Synthesis of biaryl imino/keto carboxylic acids via aryl amide directed C-H activation reaction

Chemical Communications

Volumn 49, Issue 82, 2013, Pages 9464-9466

  Zhang, Nana ^a,b   Yu, Qingzhen ^a   Chen, Ruixue ^c   Huang, Jianhui ^a,b   Xia, Yeqing ^a   Zhao, Kang ^a  

^a TIANJIN UNIVERSITY   (China)

^b Synergetic Innovation Center of Chemical Science and Engineering   (China)

^c TIANJIN UNIVERSITY OF TRADITIONAL CHINESE MEDICINE   (China)

Author keywords

[No Author keywords available]

Indexed keywords

ALDEHYDE; AMIDE; CARBON; CARBOXYLIC ACID; HYDROGEN; IMINO CARBOXYLIC ACID; KETO CARBOXYLIC ACID; OXIDIZING AGENT; PALLADIUM; UNCLASSIFIED DRUG;

ACYLATION; ARTICLE; CATALYSIS; RING OPENING; SYNTHESIS;

AMIDES; CATALYSIS; GREEN CHEMISTRY TECHNOLOGY; IMINES; KETO ACIDS; MOLECULAR STRUCTURE; PALLADIUM;

EID: 84884507884     PISSN: 13597345     EISSN: 1364548X     Source Type: Journal    
DOI: 10.1039/c3cc45449e     Document Type: Article

References (28)

1. D. A. Colby, R. G. Bergman, J. A. Ellman, Chem. Rev, 2010, 110, 624
2. P. B. Arockiam, C. Bruneau, P. H. Dixneuf, Chem. Rev, 2012, 112, 5879
3. B.-J. Li, Z.-J. Shi, Chem. Soc. Rev, 2012, 41, 5588
4. D.-G. Yu, M. Suri, F. Glorius, J. Am. Chem. Soc, 2013, 135, 8802
5. X.-F. Cheng, Y. Li, Y.-M. Su, F. Yin, J.-Y. Wang, J. Sheng, H. U. Vora, X.-S. Wang, J.-Q. Yu, J. Am. Chem. Soc, 2013, 135, 1236
6. K. D. Hesp, R. G. Bergman, J. A. Ellman, J. Am. Chem. Soc, 2011, 133, 11430
7. H. Wang, N. Schrçder, F. Glorius, Angew. Chem, Int. Ed, 2013, 52, 5386
8. A. S. Tsai, M. E. Tauchert, R. G. Bergman, J. A. Ellman, J. Am. Chem. Soc, 2011, 133, 1248
9. O. Basl, J. Bidange, Q. Shuai, C.-J. Li, Adv. Synth. Catal, 2010, 352, 1145
10. Y. Yang, B. Zhou, Y. Li, Adv. Synth. Catal, 2012, 354, 2916
11. C. Li, L. Wang, P. Li, W. Zhou, Chem.-Eur. J, 2011, 17, 10208
12. J. Park, E. Park, A. Kim, Y. Lee, K.-W. Chi, J. H. Kwak, Y. H. Jung, I. S. Kim, Org. Lett, 2011, 13, 4390
13. M. Li, H. Ge, Org. Lett, 2010, 12, 3464
14. M. Kim, J. Park, S. Sharma, A. Kim, E. Park, J. H. Kwak, Y. H. Jung, I. S. Kim, Chem. Commun, 2013, 49, 925
15. H. Wang, L.-N. Guo, X.-H. Duan, Org. Lett, 2012, 14, 4358
16. J. Park, M. Kim, S. Sharma, E. Park, A. Kim, S. H. Lee, J. H. Kwak, Y. H. Jung, I. S. Kim, Chem. Commun, 2013, 49, 1654
17. S. Guin, S. K. Rout, A. Banerjee, S. Nandi, B. K. Patel, Org. Lett, 2012, 14, 5294
18. Y.-H. Zhang, J.-Q. Yu, J. Am. Chem. Soc, 2009, 131, 14654
19. T.-S. Mei, R. Giri, N. Maugel, J.-Q. Yu, Angew. Chem, Int. Ed, 2008, 47, 5215
20. P. Mamone, G. Danoun, L. J. Gooßen, Angew. Chem, Int. Ed, 2013, 52, 6704
21. J. Miao, H. Ge, Org. Lett, 2013, 15, 2930
22. Q. Yu, N. Zhang, J. Huang, S. Lu, Y. Zhu, X. Yu, K. Zhao, Chem.-Eur. J, 2013, 19, 1118410.1002/chem.201302031
23. N. N. Smolyar, Y. M. Yutilov, Russ. J. Org. Chem, 2008, 44, 274
24. C. B. Aakeröy, A. S. Sinha, K. N. Epa, C. L. Spartz, J. Desper, Chem. Commun, 2012, 48, 11289
25. L. J. Gooßen, F. Manjolinho, B. A. Khan, N. Rodríguez, J. Org. Chem, 2009, 74, 2620
26. M. Rudzki, A. Alcalde-Aragonés, W. I. Dzik, N. Rodríguez, L. J. Gooßen, Synthesis, 2012, 184
27. L. J. Gooßen, W. R. Thiel, N. Rodríguez, C. Linder, B. Melzer, Adv. Synth. Catal, 2007, 349, 2241
28. F. Xiao, Q. Shuai, F. Zhao, O. Baslé, G. Deng, C.-J. Li, Org. Lett, 2011, 13, 1614