Erratum: Modular bifunctional chiral thioureas as versatile organocatalysts for highly enantioselective aza-henry reaction and michael addition (Advanced Synthesis and Catalysis (2012) 11 (2264-2274) DOI: 10.1002/adsc.201200144);Modular bifunctional chiral thioureas as versatile organocatalysts for highly enantioselective aza-Henry reaction and michael addition

Advanced Synthesis and Catalysis

Volumn 354, Issue 11-12, 2012, Pages 2264-2274

  Li, Hua ^a   Zhang, Xu ^a   Shi, Xin ^a   Ji, Nan ^a   He, Wei ^a   Zhang, Shengyong ^a   Zhang, Bangle ^a  

^a FOURTH MILITARY MEDICAL UNIVERSITY   (China)

Author keywords

asymmetric catalysis; aza Henry reaction; C C bond formation; Michael addition; organic catalysis

Indexed keywords

EID: 84865014487     PISSN: 16154150     EISSN: 16154169     Source Type: Journal    
DOI: 10.1002/adsc.201290028     Document Type: Erratum

References (83)

1. J. F. Teichert, B. L. Feringa, Angew. Chem. 2010, 122, 2538-2582
2. Angew. Chem. Int. Ed. 2010, 49, 2486-2528
3. W. Zhuang, T. B. Poulsen, K. A. Jøgensen, Org. Biomol. Chem. 2005, 3, 3284-3289
4. S. Kobayashi, M. Ueno, S. Saito, Y. Mizuki, H. Ishitani, Y. Yamashita, Proc. Natl. Acad. Sci. USA 2004, 101, 5476-5481
5. J.-Y. Li, S.-Z. Luo, J.-P. Cheng, J. Org. Chem. 2009, 74, 1747-1750
6. G.-Q. Zhang, E. Yashima, W.-D. Woggon, Adv. Synth. Catal. 2009, 351, 1255-1262
7. W.-P. Ye, Z.-Y. Jiang, Y.-J. Zhao, S. L. M. Goh, D. S. Leow, Y.-T. Soh, C.-H. Tan, Adv. Synth. Catal. 2007, 349, 2454-2458.
8. B. List, Chem. Rev. 2007, 107, 5413-5415
9. P. I. Dalko, L. Moisan, Angew. Chem. 2004, 116, 5248-5286
10. Angew. Chem. Int. Ed. 2004, 43, 5138-5175
11. B. List, Angew. Chem. 2010, 122, 1774-1779
12. Angew. Chem. Int. Ed. 2010, 49, 1730-1734
13. S. Bertelsen, K. A. Jorgensen, Chem. Soc. Rev. 2009, 38, 2178-2189
14. G. Lelais, D. W. C. MacMillan, Aldrichimica Acta 2006, 39, 79-87.
15. P. I. Dalko, L. Moisan, Angew. Chem. 2001, 113, 3840-3864
16. Angew. Chem. Int. Ed. 2001, 40, 3726-3748
17. K. Maruoka, Asymmetric Phase Transfer Catalysis, Wiley-VCH Verlag, Weinheim, 2008
18. A. Berkessel, H. Gröger, Asymmetric Organocatalysis: From Biomimetic Concepts to Applications in Asymmetric Synthesis Wiley-VCH, Weinheim, 2005
19. Enantioselective Organocatalysis, (Ed.:, P. I. Dalko,), Wiley-VCH, Weinheim, 2007
20. C. E. Song, Cinchona Alkaloids in Synthesis and Catalysis, Wiley-VCH, Weinheim, 2009
21. H. Pellissier, Recent Developments in Asymmetric Organocatalysis, Royal Society of Chemistry, Cambridge, UK, 2010
22. P. M. Pihko, Hydrogen Bonding in Organic Synthesis Wiley-VCH, Weinheim, 2009
23. Asymmetric Organocatalysis, 2 Vols., (Eds:, B. List, K. Maruoka,), Thieme, Stuttgart, 2011.
24. T. P. Yoon, E. N. Jacobsen, Angew. Chem. 2005, 117, 470-472
25. Angew. Chem. Int. Ed. 2005, 44, 466-468
26. Y. Takemoto, Chem. Pharm. Bull. 2010, 58, 593-601
27. D. H. Paull, E. Alden-Danforth, J. Wolfer, C. Dogo-Isonagie, C. J. Abraham, T. Lectka, J. Org. Chem. 2007, 72, 5380-5382
28. J. Wang, H. Li, X.-H. Yu, L.-S. Zu, W. Wang, Org. Lett. 2005, 7, 4293-4296
29. V. N. Wakchaure, B. List, Angew. Chem. 2010, 122, 4230-4233
30. Angew. Chem. Int. Ed. 2010, 49, 4136-4139
31. T. Okino, S. Nakamura, T. Furukawa, Y. Takemoto, Org. Lett. 2004, 6, 625-627
32. S. J. Connon, Chem. Commun. 2008, 2499-2510.
33. H. Gröger, J. Wilken, Angew. Chem. 2001, 113, 545-548
34. Angew. Chem. Int. Ed. 2001, 40, 529-532
35. S.-K. Tian, Y.-G. Chen, J.-F. Hang, L. Tang, P. Mcdaid, L. Deng, Acc. Chem. Res. 2004, 37, 621-631
36. E. M. O. Yeboah, S. O. Yeboah, G. S. Singh, Tetrahedron 2011, 67, 1725-1762
37. K. Sakthivel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260-5267
38. Y. Wang, X.-F. Liu, L. Deng, J. Am. Chem. Soc. 2006, 128, 3928-3930
39. T. P. Yoon, E. N. Jacobsen, Science 2003, 299, 1691-1693
40. H. M. R. Hoffmann, J. Frackenpohl, Eur. J. Org. Chem. 2004, 4293-4312.
41. X. Xu, T. Furukawa, T. Okino, H. Miyabe, Y. Takemoto, Chem. Eur. J. 2006, 12, 466-476
42. C. Rampalakos, W. D. Wulff, Adv. Synth. Catal. 2008, 350, 1785-1790
43. M. T. Robak, M. Trincado, J. A. Ellman, J. Am. Chem. Soc. 2007, 129, 15110-15111
44. B. Han, Q.-P. Liu, R. Li, X. Tian, X.-F. Xiong, J.-G. Deng, Y.-C. Chen, Chem. Eur. J. 2008, 14, 8094-8097
45. C.-J. Wang, X.-Q. Dong, Z.-H. Zhang, Z.-Y. Xue, H.-L. Teng, J. Am. Chem. Soc. 2008, 130, 8606-8607
46. B. M. Nugent, R. A. Yoder, J. N. Johnston, J. Am. Chem. Soc. 2004, 126, 3418-3419
47. A. Singh, J. N. Johnston, J. Am. Chem. Soc. 2008, 130, 5866-5867
48. D. Uraguchi, K. Koshimoto, T. Ooi, J. Am. Chem. Soc. 2008, 130, 10878-10879
49. M. Rueping, A. P. Antonchick, Org. Lett. 2008, 10, 1731-1734
50. Y. Wei, W. He, Y.-L. Liu, P. Liu, S.-Y. Zhang, Org. Lett. 2012, 14, 704-707
51. L. Bernardi, F. Fini, R. P. Herrera, A. Ricci, V. Sgarzani, Tetrahedron 2006, 62, 375-380.
52. T. Okachi, K. Fujimoto, M. Onaka, Org. Lett. 2002, 4, 1667-1669
53. X. Li, Z. Xi, S. Luo, J.-P. Cheng, Adv. Synth. Catal. 2010, 352, 1097-1101
54. Y.-H. Liao, X.-L. Liu, Z.-J. Wu, X.-L. Du, X.-M. Zhang, W.-C. Yuan, Adv. Synth. Catal. 2011, 353, 1720-1728
55. D. Yang, S. Gu, Y.-L. Yan, N.-Y. Zhu, K.-K. Cheung, J. Am. Chem. Soc. 2001, 123, 8612-8613.
56. E. Gomez-Bengoa, A. Linden, R. Lõpez, I. Múgica-Mendiola, M. Oiarbide, C. Palomo. , J. Am. Chem. Soc. 2008, 130, 7955-7966
57. M.-L. Eugenia, P. Merino, T. Tejero, R. P. Herrera, Eur. J. Org. Chem. 2009, 2401-2420
58. Z. Chen, H. Morimoto, S. Matsunaga, M. Shibasaki, J. Am. Chem. Soc. 2008, 130, 2170-2171
59. B. M. Trost, D. W. Lupton, Org. Lett. 2007, 9, 2023-2026.
60. K. R. Knudsen, T. Risgaard, N. Nishiwaki, K. V. Gothelf, K. A. Jørgensen, J. Am. Chem. Soc. 2001, 123, 5843-5844
61. S. Handa, V. Gnanadesikan, S. Matsunaga, M. Shibasaki, J. Am. Chem. Soc. 2007, 129, 4900-4901
62. C. Palomo, M. Oiarbide, R. Halder, A. Laso, R. Lõpez, Angew. Chem. 2006, 118, 123-126
63. Angew. Chem. Int. Ed. 2006, 45, 117-120.
64. T. Okino, Y. Hoashi, Y. Takemoto, J. Am. Chem. Soc. 2003, 125, 12672-12673.
65. H.-M. Guo, J.-G. Li, G.-R. Qu, X.-M. Zhang, W.-C. Yuan, Chirality 2011, 23, 514-518
66. C.-L. Cao, M.-C. Ye, X.-L. Sun, Y. Tang, Org. Lett. 2006, 8, 2901-2904
67. T. Okino, Y. Hoashi, T. Furukawa, X. Xu, Y. Takemoto, J. Am. Chem. Soc. 2005, 127, 119-125
68. T. Inokuma, Y. Hoashi, Y. Takemoto, J. Am. Chem. Soc. 2006, 128, 9413-9419
69. Y.-H. Liao, W.-B. Chen, Z.-J. Wu, X.-L. Du, L.-F. Cun, X.-M. Zhang, W.-C. Yuana, Adv. Synth. Catal. 2010, 352, 827-832.
70. K. Sakthivel, W. Notz, T. Bui, C. F. Barbas III, J. Am. Chem. Soc. 2001, 123, 5260-5267.
71. B. List, P. Pojarliev, H. J. Martin, Org. Lett. 2001, 3, 2423-2425.
72. H. Huang, E. N. Jacobsen, J. Am. Chem. Soc. 2006, 128, 7170-7171
73. S. B. Tsogoeva, S. W. Wei, Chem. Commun. 2006, 1451-1453
74. D. A. Yalalov, S. B. Tsogoeva, S. Schmatz, Adv. Synth. Catal. 2006, 348, 826-832
75. Z.-G. Yang, J. Liu, X.-H. Liu, Z. Wang, X.-M. Feng, Z.-S. Su, C.-W. Hu, Adv. Synth. Catal. 2008, 350, 2001-2006
76. T. Mandal, C.-G. Zhao, Angew. Chem. 2008, 120, 7828-7831
77. Angew. Chem. Int. Ed. 2008, 47, 7714-7717
78. C. G. Kokotosa, G. Kokotos, Adv. Synth. Catal. 2009, 351, 1355-1362
79. L. Peng, X.-Y. Xu, L.-L. Wang, J. Huang, J.-F. Bai, Q.-C. Huang, L.-X. Wang, Eur. J. Org. Chem. 2010, 1849-1853
80. A.-D. Lu, T. Liu, R.-H. Wu, Y.-M. Wang, Z.-H. Zhou, G.-P. Wu, J.-X. Fang, C-.C. Tang, Eur. J. Org. Chem. 2010, 5777-5781
81. A.-D. Lu, T. Liu, R.-H. Wu, Y.-M. Wang, G.-P. Wu, Z-H. Zhou, J.-X. Fang, C.-C. Tang, J. Org. Chem. 2011, 76, 3872-3879.
82. M. Tsakos, C. G. Kokotos, G. Kokotos, Adv. Synth. Catal. 2012, 354, 740-746.
83. CCDC 862556 and CCDC 862557 contain the crystallographic data for organocatalyst 1c and 5-nitro-4- (2-chlorophenyl) pentan-2-one 10h. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data-request/cif.