Corrigendum to: Efficient Cross-Coupling Reactions of Nitrogen Nucleophiles with Aryl Halides in Water (Advanced Synthesis & Catalysis, (2009), 351, 5, (720-724), 10.1002/adsc.200800746);Efficient cross-coupling reactions of nitrogen nucleophiles with aryl halides in water

Advanced Synthesis and Catalysis

Volumn 351, Issue 5, 2009, Pages 720-724

  Teo, Yong Chua ^a  

^a NANYANG TECHNOLOGICAL UNIVERSITY   (Singapore)

Author keywords

Arylation; Cross coupling; Heterogeneous catalysis; Iron; Water; cross coupling; iron; arylation; heterogeneous catalysis; water

Indexed keywords

EID: 63349110330     PISSN: 16154150     EISSN: 15213897     Source Type: Journal    
DOI: 10.1002/adsc.200990017     Document Type: Erratum

References (68)

1. a) V. Ritleng, C. Sirlin, M. Pfeffer, Chem. Rev. 2002, 102, 1731;
2. b) A. R. Muci, S. L. Buchwald, Top. Curr. Chem. 2002, 219, 131;
3. c) Metal-Catalyzed Cross-Coupling Reactions, (Eds.: F. Diederich, A. deMeijere), Wiley-VCH, Weinheim, 2004;
4. d) O. Daugulis, V. G. Zaitsev, D. Shabashov, Q.-N. Pham, A. Lazareva, Synlett 2006, 3382;
5. e) K. Godula, D. Sames, Science 2006, 312, 67;
6. f) A. R. Dick, M. S. Sanford, Tetrahedron 2006, 62, 2439;
7. g) J. F. Hartwig, Synlett 2006, 1283;
8. h) D. Alberico, M. E. Scott, M. Lautens, Chem. Rev. 2007, 107, 174;
9. i) I. V. Seregin, V. Gevorgyan, Chem. Soc. Rev. 2007, 36, 1173,
10. j) H. M. L. Davies, J. R. Manning, Nature 2008, 451, 417.
11. For reviews, see: a) K. Kunz, U. Scholz, D. Ganzer, Synlett 2003, 2428;
12. b) S.V. Ley, A.W. Thomas, Angew. Chem. 2003, 115, 5558;
13. Angew. Chem. Int. Ed. 2003, 42, 5400;
14. c) I. P. Beletskaya, A. V. Cheprakov, Coord. Chem. Rev. 2004, 248, 2337;
15. d) J.-P. Corbet, G. Mignani, Chem. Rev. 2006, 106, 2651.
16. For general reviews, see: a) C. Bolm, J. Legros, J. LePaih, L. Zani, Chem. Rev. 2004, 104, 6217;
17. b) A. Fürstner, R. Martin, Chem. Lett. 2005, 34, 624;
18. c) E. B. Bauer, Curr. Org. Chem. 2008, 12, 1341.
19. For recent contributions on iron catalysis, see: a) A. Fürstner, A. Leitner, M. Méndez, H. Krause, J. Am. Chem. Soc. 2002, 124, 13856;
20. b) A. Fürstner, A. Leitner, Angew. Chem. 2002, 114, 632;
21. Angew. Chem. Int. Ed. 2002, 41, 609;
22. c) J. Legros, C. Bolm, Angew. Chem. 2003, 115, 5645;
23. Angew. Chem. Int. Ed. 2003, 42, 5487;
24. d) J. Legros, C. Bolm, Angew. Chem. 2004, 116, 4321;
25. Angew. Chem. Int. Ed. 2004, 43, 4225;
26. e) B. Scheiper, M. Bonnekessel, H. Krause, A. Fürstner, J. Org. Chem. 2004, 69, 3943;
27. f) R. Martin, A. Fürstner, Angew. Chem. 2004, 116, 4045;
28. Angew. Chem. Int. Ed. 2004, 43, 3955;
29. g) J. Legros, C. Bolm, Chem. Eur. J. 2005, 11, 1086;
30. h) I. Sapountzis, W. Lin, C. C. Kofink, C. Despotopoulou, P. Knochel, Angew. Chem. 2005, 117, 1682;
31. Angew. Chem. Int. Ed. 2005, 44, 1654;
32. i) K. Komeyama, T. Morimoto, K. Takaki, Angew. Chem. 2006, 118, 3004;
33. Angew. Chem. Int. Ed. 2006, 45, 2938;
34. j) B. Plietker, Angew. Chem. 2006, 118, 6200;
35. Angew. Chem. Int. Ed. 2006, 45, 6053;
36. k) J. Kischel, I. Jovel, K. Mertins, A. Zapf, M. Beller, Org. Lett. 2006, 8, 19;
37. l) O. G. Mancheno, C. Bolm, Org. Lett. 2006, 8, 2349;
38. m) C. C. Kofink, B. Blank, S. Pagano, N. Gotz, P. Knochel, Chem. Commun. 2007, 1954;
39. n) G. Anilkumar, B. Bitterlich, F. G. Gelalcha, M. K. Tse, M. Beller, Chem. Commun. 2007, 289;
40. o) K. Komeyama, Y. Mieno, S. Yukawa, T. Morimoto, K. Takaki, Chem. Lett. 2007, 36, 752;
41. p) H. Egami, T. Katsuki, J. Am. Chem. Soc. 2007, 129, 8940;
42. q) M. Nakanishi, C. Bolm, Adv. Synth. Catal. 2007, 349, 861;
43. r) A. Correa, C. Bolm, Angew. Chem. 2007, 119, 9018;
44. Angew. Chem. Int. Ed. 2007, 46, 8862;
45. s) A. Correa, C. Bolm. Adv. Synth. Catal. 2008, 350, 391;
46. t) A. Correa, M. Carril, C. Bolm, Angew. Chem. 2008, 120, 2922;
47. Angew. Chem. Int. Ed. 2008, 47, 2880;
48. u) A. Correa, M. Carril, C. Bolm, Chem. Eur. J. 2008, 14, 10919;
49. v) D. Guo, H. Huang, J. Xu, H, Jiang, H. Liu, Org. Lett. 2008, 10, 4513.
50. a) M. Tamura, J. K. Kochi, J. Am. Chem. Soc. 1971, 93, 1487;
51. b) M. Tamura, J. K. Kochi, Synthesis 1971, 303;
52. c) M. Tamura, J. K. Kochi, J. Organomet. Chem. 1971, 31, 289.
53. a) Organic Synthesis in Water, (Ed. : P. A. Grieco), Blackie A & P, London, 1998;
54. b) U. M. Lindstrom, Chem. Rev. 2002, 102, 2751;
55. c) S. Kobayahi, K, Manabe, Acc. Chem. Res. 2002, 35, 209;
56. d) C.-J. Li, Chem. Rev. 2005, 105, 3095.
57. D. Sinou, Adv. Synth. Catal. 2002, 344, 221.
58. a) H. Nakai, S. Ogo, Y. Watanabe, Organometallics 2002, 21, 1674;
59. b) Y. Uozumi, Y. Kobayashi, Heterocycles 2003, 59, 71;
60. c) K. Manabe, K. Nakada, N. Aoyama, S. Kobayashi, Adv. Synth. Catal. 2005, 347, 1499;
61. d) F. Chanthavong, N. E. Leadbeater, Tetrahedron Lett. 2006, 47, 1909;
62. e) J, Yan, M. Zhu, Z. Zhou, Eur. J. Org. Chem. 2006, 2060;
63. f) M. D. Crozet, C. Castera-Ducros, P. Vanelle, Tetrahedron Lett. 2006, 47, 7061;
64. g) W.-Y. Wu, S.-N. Chen, F.-Y. Tsai, Tetrahedron Lett. 2006, 47, 9267;
65. h) N. Inoue, O. Sugimoto, K.-I. Tanji, Heterocycles 2007, 72, 665;
66. i) B.-W. Xin, Y.-H. Zhang, K. Cheng, Synthesis 2007, 1970;
67. j) M. Carril, R. SanMartin, E. Dominguez, Org. Lett. 2006, 8, 1467;
68. k) T. Kymala, A. Valkonen, K. Rissanen, Y. Xu, R. Franzen, Tetrahedron Lett. 2008, 49, 6679.