References
- Basavaiah, D.; Rao, A. J.; Satyanarayana, T. Chem. Rev. 2003, 103, 811-891. https://doi.org/10.1021/cr010043d
- Gowrisankar, S.; Lee, H. S.; Kim, S. H.; Lee, K. Y.; Kim, J. N. Tetrahedron 2009, 65, 8769-8780. https://doi.org/10.1016/j.tet.2009.07.034
- Kim, J. N.; Lee, K. Y. Curr. Org. Chem. 2002, 6, 627-645. https://doi.org/10.2174/1385272023374094
- Lee, K. Y.; Gowrisankar, S.; Kim, J. N. Bull. Korean Chem. Soc. 2005, 26, 1481-1490. https://doi.org/10.5012/bkcs.2005.26.10.1481
- Radha Krishna, P.; Sachwani, R.; Reddy, P. S. Synlett 2008, 2897-2912.
- Declerck, V.; Martinez, J.; Lamaty, F. Chem. Rev. 2009, 109, 1-48. https://doi.org/10.1021/cr068057c
- Singh, V.; Batra, S. Tetrahedron 2008, 64, 4511-4574. https://doi.org/10.1016/j.tet.2008.02.087
- Basavaiah, D.; Reddy, B. S.; Badsara, S. S. Chem. Rev. 2010, 110, 5447-5674 and further references cited therein. https://doi.org/10.1021/cr900291g
- Song, Y.; Ke, H.; Wang, N.; Wang, L.; Zou, G. Tetrahedron 2009, 65, 9086-9090. https://doi.org/10.1016/j.tet.2009.09.049
- Hsu, J.-C.; Yen, Y.-H.; Chu, Y.-H. Tetrahedron Lett. 2004, 45, 4673-4676. https://doi.org/10.1016/j.tetlet.2004.04.099
- Jeong, Y.; Ryu, J.-S. J. Org. Chem. 2010, 75, 4183-4191. https://doi.org/10.1021/jo100618d
- Johnson, C. L.; Donkor, R. E.; Nawaz, W.; Karodia, N. Tetrahedron Lett. 2004, 45, 7359-7361. https://doi.org/10.1016/j.tetlet.2004.07.155
- Rosa, J. N.; Afonso, C. A. M.; Santos, A. G. Tetrahedron 2001, 57, 4189-4193. https://doi.org/10.1016/S0040-4020(01)00316-7
- Chandrasekhar, S.; Narsihmulu, C.; Sartitha, B.; Sultana, S. S. Tetrahedron Lett. 2004, 45, 5865-5867. https://doi.org/10.1016/j.tetlet.2004.05.153
- Cho, J.-H.; Ko, S. Y.; Oh, E.; Park, J. C.; Yoo, J. U. Helv. Chim. Acta 2002, 85, 3994-3999. https://doi.org/10.1002/1522-2675(200211)85:11<3994::AID-HLCA3994>3.0.CO;2-2
- Lee, W.-D.; Yang, K.-S.; Chen, K. Chem. Commun. 2001, 1612-1613.
- Nakano, A.; Kawahara, S.; Akamatsu, S.; Morokuma, K.; Nakatani, M.; Iwabuchi, Y.; Takahashi, K.; Ishihara, J.; Hatakeyama, S. Tetrahedron 2006, 62, 381-389. https://doi.org/10.1016/j.tet.2005.09.072
- Iwabuchi, Y.; Nakatani, M.; Yokoyama, N.; Hatakeyama, S. J. Am. Chem. Soc. 1999, 121, 10219-10220. https://doi.org/10.1021/ja992655+
- Leadbeater, N. E.; van der Pol, C. J. Chem. Soc., Perkin Trans. 1 2001, 2831-2835.
- Kawamura, M.; Kobayashi, S. Tetrahedron Lett. 1999, 40, 1539-1542. https://doi.org/10.1016/S0040-4039(98)02705-1
- Bhuniya, D.; Narayanan, S.; Lamba, T. S.; Krishna Reddy, K. V. S. R. Synth. Commun. 2003, 33, 3717-3726. https://doi.org/10.1081/SCC-120025180
- Maher, D. J.; Connon, S. J. Tetrahedron Lett. 2004, 45, 1301-1305. https://doi.org/10.1016/j.tetlet.2003.11.062
- Shi, M.; Liu, X.-G. Org. Lett. 2008, 10, 1043-1046. https://doi.org/10.1021/ol7028806
- Amarante, G. W.; Benassi, M.; Milagre, H. M. S.; Braga, A. A. C.; Maseras, F.; Eberlin, M. N.; Coelho, F. Chem. Eur. J. 2009, 15, 12460-12469. https://doi.org/10.1002/chem.200900966
- Aggarwal, V. K.; Emme, I.; Fulford, S. Y. J. Org. Chem. 2003, 68, 692-700. https://doi.org/10.1021/jo026671s
- Aggarwal, V. K.; Dean, D. K.; Mereu, A.; Williams, R. J. Org. Chem. 2002, 67, 510-514. https://doi.org/10.1021/jo016073y
- Yu, C.; Liu, B.; Hu, L. J. Org. Chem. 2001, 66, 5413-5418. https://doi.org/10.1021/jo015628m
- de Souza, R. O. M. A.; Pereira, V. L. P.; Esteves, P. M.; Vasconcellos, M. L. A. A. Tetrahedron Lett. 2008, 49, 5902-5905. https://doi.org/10.1016/j.tetlet.2008.07.140
- Gruttadauria, M.; Giacalone, F.; Meo, P. L.; Marculescu, A. M.; Riela, S.; Noto, R. Eur. J. Org. Chem. 2008, 1589-1596.
- Aggarwal, V. K.; Mereu, A.; Tarver, G. J.; McCague, R. J. Org. Chem. 1998, 63, 7183-7189. https://doi.org/10.1021/jo980421n
- Yang, K.-S.; Lee, W.-D.; Pan, J.-F.; Chen, K. J. Org. Chem. 2003, 68, 915-919. https://doi.org/10.1021/jo026318m
- Yukawa, T.; Seelig, B.; Xu, Y.; Morimoto, H.; Matsunaga, S.; Berkessel, A.; Shibasaki, M. J. Am. Chem. Soc. 2010, 132, 11988-11992. https://doi.org/10.1021/ja103294a
- Shi, M.; Liu, Y.-H. Org. Biomol. Chem. 2006, 1468-1470.
- Shi, M.; Chen, L.-H.; Li, C.-Q. J. Am. Chem. Soc. 2005, 127, 3790-3800. https://doi.org/10.1021/ja0447255
- Liu, Y.-h.; Shi, M. Adv. Synth. Catal. 2008, 350, 122-128. https://doi.org/10.1002/adsc.200700338
- Yamada, Y. M. A.; Ikegami, S. Tetrahedron Lett. 2000, 41, 2165-2169. https://doi.org/10.1016/S0040-4039(00)00125-8
- Zhong, W.; Zheng, Y.; Zhou, J.; Shen, Y. Synlett 2010, 3057-3060.
- Garnier, J.-M.; Anstiss, C.; Liu, F. Adv. Synth. Catal. 2009, 351, 331-338. https://doi.org/10.1002/adsc.200800679
- McDougal, N. T.; Schaus, S. E. J. Am. Chem. Soc. 2003, 125, 12094-12095. https://doi.org/10.1021/ja037705w
- McDougal, N. T.; Trevellini, W. L.; Rodgen, S. A.; Kliman, L. T.; Schaus, S. E. Adv. Synth. Catal. 2004, 346, 1231-1240. https://doi.org/10.1002/adsc.200404122
- Narender, P.; Gangadasu, B.; Ravinder, M.; Srinivas, U.; Swamy, G. Y. S. K.; Ravikumar, K.; Rao, V. J. Tetrahedron 2006, 62, 954-959. https://doi.org/10.1016/j.tet.2005.10.032
- Grainger, R. S.; Leadbeater, N. E.; Pamies, A. M. Catal. Commun. 2002, 3, 449- 452. https://doi.org/10.1016/S1566-7367(02)00178-4
- Abermil, N.; Masson, G.; Zhu, J. Org. Lett. 2009, 11, 4648-4651. https://doi.org/10.1021/ol901920s
- Abermil, N.; Masson, G.; Zhu, J. J. Am. Chem. Soc. 2008, 130, 12596-12597. https://doi.org/10.1021/ja805122j
- Cai, J.; Zhou, Z.; Zhao, G.; Tang, C. Org. Lett. 2002, 4, 4723-4725. https://doi.org/10.1021/ol027197f
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