Browse > Article
http://dx.doi.org/10.5012/bkcs.2013.34.12.3539

Organocatalytic Enantioselective Friedel-Crafts Reaction of Naphthol with β,γ-Unsaturated α-Keto Esters  

Lee, Hyun A (Department of Chemistry, Soonchunhyang University)
Kim, Dae Young (Department of Chemistry, Soonchunhyang University)
Publication Information
Keywords
Asymmetric catalysis; ${\beta},{\gamma}$-Unsaturated ${\alpha}$-keto esters; Friedel-Crafts reaction; Organocatalysis; Chromanes;
Citations & Related Records
Times Cited By KSCI : 8  (Citation Analysis)
연도 인용수 순위
1 (e) Shi, Z.-H.; Sheng, H.; Yang, K.-F.; Jiang, J.-X.; Lai, G.-Q.; Lu, Y.; Xu, L.-W. Eur. J. Org. Chem. 2011, 66.
2 (a) Wang, X.-S.; Zheng, C.-W.; Zhao, S.-L.; Chai, Z.; Zhao, G.; Yang, G.-S. Tetrahedron: Asymmetry 2008, 19, 2699.   DOI   ScienceOn
3 (b) Jiang, X.; Wu, L.; Xing, Y.; Wang, L.; Wang, S.; Chen, Z.; Wang, R. Chem. Commun. 2012, 48, 446.   DOI   ScienceOn
4 (a) Kang, Y. K.; Kim, S. M.; Kim, D. Y. J. Am. Chem. Soc. 2010, 132, 11847.   DOI   ScienceOn
5 (b) Kang, S. H.; Kim, D. Y. Adv. Synth. Catal. 2010, 352, 2783.   DOI   ScienceOn
6 (c) Kang, Y. K.; Kim, D. Y. Curr. Org. Chem. 2010, 14, 917.   DOI   ScienceOn
7 (d) Moon, H. W.; Kim, D. Y. Tetrahedron Lett. 2010, 51, 2906.   DOI   ScienceOn
8 (e) Kang, Y. K. Kim, D. Y. Tetrahedron Lett. 2011, 52, 2356.   DOI   ScienceOn
9 (f) Lee, H. J. Kang, S. H.; Kim, D. Y. Synlett 2011, 1559.
10 (g) Woo, S. B.; Kim, D. Y. Beilstein J. Org. Chem. 2012, 8, 699.   DOI   ScienceOn
11 (h) Lee, H. J.; Woo, S. B.; Kim, D. Y. Tetrahedron Lett. 2012, 53, 3374.   DOI   ScienceOn
12 (i) Moon, H. W.; Kim, D. Y. Bull. Korean Chem. Soc. 2012, 33, 2845.   DOI   ScienceOn
13 (j) Lee, H. J.; Woo, S. B.; Kim, D. Y. Molecules 2012, 17, 7523.   DOI   ScienceOn
14 (k) Lee, H. J.; Kim, S. M.; Kim, D. Y. Tetrahedron Lett. 2012, 53, 3437.   DOI   ScienceOn
15 (l) Lee, H. J.; Kim, D. Y. Bull. Korean Chem. Soc. 2012, 33, 3171.   DOI   ScienceOn
16 (m) Moon, H. W.; Kim, D. Y. Tetrahedron Lett. 2012, 53, 6569.   DOI   ScienceOn
17 (n) Kang, Y. K.; Kim, H. H.; Koh, K. O.; Kim, D. Y. Tetrahedron Lett. 2012, 53, 3811.   DOI   ScienceOn
18 (o) Kwon, B. K.; Mang, J. Y.; Kim, D. Y. Bull. Korean Chem. Soc. 2012, 33, 2481.   DOI   ScienceOn
19 (p) Lee, H. J.; Kim, D. Y. Tetrahedron Lett. 2012, 53, 6984.   DOI   ScienceOn
20 (q) Lim, Y. J.; Kim, D. Y. Bull. Korean Chem. Soc. 2012, 33, 1825.   DOI   ScienceOn
21 (s) Lim, Y. J.; Kim, D. Y. Bull. Korean Chem. Soc. 2013, 34, 1955.   DOI   ScienceOn
22 (t) Woo, S. B.; Suh, C. W.; Koh, K. O.; Kim, D. Y. Tetrahedron Lett. 2013, 54, 3359.   DOI   ScienceOn
23 (u) Suh, C. W.; Chang, C. W.; Choi, K. W.; Lim, Y. J.; Kim, D. Y. Tetrahedron Lett. 2013, 54, 3651.   DOI   ScienceOn
24 (a) Shi, Z.; He, C. J. Am. Chem. Soc. 2004, 126, 13596.   DOI   ScienceOn
25 (a) Kang, S. H.; Kwon, B. K. Kim, D. Y. Tetrahedron Lett. 2011, 52, 3247.   DOI   ScienceOn
26 (a) Ellis, G. P.; Lockhart, I. M. The Chemistry of Heterocyclic Compounds, Chromenes,Chromanones, and Chromones; Ellis,G. P., Ed.; Wiley-VCH: New York, 2007; Vol. 31, pp 1-1196.
27 (b) Horton, D. A.; Bourne, G. T.; Smythe, M. L. Chem. Rev. 2003, 103, 893.   DOI   ScienceOn
28 (b) Ulgheri, F.; Marchetti, M.; Piccolo, O. J. Org. Chem. 2007, 72, 6056.   DOI   ScienceOn
29 (c) Jagdale, A. R.; Sudalai, A. Tetrahedron Lett. 2007, 48, 4895.   DOI   ScienceOn
30 (a) Hayashi, T. Pure. Appl. Chem. 2004, 76, 465.   DOI   ScienceOn
31 (b) Paquin, J. F.; Defieber, C.; Stephenson, C. R.; Carreira, E. M. J. Am. Chem. Soc. 2005, 127, 10850.   DOI   ScienceOn
32 (c) Fessard, T. C.; Andrews, S. P.; Motoyoshi, H.; Carreira, E. M. Angew. Chem., Int. Ed. 2007, 46, 9331.   DOI   ScienceOn
33 (a) Poulsen, T. B.; Jorgensen, K. A. Chem. Rev, 2008, 108, 2903.   DOI   ScienceOn
34 (b) You, S.-L.; Cai, Q.; Zeng, M. Chem. Soc. Rev. 2009, 38, 210.
35 (c) Bandini, M.; Umani-Ronchi, A. Catalytic Asymmetric Friedel-Crafts Alkylations; Wiley-VCH: Weinheim, 2009.
36 (a) Evans, D. A.; Fandrick, K. R.; Song, H.-J. J. Am. Chem. Soc. 2005, 127, 8942.   DOI   ScienceOn
37 (b) Palomo, C.; Oiarbide, M.; Kardak, B. G.; Garcia J. M.; Linden, A. J. Am. Chem. Soc. 2005, 127, 4154.   DOI   ScienceOn
38 (e) Singh, P. K.; Singh, V. K. Org. Lett. 2008, 10, 4121.   DOI   ScienceOn
39 (c) Yang, H.; Hong, Y.-T.; Kim, S. Org. Lett. 2007, 9, 2281.   DOI   ScienceOn
40 (d) Blay, G.; Fernandez, I.; Pedro, J. R.; Vila, C. Org. Lett. 2007, 9, 2601.   DOI   ScienceOn
41 (a) Cai, C.; Zhao, Z.-A.; You, S.-L. Angew. Chem., Int. Ed. 2009, 48, 7428.   DOI   ScienceOn
42 (b) Sheng, Y.-F.; Gu, Q.; Zhang, A.-J.; You, S.-L. J. Org. Chem. 2009, 74, 6899.   DOI   ScienceOn
43 (c) Jiang, H.; Paixoa, M. W.; Monge, D.; Jorgensen, K. A. J. Am. Chem. Soc. 2010, 132, 2775.   DOI   ScienceOn
44 (d) Bachu P.; Akiyama, T. Chem. Commun. 2010, 46, 4112.   DOI   ScienceOn
45 (b) Kang, Y. K.; Suh, K. H.; Kim, D. Y. Synlett 2011, 1125.
46 (c) Kang, Y. K.; Suh, K. H.; Kim, D. Y. Synlett 2011, 1125.
47 (d) Lee, H. J.; Kim, D. Y. Bull. Korean Chem. Soc. 2012, 33, 3537.   DOI   ScienceOn
48 (e) Lee, H. J.; Kim, D. Y. Synlett 2012, 1629.
49 (f) Suh, C. W.; Han, T. H.; Kim, D. Y. Bull. Korean Chem. Soc. 2013, 34, 1623.   DOI   ScienceOn
50 (g) Lee, J. H.; Kim, D. Y. Bull. Korean Chem. Soc. 2013, 34, 1619.   DOI   ScienceOn
51 (r) Kang, Y. K.; Lee, H. J.; Moon, H. W.; Kim, D. Y. RSC Adv. 2013, 3, 1332.   DOI