References
- White, A. W.; Curtin, N. J.; Eastman, B. W.; Golding, B. T.; Hostomsky, Z.; Kyle, S.; Maegley, K. A.; Skalitzki, D. J.; Webber, S. E.; Yu, X.-H.; Griffin, R. J. Bioorg. Med. Chem. Lett. 2004, 14, 2433 https://doi.org/10.1016/j.bmcl.2004.03.017
- Lee-Dutra, A.; Arienti, K. L.; Buzard, D. J.; Hack, M. D.; Khatuya, H.; Desai, P. J.; Nguyen, S.; Thurmond, R. L.; Karlsson, L.; Edwards, J. P.; Breitenbucher, J. G. Bioorg. Med. Chem. Lett. 2006, 16, 6043 https://doi.org/10.1016/j.bmcl.2006.08.117
- Cedillo-Rivera, R.; Munoz, O. J. Med. Microbiol. 1992, 37, 221 https://doi.org/10.1099/00222615-37-3-221
-
G
$\ddot{u}$ ng$\ddot{o}$ r, T.; Fouquet, A.; Teulon, J.-M.; Provost, D.; Cazes, M.; Cloarec, A. J. Med. Chem. 1992, 35, 4455 https://doi.org/10.1021/jm00101a024 - Denny, W. A.; Rewcastle, G. W.; Baguley, B. C. J. Med. Chem. 1990, 33, 814 https://doi.org/10.1021/jm00164a054
- Seyhan, E.; Sultan, N.; Nilgun, A.; Noyanalpan, N. Arzneimittel Forschung 1997, 47, 410
- Ries, U. J.; Mihm, G.; Narr, B.; Hasselbach, K. M.; Wittneben, H.; Entzeroth, M.; van Meel, J. C. A.; Wienen, W.; Hauel, N. H. J. Med. Chem. 1993, 36, 4040 https://doi.org/10.1021/jm00077a007
- Wang, R.; Lu, X.-X.; Yu, X.-Q.; Shi, L.; Sun, Y. J. Mol. Cat. A: Chem. 2007, 266, 198 https://doi.org/10.1016/j.molcata.2006.04.071
- Grimmet, M. R. In Comprehensive Heterocyclic Chemistry; Katritzky, A. R.; Rees, C. W., Eds.; Pergamon Press: Oxford, 1984; Vol. 5, p 457
- Hisano, T.; Ichikawa, M.; Tsumoto, K.; Tasaki, M. Chem. Pharm. Bull. 1982, 30, 2996 https://doi.org/10.1248/cpb.30.2996
- Tidwell, R. R.; Geratz, J. D.; Dann, O.; Volz, G.; Zeh, D.; Loewe, H. J. Med. Chem. 1978, 21, 613 https://doi.org/10.1021/jm00205a005
- Failey, T. A.; Tidwell, R. R.; Donkor, I.; Naiman, N. A.; Ohemeng, K. A.; Lombardy, R. J.; Bentley, J. A.; Cory, M. J. Med. Chem. 1993, 36, 1746 https://doi.org/10.1021/jm00064a008
- Dubey, P. K.; Ratnam, C. V. Indian J. Chem. Sect. B: Org. Chem. Incl. Med. Chem. 1979, 18, 428
- Yadagiri, B.; Lown, J. W. Synth. Commun. 1990, 20, 955 https://doi.org/10.1080/00397919008052798
- Harapanhalli, R. S.; McLaughlin, L. W.; Howell, R. W.; Rao, D. V.; Adelstein, S. J.; Kassis, A. I. J. Med. Chem. 1996, 39, 4804 https://doi.org/10.1021/jm9602672
- Kumar, S.; Kansal, V.; Bhaduri, A. Indian J. Chem. Sect. B: Org. Chem. Incl. Med. Chem. 1991, 20, 254
- Verner, E.; Katz, B. A.; Spencer, J. R.; Allen, D.; Hataye, J.; Hruzewicz, W.; Hui, H. C.; Kolesnikov, A.; Li, Y.; Luong, C.; Martelli, A.; Radika, K.; Rai, R.; She, M.; Schrader, W.; Sprengeler, P. A.; Trapp, S.; Wang, J.; Young, W. B.; Mackman, R. L. J. Med. Chem. 2001, 44, 2753 https://doi.org/10.1021/jm0100638
- vanden Enynde, J. J.; Delfosse, F.; Lor, P.; van Harverbeke, Y. Tetrahedron 1995, 51, 5813 https://doi.org/10.1016/0040-4020(95)00252-4
- Lee, K. J.; Janda, K. D. Can. J. Chem. 2001, 79, 1556 https://doi.org/10.1139/cjc-79-11-1556
- Bhatnagar, I.; George, M. V. Tetrahedron 1968, 24, 1293 https://doi.org/10.1016/0040-4020(68)88080-9
- Patzold, F.; Zeuner, F.; Heyer, T. H.; Niclas, H. J. Synth. Commun. 1992, 22, 281 https://doi.org/10.1080/00397919208021304
- Chikashita, H.; Nishida, S.; Miyasaki, M.; Morita, Y.; Itoh, K. Bull. Chem. Soc. Jpn. 1987, 60, 737 https://doi.org/10.1246/bcsj.60.737
- Breaulieu, P. L.; Hache, B.; von Moos, E. Synthesis 2003, 22, 1683
- Stephens, F. F.; Bower, J. D. J. Chem. Soc. 1949, 2971
- Weidner-Wells, M. A.; Ohemerg, K. A.; Nguyen, V. N.; Fraga-Spano, S.; Macielag, M. J.; Werblood, H. M.; Foleno, B. D.; Webb, G. C.; Barrett, J. F.; Hlasta, D. J. Bioorg. Med. Chem. Lett. 2001, 11, 1545 https://doi.org/10.1016/S0960-894X(01)00024-5
- Austen, S. C.; Kane, J. M. J. Heterocycl. Chem. 2001, 38, 979 https://doi.org/10.1002/jhet.5570380427
- Ridley, H. F.; Spickett, R. G. W.; Timmis, G. M. J. Heterocycl. Chem. 1965, 2, 453 https://doi.org/10.1002/jhet.5570020424
- Neelakantan, L.; Hartung, W. H. J. Org. Chem. 1959, 24, 1943 https://doi.org/10.1021/jo01094a029
- Lombardy, R. L.; Tanious, F. A.; Ramachardran, K.; Tidwell, R. R.; Wilson, W. D. J. Med. Chem. 1996, 39, 1452 https://doi.org/10.1021/jm9507946
- Lin, S.; Yang, L. Tetrahedron Lett. 2005, 46, 4315 https://doi.org/10.1016/j.tetlet.2005.04.101
- Gogoi, P.; Konwar, D. Tetrahedron Lett. 2006, 47, 79 https://doi.org/10.1016/j.tetlet.2005.10.134
- Yang, D.; Fokas, D.; Li, J.; Yu, L.; Baldino, C. M. Synthesis 2005, 47
- Bahrami, K.; Khodaei, M. M.; Kavianinia, I. Synthesis 2007, 547
- Lopez, S. E.; Rosales, M. E.; Urdaneta, N.; Godoy, M. V.; Charris, J. E. J. Chem. Res. (S) 2000, 258
- Lee, K. H.; Fokas, D.; Li, J.; Yu, L.; Baldino, C. M. J. Med. Chem. 2000, 43, 1257 https://doi.org/10.1021/jm000081+
- Belomestnykh, I. P.; Rozhdestvenskaya, N. N.; Isagulyants, G. V. Khimiya Geterotsiklicheskikh Soedinenii 1994, 802. Chem. Abstr. 122:31287
- Tibilov, S. G.; Lobachev, L. V.; Poletaeva, G. N. Khimicheskaya Promyshlennost (Moscow) 1995, 107. Chem. Abstr. 125:14579
- Sluka, J. Coll. Czch. Chem. Commun. 1981, 46, 2703 https://doi.org/10.1135/cccc19812703
- Lewis, J. C.; Berman, A. M.; Bergman, R. G.; Ellmann, J. A. J. Am. Chem. Soc. 2008, 130, 2493 https://doi.org/10.1021/ja0748985
- Du, L.-H.; Wang, Y.-G. Synthesis 2007, 675
- Sahu, D. P.; Ponnala, S. Synth. Commun. 2006, 36, 2189 https://doi.org/10.1080/00397910600638879
- Prokopcova, H.; Kappe, O. J. Org. Chem. 2007, 72, 4440 https://doi.org/10.1021/jo070408f
- Lee, I.-S. H.; Kil, H. J.; Jik, Y. R. J. Phys. Org. Chem. 2007, 20, 484 https://doi.org/10.1002/poc.1182
- Itoh, T.; Nagata, K.; Ishikawa, H.; Ohsawa, A. Heterocycles 2004, 63, 2769 https://doi.org/10.3987/COM-04-10215
- Fukuhara, T.; Hasegawa, C.; Hara, S. Synthesis 2007, 1528
- Navarrete-Vasquez, G.; Moreno-Diaz, H.; Estrado-Soto, S.; Torres-Piedra, M.; Leon-Rivera, I.; Tlahuext, H.; Munoz-Muniz, O.; Torres-Gomez, H. Synth. Commun. 2007, 37, 2815 https://doi.org/10.1080/00397910701473325
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