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14
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39049142195
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For recent syntheses:
-
For recent syntheses:. Beylin V., Boyles D.C., Curran T.T., Macikenas D., Parlett IV R.V., and Vrieze D. Org. Proc. Res. Dev. 11 (2007) 441-449
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3843124412
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Tran T.P., Ellsworth E.L., Stier M.A., Domagala J.M., Showalter H.D.H., Gracheck S.J., Shapiro M.A., Joannides T.E., and Singh R. Bioorg. Med. Chem. Lett. 14 (2004) 4405-4409
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19
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33750436245
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Ellsworth E., Tran T., Showalter H.H., Sanchez J., Watson B., Stier M., Domagala S., Gracheck E., Joannides E., Shapiro M., Dunham S., Hanna D., Huband M., Gage J., Bronstein J., Liu J., Nguyen D., and Singh R. J. Med. Chem. 49 (2006) 6435-6438
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Gracheck, S.J.11
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21
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33846897468
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Tran T., Ellsworth E., Sanchez J., Watson B., Stier M., Showalter H., Domagala J., Shapiro M., Joannides E., Gracheck S., Nguyen D., Bird P., Yip J., Sharadendu A., Ha C., Ramezani S., Wu X., and Singh R. Bioorg. Med. Chem. Lett. 17 (2007) 1312-1320
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Ha, C.15
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22
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23
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58049164499
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One patent describes, in part, the synthesis of some 2-amino-6-chloro-4-cyclopropyl-7-fluoro-pyrido[1,2-c]pyrimidine-1,3-dione core ring intermediates toward preparing C-6 variants as fluoroquinolone analogs. Ellsworth, E. L.; Showalter, H. D. H. U.S. Patent 0114458 A1, 2003.
-
One patent describes, in part, the synthesis of some 2-amino-6-chloro-4-cyclopropyl-7-fluoro-pyrido[1,2-c]pyrimidine-1,3-dione core ring intermediates toward preparing C-6 variants as fluoroquinolone analogs. Ellsworth, E. L.; Showalter, H. D. H. U.S. Patent 0114458 A1, 2003.
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24
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18244392176
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Malik M., Lu T., Zhao X., Singh A., Hattan C., Domagala J., Kerns R., and Drlica K. Antimicrob. Agents Chemother. 49 (2005) 2008-2014
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Kerns, R.7
Drlica, K.8
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0033150538
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Li Q., Sowin T., Claiborne A., Lijewski L., Zhang X., Raye K., Mazdiyasni H., Arnold W., Melcher L.M., Wang W., Hasvold L., Fung A., Chu D.T.W., and Plattner J.J. Heterocycles 51 (1999) 1345-1353
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Plattner, J.J.14
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27
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9344236011
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Li Q., Chu D.T.W., Claiborne A., Cooper C.S., Lee C.M., Raye K., Berst K.B., Donner P., Wang W., Hasvold L., Fung A., Ma Z., Tufano M., Flamm R., Shen L.L., Baranowski J., Nilius A., Alder J., Meulbroek J., Marsh K., Cowell D., Hui Y., Seif L., Melcher L.M., Henry R., Spanton S., Faghih R., Klein L.L., Tanaka S.K., and Plattner J.J. J. Med. Chem. 39 (1996) 3070-3088
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Li, Q.1
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Lee, C.M.5
Raye, K.6
Berst, K.B.7
Donner, P.8
Wang, W.9
Hasvold, L.10
Fung, A.11
Ma, Z.12
Tufano, M.13
Flamm, R.14
Shen, L.L.15
Baranowski, J.16
Nilius, A.17
Alder, J.18
Meulbroek, J.19
Marsh, K.20
Cowell, D.21
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Melcher, L.M.24
Henry, R.25
Spanton, S.26
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Klein, L.L.28
Tanaka, S.K.29
Plattner, J.J.30
more..
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30
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84945736528
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One early report of an unrelated 1,3-dione core, having no 5-methoxy group and not suitable for requisite substitution purposes, was found:
-
One early report of an unrelated 1,3-dione core, having no 5-methoxy group and not suitable for requisite substitution purposes, was found:. Hunger A., and Hoffmann K. Helv. Chim. Acta 40 (1957) 1319-1330
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(1957)
Helv. Chim. Acta
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, pp. 1319-1330
-
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Hunger, A.1
Hoffmann, K.2
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31
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58049148476
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note
-
5, 463.2231; m/z found, 463.2227.
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