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1 . compound 20 C16H20NO3F ÏàËÆ¶È:63.6% Tetrahedron 2011 67 10082-10088 Enantioenriched synthesis of Escitalopram using lithiation¨Cborylation methodology Benjamin M. Partridge, Stephen P. Thomas, Varinder K. Aggarwal Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . tryptorheedei A C11H12O5N2S ÏàËÆ¶È:63.6% Fitoterapia 2013 87 37-42 Two new tryptophan derivatives from the seed kernels of Entada rheedei: Effects on cell viability and HIV infectivity L.K. Nzowa, R.B. Teponno, L.A. Tapondjou, L. Verotta, Z. Liao, D. Graham, M.-C. Zink, L. Barboni Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |

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²éѯ½á¹û£º¹²²éµ½84¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . compound 20 C16H20NO3F ÏàËÆ¶È:63.6% Tetrahedron 2011 67 10082-10088 Enantioenriched synthesis of Escitalopram using lithiation¨Cborylation methodology Benjamin M. Partridge, Stephen P. Thomas, Varinder K. Aggarwal Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . tryptorheedei A C11H12O5N2S ÏàËÆ¶È:63.6% Fitoterapia 2013 87 37-42 Two new tryptophan derivatives from the seed kernels of Entada rheedei: Effects on cell viability and HIV infectivity L.K. Nzowa, R.B. Teponno, L.A. Tapondjou, L. Verotta, Z. Liao, D. Graham, M.-C. Zink, L. Barboni Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 3-ôǼ׻ù-¦Â-¿¨°ÍÁÖ(3-hydroxymethyl-¦Â-carboline) C12H10N2O ÏàËÆ¶È:58.3% Chinese Journal of Marine Drugs 2011 30(4) 29-33 Studies on the cytotoxic constituents from marine actinomycete Micromonospora sp. (M2DG17) HUANG Zhi-yun,T ANG Jin-shan,GAO Hao,LI Yan-jun,HONG Kui,LI Jia,YAO Xin-sheng Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . abrine ÏàËÆ¶È:58.3% Chinese Traditional and Herbal Drugs 2006 37 1610-1613 Chemical constituents of Abrus cantoniensis SHI Hai-ming; WEN Jing; TU Peng-fei Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . (S)-3-(2-allenylphenoxy)propane-1,2-diol ÏàËÆ¶È:58.3% Russian Journal of Organic Chemistry 2002 38 213-219 Cyclic Sulfites, Key Intermediates in Synthesis of 1-Alkylamino-3-aryloxy-2-propanols from Glycidol Z. A. Bredikhina, D. V. Savel'ev and A. A. Bredikhin Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 3-(hydroxymethyl)-6-[[(2-hydroxyphenyl)oxy]methyl]-1,2-dithiin C12H12O3S2 ÏàËÆ¶È:58.3% Journal of Medicinal Chemistry 1995 38 2628-2648 Novel 1,2-Dithiins: Synthesis, Molecular Modeling Studies, and Antifungal Activity Donald E. Bierer, Jeffrey M. Dener, Larisa G. Dubenko, R. Eric Gerber, Joane Litvak, Stefan Peterli, Patricia Peterli-Roth, Thien V. Truong, Guohua Mao, Barr E. Bauer Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 3-ethyl-4-hydroxy-1-methylquinolin-2(1H)-one C12H13NO2 ÏàËÆ¶È:58.3% Tetrahedron 2013 69 10826-10835 Oxidative ring opening of 3-hydroxyquinoline-2,4(1H,3H)-diones into N-(¦Á-ketoacyl)anthranilic acids Stanislav Kafka, Karel Proisl, V¨§ra Kašp¨¢rkov¨¢, Damijana Urankar, Roman Kimmel, Janez Košmrlj Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . Scopoline phenyl ether ÏàËÆ¶È:58.3% Magnetic Resonance in Chemistry 1989 27 1097-1099 Proton and carbon-13 NMR study of scopoline and its derivatives P. Scheiber and K. N¨¢dor Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . hydroxytyrosol acetate(ôÇ»ùÀÒ´¼ÒÒõ£õ¥) ÏàËÆ¶È:54.5% Chinese Traditional and Herbal Drugs 2011 42(5) 848-851 Polyphenols from leaves of Olea europaea WANG Xiao-fei, LI Chen ,ZHENG Yuan-yuan,DI Duo-long Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . ¦Â-¿¨°ÍÁÖ(¦Â-carboline) C11H8N2 ÏàËÆ¶È:54.5% Chinese Journal of Marine Drugs 2011 30(4) 29-33 Studies on the cytotoxic constituents from marine actinomycete Micromonospora sp. (M2DG17) HUANG Zhi-yun,T ANG Jin-shan,GAO Hao,LI Yan-jun,HONG Kui,LI Jia,YAO Xin-sheng Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . furo[3,2-c]quinolin-4(5H)-one ÏàËÆ¶È:54.5% Journal of Heterocyclic Chemistry 2010 47 998-1003 Carbene induced rearrangement products from two furoquinolinone scaffolds Karl-Fredrik Lindahl, Anthony Carroll, Ronald J. Quinn and Justin A. Ripper Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . compound 8 C14H16S3 ÏàËÆ¶È:54.5% Heterocycles 2008 75 1417-1424 Reaction of Dithiolactones with Benzyne: A Novel Synthesis of Benzo-1, 3-dithioles Kentaro Okuma, Akiko Nojima, and Yoshinobu Yokomori Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . spiro[1,3-benzodithiole-2,2'-[3',3']dimethyl-[2']-(propan-[2'']-ylidene)thietane] C14H16S3 ÏàËÆ¶È:54.5% Heterocycles 2005 65 1553-1556 Reaction of 3,3,5,5-Tetramethylthiolane-2,4-dithione with Benzyne: Novel Formation of Benzodithiole Kentaro Okuma,* Taeko Tsubone, Toshiyuki Shigetomi, Kosei Shioji, and Yoshinobu Yokomori Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . 4,5-Dihydro-5-hydroxythieno[3,4-c]chinolin-4-on C11H7NO2S ÏàËÆ¶È:54.5% Pharmazie 2006 61 901-907 Thieno[3,4-c]chinolin-4-yl-amine ¨C Synthese und Pr¨¹fung auf Wirksamkeit gegen Malaria / Thieno[3,4-c]quinoline-4-yl-amines ¨C synthesis and investigation of activity against malaria K. Görlitzer, B. Gabriel, H. Jomaa and J. Wiesner Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . 2-(4-Trifluoromethylbenzoyl)-1,3-cyclopentanedione ÏàËÆ¶È:54.5% Archives of Pharmacal Research 2003 26 192-196 Synthesis and immunosuppressive activity of novel succinylacetone analogues Taek Hyeon Kim, Dong Ryun Oh, Hee Sam Na and Hyun Chul Lee Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . compound 11 C11H12N2O1S2 ÏàËÆ¶È:54.5% Tetrahedron Letters 2002 43 1825-1828 Access to 3,4-furan dithiolate: towards 3,4-dialkylsulfanylfurans and their Diels¨CAlder adducts with acrylonitrile Pierre Fr¨¨re, Nuria Gallego-Planas, Philippe Blanchard, Gilles Mabon, David Rondeau Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . t-Butyl Z-3-(2-fluoro)phenylglycidate C13H16O3F ÏàËÆ¶È:54.5% Tetrahedron Letters 2003 44 2359-2361 Convenient synthesis of t-butyl Z-3-substituted glycidates under conditions of phase-transfer catalysis Andrzej Jonczyk, Tomasz Zomerfeld Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . 6-Bromo-3-(methylthiomethyl)-1H-indole C10H10BrNS ÏàËÆ¶È:54.5% Tetrahedron 2012 68 1560-1565 A novel NH4OAc and CuBr(PPh3)3-induced intermolecular Pummerer-type reaction between free (NH)-indoles and dimethylsulfoxide: facile synthesis of 3-methylthiomethyl substituted indoles Jin Liu, Xianxue Wang, Han Guo, Xiaokang Shi, Xiaoyu Ren, Guosheng Huang Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . 1-(2-(5-Nitrofuran-2-yl)-5-(chlorophenyl)-1,3,4-oxadiazol-3(2H)-yl)ethanone ÏàËÆ¶È:54.5% Molecules 2012 17 5095-5107 Synthesis, Molecular Properties Prediction, and Anti-staphylococcal Activity of N-Acylhydrazones and New 1,3,4-Oxadiazole Derivatives Cledualdo Soares de Oliveira, Bruno Freitas Lira, Vivyanne dos Santos Falcão-Silva, Jose Pinto Siqueira-Junior, Jose Maria Barbosa-Filho and Petronio Filgueiras de Athayde-Filho Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . N-{2-[(3-methoxyphenyl)thio]ethyl}acetamide C11H15NO2S ÏàËÆ¶È:54.5% Bioorganic & Medicinal Chemistry 2010 18 6496-6511 Design, synthesis, and pharmacological effects of structurally simple ligands for MT1 and MT2 melatonin receptors Alessia Carocci, Alessia Catalano, Angelo Lovece, Giovanni Lentini, Andrea Duranti, Valeria Lucini, Marilou Pannacci, Francesco Scaglione, Carlo Franchini Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . compound 2c ÏàËÆ¶È:54.5% Tetrahedron 2012 68 6513-6516 S-Benzyl isothiouronium chloride as a recoverable organocatalyst for the reduction of conjugated nitroalkenes with Hantzsch ester Quynh Pham Bao Nguyen, Jae Nyoung Kim, Taek Hyeon Kim Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . 7-nitro-2-n-propyl-5-trifluoromethyl-1H-benzimidazole 3-oxide C11H10N3O3F3 ÏàËÆ¶È:54.5% Canadian Journal of Chemistry 2004 82 1322-1327 A simple synthesis of benzimidazole N-oxides from 2-nitroaniline derivatives Scope and limitations Elba I Buj¨¢n, Mar¨ªa Laura Salum Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . 2-(bis((1'H-benzo[d]imidazol-2'-yl)methylthio)methylene)malononitrile C20H14N6S2 ÏàËÆ¶È:54.5% Archiv der Pharmazie 2012 345 745-752 Synthesis and Antioxidant Activity of a New Class of Bis and Tris Heterocycles Venkatapuram Padmavathi, Bhumireddy Chinnachennaiahgari Venkatesh, Akkarapalli Muralikrishna and Adivireddy Padmaja Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . (3-methoxybenzyl)(trifluoromethyl)sulfane C9H9SF3O ÏàËÆ¶È:54.5% Tetrahedron 2013 69 6046-6050 Room temperature nucleophilic trifluoromethylthiolation of benzyl bromides with (bpy)Cu(SCF3) Dedao Kong, Zhou Jiang, Shaogang Xin, Zhengshuai Bai, Yaofeng Yuan, Zhiqiang Weng Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . tert-butyl 1H-indole-1-carboxylate C13H15NO2 ÏàËÆ¶È:54.5% Tetrahedron 2013 69 7211-7219 Microwave-assisted synthesis of 3-substituted indoles via intramolecular arene¨Calkene coupling of o-iodoanilino enamines Original Research Article Won-Il Lee, Jong-Wha Jung, Jaehoon Sim, Hongchan An, Young-Ger Suh Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . compound 11 ÏàËÆ¶È:54.5% Canadian Journal of Chemistry 1975 53 2748-2754 Carbon-13 Nuclear Magnetic Resonance Spectra of Some Dendroketose and Other Furanose Derivatives Dolatrai M. Vyas, Harold C. Jarrell, Walter A. Szarek Structure 13C NMR ̼Æ×Ä£Äâͼ 27 . 3-ethyl-4-hydroxyquinolin-2(1H)-one C11H11NO2 ÏàËÆ¶È:54.5% Tetrahedron 2013 69 10826-10835 Oxidative ring opening of 3-hydroxyquinoline-2,4(1H,3H)-diones into N-(¦Á-ketoacyl)anthranilic acids Stanislav Kafka, Karel Proisl, V¨§ra Kašp¨¢rkov¨¢, Damijana Urankar, Roman Kimmel, Janez Košmrlj Structure 13C NMR ̼Æ×Ä£Äâͼ 28 . compound 4 ÏàËÆ¶È:54.5% Magnetic Resonance in Chemistry 1986 24 829-831 13C NMR spectra of substituted indoles Gerardo Burton, Alberto A. Ghini and Eduardo G. Gros Structure 13C NMR ̼Æ×Ä£Äâͼ 29 . compound 3l ÏàËÆ¶È:54.5% Magnetic Resonance in Chemistry 1986 24 21-30 NMR investigations on benzheteroazoles. 2¡ªNMR investigations of N-acylated 2-aminobenzimidazoles E. Gr¨¹ndemann, H. Graubaum, D. Martin and E. Schiewald Structure 13C NMR ̼Æ×Ä£Äâͼ 30 . phenethyl pyrrole-2-carboxylate C13H13NO2 ÏàËÆ¶È:54.5% Natural Medicines 1995 49 24-28 Studies on the Constituents and Anatomical Characteristics of the Sparganii Rhizome Derived from Sparganium stoloniferum BUCH.-HAM. MIYAICHI YUKINORI,MATSUURA YOKO,YAMAJI SEIICHI,NAMBA TSUNEO,TOMIMORI TSUYOSHI Structure 13C NMR ̼Æ×Ä£Äâͼ |

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