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£¨5-9-1£©13C NMR (cdcl3) ¦Ä 191.62, 140.13, 137.44, 129.38, 127.72, 127.19, 123.87, 121.15, 120.87, 119.64, 119.54, 108.45, 107.99, 64.21, 29.75. |
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1 . N-methoxy-3-formylcarbazole C14H11NO2 ÏàËÆ¶È:86.6% Chemical & Pharmaceutical Bulletin 1988 36 2377-2380 New Carbazole Alkaloids from Murraya euchrestifolia CHIHIRO ITO,TIAN-SHUNG WU and HIROSHI FURUKAWA Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 9-methoxycarbazole-3-carbaldehyde C14H11NO2 ÏàËÆ¶È:86.6% Tetrahedron Letters 2003 44 7071-7074 An efficient total synthesis of 9-methoxycarbazole-3-carbaldehyde based on a novel methodology for the preparation of methoxyindoles N. Selvakumar, Manoj Kumar Khera, B.Yadi Reddy, D. Srinivas, A.Malar Azhagan, Javed Iqbal Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 3-acetyl-4-chloro-5-hydroxy-1-methyl-1H-benzo[g]indole C15H12ClNO2 ÏàËÆ¶È:73.3% Journal of Heterocyclic Chemistry 2005 42 147-151 A simple synthesis of 4-chloro-5-hydroxy-1H-benzo[g]indoles Hyung-Woo Yi,Hyun In Cho and Kee-Jung Lee Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 9-Methyl-9H-carbazole-3-carbonitrile ÏàËÆ¶È:73.3% Tetrahedron 2012 68 4588-4595 Practical one-pot transformation of electron-rich aromatics into aromatic nitriles with molecular iodine and aq NH3 using Vilsmeier¨CHaack reaction Sousuke Ushijima, Katsuhiko Moriyama, Hideo Togo Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 3,3'-[oxybis(methylene)]bis(9-methoxy-9H-carbazole) C28H24N2O3 ÏàËÆ¶È:66.6% Phytochemistry 2005 66 1601-1606 A benzoisofuranone derivative and carbazole alkaloids from Murraya koenigii and their antimicrobial activity M. Mukhlesur Rahman, Alexander I. Gray Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . Bis(1H-3-indolyl)(p-tolyl)methane ÏàËÆ¶È:66.6% 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 ̼Æ×Ä£Äâͼ 7 . 3-acetyl-4-chloro-5-hydroxy-1H-benzo[g]indole C14H10ClNO2 ÏàËÆ¶È:66.6% Journal of Heterocyclic Chemistry 2005 42 147-151 A simple synthesis of 4-chloro-5-hydroxy-1H-benzo[g]indoles Hyung-Woo Yi,Hyun In Cho and Kee-Jung Lee Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . bis(3-indolyl)-tolylmethane ÏàËÆ¶È:66.6% Chinese Chemical Letters 2011 22 515-518 Pyridinium tribromide catalyzed condensation of indoles and aldehydes to form bisindolylalkanes Qin Yang, Zheng Lan Yin, Ban Lai Ouyang, Yi Yuan Peng Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . (¡À)-trans-2,3-Dihydro-3-(1H-imidazol-1-yl)-2-(4-methylphenyl)-4H-1-benzopyran-4-one C19H16N2O2 ÏàËÆ¶È:62.5% Archiv der Pharmazie 2009 342 541-545 3-Imidazolyl-Substituted Flavans as Potential Antifungal Agents: Synthesis,Stereochemical Properties,and Antifungal Activity Saeed Emami and Alireza Foroumadi Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 8-methyl-2-(2-thienyl)-8H-thieno[2,3-b]indole-3-carbonitrile C16H10N2S2 ÏàËÆ¶È:62.5% European Journal of Organic Chemistry 2011 4001-4007 Novel Radical Cyclization Approach to Thieno-Fused Heterocycles Prabal P. Singh, Ashok K. Yadav, Hiriyakkanavar Ila and Hiriyakkanavar Junjappa Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . N-Pentyl-3-carbazolyl Carboxyaldehyde ÏàËÆ¶È:61.1% Marine drugs 2011 9 256-277 Synthesis of 1-Substituted Carbazolyl-1,2,3,4-tetrahydro- and Carbazolyl-3,4-dihydro-¦Â-carboline Analogs as Potential Antitumor Agents Ya-Ching Shen,Yao-To Chang,Chun-Ling Lin,Chia-Ching Liaw,Yao Haur Kuo,Lan-Chun Tu,Sheau Farn Yeh and Ji-Wang Chern Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . Isoquinolin-1-yl-phenyl-amine C15H12N2 ÏàËÆ¶È:60% 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 ̼Æ×Ä£Äâͼ 13 . Isoquinolin-1-yl-(4-trifluoromethyl-phenyl)-amine C16H11F3N2 ÏàËÆ¶È:60% 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 ̼Æ×Ä£Äâͼ 14 . N,N-Bis(thiophen-2-yl-methyl)tryptamine N12-oxide C20H20N2OS2 ÏàËÆ¶È:60% 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 15 . 3-bromo-9-methyl-9H-carbazole C15H15N ÏàËÆ¶È:60% Canadian Journal of Chemistry 2005 83 63-67 N-Iodosuccinimide-An effective reagent for regioselective heterocyclization of o-cyclohex-2'-enylanilines for the synthesis of hexahydrocarbazoles K.C. Majumdar, U.K. Kundu, U. Das, N.K. Jana, and B. Roy Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . N-(4-(3,5-Bis(trifluoromethyl)-1H-pyrazol-1-yl)phenyl)-4-methylbenzenesulfonamide C18H13O2N3F6S ÏàËÆ¶È:60% The Journal of Organic Chemistry 2011 76 6657-6669 Microwave-Assisted and Continuous Flow Multistep Synthesis of 4-(Pyrazol-1-yl)carboxanilides David Obermayer, Toma N. Glasnov, and C. Oliver Kappe Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . N,N-dibenzyl-N'-phenyl-o-phenylenediamine C26H24N2 ÏàËÆ¶È:60% Journal of Heterocyclic Chemistry 2008 45 837-843 Thermal reactions of N-alkyl-2-benzylaniline and N-alkyl-N'-phenyl-o-phenylenediamine: An unusual route to 2-phenylindole and 2-phenylbenzimidazole Evelyn Cuevas Creencia,Kei Taguchi and Takaaki Horaguchi Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . 9-benzylcarbazole C19H15N ÏàËÆ¶È:60% Journal of Heterocyclic Chemistry 2006 43 1441-1446 Thermal decomposition reactions of n-alkylated 2-aminobiphenyls to carbazole and phenanthridine Evelyn Cuevas Creencia and Takaaki Horaguchi Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . compound 1c ÏàËÆ¶È:60% 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 20 . bis(indol-3-yl)(4'-trifluoromethoxyphenyl)methane C24H17N2OF3 ÏàËÆ¶È:60% Heterocycles 2006 68 331-338 A New Catalytic Application of a Keggin Acid in the Synthesis of Symmetrical Bis(indolyl)alkanes Manas Chakrabarty,* Ajanta Mukherji, Sulakshana Karmakar, Shiho Arima, and Yoshihiro Harigaya Structure 13C NMR ̼Æ×Ä£Äâͼ |
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