Amino-functionalized ionic liquid as catalytically active solvent for microwave-assisted synthesis of 4H-pyrans

Catalysis Communications

Volumn 8, Issue 2, 2007, Pages 111-114

  Peng, Yanqing ^a   Song, Gonghua ^a  

^a EAST CHINA UNIVERSITY OF SCIENCE AND TECHNOLOGY   (China)

Author keywords

4H pyrans; Functional ionic liquid; Green chemistry; Microwave; Water

Indexed keywords

DERIVATIVES; ION SOURCES; NITROGEN COMPOUNDS; ORGANIC SOLVENTS; REACTION KINETICS; SYNTHESIS (CHEMICAL); WATER;

FUNCTIONAL IONIC LIQUIDS; GREEN CHEMISTRY; MICROWAVE IRRADIATION;

CATALYSTS;

EID: 33845955177     PISSN: 15667367     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.catcom.2006.05.031     Document Type: Article

References (35)

1. Poliakoff M., Fitzpatrick J.M., Farren T.R., and Anastas P.T. Science 297 (2002) 807
2. Li C.-J. Chem. Rev. 93 (1993) 2023
3. Lindström U.M. Chem. Rev. 102 (2002) 2751
4. Seddon K.R. J. Chem. Technol. Biotechnol. 68 (1997) 351
5. Welton T. Chem. Rev. 99 (1999) 2071
6. Davis Jr. J.H., and Fox P.A. Chem. Commun. (2003) 1209
7. Davis Jr. J.H. Chem. Lett. 33 (2004) 1072
8. Davis Jr. J.H., and Forrester K.J. Tetrahedron Lett. 40 (1999) 1621
9. Lee S., Zhang Y.J., Piao J.Y., Yoon H., Song C.E., Choi J.H., and Hong J. Chem. Commun. (2003) 2624
10. Geldbach T.J., and Dyson P.J. J. Am. Chem. Soc. 126 (2004) 8114
11. Cole A.C., Jensen J.L., Ntai I., Tran K.L.T., Weaver K.J., Forbes D.C., and Davis Jr. J.H. J. Am. Chem. Soc. 124 (2002) 5962
12. Qiao K., and Yokoyama C. Chem. Lett. 33 (2004) 472
13. Qiao K., and Yokoyama C. Chem. Lett. 33 (2004) 808
14. Li D., Shi F., Peng J., Guo S., and Deng Y. J. Org. Chem. 69 (2004) 3582
15. Li D., Shi F., Guo S., and Deng Y. Tetrahedron Lett. 45 (2004) 265
16. Xie H., Zhang S., and Duan H. Tetrahedron Lett. 45 (2004) 2013
17. Jiang T., Gao H., Han B., Zhao G., Chang Y., Wu W., Gao L., and Yang G. Tetrahedron Lett. 45 (2004) 2699
18. Mi X., Luo S., and Cheng J. J. Org. Chem. 70 (2005) 2338
19. Li J., Peng Y., and Song G. Catal. Lett. 102 (2005) 159
20. Peng Y., Cai Y., Song G., and Chen J. Synlett (2005) 2147
21. Kappe C.O. Angew. Chem. Int. Edit. 43 (2004) 6250
22. Mayo K.G., Nearhoof E.H., and Kiddle J.J. Org. Lett. 4 (2002) 1567
23. Vallin K.S.A., Emilsson P., Larhed M., and Hallberg A. J. Org. Chem. 67 (2002) 6243
24. Lee S.-G., Lee J.K., Song C.E., and Kim D.-C. Bull. Korean Chem. Soc. 23 (2002) 667
25. Berthold H., Schotten T., and Hönig H. Synthesis (2002) 1607
26. Lee J.K., Kim D.-C., Song C.E., and Lee S. Synth. Commun. 33 (2003) 2301
27. Arfan A., and Bazureau J.P. Org. Proc. Res. Devel. 9 (2005) 743
28. Peng Y., and Song G. Tetrahedron Lett. 45 (2004) 5313
29. Zamocka J., Misikova E., and Durinda J. Pharmazie 46 (1991) 610
30. Wang J.L., Liu D., Zhang Z.J., Shan S., Han X., Srinivasula S.M., Croce C.M., Alnemri E.S., and Huang Z. Proc. Natl. Acad. Sci. USA 97 (2000) 7124
31. Martin N., Pascual C., Seoane C., and Soto J.L. Heterocycles 26 (1987) 2811
32. Quintela J.M., Peinador C., and Moreira M.J. Tetrahedron 51 (1995) 5901
33. Peng Y., Song G., and Huang F. Monatsh. Chem. 136 (2005) 727
34. Elnagdi M.H., Adbel-Motaleb R.M., and Mustafa M. J. Heterocyclic Chem. 24 (1987) 1677
35. Soto J.L., Seoane C., Martin N., and Quinteiro M. Heterocycles 22 (1984) 1