Basic ionic liquid as catalyst for the rapid and green synthesis of substituted 2-amino-2-chromenes in aqueous media

Catalysis Communications

Volumn 9, Issue 5, 2008, Pages 650-653

  Gong, Kai ^a   Wang, Hua Lan ^a   Fang, Dong ^a   Liu, Zu Liang ^a  

^a NANJING UNIVERSITY OF SCIENCE AND TECHNOLOGY   (China)

Author keywords

2 Amino 2 chromenes; Aqueous media; Catalyze; Functional ionic liquid

Indexed keywords

ALDEHYDES; CONDENSATION REACTIONS; SYNTHESIS (CHEMICAL);

AQUEOUS REACTION MEDIA;

IONIC LIQUIDS;

EID: 38849106907     PISSN: 15667367     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.catcom.2007.07.010     Document Type: Article

References (29)

1. Welton T. Chem. Rev. 99 (1999) 2071
2. Wasserscheid P., and Keim W. Angew. Chem. Int. Ed. 39 (2000) 377
3. Earle M.J., Mccormac P.B., and Seddon K.R. Chem. Commun. (1998) 2245
4. Yang S.D., Wu L.Y., and Liang Y.M. J. Mol. Catal. A: Chem. 268 (2007) 107
5. Li C. J. Chem. Rev. 105 (2005) 3095
6. Grieco P.A. Organic Synthesis in Water (1998), Blackie, London
7. Wei W., Li C.J., and Varma R.S. Clean Tech. Environ. Policy 7 (2005) 62
8. Narayan S., Muldoon J., and Finn M.G. Angew. Chem. Int. Ed. 44 (2005) 3275
9. Hafez E.A.A., and Elnagdi M.H. Heterocycles 26 (1987) 903
10. Kidwai M., and Saxena S. Bioorg. Med. Chem. Lett. 15 (2005) 4295
11. Shestopalov A.M., Niazimbetova Z.I., and Evans D.H. Heterocycles 51 (1999) 1101
12. Bloxham J., Dell C.P., and Smith C.W. Heterocycles 38 (1994) 399
13. Zhuang Q.Y., Shi D.Q., and Tu S.J. Chin. J. Appl. Chem. 19 (2002) 1018
14. Zhuang Q.Y., Rong L.C., and Shi D.Q. Chin. J. Org. Chem. 23 (2003) 671
15. Ballini R., Bosica G., and Conforti M.L. Tetrahedron 57 (2001) 1395
16. Ballini R., Bigi F., and Conforti M.L. Catal. Today 60 (2000) 305
17. Wang X., Shi D., and Tu S. Synth. Commun. 34 (2004) 509
18. Kumar B.S., Srinivasulu N., and Udupi R.H. Russ. J. Org. Chem. 42 (2006) 1813
19. Shestopalov A.M., Emelianova Y.M., and Nesterov V.N. Russ.Chem. Bull. Int. Ed. 51 (2002) 2239
20. Maggi R., Ballini R., and Sartori G. Tetrahedron Lett. 45 (2004) 2297
21. Kumar D., Reddy V.B., and Mishra B.G. Tetrahedron 63 (2007) 3093
22. Zhang A., Zhang M., and Chen H. Synth. Commun. 37 (2007) 231
23. Fang D., Gong K., and Liu Z. Catal. Commun. 8 (2007) 1463
24. Fang D., Zhou X., and Liu Z. Ind. Eng. Chem. Res. 45 (2006) 7982
25. Ranu B.C., and Banerjee S. Org. Lett. 7 (2005) 3049
26. Xu J.M., Liu B.K., and Lin X.F. J. Org. Chem. 71 (2006) 3991
27. Fang D., Gong K., and Liu Z.L. Chin. Reagent. 29 (2007) 4
28. Shi D.Q., Zhang Z., and Tu S.J. Chin. J. Org. Chem. 23 (2003) 809
29. Hangarge R.V., Jarikote D.V., and Shigare M.S. Green Chem. 4 (2002) 266