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1 .     carbazole
    ÏàËÆ¶È:78.5%
Phytochemistry          1985          24          3041-3043
Koenoline, a further cytotoxic carbazole alkaloid from Murraya koenigii
Manfred Fiebig, John M. Pezzuto, Djaja D. Soejarto, A.Douglas Kinghorn
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     2,2-Di(3-indolyl)-3-indolone
C24H17N3O     ÏàËÆ¶È:73.3%
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
3 .     4-(1H-indol-3-yl)-Nmethylcyclohex-3-enamine
    ÏàËÆ¶È:73.3%
Bioorganic & Medicinal Chemistry Letters          2011          21          1678-1682
Biotin tethered homotryptamine derivatives: High affinity probes of the human serotonin transporter (hSERT)
Ian D. Tomlinson , Hideki Iwamoto, Randy D. Blakely , Sandra J. Rosenthal
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     4-(1H-indol-3-yl)-1H-pyrrole-2-carboxylic acid ethyl ester
C15H14N2O2     ÏàËÆ¶È:73.3%
Tetrahedron          2013          69          5829-5840
Preparation of indole containing building blocks for the regiospecific construction of indole appended pyrazoles and pyrroles
John T. Gupton, Nakul Telang, Dominic F. Gazzo, Peter J. Barelli, Kristin E. Lescalleet, Jonathan W. Fagan, Brandon J. Mills, Kara L. Finzel, Rene P.F. Kanters, Kyle R. Crocker, Sean T. Dudek, Corinne M. Lariviere, Stanton Q. Smith, Kartik M. Keertikar
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     compound 2
    ÏàËÆ¶È:71.4%
Biochemical Systematics and Ecology          2006          34          453-456
Indole alkaloids from a sponge Sarcotragus species
Yonghong Liu, Jee H. Jung, Si Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     1-methyl-carbazole
C13H11N     ÏàËÆ¶È:71.4%
Journal of Natural Products          1991          Vol 54          1056
Aromatic Secondary Metabolites from the Sponge Tedania ignis
Rhonda L. Dillman, John H. Cardellina II.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     1-methyl-3-(trifluoromethyl)-1H-indole
    ÏàËÆ¶È:71.4%
Journal of Heterocyclic Chemistry          2008          45          969-972
Synthesis of new 3-(trifluoromethyl)-1H-indoles by reduction of trifluoromethyloxoindoles
Moônica M. Bastos,L¨²cia M. U. Mayer,Elza C. S. Figueira,Marcio Soares,N¨²bia Boechat and Warner B. Kover
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     compound 3
    ÏàËÆ¶È:71.4%
Journal of Heterocyclic Chemistry          2005          42          867-875
A study of substituent effect on 1H and 13C NMR spectra of mono,di and poly substituted carbazoles
Sergio M. Bonesi,Maria A. Ponce and Rosa Erra-Balsells
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     compound 4
    ÏàËÆ¶È:71.4%
Journal of Heterocyclic Chemistry          2005          42          867-875
A study of substituent effect on 1H and 13C NMR spectra of mono,di and poly substituted carbazoles
Sergio M. Bonesi,Maria A. Ponce and Rosa Erra-Balsells
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     compound 2c
    ÏàËÆ¶È:71.4%
Journal of Heterocyclic Chemistry          2004          41          161-171
A study of substituent effect on 1H and 13C nmr spectra of N-and C-substituted carbazoles
Sergio M. Bonesi,Maria A. Ponce and Rosa Erra-Balsells
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     compound 3b
    ÏàËÆ¶È:71.4%
Journal of Heterocyclic Chemistry          2004          41          161-171
A study of substituent effect on 1H and 13C nmr spectra of N-and C-substituted carbazoles
Sergio M. Bonesi,Maria A. Ponce and Rosa Erra-Balsells
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     compound 4a
C14H13N3S     ÏàËÆ¶È:71.4%
Heterocycles          2004          62          779-786
A Novel, Expedient Synthesis of Thiazolo[4,5-c]- and -[5,4-b]carbazoles
Manas Chakrabarty,* Nandita Ghosh, and Yoshihiro Harigaya
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     3-(3-Indolyl)butanenitrile
C12H12N2O     ÏàËÆ¶È:71.4%
Phytochemistry          2010          71          1952-1962
Indolyl-3-acetaldoxime dehydratase from the phytopathogenic fungus Sclerotinia sclerotiorum: Purification, characterization, and substrate specificity
M. Soledade C. Pedras, Zoran Minic, Premila D. Thongbam, Vangala Bhaskar, Sabine Montaut
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     Methyl carbazole-3-carboxylate
C14H11NO2     ÏàËÆ¶È:71.4%
Archives of Pharmacal Research          2010          33          675-680
Biological activity of chemical constituents from Clausena harmandiana
Tula Thongthoom, Uraiwan Songsiang, Chanokbhorn Phaosiri and Chavi Yenjai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     3-[3-(N-acetyl)aminothien-2-yl)]indole
C14H12N2OS     ÏàËÆ¶È:71.4%
Heterocycles          2002          57          1831-1840
Synthesis of Some Thiophene-fused Azepino[5,4,3-cd]indoles
Basem A. Moosa, Kayed A. Abu Safieh, and Mustafa M. El-Abadelah*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     N-[2,2,2-trichloro-1-(1H-indol-3-yl)ethyl]trifluoromethanesulfonamide
    ÏàËÆ¶È:71.4%
Russian Journal of Organic Chemistry          2008          44          86-94
Reactions of N-(Polychloroethylidene)arene-and - trifluoromethanesulfonamides with indoles
E. V. Kondrashov, E. V. Rudyakova, I. B. Rozentsveig, I. V. Ushakova and G. N. Rozentsveig, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     3,6-di(1H-indol-2-yl)-9H-carbazole
C28H19N3     ÏàËÆ¶È:71.4%
Tetrahedron          2012          68          9050-9055
Synthesis of macrocyclic systems derived from di-(2-indolyl)heteroarenes
Ibrahim F. Sengul, Kasey Wood, Naresh Kumar, David StC. Black
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     2,2'-dithiobis[3-(2-furoyl)-1-methyl-1H-indole]
C28H30N2O4     ÏàËÆ¶È:71.4%
Journal of Medicinal Chemistry          1995          38          58-67
Tyrosine Kinase Inhibitors. 4. Structure-Activity Relationships among N- and 3-Substituted 2,2'-Dithiobis(1H-indoles) for in vitro Inhibition of Receptor and Nonreceptor Protein Tyrosine Kinases
Brian D. Palmer, Gordon W. Rewcastle, Andrew M. Thompson, Maruta Boyd, H. D. Hollis Showalter, Anthony D. Sercel, David W. Fry, Alan J. Kraker, William A. Denny
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     1,4-dimethylcarbazole
    ÏàËÆ¶È:71.4%
Organic Magnetic Resonance          1982          18          117-119
Chemistry of 6H-pyrido [4, 3-b] carbazoles. Part 10¡ªCarbon-13 nuclear magnetic resonance spectra of ellipticines and some model compounds
M. Sainsbury, D. Watkins and D. K. Weerasinghe
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     Methyl 9H-carbazole-3-carboxylate
C14H11NO2     ÏàËÆ¶È:71.4%
Journal of Heterocyclic Chemistry          2012          49          913-918
An Improved Synthesis of Carbazoles via Domino Reaction of N-Protected-2-methylindoles with DMF-DMA/DMA-DMA
Radhakrishnan Sureshbabu and Arasambattu K. Mohanakrishnan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     N-(Indol-3-ylmethyl)-N'-phenylurea
C16H15N3O     ÏàËÆ¶È:71.4%
Bioorganic & Medicinal Chemistry          2006          14          4958-4979
Toward the control of Leptosphaeria maculans: Design, syntheses, biological activity, and metabolism of potential detoxification inhibitors of the crucifer phytoalexin brassinin
M. Soledade C. Pedras, Mukund Jha
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     compound 5
    ÏàËÆ¶È:70.5%
Tetrahedron Letters          2005          46          5387-5391
Facile synthesis of 2H-indazole derivatives starting from the Baylis-Hillman adducts of 2-cyclohexen-1-one
Ka Young Lee, Saravanan Gowrisankar, Jae Nyoung Kim
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     compound 5c
    ÏàËÆ¶È:68.7%
Tetrahedron Letters          2002          43          1351-1353
Novel clay-mediated, tandem addition¨Celimination-(Michael) addition reactions of indoles with 3-formylindole: an eco-friendly route to symmetrical and unsymmetrical triindolylmethanes
Manas Chakrabarty, Sandipan Sarkar
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
24 .     8-methyl-1,10-dihydropyrrolo[2,3-a]carbazole-3-carbaldehyde
C16H12N2O     ÏàËÆ¶È:68.7%
Bioorganic & Medicinal Chemistry          2010          18          6865-6873
Synthesis, Pim kinase inhibitory potencies and in vitro antiproliferative activities of diversely substituted pyrrolo[2, 3-a]carbazoles
Rufine Aku¨¦-G¨¦du, Lionel Nauton, Vincent Th¨¦ry, Jenny Bain, Philip Cohen, Fabrice Anizon, Pascale Moreau
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
25 .     9-trifluoromethyl-1,10-dihydropyrrolo[2,3-a]carbazole-3-carbaldehyde
C16H9F3N2O     ÏàËÆ¶È:68.7%
Bioorganic & Medicinal Chemistry          2010          18          6865-6873
Synthesis, Pim kinase inhibitory potencies and in vitro antiproliferative activities of diversely substituted pyrrolo[2, 3-a]carbazoles
Rufine Aku¨¦-G¨¦du, Lionel Nauton, Vincent Th¨¦ry, Jenny Bain, Philip Cohen, Fabrice Anizon, Pascale Moreau
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
26 .     2-(1H-Indol-3-yl)ethyl 5-hydroxypentanoate
C15H19NO3     ÏàËÆ¶È:66.6%
Journal of Natural Products          2009          72          2069-2071
Indole Derivatives from a Marine Sponge-Derived Yeast as DPPH Radical Scavengers
Yasumasa Sugiyama, Yuki Ito, Motofumi Suzuki, and Akira Hirota
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
27 .     compound 4
C15H19NO3     ÏàËÆ¶È:66.6%
Journal of Natural Products          1996          59          481-484
Biotransformation of Chanoclavine by Euphorbia calyptrata Cell Culture
Vladim¨ªr Křen, Petr Sedmera, and V¨§ra Přikrylov¨¢
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
28 .     3,3-Bis(indolyl)-4-isopropylphenylmethane
C26H24N2     ÏàËÆ¶È:66.6%
Canadian Journal of Chemistry          2006          84          1541-1545
Efficient RuIII-catalyzed condensation of indoles and aldehydes or ketones
Khalil Tabatabaeian, Manouchehr Mamaghani, Nosratollah Mahmoodi, and Alireza Khorshidi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
29 .     compound 3i
C15H13NO     ÏàËÆ¶È:66.6%
Journal of Heterocyclic Chemistry          2004          41          161-171
A study of substituent effect on 1H and 13C nmr spectra of N-and C-substituted carbazoles
Sergio M. Bonesi,Maria A. Ponce and Rosa Erra-Balsells
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
30 .     compound 4
    ÏàËÆ¶È:66.6%
Journal of Heterocyclic Chemistry          2010          47          1398-1405
Trichloroisocyanuric acid-catalyzed reaction of indoles: An expeditious synthesis of bis-indolyl, tris-indolyl, di(bis-indolyl), tri(bis-indolyl), and tetra(bis-indolyl)methane under solid-state conditions
Hojat Veisi, Reza Gholbedaghi, Javad Malakootikhah, Alireza Sedrpoushan, Behrooz Maleki and Davood Kordestani
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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