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jiujiupy: ½ð±Ò+8, ¡ï¡ï¡ïºÜÓаïÖú 2014-11-28 13:22:43
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     Ì¼Æ×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     Ì¼Æ×Ä£Äâͼ
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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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×Ä£Äâͼ
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