참고문헌
- Kuethe, J. T.; Wong, A.; Qu, C.; Smitrovich, J.; Davis, I. W.; Hughes, D. L. J. Org. Chem. 2005, 70, 504.
- Varvaresou, A.; Tsantili-Kakoulidou, A.; Siatra-Papastaikoudi, T.; Tiligada, E. Arzneim Forsch 2000, 50, 48-54.
- Mohan, J.; Kataria, S. Indian Chem. J. Sect. B 1996, 35, 456-458.
- Palluotto, F.; Carotti, A.; Casini, G.; Ferappi, M.; Rosata, A.; Vitali, C.; Campagna, F. Farmaco 1999, 54(3), 191-194. https://doi.org/10.1016/S0014-827X(99)00021-X
- Dzurilla, M.; Ruzinsky, M.; Kutschy, P.; Tewari, J.; Kovacik, V. Collect. Czech. Chem. Commun. 1999, 64, 1448-1456. https://doi.org/10.1135/cccc19991448
- Kutsky, P.; Dzurilla, T. M.; Sabova, A. Collect. Czech. Chem. Commun. 1999, 64, 348-362. https://doi.org/10.1135/cccc19990348
- Kutsky, P.; Dzurilla, M.; Takasugi, M.; Toerock, M.; Achbergerova, I. Tetrahedron 1998, 54, 3549-3566. https://doi.org/10.1016/S0040-4020(98)00088-X
- Khan, M. H.; Twari, S.; Begum, K.; Nizamuddin, 0, Indian Chem. J. Sect. B 1998, 37, 1075-1077.
- Machia, M.; Mamera, C.; Nencetti, S.; Rossello, A.; Broccali, G.; Limonta, D. Farmaco 1996, 51, 75-78.
- Garuti, L.; Roberti, M.; Rossi, T.; Castelli, M.; Malagoli, M. Eur. J. Med. Chem. Chem. 1998, Ther. 33, 43-46. https://doi.org/10.1016/S0223-5234(99)80074-9
- Draheim, S. A.; Bach, N. J.; Dillard, R. D.; Berry, D. R.; Carlson, D. G. J. Med. Chem. 1996, 39, 5159-5175. https://doi.org/10.1021/jm960487f
- Battagba, S.; Boldrini, E.; Settimo, F. D.; Dondio, G.; Motta, C. L. Eur. J. Med. Chem. Chim. Ther. 1999, 34, 93-106. https://doi.org/10.1016/S0223-5234(99)80044-0
- Zotova, S. A.; Korneeva, T. M.; Shvedov, V. I.; Fadaeva, N. I.; Leneva, I. A. Pharm. Chem. J. 1995, 29, 57-59. https://doi.org/10.1007/BF02219467
- Lai, G.; Anderson, W. K. Tetrahedron 2000, 56, 2583-2590. https://doi.org/10.1016/S0040-4020(00)00177-0
- Amir, M.; Dhar, N.; Tiwari, S. K. Indian. J. Chem. Sect. B 1997, 36, 96-98.
- Grasso, S.; Molica, C.; Monforte, A. M.; Monforte, P.; Zappala, M. Farmaco 1995, 50, 113-118.
- Katayama, M.; Gautam, R. K. Biosci. Biotechnol. Biochem. 1996, 60, 755-759. https://doi.org/10.1271/bbb.60.755
- Riyadh, S. M.; Farghaly, T. A.; Gomha, S. M. Arch. Pharm. Res. 2010, 33, 1721. https://doi.org/10.1007/s12272-010-1102-8
- Gomha, S. M.; Riyadh, S. M. ARKIVOC 2009, xi, 58-68.
- Abbas, I. M.; Riyadh, S. M.; Abdallah, M. A.; Gomha, S. M. J. Het. Chem. 2006, 43, 935-942. https://doi.org/10.1002/jhet.5570430419
- Abdel-Aziz, H. A.; Saleh, T. S.; El-Zahabi, H. S. A. Arch. Pharm. 2010, 343, 24-30.
- Abdel-Aziz, H. A.; Hamdy, N. A.; Gamal-Eldeen, A. M.; Fakhr, I. M. I. Z. Naturforsch C 2011, 66, 7. https://doi.org/10.5560/ZNB.2011.66c0007
- Acheson, R. M.; Prince, R. J.; Procter, G. J. Chem. Soc., Perkin Trans. 1 1979, 3, 595-599.
- Cowper, R. M.; Davidson, L. H. Org. Syn., Coll. 1943, II, 840.
- Dieckmann, W.; Platz, O. Chem. Ber. 1906, 38, 2989.
- Hegarty, A. F.; Cashoman, M. P.; Scott, F. L. Chem. Commun. 1971, 13, 684.
- National Committee for Clinical Laboratory Standards (NCCLS), "Standard Methods for Dilution Antimicrobial Susceptibility Tests for Bacteria, Which Grows Aerobically," Nat. Comm. Lab. Stands. Villanova, 1982; p 242.
- Habib, N. S.; Rida, S. M.; Badawey, E. A. M.; Fahmy, H. T. Y.; Ghozlan, H. A. Pharmazie 1997, 52, 346-350.
- Bondock, S.; Fadaly, W.; Metwally, M. A. Eur. J. Med. Chem. 2010, 45, 3692. https://doi.org/10.1016/j.ejmech.2010.05.018
- Rostom, S. A. F.; El-Ashmawy, I. M.; Abd El Razik, H. A.; Badr, M. H.; Ashour, H. M. A. Bioorg. Med. Chem. 2009, 17, 882. https://doi.org/10.1016/j.bmc.2008.11.035
- Farag, A. M.; Dawood, K. M.; Kandeel, Z. E. Tetrahedron 1997, 53, 161. https://doi.org/10.1016/S0040-4020(96)00959-3
- Hamdy, N. A.; Abdel-Aziz, H. A.; Farag, A. M.; Fakhr, I. M. I. Monatsh. fur Chem. 2007, 138, 1001-1010. https://doi.org/10.1007/s00706-007-0717-z
- Dawood, K. M.; Farag, A. M.; Abdel-Aziz, H. A. J. Chem. Res. 2005, 378-381.
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