References
- North, M. In Comprehensive Organic Functional Group Transformation; Katritzky, A. R., Meth-Cohn, O., Rees, C. W., Eds.; Pergamon: Oxford, 1995.
- Allen, C. L.; Lapkin, A. A.; Williams, J. M. J. Tetrahedron Lett. 2008, 50, 4262.
- Yeom, S.-J.; Kim, H. J.; Oh, D.-K. Enzyme Microb. Technol. 2007, 41, 842. https://doi.org/10.1016/j.enzmictec.2007.07.007
- Addis, D.; Enthaler, S.; Junge, K.; Wendt, B.; Beller, M. Tetrahedron Lett. 2009, 50, 3654. https://doi.org/10.1016/j.tetlet.2009.03.108
- Caddick, S.; Haynes, K. K.; Judd, D. B.; Williams, M. R. V. Tetrahedron Lett. 2000, 41, 3513. https://doi.org/10.1016/S0040-4039(00)00410-X
- Hegedûs, L.; Máthe, T. Applied Catalysis A: General 2005, 296, 209. https://doi.org/10.1016/j.apcata.2005.08.024
- Hegedûs, L.; Mathe, T.; Karpati, T. Applied Catalysis A: General 2008, 349, 40.
- Gregg, B. T.; Golden, K. C.; Quinn, J. F.; Wang, H.-J.; Zhang, W.; Wang, R.; Wekesa, F.; Tymoshenko, D. O. Tetrahedron Lett. 2009, 50, 3978. https://doi.org/10.1016/j.tetlet.2009.04.081
- Khosropour, A. R.; Noei, J.; Mirjafari, A. J. Iran. Chem. Soc. 2010, 7, 752. https://doi.org/10.1007/BF03246065
- Amantini, D.; Beleggia, R.; Fringuelli, F.; Pizzo, F.; Vaccaro, L. J. Org. Chem. 2004, 69, 2896. https://doi.org/10.1021/jo0499468
- Iida, S.; Ohmura, R.; Togo, T. Tetrahedron 2009, 65, 6257. https://doi.org/10.1016/j.tet.2009.05.001
- Mori, N.; Togo, H. Synlett 2005, 1456.
- Iida, S.; Togo, T. Tetrahedron 2007, 63, 8274. https://doi.org/10.1016/j.tet.2007.05.106
- Rajagopal, G.; Kim S. S. Tetrahedron 2009, 65, 4351. https://doi.org/10.1016/j.tet.2009.03.073
- Movassagh, B.; Shokri, S. Tetrahedron Lett. 2005, 46, 6923. https://doi.org/10.1016/j.tetlet.2005.08.007
- Arote, N. D.; Bhalerao, D. S.; Akamanchi, K. G. Tetrahedron Lett. 2007, 48, 3651. https://doi.org/10.1016/j.tetlet.2007.03.137
- iHuber, V.; Bartsch, R. A. Tetrahedron 1998, 54, 9281. https://doi.org/10.1016/S0040-4020(98)00581-X
- Kangani, C. O.; Dayb, B. W.; Kelley, D. E. Tetrahedron Lett. 2007, 48, 5933. https://doi.org/10.1016/j.tetlet.2007.06.119
- Telvekar, V. N.; Rane, R. A. Tetrahedron Lett. 2007, 48, 6051. https://doi.org/10.1016/j.tetlet.2007.06.108
- Anand, N.; Owston, N. A.; Parker, A. J.; Slatford, P. A.; Williams, J. M. J. Tetrahedron Lett. 2007, 48, 7761. https://doi.org/10.1016/j.tetlet.2007.09.028
- Saedny, A. Synthesis 1985, 184.
- Kuo, C. W.; Zhu, J. L.; Wu, J. D.; Chu, C. M.; Yao, C. F.; Shia, K. S. Chem. Commun. 2007, 301.
- Zhou, S.; Addis, A.; Das, S.; Junge, K.; Beller, M. Chem. Commun. 2009, 4883.
- Chen, F.; Kuang, Y.; Dai, H.; Lu, L.; Huo, M. Synthesis 2003, 2629.
- Yamaguchi, K.; Mizuno, N. Angew. Chem., Int. Ed. 2003, 42, 1480. https://doi.org/10.1002/anie.200250779
- Elkaim, L.; Gacon, A. Tetrahedron Lett. 1997, 38, 3391. https://doi.org/10.1016/S0040-4039(97)00627-8
- Hendricson, J. B.; Hussoin, M. S. J. Org. Chem. 1987, 52, 4137. https://doi.org/10.1021/jo00227a041
- Wang, E.-C.; Lin, G.-J. Tetrahedron Lett. 1998, 39, 4047. https://doi.org/10.1016/S0040-4039(98)00654-6
- Smith, M.; March, J. Advanced Organic Chemistry: Structure, 6th ed.; Wiley Interscience: Chichester, 2007.
- Yale, H. L.; Spitzmiller, E. R. J. Heterocycl. Chem. 1978, 15, 1373. https://doi.org/10.1002/jhet.5570150825
- Chandrasekhar, S.; Gopalaiah, K. Tetrahedron Lett. 2003, 44, 7437. https://doi.org/10.1016/j.tetlet.2003.08.038
- Li, D.; Shi, F.; Guo, S.; Deng, Y. Tetrahedron Lett. 2005, 46, 671. https://doi.org/10.1016/j.tetlet.2004.11.116
- Gucma, M.; Golebiewski, W. M. Synthesis 2008, 1997.
- Yadav, L. D. S.; Srivastava, V. P.; Patel, R. Tetrahedron Lett. 2009, 50, 5532. https://doi.org/10.1016/j.tetlet.2009.07.100
- Kalkhambkar, R. G.; Bunge, S. D.; Laali, K. K. Tetrahedron Lett. 2011, 52, 5184. https://doi.org/10.1016/j.tetlet.2011.07.135
- Tamami, B.; Kiasat, A. R. Synth. Commun. 2000, 30, 235. https://doi.org/10.1080/00397910008087314
- Wang, X. C.; Li, L.; Quan, Z. J.; Gong, H. P.; Ye, H. L.; Cao, X. F. Chin. Chem. Lett. 2009, 20, 651.
- Makarycheva-Mikhailova, A. V.; Bokach, N. A.; Haukka, M.; Kukushkin, V. Y. Inorg. Chim. Acta 2003, 356, 382. https://doi.org/10.1016/S0020-1693(03)00275-5
- Yang, S. H.; Chang, S. Org. Lett. 2001, 3, 4209. https://doi.org/10.1021/ol0168768
- Choi, E.; Lee, C.; Na, Y.; Chang, S. Org. Lett. 2002, 4, 2369.
- Ishihara, K.; Furuya, Y.; Yamamoto, H. Angew. Chem., Int. Ed. 2002, 41, 2983. https://doi.org/10.1002/1521-3773(20020816)41:16<2983::AID-ANIE2983>3.0.CO;2-X
- Yan, P.; Batamack, P.; Prakash, G. K. S.; Olah, G. A. Catal. Lett. 2005, 101, 141. https://doi.org/10.1007/s10562-005-4880-8
- Yamaguchi, K.; Fujiwara, H.; Ogasawara, Y.; Kotani, M.; Mizuno, N. Angew. Chem., Int. Ed. 2007, 46, 3922. https://doi.org/10.1002/anie.200605004
- Attanasi, O.; Palma, P.; Serra-Zanetti, F. Synthesis 1983, 741.
- Kim, H. S.; Kim, S. H.; Kim, J. N. Tetrahedron Lett. 2009, 50, 1717. https://doi.org/10.1016/j.tetlet.2009.01.150
- Saha, D.; Saha, A.; Ranu, B. C. Tetrahedron Lett. 2009, 50, 6088. https://doi.org/10.1016/j.tetlet.2009.08.069
- Iranpoor, N.; Zeynizadeh, B. Synth. Commun. 1999, 29, 2747. https://doi.org/10.1080/00397919908086440
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