Silver-catalyzed oxidative coupling/cyclization of acrylamides with 1,3-dicarbonyl compounds

Chemical Communications

Volumn 49, Issue 88, 2013, Pages 10370-10372

  Wang, Hua ^a   Guo, Li Na ^a   Duan, Xin Hua ^a  

^a Xi pan Jiaotong University   (China)

Author keywords

[No Author keywords available]

Indexed keywords

1,2 DICARBONYL DERIVATIVE; ACRYLAMIDE; KETONE DERIVATIVE; RADICAL; SILVER;

ADDITION REACTION; ARTICLE; CATALYSIS; CATALYST; CHEMICAL BOND; CYCLIZATION; OXIDATIVE COUPLING; QUANTUM YIELD; REACTION ANALYSIS;

EID: 84885451302     PISSN: 13597345     EISSN: 1364548X     Source Type: Journal    
DOI: 10.1039/c3cc46114a     Document Type: Article

References (39)

1. X. Chen, K. M. Engle, D.-H. Wang, J.-Q. Yu: Angew. Chem., Int. Ed. 2009 48, 5094.
2. L. Ackermann, R. Vicente, A. R. Kapdi: Angew. Chem., Int. Ed. 2009 48, 9792.
3. J. A. Ashenhurst: Chem. Soc. Rev. 2010 39, 540.
4. T. W. Lyons, M. S. Sanford: Chem. Rev. 2010 110, 1147.
5. J. Le Bras, J. Muzart: Chem. Rev. 2011 111, 1170.
6. C. S. Yeung, V. M. Dong: Chem. Rev. 2011 111, 1215.
7. C. Liu, H. Zhang, W. Shi, A. Lei: Chem. Rev. 2011 111, 1780.
8. J. Wencel-Delord, T. Dröge, F. Liu, F. Glorius: Chem. Soc. Rev. 2011 40, 4740.
9. S. H. Cho, J. Y. Kim, J. Kwak, S. Chang: Chem. Soc. Rev. 2011 40, 5068.
10. P. B. Arockiam, C. Bruneau, P. H. Dixneuf: Chem. Rev. 2012 112, 5879.
11. G. Song, F. Wang, X. Li: Chem. Soc. Rev. 2012 41, 3651.
12. B.-J. Li, Z.-J. Shi: Chem. Soc. Rev. 2012 41, 5588.
13. K. R. Campos: Chem. Soc. Rev. 2007 36, 1069.
14. C.-J. Li: Acc. Chem. Res. 2009 42, 335.
15. C. J. Scheuermann: Chem.-Asian J. 2010 5, 436.
16. F. Bellina, R. Rossi: Chem. Rev. 2010 110, 1082.
17. R. Jazzar, J. Hitce, A. Renaudat, J. Sofack-Kreutzer, O. Baudoin: Chem.-Eur. J. 2010 16, 2654.
18. O. Baudoin: Chem. Soc. Rev. 2011 40, 4902.
19. T. A. Ramirez, B. Zhao, Y. Shi: Chem. Soc. Rev. 2012 41, 931.
20. Z. Li, C.-J. Li: J. Am. Chem. Soc. 2006 128, 56.
21. N. Borduas, D. A. Powell: J. Org. Chem. 2008 73, 7822.
22. Z. Li, L. Cao, C.-J. Li: Angew. Chem., Int. Ed. 2007 46, 6505.
23. Z. Li, R. Yu, H. Li: Angew. Chem., Int. Ed. 2008 47, 7497.
24. C. He, S. Guo, J. Ke, J. Hao, H. Xu, H. Chen, A. Lei: J. Am. Chem. Soc. 2012 134, 5766.
25. D. Cheng, W. Bao: J. Org. Chem. 2008 73, 6881.
26. J. Xie, H. Jiang, Y. Cheng, C. Zhu: Chem. Commun. 2012 48, 979.
27. C. Marti, E. M. Carreira: Eur. J. Org. Chem. 2003 2209.
28. H. Lin, S. J. Danishefsky: Angew. Chem., Int. Ed. 2003 42, 36.
29. C. V. Galliford, K. A. Scheidt: Angew. Chem., Int. Ed. 2007 46, 8748.
30. G. S. Singh, Z. Y. Desta: Chem. Rev. 2012 112, 6104.
31. K. Shen, X. Liu, L. Lin, X. Feng: Chem. Sci. 2012 3, 327.
32. R. Dalpozzo, G. Bartoli, G. Bencivenni: Chem. Soc. Rev. 2012 41, 7247.
33. N. R. Ball-Jones, J. J. Badillo, A. K. Franz: Org. Biomol. Chem. 2012 10, 5165.
34. L. Hong, R. Wang: Adv. Synth. Catal. 2013 355, 1023.
35. F. Zhou, Y.-L. Liu, J. Zhou: Adv. Synth. Catal. 2010 352, 1381.
36. J. E. M. N. Klein, R. J. K. Taylor: Eur. J. Org. Chem. 2011 6821.
37. J. Iqbal, B. Bhatia, N. K. Nayyar: Chem. Rev. 1994 94, 519.
38. B. B. Snider: Chem. Rev. 1996 96, 339.
39. A. Citterio, A. Gentile, F. Minisci: Tetrahedron Lett. 1982 23, 5587.