참고문헌
- Larock, R. C. Comprehensive Organic Transformations, 2nd ed.; VCH Publishers Inc: New York, U.S.A., 1999; p 717.
- Stotter, P. L.; Hill, K. A. Tetrahedron Lett. 1972, 13, 4067. https://doi.org/10.1016/S0040-4039(01)94239-X
- Yoshida, J.; Yano, S.; Ozawa, T.; Kawabata, N. Tetrahedron Lett. 1984, 25, 2817. https://doi.org/10.1016/S0040-4039(01)81298-3
- Coats, S. J.; Wasserman, H. H. Tetrahedron Lett. 1995, 36, 7735. https://doi.org/10.1016/0040-4039(95)01576-4
- Ishida, J.; Ohtsu, H.; Tachibana, Y.; Nakanishi, Y.; Bastow, K. F.; Nagai, M.; Wang, H. K.; Itokawa, H.; Lee, K. H. Bioorg. Med. Chem. 2002, 10, 3481. https://doi.org/10.1016/S0968-0896(02)00249-3
- Hakam, K.; Thielmann, M.; Thielmann, T.; Winterfeldt, E. Tetrahedron 1987, 43, 2035. https://doi.org/10.1016/S0040-4020(01)86785-5
- Karimi, S.; Grohmann, K. G. J. Org. Chem. 1995, 60, 554. https://doi.org/10.1021/jo00108a016
- Bateson, J. H.; Quinn, A. M.; Southgate, R. J. Chem. Soc. Chem. Commun. 1986, 1151.
- Yang, D.; Yan, Y.; Lui, B. J. Org. Chem. 2002, 67, 7429. https://doi.org/10.1021/jo026025t
- Meshram, H. M.; Reddy, P. N.; Sadashiv, K.; Yadav, J. S. Tetrahedron Lett. 2005, 46, 623. https://doi.org/10.1016/j.tetlet.2004.11.140
- Das, B.; Venkateswarlu, K.; Mahender, G.; Mahender, I. Tetrahedron Lett. 2005, 46, 3041. https://doi.org/10.1016/j.tetlet.2005.03.020
- Meshram, H. M.; Reddy, P. N.; Vishnu, K.; Sadashiv, K.; Yadav, J. S. Tetrahedron Lett. 2006, 47, 991. https://doi.org/10.1016/j.tetlet.2005.11.141
- Das, B.; Venkateswarlu, K.; Holla, H.; Krishnaiah, M. J. Mol. Catal. 2006, 253, 107. https://doi.org/10.1016/j.molcata.2006.03.011
- Pravst, I.; Zupan, M.; Stavber, S. Green Chem. 2006, 8, 1001. https://doi.org/10.1039/b608446j
- Khan, A. T.; Ali, M. A.; Goswami, P.; Choudhury, L. H. J. Org. Chem. 2006, 71, 8961. https://doi.org/10.1021/jo061501r
- Hosseinzadeh, R.; Tajbakhsh, M.; Mohadjerani, M.; Lasemi, Z. Monatsh Chem. 2009, 140, 57. https://doi.org/10.1007/s00706-008-0020-7
- Podgorsek, A.; Stavber, S.; Zupan, M.; Iskra, J. Green Chem. 2007, 9, 1212. https://doi.org/10.1039/b707065a
- Khan, A. T.; Goswami, P.; Choudhury, L. H. Tetrahedron Lett. 2006, 47, 2751. https://doi.org/10.1016/j.tetlet.2006.02.075
- Mendonça, G. F.; Sindra, H. C.; de Almeida, L. S.; Esteves, P. M.; de Mattos, M. C. S. Tetrahedron Lett. 2009, 50, 473. https://doi.org/10.1016/j.tetlet.2008.11.045
- Sarrafi, Y.; Sadatshahabi, M.; Alimohammadi, K. Chinese Chem. Lett. 2009, 20, 393. https://doi.org/10.1016/j.cclet.2008.11.022
- Pandey, K. L. Synlett. 2008, 947.
- Firouzabadi, H.; Iranpoor, N.; Ebrahimzadeh, F. Tetrahedron Lett. 2006, 47, 1771. https://doi.org/10.1016/j.tetlet.2006.01.033
- Khazaei, A.; Rostami, A.; Aminimanesh, A. J. Chin. Chem. Soc. 2006, 53, 437. https://doi.org/10.1002/jccs.200600056
- De Souza, S. P. L.; Da Silva, J. F. M.; De Mattos, M. C. S. J. Braz.Chem. Soc. 2003, 14, 832. https://doi.org/10.1590/S0103-50532003000500021
- Khazaei, A.; Aminimanesh, A.; Rostami, A. Phosphorus Sulfur Relat. Elem. 2004, 179, 2483. https://doi.org/10.1080/10426500490485471
- Shchez, E. I.; Fumarola, M. J. J. Org. Chem. 1982, 47, 1588. https://doi.org/10.1021/jo00347a048
- Yang, D.; Ye, X. Y.; Xu, M.; Pang, K. W.; Cheung, K. K. J. Am. Chem.Soc. 2000, 122, 1658. https://doi.org/10.1021/ja993598n
- Tateiwa, J. I.; Hosomi, A. Eur. J. Org. Chem. 2001, 1445.
- Arcus, C. L.; Barrett, G. C. J. Chem. Soc. 1960, 2098. https://doi.org/10.1039/jr9600002098
- Cherbuliez, E.; Weber, G.; Rabinowitz, J. Helv. Chim. Acta 1965, 48, 1423. https://doi.org/10.1002/hlca.19650480623
- Shahak, I.; Bergmann, E. D. J. Chem. Soc. 1960, 3225. https://doi.org/10.1039/jr9600003225
- De Souza, S. P. L.; Da Silva, J. F. M.; De Mattos, M. C. S. Synth. Commun. 2003, 33, 935. https://doi.org/10.1081/SCC-120016353
피인용 문헌
- ChemInform Abstract: Selective Monobromination of 1,3-Diones with N-Bromosaccharin/Mg(ClO4)2 System in Solution and under Solvent-Free Conditions. vol.42, pp.43, 2011, https://doi.org/10.1002/chin.201143037
- An Efficient Method for Multicomponent Synthesis of Spiro[4H-pyran-oxindole] Derivatives Catalyzed by Magnesium Perchlorate vol.34, pp.8, 2013, https://doi.org/10.5012/bkcs.2013.34.8.2431
- Use of Bromine and Bromo-Organic Compounds in Organic Synthesis vol.116, pp.12, 2016, https://doi.org/10.1021/acs.chemrev.5b00400
- An Efficient Synthesis of Spiro[indoline-3,9′-xanthene]trione Derivatives Catalyzed by Magnesium Perchlorate vol.22, pp.8, 2017, https://doi.org/10.3390/molecules22081295
- Structures in solid state and solution of dimethoxy curcuminoids: regioselective bromination and chlorination vol.7, pp.None, 2011, https://doi.org/10.1186/1752-153x-7-107
- Trihaloisocyanuric Acids as Atom‐Economic Reagents for Halogenation of Aromatics and Carbonyl Compounds in the Solid State by Ball Milling vol.2015, pp.12, 2015, https://doi.org/10.1002/ejoc.201403463
- Artificial sugar saccharin and its derivatives: role as a catalyst vol.10, pp.60, 2011, https://doi.org/10.1039/d0ra05974a