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1 .     1,4-dihydro-1-benzaz[3,2-c]-1,2-benzopyrone
C16H11O2N     ÏàËÆ¶È:75%
Journal of Natural Products          1993          Vol 56          1402
The Reaction of Dicoumarol with Aniline
Glen M. Colin, James R. Gear
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     2,3-dihydro-1H,1'H-[2,3']biindolyl
    ÏàËÆ¶È:75%
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

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3 .     6-Bromo-3-(2-methyl-2,3-dihydrobenzo[d]thiazol-2-yl)-2H-chromen-2-one
C17H12BrNO2S     ÏàËÆ¶È:70.5%
Archiv der Pharmazie          2011          344          588-594
Synthesis and Free Radical Scavenging Activity of Coumarin Derivatives Containing a 2-Methylbenzothiazoline Motif
Mehdi Khoobi, Saeed Emami, Gholamreza Dehghan, Alireza Foroumadi, Ali Ramazani, and Abbas Shafiee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     4-[2-[4-(dimethylamino)phenyl]imidazo[4,5-b]indol-3(4H)-yl]phenol
C23H20N4O     ÏàËÆ¶È:70.5%
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

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5 .     wuzhuyurutine A
C17H11N3O2     ÏàËÆ¶È:70.5%
Heterocycles          2006          68          1691-1698
Two New Indoloquinazoline Alkaloids from the Unripe Fruits of Evodia rutaecarpa
Jie Teng and Xiu-Wei Yang*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     3-(2-methyl-1H-indol-3-yl)-6-(4-methylphenyl)-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazole
C19H15N5S     ÏàËÆ¶È:70.5%
Molecules          2011          16          8244-8256
Synthesis under Microwave Irradiation of [1,2,4]Triazolo[3,4-b] [1,3,4]thiadiazoles and Other Diazoles Bearing Indole Moieties and Their Antimicrobial Evaluation
Sobhi M. Gomha and Sayed M. Riyadh
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     2-(Trifluoromethyl)-2-(4-nitrophenylthio)-3-ethoxycarbonyl-6-bromo-2H-chromene
C19H13BrF3NO5S     ÏàËÆ¶È:70.5%
Tetrahedron          2012          68          8011-8017
Reactions of 2-(trifluoromethyl)-2-hydroxy-2H-chromenes with thiophenols promoted by Lewis acid
Xinjin Li, Jingwei Zhao, Zhongwei Wang, Jianwei Han, Jian Zhao, Shizheng Zhu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     1-Ethyl-4-hydroxy-3-(5-nitro-2-oxo-3-cyanopyridin-6-yl)quinolin-2(1H)-one
C17H12N4O5     ÏàËÆ¶È:70.5%
Heterocycles          2013          87          369-380
Synthesis of Some Novel Binuclear Heterocyclic Compounds from 6-Ethyl-3-nitropyrano[3,2-c]quinoline-4,5(6H)-dione
Hany M. Hassanin* and Dalia Abdel-Kader
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     3-(2''-methoxy-3''-hydroxyphenyl)-1-(2'-hydroxyphenyl)-propenone
C16H14O4     ÏàËÆ¶È:68.7%
Journal of Natural Products          2004          67          553-558
Microbial Transformations of Chalcones: Hydroxylation,O-Demethylation, and Cyclization to Flavanones
M. Sanchez-Gonzalez, and J. P. N. Rosazza
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     2,2-Di(3-indolyl)-3-indolone
C24H17N3O     ÏàËÆ¶È:68.7%
Journal of Natural Products          1994          Vol 57          1587
Vibrindole A, a Metabolite of the Marine Bacterium, Vibrio parahaemolyticus, Isolated from the Toxic Mucus of the Boxfish Ostracion cubicus
Ronit Bell, Shmuel Carmeli, Nehemia Sar
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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11 .     Isoquinolin-1-yl-phenyl-amine
C15H12N2     ÏàËÆ¶È:68.7%
Bioorganic & Medicinal Chemistry          2011          19          939-950
Microwave-assisted synthesis of quinoline, isoquinoline, quinoxaline and quinazoline derivatives as CB2 receptor agonists
Raimo Saari, Jonna-Carita Törmä, Tapio Nevalainen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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12 .     N,N-Bis(pyridin-2-yl-methyl)tryptamine N12-oxide
C22H22N4O     ÏàËÆ¶È:68.7%
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

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13 .     (Z)-N'-(2-Oxo-1-phenylindolin-3-ylidene)isonicotinohydrazide
C20H14N4O2     ÏàËÆ¶È:68.7%
Molecules          2011          16          7864-7879
Schiff Bases of Indoline-2, 3-dione: Potential Novel Inhibitors of Mycobacterium Tuberculosis (Mtb) DNA Gyrase
Tarek Aboul-Fadl, Hatem A. Abdel-Aziz, Mohammed K. Abdel-Hamid, Tilal Elsaman, Jane Thanassi and Michael J. Pucci
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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14 .     3-(2-Methyl-2,3-dihydrobenzo[d]thiazol-2-yl)-2H-chromen-2-one
C17H13NO2S     ÏàËÆ¶È:68.7%
Archiv der Pharmazie          2011          344          588-594
Synthesis and Free Radical Scavenging Activity of Coumarin Derivatives Containing a 2-Methylbenzothiazoline Motif
Mehdi Khoobi, Saeed Emami, Gholamreza Dehghan, Alireza Foroumadi, Ali Ramazani, and Abbas Shafiee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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15 .     3-(benzo[d]thiazol-2-yl)-2H-chromen-2-one
C16H9NO2S     ÏàËÆ¶È:68.7%
Archiv der Pharmazie          2011          344          588-594
Synthesis and Free Radical Scavenging Activity of Coumarin Derivatives Containing a 2-Methylbenzothiazoline Motif
Mehdi Khoobi, Saeed Emami, Gholamreza Dehghan, Alireza Foroumadi, Ali Ramazani, and Abbas Shafiee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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16 .     (E)-3,3-Bis(1H-3-indolyl)-1-(p-tolyl)propene
    ÏàËÆ¶È:68.7%
Tetrahedron Letters          2012          53          752-757
An original route to newly-functionalized indoles and carbazoles starting from the ring-opening of nitrothiophenes
Lara Bianchi,Gianluca Giorgi,Massimo Maccagno,Giovanni Petrillo,Carlo Scapolla,Cinzia Tavani
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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17 .     4-[2-(4-chlorophenyl)imidazo[4,5-b]indol-3(4H)-yl]phenol
C21H14ClN3O     ÏàËÆ¶È:68.7%
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

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18 .     3-[(2-mercaptophenyl)amino]-2-benzofuran-1(3H)-one
C14H11NO2S     ÏàËÆ¶È:68.7%
Journal of Heterocyclic Chemistry          2007          44          617-626
Reaction of phthalaldehydic acid with different substituted aniline as well as hydrazine derivatives
Sherine N. Khattab,Seham Y. Hassan,Ayman El-Faham,Abdel Moneim M. El Massry and Adel Amer
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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19 .     4-(9,10-dihydroacridin-9-ylidene)-2-methylsemicarbazide
C15H14N4O     ÏàËÆ¶È:68.7%
Journal of Heterocyclic Chemistry          2006          43          633-643
Tautomerism,regioisomerism,and cyclization reactions of acridinyl thiosemicarbazides
Karel D. Klika,Eva Balentov¨¢,Kalevi Pihlaja,Juraj Bern¨¢t,J¨¢n Imrich,Martina Vavrušov¨¢,Erich Kleinpeter and Andreas Koch
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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20 .     ethyl (1,3,4,10-tetrahydro-1-oxo-2H-azepino[3,4-b]indol-5-yli-dene)acetate
C16H16N2O3     ÏàËÆ¶È:68.7%
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   Ì¼Æ×Ä£Äâͼ
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34.3,36.2,36.8,37.3,38.9,40.9,42.4,45.9,50.3,56.2,56.8,63.3,70.3,73.7,
74.0,76.2,79.6,102.2,122.2,140.4,174.5
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34.3,36.2,36.8,37.3,38.9,40.9,42.4,45.9,50.3,56.2,56.8,63.3,70.3,73.7,
74.0,76.2,79.6,102.2,122.2,140.4,174.5
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