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For the synthesis of fluoroquinolines, see: a) R. D. Chambers, M. Parsons, G. Sandford, C. J. Skinner, M. J. Atherton, and J. S. Moilliet, J. Chem. Soc., Perkin Trans. 1, 1999, 803 and references therein, b) L. Strekowski, A. S. Kiselyov, and M. Hojjat, J. Org. Chem., 59, 5886 (1994). c) G.-Q. Shi, S. Takagishi, and M. Schlosser, Tetrahedron, 50, 1129 (1994).
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For recent reports on quinoline synthesis, see: a) K. Kobayashi, K. Yoneda, T. Mizumoto, H. Umakoshi, O. Morikawa, and H. Konishi, Tetrahedron Lett., 44, 4733 (2003) and references therein. b) J. N. Kim, H. J. Lee, K. Y. Lee, and H. S. Kim, Tetrahedron Lett., 42, 3737 (2001). c) C. S. Cho, B. H. Oh, J. S. Kim, T.-J. Kim, and S. C. Shim, Chem. Commun., 2000, 1885 and references therein.
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For recent reports on quinoline synthesis, see: a) K. Kobayashi, K. Yoneda, T. Mizumoto, H. Umakoshi, O. Morikawa, and H. Konishi, Tetrahedron Lett., 44, 4733 (2003) and references therein. b) J. N. Kim, H. J. Lee, K. Y. Lee, and H. S. Kim, Tetrahedron Lett., 42, 3737 (2001). c) C. S. Cho, B. H. Oh, J. S. Kim, T.-J. Kim, and S. C. Shim, Chem. Commun., 2000, 1885 and references therein.
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For recent reports on quinoline synthesis, see: a) K. Kobayashi, K. Yoneda, T. Mizumoto, H. Umakoshi, O. Morikawa, and H. Konishi, Tetrahedron Lett., 44, 4733 (2003) and references therein. b) J. N. Kim, H. J. Lee, K. Y. Lee, and H. S. Kim, Tetrahedron Lett., 42, 3737 (2001). c) C. S. Cho, B. H. Oh, J. S. Kim, T.-J. Kim, and S. C. Shim, Chem. Commun., 2000, 1885 and references therein.
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24
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0842279785
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note
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A similar intramolecular substitution with imidoyl anions proceeded at room temperature. See Ref. 8b.
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