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aiwen747: ½ð±Ò+10, ¡ïÓаïÖú, лл 2013-10-26 00:17:36
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²éѯ½á¹û£º¹²²éµ½696¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . elipticina C17H14N2 ÏàËÆ¶È:64.7% Qu¨ªmica Nova 2010 33 284-287 Indole alkaloids from the bark of Aspidosperma vargasii and A. desmanthum Henrique, Marycleuma Campos; Nunomura, Sergio Massayoshi; Pohlit, Adrian Martin Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . palmatine ÏàËÆ¶È:64.7% Chemistry of Natural Compounds 2011 47 154-156 Alkaloids of Phellodendrone lavallei introduced to Western Georgia M. B. Meskheli, V. Yu. Vachnadze, N. S. Vachnadze and A. J. Bakuridze Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . N,N-Bis(furan-2-yl-methyl)tryptamine N12-oxide C20H20N2O3 ÏàËÆ¶È:62.5% Bioorganic & Medicinal Chemistry 2011 19 3120-3127 Tryptamine derivatives as novel non-nucleosidic inhibitors against hepatitis B virus Shi-Jin Qu , Gui-Feng Wang ,Wen-Hu Duan,Shan-Yan Yao, Jian-Ping Zuo , Chang-Heng Tan ,Da-Yuan Zhu Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 4-[2-(4-chlorophenyl)imidazo[4,5-b]indol-3(4H)-yl]phenol C21H14ClN3O ÏàËÆ¶È:62.5% Chemical & Pharmaceutical Bulletin 2010 58 375-380 Microwave-Assisted, Solvent-Free and Parallel Synthesis of Some Novel Substituted Imidazoles of Biological Interest Gyanendra Kumar Sharma and Devender Pathak Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 2,3-dihydro-1H,1'H-[2,3']biindolyl ÏàËÆ¶È:62.5% Heterocycles 2008 75 1407-1416 Hf(OTf)4-Catalyzed 1, 4-Addition Reactions of Indole to Enone in the Presence of Meso and Chiral Pyridinediamine Ligands Sachiko Aburatani and Jun'ichi Uenishi Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 5-Benzyl-1,3,4,5-tetrahydro-7H-azepino[5,4,3-cd]indol-7-one C18H16N2O ÏàËÆ¶È:62.5% Heterocycles 2011 83 815-826 Facile Synthesis of Pyrano[3,2-e]indoles via the Base-Promoted Pictet-Spengler Reaction of Nb-Benzylserotonin Koji Yamada, Sayaka Yamaguchi, Noriyuki Hatae, Takumi Abe, Tatsunori Iwamura, and Minoru Ishikura Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 10-methyl-3-phenyl-4H-indolo[3,2-e][1,2,3]triazolo[1,5-a]pyrimidin-5(10H)-one C18H13N5O ÏàËÆ¶È:62.5% Heterocycles 2003 60 2669-2675 A New Tetracyclic Ring System of Biological Interest. Indolo[3,2-e][1,2,3]triazolo[1,5-a]pyrimidines through Domino Reactions of 2-Azidoindole Antonino Lauria, Chiara Patella, Patrizia Diana, Paola Barraja, Alessandra Montalbano, Girolamo Cirrincione, Gaetano Dattolo, and Anna Maria Almerico* Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . compound 7 C16H20N2O2 ÏàËÆ¶È:62.5% Tetrahedron 1996 52 9925-9930 Acid-catalysed epimerization of 1-substituted indolo[2,3-a]quinolizidines: Stereoselective routes to cis- and trans-deethyleburnamonine starting from the same ester intermediate Mauri Lounasmaa, Lars Miikki, Arto Tolvanen Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . 4'-hydroxy-3'-trifluoromethylflavonol C16H9F3O4 ÏàËÆ¶È:62.5% Journal of Medicinal Chemistry 2008 51 1874-1884 Understanding the Cardioprotective Effects of Flavonols: Discovery of Relaxant Flavonols without Antioxidant Activity Cheng Xue Qin, Xingqiang Chen, Richard A. Hughes, Spencer J. Williams and Owen L. Woodman Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 2-((1s,4s)-4-aminocyclohexyl)-N-(3,4-dichlorophenyl)-1H-imidazo[4,5-c]quinolin-4-amine C22H21Cl2N5 ÏàËÆ¶È:62.5% Journal of Medicinal Chemistry 2009 52 2098-2108 Novel 2- and 4-Substituted 1H-Imidazo[4,5-c]quinolin-4-amine Derivatives as Allosteric Modulators of the A3 Adenosine Receptor Yoonkyung Kim, Sonia de Castro, Zhan-Guo Gao, Adriaan P. IJzerman and Kenneth A. Jacobson Structure 13C NMR ̼Æ×Ä£Äâͼ |
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