Aminosulfonylation of aromatic amines, sulfur dioxide and hydrazines

Chemical Communications

Volumn 50, Issue 64, 2014, Pages 8886-8888

  Zheng, Danqing ^a   Li, Ying ^a   An, Yuanyuan ^a   Wu, Jie ^a,b  

^a FUDAN UNIVERSITY   (China)

^b SHANGHAI INSTITUTE OF ORGANIC CHEMISTRY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

2 AMINOPYRIDINE; 3 AMINOPYRIDINE; AROMATIC AMINE; DIAZONIUM COMPOUND; FUNCTIONAL GROUP; HYDRAZINE DERIVATIVE; INDOLE DERIVATIVE; QUINOLINE DERIVATIVE; SULFUR DIOXIDE;

AMINATION; AMINOSULFONYLATION; ARTICLE; ARYLATION; CHEMICAL PROCEDURES; ELECTRON; SYNTHESIS; TEMPERATURE;

EID: 84904439023     PISSN: 13597345     EISSN: 1364548X     Source Type: Journal    
DOI: 10.1039/c4cc03032j     Document Type: Article

References (37)

1. D. Surry, S. Buchwald, Angew. Chem., Int. Ed., 2008, 47:6338
2. F. Mo, G. Dong, Y. Zhang, J. Wang, Org. Biomol. Chem., 2013, 11:1582
3. D. P. Hari, B. König, Angew. Chem., Int. Ed., 2013, 52:4734
4. M. P. Doyle, B. Siegfried, R. C. Elliott, J. F. Dellaria, J. Org. Chem., 1977, 42:2431
5. A. Honraedt, M.-A. Raux, E. L. Grognec, D. Jacquemin, F.-X. Felpin, Chem. Commun., 2014, 50:5236
6. A. Honraedt, F. L. Callonnec, E. L. Grongnec, V. Fernandez, F.-X. Felpin, J. Org. Chem., 2013, 78:4604
7. M. B. Andrus, C. Song, J. Zhang, Org. Lett., 2002, 4:2079
8. X.-F. Wu, H. Neumann, M. Beller, Chem. Commun., 2011, 47:7959
9. F. Mo, D. Qiu, Y. Jiang, J. Wang, Tetrahedron Lett., 2011, 52:518
10. F. L. Callonec, E. Fouquet, F.-X. Felpin, Org. Lett., 2011, 13:2646
11. N. Susperregui, K. Miqueu, J.-M. Sotiropoulos, F. L. Callonnec, E. Fouqet, F.-X. Felpin, Chem. Eur. J., 2012, 18:7210
12. Z. Xia, J. Huang, Y. He, J. Zhao, J. Lei, Q. Zhu, Org. Lett., 2014, 16:2546
13. N. Chernyak, S. Buchwald, J. Am. Chem. Soc., 2012, 134:12466
14. X. Wang, Y. Xu, F. Mo, G. Ji, D. Qiu, J. Feng, Y. Ye, S. Zhang, Y. Zhang, J. Wang, J. Am. Chem. Soc., 2013, 135:10330
15. J.-J. Dai, C. Fang, B. Xiao, J. Yi, J. Xu, Z.-J. Liu, L. Liu, Y. Fu, J. Am. Chem. Soc., 2013, 135:8436
16. D. L. Browne, Angew. Chem., Int. Ed., 2014, 53:1482
17. F. Mo, Y. Jiang, D. Qiu, Y. Zhang, J. Wang, Angew. Chem., Int. Ed., 2010, 49:1846
18. D. Qiu, L. Jin, Z. Zheng, H. Meng, F. Mo, X. Wang, Y. Zhang, J. Wang, J. Org. Chem., 2013, 78:1923
19. D. Qiu, H. Meng, L. Jin, S. Wang, S. Tang, X. Wang, F. Mo, Y. Zhang, J. Wang, Angew. Chem., Int. Ed., 2013, 52:11581
20. M. Bartholow, Top 200 Drugs of 2011. Pharmacy Times. http://www.pharmacytimes.com/publications/issue/2012/July2012/Top-200-Drugs-of-2011, accessed on Jan 9, 2013
21. J. Drews, Science, 2000, 287:1960
22. J. R. DeBergh, N. Niljianskul, S. L. Buchwald, J. Am. Chem. Soc., 2013, 135:10638
23. B. Nguyen, E. J. Emmet, M. C. Willis, J. Am. Chem. Soc., 2010, 132:16372
24. A. J. Emmet, C. S. Richards-Taylor, B. Nguyen, A. B. Garcia-Rubia, R. Hayter, M. C. Willis, Org. Biomol. Chem., 2012, 10:4007
25. C. S. Richards-Taylor, D. C. Blakemore, M. C. Willis, Chem. Sci., 2014, 5:222
26. E. J. Emmett, B. R. Hayter, M. C. Willis, Angew. Chem., Int. Ed., 2013, 52:12679
27. A. S. Deeming, C. J. Rusell, A. J. Hennessy, M. C. Willis, Org. Lett., 2014, 16:150
28. B. N. Rocke, K. B. Bahnck, M. Herr, S. Lavergne, V. Mascitti, C. Perreault, J. Polivkova, A. Shavnya, Org. Lett., 2014, 16:154
29. S. Ye, J. Wu, Chem. Commun., 2012, 48:7753
30. S. Ye, J. Wu, Chem. Commun., 2012, 48:10037
31. D. Zheng, Y. An, Z. Li, J. Wu, Angew. Chem., Int. Ed., 2014, 53:2451
32. M. W. Johnson, S. W. Bagley, N. P. Mankad, R. G. Bergman, V. Mascitti, F. D. Toste, Angew. Chem., Int. Ed., 2014, 53:4404
33. P. Bisseret, N. Blanchard, Org. Biomol. Chem., 2013, 11:5393
34. L. Martial, Synlett, 2013, 1595
35. W. Li, H. Li, P. Langer, M. Beller, X.-F. Wu, Eur. J. Org. Chem., 2014, 3101
36. F. Mo, G. Dong, Y. Zhang, J. Wang, Org. Biomol. Chem., 2013, 11:1582
37. F. L. Callonnec, E. Fouquet, F.-X. Felpin, Org. Lett., 2011, 13:2646