pharmaceutica Sinica 2010 45 471-474 Monomeric indole alkaloids from the aerial parts of Catharanthus roseus ZHONG Xiang-zhang, WANG Guo-cai, WANG Ying, ZHANG Xiao-qi, YE Wen-cai* Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . coronaridine ÏàËÆ¶È:76.1% 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 -------------------------------------------------------------------------------- 3 . Coronaridine ÏàËÆ¶È:76.1% Phytochemistry 1980 19 1213-1218 Anticancer indole alkaloids of Ervatamia heyneana Sarath P. Gunasekera, Geoffrey Cordell, Norman R. Farnsworth Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . compound 1 C21H26N2O2 ÏàËÆ¶È:71.4% Chemical & Pharmaceutical Bulletin 1992 40 2041-2043 Indonesian Medicinal Plants. II. Chemical Structures of Pongapinones A and B, Two New Phenylpropanoids from the Bark of Pongamia pinnata (Papilionaceae) Isao KITAGAWA,Ru-song ZHANG,Kazuyuki HORI,Katsutoshi TSUCHIYA and Hirotaka SHIBUYA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . coronaridine ÏàËÆ¶È:71.4% 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 -------------------------------------------------------------------------------- 6 . N1-methyl-isovoacangine ÏàËÆ¶È:69.5% Journal of Natural Products 1981 Vol 44 459-465 Contribution A L'¨¦tude des Tabernaemontan¨¦es Am¨¦ricaines. III. Alcaloides de Anartia cf. meyeri F. Ladhar, M. Damak, A. Ahond, C. Poupat, P. Potier, C. Moretti Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . voacangine ÏàËÆ¶È:68.1% 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 -------------------------------------------------------------------------------- 8 . voacangine ÏàËÆ¶È:68.1% Chemical & Pharmaceutical Bulletin 1992 40 2041-2043 Indonesian Medicinal Plants. II. Chemical Structures of Pongapinones A and B, Two New Phenylpropanoids from the Bark of Pongamia pinnata (Papilionaceae) Isao KITAGAWA,Ru-song ZHANG,Kazuyuki HORI,Katsutoshi TSUCHIYA and Hirotaka SHIBUYA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . voacangine ÏàËÆ¶È:68.1% 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 -------------------------------------------------------------------------------- 10 . Voacangine ÏàËÆ¶È:68.1% Phytochemistry 1980 19 1213-1218 Anticancer indole alkaloids of Ervatamia heyneana Sarath P. Gunasekera, Geoffrey Cordell, Norman R. Farnsworth Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . voacangine ÏàËÆ¶È:68.1% 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 -------------------------------------------------------------------------------- 12 . voacangine ÏàËÆ¶È:68.1% Journal of the Chemical Society, Perkin Transactions 1 1976 1432-1438 Structures of tabernaelegantines A¨CD and tabernaelegantinines A and B, new indole alkaloids from Tabernaemontana elegans Ezio Bombardelli, Attilio Bonati, Bruno Gabetta, Ernesto M. Martinelli, Giuseppe Mustich and Bruno Danieli Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . coronaridine ÏàËÆ¶È:66.6% Journal of Natural Products 1988 Vol 51 528 Heyneanine Hydroxyindolenine, A New Indole Alkaloid from Ervatamia coronaria var. plena Perveen Sharma, Geoffrey A. Cordell Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . coronaridine ÏàËÆ¶È:66.6% 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 -------------------------------------------------------------------------------- 15 . 19S-Heyneanine ÏàËÆ¶È:66.6% Phytochemistry 1980 19 1213-1218 Anticancer indole alkaloids of Ervatamia heyneana Sarath P. Gunasekera, Geoffrey Cordell, Norman R. Farnsworth Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . (-)-3R-Methoxycoronaridine ÏàËÆ¶È:63.6% Phytochemistry 1994 37 1729-1735 Indole alkaloids and terpenoids fromTabernaemontana markgrafiana Helene B. Nielsen, Alan Hazell, Rita Hazell, Felipe Ghia, Kurt B.G. Torssell Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . voacangine ÏàËÆ¶È:63.6% 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 -------------------------------------------------------------------------------- 18 . alstoyunine A C20H24N2O3 ÏàËÆ¶È:61.9% 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 -------------------------------------------------------------------------------- 19 . 19-Heyneanine C21H26N2O3 ÏàËÆ¶È:61.9% 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 -------------------------------------------------------------------------------- 20 . compound 18 ÏàËÆ¶È:61.9% Natural Product Research 1996 8 75-82 Studies on the Synthesis of Strychnos Alkaloids Daniele Passarella; Swargam Sathyanarayana; Mercedes Amat; Joan Bosch Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 21 . 19-heyneanine ÏàËÆ¶È:61.9% 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 -------------------------------------------------------------------------------- 22 . 5,6-Dehydrocoronaridine ÏàËÆ¶È:61.9% Phytochemistry 1994 37 1729-1735 Indole alkaloids and terpenoids fromTabernaemontana markgrafiana Helene B. Nielsen, Alan Hazell, Rita Hazell, Felipe Ghia, Kurt B.G. Torssell Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 23 . leepacine C21H22N2O3 ÏàËÆ¶È:61.9% 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 -------------------------------------------------------------------------------- 24 . stapfinine ÏàËÆ¶È:61.9% Phytochemistry 1986 25 1781-1782 Stapfinine, an indole alkaloid from Ervatamia coronaria Atta-ur-Rahman, Anjum Muzaffar, Nader Daulatabadi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 25 . conopharyngine ÏàËÆ¶È:60.8% Journal of Natural Products 1985 Vol 48 400-423 Antimicrobially Active Alkaloids from Tabernaemontana chippii Teris A. Van Beek, Robert Verpoorte, Anders Baerheim Svendsen, Roel Fokkens Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 26 . Conopharyngine ÏàËÆ¶È:60.8% Phytochemistry 1984 23 1771-1778 Antimicrobially active alkaloids from Tabernaemontana pachysiphon T. A. van Beek, F. L. C. Kuijlaars, P. H. A. M. Thomassen, R. Verpoorte, A. Baerheim Svendsen Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 27 . pseudoakuammigine ÏàËÆ¶È:59.0% Planta Medica 1989 55 463-466 Indole Alkaloids from Aistonia angustjfolia Wen-lan Hi, Ji-ping Zhu, and Manfred Hesse Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 28 . (-)-akuammicin ÏàËÆ¶È:59.0% Planta Medica 1989 55 463-466 Indole Alkaloids from Aistonia angustjfolia Wen-lan Hi, Ji-ping Zhu, and Manfred Hesse Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 29 . voacristine ÏàËÆ¶È:59.0% Planta Medica 1983 49 148-150 Tertiary Indole Alkaloids from Leaves of Tabernaemontana dichotoma Premila Perera, Gunnar Samuelsson, Tens A. van Beek and Robert Verpoorte Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 30 . 10-deoxyakuammine ÏàËÆ¶È:59.0% Journal of Natural Products 1992 Vol 55 380 Akuammine and Dihydroakuammine, Two Indolomonoterpene Alkaloids Displaying Affinity for Opioid Receptors Guy Lewin, Patrick Le M¨¦nez, Yves Rolland, Anne Renouard, Eva Giesen-Crouse Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 31 . Voacangarine ÏàËÆ¶È:59.0% Phytochemistry 1980 19 1213-1218 Anticancer indole alkaloids of Ervatamia heyneana Sarath P. Gunasekera, Geoffrey Cordell, Norman R. Farnsworth Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 32 . 3-(2-oxopropyl)coronaridine ÏàËÆ¶È:58.3% 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 -------------------------------------------------------------------------------- 33 . 17-O-aaztyl-19,20-dihydrovoachalotine C24H30N2O4 ÏàËÆ¶È:58.3% Phytochemistry 1976 15 2021-2022 17-O-acetyl-19,20-dihydrovoachalotine, a new alkaloid from Voacanga chalotiana Ezio Bombardelli, Attilio Bonati, Bruno Gabetta, Ernesto Martinelli, Giuseppe Mustich, Bruno Danieli Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 34 . flabelliformine C21H26N2O3 ÏàËÆ¶È:57.1% Helvetica Chimica Acta 2008 Vol. 91 239 Three New Monoterpenoid Indole Alkaloids from Ervatamia flabelliformis Shuang Liang, Hai-Sheng Chen, Yun-Heng Shen, Wei-Dong Zhang, Yong-Sheng Jin, and Run-Hui Liu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 35 . yohimbine ÏàËÆ¶È:57.1% Journal of Natural Products 2001 64 193-195 Hydroxylation of Yohimbine in Superacidic Media: One-Step Access to Human Metabolites 10 and 11-Hydroxyyohimbine Alain Duflos,Florence Redoules,Jacques Fahy, Jean-Claude Jacquesy, and Marie-Paule Jouannetaud Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 36 . compound 19 ÏàËÆ¶È:57.1% 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 -------------------------------------------------------------------------------- 37 . 10,11-demethoxychippiine ÏàËÆ¶È:57.1% Natural Product Research 1999 13 143-146 Dippinine A, A New Alkaloid of the Chippiinetype From A Malayan Tabernaemontana Toh-Seok Kam; Kooi-Mow Sim Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 38 . Vinblastine ÏàËÆ¶È:57.1% Journal of Natural Products 1992 Vol 55 269 Metabolism of the Catharanthus Alkaloids: from Streptomyces griseus to Monoamine Oxidase B John P. N. Rosazza, Michael W. Duffel, Sayed El-Marakby, Sung Ho Ahn Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 39 . undulifoline C20H24N2O3 ÏàËÆ¶È:57.1% Phytochemistry 1992 31 1078-1079 Alkaloids from alstonia undulifolia Georges Massiot, Ahcene Boumendjel, Jean-Marc Nuzillard, Bernard Richard, Louisette Le Men-Olivier, Bruno David, Hamid A. Hadi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 40 . heyneanine ÏàËÆ¶È:57.1% 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 -------------------------------------------------------------------------------- 41 . cleavamine ÏàËÆ¶È:57.1% 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 -------------------------------------------------------------------------------- 42 . 16¦Á-carbomethoxy-15,20¦Â-dihydrocleavamine ÏàËÆ¶È:57.1% 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 -------------------------------------------------------------------------------- 43 . 16-epivoacarpine ÏàËÆ¶È:57.1% Chemical & Pharmaceutical Bulletin 1987 35 4668-4671 INDOLE ALKALOIDS ISOLATED FROM GELSEMIUM ELEGANS (THAILAND) : 19- (Z) -AKUAMMIDINE, 16-EPI-VOACARPINE, 19-HYDROXYDIHYDRO-GELSEVIRINE, AND THE REVISED STRUCTURE OF KOUMIDINE Shin-ichiro Sakai,Sumphan Wongseripipatana,Dhavadee Ponglux,Masaki Yokota,Koreharu Ogata,Hiromitsu Takayama and Norio Aimi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 44 . 3-hydroxy-3,4-secocoronaridine C21H28O3N2 ÏàËÆ¶È:57.1% 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 -------------------------------------------------------------------------------- 45 . compound 33 ÏàËÆ¶È:57.1% 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 -------------------------------------------------------------------------------- 46 . 19Z-16-epi-Voacarpine C21H25N2O4 ÏàËÆ¶È:57.1% Tetrahedron Letters 2005 46 5857-5861 Six new indole alkaloids from Gelsemium sempervirens Ait. f. Noriyuki Kogure, Chika Nishiya, Mariko Kitajima, Hiromitsu Takayama Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 47 . 16-epi-voacarpine ÏàËÆ¶È:57.1% Tetrahedron Letters 2005 46 5857-5861 Six new indole alkaloids from Gelsemium sempervirens Ait. f. Noriyuki Kogure, Chika Nishiya, Mariko Kitajima, Hiromitsu Takayama Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 48 . compound 7a ÏàËÆ¶È:57.1% Bulletin of the Chemical Society of Japan 1989 62 880-887 Isolation of Four 2,3,5,6,11,11b-Hexahydro-3-oxo-1H-indolizino[8,7-b]indole-5-carboxylic Acids from Clerodendron Trichotomum Thunb and Properties of Their Derivatives Hajime Irikawa, Yasuhiro Toyoda, Hiroaki Kumagai, Yasuaki Okumura Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 49 . (16R,17S)-14¦Á-hydroxy-3-isorauniticine methyl acetal C22H28N2O5 ÏàËÆ¶È:54.5% 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 -------------------------------------------------------------------------------- 50 . (¡À)-(8¦Â,9¦Á,14¦Á)-2-Methoxy-11¦Â-methoxymethyl-17-acetylgona-1,3,5(10),13(17)-tetraene C22H28O3 ÏàËÆ¶È:54.5% 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 2........ 21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2 12.2,28.0,28.8,33.1,34.9,38.2,39.4,50.1,50.5,53.3,57.4,59.6,89.1,121.1,123.0,128.1,130.4,174.3 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£º¹²²éµ½78¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . coronaridine hydroxyindolenine C21H26N2O3 ÏàËÆ¶È:66.6% 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 -------------------------------------------------------------------------------- 2 . coronaridine hydroxyindolenine ÏàËÆ¶È:66.6% 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 -------------------------------------------------------------------------------- 3 . Coronaridine hydroxyindolenine ÏàËÆ¶È:65% Phytochemistry 1994 37 1729-1735 Indole alkaloids and terpenoids fromTabernaemontana markgrafiana Helene B. Nielsen, Alan Hazell, Rita Hazell, Felipe Ghia, Kurt B.G. Torssell Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . vocangine-7-hydroxyindolenine ÏàËÆ¶È:61.9% Planta Medica 1988 54 364 Alkaloids from Trachelospermum jasmino ides Atta-ur-Rahman , T. Fatima, George Crank, and Shaheen Wasti Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . (2RS,7SR)-7,9,10,11-Tetrahydro-10,10-dimethyl-3-phenyl-2,7-methano-1-benzoxonin-8(2H)-one C21H22O2 ÏàËÆ¶È:57.8% Helvetica Chimica Acta 2011 Vol. 94 1431-1439 Manganese(III) Acetate Catalyzed Oxidative Radical Additions of ¦Á-Dicarbonyl Compounds to 1- and 2-Phenylcyclohepta-1, 3, 5-triene Esra Findik and Mustafa Ceylan Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . ketotriester ÏàËÆ¶È:55.5% Journal of Natural Products 1984 Vol 47 592-599 Cmr Spectroscopy of Labdanic Diterpenes and Related Substances Josette Bastard, Do Khac Duc, Marcel Fetizon, Malcolm J. Francis, Peter K. Grant, Rex T. Weavers, Chikara Kaneko, G. Vernon Baddeley, Jean-Marie Bernassau, Ivor R. Burfitt, Peter M. Wovkulich, Ernest Wenkert Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . N-((N-Boc-amino)hexanoyl)-para-hydroxyphenyl-L-para-tyrosinamide C26H35N3O6 ÏàËÆ¶È:55.5% Steroids 2012 77 403-412 Design of novel tyrosine-nitrogen mustard hybrid molecules active against uterine, ovarian and breast cancer cell lines Caroline Descôteaux, Kevin Brasseur, Val¨¦rie Leblanc, Sophie Parent, Éric Asselin, Gervais B¨¦rub¨¦ Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . Compound 2g ÏàËÆ¶È:55.5% Magnetic Resonance in Chmesitry 2001 39 105-108 1H and 13C spectral assignment of 1, 4, 5, 6, 7, 8-hexahydroquinolines and their oxa-analogues 5, 6, 7, 8-tetrahydro-4H-chromenes Margarita Su¨¢rez, Dolores Molero, Esperanza Salfran, Nazario Mart¨ªn, Yamila Verdecia, Roberto Martinez, Estael Ochoa, Livan Alba, Margarita Quinteiro and Carlos Seoane Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . circinatin C20H31O7N3 ÏàËÆ¶È:55% Experientia 1990 46 1206-1209 The structure of circinatin, a non-toxic metabolite from the plant pathogenic fungusPericonia circinata V. Macko, M. B. Stimmel, H. Peeters, T. J. Wolpert and L. D. Dunkle, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . methyl 4-[(3,4-dihydro-2H-[1,3]oxazino[3,2-a]indole-10-carbonyl)amino]-1-methylpiperidinylpentanoate C24H33N3O4 ÏàËÆ¶È:54.5% Bioorganic & Medicinal Chemistry 2010 18 8600-8613 Synthesis and pharmacological properties of novel hydrophilic 5-HT4 receptor antagonists Bjarne Brudeli, Lise Rom¨¢n Moltzau, Kjetil Wessel Andressen, Kurt A. Krobert, Jo Klaveness, Finn Olav Levy Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . rauflorine ÏàËÆ¶È:52.6% Planta Medica 1996 62 577-579 A1H- and 13C-NMR Study of Seven Ajma line-Type Alkaloids Reija Jokela and Mauri Lounasmaa Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . (3aS,8aR)-3a-Ethyl-1,2,3,3a,8,8a-hexahydro-1,8-dimethyl-5-[4-(pyrrolidin-1-ylmethyl)-1H-1,2,3-triazol-1-yl]pyrrolo[2,3-b]indole C21H30N6 ÏàËÆ¶È:52.6% Helvetica Chimica Acta 2011 Vol. 94 1496-1505 An Efficient Synthesis of a (-)-Physostigmine s Library for Identifying Potential Anti-Alzheimer s Agents Yi Wu, Fusheng Wang, Hao Song, and Yong Qin Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . compound 2c ÏàËÆ¶È:52.6% Phytochemistry 1987 26 745-747 Oxygenated fatty acids from Lemna trisulca Pietro Monaco,Lucio Previtera Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . compound 44 C21H25NO4 ÏàËÆ¶È:52.6% Heterocycles 2006 70 423-459 Aza-[3+3] Annulations. Part 6. Total Synthesis of Putative (-)-Lepadiformine and (-)-Cylindricine C Jiashi Wang, Jacob J. Swidorski, Nadiya Sydorenko, Richard P. Hsung,* Heather A. Coverdale, Jennifer M. Kuyava, and Jia Liu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . 2-(Benzhydrylsulfinyl)acetic acid-1-{(3-cyclohexyl-propyl)-1H-[1,2,3]triazol-4-yl}methyl ester C27H33N3O3S ÏàËÆ¶È:52.6% Molecules 2011 16 10409-10419 Convenient Synthesis and Biological Evaluation of Modafinil Derivatives: Benzhydrylsulfanyl and Benzhydrylsulfinyl [1,2,3]triazol-4-yl-methyl Esters Jae-Chul Jung, Yeonju Lee, Jee-Young Son, Eunyoung Lim, Mankil Jung and Seikwan Oh Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . 5-methoxystrictamine C21H24N2O3 ÏàËÆ¶È:52.3% Helvetica Chimica Acta 2005 Vol. 88 2508 Three New Indole Alkaloids from the Leaves of Alstonia scholaris Hua Zhou, Hong-Ping He, Xiao-Dong Luo, Yue-Hu Wang, Xian-Wen Yang, Ying-Tong Di,and Xiao-Jiang Hao Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . 16¦Á-carbomethoxy-15,20¦Á-dihydrocleavamine ÏàËÆ¶È:52.3% 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 -------------------------------------------------------------------------------- 18 . (¡À)-iboxyphylline C21H26N2O3 ÏàËÆ¶È:52.3% Heterocycles 2008 75 65-76 Synthesis of Vinca Alkaloids and Related Compounds. Part 109. An Intramolecular [4+2] Cycloaddition Mediated Biomimetic Synthesis of (¡À)-Iboxyphylline Fl¨®ri¨¢n T¨®th, György Kalaus, Gergely Pipa, Istv¨¢n Greiner, Áron Szollosy, Attila Rill, Ágnes Gömöry, L¨¢szl¨® Hazai, and Csaba Sz¨¢ntay Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . tacamine ÏàËÆ¶È:52.3% Tetrahedron letters 1982 23 4827-4830 Tacamine, the first example of a new class of indole alkaloids T.A. Van Beek, P.P. Lankhorst, R. Verpoorte, A.Baerheim Svendsen Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . methyl 4-[(3,4-dihydro-2H-[1,3]oxazino[3,2-a]indole-10-carbonyl)amino]-1-methylpiperidinylhexanoate C25H35N3O4 ÏàËÆ¶È:52.1% Bioorganic & Medicinal Chemistry 2010 18 8600-8613 Synthesis and pharmacological properties of novel hydrophilic 5-HT4 receptor antagonists Bjarne Brudeli, Lise Rom¨¢n Moltzau, Kjetil Wessel Andressen, Kurt A. Krobert, Jo Klaveness, Finn Olav Levy Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 21 . 4-[(3,4-dihydro-2H-[1,3]oxazino[3,2-a]indole-10-car-bonyl)amino]-1-methylpiperidinylpropanoic acid C21H27N3O4 ÏàËÆ¶È:52.1% Bioorganic & Medicinal Chemistry 2010 18 8600-8613 Synthesis and pharmacological properties of novel hydrophilic 5-HT4 receptor antagonists Bjarne Brudeli, Lise Rom¨¢n Moltzau, Kjetil Wessel Andressen, Kurt A. Krobert, Jo Klaveness, Finn Olav Levy Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 22 . panduratin H C20H26O2 ÏàËÆ¶È:50% Chemical & Pharmaceutical Bulletin 2008 56(4) 491-496 Panduratins D¡ªI, Novel Secondary Metabolites from Rhizomes of Boesenbergia pandurata Nwet Nwet WIN,Suresh AWALE,Hiroyasu ESUMI,Yasuhiro TEZUKA,and Shigetoshi KADOTA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 23 . demethoxypurpeline C20H22N2O ÏàËÆ¶È:50% Phytochemistry 2002 60 315-320 Indole alkaloids from Rauvolfia bahiensis A.DC. (Apocynaceae) Lucilia Kato, Raquel Marques Braga, Ingrid Koch, Luiza Sumiko Kinoshita Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 24 . phlogacantholide B C20H28O4 ÏàËÆ¶È:50% Journal of Natural Products 2005 68 86-89 Two Diterpenes and Three Diterpene Glucosides from Phlogacanthus curviflorus Xiao-Hong Yuan, Bo-Gang Li, Xiu-Yun Zhang, Hua-Yi Qi, Min Zhou, and Guo-Lin Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 25 . 9¦Â-hydroxy-2¦Â-methoxyclovan-10-one C16H26O3 ÏàËÆ¶È:50% Journal of Natural Products 2004 67 793-798 Structure−Activity Relationships in the Fungistatic Activity against Botrytis cinerea of Clovanes Modified on Ring C Athina Deligeorgopoulou, Antonio J. Macas-Snchez, Daniel J.Mobbs, Peter B. Hitchcock, James R. Hanson, and Isidro G. Collado Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 26 . 5(6)-dihydro-6-methoxyterreyclic acid A C16H24O4 ÏàËÆ¶È:50% Journal of Natural Products 2003 66 1567-1573 Cytotoxic Constituents of Aspergillus terreus from the Rhizosphere of Opuntia versicolor of the Sonoran Desert E. M. Kithsiri Wijeratne,Thomas J. Turbyville,Zhongge Zhang, Donna Bigelow,Leland S. Pierson, III,Hans D. VanEtten, Luke Whitesell,Louise M. Canfield, and A. A. Leslie Gunatilaka Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 27 . 8¦Á,14-dihydro-7-oxohelioscopinolide A C20H28O4 ÏàËÆ¶È:50% Journal of Natural Products 1998 61 749-756 Macrocyclic Diterpenoids from Euphorbia semiperfoliata Giovanni Appendino, Sven Jakupovic, Gian Cesare Tron, Jasmin Jakupovic, Veronique Milon, and Mauro Ballero Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 28 . ent-1¦Á-hydroxykauran-12-one C20H32O2 ÏàËÆ¶È:50% Journal of Natural Products 1997 60 421-424 1-Hydroxyditerpenes from Two New Zealand Liverworts, Paraschistochila pinnatifolia and Trichocolea mollissima Stephen D. Lorimer, Nigel B. Perry, Elaine J. Burgess, and Lysa M. Foster Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 29 . Voacangine hydroxyindolenine C22H28N2O4 ÏàËÆ¶È:50% 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 -------------------------------------------------------------------------------- 30 . 4-epiabietic acid C20H30O2 ÏàËÆ¶È:50% Acta Bot. Boreal. -Occident. Sin. 2009 29 2326-2330 Isolation and identification of Antifungal Components from Juniperus chinensis cv. Kaizuca NIU Xin-wei, LUO Lan, SUN Jia-long, LU Shi-wei, YUAN Zhong-lin Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 31 . parvineostemonine C17H25NO2 ÏàËÆ¶È:50% Chinese Chemical Letters 2003 14 173-175 A Novel Alkaloid from Stemona parviflora Chang Qiang KE, Zhi Sheng HE, Yi Ping YANG, Yang YE Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 32 . compound 5g ÏàËÆ¶È:50% Chinese Chemical Letters 2006 17 150-152 Multicomponent Reaction in Ionic Liquid: A Novel and Green Synthesis of 1, 4-Dihydropyridine Derivatives Xin Ying ZHANG, Yan Zhen LI, Xue Sen FAN, Gui Rong QU,Xue Yuan HU, Jian Ji WANG Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 33 . Methyl 2-(1-naphthyl)tetrahydro-1H-thieno[3,4-b]pyrrole-6a(6H)-carboxylate C18H19NO2S ÏàËÆ¶È:50% Molecules 1998 3 60-63 Intramolecular Cycloaddition of Imines of Cysteine Derivatives Ana M. T. D. P. V. Cabral, Antonio M. d'A Rocha Gonsalves and Teresa M. V. D. Pinho e Melo Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 34 . (20R,23S,25S)-De-A,B-25-Trimethylsilylhydroxy-cholestane-8-one-26,23-N-methyl lactam ÏàËÆ¶È:50% Molecules 2003 8 488-499 Novel Heteroatom-containing Vitamin D3 Analogs: Efficient Synthesis of 1¦Á, 25-Dihydroxyvitamin D3-26, 23-lactam Yuko Kato, Yuichi Hashimoto and Kazuo Nagasawa Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 35 . (2S,3'S)-2-(2-oxo-2,3,4,5-tetrahydro-1H-benzoazepin-3-ylamino)-4-phenylbutyricacid ethyl ester C22H26N2O3 ÏàËÆ¶È:50% Molecules 2006 11 641-648 Formal Synthesis of the ACE Inhibitor Benazepril¡¤HCl via an Asymmetric Aza-Michael Reaction Luo-Ting Yu, Ji-Ling Huang, Ching-Yao Chang and Teng-Kuei Yang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 36 . 3¦Á,8¦Á,9¦Á-trihydroxycedrane ÏàËÆ¶È:50% Phytochemistry 1996 42 1583-1586 Biotransformation of cedrol and related compounds by Mucor plumbeus Braulio M. Fraga, Ricardo Guillermo, James R. Hanson, Almaz Truneh Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 37 . heteroscyphic acid A C20H32O2 ÏàËÆ¶È:50% Phytochemistry 1994 37 1263-1268 Diterpenes of the clerodane-type from cultured cells of Heteroscyphus planus Kensuke Nabeta, Tadashi Oohata, Noriko Izumi, Kenji Katoh Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 38 . 13¦Á-(4'hydroxytigloyloxy)lupanine C20H30N2O4 ÏàËÆ¶È:50% Phytochemistry 1993 32 1603-1605 (+)-13¦Á-(4'-Hydroxytigloyloxy) lupanine from Ormosia krugii Martua P. Nasution, A.Douglas Kinghorn Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 39 . pearsonine ÏàËÆ¶È:50% Phytochemistry 1991 30 3631-3634 Co-occurrence of hydroxylated lupanines and their corresponding angelate esters inPearsonia species Gerhard H. Verdoorn, Ben-Erik van Wyk Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 40 . Dimethyl 2,2-dimethoxy-4-(3-nitrobenzyl)glutarate C16H21NO8 ÏàËÆ¶È:50% Chemical Research in Chinese Universities 2007 23 284-288 Syntheses and Bioactivities of 4-Ar-2-oxo-glutaric Acids CHEN Qiu-yun,ZHANG Rong-xian, LIU Qing-shan and Scho field Christopher Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 41 . 2-{1-[(3aS,8aR)-3a-Ethyl-1,2,3,3a,8,8a-hexahydro-1,8-dimethylpyrrolo[2,3-b]indol-5-yl]-1H-1,2,3-triazol-4-yl}ethanol C18H25N5O ÏàËÆ¶È:50% Helvetica Chimica Acta 2011 Vol. 94 1496-1505 An Efficient Synthesis of a (-)-Physostigmine s Library for Identifying Potential Anti-Alzheimer s Agents Yi Wu, Fusheng Wang, Hao Song, and Yong Qin Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 42 . 15S-Hydroxy-7S-methoxy-2-methyl-2E,4E,10E-hexadecatrienoic Acid C18H30O4 ÏàËÆ¶È:50% Journal of Natural Products 2001 64 472-479 Synthesis of (7S,15S)- and (7R,15S)-Dolatrienoic Acid Jonathan J. Duffield and George R. Pettit Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 43 . 15S-Hydroxy-7R-methoxy-2-methyl-2E,4E,10E-hexadecatrienoic acid C18H30O4 ÏàËÆ¶È:50% Journal of Natural Products 2001 64 472-479 Synthesis of (7S,15S)- and (7R,15S)-Dolatrienoic Acid Jonathan J. Duffield and George R. Pettit Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 44 . compound [2H3]-9 ÏàËÆ¶È:50% Chemical & Pharmaceutical Bulletin 2009 57 1421-1424 A Facile Method for Preparation of [2H3]-Sufentanil and Its Metabolites Sankareswaran Srimurugan, Kaliyappan Murugan and Chinpiao Chen Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 45 . compound 3 ÏàËÆ¶È:50% Tetrahedron Letters 2000 41 603-607 Documentation of a rare example of an intramolecular 1,2-addition of a trialkylborane to a carbonyl group Robert K. BoeckmanJr., Lorna H. Mitchell, Pengcheng Shao, Rene J. Lachicotte Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 46 . pearsonine ÏàËÆ¶È:50% Phytochemistry 1990 29 1297-1302 Esters of quinolizidine alkaloids from the genus Pearsonia Gerhard H. Verdoorn,Ben-Erik van Wyk Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 47 . 3-hydroxy-3,4-secocoronaridine C21H28O3N2 ÏàËÆ¶È:50% 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 -------------------------------------------------------------------------------- 48 . 1,9,17,25-tetraazapentacyclo[23.7.1.19,17.010,15.027,32]tetra-triaconta-10(15),11,13,27(32),28,30-hexaene-16,26,33,34-tetrone C30H36N4O4 ÏàËÆ¶È:50% Journal of Heterocyclic Chemistry 2007 44 1501-1504 Synthesis of quinazolinophanes containing bridgehead nitrogen atoms from quinazoline-2,4(1H,3H)-dione R. L. Sharam,Jasbir Singh,Surinder Kumar,Daljeet Kour,Anand Sachar,Shallu,Poonam and Bhawana Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 49 . methyl 2-tert-butoxycarbonylamino-5-[(3-iodo-1H-indole-2-yl)carbonylamino]pent-2-enoate ÏàËÆ¶È:50% Journal of Heterocyclic Chemistry 2005 42 1433-1441 Preparation and reactivity of 5-substituted azepino[3,4-b]indoles C. Montagne,N. Laurent,B. Joseph and J.-Y. M¨¦rour Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 50 . compound 9b C20H24IN3O5 ÏàËÆ¶È:50% Journal of Heterocyclic Chemistry 2005 42 1433-1441 Preparation and reactivity of 5-substituted azepino[3,4-b]indoles C. Montagne,N. Laurent,B. Joseph and J.-Y. M¨¦rour Structure 13C NMR ̼Æ×Ä£Äâͼ |
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