One-pot sequential C–N coupling and cross dehydrogenative couplings: Synthesis of novel azole fused imidazo[1,2-a]pyridines

Chemical Communications

Volumn 49, Issue 28, 2013, Pages 2924-2926

  Pericherla, Kasiviswanadharaju ^a   Khedar, Poonam ^a   Khungar, Bharti ^a   Kumar, Anil ^a  

^a BIRLA INSTITUTE OF TECHNOLOGY AND SCIENCE   (India)

Author keywords

[No Author keywords available]

Indexed keywords

ALPIDEM; GSK 812397; HUMAN IMMUNODEFICIENCY VIRUS ANTIBODY; IMIDAZO[1,2 A]PYRIDINE DERIVATIVE; MIROPROFEN; PYRROLE DERIVATIVE; UNCLASSIFIED DRUG; ZOLPIDEM;

ARTICLE; CHEMICAL STRUCTURE; CROSS COUPLING REACTION; DEHYDROGENATION; ONE POT SYNTHESIS;

EID: 84875046027     PISSN: 13597345     EISSN: 1364548X     Source Type: Journal    
DOI: 10.1039/c3cc39206f     Document Type: Article

References (23)

1. S. W. Fewell, J. L. Woolford, Mol. Cell. Biol, 1999, 19, 826-834
2. A. S. Howard, in Comprehensive Heterocyclic Chemistry II, ed. R. K. Alan, W. R. Charles and F. V. S. Eric, Pergamon, Oxford, 1996, pp. 249-286
3. L. Albrecht, A. Albrecht, L. K. Ransborg, K. A. Jorgensen, Chem. Sci, 2011, 2, 1273-1277
4. B. Narasimhan, D. Sharma, P. Kumar, Med. Chem. Res, 2011, 20, 1119-1140
5. P. Molina, A. Tarraga, F. Oton, Org. Biomol. Chem. 2012, 10, 1711-1724
6. C. Liu, H. Zhang, W. Shi, A. Lei, Chem. Rev, 2011, 111, 1780-1824
7. C. S. Yeung, V. M. Dong, Chem. Rev, 2011, 111, 1215-1292
8. C.-J. Li, Acc. Chem. Res, 2008, 42, 335-344
9. C. J. Scheuermann, Chem.-Asian J, 2010, 5, 436-451
10. M. Sun, H. Wu, J. Zheng, W. Bao, Adv. Synth. Catal, 2012, 354, 835-838
11. X. Qin, B. Feng, J. Dong, X. Li, Y. Xue, J. Lan, J. You, J. Org. Chem. 2012, 77, 7677-7683
12. J. Dong, Y. Huang, X. Qin, Y. Cheng, J. Hao, D. Wan, W. Li, X. Liu, J. You, Chem.-Eur. J, 2012, 18, 6158-6162
13. C. C. Malakar, D. Schmidt, J. R. Conrad, U. Beifuss, Org. Lett, 2011, 13, 1378-1381
14. T. A. Dwight, N. R. Rue, D. Charyk, R. Josselyn, B. DeBoef, Org. Lett, 2007, 9, 3137-3139
15. X. Bugaut, F. Glorius, Angew. Chem. Int. Ed, 2011, 50, 7479-7481
16. S. Fan, Z. Chen, X. Zhang, Org. Lett, 2012, 14, 4950-4953
17. H. Xu, H. Fu, Chem.-Eur. J, 2012, 18, 1180-1186
18. P. Xi, F. Yang, S. Qin, D. Zhao, J. Lan, G. Gao, C. Hu, J. You, J. Am. Chem. Soc. 2010, 132, 1822-1824
19. C.-Y. He, S. Fan, X. Zhang, J. Am. Chem. Soc. 2010, 132, 12850-12852
20. K. Pericherla, B. Khungar, A. Kumar, Tetrahedron Lett, 2012, 53, 1253-1257
21. Y. Aubin, C. Fischmeister, C. M. Thomas, J.-L. Renaud, Chem. Soc. Rev, 2010, 39, 4130-4145
22. H. Zhao, H. Fu, R. Qiao, J. Org. Chem. 2010, 75, 3311-3316
23. W. Han, P. Mayer, A. R. Ofial, Angew. Chem. Int. Ed, 2011, 50, 2178-2182