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http://dx.doi.org/10.5012/bkcs.2006.27.2.319

Synthesis of Cyclopropane Derivatives Starting from the Baylis-Hillman Adducts Using Sulfur Ylide Chemistry  

Lee, Ka-Young (Department of Chemistry and Institute of Basic Science, Chonnam National University)
Kim, Seung-Chan (Department of Chemistry and Institute of Basic Science, Chonnam National University)
Kim, Jae-Nyoung (Department of Chemistry and Institute of Basic Science, Chonnam National University)
Publication Information
Bulletin of the Korean Chemical Society / v.27, no.2, 2006 , pp. 319-321 More about this Journal
Keywords
Cyclopropane; Baylis-Hillman adducts; Sulfur ylide; Michael acceptor;
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1 Donaldson, W. A. Tetrahedron 2001, 57, 8589   DOI   ScienceOn
2 Salaun, J. Chem. Rev. 1989, 89, 1247   DOI
3 Li, A.-H.; Dai, L.-X.; Aggarwal, V. K. Chem. Rev. 1997, 97, 2341   DOI   ScienceOn
4 Midura, W. H.; Mikolajczyk, M. Tetrahedron Lett. 2002, 43, 3061   DOI   ScienceOn
5 Cebula, R. E. J.; Hanna, M. R.; Theberge, C. R.; Verbicky, C. A.; Zercher, C. K. Tetrahedron Lett. 1996, 37, 8341   DOI   ScienceOn
6 Bremeyer, N.; Smith, S. C.; Ley, S. V.; Gaunt, M. J. Angew. Chem. Int. Ed. 2004, 43, 2681   DOI   ScienceOn
7 Oswald, M. F.; Raw, S. A.; Taylor, R. J. K. Chem. Commun. 2005, 2253
8 Oswald, M. F.; Raw, S. A.; Taylor, R. J. K. Org. Lett. 2004, 6, 3997   DOI   ScienceOn
9 Jain, S. L.; Sain, B. Tetrahedron Lett. 2005, 46, 37   DOI   ScienceOn
10 Papageorgiou, C. D.; Ley, S. V.; Gaunt, M. J. Angew. Chem. Int. Ed. 2003, 42, 828   DOI   ScienceOn
11 Liao, W.-W.; Li, K.; Tang, Y. J. Am. Chem. Soc. 2003, 125, 13030   DOI   ScienceOn
12 Avery, T. D.; Fallon, G.; Greatrex, B. W.; Pyke, S. M.; Taylor, D. K.; Tiekink, E. R. T. J. Org. Chem. 2001, 66, 7955   DOI   ScienceOn
13 Ye, S.; Huang, Z.-Z.; Xia, C.-A.; Tang, Y.; Dai, L.-X. J. Am. Chem. Soc. 2002, 124, 2432   DOI   ScienceOn
14 Kowalkowska, A.; Sucholbiak, D.; Jonczyk, A. Eur. J. Org. Chem. 2005, 925
15 Lee, P. H.; Kim, J. S.; Kim, Y. C.; Kim, S. Tetrahedron Lett. 1993, 34, 7583   DOI   ScienceOn
16 Bernard, A. M.; Frongia, A.; Piras, P. P.; Secci, F.; Spiga, M. Org. Lett. 2005, 7, 4565   DOI   ScienceOn
17 Gowrisankar, S.; Lee, K. Y.; Kim, J. N. Tetrahedron Lett. 2005, 46, 4859   DOI   ScienceOn
18 Lee, K. Y.; Gowrisankar, S.; Kim, J. N. Tetrahedron Lett. 2005, 46, 5387   DOI   ScienceOn
19 Basavaiah, D.; Hyma, R. S.; Padmaja, K.; Krishnamacharyulu, M. Tetrahedron 1999, 55, 6971   DOI   ScienceOn
20 Crist, R. M.; Reddy, P. V.; Borhan, B. Tetrahedron Lett. 2001, 42, 619   DOI   ScienceOn
21 Buchholz, R.; Hoffmann, H. M. R. Helv. Chim. Acta 1991, 74, 1213   DOI
22 Lee, K. Y.; Gowrisankar, S.; Kim, J. N. Bull. Korean Chem. Soc. 2005, 26, 1481 and further references cited therein   DOI   ScienceOn
23 Muller, P.; Ghanem, A. Org. Lett. 2004, 6, 4347   DOI   ScienceOn
24 Lee, C. G.; Lee, K. Y.; Lee, S.; Kim, J. N. Tetrahedron 2005, 61, 1493   DOI   ScienceOn
25 Kondo, K.; Matsui, K.; Takahatake, Y. Tetrahedron Lett. 1976, 17, 4359   DOI   ScienceOn
26 Jonczyk, A.; Konarska, A. Synlett 1999, 1085
27 Honda, M.; Naitou, T.; Hoshino, H.; Takagi, S.; Segi, M.; Nakajima, T. Tetrahedron Lett. 2005, 46, 7345   DOI   ScienceOn
28 Leroy, B. Tetrahedron Lett. 2005, 46, 7563   DOI   ScienceOn
29 Hubner, J.; Liebscher, J.; Patzel, M. Tetrahedron 2002, 58, 10485   DOI   ScienceOn