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²éѯ½á¹û£º¹²²éµ½456¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . (-)-tetrahydroalstonine ÏàËÆ¶È:100% 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 2 . tetrahydroalstonine ÏàËÆ¶È:100% 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 3 . 11-methoxytetrahydroalstonine C22H26N2O4 ÏàËÆ¶È:77.2% Phytochemistry 1991 30 2447-2449 11-Methoxytetrahydroalstonine, a heteroyohimbinoid alkaloid from Vinca major Gobinda Mukhopadhyay, Biswapati Mukherjee, Amarendra Patra, Asima Chatterjee, Ratna Ghosh, Priyobroto Roychowdhury, H. Kawazura Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 10-Methoxytetrahydroalstonine C22H26N2O4 ÏàËÆ¶È:77.2% Journal of Separation Science 2013 36 407-413 Large-scale separation of antipsychotic alkaloids from Rauwolfia tetraphyllaL. by pH-zone-refining fast centrifugal partition chromatography Anupam Maurya, Shikha Gupta and Santosh K. Srivastava Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 3-isorauniticine ÏàËÆ¶È:76.1% 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 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 . 17-epi-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 8 . 14¦Á-hydroxyrauniticine 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 9 . ¦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 10 . (+)-vincadine ÏàËÆ¶È:71.4% 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 11 . 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 12 . 14-¦Â-Hydroxy-3-iso-rauniticine C21H24N2O4 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 13 . 14¦Á-hydroxyrauniticine ÏàËÆ¶È:71.4% Australian Journal of Chemistry 1998 51 961-964 The Alkaloids of Uncaria cf. glabrata Dayar Arbain, Afrida, Satria Ibrahim, Melvyn V. Sargent, Brian W. Skelton and Allan H. White Structure 13C NMR ̼Æ×Ä£Äâͼ |
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zengjundeyo: ½ð±Ò+15, ¡ï¡ï¡ïºÜÓаïÖú, ллÄã 2013-09-02 14:55:39
zengjundeyo: ½ð±Ò+15, ¡ï¡ï¡ïºÜÓаïÖú, ллÄã 2013-09-02 14:55:39
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²éѯ½á¹û£º¹²²éµ½371¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . compound 1 C21H26N2O2 ÏàËÆ¶È:100% 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 2 . coronaridine ÏàËÆ¶È:100% 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 3 . coronaridine ÏàËÆ¶È:100% 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 4 . coronaridine ÏàËÆ¶È:100% 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 5 . coronaridine ÏàËÆ¶È:100% Qu¨ªmica Nova 2008 31 20-24 Chemical constituents from Tabernaemontana catharinensis root bark: a brief NMR review of indole alkaloids and in vitro cytotoxicity Pereira, Paulo S¨¦rgio; França, Suzelei de Castro; Oliveira, Paulo Vinicius Anderson de; Breves, Camila Moniz de Souza; Pereira, Sarazete Izidia Vaz; Sampaio, Suely Vilela; Nomizo, Auro; Dias, Diones Aparecida Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . coronaridine ÏàËÆ¶È:100% 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 7 . coronaridine ÏàËÆ¶È:95.2% 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 8 . coronaridina ÏàËÆ¶È:95.2% 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 9 . coronaridine C21H26O2N2 ÏàËÆ¶È:95.2% Academic Journal of Second Military Medical University 2006 27 92-96 Antiaddictive indole alkaloids in Ervatamia yunnanensis and their bioactivity XUAN Wei-dong, CHEN Hai-sheng, YUAN Zhi-xian, ZHANG Xiao-dong, HUANG Mao Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . Coronaridine ÏàËÆ¶È:90.4% 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 . 3-R-ethoxycoronaridine C23H30N2O3 ÏàËÆ¶È:85.7% Academic Journal of Second Military Medical University 2006 27 92-96 Antiaddictive indole alkaloids in Ervatamia yunnanensis and their bioactivity XUAN Wei-dong, CHEN Hai-sheng, YUAN Zhi-xian, ZHANG Xiao-dong, HUANG Mao Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . 19-R-hyyneanine ÏàËÆ¶È:80.9% Natural Product Sciences 1997 3 42-48 Alkaloids from The Roots of Tabernaemontana Macrocarpa Jack Husain, Khairana; Said, Ikram M.; Din, Laily B.; Takayama, Hiromitsu; Kitajima, Mariko; Aimi, Norio Structure 13C NMR ̼Æ×Ä£Äâͼ |
3Â¥2013-09-02 12:48:06














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