참고문헌
- Bell, R.; Carmeli, S.; Sar, N. J. Nat. Prod. 1994, 57, 1587 https://doi.org/10.1021/np50113a022
- Fahy, E.; Porn, B. C. M.; Faulkner, D. J.; Smith, K. J. Nat. Prod. 1991, 54, 564 https://doi.org/10.1021/np50074a032
- Garbe, T. R.; Kobayashi, M.; Shimizu, N.; Takesue, N.; Ozawa, M.; Yukawa, H. J. Nat. Prod. 2000, 63, 596 https://doi.org/10.1021/np990517s
- Sundberg, R. J. The Chemistry of Indoles; Academic: Newyork, 1996
- Ge, X.; Yannai, S.; Rennert, G.; Gruener, N.; Fares, F. A. Biochem. Biophys. Res. Commun. 1996, 228, 153 https://doi.org/10.1006/bbrc.1996.1631
- Chakrabarty, M.; Basak, R.; Harigaya, Y. Heterocycles 2001, 55, 2431 https://doi.org/10.3987/REV-01-541
- Kamal, A.; Qureshi, A. A. Tetrahedron 1963, 19, 513 https://doi.org/10.1016/S0040-4020(01)98540-0
- Babu, G.; Sridhar, N.; Perumal, P. T. Synth. Commun. 2000, 30, 1609 https://doi.org/10.1080/00397910008087197
- Nagarajan, R.; Perumal, P. T. Tetrahedron 2002, 58, 1229 https://doi.org/10.1016/S0040-4020(01)01227-3
- Bandgar, B. P.; Shaikh, K. A. J. Chem. Res. Synop. 2004, 34
- Mi, X. L.; Luo, S. Z.; He, J. Q.; Cheng, J. P. Tetrahedron Lett. 2004, 45, 4567 https://doi.org/10.1016/j.tetlet.2004.04.039
- Chen, D.; Yu, L.; Wang, P. G. Tetrahedron Lett. 1996, 37, 4467 https://doi.org/10.1016/0040-4039(96)00958-6
- Yadav, J. S.; Reddy, B. V. S.; Murthy, V. S. R.; Kumar, G. M.; Madan, C. Synthesis 2001, 783
- Xia, M.; Wang, S. B.; Yuan, W. B. Synth. Commun. 2004, 34, 3175 https://doi.org/10.1081/SCC-200028611
- Ji, S. J.; Wang, S. Y.; Zhang, Y.; Loh, T. P. Tetrahedron 2004, 60, 2051 https://doi.org/10.1016/j.tet.2003.12.060
- Bandgar, B. P.; Shaikh, K. A. Tetrahedron Lett. 2003, 44, 1956
- Koshima, H.; Matsuaka, W. J. Heterocyclic Chem. 2002, 39, 1089 https://doi.org/10.1002/jhet.5570390539
- Nagarajan, R.; Perumal, P. T. Chem. Lett. 2004, 33, 288 https://doi.org/10.1246/cl.2004.288
- Ramesh, C.; Banerjee, J.; Pal, R.; Das, B. Adv. Synth. Catal. 2003, 345, 557 https://doi.org/10.1002/adsc.200303022
- Nagarajan, R.; Perumal, P. T. Synth. Commun. 2002, 32, 105 https://doi.org/10.1081/SCC-120001515
- Ramesh, C.; Ravindranath, N.; Das, B. J. Chem. Res. Synop. 2003, 72
- Karthik, M.; Tripathi, A. K.; Gupta, N. M.; Palanichamy, M.; Murugesan, V. Catal. Commn. 2004, 5, 371 https://doi.org/10.1016/j.catcom.2004.04.007
- Reddy, A. V.; Ravinder, R.; Reddy, V. L. N.; Goud, T. V.; Ravikanth, V.; Venkateseswarlu, Y. Synth. Commun. 2003, 33, 3687 https://doi.org/10.1081/SCC-120025177
- Chakrabarty, M.; Gosh, N.; Basak, R.; Harigaya, Y. Tetrahedron Lett. 2002, 43, 4075 https://doi.org/10.1016/S0040-4039(02)00682-2
- Penieres-Carrillo, G.; Garcia-Estrada, J. G.; Gutierrez-Ramirez, J. L.; Alvarez-Toledano, C. Green Chem. 2003, 5, 337
- Zolfigol, M. A.; Salehi, P.; Shirl, M. Phosphorus, Sulfur Silicon Relat. Elem. 2004, 179, 2273 https://doi.org/10.1080/10426500490484904
- Yadav, J. S.; Reddy, B. V. S.; Sunitha, S. Adv. Synth. Catal. 2003, 345, 349 https://doi.org/10.1002/adsc.200390038
- Wang, L. M.; Han, J. W.; Tian, H.; Sheng, J.; Fan, Z. Y.; Tang, X. P. Synlett 2005, 337
- Sharma, G. V. M.; Reddy, J. J.; Lakshmi, P. S.; Krishna, P. R. Tetrahedron Lett. 2004, 45, 7729 https://doi.org/10.1016/j.tetlet.2004.08.084
- Bandgar, B. P.; Bettigeri, S. V.; Joshi, N. S. Monatsh. Chem. 2004, 135, 1265 https://doi.org/10.1007/s00706-004-0206-6
- Feng, X. L.; Guan, C. J.; Zhao, C. X. Synth. Commun. 2004, 34, 487 https://doi.org/10.1081/SCC-120027288
- Ji, S. J.; Zhou, M. F.; Gu, D. G.; Wang, S. Y.; Loh, T. P. Synlett 2003, 2077
- Ji, S. J.; Zhou, M. F.; Gu, D. G.; Jiang, Z. Q.; Loh, T. P. Eur. J. Org. Chem. 2004, 1584
- Lenarsic, R.; Kocevar, M.; Polanc, S. J. Org. Chem. 1999, 64, 2558 https://doi.org/10.1021/jo9821170
- Firouzabadi, H.; Iranpoor, N.; Karimi, B. Synlett 1999, 3, 319
- Chary, K. P.; Mohan, G. H.; Iyengar, D. S. Chem. Lett. 1999, 12, 1339
- Chary, K. P.; Ram, S. R.; Mohan, G. H.; Iyengar, D. S. Synlett 2000, 5, 683
- Karimi, B.; Seradj, H. Synlett 2000, 6, 805
- Reddy, V.; Mahesh, M.; Raju, P. V. K.; Ramesh, T.; Narayana Reddy, V. V. Tetrahedron Lett. 2002, 43, 2657 https://doi.org/10.1016/S0040-4039(02)00280-0
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