(m, 2H), 1.39–1.24 (m, 30H), 0.91–0.86 (m, 3H); 13C NMR
(75 MHz, CDCl3): d 148.6, 129.1, 117.0, 112.6, 43.9, 31.9, 29.7,
29.6, 29.5, 29.4, 29.3, 27.2, 22.7, 14.1.
T. J. P. Adolfs, A. C. McCreary, H. G. Keizer, H. C. Wals, W. Veerman,
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Wexler, J. Med. Chem., 2005, 48, 1729; (e) S. D. Barche´chath, R. I.
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3-Phenyloxazolidin-2-one (3na)32
1H NMR (300 MHz, CDCl3): d 7.55–7.53 (m, 2H), 7.40–7.35 (m,
2H), 7.17–7.12 (m, 1H), 4.49–4.44 (m, 2H), 4.07–4.02 (m, 2H); 13
C
NMR (75 MHz, CDCl3): d 155.3, 138.2, 129.0, 124.0, 118.2, 61.3,
45.1.
2-Methyl-N-phenylaniline (3oa)33
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Res., 1998, 31, 805.
1H NMR (300 MHz, CDCl3): d 7.29–7.20 (m, 5H), 6.99–6.89
(m, 4H), 5.39 (s, 1H), 2.27 (s, 3H); 13C NMR (75 MHz, CDCl3):
d 148.7, 146.0, 135.7, 134.1, 133.0, 131.5, 126.7, 125.2, 123.5, 122.2,
22.7.
5 J. F. Hartwig, Angew. Chem., Int. Ed., 1998, 37, 2046.
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1429.
N-(4-Methoxyphenyl)benzenamine (3pa)34
1H NMR (300 MHz, CDCl3): d 7.24–7.18 (m, 2H), 7.08–7.05
(m, 2H), 6.91–6.83 (m, 5H), 5.48 (s, 1H), 3.78 (s, 3H); 13C NMR
(75 MHz, CDCl3): d 135.7, 129.3, 124.3, 122.2, 119.5, 115.6, 114.6,
114.1, 55.6.
2-Methoxy-N-phenylaniline (3qa)25
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B. Nguyen, T. L. Lau, M. H. McNeill, J. E. Dalgard, J. H. Chen,
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7137; (e) Y. H. Liu, C. Chen and L. M. Yang, Tetrahedron Lett., 2006,
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Ma¨eorg, Tetrahedron Lett., 2007, 48, 1155; (g) N. S. Nandurkar, M. J.
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1H NMR (300 MHz, CDCl3): d 7.31–7.25 (m, 2H), 7.16 (d, J =
7.6 Hz, 2H), 6.95–6.87 (m, 5H), 6.16 (s, 1H), 3.89 (s, 3H); 13C NMR
(75 MHz, CDCl3): d 148.2, 142.7, 132.9, 129.3, 121.1, 120.8, 119.9,
118.5, 114.6, 110.5, 55.6.
4-Phenylmorpholine (3ra)33
1H NMR (300 MHz, CDCl3): d 7.30–7.25 (m, 2H), 6.93–6.88 (m,
3H), 3.87–3.84 (m, 2H), 3.17–3.13 (m, 2H); 13C NMR (75 MHz,
CDCl3): d 151.3, 129.2, 120.1, 115.7, 66.9, 49.3.
9 C. Bolm and A. Correa, Angew. Chem., Int. Ed., 2007, 46, 8862.
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3-Methyl-N-phenylbenzenamine (3cd)35
1H NMR (300 MHz, CDCl3): d 7.27–7.22 (m, 3H), 7.13–7.11 (m,
1H), 7.06–7.03 (m, 2H), 6.90–6.86 (m, 2H), 6.74–6.72 (m, 1H),
5.65 (s, 1H), 2.30 (s, 3H); 13C NMR (75 MHz, CDCl3): d 135.0,
131.3, 129.3, 129.2, 121.9, 120.8, 119.5, 118.5, 117.8, 114.9. 21.5.
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Tetrahedron Lett., 1998, 39, 2933; (b) P. Y. S. Lam, C. G. Clark, S.
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14 P. Y. S. Lam, C. G. Clark, S. Saubern, J. Adams, K. M. Averill, D. M. T.
Chan and A. Combs, Synlett, 2000, 674.
N-Phenylnaphthalen-1-amine (3ce)36
1H NMR (300 MHz, CDCl3): d 7.99–7.98 (m, 1H), 7.90–7.82 (m,
3H), 7.52–7.44 (m, 5H), 6.98–6.88 (m, 3H), 5.89 (s, 1H); 13C NMR
(75 MHz, CDCl3): d 131.0, 129.3, 129.1, 128.5, 126.1, 126.0, 125.7,
122.9, 122.8, 121.8, 120.5, 117.3, 115.8.
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3994.
16 E. J. G. Anctil and V. Snieckus, in Metal-Catalyzed Cross-Coupling
Reactions, ed. A. de Mejijere and F. Diederich, Wiley-VCH, Weinheim,
2004, vol. 2, pp. 761–814.
Acknowledgements
17 T. N. Mitchell, in Metal-Catalyzed Cross-Coupling Reactions, ed. A.
de Mejijere and F. Diederich, Wiley-VCH, Weinheim, 2004, vol. 1,
pp. 125–162.
We thank the National Natural Science Foundation of China (No.
20504023) for financial support.
18 R. J. Song, C. L. Deng, Y. X. Xie and J. H. Li, Tetrahedron Lett., 2007,
48, 7845.
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