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13
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77955663898
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We found that higher yields were achieved by using chloroacetaldehyde freshly prepared from the corresponding diethylacetal rather than using commercially available aqueous choroacetaldehyde
-
We found that higher yields were achieved by using chloroacetaldehyde freshly prepared from the corresponding diethylacetal rather than using commercially available aqueous choroacetaldehyde.
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14
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77955664310
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U.S. 2006/106023 (A1)
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Guzi, T.; Paruch, K.; Dwyer, M.; Zhao, L.; Curran, P. J.; Belanger, D. B.; Hamann, B.; Reddy, P. A.; Siddiqui, M. A. U.S. 2006/106023 (A1).
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Guzi, T.1
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Siddiqui, M.A.9
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15
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77955655172
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US/2004/0220189
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Sun, C. L.; Liang, C.; Huang, P.; Harris, G. D.; Guan, H. US/2004/0220189
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Sun, C.L.1
Liang, C.2
Huang, P.3
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16
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77955655993
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US/2005/009832
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Sun, C. L.; Liang, C.; Huang, P.; Harris, G. D.; Guan, H. US/2005/009832.
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Sun, C.L.1
Liang, C.2
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17
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77955659281
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3-Bromo-8-(methylsulfonyl)imidazo[1,2-a]pyrazine 4 is a stable solid that can be stored cold for months without decomposition
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3-Bromo-8-(methylsulfonyl)imidazo[1,2-a]pyrazine 4 is a stable solid that can be stored cold for months without decomposition.
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-
-
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18
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77955665691
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The coordinates for compound 1j have been deposited in the RCSB Protein Data Bank under the Accession Code 3NRM
-
The coordinates for compound 1j have been deposited in the RCSB Protein Data Bank under the Accession Code 3NRM.
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19
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1842848073
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J. Nowakowski, C.N. Cronin, D.E. McRee, M.W. Knuth, C.G. Nelson, N.P. Pavletich, J. Rogers, B.-C. Sang, D.N. Scheibe, R.V. Swanson, and D.A. Thompson Structure 10 2002 1659
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22
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77956159549
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Subsequent X-ray data with related imidazo[1,2-a]pyrazine inhibitors revealed a water mediated hydrogen bond between the enzyme and the 3-(4-pyrazolo) group
-
Subsequent X-ray data with related imidazo[1,2-a]pyrazine inhibitors revealed a water mediated hydrogen bond between the enzyme and the 3-(4-pyrazolo) group. Yu, T.; Tagat, J. R.; Kerekes, A. D.; Doll, R. J.; Zhang, Y.; Xiao, Y.; Esposite, S.; Belanger, D. B.; Curran, P. J.; Amit K. Mandal; Siddiqui, M. A.; Shih, N-Y.; Basso, A. D.; Liu, M.; Gray, K.; Tevar, S.; Jones, J.; Lee, S.; Ponery, S.; Smith, E. B.; Hruza, A.; Voigt, J.; Ramanathan, L.; Prosise, W.; Hu, M. J. Med. Chem. Lett. 2010, http://pubs.acs.org/doi/abs/10. 1021/ml100063w.
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Mandal, A.K.10
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Shih, N.-Y.12
Basso, A.D.13
Liu, M.14
Gray, K.15
Tevar, S.16
Jones, J.17
Lee, S.18
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Ramanathan, L.23
Prosise, W.24
Hu, M.25
more..
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23
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13944252481
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The conformational preference of thiazoles in related systems has been documented. A.C. Pierce, E. ter Haar, H.M. Binch, D.P. Kay, S.R. Patel, and P. Li J. Med. Chem. 48 2005 1278
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32344437258
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F.H. Jung, G. Pasquet, C. Lambert-van der Brempt, J.J. Lohmann, N. Warin, F. Renaud, H. Germain, C. De Savi, N. Roberts, T. Johnson, C. Dousson, G.B. Hill, A.A. Mortlock, N. Heron, R.W. Wilkinson, S.R. Wedge, S.P. Heaton, R. Odedra, N.J. Keen, S. Green, E. Brown, K. Thompson, and S. Brightwell J. Med. Chem. 49 2006 955
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Germain, H.7
De Savi, C.8
Roberts, N.9
Johnson, T.10
Dousson, C.11
Hill, G.B.12
Mortlock, A.A.13
Heron, N.14
Wilkinson, R.W.15
Wedge, S.R.16
Heaton, S.P.17
Odedra, R.18
Keen, N.J.19
Green, S.20
Brown, E.21
Thompson, K.22
Brightwell, S.23
more..
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25
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77955659405
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note
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50 values were derived by nonlinear regression analysis.
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27
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17344373426
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S. Sorota, X.S. Zhang, M. Margulis, K. Tucker, and T. Priestley Assay Drug Dev. Technol. 3 2005 47
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Priestley, T.5
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