A green method for the synthesis of thiochromene derivatives in ionic liquids

Journal of Heterocyclic Chemistry

Volumn 48, Issue 5, 2011, Pages 1056-1060

  Wang, Xiang Shan ^a   Wu, Jian Rong ^a   Zhou, Jie ^a   Zhang, Mei Mei ^a  

^a JIANGSU NORMAL UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

6H BENZO[C]THIOCHROMENE 8,10 DICARBONITRILE DERIVATIVE; 6H BENZO[C]THIOCHROMENE 8,8,10(7H) TRICARBONITRILE DERIVATIVE; ALDEHYDE; ANION; CHROMENE DERIVATIVE; IONIC LIQUID; MALONONITRILE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL REACTION; PH; ROOM TEMPERATURE; SYNTHESIS;

EID: 80053216881     PISSN: 0022152X     EISSN: 19435193     Source Type: Journal    
DOI: 10.1002/jhet.688     Document Type: Article

References (26)

1. (a), Erkkila, A.; Majander, I.; Pihko, P. M., Chem Rev 2007, 107, 5416
2. (b), Beak, P.; Anderson, D. R.; Curtis, M. D.; Laumer, J. M.; Pippel, D. J.; Weisenburger, G. A., Acc Chem Res 2000, 33, 715.
3. (a), Liéby-Muller, F.; Constantieux, T.; Jean Rodriguez, J., J Am Chem Soc 2005, 127, 17176
4. (b), Chebanov, V. A.; Saraev, V. E.; Desenko, S. M.; Chernenko, V. N.; Knyazeva, I. V.; Groth, U.; Glasnov, T. N.; Kappe, C. O., J Org Chem 2008, 73, 5110
5. (c), Sunderhaus, J. D.; Dockendorff, C.; Martin, S. F., Org Lett 2007, 9, 4223.
6. (a), Wang, Z.; Zhou, L.; El-Boubbou, K.; Ye, X.-S.; Huang, X., J Org Chem 2007, 72, 6409
7. (b), Heravi, M. M.; Baghernejad, B.; Oskooie, H. A.; Hekmatshoar, R., Tetrahedron Lett 2008, 49, 6101
8. (c), Willy, B.; Müller, T. J. J., Eur J Org Chem 2008, 4157
9. (d), Umkehrer, M.; Kolb, J.; Burdack, C.; Hiller, W., Synlett 2005, 79.
10. (a), Welton, T., Chem Rev 1999, 99, 2071
11. (b), Dupont, J.; de Souza, R. F.; Suarez, P. A. Z., Chem Rev 2002, 102, 3667
12. (c), Martins, M. A. P.; Frizzo, C. P.; Moreira, D. N.; Zanatta, N.; Bonacorso, H. G., Chem Rev 2008, 108, 2015.
13. (a), Campbell, J. L. E.; Johnson, K. E., J Am Chem Soc 1995, 117, 7791
14. (b), Gu, Y. L.; Peng, J. J.; Qiao, K.; Yang, H. Z.; Shi, F.; Deng, Y. Q., Prog Chem 2003, 15, 222.
15. (a), Fang, D.; Luo, J.; Zhou, X. L.; Liu, Z. L., Catal Lett 2007, 116, 76
16. (b), Yavari, I.; Kowsari, E., Synlett 2008, 897
17. (c), Hajipour, A. R.; Ghayeb, Y.; Sheikhan, N.; Ruoho, A. E., Tetrahedron Lett 2009, 50, 5649
18. (d), Huang, B. H.; Li, Z. J.; Shi, N.; Xu, X. L.; Zhang, K.; Fang, Y. X., Youji Huaxue 2009, 29, 770
19. (e), Shi, D. Q.; Ni, S. N.; Yang, F.; Ji, S. J., J Heterocycl Chem 2008, 45, 1275
20. (f), Valizadeh, H.; Shockravi, A.; Gholipur, H., J Heterocycl Chem 2007, 44, 867.
21. (a), Wang, X. S.; Zhang, M. M.; Jiang, H.; Shi, D. Q.; Tu, S. J.; Wei, X. Y.; Zong, Z. M., Synthesis 2006, 4187
22. (b), Wang, X. S.; Zhang, M. M.; Jiang, H.; Yao, C. S.; Tu, S. J., Tetrahedron 2007, 63, 4439
23. (c), Wang, X. S.; Wu, J. R.; Li, Q.; Yao, C. S.; Tu, S. J., Synlett 2008, 1185
24. (d), Wang, X. S.; Zhang, M. M.; Shi, D. Q.; Tu, S. J.; Wei, X. Y.; Zong, Z. M., J Heterocycl Chem 2008, 45, 71
25. (e), Wang, X. S.; Wu, J. R.; Li, Q.; Zhang, M. M., J Heterocycl Chem 2009, 46, 1355.
26. Wang, X. S.; Zhang, M. M.; Li, Q.; Yao, C. S.; Tu, S. J., Tetrahedron 2007, 63, 5265.