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[3a] For the synthesis of quinolines catalyzed by transition metals such as Pd, Rh, Ru and Fe, see: C. S. Cho, B. H. Oh, J. S. Kim, T.-J. Kim and S. C. Shim, Chem. Commun., 1885 (2000) and references cited therein;
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Chem. Commun.
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Cho, C.S.1
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[4a] C. S. Cho, H. K. Lim, S. C. Shim, T. J. Kim and H.-J. Choi, Chem. Commun., 995 (1998);
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Chem. Commun.
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Cho, C.S.1
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[c] C. S. Cho, J. H. Kim, T.-J. Kim and S. C. Shim, Tetrahedron, 57, 3321 (2001).
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Tetrahedron
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Cho, C.S.1
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[b] C. S. Cho, B. H. Oh, S. C. Shim and D. H. Oh, J. Heterocyclic Chem., 37, 1315 (2000);
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[c] C. S. Cho, J. S. Kim, B. H. Oh, T.-J. Kim, S. C. Shim and N. S. Yoon, Tetrahedron, 56, 7747 (2000);
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[e] C. S. Cho, D. T. Kim, T.-J. Kim and S. C. Shim, Bull. Korean Chem. Soc., 24, 1026 (2003).
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Bull. Korean Chem. Soc.
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Cho, C.S.1
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13
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45449092575
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C. S. Cho, B. T. Kim, M. J. Lee, T.-J. Kim and S. C. Shim, Angew. Chem. Int. Ed. Engl., 40, 958 (2001).
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Angew. Chem. Int. Ed. Engl.
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[7a] C. S. Cho, B. T. Kim, T.-J. Kim and S. C. Shim, J. Org. Chem., 66, 9020 (2001);
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[b] C. S. Cho, B. T. Kim, T.-J. Kim and S. C. Shim, Tetrahedron Letters, 43, 7987 (2002);
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Tetrahedron Letters
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16
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[c] C. S. Cho, B. T. Kim, H.-S. Kim, T.-J. Kim and S. C. Shim, Organometallics, 22, 3608 (2003).
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Organometallics
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C. S. Cho, J. H. Park, T.-J. Kim and S. C. Shim, Bull. Korean Chem. Soc., 23, 23 (2002).
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Bull. Korean Chem. Soc.
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Cho, C.S.1
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19
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C. S. Cho, J. H. Kim, H.-J. Choi, T.-J. Kim and S. C. Shim, Tetrahedron Letters, 44, 2975 (2003).
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Tetrahedron Letters
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20
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0001184450
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[16a] Our recent examples for the direct application of nitroarenes to amine exchange reaction leading to indoles and quinolines: C. S. Cho, T. K. Kim, S. W. Yoon, T.-J. Kim, S. C. Shim, Bull. Korean Chem. Soc., 22, 545 (2001);
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[b] C. S. Cho, T. K. Kim, T.-J. Kim, S. C. Shim and N. S. Yoon, J. Heterocyclic Chem., 39, 291 (2002);
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[19a] Our recent reports on the discovery of additive activity of tin(II) chloride in organic reactions: C. S. Cho, J. S. Kim, H. S. Kim, T.-J. Kim and S. C. Shim, Synth. Commun., 31, 3791 (2001);
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