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aiwen747: ½ð±Ò+10, ¡ïÓаïÖú, лл 2013-10-26 00:17:36
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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×Ä£Äâͼ
2Â¥2013-10-25 19:51:21
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