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aiwen747: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú, xiexie 2013-08-20 14:40:40
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aiwen747: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú, xiexie 2013-08-20 14:40:40
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²éѯ½á¹û£º¹²²éµ½2717¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×Ä£Äâͼ |
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