Efficient synthesis of 2,4-diarylquinolines VIA Fe(III) trifluoroacetate catalyzed three-component reactions under solvent-free conditions

Heterocycles

Volumn 85, Issue 3, 2012, Pages 639-649

  Zhang, Min ^a   Wang, Ting ^a   Xiong, Biao ^a   Yan, Fengxia ^a   Wang, Xiaoting ^a   Ding, Yuqiang ^a   Song, Qijun ^a  

^a JIANGNAN UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 84863287981     PISSN: 03855414     EISSN: 18810942     Source Type: Journal    
DOI: 10.3987/COM-12-12433     Document Type: Article

References (38)

1. C. Praveen, P. Dheenkumar, D. Muralidharan, and P. T. Perumal, Bioorg. Med. Chem. Lett., 2010, 20, 7292.
2. S. Ou, Z. H. Lin, C. Y. Duan, H. T. Zhang, and Z. P. Bai, Chem. Commun., 2006, 42, 4392.
3. (a) E. F. Flegeau, C. Bruneau, P. H. Dixneuf, and A. Justand, J. Am. Chem. Soc., 2011, 133, 10161;
4. (b) P. B. Arockiam, C. Fischmeister, C. Bruneau, and P. H. Dixneuf, Angew. Chem. Int. Ed., 2010, 49, 6629;
5. (c) I. Ozdemir, S. Demir, B. Cetinkaya, C. Gourlaouen, F. Maseras, C. Bruneau, and P. H. Dixneuf, J. Am. Chem. Soc., 2008, 130, 1156.
6. (a) F. Gartner, A. Boddien, E. Barsch, K. Fumino, S. Losse, H. Junge, D. Hollmann, A. Bruckner, R. Ludwig, and M. Beller, Chem. Eur. J., 2011, 17, 6425;
7. (b) S. C. Lee and Y. S. Kim, Mol. Cryst. Liq. Cryst., 2009, 509, 1034.
8. Z. H. Skraup, Ber. Dtsch. Chem. Ges., 1880, 13, 2086.
9. (a) H. M. Wang, R. S. Hou, H. D. Du, I. J. Kang, and L. C. Chen, Heterocycles, 2011, 83, 331;
10. (b) M. Dabiri and S. Bashiribod, Molecules, 2009, 14, 1126;
11. (c) P. Friedländer, Ber. Dtsch. Chem. Ges., 1882, 15, 2572.
12. A. Combes, Bull. Soc. Chim. Fr., 1888, 49, 89.
13. (a) I. M. Baltork, S. Tangestaninejad, M. Moghadam, V. Mirkhani, S. Anvar, and A. Mirjafari, Synlett, 2010, 20, 3104;
14. (b) B. Gabriele, R. Mancuso, E. Lupinacci, R. Spina, G. Salerno, L. Veltri, and A. Dibenedetto, Tetrahedron, 2009, 65, 8507;
15. (c) J. Horn, S. P. Marsden, A. Nelson, D. House, and G. G. Weingarten, Org. Lett., 2008, 10, 4117;
16. (d) R. Sarma and D. Prajaparti, Synlett, 2008, 19, 3001;
17. (e) B. Gabriele, R. Mancuso, G. Salerno, G. Ruffolo, and P. Plastina, J. Org. Chem., 2007, 72, 6873;
18. (f) X. Y. Liu, P. Ding, J. S. Huang, and C. M. Che, Org. Lett., 2007, 9, 2645;
19. (g) C. S. Cho and J. U. Kim, Tetrahedron Lett., 2007, 48, 3775;
20. (h) R. P. Korivi and C. H. Cheng, J. Org. Chem., 2006, 71, 7079.
21. (a) X. Zhang, B. Q. Liu, X. Shu, Y. Gao, H. P. Lv, and J. Zhu, J. Org. Chem., 2012, 77, 501;
22. (b) J. Tang, L. M. Wang, D. Mao, W. B. Wang, L. Zhang, S. Y. Wu, and Y. S. Xie, Tetrahedron, 2011, 67, 8465;
23. (c) X. J. Li, Z. J. Mao, Y. G. Wang, W. X. Chen, and X. F. Lin, Tetrahedron, 2011, 67, 3858;
24. (d) A. Kumar and V. K. Rao, Synlett, 2011, 2157;
25. (e) A. Kulkarni and B. Torok, Green. Chem., 2010, 12, 875;
26. (f) K. Cao, F. M. Zhang, Y. Q. Tu, X. T. Zhuo, and C. A. Fan, Chem. Eur. J., 2009, 15, 6332;
27. (g) S. K. Guchhait, K. Jadeja, and C. Madaan, Tetrahedron Lett., 2009, 50, 6861;
28. (h) H. Huang, H. L. Jiang, K. X. Chen, and H. Liu, J. Org. Chem., 2009, 74, 5476;
29. (i) S. Kikuchi, M. Iwai, and S.-i. Fukuzawa, Synlett, 2007, 2639.
30. (a) M. Zhang, T. Roisnel, and P. H. Dixneuf, Adv. Synth. Catal., 2010, 352, 1896;
31. (b) M. Zhang, B. Xiong, T. Wang, Y. Q. Ding, and L. Wang, Heterocycles, 2011, 83, 2289;
32. (c) M. Zhang, B. Xiong, W. Yang, D. N. T. Kumar, and Y. Q. Ding, Monatsh. Chem., 2012, 143, 471.
33. W. Yang, H. Fu, Q. J. Song, M. Zhang, and Y. Q. Ding, Organometallics, 2011, 30, 77.
34. M. Zhang, B. Xiong, W. Yang, L. Chen, F. Wu, Q. Wang, and Y. Q. Ding, Synth. Commun., 2011, DOI:10.1080/00397911.2011.569866.
35. (a) S. Enthaler, K. Junge, and M. Beller, Angew. Chem. Int. Ed., 2008, 47, 3317;
36. (b) A. Correa, G. O. Mancheno, and C. Bolm, Chem. Soc. Rev., 2008, 37, 1108.
37. (a) H. Adibi, H. A. Samimi, and M. Beygzadeh, Catal. Commun., 2007, 8, 2119;
38. (b) N. Iranpoor and H. Adibi, Bull. Chem. Soc. Jpn., 2000, 73, 675.