A practical and efficient synthesis of quinoxaline derivatives catalyzed by task-specific ionic liquid

Catalysis Communications

Volumn 9, Issue 2, 2008, Pages 317-320

  Dong, Fang ^a,b   Kai, Gong ^b   Zhenghao, Fei ^a   Xinli, Zhou ^b   Zuliang, Liu ^b  

^a Jiangsu Provincial Key Laboratory of Coastal Wetland Bioresources and Environmental Protection   (China)

^b NANJING UNIVERSITY OF SCIENCE AND TECHNOLOGY   (China)

Author keywords

Ionic liquid; Quinoxaline derivatives; Synthesis

Indexed keywords

CATALYST ACTIVITY; DERIVATIVES; FILTRATION; IONIC LIQUIDS; ORGANIC SOLVENTS; SYNTHESIS (CHEMICAL);

QUINOXALINE DERIVATIVES; TASK-SPECIFIC IONIC LIQUIDS;

NITROGEN COMPOUNDS;

EID: 36248989701     PISSN: 15667367     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.catcom.2007.07.003     Document Type: Article

References (42)

1. Shivaji V.M., Sastry M.N.V., Wang C.C., and Ching-Fa Y. Tetrahedron Lett. 46 (2005) 6345
2. Hui X., Desrivot J., Bories C., Loiseau P.M., Franck X., Hocquemiller R., and Figadere B. Bioorg. Med. Chem. Lett. 16 (2006) 815
3. Sato N. In: Katritzky A.R., Rees C.W., and Scriven E.F.V. (Eds). Comprihensive Heterocyclic Chemistry II vol. 6 (1996), Pergamon, Oxford 233
4. Sakata G., Makino K., and Kurasama Y. Heterocycles 27 (1988) 2481
5. Cheeseman G.W.H., and Werstiuk E.S.G. Adv. Heterocycl. Chem. 22 (1978) 367
6. Seitz L.E., Suling W.J., and Reynolds R.C. J. Med. Chem. 45 (2002) 5604
7. Gazit A., App H., McMahon G., Chen A., Levitzki A., and Bohmer F.D. J. Med. Chem. 39 (1996) 2170
8. Monge A., Palop J.A., Del Castillo J.C., Caldero J.M., Roca J., Romero G., Del Rio J., and Lasheras B. J. Med. Chem. 36 (1993) 2745
9. Toshima K., Takano R., Ozawa T., and Matsumara S. Chem. Commun. (2002) 212
10. Lee J., Murray W.V., and Rivero R.A. J. Org. Chem. 62 (1997) 3874
11. Holland R.J., Hardcastle I.R., and Jarman M. Tetrahedron Lett. 43 (2002) 6435
12. Krehnak V., Smith J., and Vagner J. Tetrahedron Lett. 41 (2000) 2835
13. Uxey T., Tempest P., and Hulme C. Tetrahedron Lett. 43 (2002) 1637
14. Zaragoza F., and Stephensen H. J. Org. Chem. 64 (1999) 2555
15. Dailey S., Feast J.W., Peace R.J., Sage I.C., Till S., and Wood E.L. J. Mater. Chem. 11 (2001) 2238
16. Mizuno T., Wei W.H., Eller L.R., and Sessler J.L. J. Am. Chem. Soc. 124 (2002) 1134
17. Elwahy A.H.M. Tetrahedron 56 (2000) 897
18. Crossley J.C., and Johnston L.A. Chem. Commun. (2002) 1122
19. Brown D.J. Quinoxalines: supplement II. In: Taylor E.C., and Wipf P. (Eds). The Chemistry of Heterocyclic Compounds (2004), John Wiley & Sons, New Jersey
20. Antoniotti S., and Donach E. Tetrahedron Lett. 43 (2002) 3971
21. Robinson R.S., and Taylor R.J.K. Synlett (2005) 1003
22. Raw S.A., Wilfred C.D., and Taylor R.J.K. Org. Biomol. Chem. 2 (2004) 788
23. Raw S.A., Wilfred C.D., and Taylor R.J.K. Chem. Commun. (2003) 2286
24. Venkatesh C., Singh B., Mahata P.K., Ha H., and Junjappa H. Org. Lett. 7 (2005) 2169
25. Wu Z., and Ede N.J. Tetrahedron Lett. 42 (2001) 8115
26. Xekoukoulotakis N.P., Hadjiantonious M.C.P., and Maroulis A.J. Tetrahedron Lett. 41 (2000) 10299
27. Zhao Z., Wisnoski D.D., Wolkenberg S.E., Leister W.H., Wang Y., and Lindsley C.W. Tetrahedron Lett. 45 (2004) 4873
28. Bhosale R.S., Sarda S.R., Ardhapure S.S., Jadhav W.N., Bhusare S.R., and Pawar R.P. Tetrahedron Lett. 46 (2005) 7183
29. More S.N., Sastry M.N.V., Wang C.C., and Yao C.F. Tetrahedron Lett. 46 (2005) 6345
30. Heravi M.M., Taheri S., Bakhtiari K., and Oskooie H.A. Catal. Commun. 8 (2007) 211
31. Heravi M.M., Tehrani M.H., Bakhtiari K., and Oskooie H.A. Catal. Commun. 8 (2007) 1341
32. Wasserscheid P., and Hal R. Green Chem. 4 (2002) 400
33. Fraga-Dubreuil J., Bourahla K., Rahmouni M., Bazureau J.P., and Hamelin J. J. Catal. Commun. 3 (2002) 185
34. Garcia M.T., Gathergood N., and Scammells P.J. Green Chem. 7 (2005) 9
35. Cole A.C., Jensen J.L., Ntai I., Tran T., Weaver K.J., Forbes D.C., and Davis Jr. J.H. J. Am. Chem. Soc. 124 (2002) 5962
36. Wu H., Yang F., Cui P., Tang J., and He M. Tetrahedron Lett. 45 (2004) 4963
37. Xing H., Wang T., Zhou Z., and Dai Y. Ind. Eng. Chem. Res. 44 (2005) 4147
38. Atef A., and Jean P.B. Org. Process Res. Dev. 5 (2005) 743
39. Zhang F., Qian D., Luo S., Liu B., Du X., and Xu Z. J. Chem. Res. 11 (2004) 773
40. Fang D., Gong K., Shi Q.R., and Liu Z.L. Catal. Commun. 8 (2007) 1463
41. Fang D., Chen K.Q., Lu Z.E., and Sun D.Q. Chin. J. Appl. Chem. 12 (1995) 109
42. D. Fang, J. Luo, X.L. Zhou, Z.L. Liu, Catal. Lett. DOI: 10.1007/s10562-007-9095-8.