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http://dx.doi.org/10.5012/bkcs.2004.25.1.033

A Facile Synthesis of 4-Arylidene-2-substituted Isoxazolidin-5-ones from Baylis-Hillman Acetates  

Lee, Ka-Young (Department of Chemistry and Institute of Basic Science, Chonnam National University)
Lee, Chang-Gon (Department of Chemistry and Institute of Basic Science, Chonnam National University)
Kim, Taek-Hyeon (Faculty of Applied Chemistry, 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.25, no.1, 2004 , pp. 33-34 More about this Journal
Keywords
Baylis-Hillman acetates; Isoxazolidin-5-ones; N-Alkylhydroxylamines; Lithium perchlorate;
Citations & Related Records
Times Cited By KSCI : 2  (Citation Analysis)
Times Cited By Web Of Science : 6  (Related Records In Web of Science)
Times Cited By SCOPUS : 6
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[] / The cyclization of 3a is not effective in the presence of p-TsOH or acetic acid in benzene or in toluene
2 Lee, K. Y.; Kim, J. M.; Kim, J. N. Tetrahedron Lett. 2003, 44, 6737.   DOI   ScienceOn
3 Lee, H.- S.; Park, J.-S.; Kim, B. M.; Gellman, S. H. J. Org. Chem. 2003, 68, 1575.   DOI   ScienceOn
4 Shindo, M.; Itoh, K.; Tsuchiya, C.; Shishido, K. Org. Lett. 2002, 4, 3119.   DOI   ScienceOn
5 Ishikawa, T.; Kudoh, T.; Yoshida, J.; Yasuhara, A.; Manabe, S.; Saito, S. Org. Lett. 2002, 4, 1907.   DOI   ScienceOn
6 Im, Y. J.; Lee, C. G.; Kim, H. R.; Kim, J. N. Tetrahedron Lett. 2003, 44, 2987.   DOI   ScienceOn
7 Im, Y. J.; Kim, J. M.; Kim, J. N. Bull. Korean Chem. Soc. 2002, 23, 1361.   DOI   ScienceOn
8 Niu, D.; Zhao, K. J. Am. Chem. Soc. 1999, 121, 2456.   DOI   ScienceOn
9 Basanaiah, D.; Rao, A. J.; Satyanarayana, T. Chem. Rev. 2003, 103, 811 and further references cited therein.   DOI   ScienceOn
10 Stamm, H.; Hoenicke, J. Ann. 1971, 748, 143.
11 Im, Y. J.; Na, J. E.; Kim, J. N. Bull. Korean Chem. Soc. 2003, 24, 511.   DOI   ScienceOn
12 Maciejewski, P. I.; Belzecki, C.; Chmielewski, M. Tetrahedron 1992, 48, 10363.   DOI   ScienceOn
13 Pan, S.; Wang, J.; Zhao, K. J. Org. Chem. 1999, 64, 4.   DOI   ScienceOn
14 Sibi, M. P.; Liu, M. Org. Lett. 2000, 2, 3393.   DOI   ScienceOn
15 Baldwin, J. E.; Harwood, L. M.; Lombard, M. J. Tetrahedron 1984, 40, 4363.   DOI   ScienceOn
16 Kang, H. Y.; Cho, Y. S.; Koh, H. Y.; Chang, M. H. Chem. Lett. 1991, 1333.
17 Moglioni, A. G.; Muray, E.; Castillo, J. A.; Alvarez-Larena, A.; Moltrasio, G. Y.; Branchadell, V.; Ortuno, R. M. J. Org. Chem. 2002, 67, 2402.   DOI   ScienceOn
18 Baldwin, S. W.; Aube, J. Tetrahedron Lett. 1987, 28, 179.   DOI   ScienceOn
19 Xiang, Y.; Gi, H.-J.; Niu, D.; Schinazi, R. F.; Zhao, K. J. Org. Chem. 1997, 62, 7430.   DOI   ScienceOn
20 Langlois, N.; Calvez, O.; Radom, M.-O. Tetrahedron Lett. 1997, 38, 8037.   DOI   ScienceOn
21 Merino, P.; Franco, S.; Merchan, F. L.; Tejero, T. J. Org. Chem. 2000, 65, 5575.   DOI   ScienceOn
22 Ishikawa, T.; Nagai, K.; Kudoh, T.; Saito, S. Synlett 1998, 1291.
23 Kim, J. N.; Kim, J. M.; Lee, K. Y. Synlett 2003, 821.