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52.87,118.59,122.07,123.61,124.46,125.81,126.15,127.26,127.66,127.88,128.66,129.04,129.41,130.97,133.18,134.51,137.13,137.53,138.24,139.49,144.87,166.57,167.91
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sujianwei: ½ð±Ò+10 2013-01-24 21:42:24
1 .     (6,8-Dichloroindolizine-1,2,3-triyl)tris(phenylmethanone)
C29H17Cl2NO3     ÏàËÆ¶È:78.2%
Tetrahedron          2012          68          7338-7344
Convergent domino synthesis of 1,2,3-triaroylindolizines from methyl ketones and pyridines via self-division of labor strategy
Yan Yang, Meng Gao, Dong-Xue Zhang, Liu-Ming Wu, Wen-Ming Shu, An-Xin Wu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     3-(4-chrolophenyl)-2,3-dihydro-2,2-diphenyl-1-oxo-1H-pyrido[2,1-b]benzothiazol-4-carbonitrile
C30H19N2OSCl     ÏàËÆ¶È:73.9%
Heterocycles          2009          77          409-416
[4+2] Cycloaddition of Diphenylketene to 1-Aza-1,3-dienes
Masanori Sakamoto, Tatsuya Nakai, Hiroaki Yanagisawa, and Tomomi Kawasaki
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     6-naphthalen-2-yl-3-nitro-2-phenylsulfonylmethylimidazo[1,2-a]pyridine
C24H17N3O4S     ÏàËÆ¶È:73.9%
Heterocycles          2005          65          2979-2989
An Efficient Synthetic Route to New Imidazo[1,2-a]pyridines by Cross-Coupling Reactions in Aqueous Medium
Caroline Castera, Maxime D. Crozet, and Patrice Vanelle*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     6-Chloro-2-(2-naphthyl)-4-phenyl-1,2-dihydroquinazoline N3-oxide
C24H17N2OCl     ÏàËÆ¶È:73.9%
Archiv der Pharmazie          2004          337          239-246
New Derivatives of Quinazoline and 1,2-Dihydroquinazoline N3-Oxide with Expected Antitumor Activity
Elżbieta Mikiciuk-Olasik, Katarzyna Baszczak-Światkiewiz, Elżbieta Żurek, Urszula Krajewska, Marek R¨®żalski, Rafał Kruszy¨½ski and Tadeusz J. Bartczak
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     6-amidino-7,8-dihydro-2-naphthyl-2-naphthoate methanesulfonate
    ÏàËÆ¶È:73.9%
Bioorganic & Medicinal Chemistry          1997          5          971-985
New serine protease inhibitors with leukotriene B4 (LTB4) receptor binding affinity
Yoshisuke Nakayama, Kazuhiko Senokuchi, Katsuhito Sakaki, Masashi Kato, Toru Maruyama, Toru Miyazaki, Hidenori Ito, Hisao Nakai, Masanori Kawamura
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     N-(tert-butoxycarbonyl)-(Z)-¦Â-(dibenzothien-4-yl)dehydrophenylalanine
C27H25NO4S     ÏàËÆ¶È:73.9%
Bioorganic & Medicinal Chemistry          2008          16          5584-5589
Synthesis of new heteroaryl and heteroannulated indoles from dehydrophenylalanines: Antitumor evaluation
Maria-João R.P. Queiroz, Ana S. Abreu, M. Solange D. Carvalho, Paula M.T. Ferreira, Nair Nazareth, M. São-Jos¨¦ Nascimento
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     compound 16d
C27H19NO2S     ÏàËÆ¶È:73.9%
European Journal of Organic Chemistry          2011                   922-935
Lewis Acid Mediated One-Pot Synthesis of Aryl/Heteroaryl-Fused Carbazoles Involving a Cascade Friedel¨CCrafts Alkylation/Electrocyclization/Aromatization Reaction Sequence
Radhakrishnan Sureshbabu, Velu Saravanan, Vasudevan Dhayalan and Arasambattu K. Mohanakrishnan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     5,11-dihydro-3,3-dimethyl-6,12-diphenyl-1H-fluoreno[3,2-e][1,3]dioxepine
     ÏàËÆ¶È:73.9%
Heterocycles          2012          85          1077-1088
Synthesis of Fluorene- and Spirobifluorene-Fused Thiophenes
Wen Yao, Qiancai Liu,* Yingbo Shi, and Jie Tang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     1,4-diphenyl-2,3-bis(bromomethyl)-9-fluorene
    ÏàËÆ¶È:73.9%
Heterocycles          2012          85          1077-1088
Synthesis of Fluorene- and Spirobifluorene-Fused Thiophenes
Wen Yao, Qiancai Liu,* Yingbo Shi, and Jie Tang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     4'-benzyloxy-3'-trifluoromethylflavonol
    ÏàËÆ¶È:73.9%
Journal of Medicinal Chemistry          2008          51          1874-1884
Understanding the Cardioprotective Effects of Flavonols: Discovery of Relaxant Flavonols without Antioxidant Activity
Cheng Xue Qin, Xingqiang Chen, Richard A. Hughes, Spencer J. Williams and Owen L. Woodman
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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11 .     1-phenylsulfonyl-3-(1-methoxycarbonylbenzene-2-yl)-carbonylindole
C23H17NO5S     ÏàËÆ¶È:73.9%
Journal of Medicinal Chemistry          2004          47          4958-4963
Synthesis, Electrochemistry, and Bioactivity of the Cyanobacterial Calothrixins and Related Quinones
Paul H. Bernardo, Christina L. L. Chai, Graham A. Heath, Peter J. Mahon, Geoffrey D. Smith, Paul Waring, and Bronwyn A. Wilkes
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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12 .     2,3-dihydro-2,2-diphenyl-1-oxo-1H-3-(p-tolyl)-pyrido[2,1-b]benzothiazol-4-carbonitrile
C31H22N2OS     ÏàËÆ¶È:72%
Heterocycles          2009          77          409-416
[4+2] Cycloaddition of Diphenylketene to 1-Aza-1,3-dienes
Masanori Sakamoto, Tatsuya Nakai, Hiroaki Yanagisawa, and Tomomi Kawasaki
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     2-[3-(1-{2-[3-(4,5-diphenyl-1H-imidazol-2-yl)-phenyl]-4,5-diphenyl-2H-imidazol-2-yl}-4,5-diphenyl-1H-imidazol-2-yl]phenyl)-4,5-diphenyl-1H-imidazol
C36H24N4     ÏàËÆ¶È:72%
Russian Journal of Organic Chemistry          2011          47          1723-1726
Synthesis of radicals underlain by 1,3-bis(4,5-diphenylimidazol-2-yl)benzene
B. S. Tanaseichuk, M. K. Pryanichnikova, A. A. Burtasov, A. V. Dolganov and O. A. Tsyplenkova, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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14 .     5,15-bis(4-methoxycarbonylphenyl)-10,20-bis(1-naphthyl)porphyrin
C56H38N4O4     ÏàËÆ¶È:71.4%
European Journal of Organic Chemistry          2011                   5797-5816
5,15-A2B2- and 5,15-A2BC-Type Porphyrins with Donor and Acceptor Groups for Use in Nonlinear Optics and Photodynamic Therapy
Mathias O. Senge, Marijana Fazekas, Monica Pintea, Monika Zawadzka and Werner J. Blau
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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15 .     (E)-3-benzyl-1-but-3-enoyl-2-styryl-2,3-dihydroquinazolin-4(1H)-one
C27H24N2O2     ÏàËÆ¶È:70.8%
Heterocycles          2009          78          635-644
Efficient Syntheses of 1-Azatricyclic Ring Systems from Anthranylamide
Daniele Muroni, Mauro Mucedda, and Antonio Saba
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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16 .     3-chloro-N-(6-{[(4-chloroanilino)carbonyl]amino}-2-methylquinolin-4-yl)benzamide
C24H18Cl2N4O2     ÏàËÆ¶È:70.8%
Bioorganic & Medicinal Chemistry          2009          17          203-221
Search for new pharmacophores for antimalarial activity. Part I: Synthesis and antimalarial activity of new 2-methyl-6-ureido-4-quinolinamides
S. Madapa, Z. Tusi, D. Sridhar, A. Kumar, M.I. Siddiqi, K. Srivastava, A. Rizvi, R. Tripathi, S.K. Puri, G.B. Shiva Keshava, P.K. Shukla, S. Batra
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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17 .     2,2-Diphenyl-2H,7H-benzo[7,8]fluoreno[4,3-b]pyran-7-one
    ÏàËÆ¶È:69.5%
Helvetica Chimica Acta          2003          Vol. 86          570
Photochromic Properties of New Benzoindene-Fused 2H-Chromenes
Cristina I. Martins, Paulo J. Coelho, Luis M. Carvalho, Ana M.F. Oliveira-Campos,Andr¨¦ Samat, and Robert Guglielmetti
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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18 .     (Z)-5-benzylidene-2-(diphenylmethylidene)-3-phenyl-1,3-thiazolidin-4-one
C29H21NOS     ÏàËÆ¶È:69.5%
Helvetica Chimica Acta          2009          92          1800-1816
Chemoselectivity of the Reactions of Diazomethanes with 5-Benzylidene-3-phenylrhodanine
Martin S. Seyfried, Anthony Linden, Grzegorz Mlosto, Heinz Heimgartner
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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19 .     6-(Dibenzo[b,d]thiophen-4-yl)-2-hydroxyisoquinoline-1,3(2H,4H)-dione
C21H13NO3S     ÏàËÆ¶È:69.5%
Bioorganic & Medicinal Chemistry          2012          20          467-479
The design, synthesis and biological evaluations of C-6 or C-7 substituted 2-hydroxyisoquinoline-1,3-diones as inhibitors of hepatitis C virus
Yue-Lei Chen, Jing Tang, Matthew J. Kesler, Yuk Y. Sham, Robert Vince, Robert J. Geraghty,Zhengqiang Wang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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20 .     2,3-diphenyl-1-(phenylsulfonyl)indole
C26H19NO2S     ÏàËÆ¶È:69.5%
Tetrahedron Letters          2000          41          8717-8721
Bis-Suzuki reactions of 2,3-dihaloindoles. A convenient synthesis of 2,3-diarylindoles
Yanbing Liu, Gordon W. Gribble
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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21 .     11b,12-dihydro-5,11b-thioepoxy[2',1']-naphthaleno-5H-isoindolo[2,1-b]isoquinolin-7-one
C26H16NOS     ÏàËÆ¶È:69.5%
Organic letters          2000          2          1201-1204
Formation of New 5,11b-Bridged Isoindolo[2,1-b]isoquinolinones Alkaloids through a Tandem Pummerer/¦Ð-Cationic Cyclization
Nicolas Hucher, Adam Daich, and Bernard Decroix
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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