References
- Leonard, J. Contemp. Org. Synth. 1994, 1, 387. https://doi.org/10.1039/co9940100387
- Perlmutter, P. Conjugate Addition Reactions in Organic Synthesis; Pergamon: Oxford, 1992.
- Krause, N.; Hoffmann-Röder, A. Synthesis 2001, 171.
- Berner, O. M.; Tedeschi, L.; Enders, D. Eur. J. Org. Chem. 2002, 1877.
- Christoffers, J.; Baro, A. Angew. Chem., Int. Ed. 2003, 42, 1688. https://doi.org/10.1002/anie.200201614
- Connon, S. J. Angew. Chem., Int. Ed. 2006, 45, 3909. https://doi.org/10.1002/anie.200600529
- Doyle, A. G.; Jacobsen, E. N. Chem. Rev. 2007, 107, 5713. https://doi.org/10.1021/cr068373r
- Yu, X.; Wang, W. Chem. Asian J. 2008, 3, 516. https://doi.org/10.1002/asia.200700415
- Connon, S. J. Synlett 2009, 354.
- Tsogoeva, S. B. Eur. J. Org. Chem. 2007, 1701.
- Almasi, D.; Alonso, D. A.; Najera, D. Tetrahedron: Asymmetry 2007, 18, 299. https://doi.org/10.1016/j.tetasy.2007.01.023
- Ogawa, C.; Kizu, K.; Shimizu, H.; Takeuchi, M.; Kobayashi, S. Chem. Asian J. 2006, 1-2, 121.
- Wu, F.; Li, H.; Hong, R.; Deng, L. Angew. Chem., Int. Ed. 2006, 45, 947. https://doi.org/10.1002/anie.200502658
- Yang, J.; Li, W.; Jin, Z.; Liang, X.; Ye, J. Org. Lett. 2010, 12, 5218. https://doi.org/10.1021/ol102256v
- Wingard, L. B.; OReilly, R. A.; Levy, G. Clin. Pharmacol. Ther. 1978, 23, 212.
- Thomassigny, C.; Prim, D.; Greck, C. Tetrahedron Lett. 2006, 47, 1117. https://doi.org/10.1016/j.tetlet.2005.12.028
- Cravotto, G.; Nano, G. M.; Palmisano, G.; Tagliapietra, S. Tetrahedron: Asymmetry 2001, 12, 707. https://doi.org/10.1016/S0957-4166(01)00124-0
- Tsuchiya, Y.; Hamashima, Y.; Sodeoka, M. Org. Lett. 2006, 8, 485.
- Dong, Z.-H.; Wang, L.-J.; Chen, X.-H.; Liu, X.-H.; Lin, L.-L.; Feng, X.-M. Eur. J. Org. Chem. 2009, 5192.
- Rogozinska, M.; Adamkiewicz, A.; Mlynarski, J. Green Chem. 2010, 13, 1155.
- Mei, R.-Q.; Xu, X.-Y.; Li, Y.-C.; Fu, J.-Y.; Huang, Q.-C.; Wang, L.-X. Tetrahedron Lett. 2011, 52, 1566. https://doi.org/10.1016/j.tetlet.2011.01.054
- Zhu, X.; Lin, A.; Shi, Y.; Guo, J.; Zhu, C.; Cheng, Y. Org. Lett. 2011, 13, 4382. https://doi.org/10.1021/ol201715h
- Kim, D. Y.; Park E. J. Org. Lett. 2002, 4, 545. https://doi.org/10.1021/ol010281v
- Park, E. J.; Kim, M. H.; Kim, D. Y. J. Org. Chem. 2004, 69, 6897. https://doi.org/10.1021/jo0401772
- Kim, S. M.; Kim, H. R.; Kim, D. Y. Org. Lett. 2005, 7, 2309. https://doi.org/10.1021/ol050413a
- Kim, H. R.; Kim, D. Y. Tetrahedron Lett. 2005, 46, 3115. https://doi.org/10.1016/j.tetlet.2005.02.164
- Kang, Y. K; Cho, M. J.; Kim, S. M.; Kim, D. Y. Synlett 2007, 1135.
- Lee, J. H.; Kim, D. Y. Adv. Synth. Catal. 2009, 351, 1779. https://doi.org/10.1002/adsc.200900268
- Kang, Y. K.; Kim, D. Y. J. Org. Chem. 2009, 74, 5734. https://doi.org/10.1021/jo900880t
- Kang, Y. K.; Kim, S. M.; Kim, D. Y. J. Am. Chem. Soc. 2010, 132, 11847. https://doi.org/10.1021/ja103786c
- Kang, S. H.; Kim, D. Y. Adv. Synth. Catal. 2010, 352, 2783. https://doi.org/10.1002/adsc.201000515
- Kang, Y. K.; Kim, D. Y. Curr. Org. Chem. 2010, 14, 917. https://doi.org/10.2174/138527210791111768
- Kang, Y. K. Kim, D. Y. Tetrahedron Lett. 2011, 52, 2356. https://doi.org/10.1016/j.tetlet.2011.02.087
- Lee, H. J.; Kim, J. H.; Kim, D. Y. Bull. Korean Chem. Soc. 2011, 32, 785. https://doi.org/10.5012/bkcs.2011.32.3.785
- Lee, H. J.; Kang, S. H.; Kim, D. Y. Bull. Korean Chem. Soc. 2011, 32, 1125. https://doi.org/10.5012/bkcs.2011.32.4.1125
- Kang, Y. K.; Yoon, S. J.; Kim, D. Y. Bull. Korean Chem. Soc. 2011, 32, 1195. https://doi.org/10.5012/bkcs.2011.32.4.1195
- Kwon, Y. K.; Kang, Y. K.; Kim, E. Y. Bull. Korean Chem. Soc. 2011, 32, 1773. https://doi.org/10.5012/bkcs.2011.32.5.1773
- Kim, D. Y.; Huh, S. C.; Kim, S. M. Tetrahedron Lett. 2001, 42, 6299.
- Kim, D. Y.; Huh, S. C. Tetrahedron 2001, 57, 8933. https://doi.org/10.1016/S0040-4020(01)00891-2
- Kang, Y. K.; Kim, D. Y. Tetrahedron Lett. 2006, 47, 4565. https://doi.org/10.1016/j.tetlet.2006.05.003
- Lee, J. H.; Bang, H. T.; Kim, D. Y. Synlett 2008, 1821.
- Kim, S. M.; Lee, J. H.; Kim, D. Y. Synlett 2008, 2659.
- Jung, S. H.; Kim, D. Y. Tetrahedron Lett. 2008, 49, 5527. https://doi.org/10.1016/j.tetlet.2008.07.041
- Kwon, B. K.; Kim, S. M.; Kim, D. Y. J. Fluorine Chem. 2009, 130, 759. https://doi.org/10.1016/j.jfluchem.2009.06.002
- Mang, J. Y.; Kwon, D. G.; Kim, D. Y. J. Fluorine Chem. 2009, 130, 259. https://doi.org/10.1016/j.jfluchem.2008.11.001
- Oh, Y.; Kim, S. M.; Kim, D. Y. Tetrahedron Lett. 2009, 50, 4674. https://doi.org/10.1016/j.tetlet.2009.06.003
- Kang, S. H.; Kang, Y. K.; Kim, D. Y. Tetrahedron, 2009, 65, 5676. https://doi.org/10.1016/j.tet.2009.05.037
- Moon, H. W.; Kim, D. Y. Tetrahedron Lett. 2010, 51, 2906. https://doi.org/10.1016/j.tetlet.2010.03.105
- Moon, H. W.; Cho, M. J.; Kim, D. Y. Tetrahedron Lett. 2009, 50, 4896. https://doi.org/10.1016/j.tetlet.2009.06.056
- Lee, H. J. Kang, S. H.; Kim, D. Y. Synlett 2011, 1559.
- Kang, S. H.; Kwon, B. K.; Kim, D. Y. Tetrahedron Lett. 2011, 52, 3247. https://doi.org/10.1016/j.tetlet.2011.04.084
- Kang, Y. K.; Suh, K. H.; Kim, D. Y. Synlett 2011, 1125.
- Moon, H. W.; Kim, D. Y. Bull. Korean Chem. Soc. 2011, 32, 291. https://doi.org/10.5012/bkcs.2011.32.1.291
- Lee, H. J.; Chae, Y. M.; Kim, D. Y. Bull. Korean Chem. Soc. 2011, 32, 2875. https://doi.org/10.5012/bkcs.2011.32.8.2875
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