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21.86,27.32,29.62,29.72,52.84,52.88,111.76,116.22,117.55,119.72,120.77,124.48,124.66,129.77,130.63,131.01,133.45,168.86,172.47
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1 .     Dimethyl (3R*,4R*)-1-[2-(4-Oxo-4H-chromen-2-yl)phenyl]pyrrolidine-3,4-dicarboxylate
C23H21NO6     ÏàËÆ¶È:68.4%
European Journal of Organic Chemistry          2012                   132-143
Flavone¨CNitrogen Heterocycle Conjugate Formation by 1,3-Dipolar Cycloadditions
Regina M. S. Sousa, Diana C. G. A. Pinto, Artur M. S. Silva, Vanda Vaz Serra, Ana I. R. N. A. Barros, Maria A. F. Faustino, Maria G. P. M. S. Neves and Jos¨¦ A. S. Cavaleiro
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     N-acetyl-benz[g]tryptophan methyl ester
C18H18N2O3     ÏàËÆ¶È:63.1%
Bioorganic & Medicinal Chemistry          2013          21          1159-1165
Synthesis and biological evaluation of novel tryptoline derivatives as indoleamine 2,3-dioxygenase (IDO) inhibitors
Minoru Tanaka, Xin Li, Hidemasa Hikawa, Takafumi Suzuki, Katsuhiko Tsutsumi, Masashi Sato, Osamu Takikawa, Hideharu Suzuki, Yuusaku Yokoyama
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     cypermethrin II A
    ÏàËÆ¶È:60%
Chemistry of Natural Compounds          1988          24          246-250
1H AND 13C NMR SPECTRA OF BIOLOGICALLY ACTIVE COMPOUNDS."IV. DIASTEREOMERS OF PYRETHROIDS AND THEIR INSECTICIDAL ACTIVITY
G. A. Tolstikov, L. M. Khalilov,F. Z. Galin, E. V. Vasil'eva,D. B. Amirkhanov, M. G. Migranov,and A. A. Panasenko
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     cypermethrin II C
    ÏàËÆ¶È:60%
Chemistry of Natural Compounds          1988          24          246-250
1H AND 13C NMR SPECTRA OF BIOLOGICALLY ACTIVE COMPOUNDS."IV. DIASTEREOMERS OF PYRETHROIDS AND THEIR INSECTICIDAL ACTIVITY
G. A. Tolstikov, L. M. Khalilov,F. Z. Galin, E. V. Vasil'eva,D. B. Amirkhanov, M. G. Migranov,and A. A. Panasenko
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     4-(N-methoxycarbonyl)amino-5,5-ethylenedioxy-1-(toluene-4-sulfonyl)-3,4-dihydro-1H-benzo[c,d]-indole
C22H22N2O6S     ÏàËÆ¶È:60%
Heterocycles          2004          64          153-175
Chemistry of Indoles Carrying a Basic Function. Part IX. Unexpected Cyclizations of Diketones Derived from Uhle's Ketone
Istv¨¢n Moldvai,* Eszter G¨¢cs-Baitz, Eszter Temesv¨¢ri-Major, M¨¢ria Incze, L¨¢szl¨® Poppe, and Csaba Sz¨¢ntay*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     compound 6a
C26H36N2O2S     ÏàËÆ¶È:57.8%
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   Ì¼Æ×Ä£Äâͼ
7 .     methyl-3-(4'-(p-methylphenyl)-1'H-pyrrol-3'-ylsulfonyl)-4-(pchlorophenyl)-3H-pyrrole-3-carboxylate
C23H19ClN2O4S     ÏàËÆ¶È:57.8%
Chemical & Pharmaceutical Bulletin          2009          57          1200-1205
Synthesis and Biological Activity of a New Class of Sulfone-Linked Pyrrolylpyrazoles and Pyrrolylisoxazoles from Methyl-3-aryl-2-(E-arylethenesulfonyl)acrylate
Venkatapuram Padmavathi, Thunga Radha Lakshmi, Konda Mahesh and Adivireddy Padmaja
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     12-chloro-7,8,9,10-tetrahydrobenzonaphtho[2,3-f]oxepin-13-carbaldehyde
C19H15ClO2     ÏàËÆ¶È:57.8%
Heterocycles          2010          81          2269-2290
Synthesis of Naphtho[2,3-b]- and Naphtho[1,2-b]-fused Thieno[2,3-d][1]benzoxepins and Thieno[2,3-d][1]benzothiepins
Ivana Ozimec Landek, Dijana Pešić, Rudolf Trojko, Maja Devčić Bogdanović, Mladen Merćep, and Milan Mesić
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     (2S)-3-(1H-indol-3-yl)-2-[(3-phenyl-2-propynoyl)amino]propanoic acid
C20H16N2O3     ÏàËÆ¶È:57.8%
Heterocycles          2009          77          1249-1259
Preparation and Synthetic Applications of N-(¦Á,¦Â-Unsaturated Acyl)-¦Á-amino Acid Derivatives
Alan R. Katritzky, Reena Gyanda, Nabin K. Meher, and Yuming Song
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     compound (S)-H4-BINOL
    ÏàËÆ¶È:57.8%
Chinese Chemical Letters          2010          21          1277-1280
Convenient synthesis of chiral H_4-BINOL via direct hydrogenation of BINOL
Qian Chang Ding; Yun Feng Du; Xin Sheng Li; Dong Cheng Xu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     7-(Pentyloxy)-5-phenyl-[1,2,4]-triazolo[4,3-a]quinoline
C21H21N3O     ÏàËÆ¶È:57.8%
Archiv der Pharmazie          2008          341          774-779
Synthesis and Anticonvulsant Activity of 5-Phenyl-[1,2,4]-triazolo[4,3-a]quinolines
Li-Ping Guan, Qing-Hao Jin, Shou-Feng Wang, Fu-Nan Li and Zhe-Shan Quan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     compound 6a
    ÏàËÆ¶È:57.8%
Tetrahedron          1990          46          6831-6838
New intermediates of phaeomelanogenesis in vitro beyond the 1,4-benzothiazine stage
C. Costantini, O. Crescenzi, G. Prota, A. Palumbo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     (R)-methyl 2-(pentylcarbamoyl)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole-3-carboxylate
C19H25N3O3     ÏàËÆ¶È:57.8%
Bioorganic & Medicinal Chemistry          2011          19          6182-6195
Design, synthesis, and biological evaluation of callophycin A and analogues as potential chemopreventive and anticancer agents
Li Shen, Eun-Jung Park, Tamara P. Kondratyuk, Daniela Guendisch, Laura Marler, John M. Pezzuto, Anthony D. Wright, Dianqing Sun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     5-methyl-12-phenyl-5H-pyrido[1',2':1,2]pyrimido[4,5-b]-indol-11-ium iodide
    ÏàËÆ¶È:57.8%
The Journal of Organic Chemistry          2002          67          7797-7801
Thermolysis of Benzannulated Enyne−Carbodiimides. Application in the Synthesis of Pyrido[1¡®,2¡®:1,2]pyrimido[4,5-b]indoles and Related Heteroaromatic Compounds
Xiaoling Lu, Jeffrey L. Petersen, and Kung K. Wang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     (¡À)-(3¦Á,16¦Â)-desethyleburnamonine
C17H18N2O     ÏàËÆ¶È:57.8%
European Journal of Organic Chemistry          2011                   6409-6412
Expeditious Route Towards (¡À)-Desethyleburnamonine, a Precursor of (¡À)-Vindeburnol
Laurence Jung-Deyon, Bruno Giethlen and Andr¨¦ Mann
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     3-(indolin-1-yl)-2H-chromen-2-one
    ÏàËÆ¶È:57.8%
European Journal of Organic Chemistry          2011                   5077-5088
Palladium-Catalyzed Coupling of 3-Halo-Substituted Coumarins, Chromenes, and Quinolones with Various Nitrogen-Containing Nucleophiles
Mohamed Ali Soussi, Davide Audisio, Samir Messaoudi, Olivier Provot, Jean-Daniel Brion and Mouad Alami
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     diethyl 2-[4-(cyanomethyl)-3-benzyl-3,4-dihydroquinazolin-2-yl]propanedioate
C24H25N3O4     ÏàËÆ¶È:57.8%
Heterocycles          2012          84          893-911
Expedient Synthesis of 3,4-Dihydroquinazolines via Tandem Addition ¡ª Conjugate Addition Cyclization of Carbodiimides Bearing a Michael Acceptor
Takao Saito,* Hayato Nakano, Hidenori Terada, Noriki Kutsumura, and Takashi Otani
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     juglanin B
    ÏàËÆ¶È:57.8%
Natural Product Communications          2010          5          1687 - 1708
Naturally Occurring Diarylheptanoids
Haining Lv and Gaimei She
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     myricarborin
    ÏàËÆ¶È:57.8%
Natural Product Communications          2010          5          1687 - 1708
Naturally Occurring Diarylheptanoids
Haining Lv and Gaimei She
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     (3R*,4S*)-Dimethyl 1-[2-(4-Oxo-4H-chromen-2-yl)phenyl]pyrrolidine-3,4-dicarboxylate
C23H21NO6     ÏàËÆ¶È:57.8%
European Journal of Organic Chemistry          2012                   132-143
Flavone¨CNitrogen Heterocycle Conjugate Formation by 1,3-Dipolar Cycloadditions
Regina M. S. Sousa, Diana C. G. A. Pinto, Artur M. S. Silva, Vanda Vaz Serra, Ana I. R. N. A. Barros, Maria A. F. Faustino, Maria G. P. M. S. Neves and Jos¨¦ A. S. Cavaleiro
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     tert-Butyl 3-{[(3S,5R)-5-Methoxy-5-(methoxycarbonyl)isoxazolidin-3-yl]methyl}-1H-indole-1-carboxylate
C32H44N2O11     ÏàËÆ¶È:57.8%
Helvetica Chimica Acta          2012          95          2481-2501
Synthesis of Enantiomerically Pure Isoxazolidine Monomers for the Preparation of ¦Â3-Oligopeptides by Iterative -Keto AcidHydroxylamine (KAHA) Ligations
Ying-Ling Chiang, Justin A. Russak, Nancy Carrillo and Jeffrey W. Bode
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     tert-Butyl 3-{[(3R,5S)-5-Methoxy-5-(methoxycarbonyl)isoxazolidin-3-yl]methyl}-1H-indole-1-carboxylate
C32H44N2O11     ÏàËÆ¶È:57.8%
Helvetica Chimica Acta          2012          95          2481-2501
Synthesis of Enantiomerically Pure Isoxazolidine Monomers for the Preparation of ¦Â3-Oligopeptides by Iterative -Keto AcidHydroxylamine (KAHA) Ligations
Ying-Ling Chiang, Justin A. Russak, Nancy Carrillo and Jeffrey W. Bode
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     3-(2-Phenyl-benzofuran-3-yl)-propyl 4-amino-2,3,4,6-tetradeoxy-¦Á-L-threo-hexopyranoside
C23H27NO3     ÏàËÆ¶È:57.1%
Bioorganic & Medicinal Chemistry          2011          19          1779-1789
Structure¨Cactivity relationships in glycosylated 2-phenyl-indoles,2-phenyl-benzothiophenes and 2-phenyl-benzofurans as DNA binding and potential antitumor agents
Wei Shi, Todd L. Lowary
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
24 .     juglanin B
C20H24O4     ÏàËÆ¶È:55%
Planta Medica          2008          74          754-759
Cytotoxic Diarylheptanoids from the Pericarps of Walnuts (Juglans regia)
Jun-Xi Liu, Duo-Long Di, Xiao-NingWei, Yin Han
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
25 .     cypermethrin II B
    ÏàËÆ¶È:55%
Chemistry of Natural Compounds          1988          24          246-250
1H AND 13C NMR SPECTRA OF BIOLOGICALLY ACTIVE COMPOUNDS."IV. DIASTEREOMERS OF PYRETHROIDS AND THEIR INSECTICIDAL ACTIVITY
G. A. Tolstikov, L. M. Khalilov,F. Z. Galin, E. V. Vasil'eva,D. B. Amirkhanov, M. G. Migranov,and A. A. Panasenko
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
26 .     cypermethrin II D
    ÏàËÆ¶È:55%
Chemistry of Natural Compounds          1988          24          246-250
1H AND 13C NMR SPECTRA OF BIOLOGICALLY ACTIVE COMPOUNDS."IV. DIASTEREOMERS OF PYRETHROIDS AND THEIR INSECTICIDAL ACTIVITY
G. A. Tolstikov, L. M. Khalilov,F. Z. Galin, E. V. Vasil'eva,D. B. Amirkhanov, M. G. Migranov,and A. A. Panasenko
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
27 .     juglanin B
C20H22O3     ÏàËÆ¶È:55%
Chinese Chemical Letters          2007          18          943-946
Two new diarylheptanoids from the pericarps of Juglans regia L
Xi Liu, Duo Long Di , Xin Yi Huang, Chen Li
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
28 .     myricarborin
C20H22O3     ÏàËÆ¶È:55%
Phytochemistry          2000          54          975-978
Diarylheptanoids from Myrica arborea
Mathieu Tene, Hyppolite Kamdem Wabo, Pierre Kamnaing, Apollinaire Tsopmo, Pierre Tane, Johnson Foyere Ayafor, Olov Sterner
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
29 .     juglanin B
    ÏàËÆ¶È:55%
Planta Medica          2011          77          841-845
Neuroprotective Diarylheptanoids from the Leaves and Twigs of Juglans sinensis against Glutamate-Induced Toxicity in HT22 Cells
Heejung Yang, Sang Hyun Sung, Jinwoong Kim,Young Choong Kim
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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