Silica sulfuric acid: A versatile and reusable heterogeneous catalyst for the synthesis of oxazolines and imidazolines under various reaction conditions

Catalysis Communications

Volumn 9, Issue 5, 2008, Pages 894-901

  Mohammadpoor Baltork, Iraj ^a   Mirkhani, Valiollah ^a   Moghadam, Majid ^a,b   Tangestaninejad, Shahram ^a   Zolfigol, Mohammad Ali ^c   Abdollahi Alibeik, Mohammad ^d   Khosropour, Ahmad Reza ^a   Kargar, Hadi ^a   Hojati, Seyedeh Fatemeh ^a  

^a UNIVERSITY OF ISFAHAN   (Iran)

^b YASOUJ UNIVERSITY   (Iran)

^c BU ALI SINA UNIVERSITY   (Iran)

^d YAZD UNIVERSITY   (Iran)

Author keywords

Imidazoline; Nitrile; Oxazoline; Silica sulfuric acid; Ultrasonic irradiation

Indexed keywords

ALCOHOLS; AMINES; REACTION KINETICS; SILICA; SYNTHESIS (CHEMICAL); ULTRASONICS;

IMIDAZOLINES; NITRILES; OXAZOLINES; SILICA SULFURIC ACIDS; ULTRASONIC IRRADIATION;

SULFURIC ACID;

EID: 38849162883     PISSN: 15667367     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.catcom.2007.09.017     Document Type: Article

References (35)

1. Tamagaki S., Card R.J., and Neckers D.C. J. Am. Chem. Soc. 100 (1978) 6635
2. Zolfigol M.A. Tetrahedron 57 (2001) 9509
3. Maga J.A. CRC Crit. Rev. Food Sci. Nutr. 14 (1981) 295
4. Gant T.G., and Meyers A.I. Tetrahedron 50 (1994) 2297
5. Desimoni G., Faita G., and Jorgensen K.A. Chem. Rev. 106 (2006) 3561
6. Xi X., Jiang L., Sun W., and Shen Z. Eur. Polym. J. 41 (2005) 2592
7. Cwik A., Hell Z., Hegedüs A., Finta Z., and Horvath Z. Tetrahedron Lett. 43 (2002) 3985
8. Zhou P., Blubaum J.E., Burns C.T., and Natale N.R. Tetrahedron Lett. 38 (1997) 7019
9. Clarke D.S., and Wood R. Synth. Commun. 26 (1996) 1335
10. Mohammadpoor-Baltork I., Khosropour A.R., and Hojati S.F. Synlett (2005) 2747
11. Badiang J.G., and Aube J. J. Org. Chem. 61 (1996) 2484
12. Corey E.J., and Ishihara K. Tetrahedron Lett. 33 (1992) 6807
13. Minakata S., Nishimura M., Takahashi T., Oderaotoshi Y., and Komatsu M. Tetrahedron Lett. 42 (2001) 9019
14. Vorbrüggen H., and Krolikiewicz K. Tetrahedron Lett. 22 (1981) 4471
15. Neef G., Eder U., and Sauer G. J. Org. Chem. 46 (1981) 2824
16. Levesque G., Gressier J.-C., and Proust M. Synthesis (1981) 963
17. Hill A.J., and Johnston J.V. J. Am. Chem. Soc. 76 (1954) 922
18. Salgado-Zamora H., Campos E., Jimenez R., and Cervantes H. Heterocycles 47 (1998) 1043
19. Boland N.A., Casey M., Hynes S.J., Matthews J.W., and Smyth M.P. J. Org. Chem. 67 (2002) 3919
20. Shin G.I., Lee J.I., and Kim J.-H. Bull. Korean Chem. Soc. 17 (1996) 29
21. Mohammadpoor-Baltork I., Khosropour A.R., and Hojati S.F. Catal. Commun. 8 (2007) 200
22. Mirkhani V., Moghadam M., Tangestaninejad S., and Kargar H. Tetrahedron Lett. 47 (2006) 2129
23. In: Mason T.J., Luche J.-L., Eldick I.: R.V., and Hubbard C.D. (Eds). Chemistry Under Extreme or Non-Classical Conditions (1997), Wiley, New York 317
24. Bower J.F., Martin C.J., Rawson D.J., Slawin A.M.Z., and Williams J.M.J. J. Chem. Soc. Perkin Trans. 1 (1995) 333
25. Ma J.-A., and Cahard D. Tetrahedron: Asymmetry 15 (2004) 1007
26. Oxely P., and Short W.F. J. Chem. Soc. (1947) 497
27. Witte H., and Seeliger W. Liebigs Ann. Chem. (1974) 996
28. Poindexter G.S. J. Heterocycl. Chem. 20 (1983) 1431
29. Pridgen L.N. J. Org. Chem. 47 (1982) 4319
30. Pirrung M.C., and Tumey L.N. J. Comb. Chem. 2 (2000) 675
31. George B., and Papadopoulos E.P. J. Org. Chem. 42 (1977) 441
32. Kumagai T., Kawamura Y., and Mukai T. Tetrahedron Lett. 24 (1983) 2279
33. Bandgar B.P., and Pandit S.S. Tetrahedron Lett. 44 (2003) 2331
34. Schöning A., Debaerdemaeker T., Zander M., and Friedrichsen W. Chem. Ber. 122 (1989) 1119
35. Chen L. J. Mater. Sci. Lett. 22 (2003) 953