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A. B. Dounay, K. Hatanaka, J. J. Kodanko, M. Oestreich, L. E. Overman, L. A. Pfeifer, M. M. Weiss, J. Am. Chem. Soc. 2003, 125, 6261, and references cited therein.
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Other selected examples of catalytic asymmetric synthesis of oxindoles with quaternary carbon stereocenters: a) S. Lee, J. F. Hartwig, J. Org. Chem. 2001, 66, 3402;
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a) A. Berkessel, F. Cleemann, S. Mukherjee, Angew. Chem. 2005, 117, 7632;
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b) T.-Y. Liu, H.-L. Cui, J. Long, B.-J. Li, Y. Wu, L.-S. Ding, Y.-C. Chen, J. Am. Chem. Soc. 2007, 129, 1878.
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Chen, Y.-C.7
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43
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77149168264
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7a,b]
-
7a,b]
-
-
-
-
45
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0142072631
-
-
For leading examples of catalyst 1c: a T. Okino, Y. Hoashi, Y. Takemoto, J. Am. Chem. Soc. 2003, 125, 12672;
-
For leading examples of catalyst 1c: a) T. Okino, Y. Hoashi, Y. Takemoto, J. Am. Chem. Soc. 2003, 125, 12672;
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46
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11844302258
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b) T. Okino, Y. Hoashi, T. Furukawa, X.-N. Xu, Y. Takemoto, J. Am. Chem. Soc. 2005, 127, 119;
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33746323982
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c) T. Inokuma, Y. Hoashi, Y. Takemoto, J. Am. Chem. Soc. 2006, 128, 9413;
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51
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19544393388
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For leading examples of catalyst 1e: a B. Vakulya, S. Varga, A. Csámpai, T. Soós, Org. Lett. 2005, 7, 1967;
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For leading examples of catalyst 1e: a) B. Vakulya, S. Varga, A. Csámpai, T. Soós, Org. Lett. 2005, 7, 1967;
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52
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15444366940
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e) Y.-Q. Wang, J. Song, R. Hong, H. M. Li, L. Deng, J. Am. Chem. Soc. 2006, 128, 8156;
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60
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33744823336
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For leading examples of catalyst 1f: a T.-Y. Liu, J. Long, B.-J. Li, L. Jiang, R. Li, Y. Wu, L.-S. Ding, Y.-C. Chen, Org. Biomol. Chem. 2006, 4, 2097;
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For leading examples of catalyst 1f: a) T.-Y. Liu, J. Long, B.-J. Li, L. Jiang, R. Li, Y. Wu, L.-S. Ding, Y.-C. Chen, Org. Biomol. Chem. 2006, 4, 2097;
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61
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Li, X.1
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63
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3042579804
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-
For leading example of catalyst 1g: Y. Sohtome, A. Tanatani, Y. Hashimoto, K. Nagasawa, Tetrahedron Lett. 2004, 45, 5589.
-
For leading example of catalyst 1g: Y. Sohtome, A. Tanatani, Y. Hashimoto, K. Nagasawa, Tetrahedron Lett. 2004, 45, 5589.
-
-
-
-
64
-
-
77149127821
-
-
Our catalyst 1b is also better than Takemotös catalyst 1c in the currently studied Michael addition reaction of 2b to nitrostyrene. See Scheme S1 in the Supporting Information
-
Our catalyst 1b is also better than "Takemotös catalyst" 1c in the currently studied Michael addition reaction of 2b to nitrostyrene. See Scheme S1 in the Supporting Information.
-
-
-
-
65
-
-
46949084402
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C.-J. Wang, X.-Q. Dong, Z.-H. X, H.-L. Teng, J. Am. Chem. Soc. 2008, 130, 8606.
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Teng, Z.-H.X.H.-L.3
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