참고문헌
- Tang, Y.; Oppenheimer, J.; Song, Z.; You, L.; Zhang, X.; Hsung, R. P. Tetrahedron 2006, 62, 10785. https://doi.org/10.1016/j.tet.2006.08.054
- McKee, T. C.; Fuller, R. W.; Covington, C. D.; Cardellina II, J. H.; Gulakowski, R. J.; Krepps, B. L.; McMahon, J. B.; Boyd, M. R. J. Nat. Prod. 1996, 59, 754. https://doi.org/10.1021/np9603784
- McKee, T. C.; Covington, C. D.; Fuller, R. W.; Bokesch, H. R.; Young, S.; Cardellina II, J. H.; Kadushin, M. R.; Doel Soejarto, D.; Stevens, P. F.; Cragg, G. M.; Boyd, M. R. J. Nat. Prod. 1998, 61, 1252. https://doi.org/10.1021/np980140a
- Grundon, M. F. In The Alkaloids: Quinoline Alkaloids Related to Anthranilic Acid; Academic Press: London, 1988; 32, p 341.
- Ulubelen, A.; Mericli, A. H.; Mericli, F.; Kaya, U. Phytochemistry 1994, 35, 1600. https://doi.org/10.1016/S0031-9422(00)86905-8
- Wu, S.-J.; Chen, I. -S. Phytochemistry 1993, 34, 1659. https://doi.org/10.1016/S0031-9422(00)90870-7
- Campbell, W. E.; Davidowitz, B.; Jackson, G. E. Phytochemistry 1990, 29, 1303. https://doi.org/10.1016/0031-9422(90)85447-N
- Khalid, S. A.; Waterman, P. G. Phytochemistry 1981, 20, 2761. https://doi.org/10.1016/0031-9422(81)85282-X
- Hifnawy, M. S.; Vaquette, J.; Sevenet, T.; Pousset, J.-L.; Cave, A. Phytochemistry 1977, 16, 1035. https://doi.org/10.1016/S0031-9422(00)86717-5
- Stermitz, F. R.; Sharifi, I. A. Phytochemistry 1977, 16, 2003. https://doi.org/10.1016/0031-9422(77)80113-1
- Kulesza, A.; Ebetino, F. H.; Mishra, R. K.; Cross-Doersen, D.; Mazur, A. W. Org. Lett. 2003, 5, 1163. https://doi.org/10.1021/ol027281v
- Uher, M.; Konecny, V.; Rajniakove, O. Chem. Pap. 1994, 48, 282.
- Perez-Perez, M.; Balzarini, J.; Rozenski, J.; De-Clercq, E.; Herdewijn, P. Bioorg. Med. Chem. Lett. 1995, 5, 1115. https://doi.org/10.1016/0960-894X(95)00176-T
- Aytemir, M. D.; Calis, U.; Ozalp, M. Arch. Pharm. Pharm. Med. Chem. 2004, 337, 281. https://doi.org/10.1002/ardp.200200754
- Lima, V.; Silva, C. B.; Mafezoli, J.; Bezerra, M. M.; Moraes, M. O.; Mourao, G. S. M. M.; Silva, J. N.; M. C. F. Oliveira. Fitoterapia 2006, 77, 574. https://doi.org/10.1016/j.fitote.2006.09.005
- Lee, Y. R.; Choi, J. H.; Trinh, D. T. L.; Kim, N. W. Synthesis 2005,3026.
- Chen, I. S.; Wu, S. J.; Tsai, I. L. Wu, T. S.; Pezzuto, J. M.; Lu, M. C.; Chai, H.; Suh, N.; Teng, C. M. J. Nat. Prod. 1994, 57, 1206. https://doi.org/10.1021/np50111a003
- Yu, D.; Suzuki, M.; Xie, L.; Morris-Natschke, S. L.; Lee, K.-H. Med. Res. Rev. 2003, 23, 322. https://doi.org/10.1002/med.10034
- Chen, M.; Shao, C.-L.; Fu, X.-M.; Xu, R.-F.; Zheng, J.-J.; Zhao, D.-L.; She, Z.-G.; Wang, C.-Y. J. Nat. Prod. 2013, 76, 547. https://doi.org/10.1021/np300707x
- Lee, Y. R.; Kim, D. H.; Shim, J.-J.; Kim, S. K.; Park, J. H.; Cha, J. S. Bull. Korean Chem. Soc. 2002, 23, 998. https://doi.org/10.5012/bkcs.2002.23.7.998
- Lee, Y. R.; Choi, J. H.; Trinh, D. T. L.; Kim, N. W. Synthesis 2005, 18, 3026.
- Lee, Y. R.; Kim, D. H. Synthesis 2006, 4, 603.
- Lee, Y. R.; Wang, X.; Kim, Y. M.; Shim, J. J.; Kim, B. N.; Han, D. H. Bull. Korean Chem. Soc. 2007, 28, 1735. https://doi.org/10.5012/bkcs.2007.28.10.1735
- Jung, E. J.; Lee, Y. R.; Lee, H. J. Bull. Korean Chem. Soc. 2009, 30, 2833. https://doi.org/10.5012/bkcs.2009.30.11.2833
- Kurdyumov, A. V.; Lin, N.; Hsung, R. P.; Gullickson, G. C.; Cole, K. P.; Sydorenko, N.; Swidorski, J. J. Org. Lett. 2006, 8, 191. https://doi.org/10.1021/ol0523042
- Huber, C.; Moreau, J.; Batany, J.; Duboc, A.; Hurvois, J.-P.; Renaud, J.-L. Adv. Synth. Catal. 2008, 350, 40. https://doi.org/10.1002/adsc.200700375
- Moreau, J.; Hubert, C.; Batany, J.; Toupet, L.; Roisnel, T.; Hurvois, J.-P.; Renaud, J.-L. J. Org. Chem. 2009, 74, 8963. https://doi.org/10.1021/jo901238y
- Garcia, A.; Borchardt, D.; Chang, C.-E. A.; Marsella, M. J. J. Am. Chem. Soc. 2009, 131, 16640. https://doi.org/10.1021/ja907062v
- Martinez-Palou, R. Quimica en Microondas; CEM Publishing: Mattews, NC, 2006.
- Lidstom, P.; Tierney, J. P., Eds.; Microwave-Assisted Organic Synthesis; Blackwell Scientific, 2005.
- Kappe, C. O.; Stadler, A. Microwaves in Organic and Medicinal Chemistry; Wiley- VCH: Weinheim, 2005.
- Loupy, A., Eds.; Microwaves in Organic Synthesis; Wiley-VCH: Weinheim, 2002.
- Hayes, B. L. Microwave Synthesis: Chemistry at the Speed of Light; CEM Publishing: Matthews, NC, 2002.
- Martinez-Palou, R. Mol. Diversity 2006, 10, 435. https://doi.org/10.1007/s11030-006-9021-9
- Martinez-Palou, R. J. Mex. Chem. Soc. 2007, 51, 252.
- Varma, R. S. Green Chem. 1999, 1, 43. https://doi.org/10.1039/a808223e
- Dallinger, D.; Kappe, C. O. Chem. Rev. 2007, 107, 2563. https://doi.org/10.1021/cr0509410
- Vaddula, B. R.; Varma, R. S.; Leazer, J. Eur. J. Org. Chem. 2012, 6852.
- Soares, M. I. L.; Pinho e Melo, T. M. V. D. Tetrahedron Lett. 2008, 49, 4889. https://doi.org/10.1016/j.tetlet.2008.06.013
- Borkin, D.; Morzhina, E.; Datta, S.; Rudnitskaya, A.; Sood, A.; Torok, M.; Torok, B. Org. Biomol. Chem. 2011, 9, 1394. https://doi.org/10.1039/c0ob00638f
- Qu, G.; Han, S.; Zhang, Z.; Geng, M.; Xue, F. J. Braz. Chem. Soc. 2006, 17, 915. https://doi.org/10.1590/S0103-50532006000500015
- Figiel, P. J.; Kopylovich, M. N.; Lasri, J.; Guedes da Silva, M. F. C.; Frausto da Silvaa, J. J. R.; Pombeiro, A. J. L. Chem. Commun. 2010, 46, 2766. https://doi.org/10.1039/b922738e
- Gonzalez-Arellano, C.; Yoshida, K.; Luque, R.; Gai, P. L. Green Chem. 2010, 12, 1281. https://doi.org/10.1039/c003410j
- berg, V.; Norman, F.; Chorell, E.; Westermark, A.; Olofsson, A.; Sauer-Eriksson, A. E.; Almqvist, F. Org. Biomol. Chem. 2005, 3, 2817. https://doi.org/10.1039/b503294f
- Bose, A. K.; Manhas, M. S.; Ghosh, M.; Shah, M.; Raju, V. S.; Bari, S. S.; Newaz, S. N.; Banik, B. K.; Chaudhary, A. G.; Barakat, K. J. J. Org. Chem. 1991, 56, 6968. https://doi.org/10.1021/jo00025a004
- Leonor Reyes, L.; Corona, S.; Arroyo, G.; Delgado, F.; Miranda, R. Int. J. Mol. Sci. 2010, 11, 2576. https://doi.org/10.3390/ijms11062576
- Erdelyi, M.; Gogoll, A. Synthesis 2002, 11, 1592.
- Jung, E. J.; Park, B. H.; Lee, Y. R. Green Chem. 2010, 12, 2003. https://doi.org/10.1039/c0gc00265h
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